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 3 transcript(s)...
Querying Taster for transcript #1: ENST00000346991
Querying Taster for transcript #2: ENST00000527044
Querying Taster for transcript #3: ENST00000399668
MT speed 0 s - this script 3.902039 s

Results

genesymbol	prediction	probability	model	prediction problem	splicing	ClinVar	amino acid changes	variant type	dbSNP ID	protein length	file
KNL1	polymorphism_automatic	0.0297668028189541	simple_aae		affected		M598T	single base exchange	rs11858113		show file
KNL1	polymorphism_automatic	0.0297668028189541	simple_aae		affected		M572T	single base exchange	rs11858113		show file
KNL1	polymorphism_automatic	0.999999999999906	without_aae		affected			single base exchange	rs11858113		show file

Taster files

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 0.970233197181046 (classification due to TGP/ExAC, real probability is shown anyway) (explain)

Summary

amino acid sequence changed
homozygous in TGP or ExAC
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr15:40914177T>CN/A show variant in all transcripts IGV

HGNC symbol

KNL1

Ensembl transcript ID

ENST00000346991

Genbank transcript ID

NM_170589

UniProt peptide

Q8NG31

alteration type

single base exchange

alteration region

CDS

DNA changes

c.1793T>C
cDNA.2183T>C
g.27960T>C

AA changes

M598T Score: 81 explain score(s)

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

598

frameshift

known variant

Reference ID: rs11858113

database	homozygous (C/C)	heterozygous	allele carriers
1000G	326	1108	1434
ExAC	9787	13193	22980

regulatory features

H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	1.135	1
	0.242	1
(flanking)	3.847	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
Donor marginally increased	27951	wt: 0.4935 / mu: 0.5449 (marginal change - not scored)	wt: ATCAGGTGAAAATAT mu: ATCAGGTGAAAATAC	CAGG\|tgaa
Donor increased	27952	wt: 0.47 / mu: 0.73	wt: TCAGGTGAAAATATG mu: TCAGGTGAAAATACG	AGGT\|gaaa

distance from splice site

1340

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

598

mutated

not conserved

598

Ptroglodytes

no homologue

Mmulatta

no homologue

Fcatus

no homologue

Mmusculus

all identical

ENSMUSG00000027326

552

Ggallus

no homologue

Trubripes

no alignment

ENSTRUG00000013401

n/a

Drerio

no alignment

ENSDARG00000070239

n/a

Dmelanogaster

no homologue

Celegans

no homologue

Xtropicalis

no homologue

protein features

start (aa)	end (aa)	feature	details
1	728	REGION	Interaction with BUB1 and BUB1B.	lost
601	601	MOD_RES	Phosphothreonine.	might get lost (downstream of altered splice site)
682	682	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
765	765	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
767	767	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
855	1201	REGION	2 X 104 AA approximate repeats.	might get lost (downstream of altered splice site)
885	989	REPEAT	1.	might get lost (downstream of altered splice site)
954	954	MOD_RES	Phosphothreonine.	might get lost (downstream of altered splice site)
956	956	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1039	1039	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1042	1042	MOD_RES	Phosphothreonine.	might get lost (downstream of altered splice site)
1076	1076	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1099	1201	REPEAT	2.	might get lost (downstream of altered splice site)
1232	1232	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1332	1332	CONFLICT	P -> A (in Ref. 2; BAC05691).	might get lost (downstream of altered splice site)
1357	1357	CONFLICT	N -> H (in Ref. 2; BAC05691).	might get lost (downstream of altered splice site)
1720	1720	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1756	1756	CONFLICT	N -> Y (in Ref. 2; BAC05691).	might get lost (downstream of altered splice site)
1773	1773	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1789	1803	MOTIF	Nuclear localization signal (Potential).	might get lost (downstream of altered splice site)
1818	1819	SITE	Breakpoint for translocation to form MLL- CASC5.	might get lost (downstream of altered splice site)
1834	2316	REGION	Necessary for kinetochore localization and for interaction with NSL1 and DSN1.	might get lost (downstream of altered splice site)
1845	1845	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1869	1869	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1879	1879	MOD_RES	Phosphothreonine.	might get lost (downstream of altered splice site)
1942	2133	COILED	Potential.	might get lost (downstream of altered splice site)

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

7029 / 7029

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

2343 / 2343

position of stopcodon in wt / mu cDNA

7419 / 7419

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

391 / 391

chromosome

strand

last intron/exon boundary

7305

theoretical NMD boundary in CDS

6864

length of CDS

7029

coding sequence (CDS) position

1793

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

2183

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

27960

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

40914177

original gDNA sequence snippet

ACTCTTATCAGGTGAAAATATGGATTTGACTGAAAGTCACA

altered gDNA sequence snippet

ACTCTTATCAGGTGAAAATACGGATTTGACTGAAAGTCACA

original cDNA sequence snippet

ACTCTTATCAGGTGAAAATATGGATTTGACTGAAAGTCACA

altered cDNA sequence snippet

ACTCTTATCAGGTGAAAATACGGATTTGACTGAAAGTCACA

wildtype AA sequence

MDGVSSEANE ENDNIERPVR RRHSSILKPP RSPLQDLRGG NERVQESNAL RNKKNSRRVS
FADTIKVFQT ESHMKIVRKS EMEGCSAMVP SQLQLLPPGF KRFSCLSLPE TETGENLLLI
QNKKLEDNYC EITGMNTLLS APIHTQMQQK EFSIIEHTRE RKHANDQTVI FSDENQMDLT
SSHTVMITKG LLDNPISEKS TKIDTTSFLA NLKLHTEDSR MKKEVNFSVD QNTSSENKID
FNDFIKRLKT GKCSAFPDVP DKENFEIPIY SKEPNSASST HQMHVSLKED ENNSNITRLF
REKDDGMNFT QCHTANIQTL IPTSSETNSR ESKGNDITIY GNDFMDLTFN HTLQILPATG
NFSEIENQTQ NAMDVTTGYG TKASGNKTVF KSKQNTAFQD LSINSADKIH ITRSHIMGAE
THIVSQTCNQ DARILAMTPE SIYSNPSIQG CKTVFYSSCN DAMEMTKCLS NMREEKNLLK
HDSNYAKMYC NPDAMSSLTE KTIYSGEENM DITKSHTVAI DNQIFKQDQS NVQIAAAPTP
EKEMMLQNLM TTSEDGKMNV NCNSVPHVSK ERIQQSLSNP LSISLTDRKT ELLSGENMDL
TESHTSNLGS QVPLAAYNLA PESTSESHSQ SKSSSDECEE ITKSRNEPFQ RSDIIAKNSL
TDTWNKDKDW VLKILPYLDK DSPQSADCNQ EIATSHNIVY CGGVLDKQIT NRNTVSWEQS
LFSTTKPLFS SGQFSMKNHD TAISSHTVKS VLGQNSKLAE PLRKSLSNPT PDYCHDKMII
CSEEEQNMDL TKSHTVVIGF GPSELQELGK TNLEHTTGQL TTMNRQIAVK VEKCGKSPIE
KSGVLKSNCI MDVLEDESVQ KPKFPKEKQN VKIWGRKSVG GPKIDKTIVF SEDDKNDMDI
TKSYTIEINH RPLLEKRDCH LVPLAGTSET ILYTCRQDDM EITRSHTTAL ECKTVSPDEI
TTRPMDKTVV FVDNHVELEM TESHTVFIDY QEKERTDRPN FELSQRKSLG TPTVICTPTE
ESVFFPGNGE SDRLVANDSQ LTPLEEWSNN RGPVEVADNM ELSKSATCKN IKDVQSPGFL
NEPLSSKSQR RKSLKLKNDK TIVFSENHKN DMDITQSCMV EIDNESALED KEDFHLAGAS
KTILYSCGQD DMEITRSHTT ALECKTLLPN EIAIRPMDKT VLFTDNYSDL EVTDSHTVFI
DCQATEKILE ENPKFGIGKG KNLGVSFPKD NSCVQEIAEK QALAVGNKIV LHTEQKQQLF
AATNRTTNEI IKFHSAAMDE KVIGKVVDQA CTLEKAQVES CQLNNRDRRN VDFTSSHATA
VCGSSDNYSC LPNVISCTDN LEGSAMLLCD KDEEKANYCP VQNDLAYAND FASEYYLESE
GQPLSAPCPL LEKEEVIQTS TKGQLDCVIT LHKDQDLIKD PRNLLANQTL VYSQDLGEMT
KLNSKRVSFK LPKDQMKVYV DDIYVIPQPH FSTDQPPLPK KGQSSINKEE VILSKAGNKS
LNIIENSSAP ICENKPKILN SEEWFAAACK KELKENIQTT NYNTALDFHS NSDVTKQVIQ
THVNAGEAPD PVITSNVPCF HSIKPNLNNL NGKTGEFLAF QTVHLPPLPE QLLELGNKAH
NDMHIVQATE IHNINIISSN AKDSRDEENK KSHNGAETTS LPPKTVFKDK VRRCSLGIFL
PRLPNKRNCS VTGIDDLEQI PADTTDINHL ETQPVSSKDS GIGSVAGKLN LSPSQYINEE
NLPVYPDEIN SSDSINIETE EKALIETYQK EISPYENKMG KTCNSQKRTW VQEEEDIHKE
KKIRKNEIKF SDTTQDREIF DHHTEEDIDK SANSVLIKNL SRTPSSCSSS LDSIKADGTS
LDFSTYRSSQ MESQFLRDTI CEESLREKLQ DGRITIREFF ILLQVHILIQ KPRQSNLPGN
FTVNTPPTPE DLMLSQYVYR PKIQIYREDC EARRQKIEEL KLSASNQDKL LVDINKNLWE
KMRHCSDKEL KAFGIYLNKI KSCFTKMTKV FTHQGKVALY GKLVQSAQNE REKLQIKIDE
MDKILKKIDN CLTEMETETK NLEDEEKNNP VEEWDSEMRA AEKELEQLKT EEEELQRNLL
ELEVQKEQTL AQIDFMQKQR NRTEELLDQL SLSEWDVVEW SDDQAVFTFV YDTIQLTITF
EESVVGFPFL DKRYRKIVDV NFQSLLDEDQ APPSSLLVHK LIFQYVEEKE SWKKTCTTQH
QLPKMLEEFS LVVHHCRLLG EEIEYLKRWG PNYNLMNIDI NNNELRLLFS SSAAFAKFEI
TLFLSAYYPS VPLPSTIQNH VGNTSQDDIA TILSKVPLEN NYLKNVVKQI YQDLFQDCHF
YH*

mutated AA sequence

MDGVSSEANE ENDNIERPVR RRHSSILKPP RSPLQDLRGG NERVQESNAL RNKKNSRRVS
FADTIKVFQT ESHMKIVRKS EMEGCSAMVP SQLQLLPPGF KRFSCLSLPE TETGENLLLI
QNKKLEDNYC EITGMNTLLS APIHTQMQQK EFSIIEHTRE RKHANDQTVI FSDENQMDLT
SSHTVMITKG LLDNPISEKS TKIDTTSFLA NLKLHTEDSR MKKEVNFSVD QNTSSENKID
FNDFIKRLKT GKCSAFPDVP DKENFEIPIY SKEPNSASST HQMHVSLKED ENNSNITRLF
REKDDGMNFT QCHTANIQTL IPTSSETNSR ESKGNDITIY GNDFMDLTFN HTLQILPATG
NFSEIENQTQ NAMDVTTGYG TKASGNKTVF KSKQNTAFQD LSINSADKIH ITRSHIMGAE
THIVSQTCNQ DARILAMTPE SIYSNPSIQG CKTVFYSSCN DAMEMTKCLS NMREEKNLLK
HDSNYAKMYC NPDAMSSLTE KTIYSGEENM DITKSHTVAI DNQIFKQDQS NVQIAAAPTP
EKEMMLQNLM TTSEDGKMNV NCNSVPHVSK ERIQQSLSNP LSISLTDRKT ELLSGENTDL
TESHTSNLGS QVPLAAYNLA PESTSESHSQ SKSSSDECEE ITKSRNEPFQ RSDIIAKNSL
TDTWNKDKDW VLKILPYLDK DSPQSADCNQ EIATSHNIVY CGGVLDKQIT NRNTVSWEQS
LFSTTKPLFS SGQFSMKNHD TAISSHTVKS VLGQNSKLAE PLRKSLSNPT PDYCHDKMII
CSEEEQNMDL TKSHTVVIGF GPSELQELGK TNLEHTTGQL TTMNRQIAVK VEKCGKSPIE
KSGVLKSNCI MDVLEDESVQ KPKFPKEKQN VKIWGRKSVG GPKIDKTIVF SEDDKNDMDI
TKSYTIEINH RPLLEKRDCH LVPLAGTSET ILYTCRQDDM EITRSHTTAL ECKTVSPDEI
TTRPMDKTVV FVDNHVELEM TESHTVFIDY QEKERTDRPN FELSQRKSLG TPTVICTPTE
ESVFFPGNGE SDRLVANDSQ LTPLEEWSNN RGPVEVADNM ELSKSATCKN IKDVQSPGFL
NEPLSSKSQR RKSLKLKNDK TIVFSENHKN DMDITQSCMV EIDNESALED KEDFHLAGAS
KTILYSCGQD DMEITRSHTT ALECKTLLPN EIAIRPMDKT VLFTDNYSDL EVTDSHTVFI
DCQATEKILE ENPKFGIGKG KNLGVSFPKD NSCVQEIAEK QALAVGNKIV LHTEQKQQLF
AATNRTTNEI IKFHSAAMDE KVIGKVVDQA CTLEKAQVES CQLNNRDRRN VDFTSSHATA
VCGSSDNYSC LPNVISCTDN LEGSAMLLCD KDEEKANYCP VQNDLAYAND FASEYYLESE
GQPLSAPCPL LEKEEVIQTS TKGQLDCVIT LHKDQDLIKD PRNLLANQTL VYSQDLGEMT
KLNSKRVSFK LPKDQMKVYV DDIYVIPQPH FSTDQPPLPK KGQSSINKEE VILSKAGNKS
LNIIENSSAP ICENKPKILN SEEWFAAACK KELKENIQTT NYNTALDFHS NSDVTKQVIQ
THVNAGEAPD PVITSNVPCF HSIKPNLNNL NGKTGEFLAF QTVHLPPLPE QLLELGNKAH
NDMHIVQATE IHNINIISSN AKDSRDEENK KSHNGAETTS LPPKTVFKDK VRRCSLGIFL
PRLPNKRNCS VTGIDDLEQI PADTTDINHL ETQPVSSKDS GIGSVAGKLN LSPSQYINEE
NLPVYPDEIN SSDSINIETE EKALIETYQK EISPYENKMG KTCNSQKRTW VQEEEDIHKE
KKIRKNEIKF SDTTQDREIF DHHTEEDIDK SANSVLIKNL SRTPSSCSSS LDSIKADGTS
LDFSTYRSSQ MESQFLRDTI CEESLREKLQ DGRITIREFF ILLQVHILIQ KPRQSNLPGN
FTVNTPPTPE DLMLSQYVYR PKIQIYREDC EARRQKIEEL KLSASNQDKL LVDINKNLWE
KMRHCSDKEL KAFGIYLNKI KSCFTKMTKV FTHQGKVALY GKLVQSAQNE REKLQIKIDE
MDKILKKIDN CLTEMETETK NLEDEEKNNP VEEWDSEMRA AEKELEQLKT EEEELQRNLL
ELEVQKEQTL AQIDFMQKQR NRTEELLDQL SLSEWDVVEW SDDQAVFTFV YDTIQLTITF
EESVVGFPFL DKRYRKIVDV NFQSLLDEDQ APPSSLLVHK LIFQYVEEKE SWKKTCTTQH
QLPKMLEEFS LVVHHCRLLG EEIEYLKRWG PNYNLMNIDI NNNELRLLFS SSAAFAKFEI
TLFLSAYYPS VPLPSTIQNH VGNTSQDDIA TILSKVPLEN NYLKNVVKQI YQDLFQDCHF
YH*

speed

1.01 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

polymorphism

Model: simple_aae, prob: 0.970233197181046 (classification due to TGP/ExAC, real probability is shown anyway) (explain)

Summary

amino acid sequence changed
homozygous in TGP or ExAC
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr15:40914177T>CN/A show variant in all transcripts IGV

HGNC symbol

KNL1

Ensembl transcript ID

ENST00000399668

Genbank transcript ID

NM_144508

UniProt peptide

Q8NG31

alteration type

single base exchange

alteration region

CDS

DNA changes

c.1715T>C
cDNA.1876T>C
g.27960T>C

AA changes

M572T Score: 81 explain score(s)

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

572

frameshift

known variant

Reference ID: rs11858113

database	homozygous (C/C)	heterozygous	allele carriers
1000G	326	1108	1434
ExAC	9787	13193	22980

regulatory features

H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	1.135	1
	0.242	1
(flanking)	3.847	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
Donor marginally increased	27951	wt: 0.4935 / mu: 0.5449 (marginal change - not scored)	wt: ATCAGGTGAAAATAT mu: ATCAGGTGAAAATAC	CAGG\|tgaa
Donor increased	27952	wt: 0.47 / mu: 0.73	wt: TCAGGTGAAAATATG mu: TCAGGTGAAAATACG	AGGT\|gaaa

distance from splice site

1340

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

572

mutated

not conserved

572

Ptroglodytes

no homologue

Mmulatta

no homologue

Fcatus

no homologue

Mmusculus

all identical

ENSMUSG00000027326

552

Ggallus

no homologue

Trubripes

no alignment

ENSTRUG00000013401

n/a

Drerio

no alignment

ENSDARG00000070239

n/a

Dmelanogaster

no homologue

Celegans

no homologue

Xtropicalis

no homologue

protein features

start (aa)	end (aa)	feature	details
1	728	REGION	Interaction with BUB1 and BUB1B.	lost
578	578	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
601	601	MOD_RES	Phosphothreonine.	might get lost (downstream of altered splice site)
682	682	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
765	765	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
767	767	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
855	1201	REGION	2 X 104 AA approximate repeats.	might get lost (downstream of altered splice site)
885	989	REPEAT	1.	might get lost (downstream of altered splice site)
954	954	MOD_RES	Phosphothreonine.	might get lost (downstream of altered splice site)
956	956	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1039	1039	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1042	1042	MOD_RES	Phosphothreonine.	might get lost (downstream of altered splice site)
1076	1076	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1099	1201	REPEAT	2.	might get lost (downstream of altered splice site)
1232	1232	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1332	1332	CONFLICT	P -> A (in Ref. 2; BAC05691).	might get lost (downstream of altered splice site)
1357	1357	CONFLICT	N -> H (in Ref. 2; BAC05691).	might get lost (downstream of altered splice site)
1720	1720	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1756	1756	CONFLICT	N -> Y (in Ref. 2; BAC05691).	might get lost (downstream of altered splice site)
1773	1773	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1789	1803	MOTIF	Nuclear localization signal (Potential).	might get lost (downstream of altered splice site)
1818	1819	SITE	Breakpoint for translocation to form MLL- CASC5.	might get lost (downstream of altered splice site)
1834	2316	REGION	Necessary for kinetochore localization and for interaction with NSL1 and DSN1.	might get lost (downstream of altered splice site)
1845	1845	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1869	1869	MOD_RES	Phosphoserine.	might get lost (downstream of altered splice site)
1879	1879	MOD_RES	Phosphothreonine.	might get lost (downstream of altered splice site)
1942	2133	COILED	Potential.	might get lost (downstream of altered splice site)

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

6951 / 6951

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

2317 / 2317

position of stopcodon in wt / mu cDNA

7112 / 7112

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

162 / 162

chromosome

strand

last intron/exon boundary

6998

theoretical NMD boundary in CDS

6786

length of CDS

6951

coding sequence (CDS) position

1715

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

1876

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

27960

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

40914177

original gDNA sequence snippet

ACTCTTATCAGGTGAAAATATGGATTTGACTGAAAGTCACA

altered gDNA sequence snippet

ACTCTTATCAGGTGAAAATACGGATTTGACTGAAAGTCACA

original cDNA sequence snippet

ACTCTTATCAGGTGAAAATATGGATTTGACTGAAAGTCACA

altered cDNA sequence snippet

ACTCTTATCAGGTGAAAATACGGATTTGACTGAAAGTCACA

wildtype AA sequence

MDGVSSEANE ENDNIERPVR RRHSSILKPP RSPLQDLRGG NERVQESNAL RNKKNSRRVS
FADTIKVFQT ESHMKIVRKS EMEETETGEN LLLIQNKKLE DNYCEITGMN TLLSAPIHTQ
MQQKEFSIIE HTRERKHAND QTVIFSDENQ MDLTSSHTVM ITKGLLDNPI SEKSTKIDTT
SFLANLKLHT EDSRMKKEVN FSVDQNTSSE NKIDFNDFIK RLKTGKCSAF PDVPDKENFE
IPIYSKEPNS ASSTHQMHVS LKEDENNSNI TRLFREKDDG MNFTQCHTAN IQTLIPTSSE
TNSRESKGND ITIYGNDFMD LTFNHTLQIL PATGNFSEIE NQTQNAMDVT TGYGTKASGN
KTVFKSKQNT AFQDLSINSA DKIHITRSHI MGAETHIVSQ TCNQDARILA MTPESIYSNP
SIQGCKTVFY SSCNDAMEMT KCLSNMREEK NLLKHDSNYA KMYCNPDAMS SLTEKTIYSG
EENMDITKSH TVAIDNQIFK QDQSNVQIAA APTPEKEMML QNLMTTSEDG KMNVNCNSVP
HVSKERIQQS LSNPLSISLT DRKTELLSGE NMDLTESHTS NLGSQVPLAA YNLAPESTSE
SHSQSKSSSD ECEEITKSRN EPFQRSDIIA KNSLTDTWNK DKDWVLKILP YLDKDSPQSA
DCNQEIATSH NIVYCGGVLD KQITNRNTVS WEQSLFSTTK PLFSSGQFSM KNHDTAISSH
TVKSVLGQNS KLAEPLRKSL SNPTPDYCHD KMIICSEEEQ NMDLTKSHTV VIGFGPSELQ
ELGKTNLEHT TGQLTTMNRQ IAVKVEKCGK SPIEKSGVLK SNCIMDVLED ESVQKPKFPK
EKQNVKIWGR KSVGGPKIDK TIVFSEDDKN DMDITKSYTI EINHRPLLEK RDCHLVPLAG
TSETILYTCR QDDMEITRSH TTALECKTVS PDEITTRPMD KTVVFVDNHV ELEMTESHTV
FIDYQEKERT DRPNFELSQR KSLGTPTVIC TPTEESVFFP GNGESDRLVA NDSQLTPLEE
WSNNRGPVEV ADNMELSKSA TCKNIKDVQS PGFLNEPLSS KSQRRKSLKL KNDKTIVFSE
NHKNDMDITQ SCMVEIDNES ALEDKEDFHL AGASKTILYS CGQDDMEITR SHTTALECKT
LLPNEIAIRP MDKTVLFTDN YSDLEVTDSH TVFIDCQATE KILEENPKFG IGKGKNLGVS
FPKDNSCVQE IAEKQALAVG NKIVLHTEQK QQLFAATNRT TNEIIKFHSA AMDEKVIGKV
VDQACTLEKA QVESCQLNNR DRRNVDFTSS HATAVCGSSD NYSCLPNVIS CTDNLEGSAM
LLCDKDEEKA NYCPVQNDLA YANDFASEYY LESEGQPLSA PCPLLEKEEV IQTSTKGQLD
CVITLHKDQD LIKDPRNLLA NQTLVYSQDL GEMTKLNSKR VSFKLPKDQM KVYVDDIYVI
PQPHFSTDQP PLPKKGQSSI NKEEVILSKA GNKSLNIIEN SSAPICENKP KILNSEEWFA
AACKKELKEN IQTTNYNTAL DFHSNSDVTK QVIQTHVNAG EAPDPVITSN VPCFHSIKPN
LNNLNGKTGE FLAFQTVHLP PLPEQLLELG NKAHNDMHIV QATEIHNINI ISSNAKDSRD
EENKKSHNGA ETTSLPPKTV FKDKVRRCSL GIFLPRLPNK RNCSVTGIDD LEQIPADTTD
INHLETQPVS SKDSGIGSVA GKLNLSPSQY INEENLPVYP DEINSSDSIN IETEEKALIE
TYQKEISPYE NKMGKTCNSQ KRTWVQEEED IHKEKKIRKN EIKFSDTTQD REIFDHHTEE
DIDKSANSVL IKNLSRTPSS CSSSLDSIKA DGTSLDFSTY RSSQMESQFL RDTICEESLR
EKLQDGRITI REFFILLQVH ILIQKPRQSN LPGNFTVNTP PTPEDLMLSQ YVYRPKIQIY
REDCEARRQK IEELKLSASN QDKLLVDINK NLWEKMRHCS DKELKAFGIY LNKIKSCFTK
MTKVFTHQGK VALYGKLVQS AQNEREKLQI KIDEMDKILK KIDNCLTEME TETKNLEDEE
KNNPVEEWDS EMRAAEKELE QLKTEEEELQ RNLLELEVQK EQTLAQIDFM QKQRNRTEEL
LDQLSLSEWD VVEWSDDQAV FTFVYDTIQL TITFEESVVG FPFLDKRYRK IVDVNFQSLL
DEDQAPPSSL LVHKLIFQYV EEKESWKKTC TTQHQLPKML EEFSLVVHHC RLLGEEIEYL
KRWGPNYNLM NIDINNNELR LLFSSSAAFA KFEITLFLSA YYPSVPLPST IQNHVGNTSQ
DDIATILSKV PLENNYLKNV VKQIYQDLFQ DCHFYH*

mutated AA sequence

MDGVSSEANE ENDNIERPVR RRHSSILKPP RSPLQDLRGG NERVQESNAL RNKKNSRRVS
FADTIKVFQT ESHMKIVRKS EMEETETGEN LLLIQNKKLE DNYCEITGMN TLLSAPIHTQ
MQQKEFSIIE HTRERKHAND QTVIFSDENQ MDLTSSHTVM ITKGLLDNPI SEKSTKIDTT
SFLANLKLHT EDSRMKKEVN FSVDQNTSSE NKIDFNDFIK RLKTGKCSAF PDVPDKENFE
IPIYSKEPNS ASSTHQMHVS LKEDENNSNI TRLFREKDDG MNFTQCHTAN IQTLIPTSSE
TNSRESKGND ITIYGNDFMD LTFNHTLQIL PATGNFSEIE NQTQNAMDVT TGYGTKASGN
KTVFKSKQNT AFQDLSINSA DKIHITRSHI MGAETHIVSQ TCNQDARILA MTPESIYSNP
SIQGCKTVFY SSCNDAMEMT KCLSNMREEK NLLKHDSNYA KMYCNPDAMS SLTEKTIYSG
EENMDITKSH TVAIDNQIFK QDQSNVQIAA APTPEKEMML QNLMTTSEDG KMNVNCNSVP
HVSKERIQQS LSNPLSISLT DRKTELLSGE NTDLTESHTS NLGSQVPLAA YNLAPESTSE
SHSQSKSSSD ECEEITKSRN EPFQRSDIIA KNSLTDTWNK DKDWVLKILP YLDKDSPQSA
DCNQEIATSH NIVYCGGVLD KQITNRNTVS WEQSLFSTTK PLFSSGQFSM KNHDTAISSH
TVKSVLGQNS KLAEPLRKSL SNPTPDYCHD KMIICSEEEQ NMDLTKSHTV VIGFGPSELQ
ELGKTNLEHT TGQLTTMNRQ IAVKVEKCGK SPIEKSGVLK SNCIMDVLED ESVQKPKFPK
EKQNVKIWGR KSVGGPKIDK TIVFSEDDKN DMDITKSYTI EINHRPLLEK RDCHLVPLAG
TSETILYTCR QDDMEITRSH TTALECKTVS PDEITTRPMD KTVVFVDNHV ELEMTESHTV
FIDYQEKERT DRPNFELSQR KSLGTPTVIC TPTEESVFFP GNGESDRLVA NDSQLTPLEE
WSNNRGPVEV ADNMELSKSA TCKNIKDVQS PGFLNEPLSS KSQRRKSLKL KNDKTIVFSE
NHKNDMDITQ SCMVEIDNES ALEDKEDFHL AGASKTILYS CGQDDMEITR SHTTALECKT
LLPNEIAIRP MDKTVLFTDN YSDLEVTDSH TVFIDCQATE KILEENPKFG IGKGKNLGVS
FPKDNSCVQE IAEKQALAVG NKIVLHTEQK QQLFAATNRT TNEIIKFHSA AMDEKVIGKV
VDQACTLEKA QVESCQLNNR DRRNVDFTSS HATAVCGSSD NYSCLPNVIS CTDNLEGSAM
LLCDKDEEKA NYCPVQNDLA YANDFASEYY LESEGQPLSA PCPLLEKEEV IQTSTKGQLD
CVITLHKDQD LIKDPRNLLA NQTLVYSQDL GEMTKLNSKR VSFKLPKDQM KVYVDDIYVI
PQPHFSTDQP PLPKKGQSSI NKEEVILSKA GNKSLNIIEN SSAPICENKP KILNSEEWFA
AACKKELKEN IQTTNYNTAL DFHSNSDVTK QVIQTHVNAG EAPDPVITSN VPCFHSIKPN
LNNLNGKTGE FLAFQTVHLP PLPEQLLELG NKAHNDMHIV QATEIHNINI ISSNAKDSRD
EENKKSHNGA ETTSLPPKTV FKDKVRRCSL GIFLPRLPNK RNCSVTGIDD LEQIPADTTD
INHLETQPVS SKDSGIGSVA GKLNLSPSQY INEENLPVYP DEINSSDSIN IETEEKALIE
TYQKEISPYE NKMGKTCNSQ KRTWVQEEED IHKEKKIRKN EIKFSDTTQD REIFDHHTEE
DIDKSANSVL IKNLSRTPSS CSSSLDSIKA DGTSLDFSTY RSSQMESQFL RDTICEESLR
EKLQDGRITI REFFILLQVH ILIQKPRQSN LPGNFTVNTP PTPEDLMLSQ YVYRPKIQIY
REDCEARRQK IEELKLSASN QDKLLVDINK NLWEKMRHCS DKELKAFGIY LNKIKSCFTK
MTKVFTHQGK VALYGKLVQS AQNEREKLQI KIDEMDKILK KIDNCLTEME TETKNLEDEE
KNNPVEEWDS EMRAAEKELE QLKTEEEELQ RNLLELEVQK EQTLAQIDFM QKQRNRTEEL
LDQLSLSEWD VVEWSDDQAV FTFVYDTIQL TITFEESVVG FPFLDKRYRK IVDVNFQSLL
DEDQAPPSSL LVHKLIFQYV EEKESWKKTC TTQHQLPKML EEFSLVVHHC RLLGEEIEYL
KRWGPNYNLM NIDINNNELR LLFSSSAAFA KFEITLFLSA YYPSVPLPST IQNHVGNTSQ
DDIATILSKV PLENNYLKNV VKQIYQDLFQ DCHFYH*

speed

0.84 s

mutation t@sting

documentation

Prediction

polymorphism

Model: without_aae, prob: 9.42704647865886e-14 (classification due to TGP/ExAC, real probability is shown anyway) (explain)

Summary

homozygous in TGP or ExAC
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr15:40914177T>CN/A show variant in all transcripts IGV

HGNC symbol

KNL1

Ensembl transcript ID

ENST00000527044

Genbank transcript ID

N/A

UniProt peptide

N/A

alteration type

single base exchange

alteration region

3'UTR

DNA changes

cDNA.2031T>C
g.27960T>C

AA changes

N/A

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

N/A

frameshift

N/A

known variant

Reference ID: rs11858113

database	homozygous (C/C)	heterozygous	allele carriers
1000G	326	1108	1434
ExAC	9787	13193	22980

regulatory features

H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	1.135	1
	0.242	1
(flanking)	3.847	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 549)

effect	gDNA position	score	detection sequence	exon-intron border
Donor marginally increased	27951	wt: 0.4935 / mu: 0.5449 (marginal change - not scored)	wt: ATCAGGTGAAAATAT mu: ATCAGGTGAAAATAC	CAGG\|tgaa
Donor increased	27952	wt: 0.47 / mu: 0.73	wt: TCAGGTGAAAATATG mu: TCAGGTGAAAATACG	AGGT\|gaaa

distance from splice site

1181

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

376 / 376

chromosome

strand

last intron/exon boundary

692

theoretical NMD boundary in CDS

266

length of CDS

342

coding sequence (CDS) position

N/A

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

2031

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

27960

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

40914177

original gDNA sequence snippet

ACTCTTATCAGGTGAAAATATGGATTTGACTGAAAGTCACA

altered gDNA sequence snippet

ACTCTTATCAGGTGAAAATACGGATTTGACTGAAAGTCACA

original cDNA sequence snippet

ACTCTTATCAGGTGAAAATATGGATTTGACTGAAAGTCACA

altered cDNA sequence snippet

ACTCTTATCAGGTGAAAATACGGATTTGACTGAAAGTCACA

wildtype AA sequence

MDGVSSEANE ENDNIERPVR RRHSSILKPP RSPLQDLRGG NERVQESNAL RNKKNSRRVS
FADTIKVFQT ESHMKIVRKS EMEETGENLL LIQNKKLEDN YCEITVFNYR TYP*

mutated AA sequence

N/A

speed

0.76 s

MutationTaster - study a chromosomal position

Results

Taster files

mutation t@sting

Prediction

polymorphism

mutation t@sting

Prediction

polymorphism

mutation t@sting

Prediction

polymorphism

Problems