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HomeVariants

chr2:47639682 C>T

Annotations

GeneMSH2
TranscriptNM_000251.2
cDNAc.775C>T
Proteinp.P259S
Functionmissense
Localizationexon
hg19chr2:47639682 C>T

Synonyms

TranscriptcDNAProtein
NM_001258281.1c.577C>Tp.P193S
XR_001738747.1n.847C>T
XR_939685.1n.847C>T

Frequency in gnomAD

GenomeExome
MAX0.000008959
AFR0
AMR0
ASJ0
EAS0
FIN0
NFE0.000008959
SAS0

ClinVar

IDPhenotypeEffect
RCV000228319.3Hereditary nonpolyposis colon cancerVUS
RCV000235651.2not specifiedVUS
RCV000128997.5Hereditary cancer-predisposing syndromeVUS

HGMD

IDPhenotypeEffect
CM117423Colorectal cancer, non-polyposisDM?