Details for TRRAP:c.10171A>G, p.Met3391Val

CHROMOSOME 7
GENOMIC COORDINATES
hg19hg38
9859237598994752
VARIANT EFFECT None
ANNOTATION FLAG None
GENE TRRAP
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT N.A.
CDNA CHANGE c.10171A>G
PROTEIN CHANGE p.Met3391Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.362641Polymorphism
DBSNP ID NA
1 combination linked to TRRAP:c.10171A>G, p.Met3391Val OLI1044
1 disease linked to TRRAP:c.10171A>G, p.Met3391Val Primary ovarian failure

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