Details for GALT:c.776G>A, p.Arg259Gln

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
3464884734648850
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE GALT
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_000155.3
CDNA CHANGE c.776G>A
PROTEIN CHANGE p.Arg259Gln
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign3.774525Disease causing
DBSNP ID rs886042070
1 combination linked to GALT:c.776G>A, p.Arg259Gln OLI091
1 disease linked to GALT:c.776G>A, p.Arg259Gln Primary ovarian failure

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