VWF c.7913G>C ;(p.G2638A)

Variant ID: 12-6062735-C-G

NM_000552.3(VWF):c.7913G>C;(p.G2638A)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Somatic STAT3 mutations in CD8+ T cells of healthy blood donors carrying human T-cell leukemia virus type 2.

Haematologica
Kim, Daehong D; Myllymäki, Mikko M; Kankainen, Matti M; Jarvinen, Timo T; Park, Giljun G; Bruhn, Roberta R; Murphy, Edward L EL; Mustjoki, Satu S
Publication Date: 2022-02-01

Variant appearance in text: VWF: G2638A
PubMed Link: 34706498
Variant Present in the following documents:
  • 2021_279140_KIM_SUPPL.pdf
View BVdb publication page