KMT2C c.11141A>C ;(p.K3714T)

Variant ID: 7-151859521-T-G

NM_170606.2(KMT2C):c.11141A>C;(p.K3714T)

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: N/A
PubMed Link: 36413997
Variant Present in the following documents:
View BVdb publication page



Utility of exome sequencing in routine care for metastatic colorectal cancer.

Molecular And Clinical Oncology
D'Agay, Melchior De Giraud MG; Galland, Loïck L; Tharin, Zoe Z; Truntzer, Caroline C; Ghiringhelli, Francois F
Publication Date: 2021-11

Variant appearance in text: KMT2C: 11141A>C; Lys3714Thr
PubMed Link: 34631054
Variant Present in the following documents:
  • Supplementary_Data.pdf
View BVdb publication page