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BRCA2 c.337_339del ;(p.R113del)
Variant ID: 13-32899233-TAGA-T
NM_000059.3(
BRCA2
):c.337_339del;(p.R113del)
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:
mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing.
Scientific Reports
Wang, Xiaoyuan X; Zhang, Yanqin Y; Ding, Jie J; Wang, Fang F
Publication Date: 2021-09-10
Variant appearance in text: BRCA2: r113del
PubMed Link:
34508137
Variant Present in the following documents:
41598_2021_Article_97414.pdf
View BVdb publication page