Variant #0001075599 (NC_000011.9:g.533535C>G, NM_005343.2:c.368G>C (HRAS))

Chromosome 11
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.533535C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID C11orf35_000058 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs730880464
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-28 09:32:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 ?/. - c.368G>C r.(?) p.(Arg123Pro)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.