Bibliome.ai browser hg19
Search
About
Stats
FAQ
PGM2L1 c.1513G>C ;(p.E505Q)
Variant ID: 11-74053625-C-G
NM_173582.3(
PGM2L1
):c.1513G>C;(p.E505Q)
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:
Tracing the evolution of aneuploid cancers by multiregional sequencing with CRUST.
Briefings In Bioinformatics
Chattopadhyay, Subhayan S; Karlsson, Jenny J; Valind, Anders A; Andersson, Natalie N; Gisselsson, David D
Publication Date: 2021-11-05
Variant appearance in text: PGM2L1: E505Q
PubMed Link:
34343239
Variant Present in the following documents:
supplementary_table_2_bbab292.xlsx, sheet 6
View BVdb publication page