MSH2 c.1813del ;(p.V605Lfs*30)

Variant ID: 2-47702217-TG-T

NM_000251.2(MSH2):c.1813del;(p.V605Lfs*30)

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:

Comparison of screening strategies for Lynch syndrome in patients with newly diagnosed endometrial cancer: a prospective cohort study in China.

Cancer Communications (London, England)
Chao, Xiaopei X; Li, Lei L; Wu, Ming M; Ma, Shuiqing S; Tan, Xianjie X; Zhong, Sen S; Bi, Yalan Y; Lang, Jinghe J
Publication Date: 2019-07-15

Variant appearance in text: MSH2: 1813delG; Val605Leufs
PubMed Link: 31307542
Variant Present in the following documents:
  • Main text
  • 40880_2019_Article_388.pdf
View BVdb publication page