MSH6 c.3489A>C ;(p.E1163D)

Variant ID: 2-48032099-A-C

NM_000179.2(MSH6):c.3489A>C;(p.E1163D)

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:

Germline sequence variants contributing to cancer susceptibility in South African breast cancer patients of African ancestry.

Scientific Reports
Eygelaar, Dewald D; van Rensburg, Elizabeth J EJ; Joubert, Fourie F
Publication Date: 2022-01-17

Variant appearance in text: MSH6: 3489A>C; Glu1163Asp; rs531674673
PubMed Link: 35039564
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_4791.pdf
  • 41598_2022_4791_MOESM8_ESM.xlsx, sheet 1
View BVdb publication page


Germline sequence variants contributing to cancer susceptibility in South African breast cancer patients of African ancestry.

Scientific Reports
Eygelaar, Dewald D; van Rensburg, Elizabeth J EJ; Joubert, Fourie F
Publication Date: 2022-01-17

Variant appearance in text: MSH6: 3489A>C; Glu1163Asp; rs531674673
PubMed Link: 35039564
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_4791.pdf
  • 41598_2022_4791_MOESM8_ESM.xlsx, sheet 1
View BVdb publication page