NF1 c.19G>T ;(p.V7L)

Variant ID: 17-29422346-G-T

NM_001042492.2(NF1):c.19G>T;(p.V7L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Unique ethnic features of DDX41 mutations in patients with idiopathic cytopenia of undetermined significance, myelodysplastic syndrome, or acute myeloid leukemia.

Haematologica
Choi, Eun-Ji EJ; Cho, Young-Uk YU; Hur, Eun-Hye EH; Jang, Seongsoo S; Kim, Nayoung N; Park, Han-Seung HS; Lee, Jung-Hee JH; Lee, Kyoo-Hyung KH; Kim, Si-Hwan SH; Hwang, Sang-Hyun SH; Seo, Eul-Ju EJ; Park, Chan-Jeoung CJ; Lee, Je-Hwan JH
Publication Date: 2022-02-01

Variant appearance in text: NF1: 19G>T
PubMed Link: 33626862
Variant Present in the following documents:
  • 2020_270553_CHOI_SUPPL.pdf
View BVdb publication page