Details for NKX2-1:c.7A>T, p.Met3Leu

CHROMOSOME 14
GENOMIC COORDINATES
hg19hg38
3698855636519351
VARIANT EFFECT missense
ANNOTATION FLAG manually_attributed
GENE NKX2-1
REFERENCE ALLELE T
ALTERNATE ALLELE A
TRANSCRIPT NM_003317.4
CDNA CHANGE c.7A>T
PROTEIN CHANGE p.Met3Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.131207Disease causing
DBSNP ID NA
1 combination linked to NKX2-1:c.7A>T, p.Met3Leu OLI184
1 disease linked to NKX2-1:c.7A>T, p.Met3Leu Hirschsprung disease

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