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MSH6 c.1807_1808delinsGC ;(p.K603A)
Variant ID: 2-48026929-AA-GC
NM_000179.2(
MSH6
):c.1807_1808delinsGC;(p.K603A)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Nucleosomes around a mismatched base pair are excluded via an Msh2-dependent reaction with the aid of SNF2 family ATPase Smarcad1.
Genes & Development
Terui, Riki R; Nagao, Koji K; Kawasoe, Yoshitaka Y; Taki, Kanae K; Higashi, Torahiko L TL; Tanaka, Seiji S; Nakagawa, Takuro T; Obuse, Chikashi C; Masukata, Hisao H; Takahashi, Tatsuro S TS
Publication Date: 2018-06-01
Variant appearance in text: MSH6: K603A
PubMed Link:
29899141
Variant Present in the following documents:
Main text
806.pdf
View BVdb publication page