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Details for UNC13D:c.1982A>G, p.Lys661Arg

CHROMOSOME

17

GENOMIC COORDINATES

hg19	hg38
73831011	75834930

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

T

ALTERNATE ALLELE

C

TRANSCRIPT

CDNA CHANGE

c.1982A>G

PROTEIN CHANGE

p.Lys661Arg

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	3.975365	Polymorphism

DBSNP ID

1 combination linked to UNC13D:c.1982A>G, p.Lys661Arg

1 disease linked to UNC13D:c.1982A>G, p.Lys661Arg

Primary hemophagocytic lymphohistiocytosis

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