Details for TG:c.4932dupG, p.Gln1644fs

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
133945922132933677
VARIANT EFFECT None
ANNOTATION FLAG None
GENE TG
REFERENCE ALLELE G
ALTERNATE ALLELE GG
TRANSCRIPT N.A.
CDNA CHANGE c.4932dupG
PROTEIN CHANGE p.Gln1644fs
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone3.651083Disease causing
DBSNP ID NA
1 combination linked to TG:c.4932dupG, p.Gln1644fs OLI1503
1 disease linked to TG:c.4932dupG, p.Gln1644fs Congenital hypothyroidism
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