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KMT2D c.8046+12C>T
Variant ID: 12-49433495-G-A
NM_003482.3(
KMT2D
):c.8046+12C>T
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:
Case Report: A Novel Pathomechanism in PEComa by the Loss of Heterozygosity of TP53.
Frontiers In Oncology
Butz, Henriett H; Lövey, József J; Szentkereszty, Márton M; Bozsik, Anikó A; Tóth, Erika E; Patócs, Attila A
Publication Date: 2022
Variant appearance in text: rs184322774
PubMed Link:
35419288
Variant Present in the following documents:
Table_1.xlsx, sheet 1
View BVdb publication page