Details for SHH:c.423C>A, p.Cys141Ter

CHROMOSOME 7
GENOMIC COORDINATES
hg19hg38
155592818155800124
VARIANT EFFECT None
ANNOTATION FLAG None
GENE SHH
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT NM_001310462
CDNA CHANGE c.423C>A
PROTEIN CHANGE p.Cys141Ter
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone0.663876Polymorphism
DBSNP ID NA
1 combination linked to SHH:c.423C>A, p.Cys141Ter OLI1552
1 disease linked to SHH:c.423C>A, p.Cys141Ter 46,XY disorder of sex development

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