Details for MAMLD1:c.454C>T, p.Gln152Ter

CHROMOSOME X
GENOMIC COORDINATES
hg19hg38
149638374150470102
VARIANT EFFECT nonsense
ANNOTATION FLAG automatically_attributed_and_verified
GENE MAMLD1
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_001177465.3
CDNA CHANGE c.454C>T
PROTEIN CHANGE p.Gln152Ter
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone6.01751None
DBSNP ID NA
1 combination linked to MAMLD1:c.454C>T, p.Gln152Ter OLI347
1 disease linked to MAMLD1:c.454C>T, p.Gln152Ter 46,XY disorder of sex development

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