Bibliome.ai browser hg19
Search
About
Stats
FAQ
BRCA2 c.1422T>G ;(p.L474=)
Variant ID: 13-32907037-T-G
NM_000059.3(
BRCA2
):c.1422T>G;(p.L474=)
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:
Blood-Based Next-Generation Sequencing Analysis of Appendiceal Cancers.
The Oncologist
Shaib, Walid L WL; Zakka, Katerina K; Staley, Charles C; Roberts, Ali A; Akce, Mehmet M; Wu, Christina C; Alese, Olatunji B OB; El-Rayes, Bassel F BF
Publication Date: 2020-05
Variant appearance in text: BRCA2: L474L
PubMed Link:
31784493
Variant Present in the following documents:
Main text
View BVdb publication page