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BRCA2 c.1804_1805del ;(p.G602Kfs*13)
Variant ID: 13-32907419-AGG-A
NM_000059.3(
BRCA2
):c.1804_1805del;(p.G602Kfs*13)
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:
Mutation of SPINOPHILIN (PPP1R9B) found in human tumors promotes the tumorigenic and stemness properties of cells.
Theranostics
Verdugo-Sivianes, Eva M EM; Rojas, Ana M AM; Muñoz-Galván, Sandra S; Otero-Albiol, Daniel D; Carnero, Amancio A
Publication Date: 2021
Variant appearance in text: BRCA2: G602Kfs*13
PubMed Link:
33537097
Variant Present in the following documents:
thnov11p3452s1.pdf
View BVdb publication page