Details for FIG4:c.244G>A, p.Gly82Arg

CHROMOSOME 6
GENOMIC COORDINATES
hg19hg38
110037726109716523
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE FIG4
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_014845.5
CDNA CHANGE c.244G>A
PROTEIN CHANGE p.Gly82Arg
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
1.193e-050.00.00.00.00.02.637e-050.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.941691Disease causing
DBSNP ID rs774546266
1 combination linked to FIG4:c.244G>A, p.Gly82Arg OLI660
1 disease linked to FIG4:c.244G>A, p.Gly82Arg Amyotrophic lateral sclerosis

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