Details for MTOR:c.5863C>T, p.Arg1955Cys

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
1118855811128501
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE MTOR
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_004958.3
CDNA CHANGE c.5863C>T
PROTEIN CHANGE p.Arg1955Cys
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
3.976e-060.00.00.00.00.08.79e-060.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging4.676329Disease causing
DBSNP ID rs1345837094
1 combination linked to MTOR:c.5863C>T, p.Arg1955Cys OLI859
1 disease linked to MTOR:c.5863C>T, p.Arg1955Cys Kallmann syndrome

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