Variant #0001077968 (NC_000011.9:g.532733G>A, NM_005343.2:c.473C>T (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.532733G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID HRAS_000027
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs587778400
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-05-18 10:49:07 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 ?/. - c.473C>T r.(?) p.(Thr158Met)


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