RYR1 c.3284C>A ;(p.T1095N)

Variant ID: 19-38958355-C-A

NM_000540.2(RYR1):c.3284C>A;(p.T1095N)

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:

TP53 Loss of Heterozygosity Induces De Novo SCLC Formation in EGFR-Mutated Lung Adenocarcinoma: A Case Report.

Jto Clinical And Research Reports
Kunimasa, Kei K; Hirotsu, Yosuke Y; Amemiya, Kenji K; Nakamura, Harumi H; Nishino, Kazumi K; Honma, Keiichiro K; Okami, Jiro J; Omata, Masao M; Kumagai, Toru T
Publication Date: 2022-05

Variant appearance in text: RYR1: 3284C>A; Thr1095Asn
PubMed Link: 35498386
Variant Present in the following documents:
  • mmc2.xlsx, sheet 1
View BVdb publication page