TYR c.34_36delinsGAG ;(p.S12E)

Variant ID: 11-88911155-AGT-GAG

NM_000372.4(TYR):c.34_36delinsGAG;(p.S12E)

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: S12E
PubMed Link: 31518343
Variant Present in the following documents:
  • Main text
  • pgen.1008384.pdf
View BVdb publication page