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MUTYH c.231C>T ;(p.D77=)
Variant ID: 1-45799118-G-A
NM_001048174.1(
MUTYH
):c.231C>T;(p.D77=)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Clinical relevance of pathogenic germline variants in mismatch repair genes in Chinese breast cancer patients.
Npj Breast Cancer
Hu, Li L; Sun, Jie J; Li, Zhongwu Z; Qu, Ziwei Z; Liu, Yan Y; Wan, Qiting Q; Liu, Jiaming J; Ding, Xinyun X; Zang, Fan F; Zhang, Juan J; Yao, Lu L; Xu, Ye Y; Wang, Yin Y; Xie, Yuntao Y
Publication Date: 2022-04-21
Variant appearance in text: MYH: 231C>T
PubMed Link:
35449176
Variant Present in the following documents:
41523_2022_417_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page
Molecular approach to genetic and epigenetic pathogenesis of early-onset colorectal cancer.
World Journal Of Gastrointestinal Oncology
Tezcan, Gulcin G; Tunca, Berrin B; Ak, Secil S; Cecener, Gulsah G; Egeli, Unal U
Publication Date: 2016-01-15
Variant appearance in text: MUTYH: 231C>T
PubMed Link:
26798439
Variant Present in the following documents:
Main text
View BVdb publication page