SYNJ1 c.2653G>A ;(p.V885I)

Variant ID: 21-34029139-C-T

NM_203446.2(SYNJ1):c.2653G>A;(p.V885I)

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:

Characterization of rare germline variants in familial multiple myeloma.

Blood Cancer Journal
Catalano, Calogerina C; Paramasivam, Nagarajan N; Blocka, Joanna J; Giangiobbe, Sara S; Huhn, Stefanie S; Schlesner, Matthias M; Weinhold, Niels N; Sijmons, Rolf R; de Jong, Mirjam M; Langer, Christian C; Preuss, Klaus-Dieter KD; Nilsson, Björn B; Durie, Brian B; Goldschmidt, Hartmut H; Bandapalli, Obul Reddy OR; Hemminki, Kari K; Försti, Asta A
Publication Date: 2021-02-13

Variant appearance in text: SYNJ1: V924I
PubMed Link: 33583942
Variant Present in the following documents:
  • 41408_2021_422_MOESM1_ESM.pdf
View BVdb publication page