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Details for SHH:c.1367G>C, p.Gly456Ala

CHROMOSOME

7

GENOMIC COORDINATES

hg19	hg38
155595616	155802922

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

G

TRANSCRIPT

CDNA CHANGE

c.1367G>C

PROTEIN CHANGE

p.Gly456Ala

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	Damaging	3.179604	Disease causing

DBSNP ID

1 combination linked to SHH:c.1367G>C, p.Gly456Ala

1 disease linked to SHH:c.1367G>C, p.Gly456Ala

46,XY disorder of sex development

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