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TYR c.34_35delinsCA ;(p.S12H)
Variant ID: 11-88911155-AG-CA
NM_000372.4(
TYR
):c.34_35delinsCA;(p.S12H)
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:
An approximate full-likelihood method for inferring selection and allele frequency trajectories from DNA sequence data.
Plos Genetics
Stern, Aaron J AJ; Wilton, Peter R PR; Nielsen, Rasmus R
Publication Date: 2019-09
Variant appearance in text: TYR: S12H
PubMed Link:
31518343
Variant Present in the following documents:
Main text
pgen.1008384.pdf
View BVdb publication page