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BRCA2 c.3465T>C ;(p.T1155=)
Variant ID: 13-32911957-T-C
NM_000059.3(
BRCA2
):c.3465T>C;(p.T1155=)
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:
The Gain-of-Function p53 R248W Mutant Promotes Migration by STAT3 Deregulation in Human Pancreatic Cancer Cells.
Frontiers In Oncology
Klemke, Luisa L; Fehlau, Clara F CF; Winkler, Nadine N; Toboll, Felicia F; Singh, Shiv K SK; Moll, Ute M UM; Schulz-Heddergott, Ramona R
Publication Date: 2021
Variant appearance in text: BRCA2: 3465T>C
PubMed Link:
34178628
Variant Present in the following documents:
DataSheet_1.pdf
View BVdb publication page