Details for TG:c.2307G>A, p.Trp769Ter

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
133900359132888114
VARIANT EFFECT None
ANNOTATION FLAG None
GENE TG
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE c.2307G>A
PROTEIN CHANGE p.Trp769Ter
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone7.560745Disease causing
DBSNP ID NA
1 combination linked to TG:c.2307G>A, p.Trp769Ter OLI990
1 disease linked to TG:c.2307G>A, p.Trp769Ter Congenital hypothyroidism
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