AKAP9 c.9938G>A ;(p.S3313N)

Variant ID: 7-91726211-G-A

NM_005751.4(AKAP9):c.9938G>A;(p.S3313N)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The spectrum of somatic mutations in monoclonal gammopathy of undetermined significance indicates a less complex genomic landscape than that in multiple myeloma.

Haematologica
Mikulasova, Aneta A; Wardell, Christopher P CP; Murison, Alexander A; Boyle, Eileen M EM; Jackson, Graham H GH; Smetana, Jan J; Kufova, Zuzana Z; Pour, Ludek L; Sandecka, Viera V; Almasi, Martina M; Vsianska, Pavla P; Gregora, Evzen E; Kuglik, Petr P; Hajek, Roman R; Davies, Faith E FE; Morgan, Gareth J GJ; Walker, Brian A BA
Publication Date: 2017-09

Variant appearance in text: AKAP9: S3313N
PubMed Link: 28550183
Variant Present in the following documents:
  • Main text
  • 1021617.pdf
View BVdb publication page