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DNAH11 c.2880C>T ;(p.S960=)
Variant ID: 7-21639617-C-T
NM_001277115.1(
DNAH11
):c.2880C>T;(p.S960=)
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:
Non-cancer-related pathogenic germline variants and expression consequences in ten-thousand cancer genomes.
Genome Medicine
Wang, Zishan Z; Fan, Xiao X; Shen, Yufeng Y; Pagadala, Meghana S MS; Signer, Rebecca R; Cygan, Kamil J KJ; Fairbrother, William G WG; Carter, Hannah H; Chung, Wendy K WK; Huang, Kuan-Lin KL
Publication Date: 2021-09-09
Variant appearance in text: DNAH11: 2880C>T
PubMed Link:
34503567
Variant Present in the following documents:
13073_2021_964_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page