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MSH2 c.1662C>A ;(p.S554R)
Variant ID: 2-47698104-C-A
NM_000251.2(
MSH2
):c.1662C>A;(p.S554R)
This variant was identified in 4 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
The effects of genomic germline variant reclassification on clinical cancer care.
Oncotarget
Slavin, Thomas P TP; Manjarrez, Sophia S; Pritchard, Colin C CC; Gray, Stacy S; Weitzel, Jeffrey N JN
Publication Date: 2019-01-11
Variant appearance in text: MSH2: Ser554Arg
PubMed Link:
30728895
Variant Present in the following documents:
Main text
oncotarget-10-417.pdf
View BVdb publication page
Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.
Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015
Variant appearance in text: HNPCC1: S554R
PubMed Link:
26659599
Variant Present in the following documents:
pone.0144692.s002.xlsx, sheet 1
View BVdb publication page
GESPA: classifying nsSNPs to predict disease association.
Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25
Variant appearance in text: MSH2: S554R
PubMed Link:
26206375
Variant Present in the following documents:
12859_2015_673_MOESM1_ESM.xls, sheet 3
View BVdb publication page
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Nucleic Acids Research
Ryu, Gil-Mi GM; Song, Pamela P; Kim, Kyu-Won KW; Oh, Kyung-Soo KS; Park, Keun-Joon KJ; Kim, Jong Hun JH
Publication Date: 2009-03
Variant appearance in text: MSH2: S554R
PubMed Link:
19139070
Variant Present in the following documents:
gkn1008_nar-01723-s-2008-File011.xls, sheet 4
gkn1008_nar-01723-s-2008-File009.xls, sheet 4
View BVdb publication page