TMEM43 c.882+1G>A

Variant ID: 3-14177409-G-A

NM_024334.2(TMEM43):c.882+1G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.

Ebiomedicine
Foley, Samantha B SB; Rios, Jonathan J JJ; Mgbemena, Victoria E VE; Robinson, Linda S LS; Hampel, Heather L HL; Toland, Amanda E AE; Durham, Leslie L; Ross, Theodora S TS
Publication Date: 2015-01

Variant appearance in text: TMEM43: 882+1G>A
PubMed Link: 26023681
Variant Present in the following documents:
  • mmc1.pdf
View BVdb publication page