SDHA c.771-213T>C

Variant ID: 5-230778-T-C

NM_004168.2(SDHA):c.771-213T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Interaction of germline variants in a family with a history of early-onset clear cell renal cell carcinoma.

Molecular Genetics & Genomic Medicine
Nicolas, Emmanuelle E; Demidova, Elena V EV; Iqbal, Waleed W; Serebriiskii, Ilya G IG; Vlasenkova, Ramilia R; Ghatalia, Pooja P; Zhou, Yan Y; Rainey, Kim K; Forman, Andrea F AF; Dunbrack, Roland L RL; Golemis, Erica A EA; Hall, Michael J MJ; Daly, Mary B MB; Arora, Sanjeevani S
Publication Date: 2019-03

Variant appearance in text: SDHA: 771-213T>C; rs10079760
PubMed Link: 30680959
Variant Present in the following documents:
  • MGG3-7-na-s003.xlsx, sheet 2
  • MGG3-7-na-s003.xlsx, sheet 7
  • MGG3-7-na-s003.xlsx, sheet 5
  • MGG3-7-na-s003.xlsx, sheet 4
  • MGG3-7-na-s003.xlsx, sheet 6
View BVdb publication page