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.




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