MSH6 c.3243G>T ;(p.L1081F)

Variant ID: 2-48030629-G-T

NM_000179.2(MSH6):c.3243G>T;(p.L1081F)

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:

Targeted DNA Sequencing Detects Mutations Related to Susceptibility among Familial Non-medullary Thyroid Cancer.

Scientific Reports
Yu, Yang Y; Dong, Li L; Li, Dapeng D; Chuai, Shaokun S; Wu, Zhigang Z; Zheng, Xiangqian X; Cheng, Yanan Y; Han, Lei L; Yu, Jinpu J; Gao, Ming M
Publication Date: 2015-11-04

Variant appearance in text: MSH6: L1081F
PubMed Link: 26530882
Variant Present in the following documents:
  • Main text
  • srep16129.pdf
  • srep16129-s2.xls, sheet 1
View BVdb publication page