MutationTaster - study a chromosomal position

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input seems to be ok - now mapping the variant to the different transcripts...
found 1 transcript(s)...
Querying Taster for transcript #1: ENST00000282561
MT speed 0.15 s - this script 2.256375 s

Results

genesymbol	prediction	probability	model	prediction problem	splicing	ClinVar	amino acid changes	variant type	dbSNP ID	protein length	file
GJA1	disease_causing	0.999999562156061	simple_aae		affected		R376Q	single base exchange	rs104893965		show file

Taster files

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999999562156061 (explain)

Summary

amino acid sequence changed
known disease mutation at this position (HGMD CM014192)
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr6:121769120G>AN/A show variant in all transcripts IGV

HGNC symbol

GJA1

Ensembl transcript ID

ENST00000282561

Genbank transcript ID

NM_000165

UniProt peptide

P17302

alteration type

single base exchange

alteration region

CDS

DNA changes

c.1127G>A
cDNA.1284G>A
g.12283G>A

AA changes

R376Q Score: 43 explain score(s)

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

376

frameshift

known variant

Reference ID: rs104893965

database	homozygous (A/A)	heterozygous	allele carriers
1000G	-	-	-
ExAC	0	22	22

known disease mutation at this position, please check HGMD for details (HGMD ID CM014192)

known disease mutation at this position, please check HGMD for details (HGMD ID CM014192)
known disease mutation at this position, please check HGMD for details (HGMD ID CM014192)

regulatory features

H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	3.546	1
	5.484	1
(flanking)	1.196	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 gained	12285	0.59	mu: CTCAGCCTGATGACC	CAGC\|ctga

distance from splice site

1143

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

376

mutated

all conserved

376

Ptroglodytes

all identical

ENSPTRG00000018560

376

Mmulatta

all identical

ENSMMUG00000005225

376

Fcatus

no homologue

Mmusculus

all identical

ENSMUSG00000050953

376

Ggallus

all identical

ENSGALG00000014873

375

Trubripes

no homologue

Drerio

all identical

ENSDARG00000041799

375

Dmelanogaster

no homologue

Celegans

no homologue

Xtropicalis

all identical

ENSXETG00000025411

373

protein features

start (aa)	end (aa)	feature	details
232	382	TOPO_DOM	Cytoplasmic (Potential).	lost

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

1149 / 1149

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

383 / 383

position of stopcodon in wt / mu cDNA

1306 / 1306

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

158 / 158

chromosome

strand

last intron/exon boundary

142

theoretical NMD boundary in CDS

cannot be calculated, too little distance between start ATG and last intron/exon boundary

length of CDS

1149

coding sequence (CDS) position

1127

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

1284

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

12283

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

121769120

original gDNA sequence snippet

TCGTGCCAGCAGCAGACCTCGGCCTGATGACCTGGAGATCT

altered gDNA sequence snippet

TCGTGCCAGCAGCAGACCTCAGCCTGATGACCTGGAGATCT

original cDNA sequence snippet

TCGTGCCAGCAGCAGACCTCGGCCTGATGACCTGGAGATCT

altered cDNA sequence snippet

TCGTGCCAGCAGCAGACCTCAGCCTGATGACCTGGAGATCT

wildtype AA sequence

MGDWSALGKL LDKVQAYSTA GGKVWLSVLF IFRILLLGTA VESAWGDEQS AFRCNTQQPG
CENVCYDKSF PISHVRFWVL QIIFVSVPTL LYLAHVFYVM RKEEKLNKKE EELKVAQTDG
VNVDMHLKQI EIKKFKYGIE EHGKVKMRGG LLRTYIISIL FKSIFEVAFL LIQWYIYGFS
LSAVYTCKRD PCPHQVDCFL SRPTEKTIFI IFMLVVSLVS LALNIIELFY VFFKGVKDRV
KGKSDPYHAT SGALSPAKDC GSQKYAYFNG CSSPTAPLSP MSPPGYKLVT GDRNNSSCRN
YNKQASEQNW ANYSAEQNRM GQAGSTISNS HAQPFDFPDD NQNSKKLAAG HELQPLAIVD
QRPSSRASSR ASSRPRPDDL EI*

mutated AA sequence

speed

0.15 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

MutationTaster - study a chromosomal position

Results

Taster files

mutation t@sting

Prediction

disease causing

Problems