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Details for UNC13D:c.1232G>A, p.Arg411Gln

CHROMOSOME

17

GENOMIC COORDINATES

hg19	hg38
73832719	75836638

VARIANT EFFECT

missense

ANNOTATION FLAG

manually_attributed

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

T

TRANSCRIPT

CDNA CHANGE

c.1232G>A

PROTEIN CHANGE

p.Arg411Gln

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
0.0008	0.0	0.0	0.004	0.0	0.0

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
0.0005861	0.0	0.0	0.0	0.007832	0.0	8.817e-06	0.0001632	3.266e-05

ESP
AA	EA
0.0	0.0001163

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Tolerated	Benign	2.954872	Disease causing

DBSNP ID

1 combination linked to UNC13D:c.1232G>A, p.Arg411Gln

1 disease linked to UNC13D:c.1232G>A, p.Arg411Gln

Familial hemophagocytic lymphohistiocytosis

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