chr2:47639682 C>T
Annotations
GeneMSH2
TranscriptNM_000251.2
cDNAc.775C>T
Proteinp.P259S
Functionmissense
Localizationexon
hg19chr2:47639682 C>T
dbSNPrs587781294
Synonyms
TranscriptcDNAProtein
NM_001258281.1c.577C>Tp.P193S
XR_001738747.1n.847C>T
XR_939685.1n.847C>T
Frequency in gnomAD
GenomeExome
MAX–0.000008959
AFR–0
AMR–0
ASJ–0
EAS–0
FIN–0
NFE–0.000008959
SAS–0
ClinVar
IDPhenotypeEffect
HGMD
IDPhenotypeEffect
CM117423Colorectal cancer, non-polyposisDM?