Details for NID1:c.577A>G, p.Ile193Val

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
236208932236045632
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE NID1
REFERENCE ALLELE T
ALTERNATE ALLELE C
TRANSCRIPT NM_002508.2
CDNA CHANGE c.577A>G
PROTEIN CHANGE p.Ile193Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.163537Polymorphism
DBSNP ID rs1572617750
1 combination linked to NID1:c.577A>G, p.Ile193Val OLI741
1 disease linked to NID1:c.577A>G, p.Ile193Val Isolated anencephaly

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