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Details for CRY1:c.1292G>A, p.Arg431His

CHROMOSOME

12

GENOMIC COORDINATES

hg19	hg38
107391466	106997688

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

T

TRANSCRIPT

CDNA CHANGE

c.1292G>A

PROTEIN CHANGE

p.Arg431His

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
0.0003361	0.0	0.0	9.948e-05	0.004135	0.0	3.536e-05	0.0	9.809e-05

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	3.314322	Disease causing

DBSNP ID

1 combination linked to CRY1:c.1292G>A, p.Arg431His

1 disease linked to CRY1:c.1292G>A, p.Arg431His

Normosmic congenital hypogonadotropic hypogonadism

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