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Details for MYO7A:p.Val692Met

CHROMOSOME

11

GENOMIC COORDINATES

hg19	hg38
76885940	77174894

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

N.A.

CDNA CHANGE

None

PROTEIN CHANGE

p.Val692Met

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
None	None	None	None	None	None

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
None	None	None	None	None	None	None	None	None

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	3.871259	Disease causing

DBSNP ID

1 combination linked to MYO7A:p.Val692Met

1 disease linked to MYO7A:p.Val692Met

Usher syndrome type 1

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