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MSH6 c.124C>A ;(p.P42T)
Variant ID: 2-48010496-C-A
NM_000179.2(
MSH6
):c.124C>A;(p.P42T)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genomics-Driven Precision Medicine in Pediatric Solid Tumors.
Cancers
Suthapot, Praewa P; Chiangjong, Wararat W; Chaiyawat, Parunya P; Choochuen, Pongsakorn P; Pruksakorn, Dumnoensun D; Sangkhathat, Surasak S; Hongeng, Suradej S; Anurathapan, Usanarat U; Chutipongtanate, Somchai S
Publication Date: 2023-02-23
Variant appearance in text: MSH6: P42T
PubMed Link:
36900212
Variant Present in the following documents:
Main text
cancers-15-01418.pdf
View BVdb publication page
Investigation on the role of nsSNPs in HNPCC genes--a bioinformatics approach.
Journal Of Biomedical Science
Doss, C George Priya CG; Sethumadhavan, Rao R
Publication Date: 2009-04-24
Variant appearance in text: rs34014629
PubMed Link:
19389263
Variant Present in the following documents:
Main text
1423-0127-16-42.pdf
View BVdb publication page