PTGES c.109G>A ;(p.V37M)

Variant ID: 9-132515183-C-T

NM_004878.4(PTGES):c.109G>A;(p.V37M)

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:

Whole exome sequencing identified sixty-five coding mutations in four neuroblastoma tumors.

Scientific Reports
Miller, Aubrey L AL; Garcia, Patrick L PL; Pressey, Joseph G JG; Beierle, Elizabeth A EA; Kelly, David R DR; Crossman, David K DK; Council, Leona N LN; Daniel, Richard R; Watts, Raymond G RG; Cramer, Stuart L SL; Yoon, Karina J KJ
Publication Date: 2017-12-19

Variant appearance in text: PTGES: 109G>A; Val37Met
PubMed Link: 29259192
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_17162.pdf
View BVdb publication page