SDHB c.8C>T ;(p.A3V)

Variant ID: 1-17380507-G-A

NM_003000.2(SDHB):c.8C>T;(p.A3V)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Circulating messenger RNA variants as a potential biomarker for surveillance of hepatocellular carcinoma.

Frontiers In Oncology
Block, Timothy T; Zezulinski, Daniel D; Kaplan, David E DE; Lu, Jingqiao J; Zanine, Samantha S; Zhan, Tingting T; Doria, Cataldo C; Sayeed, Aejaz A
Publication Date: 2022

Variant appearance in text: rs11203289
PubMed Link: 36582804
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



Detecting protein variants by mass spectrometry: a comprehensive study in cancer cell-lines.

Genome Medicine
Alfaro, Javier A JA; Ignatchenko, Alexandr A; Ignatchenko, Vladimir V; Sinha, Ankit A; Boutros, Paul C PC; Kislinger, Thomas T
Publication Date: 2017-07-18

Variant appearance in text: rs11203289
PubMed Link: 28716134
Variant Present in the following documents:
  • 13073_2017_454_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page



Germline and somatic SDHx alterations in apparently sporadic differentiated thyroid cancer.

Endocrine-Related Cancer
Ni, Ying Y; Seballos, Spencer S; Ganapathi, Shireen S; Gurin, Danielle D; Fletcher, Benjamin B; Ngeow, Joanne J; Nagy, Rebecca R; Kloos, Richard T RT; Ringel, Matthew D MD; LaFramboise, Thomas T; Eng, Charis C
Publication Date: 2015-04

Variant appearance in text: rs11203289
PubMed Link: 25694510
Variant Present in the following documents:
  • Main text
  • ERC140537.pdf
View BVdb publication page



PATH-SCAN: a reporting tool for identifying clinically actionable variants.

Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing
Daneshjou, Roxana R; Zappala, Zachary Z; Kukurba, Kim K; Boyle, Sean M SM; Ormond, Kelly E KE; Klein, Teri E TE; Snyder, Michael M; Bustamante, Carlos D CD; Altman, Russ B RB; Montgomery, Stephen B SB
Publication Date: 2014

Variant appearance in text: rs11203289
PubMed Link: 24297550
Variant Present in the following documents:
  • Main text
View BVdb publication page



Germline SDHx variants modify breast and thyroid cancer risks in Cowden and Cowden-like syndrome via FAD/NAD-dependant destabilization of p53.

Human Molecular Genetics
Ni, Ying Y; He, Xin X; Chen, Jinlian J; Moline, Jessica J; Mester, Jessica J; Orloff, Mohammed S MS; Ringel, Matthew D MD; Eng, Charis C
Publication Date: 2012-01-15

Variant appearance in text: rs11203289
PubMed Link: 21979946
Variant Present in the following documents:
  • ddr459.pdf
View BVdb publication page