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PAH c.1141G>T ;(p.E381*)
Variant ID: 12-103237482-C-A
NM_000277.1(
PAH
):c.1141G>T;(p.E381*)
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:
Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations.
Pigment Cell & Melanoma Research
Arbesman, Joshua J; Ravichandran, Sairekha S; Funchain, Pauline P; Thompson, Cheryl L CL
Publication Date: 2018-07
Variant appearance in text: PAH: E381*
PubMed Link:
29473999
Variant Present in the following documents:
Main text
View BVdb publication page