SLC22A11 c.1382G>C ;(p.R461P)

Variant ID: 11-64336250-G-C

NM_018484.2(SLC22A11):c.1382G>C;(p.R461P)

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:

Reliability of Whole-Exome Sequencing for Assessing Intratumor Genetic Heterogeneity.

Cell Reports
Shi, Weiwei W; Ng, Charlotte K Y CKY; Lim, Raymond S RS; Jiang, Tingting T; Kumar, Sushant S; Li, Xiaotong X; Wali, Vikram B VB; Piscuoglio, Salvatore S; Gerstein, Mark B MB; Chagpar, Anees B AB; Weigelt, Britta B; Pusztai, Lajos L; Reis-Filho, Jorge S JS; Hatzis, Christos C
Publication Date: 2018-11-06

Variant appearance in text: SLC22A11: R461P
PubMed Link: 30404001
Variant Present in the following documents:
  • NIHMS1512150-supplement-4.xlsx, sheet 1
  • NIHMS1512150-supplement-5.xlsx, sheet 1
View BVdb publication page