chr8:71215405:A>T Detail (hg38) (EYA1)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr8:72,127,640-72,127,640 View the variant detail on this assembly version.
hg38	chr8:71,215,405-71,215,405

HGVS

EYA1

Type	Transcript	Protein
RefSeq	NM_000503.5:c.1579T>A	NP_000494.2:p.Tyr527Asn
	NM_001288574.1:c.1579T>A	NP_001275503.1:p.Tyr527Asn
	NM_001288575.1:c.1579T>A	NP_001275504.1:p.Tyr527Asn
	NM_172060.3:c.1480T>A	NP_742057.1:p.Tyr494Asn
	NM_172058.3:c.1579T>A	NP_742055.1:p.Tyr527Asn
	NM_172059.3:c.1474T>A	NP_742056.1:p.Tyr492Asn
Ensemble	ENST00000303824.11:c.1561T>A	ENST00000303824.11:p.Tyr521Asn
	ENST00000340726.8:c.1579T>A	ENST00000340726.8:p.Tyr527Asn
	ENST00000388740.4:c.1480T>A	ENST00000388740.4:p.Tyr494Asn
	ENST00000388741.7:c.1477T>A	ENST00000388741.7:p.Tyr493Asn
	ENST00000388742.8:c.1579T>A	ENST00000388742.8:p.Tyr527Asn
	ENST00000388743.6:c.1576T>A	ENST00000388743.6:p.Tyr526Asn
	ENST00000419131.6:c.1474T>A	ENST00000419131.6:p.Tyr492Asn
	ENST00000643681.1:c.1666T>A	ENST00000643681.1:p.Tyr556Asn
	ENST00000644229.1:c.1561T>A	ENST00000644229.1:p.Tyr521Asn
	ENST00000644712.1:c.1558T>A	ENST00000644712.1:p.Tyr520Asn
	ENST00000645793.1:c.1579T>A	ENST00000645793.1:p.Tyr527Asn
	ENST00000647540.1:c.1579T>A	ENST00000647540.1:p.Tyr527Asn

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Likely pathogenic
Review star
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Links

EYA1

Type	Database	ID	Link
Gene	MIM	601653	OMIM
	HGNC	3519	HGNC
	Ensembl	ENSG00000104313	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely pathogenic	2017-06-20	criteria provided, single submitter	Rare genetic deafness	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.584	Branchio-Oto-Renal Syndrome	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000503.6(EYA1):c.1579T>A (p.Tyr527Asn) AND Rare genetic deafness	ClinVar	Detail
NA	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs397517918 dbSNP
Genome: hg38
Position: chr8:71,215,405-71,215,405
Variant Type: snv
Reference Allele: A
Alternative Allele: T

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