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BRCA2 c.1291_1292insT ;(p.T431Ifs*21)
Variant ID: 13-32906906-A-AT
NM_000059.3(
BRCA2
):c.1291_1292insT;(p.T431Ifs*21)
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:
Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/2 mutation detection.
Familial Cancer
van Harssel, J J T JJ; van Roozendaal, C E P CE; Detisch, Y Y; Brandão, R D RD; Paulussen, A D C AD; Zeegers, M M; Blok, M J MJ; Gómez García, E B EB
Publication Date: 2010-06
Variant appearance in text: BRCA2: 1291_1292insT
PubMed Link:
19949876
Variant Present in the following documents:
Main text
10689_2009_Article_9305.pdf
View BVdb publication page