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Details for RNF216:c.106G>A, p.Asp36Asn

CHROMOSOME

7

GENOMIC COORDINATES

hg19	hg38
5792572	5752941

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

T

TRANSCRIPT

CDNA CHANGE

c.106G>A

PROTEIN CHANGE

p.Asp36Asn

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
Deleterious	Damaging	4.074112	Polymorphism

DBSNP ID

1 combination linked to RNF216:c.106G>A, p.Asp36Asn

1 disease linked to RNF216:c.106G>A, p.Asp36Asn

Normosmic congenital hypogonadotropic hypogonadism

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