RET c.2136+374C>A

Variant ID: 10-43610558-C-A

NM_020975.4(RET):c.2136+374C>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs2742233
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease.

Plos One
Kim, Jeong-Hyun JH; Cheong, Hyun Sub HS; Sul, Jae Hoon JH; Seo, Jeong-Meen JM; Kim, Dae-Yeon DY; Oh, Jung-Tak JT; Park, Kwi-Won KW; Kim, Hyun-Young HY; Jung, Soo-Min SM; Jung, Kyuwhan K; Cho, Min Jeng MJ; Bae, Joon Seol JS; Shin, Hyoung Doo HD
Publication Date: 2014

Variant appearance in text: rs2742233
PubMed Link: 25310821
Variant Present in the following documents:
  • Main text
  • pone.0110292.pdf
View BVdb publication page