Details for NKX2-5:c.639_641dup, p.Pro214dup

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
172659905173232902
VARIANT EFFECT None
ANNOTATION FLAG None
GENE NKX2-5
REFERENCE ALLELE A
ALTERNATE ALLELE AGGC
TRANSCRIPT N.A.
CDNA CHANGE c.639_641dup
PROTEIN CHANGE p.Pro214dup
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone2.182453Polymorphism
DBSNP ID NA
1 combination linked to NKX2-5:c.639_641dup, p.Pro214dup OLI1506
1 disease linked to NKX2-5:c.639_641dup, p.Pro214dup Congenital hypothyroidism

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