Variant #0000962823 (NC_000003.11:g.49395691_49395693del, NM_001664.2:c.*1966_*1968del (RHOA))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49395691_49395693del
DNA change (hg38) -
Published as GPX1(NM_201397.3):c.36_38delGGC (p.A13_Q14delinsQSVYAFSARPLAGGEPVSLGSLRGKVLLIENVASL*)
ISCN -
DB-ID GPX1_000006 See all 2 reported entries
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPX1 NM_000581.2 -/. - c.36_38del r.? p.?
RHOA NM_001664.2 -/. - c.*1966_*1968del r.(=) p.(=)


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