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PIK3CA c.1495T>G ;(p.S499A)
Variant ID: 3-178928309-T-G
NM_006218.2(
PIK3CA
):c.1495T>G;(p.S499A)
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:
New perspectives on the biology of fragile X syndrome.
Current Opinion In Genetics & Development
Wang, Tao T; Bray, Steven M SM; Warren, Stephen T ST
Publication Date: 2012-06
Variant appearance in text: PI3K: S499A
PubMed Link:
22382129
Variant Present in the following documents:
Main text
View BVdb publication page