TLN2 c.2831C>G ;(p.S944C)

Variant ID: 15-63009842-C-G

NM_015059.2(TLN2):c.2831C>G;(p.S944C)

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:

Exome sequencing in 51 early onset non-familial CRC cases.

Molecular Genetics & Genomic Medicine
Thutkawkorapin, Jessada J; Lindblom, Annika A; Tham, Emma E
Publication Date: 2019-05

Variant appearance in text: TLN2: S944C; rs766710014
PubMed Link: 30809968
Variant Present in the following documents:
  • MGG3-7-e605-s002.xlsx, sheet 1
View BVdb publication page