Variant #0001042556 (NC_000019.9:g.1106596_1106611dup, NM_014963.2:c.*1609_*1624dup (SBNO2))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1106596_1106611dup
DNA change (hg38) -
Published as GPX4(NM_001039847.3):c.641_656dup (p.(Leu220Serfs*?))
ISCN -
DB-ID GPX4_000017
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPX4 NM_001039848.1 ?/. - c.*25_*40dup r.(=) p.(=)
GPX4 NM_002085.3 ?/. - c.*25_*40dup r.(=) p.(=)
SBNO2 NM_014963.2 ?/. - c.*1609_*1624dup r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.