Details for MSH4:c.1025C>T, p.Thr342Ile

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
7628812975822444
VARIANT EFFECT None
ANNOTATION FLAG None
GENE MSH4
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_002440.4
CDNA CHANGE c.1025C>T
PROTEIN CHANGE p.Thr342Ile
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
4.643e-060.00.00.06.579e-050.00.00.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.335728Disease causing
DBSNP ID NA
1 combination linked to MSH4:c.1025C>T, p.Thr342Ile OLI1730
1 disease linked to MSH4:c.1025C>T, p.Thr342Ile Primary ovarian failure

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