Bibliome.ai browser hg19
Search
About
Stats
FAQ
ARID1A c.4226A>C ;(p.Q1409P)
Variant ID: 1-27100944-A-C
NM_006015.4(
ARID1A
):c.4226A>C;(p.Q1409P)
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:
Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria.
European Journal Of Human Genetics : Ejhg
Adeyemo, Adebolajo A; Faridi, Rabia R; Chattaraj, Parna P; Yousaf, Rizwan R; Tona, Risa R; Okorie, Samuel S; Bharadwaj, Thashi T; Nouel-Saied, Liz M LM; Acharya, Anushree A; Schrauwen, Isabelle I; Morell, Robert J RJ; Leal, Suzanne M SM; Friedman, Thomas B TB; Griffith, Andrew J AJ; Roux, Isabelle I
Publication Date: 2022-01
Variant appearance in text: ARID1A: 4226A>C; Gln1409Pro
PubMed Link:
34837038
Variant Present in the following documents:
41431_2021_984_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page
Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria.
European Journal Of Human Genetics : Ejhg
Adeyemo, Adebolajo A; Faridi, Rabia R; Chattaraj, Parna P; Yousaf, Rizwan R; Tona, Risa R; Okorie, Samuel S; Bharadwaj, Thashi T; Nouel-Saied, Liz M LM; Acharya, Anushree A; Schrauwen, Isabelle I; Morell, Robert J RJ; Leal, Suzanne M SM; Friedman, Thomas B TB; Griffith, Andrew J AJ; Roux, Isabelle I
Publication Date: 2021-11-26
Variant appearance in text: ARID1A: 4226A>C; Gln1409Pro
PubMed Link:
34837038
Variant Present in the following documents:
41431_2021_984_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page