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PARP2 c.464A>G ;(p.N155S)
Variant ID: 14-20819248-A-G
NM_001042618.1(
PARP2
):c.464A>G;(p.N155S)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.
Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015
Variant appearance in text: rs3093906
PubMed Link:
26659599
Variant Present in the following documents:
pone.0144692.s002.xlsx, sheet 1
View BVdb publication page
Genome-wide survey of allele-specific splicing in humans.
Bmc Genomics
Nembaware, Victoria V; Lupindo, Bukiwe B; Schouest, Katherine K; Spillane, Charles C; Scheffler, Konrad K; Seoighe, Cathal C
Publication Date: 2008-06-02
Variant appearance in text: rs3093906
PubMed Link:
18518984
Variant Present in the following documents:
Main text
1471-2164-9-265.pdf
View BVdb publication page