EPHB2 c.599T>C ;(p.I200T)

Variant ID: 1-23111357-T-C

NM_017449.3(EPHB2):c.599T>C;(p.I200T)

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: EPHB2: I200T
PubMed Link: 30404001
Variant Present in the following documents:
  • NIHMS1512150-supplement-5.xlsx, sheet 1
View BVdb publication page