Bibliome.ai browser hg19
Search
About
Stats
FAQ
HR c.1010del ;(p.G337Vfs*26)
Variant ID: 8-21984944-AC-A
NM_005144.4(
HR
):c.1010del;(p.G337Vfs*26)
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:
A novel germline mutation in hMLH1 in three Korean women with endometrial cancer in a family of Lynch syndrome: case report and literature review.
Hereditary Cancer In Clinical Practice
Jung, Youn-Joon YJ; Kim, Hye Ryoun HR; Kim, Mi Kyung MK; Lee, Eun-Ju EJ
Publication Date: 2021-06-03
Variant appearance in text: HR: 1008delG
PubMed Link:
34082788
Variant Present in the following documents:
Main text
13053_2021_Article_185.pdf
View BVdb publication page