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MSH2 c.64_65delinsGA ;(p.F22D)
Variant ID: 2-47630394-TT-GA
NM_000251.2(
MSH2
):c.64_65delinsGA;(p.F22D)
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:
Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.
Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09
Variant appearance in text: MSH2: F22D
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page
Mutated CEACAMs Disrupt Transforming Growth Factor Beta Signaling and Alter the Intestinal Microbiome to Promote Colorectal Carcinogenesis.
Gastroenterology
Gu, Shoujun S; Zaidi, Sobia S; Hassan, Md Imtaiyaz MI; Mohammad, Taj T; Malta, Tathiane M TM; Noushmehr, Houtan H; Nguyen, Bryan B; Crandall, Keith A KA; Srivastav, Jigisha J; Obias, Vincent V; Lin, Paul P; Nguyen, Bao-Ngoc BN; Yao, Michael M; Yao, Ren R; King, Charles Hadley CH; Mazumder, Raja R; Mishra, Bibhuti B; Rao, Shuyun S; Mishra, Lopa L
Publication Date: 2020-01
Variant appearance in text: MSH2: F22D
PubMed Link:
31585122
Variant Present in the following documents:
Main text
View BVdb publication page