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 4 transcript(s)...
Querying Taster for transcript #1: ENST00000406846
Querying Taster for transcript #2: ENST00000304421
Querying Taster for transcript #3: ENST00000346173
Querying Taster for transcript #4: ENST00000541117
MT speed 0 s - this script 5.990948 s

Results

genesymbol	prediction	probability	model	prediction problem	splicing	ClinVar	amino acid changes	variant type	dbSNP ID	protein length	file
FSHR	disease_causing	0.99706297505512	simple_aae		affected		I160T	single base exchange	rs121909659		show file
FSHR	disease_causing	0.999995003247476	simple_aae		affected		I160T	single base exchange	rs121909659		show file
FSHR	disease_causing	1	without_aae		affected			single base exchange	rs121909659		show file
FSHR	disease_causing	1	without_aae		affected			single base exchange	rs121909659		show file

Taster files

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.99706297505512 (explain)

Summary

amino acid sequence changed
known as potential disease variant: rs16244 (probable pathogenic)
known disease mutation at this position (HGMD CM980772)
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr2:49216161A>GN/A show variant in all transcripts IGV

HGNC symbol

FSHR

Ensembl transcript ID

ENST00000346173

Genbank transcript ID

N/A

UniProt peptide

P23945

alteration type

single base exchange

alteration region

CDS

DNA changes

c.479T>C
cDNA.589T>C
g.165516T>C

AA changes

I160T Score: 89 explain score(s)

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

160

frameshift

known variant

Reference ID: rs121909659

database	homozygous (G/G)	heterozygous	allele carriers
1000G	-	-	-
ExAC	0	3	3

known as potential disease variant: rs16244 (probable pathogenic for Ovarian hyperstimulation syndrome|Ovarian dysgenesis 1|not provided) dbSNP NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM980772)

known disease mutation at this position, please check HGMD for details (HGMD ID CM980772)
known disease mutation at this position, please check HGMD for details (HGMD ID CM980772)

regulatory features

N/A

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	0.938	0.993
	3.139	0.973
(flanking)	-0.887	0.001

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 increased	165521	wt: 0.38 / mu: 0.56	wt: TTGAAAGAAATTCTT mu: CTGAAAGAAATTCTT	GAAA\|gaaa
Donor marginally increased	165510	wt: 0.8327 / mu: 0.8572 (marginal change - not scored)	wt: CATCCACACAATTGA mu: CATCCACACAACTGA	TCCA\|caca
Donor marginally increased	165516	wt: 0.8877 / mu: 0.9086 (marginal change - not scored)	wt: CACAATTGAAAGAAA mu: CACAACTGAAAGAAA	CAAT\|tgaa
Donor increased	165520	wt: 0.53 / mu: 0.91	wt: ATTGAAAGAAATTCT mu: ACTGAAAGAAATTCT	TGAA\|agaa
Donor marginally increased	165515	wt: 0.8867 / mu: 0.9637 (marginal change - not scored)	wt: ACACAATTGAAAGAA mu: ACACAACTGAAAGAA	ACAA\|ttga

distance from splice site

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

160

mutated

not conserved

160

Ptroglodytes

all identical

ENSPTRG00000011914

160

Mmulatta

all identical

ENSMMUG00000017196

160

Fcatus

not conserved

ENSFCAG00000001215

160

Mmusculus

all identical

ENSMUSG00000032937

160

Ggallus

all conserved

ENSGALG00000009100

192

Trubripes

no homologue

Drerio

all identical

ENSDARG00000071494

166

Dmelanogaster

not conserved

FBgn0016650

363

CCAFQFP

Celegans

all conserved

C50H2.1

294

Xtropicalis

all identical

ENSXETG00000025827

protein features

start (aa)	end (aa)	feature	details
18	366	TOPO_DOM	Extracellular (Potential).	lost
144	169	REPEAT	LRR 5.	lost
168	171	STRAND		might get lost (downstream of altered splice site)
170	192	REPEAT	LRR 6.	might get lost (downstream of altered splice site)
173	176	STRAND		might get lost (downstream of altered splice site)
187	192	TURN		might get lost (downstream of altered splice site)
191	191	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
193	199	STRAND		might get lost (downstream of altered splice site)
193	216	REPEAT	LRR 7.	might get lost (downstream of altered splice site)
197	198	CONFLICT	EL -> AV (in Ref. 1; AAA52477).	might get lost (downstream of altered splice site)
199	199	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
211	216	TURN		might get lost (downstream of altered splice site)
217	240	REPEAT	LRR 8.	might get lost (downstream of altered splice site)
221	224	STRAND		might get lost (downstream of altered splice site)
235	237	STRAND		might get lost (downstream of altered splice site)
241	259	REPEAT	LRR 9.	might get lost (downstream of altered splice site)
243	245	STRAND		might get lost (downstream of altered splice site)
258	260	TURN		might get lost (downstream of altered splice site)
266	268	STRAND		might get lost (downstream of altered splice site)
272	280	HELIX		might get lost (downstream of altered splice site)
293	293	CARBOHYD	N-linked (GlcNAc...) (By similarity).	might get lost (downstream of altered splice site)
295	295	CONFLICT	S -> P (in Ref. 8; CAA48179).	might get lost (downstream of altered splice site)
318	318	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
345	348	STRAND		might get lost (downstream of altered splice site)
367	387	TRANSMEM	Helical; Name=1; (Potential).	might get lost (downstream of altered splice site)
388	398	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
399	421	TRANSMEM	Helical; Name=2; (Potential).	might get lost (downstream of altered splice site)
422	443	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
442	442	DISULFID	By similarity.	might get lost (downstream of altered splice site)
444	465	TRANSMEM	Helical; Name=3; (Potential).	might get lost (downstream of altered splice site)
466	485	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
486	508	TRANSMEM	Helical; Name=4; (Potential).	might get lost (downstream of altered splice site)
509	528	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
517	517	DISULFID	By similarity.	might get lost (downstream of altered splice site)
529	550	TRANSMEM	Helical; Name=5; (Potential).	might get lost (downstream of altered splice site)
551	573	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
574	597	TRANSMEM	Helical; Name=6; (Potential).	might get lost (downstream of altered splice site)
598	608	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
609	630	TRANSMEM	Helical; Name=7; (Potential).	might get lost (downstream of altered splice site)
631	695	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

1902 / 1902

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

634 / 634

position of stopcodon in wt / mu cDNA

2012 / 2012

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

111 / 111

chromosome

strand

-1

last intron/exon boundary

779

theoretical NMD boundary in CDS

618

length of CDS

1902

coding sequence (CDS) position

479

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

589

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

165516

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

49216161

original gDNA sequence snippet

TAACATAAACATCCACACAATTGAAAGAAATTCTTTCGTGG

altered gDNA sequence snippet

TAACATAAACATCCACACAACTGAAAGAAATTCTTTCGTGG

original cDNA sequence snippet

TAACATAAACATCCACACAATTGAAAGAAATTCTTTCGTGG

altered cDNA sequence snippet

TAACATAAACATCCACACAACTGAAAGAAATTCTTTCGTGG

wildtype AA sequence

MALLLVSLLA FLSLGSGCHH RICHCSNRVF LCQESKVTEI PSDLPRNAIE LRFVLTKLRV
IQKGAFSGFG DLEKIEISQN DVLEVIEADV FSNLPKLHEI RIEKANNLLY INPEAFQNLP
NLQYLLISNT GIKHLPDVHK IHSLQKVLLD IQDNINIHTI ERNSFVGLSF ESVILWLNKN
GIQEIHNCAF NGTQLDELNL SDNNNLEELP NDVFHGASGP VILSELHPIC NKSILRQEVD
YMTQARGQRS SLAEDNESSY SRGFDMTYTE FDYDLCNEVV DVTCSPKPDA FNPCEDIMGY
NILRVLIWFI SILAITGNII VLVILTTSQY KLTVPRFLMC NLAFADLCIG IYLLLIASVD
IHTKSQYHNY AIDWQTGAGC DAAGFFTVFA SELSVYTLTA ITLERWHTIT HAMQLDCKVQ
LRHAASVMVM GWIFAFAAAL FPIFGISSYM KVSICLPMDI DSPLSQLYVM SLLVLNVLAF
VVICGCYIHI YLTVRNPNIV SSSSDTRIAK RMAMLIFTDF LCMAPISFFA ISASLKVPLI
TVSKAKILLV LFHPINSCAN PFLYAIFTKN FRRDFFILLS KCGCYEMQAQ IYRTETSSTV
HNTHPRNGHC SSAPRVTSGS TYILVPLSHL AQN*

mutated AA sequence

MALLLVSLLA FLSLGSGCHH RICHCSNRVF LCQESKVTEI PSDLPRNAIE LRFVLTKLRV
IQKGAFSGFG DLEKIEISQN DVLEVIEADV FSNLPKLHEI RIEKANNLLY INPEAFQNLP
NLQYLLISNT GIKHLPDVHK IHSLQKVLLD IQDNINIHTT ERNSFVGLSF ESVILWLNKN
GIQEIHNCAF NGTQLDELNL SDNNNLEELP NDVFHGASGP VILSELHPIC NKSILRQEVD
YMTQARGQRS SLAEDNESSY SRGFDMTYTE FDYDLCNEVV DVTCSPKPDA FNPCEDIMGY
NILRVLIWFI SILAITGNII VLVILTTSQY KLTVPRFLMC NLAFADLCIG IYLLLIASVD
IHTKSQYHNY AIDWQTGAGC DAAGFFTVFA SELSVYTLTA ITLERWHTIT HAMQLDCKVQ
LRHAASVMVM GWIFAFAAAL FPIFGISSYM KVSICLPMDI DSPLSQLYVM SLLVLNVLAF
VVICGCYIHI YLTVRNPNIV SSSSDTRIAK RMAMLIFTDF LCMAPISFFA ISASLKVPLI
TVSKAKILLV LFHPINSCAN PFLYAIFTKN FRRDFFILLS KCGCYEMQAQ IYRTETSSTV
HNTHPRNGHC SSAPRVTSGS TYILVPLSHL AQN*

speed

1.35 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: 0.999995003247476 (explain)

Summary

amino acid sequence changed
known as potential disease variant: rs16244 (probable pathogenic)
known disease mutation at this position (HGMD CM980772)
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr2:49216161A>GN/A show variant in all transcripts IGV

HGNC symbol

FSHR

Ensembl transcript ID

ENST00000406846

Genbank transcript ID

NM_000145

UniProt peptide

P23945

alteration type

single base exchange

alteration region

CDS

DNA changes

c.479T>C
cDNA.599T>C
g.165516T>C

AA changes

I160T Score: 89 explain score(s)

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

160

frameshift

known variant

Reference ID: rs121909659

database	homozygous (G/G)	heterozygous	allele carriers
1000G	-	-	-
ExAC	0	3	3

regulatory features

N/A

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	0.938	0.993
	3.139	0.973
(flanking)	-0.887	0.001

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 increased	165521	wt: 0.38 / mu: 0.56	wt: TTGAAAGAAATTCTT mu: CTGAAAGAAATTCTT	GAAA\|gaaa
Donor marginally increased	165510	wt: 0.8327 / mu: 0.8572 (marginal change - not scored)	wt: CATCCACACAATTGA mu: CATCCACACAACTGA	TCCA\|caca
Donor marginally increased	165516	wt: 0.8877 / mu: 0.9086 (marginal change - not scored)	wt: CACAATTGAAAGAAA mu: CACAACTGAAAGAAA	CAAT\|tgaa
Donor increased	165520	wt: 0.53 / mu: 0.91	wt: ATTGAAAGAAATTCT mu: ACTGAAAGAAATTCT	TGAA\|agaa
Donor marginally increased	165515	wt: 0.8867 / mu: 0.9637 (marginal change - not scored)	wt: ACACAATTGAAAGAA mu: ACACAACTGAAAGAA	ACAA\|ttga

distance from splice site

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

160

mutated

not conserved

160

Ptroglodytes

all identical

ENSPTRG00000011914

160

Mmulatta

all identical

ENSMMUG00000017196

160

Fcatus

not conserved

ENSFCAG00000001215

160

Mmusculus

all identical

ENSMUSG00000032937

160

Ggallus

all identical

ENSGALG00000009100

160

Trubripes

no homologue

Drerio

all identical

ENSDARG00000071494

166

Dmelanogaster

all identical

FBgn0016650

246

Celegans

all identical

C50H2.1

196

DLS

Xtropicalis

all identical

ENSXETG00000025827

protein features

start (aa)	end (aa)	feature	details
18	366	TOPO_DOM	Extracellular (Potential).	lost
144	169	REPEAT	LRR 5.	lost
168	171	STRAND		might get lost (downstream of altered splice site)
170	192	REPEAT	LRR 6.	might get lost (downstream of altered splice site)
173	176	STRAND		might get lost (downstream of altered splice site)
187	192	TURN		might get lost (downstream of altered splice site)
191	191	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
193	199	STRAND		might get lost (downstream of altered splice site)
193	216	REPEAT	LRR 7.	might get lost (downstream of altered splice site)
197	198	CONFLICT	EL -> AV (in Ref. 1; AAA52477).	might get lost (downstream of altered splice site)
199	199	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
211	216	TURN		might get lost (downstream of altered splice site)
217	240	REPEAT	LRR 8.	might get lost (downstream of altered splice site)
221	224	STRAND		might get lost (downstream of altered splice site)
235	237	STRAND		might get lost (downstream of altered splice site)
241	259	REPEAT	LRR 9.	might get lost (downstream of altered splice site)
243	245	STRAND		might get lost (downstream of altered splice site)
258	260	TURN		might get lost (downstream of altered splice site)
266	268	STRAND		might get lost (downstream of altered splice site)
272	280	HELIX		might get lost (downstream of altered splice site)
293	293	CARBOHYD	N-linked (GlcNAc...) (By similarity).	might get lost (downstream of altered splice site)
295	295	CONFLICT	S -> P (in Ref. 8; CAA48179).	might get lost (downstream of altered splice site)
318	318	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
345	348	STRAND		might get lost (downstream of altered splice site)
367	387	TRANSMEM	Helical; Name=1; (Potential).	might get lost (downstream of altered splice site)
388	398	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
399	421	TRANSMEM	Helical; Name=2; (Potential).	might get lost (downstream of altered splice site)
422	443	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
442	442	DISULFID	By similarity.	might get lost (downstream of altered splice site)
444	465	TRANSMEM	Helical; Name=3; (Potential).	might get lost (downstream of altered splice site)
466	485	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
486	508	TRANSMEM	Helical; Name=4; (Potential).	might get lost (downstream of altered splice site)
509	528	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
517	517	DISULFID	By similarity.	might get lost (downstream of altered splice site)
529	550	TRANSMEM	Helical; Name=5; (Potential).	might get lost (downstream of altered splice site)
551	573	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
574	597	TRANSMEM	Helical; Name=6; (Potential).	might get lost (downstream of altered splice site)
598	608	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
609	630	TRANSMEM	Helical; Name=7; (Potential).	might get lost (downstream of altered splice site)
631	695	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

2088 / 2088

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

696 / 696

position of stopcodon in wt / mu cDNA

2208 / 2208

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

-1

last intron/exon boundary

975

theoretical NMD boundary in CDS

804

length of CDS

2088

coding sequence (CDS) position

479

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

599

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

165516

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

49216161

original gDNA sequence snippet

TAACATAAACATCCACACAATTGAAAGAAATTCTTTCGTGG

altered gDNA sequence snippet

TAACATAAACATCCACACAACTGAAAGAAATTCTTTCGTGG

original cDNA sequence snippet

TAACATAAACATCCACACAATTGAAAGAAATTCTTTCGTGG

altered cDNA sequence snippet

TAACATAAACATCCACACAACTGAAAGAAATTCTTTCGTGG

wildtype AA sequence

MALLLVSLLA FLSLGSGCHH RICHCSNRVF LCQESKVTEI PSDLPRNAIE LRFVLTKLRV
IQKGAFSGFG DLEKIEISQN DVLEVIEADV FSNLPKLHEI RIEKANNLLY INPEAFQNLP
NLQYLLISNT GIKHLPDVHK IHSLQKVLLD IQDNINIHTI ERNSFVGLSF ESVILWLNKN
GIQEIHNCAF NGTQLDELNL SDNNNLEELP NDVFHGASGP VILDISRTRI HSLPSYGLEN
LKKLRARSTY NLKKLPTLEK LVALMEASLT YPSHCCAFAN WRRQISELHP ICNKSILRQE
VDYMTQARGQ RSSLAEDNES SYSRGFDMTY TEFDYDLCNE VVDVTCSPKP DAFNPCEDIM
GYNILRVLIW FISILAITGN IIVLVILTTS QYKLTVPRFL MCNLAFADLC IGIYLLLIAS
VDIHTKSQYH NYAIDWQTGA GCDAAGFFTV FASELSVYTL TAITLERWHT ITHAMQLDCK
VQLRHAASVM VMGWIFAFAA ALFPIFGISS YMKVSICLPM DIDSPLSQLY VMSLLVLNVL
AFVVICGCYI HIYLTVRNPN IVSSSSDTRI AKRMAMLIFT DFLCMAPISF FAISASLKVP
LITVSKAKIL LVLFHPINSC ANPFLYAIFT KNFRRDFFIL LSKCGCYEMQ AQIYRTETSS
TVHNTHPRNG HCSSAPRVTS GSTYILVPLS HLAQN*

mutated AA sequence

MALLLVSLLA FLSLGSGCHH RICHCSNRVF LCQESKVTEI PSDLPRNAIE LRFVLTKLRV
IQKGAFSGFG DLEKIEISQN DVLEVIEADV FSNLPKLHEI RIEKANNLLY INPEAFQNLP
NLQYLLISNT GIKHLPDVHK IHSLQKVLLD IQDNINIHTT ERNSFVGLSF ESVILWLNKN
GIQEIHNCAF NGTQLDELNL SDNNNLEELP NDVFHGASGP VILDISRTRI HSLPSYGLEN
LKKLRARSTY NLKKLPTLEK LVALMEASLT YPSHCCAFAN WRRQISELHP ICNKSILRQE
VDYMTQARGQ RSSLAEDNES SYSRGFDMTY TEFDYDLCNE VVDVTCSPKP DAFNPCEDIM
GYNILRVLIW FISILAITGN IIVLVILTTS QYKLTVPRFL MCNLAFADLC IGIYLLLIAS
VDIHTKSQYH NYAIDWQTGA GCDAAGFFTV FASELSVYTL TAITLERWHT ITHAMQLDCK
VQLRHAASVM VMGWIFAFAA ALFPIFGISS YMKVSICLPM DIDSPLSQLY VMSLLVLNVL
AFVVICGCYI HIYLTVRNPN IVSSSSDTRI AKRMAMLIFT DFLCMAPISF FAISASLKVP
LITVSKAKIL LVLFHPINSC ANPFLYAIFT KNFRRDFFIL LSKCGCYEMQ AQIYRTETSS
TVHNTHPRNG HCSSAPRVTS GSTYILVPLS HLAQN*

speed

1.32 s

mutation t@sting

documentation

Prediction

disease causing

Model: without_aae, prob: 1 (explain)

Summary

known as potential disease variant: rs16244 (probable pathogenic)
known disease mutation at this position (HGMD CM980772)
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr2:49216161A>GN/A show variant in all transcripts IGV

HGNC symbol

FSHR

Ensembl transcript ID

ENST00000304421

Genbank transcript ID

NM_181446

UniProt peptide

P23945

alteration type

single base exchange

alteration region

intron

DNA changes

g.165516T>C

AA changes

N/A

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

N/A

frameshift

N/A

known variant

Reference ID: rs121909659

database	homozygous (G/G)	heterozygous	allele carriers
1000G	-	-	-
ExAC	0	3	3

regulatory features

N/A

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	0.938	0.993
	3.139	0.973
(flanking)	-0.887	0.001

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 increased	165521	wt: 0.38 / mu: 0.56	wt: TTGAAAGAAATTCTT mu: CTGAAAGAAATTCTT	GAAA\|gaaa
Donor marginally increased	165510	wt: 0.8327 / mu: 0.8572 (marginal change - not scored)	wt: CATCCACACAATTGA mu: CATCCACACAACTGA	TCCA\|caca
Donor marginally increased	165516	wt: 0.8877 / mu: 0.9086 (marginal change - not scored)	wt: CACAATTGAAAGAAA mu: CACAACTGAAAGAAA	CAAT\|tgaa
Donor increased	165520	wt: 0.53 / mu: 0.91	wt: ATTGAAAGAAATTCT mu: ACTGAAAGAAATTCT	TGAA\|agaa
Donor marginally increased	165515	wt: 0.8867 / mu: 0.9637 (marginal change - not scored)	wt: ACACAATTGAAAGAA mu: ACACAACTGAAAGAA	ACAA\|ttga

distance from splice site

1544

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

N/A

protein features

start (aa)	end (aa)	feature	details
18	366	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
144	169	REPEAT	LRR 5.	might get lost (downstream of altered splice site)
147	153	STRAND		might get lost (downstream of altered splice site)
168	171	STRAND		might get lost (downstream of altered splice site)
170	192	REPEAT	LRR 6.	might get lost (downstream of altered splice site)
173	176	STRAND		might get lost (downstream of altered splice site)
187	192	TURN		might get lost (downstream of altered splice site)
191	191	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
193	199	STRAND		might get lost (downstream of altered splice site)
193	216	REPEAT	LRR 7.	might get lost (downstream of altered splice site)
197	198	CONFLICT	EL -> AV (in Ref. 1; AAA52477).	might get lost (downstream of altered splice site)
199	199	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
211	216	TURN		might get lost (downstream of altered splice site)
217	240	REPEAT	LRR 8.	might get lost (downstream of altered splice site)
221	224	STRAND		might get lost (downstream of altered splice site)
235	237	STRAND		might get lost (downstream of altered splice site)
241	259	REPEAT	LRR 9.	might get lost (downstream of altered splice site)
243	245	STRAND		might get lost (downstream of altered splice site)
258	260	TURN		might get lost (downstream of altered splice site)
266	268	STRAND		might get lost (downstream of altered splice site)
272	280	HELIX		might get lost (downstream of altered splice site)
293	293	CARBOHYD	N-linked (GlcNAc...) (By similarity).	might get lost (downstream of altered splice site)
295	295	CONFLICT	S -> P (in Ref. 8; CAA48179).	might get lost (downstream of altered splice site)
318	318	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
345	348	STRAND		might get lost (downstream of altered splice site)
367	387	TRANSMEM	Helical; Name=1; (Potential).	might get lost (downstream of altered splice site)
388	398	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
399	421	TRANSMEM	Helical; Name=2; (Potential).	might get lost (downstream of altered splice site)
422	443	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
442	442	DISULFID	By similarity.	might get lost (downstream of altered splice site)
444	465	TRANSMEM	Helical; Name=3; (Potential).	might get lost (downstream of altered splice site)
466	485	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
486	508	TRANSMEM	Helical; Name=4; (Potential).	might get lost (downstream of altered splice site)
509	528	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
517	517	DISULFID	By similarity.	might get lost (downstream of altered splice site)
529	550	TRANSMEM	Helical; Name=5; (Potential).	might get lost (downstream of altered splice site)
551	573	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
574	597	TRANSMEM	Helical; Name=6; (Potential).	might get lost (downstream of altered splice site)
598	608	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
609	630	TRANSMEM	Helical; Name=7; (Potential).	might get lost (downstream of altered splice site)
631	695	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)

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

N/A

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

N/A

position of start ATG in wt / mu cDNA

65 / 65

chromosome

strand

-1

last intron/exon boundary

841

theoretical NMD boundary in CDS

726

length of CDS

2010

coding sequence (CDS) position

N/A

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

N/A

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

165516

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

49216161

original gDNA sequence snippet

TAACATAAACATCCACACAATTGAAAGAAATTCTTTCGTGG

altered gDNA sequence snippet

TAACATAAACATCCACACAACTGAAAGAAATTCTTTCGTGG

original cDNA sequence snippet

N/A

altered cDNA sequence snippet

N/A

wildtype AA sequence

MALLLVSLLA FLSLGSGCHH RICHCSNRVF LCQESKVTEI PSDLPRNAIE LRFVLTKLRV
IQKGAFSGFG DLEKIEISQN DVLEVIEADV FSNLPKLHEI RIEKANNLLY INPEAFQNLP
NLQYLLISNT GIKHLPDVHK IHSLQKVLLW LNKNGIQEIH NCAFNGTQLD ELNLSDNNNL
EELPNDVFHG ASGPVILDIS RTRIHSLPSY GLENLKKLRA RSTYNLKKLP TLEKLVALME
ASLTYPSHCC AFANWRRQIS ELHPICNKSI LRQEVDYMTQ ARGQRSSLAE DNESSYSRGF
DMTYTEFDYD LCNEVVDVTC SPKPDAFNPC EDIMGYNILR VLIWFISILA ITGNIIVLVI
LTTSQYKLTV PRFLMCNLAF ADLCIGIYLL LIASVDIHTK SQYHNYAIDW QTGAGCDAAG
FFTVFASELS VYTLTAITLE RWHTITHAMQ LDCKVQLRHA ASVMVMGWIF AFAAALFPIF
GISSYMKVSI CLPMDIDSPL SQLYVMSLLV LNVLAFVVIC GCYIHIYLTV RNPNIVSSSS
DTRIAKRMAM LIFTDFLCMA PISFFAISAS LKVPLITVSK AKILLVLFHP INSCANPFLY
AIFTKNFRRD FFILLSKCGC YEMQAQIYRT ETSSTVHNTH PRNGHCSSAP RVTSGSTYIL
VPLSHLAQN*

mutated AA sequence

N/A

speed

0.94 s

mutation t@sting

documentation

Prediction

disease causing

Model: without_aae, prob: 1 (explain)

Summary

known as potential disease variant: rs16244 (probable pathogenic)
known disease mutation at this position (HGMD CM980772)
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr2:49216161A>GN/A show variant in all transcripts IGV

HGNC symbol

FSHR

Ensembl transcript ID

ENST00000541117

Genbank transcript ID

N/A

UniProt peptide

P23945

alteration type

single base exchange

alteration region

5'UTR

DNA changes

cDNA.240T>C
g.165516T>C

AA changes

N/A

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

N/A

frameshift

N/A

known variant

Reference ID: rs121909659

database	homozygous (G/G)	heterozygous	allele carriers
1000G	-	-	-
ExAC	0	3	3

regulatory features

N/A

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	0.938	0.993
	3.139	0.973
(flanking)	-0.887	0.001

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

splice sites

splice site change before start ATG (at aa -102) | splice site change before start ATG (at aa -101) |

effect	gDNA position	score	detection sequence	exon-intron border
Donor increased	165521	wt: 0.38 / mu: 0.56	wt: TTGAAAGAAATTCTT mu: CTGAAAGAAATTCTT	GAAA\|gaaa
Donor marginally increased	165510	wt: 0.8327 / mu: 0.8572 (marginal change - not scored)	wt: CATCCACACAATTGA mu: CATCCACACAACTGA	TCCA\|caca
Donor marginally increased	165516	wt: 0.8877 / mu: 0.9086 (marginal change - not scored)	wt: CACAATTGAAAGAAA mu: CACAACTGAAAGAAA	CAAT\|tgaa
Donor increased	165520	wt: 0.53 / mu: 0.91	wt: ATTGAAAGAAATTCT mu: ACTGAAAGAAATTCT	TGAA\|agaa
Donor marginally increased	165515	wt: 0.8867 / mu: 0.9637 (marginal change - not scored)	wt: ACACAATTGAAAGAA mu: ACACAACTGAAAGAA	ACAA\|ttga

distance from splice site

Kozak consensus sequence altered?

conservation
protein level for non-synonymous changes

N/A

protein features

start (aa)	end (aa)	feature	details
1	17	SIGNAL	Potential.	might get lost (downstream of altered splice site)
13	13	CONFLICT	S -> R (in Ref. 8; CAA48179).	might get lost (downstream of altered splice site)
18	18	DISULFID		might get lost (downstream of altered splice site)
18	46	DOMAIN	LRRNT.	might get lost (downstream of altered splice site)
18	366	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
21	26	STRAND		might get lost (downstream of altered splice site)
23	23	DISULFID		might get lost (downstream of altered splice site)
25	25	DISULFID		might get lost (downstream of altered splice site)
29	34	STRAND		might get lost (downstream of altered splice site)
32	32	DISULFID		might get lost (downstream of altered splice site)
49	55	STRAND		might get lost (downstream of altered splice site)
49	72	REPEAT	LRR 1.	might get lost (downstream of altered splice site)
59	61	STRAND		might get lost (downstream of altered splice site)
63	68	TURN		might get lost (downstream of altered splice site)
73	97	REPEAT	LRR 2.	might get lost (downstream of altered splice site)
74	78	STRAND		might get lost (downstream of altered splice site)
88	93	STRAND		might get lost (downstream of altered splice site)
98	118	REPEAT	LRR 3.	might get lost (downstream of altered splice site)
99	105	STRAND		might get lost (downstream of altered splice site)
112	112	CONFLICT	N -> T (in Ref. 1; AAA52477).	might get lost (downstream of altered splice site)
115	117	STRAND		might get lost (downstream of altered splice site)
119	143	REPEAT	LRR 4.	might get lost (downstream of altered splice site)
124	130	STRAND		might get lost (downstream of altered splice site)
143	145	STRAND		might get lost (downstream of altered splice site)
144	169	REPEAT	LRR 5.	might get lost (downstream of altered splice site)
147	153	STRAND		might get lost (downstream of altered splice site)
168	171	STRAND		might get lost (downstream of altered splice site)
170	192	REPEAT	LRR 6.	might get lost (downstream of altered splice site)
173	176	STRAND		might get lost (downstream of altered splice site)
187	192	TURN		might get lost (downstream of altered splice site)
191	191	CARBOHYD	N-linked (GlcNAc...).	might get lost (downstream of altered splice site)
193	199	STRAND		might get lost (downstream of altered splice site)
193	216	REPEAT	LRR 7.	might get lost (downstream of altered splice site)
197	198	CONFLICT	EL -> AV (in Ref. 1; AAA52477).	might get lost (downstream of altered splice site)
199	199	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
211	216	TURN		might get lost (downstream of altered splice site)
217	240	REPEAT	LRR 8.	might get lost (downstream of altered splice site)
221	224	STRAND		might get lost (downstream of altered splice site)
235	237	STRAND		might get lost (downstream of altered splice site)
241	259	REPEAT	LRR 9.	might get lost (downstream of altered splice site)
243	245	STRAND		might get lost (downstream of altered splice site)
258	260	TURN		might get lost (downstream of altered splice site)
266	268	STRAND		might get lost (downstream of altered splice site)
272	280	HELIX		might get lost (downstream of altered splice site)
293	293	CARBOHYD	N-linked (GlcNAc...) (By similarity).	might get lost (downstream of altered splice site)
295	295	CONFLICT	S -> P (in Ref. 8; CAA48179).	might get lost (downstream of altered splice site)
318	318	CARBOHYD	N-linked (GlcNAc...) (Potential).	might get lost (downstream of altered splice site)
345	348	STRAND		might get lost (downstream of altered splice site)
367	387	TRANSMEM	Helical; Name=1; (Potential).	might get lost (downstream of altered splice site)
388	398	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
399	421	TRANSMEM	Helical; Name=2; (Potential).	might get lost (downstream of altered splice site)
422	443	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
442	442	DISULFID	By similarity.	might get lost (downstream of altered splice site)
444	465	TRANSMEM	Helical; Name=3; (Potential).	might get lost (downstream of altered splice site)
466	485	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
486	508	TRANSMEM	Helical; Name=4; (Potential).	might get lost (downstream of altered splice site)
509	528	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
517	517	DISULFID	By similarity.	might get lost (downstream of altered splice site)
529	550	TRANSMEM	Helical; Name=5; (Potential).	might get lost (downstream of altered splice site)
551	573	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)
574	597	TRANSMEM	Helical; Name=6; (Potential).	might get lost (downstream of altered splice site)
598	608	TOPO_DOM	Extracellular (Potential).	might get lost (downstream of altered splice site)
609	630	TRANSMEM	Helical; Name=7; (Potential).	might get lost (downstream of altered splice site)
631	695	TOPO_DOM	Cytoplasmic (Potential).	might get lost (downstream of altered splice site)

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

N/A

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

N/A

position of start ATG in wt / mu cDNA

554 / 554

chromosome

strand

-1

last intron/exon boundary

616

theoretical NMD boundary in CDS

length of CDS

1296

coding sequence (CDS) position

N/A

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

240

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

165516

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

49216161

original gDNA sequence snippet

TAACATAAACATCCACACAATTGAAAGAAATTCTTTCGTGG

altered gDNA sequence snippet

TAACATAAACATCCACACAACTGAAAGAAATTCTTTCGTGG

original cDNA sequence snippet

TAACATAAACATCCACACAATTGAAAGAAATTCTTTCGTGG

altered cDNA sequence snippet

TAACATAAACATCCACACAACTGAAAGAAATTCTTTCGTGG

wildtype AA sequence

MEASLTYPSH CCAFANWRRQ ISELHPICNK SILRQEVDYM TQARGQRSSL AEDNESSYSR
GFDMTYTEFD YDLCNEVVDV TCSPKPDAFN PCEDIMGYNI LRVLIWFISI LAITGNIIVL
VILTTSQYKL TVPRFLMCNL AFADLCIGIY LLLIASVDIH TKSQYHNYAI DWQTGAGCDA
AGFFTVFASE LSVYTLTAIT LERWHTITHA MQLDCKVQLR HAASVMVMGW IFAFAAALFP
IFGISSYMKV SICLPMDIDS PLSQLYVMSL LVLNVLAFVV ICGCYIHIYL TVRNPNIVSS
SSDTRIAKRM AMLIFTDFLC MAPISFFAIS ASLKVPLITV SKAKILLVLF HPINSCANPF
LYAIFTKNFR RDFFILLSKC GCYEMQAQIY RTETSSTVHN THPRNGHCSS APRVTSGSTY
ILVPLSHLAQ N*

mutated AA sequence

N/A

speed

1.10 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

Problems