RET c.125T>C ;(p.V42A)

Variant ID: 10-43595958-T-C

NM_020975.4(RET):c.125T>C;(p.V42A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.

American Journal Of Human Genetics
Pejaver, Vikas V; Byrne, Alicia B AB; Feng, Bing-Jian BJ; Pagel, Kymberleigh A KA; Mooney, Sean D SD; Karchin, Rachel R; O'Donnell-Luria, Anne A; Harrison, Steven M SM; Tavtigian, Sean V SV; Greenblatt, Marc S MS; Biesecker, Leslie G LG; Radivojac, Predrag P; Brenner, Steven E SE; ,
Publication Date: 2022-12-01

Variant appearance in text: RET: V42A; rs773375434
PubMed Link: 36413997
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



Molecular subversion of Cdc42 signalling in cancer.

Biochemical Society Transactions
Murphy, Natasha P NP; Binti Ahmad Mokhtar, Ana Masara AM; Mott, Helen R HR; Owen, Darerca D
Publication Date: 2021-06-30

Variant appearance in text: RET: V42A
PubMed Link: 34196668
Variant Present in the following documents:
  • Main text
  • BST-49-1425.pdf
View BVdb publication page