THSD7A c.145_146delinsTG ;(p.A49W)

Variant ID: 7-11871427-GC-CA

NM_015204.2(THSD7A):c.145_146delinsTG;(p.A49W)

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:

Predicting clinical benefit of immunotherapy by antigenic or functional mutations affecting tumour immunogenicity.

Nature Communications
Kim, Kwoneel K; Kim, Hong Sook HS; Kim, Jeong Yeon JY; Jung, Hyunchul H; Sun, Jong-Mu JM; Ahn, Jin Seok JS; Ahn, Myung-Ju MJ; Park, Keunchil K; Lee, Se-Hoon SH; Choi, Jung Kyoon JK
Publication Date: 2020-02-19

Variant appearance in text: THSD7A: A49W
PubMed Link: 32075964
Variant Present in the following documents:
  • 41467_2020_14562_MOESM11_ESM.xlsx, sheet 37
View BVdb publication page