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TP53 c.543del ;(p.C182Afs*65)
Variant ID: 17-7578387-AG-A
NM_000546.5(
TP53
):c.543del;(p.C182Afs*65)
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:
Hereditary cancer syndrome-associated pathogenic variants are common in patients with hematologic malignancies subsequent to primary solid cancer.
Journal Of Cancer
Oh, Joowon J; Kim, Yu Ri YR; Kim, Yoonjung Y; Kim, Boyeon B; Park, Kyung Sun KS; Nam, Seong-Hyeuk SH; Lee, Kyung-A KA
Publication Date: 2021
Variant appearance in text: TP53: 543del
PubMed Link:
34093829
Variant Present in the following documents:
jcav12p4288s2.xlsx, sheet 3
View BVdb publication page