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MSH6 c.944C>T ;(p.S315F)
Variant ID: 2-48026066-C-T
NM_000179.2(
MSH6
):c.944C>T;(p.S315F)
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:
Predicting the functional impact of protein mutations: application to cancer genomics.
Nucleic Acids Research
Reva, Boris B; Antipin, Yevgeniy Y; Sander, Chris C
Publication Date: 2011-09-01
Variant appearance in text: MSH6: S315F
PubMed Link:
21727090
Variant Present in the following documents:
supp_gkr407_Supplement2_Table_SM1_COSMIC_mutations.xls, sheet 1
View BVdb publication page
Cooperative nuclear localization sequences lend a novel role to the N-terminal region of MSH6.
Plos One
Gassman, Natalie R NR; Clodfelter, Jill E JE; McCauley, Anita K AK; Bonin, Keith K; Salsbury, Freddie R FR; Scarpinato, Karin D KD
Publication Date: 2011-03-17
Variant appearance in text: MSH6: S315F
PubMed Link:
21437237
Variant Present in the following documents:
Main text
pone.0017907.pdf
View BVdb publication page