Variant #0001027937 (NC_000001.10:g.115258747C>A, NM_002524.4:c.35G>T (NRAS))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.115258747C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID NRAS_000006 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121913237
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-02-14 15:10:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NRAS NM_002524.4 +/. - c.35G>T r.(?) p.(Gly12Val)


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