Bibliome.ai browser hg19
Search
About
Stats
FAQ
MYL2 c.53T>G ;(p.F18C)
Variant ID: 12-111356948-A-C
NM_000432.3(
MYL2
):c.53T>G;(p.F18C)
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:
NECTAR: a database of codon-centric missense variant annotations.
Nucleic Acids Research
Gong, Sungsam S; Ware, James S JS; Walsh, Roddy R; Cook, Stuart A SA
Publication Date: 2014-01
Variant appearance in text: MYL2: 53T>G
PubMed Link:
24297257
Variant Present in the following documents:
Main text
gkt1245.pdf
View BVdb publication page