Details for ATP2B3:c.2197G>A, p.Gly733Arg

CHROMOSOME X
GENOMIC COORDINATES
hg19hg38
152821645153556187
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE ATP2B3
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_001001344.2
CDNA CHANGE c.2197G>A
PROTEIN CHANGE p.Gly733Arg
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.946588Disease causing
DBSNP ID NA
1 combination linked to ATP2B3:c.2197G>A, p.Gly733Arg OLI503
1 disease linked to ATP2B3:c.2197G>A, p.Gly733Arg X-linked cerebellar ataxia

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