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Details for MYO7A:c.2882G>A, p.Gly961Asp

CHROMOSOME

11

GENOMIC COORDINATES

hg19	hg38
76892613	77181567

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

N.A.

CDNA CHANGE

c.2882G>A

PROTEIN CHANGE

p.Gly961Asp

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
0.0001453	0.002019	2.901e-05	0.0	0.0	0.0	8.931e-06	0.0003326	3.272e-05

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	4.006922	Disease causing

DBSNP ID

1 combination linked to MYO7A:c.2882G>A, p.Gly961Asp

1 disease linked to MYO7A:c.2882G>A, p.Gly961Asp

46,XY disorder of sex development

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