Details for TG:c.5042-2A>G,

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
133953594132941349
VARIANT EFFECT splicing
ANNOTATION FLAG automatically_attributed_and_verified
GENE TG
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT NM_003235.4
CDNA CHANGE c.5042-2A>G
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone4.910688Disease causing
DBSNP ID NA
1 combination linked to TG:c.5042-2A>G, OLI031
1 disease linked to TG:c.5042-2A>G, Congenital hypothyroidism

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