Details for TPO:c.483-2A>G,

CHROMOSOME 2
GENOMIC COORDINATES
hg19hg38
14574641453692
VARIANT EFFECT splicing
ANNOTATION FLAG automatically_attributed_and_verified
GENE TPO
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT NM_000547.5
CDNA CHANGE c.483-2A>G
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone5.016392Disease causing
DBSNP ID NA
1 combination linked to TPO:c.483-2A>G, OLI031
1 disease linked to TPO:c.483-2A>G, Congenital hypothyroidism

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