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BRCA2 c.4131_4132insTGA ;(p.N1377_T1378ins*)
Variant ID: 13-32912623-C-CTGA
NM_000059.3(
BRCA2
):c.4131_4132insTGA;(p.N1377_T1378ins*)
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:
Prevalence of mutations in BRCA and MMR genes in patients affected with hereditary endometrial cancer.
Medical Oncology (Northwood, London, England)
Vietri, Maria Teresa MT; D'Elia, Giovanna G; Caliendo, Gemma G; Casamassimi, Amelia A; Federico, Alessandro A; Passariello, Luana L; Cioffi, Michele M; Molinari, Anna Maria AM
Publication Date: 2021-01-23
Variant appearance in text: BRCA2: 4131_4132insTGA; Thr1378Ter
PubMed Link:
33484353
Variant Present in the following documents:
12032_2021_Article_1454.pdf
View BVdb publication page