Details for SLC2A1:c.188C>T, p.Thr63Met

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
4339680442931133
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE SLC2A1
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_006516.2
CDNA CHANGE c.188C>T
PROTEIN CHANGE p.Thr63Met
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
9.148e-056.152e-050.00.0017860.00.02.638e-050.03.266e-05

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign1.877081Disease causing
DBSNP ID rs200828053
1 combination linked to SLC2A1:c.188C>T, p.Thr63Met OLI706
1 disease linked to SLC2A1:c.188C>T, p.Thr63Met Isolated anencephaly

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