MutationTaster - study a chromosomal position

NEVER press reload or F5 - unless you want to start from the very beginning.
input seems to be ok - now mapping the variant to the different transcripts...
found 5 transcript(s)...
Querying Taster for transcript #1: ENST00000371929
Querying Taster for transcript #2: ENST00000355699
Querying Taster for transcript #3: ENST00000356589
Querying Taster for transcript #4: ENST00000371916
Querying Taster for transcript #5: ENST00000536611
MT speed 0 s - this script 6.316778 s

Results

genesymbol	prediction	probability	model	prediction problem	splicing	ClinVar	amino acid changes	variant type	dbSNP ID	protein length	file
ADAMTS13	disease_causing_automatic	0.999987931507749	simple_aae		affected	0	R70H	single base exchange	rs121908471		show file
ADAMTS13	disease_causing_automatic	0.999995921404691	simple_aae		affected	0	R398H	single base exchange	rs121908471		show file
ADAMTS13	disease_causing_automatic	0.999995921404691	simple_aae		affected	0	R398H	single base exchange	rs121908471		show file
ADAMTS13	disease_causing_automatic	0.999999308387091	simple_aae		affected	0	R367H	single base exchange	rs121908471		show file
ADAMTS13	disease_causing_automatic	1	without_aae		affected	0		single base exchange	rs121908471		show file

Taster files

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999987931507749 (classification due to ClinVar, real probability is shown anyway) (explain)

Summary

amino acid sequence changed
known disease mutation at this position (HGMD CM012889)
known disease mutation: rs5802 (pathogenic)
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr9:136298598G>AN/A show variant in all transcripts IGV

HGNC symbol

ADAMTS13

Ensembl transcript ID

ENST00000536611

Genbank transcript ID

N/A

UniProt peptide

Q76LX8

alteration type

single base exchange

alteration region

CDS

DNA changes

c.209G>A
cDNA.829G>A
g.19121G>A

AA changes

R70H Score: 29 explain score(s)

position(s) of altered AA
if AA alteration in CDS

frameshift

known variant

Reference ID: rs121908471
Allele 'A' was neither found in ExAC nor 1000G.
known disease mutation: rs5802 (pathogenic for Upshaw-Schulman syndrome) dbSNP NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM012889)

known disease mutation at this position, please check HGMD for details (HGMD ID CM012889)
known disease mutation at this position, please check HGMD for details (HGMD ID CM012889)

regulatory features

H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
CTCF, Transcription Factor, CCCTC-binding factor
DNase1, Open Chromatin, DNase1 Hypersensitive Site

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	5.213	1
	5.213	1
(flanking)	0.373	1

explain score(s) and/or inspect your position(s) in in UCSC Genome Browser

splice sites

effect	gDNA position	score	wt detection sequence	exon-intron border
Acc increased	19127	wt: 0.33 / mu: 0.44	wt: AAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCACCA mu: AAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCACCA	cctg\|CGGA
Acc marginally increased	19124	wt: 0.8311 / mu: 0.8822 (marginal change - not scored)	wt: CCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCA mu: CCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCA	gctc\|CTGC
Acc marginally increased	19125	wt: 0.8573 / mu: 0.8611 (marginal change - not scored)	wt: CGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCAC mu: CGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCAC	ctcc\|TGCG
Acc marginally increased	19121	wt: 0.3744 / mu: 0.3895 (marginal change - not scored)	wt: TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG mu: TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG	cccg\|CTCC

distance from splice site

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

mutated

not conserved

Ptroglodytes

all identical

ENSPTRG00000022942

356

Mmulatta

all identical

ENSMMUG00000000937

394

Fcatus

no homologue

Mmusculus

all identical

ENSMUSG00000014852

403

Ggallus

no homologue

Trubripes

no homologue

Drerio

all identical

ENSDARG00000076270

397

Dmelanogaster

not conserved

FBgn0086408

667

CLYGQSR

Celegans

no homologue

Xtropicalis

no homologue

protein features

start (aa)	end (aa)	feature	details
30	74	PROPEP	/FTId=PRO_0000247510.	lost
71	71	MUTAGEN	R->K: Abolishes pro-domain removal but no loss of proteolytic activity; when associated with D-73.	might get lost (downstream of altered splice site)
73	73	MUTAGEN	R->D: Abolishes pro-domain removal but no loss of proteolytic activity; when associated with K-71.	might get lost (downstream of altered splice site)
80	286	DOMAIN	Peptidase M12B.	might get lost (downstream of altered splice site)
83	83	METAL	Calcium (Potential).	might get lost (downstream of altered splice site)
101	101	CONFLICT	E -> R (in Ref. 1; AA sequence).	might get lost (downstream of altered splice site)
142	142	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
146	146	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
173	173	METAL	Calcium (Potential).	might get lost (downstream of altered splice site)
202	202	DISULFID	By similarity.	might get lost (downstream of altered splice site)
224	224	METAL	Zinc; catalytic (By similarity).	might get lost (downstream of altered splice site)
225	225	ACT_SITE	By similarity.	might get lost (downstream of altered splice site)
228	228	METAL	Zinc; catalytic (By similarity).	might get lost (downstream of altered splice site)
234	234	METAL	Zinc; catalytic (By similarity).	might get lost (downstream of altered splice site)
242	242	DISULFID	By similarity.	might get lost (downstream of altered splice site)
265	265	DISULFID	By similarity.	might get lost (downstream of altered splice site)
281	281	DISULFID	By similarity.	might get lost (downstream of altered splice site)
281	281	METAL	Calcium (Potential).	might get lost (downstream of altered splice site)
284	284	METAL	Calcium (Potential).	might get lost (downstream of altered splice site)
287	383	DOMAIN	Disintegrin.	might get lost (downstream of altered splice site)
300	374	REGION	Cysteine-rich.	might get lost (downstream of altered splice site)
301	303	HELIX		might get lost (downstream of altered splice site)
307	314	HELIX		might get lost (downstream of altered splice site)
331	334	HELIX		might get lost (downstream of altered splice site)
337	340	STRAND		might get lost (downstream of altered splice site)
359	361	STRAND		might get lost (downstream of altered splice site)
364	367	STRAND		might get lost (downstream of altered splice site)
370	373	STRAND		might get lost (downstream of altered splice site)
374	377	HELIX		might get lost (downstream of altered splice site)
384	439	DOMAIN	TSP type-1 1.	might get lost (downstream of altered splice site)
396	396	DISULFID	By similarity.	might get lost (downstream of altered splice site)
399	401	STRAND		might get lost (downstream of altered splice site)
400	400	DISULFID	By similarity.	might get lost (downstream of altered splice site)
403	406	STRAND		might get lost (downstream of altered splice site)
411	411	DISULFID	By similarity.	might get lost (downstream of altered splice site)
417	419	STRAND		might get lost (downstream of altered splice site)
423	423	DISULFID	By similarity.	might get lost (downstream of altered splice site)
430	433	STRAND		might get lost (downstream of altered splice site)
433	433	DISULFID	By similarity.	might get lost (downstream of altered splice site)
438	438	DISULFID	By similarity.	might get lost (downstream of altered splice site)
442	451	HELIX		might get lost (downstream of altered splice site)
452	455	TURN		might get lost (downstream of altered splice site)
470	472	STRAND		might get lost (downstream of altered splice site)
474	476	TURN		might get lost (downstream of altered splice site)
479	483	HELIX		might get lost (downstream of altered splice site)
486	489	STRAND		might get lost (downstream of altered splice site)
495	497	STRAND		might get lost (downstream of altered splice site)
498	500	MOTIF	Cell attachment site (Potential).	might get lost (downstream of altered splice site)
519	523	STRAND		might get lost (downstream of altered splice site)
526	530	STRAND		might get lost (downstream of altered splice site)
534	536	STRAND		might get lost (downstream of altered splice site)
552	552	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
554	562	STRAND		might get lost (downstream of altered splice site)
556	685	REGION	Spacer.	might get lost (downstream of altered splice site)
569	576	STRAND		might get lost (downstream of altered splice site)
579	579	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
581	588	STRAND		might get lost (downstream of altered splice site)
592	599	STRAND		might get lost (downstream of altered splice site)
602	605	STRAND		might get lost (downstream of altered splice site)
608	610	STRAND		might get lost (downstream of altered splice site)
614	614	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
614	618	STRAND		might get lost (downstream of altered splice site)
623	632	STRAND		might get lost (downstream of altered splice site)
634	636	STRAND		might get lost (downstream of altered splice site)
638	647	STRAND		might get lost (downstream of altered splice site)
653	661	STRAND		might get lost (downstream of altered splice site)
663	665	HELIX		might get lost (downstream of altered splice site)
667	667	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
667	669	HELIX		might get lost (downstream of altered splice site)
673	680	STRAND		might get lost (downstream of altered splice site)
682	730	DOMAIN	TSP type-1 2.	might get lost (downstream of altered splice site)
707	707	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
742	805	DOMAIN	TSP type-1 3.	might get lost (downstream of altered splice site)
808	859	DOMAIN	TSP type-1 4.	might get lost (downstream of altered splice site)
828	828	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
896	950	DOMAIN	TSP type-1 5.	might get lost (downstream of altered splice site)
951	1011	DOMAIN	TSP type-1 6.	might get lost (downstream of altered splice site)
1012	1068	DOMAIN	TSP type-1 7.	might get lost (downstream of altered splice site)
1072	1131	DOMAIN	TSP type-1 8.	might get lost (downstream of altered splice site)
1192	1298	DOMAIN	CUB 1.	might get lost (downstream of altered splice site)
1235	1235	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
1299	1427	DOMAIN	CUB 2.	might get lost (downstream of altered splice site)
1354	1354	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

1095 / 1095

position (AA) of stopcodon in wt / mu AA sequence

365 / 365

position of stopcodon in wt / mu cDNA

1715 / 1715

poly(A) signal

N/A

conservation
nucleotide level for all changes - no scoring up to now

N/A

position of start ATG in wt / mu cDNA

621 / 621

chromosome

strand

last intron/exon boundary

2046

theoretical NMD boundary in CDS

1375

length of CDS

1095

coding sequence (CDS) position

209

cDNA position
(for ins/del: last normal base / first normal base)

829

gDNA position
(for ins/del: last normal base / first normal base)

19121

chromosomal position
(for ins/del: last normal base / first normal base)

136298598

original gDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG

altered gDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG

original cDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG

altered cDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG

wildtype AA sequence

MDMCQALSCH TDPLDQSSCS RLLVPLLDGT ECGVEKWCSK GRCRSLVELT PIAAVHGRWS
SWGPRSPCSR SCGGGVVTRR RQCNNPRPAF GGRACVGADL QAEMCNTQAC EKTQLEFMSQ
QCARTDGQPL RSSPGGASFY HWGAAVPHSQ GDALCRHMCR AIGESFIMKR GDSFLDGTRC
MPSGPREDGT LSLCVSGSCR TFGCDGRMDS QQVWDRCQVC GGDNSTCSPR KGSFTAGRAR
EYVTFLTVTP NLTSVYIANH RPLFTHLAVR IGGRYVVAGK MSISPNTTYP SLLEDGRVEY
RVALTEDRLP RLEEIRIWGP LQEDADIQVG GVRAQLMHIS WWSRPGLGER DLCARGRWPG
GSSD*

mutated AA sequence

MDMCQALSCH TDPLDQSSCS RLLVPLLDGT ECGVEKWCSK GRCRSLVELT PIAAVHGRWS
SWGPRSPCSH SCGGGVVTRR RQCNNPRPAF GGRACVGADL QAEMCNTQAC EKTQLEFMSQ
QCARTDGQPL RSSPGGASFY HWGAAVPHSQ GDALCRHMCR AIGESFIMKR GDSFLDGTRC
MPSGPREDGT LSLCVSGSCR TFGCDGRMDS QQVWDRCQVC GGDNSTCSPR KGSFTAGRAR
EYVTFLTVTP NLTSVYIANH RPLFTHLAVR IGGRYVVAGK MSISPNTTYP SLLEDGRVEY
RVALTEDRLP RLEEIRIWGP LQEDADIQVG GVRAQLMHIS WWSRPGLGER DLCARGRWPG
GSSD*

speed

0.86 s

All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999995921404691 (classification due to ClinVar, real probability is shown anyway) (explain)

Summary

amino acid sequence changed
known disease mutation at this position (HGMD CM012889)
known disease mutation: rs5802 (pathogenic)
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr9:136298598G>AN/A show variant in all transcripts IGV

HGNC symbol

ADAMTS13

Ensembl transcript ID

ENST00000371929

Genbank transcript ID

NM_139025

UniProt peptide

Q76LX8

alteration type

single base exchange

alteration region

CDS

DNA changes

c.1193G>A
cDNA.1637G>A
g.19121G>A

AA changes

R398H Score: 29 explain score(s)

position(s) of altered AA
if AA alteration in CDS

398

frameshift

known variant

regulatory features

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	5.213	1
	5.213	1
(flanking)	0.373	1

explain score(s) and/or inspect your position(s) in in UCSC Genome Browser

splice sites

effect	gDNA position	score	wt detection sequence	exon-intron border
Acc increased	19127	wt: 0.33 / mu: 0.44	wt: AAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCACCA mu: AAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCACCA	cctg\|CGGA
Acc marginally increased	19124	wt: 0.8311 / mu: 0.8822 (marginal change - not scored)	wt: CCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCA mu: CCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCA	gctc\|CTGC
Acc marginally increased	19125	wt: 0.8573 / mu: 0.8611 (marginal change - not scored)	wt: CGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCAC mu: CGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCAC	ctcc\|TGCG
Acc marginally increased	19121	wt: 0.3744 / mu: 0.3895 (marginal change - not scored)	wt: TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG mu: TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG	cccg\|CTCC

distance from splice site

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

398

mutated

not conserved

398

Ptroglodytes

all identical

ENSPTRG00000022942

356

Mmulatta

all identical

ENSMMUG00000000937

394

Fcatus

no homologue

Mmusculus

all identical

ENSMUSG00000014852

403

Ggallus

no homologue

Trubripes

no homologue

Drerio

all identical

ENSDARG00000076270

397

Dmelanogaster

not conserved

FBgn0086408

674

CLYGQSRRLLEG

Celegans

no homologue

Xtropicalis

no homologue

protein features

start (aa)	end (aa)	feature	details
384	439	DOMAIN	TSP type-1 1.	lost
399	401	STRAND		might get lost (downstream of altered splice site)
400	400	DISULFID	By similarity.	might get lost (downstream of altered splice site)
403	406	STRAND		might get lost (downstream of altered splice site)
411	411	DISULFID	By similarity.	might get lost (downstream of altered splice site)
417	419	STRAND		might get lost (downstream of altered splice site)
423	423	DISULFID	By similarity.	might get lost (downstream of altered splice site)
430	433	STRAND		might get lost (downstream of altered splice site)
433	433	DISULFID	By similarity.	might get lost (downstream of altered splice site)
438	438	DISULFID	By similarity.	might get lost (downstream of altered splice site)
442	451	HELIX		might get lost (downstream of altered splice site)
452	455	TURN		might get lost (downstream of altered splice site)
470	472	STRAND		might get lost (downstream of altered splice site)
474	476	TURN		might get lost (downstream of altered splice site)
479	483	HELIX		might get lost (downstream of altered splice site)
486	489	STRAND		might get lost (downstream of altered splice site)
495	497	STRAND		might get lost (downstream of altered splice site)
498	500	MOTIF	Cell attachment site (Potential).	might get lost (downstream of altered splice site)
519	523	STRAND		might get lost (downstream of altered splice site)
526	530	STRAND		might get lost (downstream of altered splice site)
534	536	STRAND		might get lost (downstream of altered splice site)
552	552	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
554	562	STRAND		might get lost (downstream of altered splice site)
556	685	REGION	Spacer.	might get lost (downstream of altered splice site)
569	576	STRAND		might get lost (downstream of altered splice site)
579	579	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
581	588	STRAND		might get lost (downstream of altered splice site)
592	599	STRAND		might get lost (downstream of altered splice site)
602	605	STRAND		might get lost (downstream of altered splice site)
608	610	STRAND		might get lost (downstream of altered splice site)
614	614	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
614	618	STRAND		might get lost (downstream of altered splice site)
623	632	STRAND		might get lost (downstream of altered splice site)
634	636	STRAND		might get lost (downstream of altered splice site)
638	647	STRAND		might get lost (downstream of altered splice site)
653	661	STRAND		might get lost (downstream of altered splice site)
663	665	HELIX		might get lost (downstream of altered splice site)
667	667	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
667	669	HELIX		might get lost (downstream of altered splice site)
673	680	STRAND		might get lost (downstream of altered splice site)
682	730	DOMAIN	TSP type-1 2.	might get lost (downstream of altered splice site)
707	707	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
742	805	DOMAIN	TSP type-1 3.	might get lost (downstream of altered splice site)
808	859	DOMAIN	TSP type-1 4.	might get lost (downstream of altered splice site)
828	828	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
896	950	DOMAIN	TSP type-1 5.	might get lost (downstream of altered splice site)
951	1011	DOMAIN	TSP type-1 6.	might get lost (downstream of altered splice site)
1012	1068	DOMAIN	TSP type-1 7.	might get lost (downstream of altered splice site)
1072	1131	DOMAIN	TSP type-1 8.	might get lost (downstream of altered splice site)
1192	1298	DOMAIN	CUB 1.	might get lost (downstream of altered splice site)
1235	1235	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
1299	1427	DOMAIN	CUB 2.	might get lost (downstream of altered splice site)
1354	1354	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

4284 / 4284

position (AA) of stopcodon in wt / mu AA sequence

1428 / 1428

position of stopcodon in wt / mu cDNA

4728 / 4728

poly(A) signal

N/A

conservation
nucleotide level for all changes - no scoring up to now

N/A

position of start ATG in wt / mu cDNA

445 / 445

chromosome

strand

last intron/exon boundary

4522

theoretical NMD boundary in CDS

4027

length of CDS

4284

coding sequence (CDS) position

1193

cDNA position
(for ins/del: last normal base / first normal base)

1637

gDNA position
(for ins/del: last normal base / first normal base)

19121

chromosomal position
(for ins/del: last normal base / first normal base)

136298598

original gDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG

altered gDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG

original cDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG

altered cDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG

wildtype AA sequence

MHQRHPRARC PPLCVAGILA CGFLLGCWGP SHFQQSCLQA LEPQAVSSYL SPGAPLKGRP
PSPGFQRQRQ RQRRAAGGIL HLELLVAVGP DVFQAHQEDT ERYVLTNLNI GAELLRDPSL
GAQFRVHLVK MVILTEPEGA PNITANLTSS LLSVCGWSQT INPEDDTDPG HADLVLYITR
FDLELPDGNR QVRGVTQLGG ACSPTWSCLI TEDTGFDLGV TIAHEIGHSF GLEHDGAPGS
GCGPSGHVMA SDGAAPRAGL AWSPCSRRQL LSLLSAGRAR CVWDPPRPQP GSAGHPPDAQ
PGLYYSANEQ CRVAFGPKAV ACTFAREHLD MCQALSCHTD PLDQSSCSRL LVPLLDGTEC
GVEKWCSKGR CRSLVELTPI AAVHGRWSSW GPRSPCSRSC GGGVVTRRRQ CNNPRPAFGG
RACVGADLQA EMCNTQACEK TQLEFMSQQC ARTDGQPLRS SPGGASFYHW GAAVPHSQGD
ALCRHMCRAI GESFIMKRGD SFLDGTRCMP SGPREDGTLS LCVSGSCRTF GCDGRMDSQQ
VWDRCQVCGG DNSTCSPRKG SFTAGRAREY VTFLTVTPNL TSVYIANHRP LFTHLAVRIG
GRYVVAGKMS ISPNTTYPSL LEDGRVEYRV ALTEDRLPRL EEIRIWGPLQ EDADIQVYRR
YGEEYGNLTR PDITFTYFQP KPRQAWVWAA VRGPCSVSCG AGLRWVNYSC LDQARKELVE
TVQCQGSQQP PAWPEACVLE PCPPYWAVGD FGPCSASCGG GLRERPVRCV EAQGSLLKTL
PPARCRAGAQ QPAVALETCN PQPCPARWEV SEPSSCTSAG GAGLALENET CVPGADGLEA
PVTEGPGSVD EKLPAPEPCV GMSCPPGWGH LDATSAGEKA PSPWGSIRTG AQAAHVWTPA
AGSCSVSCGR GLMELRFLCM DSALRVPVQE ELCGLASKPG SRREVCQAVP CPARWQYKLA
ACSVSCGRGV VRRILYCARA HGEDDGEEIL LDTQCQGLPR PEPQEACSLE PCPPRWKVMS
LGPCSASCGL GTARRSVACV QLDQGQDVEV DEAACAALVR PEASVPCLIA DCTYRWHVGT
WMECSVSCGD GIQRRRDTCL GPQAQAPVPA DFCQHLPKPV TVRGCWAGPC VGQGTPSLVP
HEEAAAPGRT TATPAGASLE WSQARGLLFS PAPQPRRLLP GPQENSVQSS ACGRQHLEPT
GTIDMRGPGQ ADCAVAIGRP LGEVVTLRVL ESSLNCSAGD MLLLWGRLTW RKMCRKLLDM
TFSSKTNTLV VRQRCGRPGG GVLLRYGSQL APETFYRECD MQLFGPWGEI VSPSLSPATS
NAGGCRLFIN VAPHARIAIH ALATNMGAGT EGANASYILI RDTHSLRTTA FHGQQVLYWE
SESSQAEMEF SEGFLKAQAS LRGQYWTLQS WVPEMQDPQS WKGKEGT*

mutated AA sequence

MHQRHPRARC PPLCVAGILA CGFLLGCWGP SHFQQSCLQA LEPQAVSSYL SPGAPLKGRP
PSPGFQRQRQ RQRRAAGGIL HLELLVAVGP DVFQAHQEDT ERYVLTNLNI GAELLRDPSL
GAQFRVHLVK MVILTEPEGA PNITANLTSS LLSVCGWSQT INPEDDTDPG HADLVLYITR
FDLELPDGNR QVRGVTQLGG ACSPTWSCLI TEDTGFDLGV TIAHEIGHSF GLEHDGAPGS
GCGPSGHVMA SDGAAPRAGL AWSPCSRRQL LSLLSAGRAR CVWDPPRPQP GSAGHPPDAQ
PGLYYSANEQ CRVAFGPKAV ACTFAREHLD MCQALSCHTD PLDQSSCSRL LVPLLDGTEC
GVEKWCSKGR CRSLVELTPI AAVHGRWSSW GPRSPCSHSC GGGVVTRRRQ CNNPRPAFGG
RACVGADLQA EMCNTQACEK TQLEFMSQQC ARTDGQPLRS SPGGASFYHW GAAVPHSQGD
ALCRHMCRAI GESFIMKRGD SFLDGTRCMP SGPREDGTLS LCVSGSCRTF GCDGRMDSQQ
VWDRCQVCGG DNSTCSPRKG SFTAGRAREY VTFLTVTPNL TSVYIANHRP LFTHLAVRIG
GRYVVAGKMS ISPNTTYPSL LEDGRVEYRV ALTEDRLPRL EEIRIWGPLQ EDADIQVYRR
YGEEYGNLTR PDITFTYFQP KPRQAWVWAA VRGPCSVSCG AGLRWVNYSC LDQARKELVE
TVQCQGSQQP PAWPEACVLE PCPPYWAVGD FGPCSASCGG GLRERPVRCV EAQGSLLKTL
PPARCRAGAQ QPAVALETCN PQPCPARWEV SEPSSCTSAG GAGLALENET CVPGADGLEA
PVTEGPGSVD EKLPAPEPCV GMSCPPGWGH LDATSAGEKA PSPWGSIRTG AQAAHVWTPA
AGSCSVSCGR GLMELRFLCM DSALRVPVQE ELCGLASKPG SRREVCQAVP CPARWQYKLA
ACSVSCGRGV VRRILYCARA HGEDDGEEIL LDTQCQGLPR PEPQEACSLE PCPPRWKVMS
LGPCSASCGL GTARRSVACV QLDQGQDVEV DEAACAALVR PEASVPCLIA DCTYRWHVGT
WMECSVSCGD GIQRRRDTCL GPQAQAPVPA DFCQHLPKPV TVRGCWAGPC VGQGTPSLVP
HEEAAAPGRT TATPAGASLE WSQARGLLFS PAPQPRRLLP GPQENSVQSS ACGRQHLEPT
GTIDMRGPGQ ADCAVAIGRP LGEVVTLRVL ESSLNCSAGD MLLLWGRLTW RKMCRKLLDM
TFSSKTNTLV VRQRCGRPGG GVLLRYGSQL APETFYRECD MQLFGPWGEI VSPSLSPATS
NAGGCRLFIN VAPHARIAIH ALATNMGAGT EGANASYILI RDTHSLRTTA FHGQQVLYWE
SESSQAEMEF SEGFLKAQAS LRGQYWTLQS WVPEMQDPQS WKGKEGT*

speed

1.49 s

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999995921404691 (classification due to ClinVar, real probability is shown anyway) (explain)

Summary

amino acid sequence changed
known disease mutation at this position (HGMD CM012889)
known disease mutation: rs5802 (pathogenic)
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr9:136298598G>AN/A show variant in all transcripts IGV

HGNC symbol

ADAMTS13

Ensembl transcript ID

ENST00000355699

Genbank transcript ID

NM_139027

UniProt peptide

Q76LX8

alteration type

single base exchange

alteration region

CDS

DNA changes

c.1193G>A
cDNA.1313G>A
g.19121G>A

AA changes

R398H Score: 29 explain score(s)

position(s) of altered AA
if AA alteration in CDS

398

frameshift

known variant

regulatory features

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	5.213	1
	5.213	1
(flanking)	0.373	1

explain score(s) and/or inspect your position(s) in in UCSC Genome Browser

splice sites

effect	gDNA position	score	wt detection sequence	exon-intron border
Acc increased	19127	wt: 0.33 / mu: 0.44	wt: AAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCACCA mu: AAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCACCA	cctg\|CGGA
Acc marginally increased	19124	wt: 0.8311 / mu: 0.8822 (marginal change - not scored)	wt: CCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCA mu: CCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCA	gctc\|CTGC
Acc marginally increased	19125	wt: 0.8573 / mu: 0.8611 (marginal change - not scored)	wt: CGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCAC mu: CGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCAC	ctcc\|TGCG
Acc marginally increased	19121	wt: 0.3744 / mu: 0.3895 (marginal change - not scored)	wt: TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG mu: TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG	cccg\|CTCC

distance from splice site

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

398

mutated

not conserved

398

Ptroglodytes

all identical

ENSPTRG00000022942

356

Mmulatta

all identical

ENSMMUG00000000937

394

Fcatus

no homologue

Mmusculus

all identical

ENSMUSG00000014852

403

Ggallus

no homologue

Trubripes

no homologue

Drerio

all identical

ENSDARG00000076270

397

Dmelanogaster

not conserved

FBgn0086408

674

CLYGQSRRLLEG

Celegans

no homologue

Xtropicalis

no homologue

protein features

start (aa)	end (aa)	feature	details
384	439	DOMAIN	TSP type-1 1.	lost
399	401	STRAND		might get lost (downstream of altered splice site)
400	400	DISULFID	By similarity.	might get lost (downstream of altered splice site)
403	406	STRAND		might get lost (downstream of altered splice site)
411	411	DISULFID	By similarity.	might get lost (downstream of altered splice site)
417	419	STRAND		might get lost (downstream of altered splice site)
423	423	DISULFID	By similarity.	might get lost (downstream of altered splice site)
430	433	STRAND		might get lost (downstream of altered splice site)
433	433	DISULFID	By similarity.	might get lost (downstream of altered splice site)
438	438	DISULFID	By similarity.	might get lost (downstream of altered splice site)
442	451	HELIX		might get lost (downstream of altered splice site)
452	455	TURN		might get lost (downstream of altered splice site)
470	472	STRAND		might get lost (downstream of altered splice site)
474	476	TURN		might get lost (downstream of altered splice site)
479	483	HELIX		might get lost (downstream of altered splice site)
486	489	STRAND		might get lost (downstream of altered splice site)
495	497	STRAND		might get lost (downstream of altered splice site)
498	500	MOTIF	Cell attachment site (Potential).	might get lost (downstream of altered splice site)
519	523	STRAND		might get lost (downstream of altered splice site)
526	530	STRAND		might get lost (downstream of altered splice site)
534	536	STRAND		might get lost (downstream of altered splice site)
552	552	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
554	562	STRAND		might get lost (downstream of altered splice site)
556	685	REGION	Spacer.	might get lost (downstream of altered splice site)
569	576	STRAND		might get lost (downstream of altered splice site)
579	579	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
581	588	STRAND		might get lost (downstream of altered splice site)
592	599	STRAND		might get lost (downstream of altered splice site)
602	605	STRAND		might get lost (downstream of altered splice site)
608	610	STRAND		might get lost (downstream of altered splice site)
614	614	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
614	618	STRAND		might get lost (downstream of altered splice site)
623	632	STRAND		might get lost (downstream of altered splice site)
634	636	STRAND		might get lost (downstream of altered splice site)
638	647	STRAND		might get lost (downstream of altered splice site)
653	661	STRAND		might get lost (downstream of altered splice site)
663	665	HELIX		might get lost (downstream of altered splice site)
667	667	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
667	669	HELIX		might get lost (downstream of altered splice site)
673	680	STRAND		might get lost (downstream of altered splice site)
682	730	DOMAIN	TSP type-1 2.	might get lost (downstream of altered splice site)
707	707	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
742	805	DOMAIN	TSP type-1 3.	might get lost (downstream of altered splice site)
808	859	DOMAIN	TSP type-1 4.	might get lost (downstream of altered splice site)
828	828	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
896	950	DOMAIN	TSP type-1 5.	might get lost (downstream of altered splice site)
951	1011	DOMAIN	TSP type-1 6.	might get lost (downstream of altered splice site)
1012	1068	DOMAIN	TSP type-1 7.	might get lost (downstream of altered splice site)
1072	1131	DOMAIN	TSP type-1 8.	might get lost (downstream of altered splice site)
1192	1298	DOMAIN	CUB 1.	might get lost (downstream of altered splice site)
1235	1235	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
1299	1427	DOMAIN	CUB 2.	might get lost (downstream of altered splice site)
1354	1354	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

4116 / 4116

position (AA) of stopcodon in wt / mu AA sequence

1372 / 1372

position of stopcodon in wt / mu cDNA

4236 / 4236

poly(A) signal

N/A

conservation
nucleotide level for all changes - no scoring up to now

N/A

position of start ATG in wt / mu cDNA

121 / 121

chromosome

strand

last intron/exon boundary

4030

theoretical NMD boundary in CDS

3859

length of CDS

4116

coding sequence (CDS) position

1193

cDNA position
(for ins/del: last normal base / first normal base)

1313

gDNA position
(for ins/del: last normal base / first normal base)

19121

chromosomal position
(for ins/del: last normal base / first normal base)

136298598

original gDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG

altered gDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG

original cDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG

altered cDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG

wildtype AA sequence

MHQRHPRARC PPLCVAGILA CGFLLGCWGP SHFQQSCLQA LEPQAVSSYL SPGAPLKGRP
PSPGFQRQRQ RQRRAAGGIL HLELLVAVGP DVFQAHQEDT ERYVLTNLNI GAELLRDPSL
GAQFRVHLVK MVILTEPEGA PNITANLTSS LLSVCGWSQT INPEDDTDPG HADLVLYITR
FDLELPDGNR QVRGVTQLGG ACSPTWSCLI TEDTGFDLGV TIAHEIGHSF GLEHDGAPGS
GCGPSGHVMA SDGAAPRAGL AWSPCSRRQL LSLLSAGRAR CVWDPPRPQP GSAGHPPDAQ
PGLYYSANEQ CRVAFGPKAV ACTFAREHLD MCQALSCHTD PLDQSSCSRL LVPLLDGTEC
GVEKWCSKGR CRSLVELTPI AAVHGRWSSW GPRSPCSRSC GGGVVTRRRQ CNNPRPAFGG
RACVGADLQA EMCNTQACEK TQLEFMSQQC ARTDGQPLRS SPGGASFYHW GAAVPHSQGD
ALCRHMCRAI GESFIMKRGD SFLDGTRCMP SGPREDGTLS LCVSGSCRTF GCDGRMDSQQ
VWDRCQVCGG DNSTCSPRKG SFTAGRAREY VTFLTVTPNL TSVYIANHRP LFTHLAVRIG
GRYVVAGKMS ISPNTTYPSL LEDGRVEYRV ALTEDRLPRL EEIRIWGPLQ EDADIQVYRR
YGEEYGNLTR PDITFTYFQP KPRQAWVWAA VRGPCSVSCG AGLRWVNYSC LDQARKELVE
TVQCQGSQQP PAWPEACVLE PCPPYWAVGD FGPCSASCGG GLRERPVRCV EAQGSLLKTL
PPARCRAGAQ QPAVALETCN PQPCPARWEV SEPSSCTSAG GAGLALENET CVPGADGLEA
PVTEGPGSVD EKLPAPEPCV GMSCPPGWGH LDATSAGEKA PSPWGSIRTG AQAAHVWTPA
AGSCSVSCGR GLMELRFLCM DSALRVPVQE ELCGLASKPG SRREVCQAVP CPARWQYKLA
ACSVSCGRGV VRRILYCARA HGEDDGEEIL LDTQCQGLPR PEPQEACSLE PCPPRWKVMS
LGPCSASCGL GTARRSVACV QLDQGQDVEV DEAACAALVR PEASVPCLIA DCTYRWHVGT
WMECSVSCGD GIQRRRDTCL GPQAQAPVPA DFCQHLPKPV TVRGCWAGPC VGQGACGRQH
LEPTGTIDMR GPGQADCAVA IGRPLGEVVT LRVLESSLNC SAGDMLLLWG RLTWRKMCRK
LLDMTFSSKT NTLVVRQRCG RPGGGVLLRY GSQLAPETFY RECDMQLFGP WGEIVSPSLS
PATSNAGGCR LFINVAPHAR IAIHALATNM GAGTEGANAS YILIRDTHSL RTTAFHGQQV
LYWESESSQA EMEFSEGFLK AQASLRGQYW TLQSWVPEMQ DPQSWKGKEG T*

mutated AA sequence

MHQRHPRARC PPLCVAGILA CGFLLGCWGP SHFQQSCLQA LEPQAVSSYL SPGAPLKGRP
PSPGFQRQRQ RQRRAAGGIL HLELLVAVGP DVFQAHQEDT ERYVLTNLNI GAELLRDPSL
GAQFRVHLVK MVILTEPEGA PNITANLTSS LLSVCGWSQT INPEDDTDPG HADLVLYITR
FDLELPDGNR QVRGVTQLGG ACSPTWSCLI TEDTGFDLGV TIAHEIGHSF GLEHDGAPGS
GCGPSGHVMA SDGAAPRAGL AWSPCSRRQL LSLLSAGRAR CVWDPPRPQP GSAGHPPDAQ
PGLYYSANEQ CRVAFGPKAV ACTFAREHLD MCQALSCHTD PLDQSSCSRL LVPLLDGTEC
GVEKWCSKGR CRSLVELTPI AAVHGRWSSW GPRSPCSHSC GGGVVTRRRQ CNNPRPAFGG
RACVGADLQA EMCNTQACEK TQLEFMSQQC ARTDGQPLRS SPGGASFYHW GAAVPHSQGD
ALCRHMCRAI GESFIMKRGD SFLDGTRCMP SGPREDGTLS LCVSGSCRTF GCDGRMDSQQ
VWDRCQVCGG DNSTCSPRKG SFTAGRAREY VTFLTVTPNL TSVYIANHRP LFTHLAVRIG
GRYVVAGKMS ISPNTTYPSL LEDGRVEYRV ALTEDRLPRL EEIRIWGPLQ EDADIQVYRR
YGEEYGNLTR PDITFTYFQP KPRQAWVWAA VRGPCSVSCG AGLRWVNYSC LDQARKELVE
TVQCQGSQQP PAWPEACVLE PCPPYWAVGD FGPCSASCGG GLRERPVRCV EAQGSLLKTL
PPARCRAGAQ QPAVALETCN PQPCPARWEV SEPSSCTSAG GAGLALENET CVPGADGLEA
PVTEGPGSVD EKLPAPEPCV GMSCPPGWGH LDATSAGEKA PSPWGSIRTG AQAAHVWTPA
AGSCSVSCGR GLMELRFLCM DSALRVPVQE ELCGLASKPG SRREVCQAVP CPARWQYKLA
ACSVSCGRGV VRRILYCARA HGEDDGEEIL LDTQCQGLPR PEPQEACSLE PCPPRWKVMS
LGPCSASCGL GTARRSVACV QLDQGQDVEV DEAACAALVR PEASVPCLIA DCTYRWHVGT
WMECSVSCGD GIQRRRDTCL GPQAQAPVPA DFCQHLPKPV TVRGCWAGPC VGQGACGRQH
LEPTGTIDMR GPGQADCAVA IGRPLGEVVT LRVLESSLNC SAGDMLLLWG RLTWRKMCRK
LLDMTFSSKT NTLVVRQRCG RPGGGVLLRY GSQLAPETFY RECDMQLFGP WGEIVSPSLS
PATSNAGGCR LFINVAPHAR IAIHALATNM GAGTEGANAS YILIRDTHSL RTTAFHGQQV
LYWESESSQA EMEFSEGFLK AQASLRGQYW TLQSWVPEMQ DPQSWKGKEG T*

speed

1.63 s

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999999308387091 (classification due to ClinVar, real probability is shown anyway) (explain)

Summary

amino acid sequence changed
known disease mutation at this position (HGMD CM012889)
known disease mutation: rs5802 (pathogenic)
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr9:136298598G>AN/A show variant in all transcripts IGV

HGNC symbol

ADAMTS13

Ensembl transcript ID

ENST00000356589

Genbank transcript ID

NM_139026

UniProt peptide

Q76LX8

alteration type

single base exchange

alteration region

CDS

DNA changes

c.1100G>A
cDNA.1220G>A
g.19121G>A

AA changes

R367H Score: 29 explain score(s)

position(s) of altered AA
if AA alteration in CDS

367

frameshift

known variant

regulatory features

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	5.213	1
	5.213	1
(flanking)	0.373	1

explain score(s) and/or inspect your position(s) in in UCSC Genome Browser

splice sites

effect	gDNA position	score	wt detection sequence	exon-intron border
Acc increased	19127	wt: 0.33 / mu: 0.44	wt: AAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCACCA mu: AAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCACCA	cctg\|CGGA
Acc marginally increased	19124	wt: 0.8311 / mu: 0.8822 (marginal change - not scored)	wt: CCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCA mu: CCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCA	gctc\|CTGC
Acc marginally increased	19125	wt: 0.8573 / mu: 0.8611 (marginal change - not scored)	wt: CGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCAC mu: CGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCAC	ctcc\|TGCG
Acc marginally increased	19121	wt: 0.3744 / mu: 0.3895 (marginal change - not scored)	wt: TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG mu: TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG	cccg\|CTCC

distance from splice site

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

367

mutated

not conserved

367

Ptroglodytes

all identical

ENSPTRG00000022942

356

Mmulatta

all identical

ENSMMUG00000000937

394

Fcatus

no homologue

Mmusculus

all identical

ENSMUSG00000014852

403

Ggallus

no homologue

Trubripes

no homologue

Drerio

all identical

ENSDARG00000076270

397

Dmelanogaster

not conserved

FBgn0086408

677

CLYGQSRRLLEG

Celegans

no homologue

Xtropicalis

no homologue

protein features

start (aa)	end (aa)	feature	details
287	383	DOMAIN	Disintegrin.	lost
300	374	REGION	Cysteine-rich.	lost
364	367	STRAND		lost
370	373	STRAND		might get lost (downstream of altered splice site)
374	377	HELIX		might get lost (downstream of altered splice site)
384	439	DOMAIN	TSP type-1 1.	might get lost (downstream of altered splice site)
396	396	DISULFID	By similarity.	might get lost (downstream of altered splice site)
399	401	STRAND		might get lost (downstream of altered splice site)
400	400	DISULFID	By similarity.	might get lost (downstream of altered splice site)
403	406	STRAND		might get lost (downstream of altered splice site)
411	411	DISULFID	By similarity.	might get lost (downstream of altered splice site)
417	419	STRAND		might get lost (downstream of altered splice site)
423	423	DISULFID	By similarity.	might get lost (downstream of altered splice site)
430	433	STRAND		might get lost (downstream of altered splice site)
433	433	DISULFID	By similarity.	might get lost (downstream of altered splice site)
438	438	DISULFID	By similarity.	might get lost (downstream of altered splice site)
442	451	HELIX		might get lost (downstream of altered splice site)
452	455	TURN		might get lost (downstream of altered splice site)
470	472	STRAND		might get lost (downstream of altered splice site)
474	476	TURN		might get lost (downstream of altered splice site)
479	483	HELIX		might get lost (downstream of altered splice site)
486	489	STRAND		might get lost (downstream of altered splice site)
495	497	STRAND		might get lost (downstream of altered splice site)
498	500	MOTIF	Cell attachment site (Potential).	might get lost (downstream of altered splice site)
519	523	STRAND		might get lost (downstream of altered splice site)
526	530	STRAND		might get lost (downstream of altered splice site)
534	536	STRAND		might get lost (downstream of altered splice site)
552	552	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
554	562	STRAND		might get lost (downstream of altered splice site)
556	685	REGION	Spacer.	might get lost (downstream of altered splice site)
569	576	STRAND		might get lost (downstream of altered splice site)
579	579	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
581	588	STRAND		might get lost (downstream of altered splice site)
592	599	STRAND		might get lost (downstream of altered splice site)
602	605	STRAND		might get lost (downstream of altered splice site)
608	610	STRAND		might get lost (downstream of altered splice site)
614	614	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
614	618	STRAND		might get lost (downstream of altered splice site)
623	632	STRAND		might get lost (downstream of altered splice site)
634	636	STRAND		might get lost (downstream of altered splice site)
638	647	STRAND		might get lost (downstream of altered splice site)
653	661	STRAND		might get lost (downstream of altered splice site)
663	665	HELIX		might get lost (downstream of altered splice site)
667	667	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
667	669	HELIX		might get lost (downstream of altered splice site)
673	680	STRAND		might get lost (downstream of altered splice site)
682	730	DOMAIN	TSP type-1 2.	might get lost (downstream of altered splice site)
707	707	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
742	805	DOMAIN	TSP type-1 3.	might get lost (downstream of altered splice site)
808	859	DOMAIN	TSP type-1 4.	might get lost (downstream of altered splice site)
828	828	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
896	950	DOMAIN	TSP type-1 5.	might get lost (downstream of altered splice site)
951	1011	DOMAIN	TSP type-1 6.	might get lost (downstream of altered splice site)
1012	1068	DOMAIN	TSP type-1 7.	might get lost (downstream of altered splice site)
1072	1131	DOMAIN	TSP type-1 8.	might get lost (downstream of altered splice site)
1192	1298	DOMAIN	CUB 1.	might get lost (downstream of altered splice site)
1235	1235	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
1299	1427	DOMAIN	CUB 2.	might get lost (downstream of altered splice site)
1354	1354	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

4023 / 4023

position (AA) of stopcodon in wt / mu AA sequence

1341 / 1341

position of stopcodon in wt / mu cDNA

4143 / 4143

poly(A) signal

N/A

conservation
nucleotide level for all changes - no scoring up to now

N/A

position of start ATG in wt / mu cDNA

121 / 121

chromosome

strand

last intron/exon boundary

3937

theoretical NMD boundary in CDS

3766

length of CDS

4023

coding sequence (CDS) position

1100

cDNA position
(for ins/del: last normal base / first normal base)

1220

gDNA position
(for ins/del: last normal base / first normal base)

19121

chromosomal position
(for ins/del: last normal base / first normal base)

136298598

original gDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG

altered gDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG

original cDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG

altered cDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG

wildtype AA sequence

MHQRHPRARC PPLCVAGILA CGFLLGCWGP SHFQQSCLQA LEPQAVSSYL SPGAPLKGRP
PSPGFQRQRQ RQRRAAGGIL HLELLVAVGP DVFQAHQEDT ERYVLTNLNI GAELLRDPSL
GAQFRVHLVK MVILTEPEGA PNITANLTSS LLSVCGWSQT INPEDDTDPG HADLVLYITR
FDLELPDGNR QVRGVTQLGG ACSPTWSCLI TEDTGFDLGV TIAHEIGHSF GLEHDGAPGS
GCGPSGHVMA SDGAAPRAGL AWSPCSRRQL LSLLSANEQC RVAFGPKAVA CTFAREHLDM
CQALSCHTDP LDQSSCSRLL VPLLDGTECG VEKWCSKGRC RSLVELTPIA AVHGRWSSWG
PRSPCSRSCG GGVVTRRRQC NNPRPAFGGR ACVGADLQAE MCNTQACEKT QLEFMSQQCA
RTDGQPLRSS PGGASFYHWG AAVPHSQGDA LCRHMCRAIG ESFIMKRGDS FLDGTRCMPS
GPREDGTLSL CVSGSCRTFG CDGRMDSQQV WDRCQVCGGD NSTCSPRKGS FTAGRAREYV
TFLTVTPNLT SVYIANHRPL FTHLAVRIGG RYVVAGKMSI SPNTTYPSLL EDGRVEYRVA
LTEDRLPRLE EIRIWGPLQE DADIQVYRRY GEEYGNLTRP DITFTYFQPK PRQAWVWAAV
RGPCSVSCGA GLRWVNYSCL DQARKELVET VQCQGSQQPP AWPEACVLEP CPPYWAVGDF
GPCSASCGGG LRERPVRCVE AQGSLLKTLP PARCRAGAQQ PAVALETCNP QPCPARWEVS
EPSSCTSAGG AGLALENETC VPGADGLEAP VTEGPGSVDE KLPAPEPCVG MSCPPGWGHL
DATSAGEKAP SPWGSIRTGA QAAHVWTPAA GSCSVSCGRG LMELRFLCMD SALRVPVQEE
LCGLASKPGS RREVCQAVPC PARWQYKLAA CSVSCGRGVV RRILYCARAH GEDDGEEILL
DTQCQGLPRP EPQEACSLEP CPPRWKVMSL GPCSASCGLG TARRSVACVQ LDQGQDVEVD
EAACAALVRP EASVPCLIAD CTYRWHVGTW MECSVSCGDG IQRRRDTCLG PQAQAPVPAD
FCQHLPKPVT VRGCWAGPCV GQGACGRQHL EPTGTIDMRG PGQADCAVAI GRPLGEVVTL
RVLESSLNCS AGDMLLLWGR LTWRKMCRKL LDMTFSSKTN TLVVRQRCGR PGGGVLLRYG
SQLAPETFYR ECDMQLFGPW GEIVSPSLSP ATSNAGGCRL FINVAPHARI AIHALATNMG
AGTEGANASY ILIRDTHSLR TTAFHGQQVL YWESESSQAE MEFSEGFLKA QASLRGQYWT
LQSWVPEMQD PQSWKGKEGT *

mutated AA sequence

MHQRHPRARC PPLCVAGILA CGFLLGCWGP SHFQQSCLQA LEPQAVSSYL SPGAPLKGRP
PSPGFQRQRQ RQRRAAGGIL HLELLVAVGP DVFQAHQEDT ERYVLTNLNI GAELLRDPSL
GAQFRVHLVK MVILTEPEGA PNITANLTSS LLSVCGWSQT INPEDDTDPG HADLVLYITR
FDLELPDGNR QVRGVTQLGG ACSPTWSCLI TEDTGFDLGV TIAHEIGHSF GLEHDGAPGS
GCGPSGHVMA SDGAAPRAGL AWSPCSRRQL LSLLSANEQC RVAFGPKAVA CTFAREHLDM
CQALSCHTDP LDQSSCSRLL VPLLDGTECG VEKWCSKGRC RSLVELTPIA AVHGRWSSWG
PRSPCSHSCG GGVVTRRRQC NNPRPAFGGR ACVGADLQAE MCNTQACEKT QLEFMSQQCA
RTDGQPLRSS PGGASFYHWG AAVPHSQGDA LCRHMCRAIG ESFIMKRGDS FLDGTRCMPS
GPREDGTLSL CVSGSCRTFG CDGRMDSQQV WDRCQVCGGD NSTCSPRKGS FTAGRAREYV
TFLTVTPNLT SVYIANHRPL FTHLAVRIGG RYVVAGKMSI SPNTTYPSLL EDGRVEYRVA
LTEDRLPRLE EIRIWGPLQE DADIQVYRRY GEEYGNLTRP DITFTYFQPK PRQAWVWAAV
RGPCSVSCGA GLRWVNYSCL DQARKELVET VQCQGSQQPP AWPEACVLEP CPPYWAVGDF
GPCSASCGGG LRERPVRCVE AQGSLLKTLP PARCRAGAQQ PAVALETCNP QPCPARWEVS
EPSSCTSAGG AGLALENETC VPGADGLEAP VTEGPGSVDE KLPAPEPCVG MSCPPGWGHL
DATSAGEKAP SPWGSIRTGA QAAHVWTPAA GSCSVSCGRG LMELRFLCMD SALRVPVQEE
LCGLASKPGS RREVCQAVPC PARWQYKLAA CSVSCGRGVV RRILYCARAH GEDDGEEILL
DTQCQGLPRP EPQEACSLEP CPPRWKVMSL GPCSASCGLG TARRSVACVQ LDQGQDVEVD
EAACAALVRP EASVPCLIAD CTYRWHVGTW MECSVSCGDG IQRRRDTCLG PQAQAPVPAD
FCQHLPKPVT VRGCWAGPCV GQGACGRQHL EPTGTIDMRG PGQADCAVAI GRPLGEVVTL
RVLESSLNCS AGDMLLLWGR LTWRKMCRKL LDMTFSSKTN TLVVRQRCGR PGGGVLLRYG
SQLAPETFYR ECDMQLFGPW GEIVSPSLSP ATSNAGGCRL FINVAPHARI AIHALATNMG
AGTEGANASY ILIRDTHSLR TTAFHGQQVL YWESESSQAE MEFSEGFLKA QASLRGQYWT
LQSWVPEMQD PQSWKGKEGT *

speed

1.43 s

mutation t@sting

documentation

Prediction

disease causing

Model: without_aae, prob: 1 (classification due to ClinVar, real probability is shown anyway) (explain)

Summary

known disease mutation at this position (HGMD CM012889)
known disease mutation: rs5802 (pathogenic)
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr9:136298598G>AN/A show variant in all transcripts IGV

HGNC symbol

ADAMTS13

Ensembl transcript ID

ENST00000371916

Genbank transcript ID

N/A

UniProt peptide

N/A

alteration type

single base exchange

alteration region

3'UTR

DNA changes

cDNA.1336G>A
g.19121G>A

AA changes

N/A

position(s) of altered AA
if AA alteration in CDS

N/A

frameshift

N/A

known variant

regulatory features

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	5.213	1
	5.213	1
(flanking)	0.373	1

explain score(s) and/or inspect your position(s) in in UCSC Genome Browser

splice sites

splice site change occurs after stopcodon (at aa 299)

effect	gDNA position	score	detection sequence	exon-intron border
Acc increased	19127	wt: 0.33 / mu: 0.44	wt: AAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCACCA mu: AAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCACCA	cctg\|CGGA
Acc marginally increased	19124	wt: 0.8311 / mu: 0.8822 (marginal change - not scored)	wt: CCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCA mu: CCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCA	gctc\|CTGC
Acc marginally increased	19125	wt: 0.8573 / mu: 0.8611 (marginal change - not scored)	wt: CGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCAC mu: CGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGGTCAC	ctcc\|TGCG
Acc marginally increased	19121	wt: 0.3744 / mu: 0.3895 (marginal change - not scored)	wt: TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG mu: TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG	cccg\|CTCC

distance from splice site

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

N/A

protein features

N/A

length of protein

N/A

AA sequence altered

N/A

position of stopcodon in wt / mu CDS

N/A

position (AA) of stopcodon in wt / mu AA sequence

N/A

position of stopcodon in wt / mu cDNA

N/A

poly(A) signal

signal is predicted to be ok

conservation
nucleotide level for all changes - no scoring up to now

N/A

position of start ATG in wt / mu cDNA

445 / 445

chromosome

strand

last intron/exon boundary

4221

theoretical NMD boundary in CDS

3726

length of CDS

831

coding sequence (CDS) position

N/A

cDNA position
(for ins/del: last normal base / first normal base)

1336

gDNA position
(for ins/del: last normal base / first normal base)

19121

chromosomal position
(for ins/del: last normal base / first normal base)

136298598

original gDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG

altered gDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG

original cDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGG

altered cDNA sequence snippet

TCCCCGAAGTCCTTGCTCCCACTCCTGCGGAGGAGGTGTGG

wildtype AA sequence

mutated AA sequence

N/A

speed

1.35 s

MutationTaster - study a chromosomal position

Results

Taster files

mutation t@sting

Prediction

disease causing

mutation t@sting

Prediction

disease causing

mutation t@sting

Prediction

disease causing

mutation t@sting

Prediction

disease causing

mutation t@sting

Prediction

disease causing

Problems