DSCAML1 c.2977G>A ;(p.V993I)

Variant ID: 11-117340673-C-T

NM_020693.2(DSCAML1):c.2977G>A;(p.V993I)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic Variants.

Scientific Reports
Theisen, J Graham JG; Sundaram, Viji V; Filchak, Mary S MS; Chorich, Lynn P LP; Sullivan, Megan E ME; Knight, James J; Kim, Hyung-Goo HG; Layman, Lawrence C LC
Publication Date: 2019-12-27

Variant appearance in text: DSCAML1: V1053I
PubMed Link: 31882810
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_53500.pdf
View BVdb publication page



Protein domain-level landscape of cancer-type-specific somatic mutations.

Plos Computational Biology
Yang, Fan F; Petsalaki, Evangelia E; Rolland, Thomas T; Hill, David E DE; Vidal, Marc M; Roth, Frederick P FP
Publication Date: 2015-03

Variant appearance in text: DSCAML1: V1053I
PubMed Link: 25794154
Variant Present in the following documents:
  • pcbi.1004147.s001.xlsx, sheet 1
View BVdb publication page