Variant #0000856891 (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 NRAS(NM_002524.4):c.35G>T (p.(Gly12Val))
ISCN -
DB-ID NRAS_000006 See all 4 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +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     
NRAS NM_002524.4 +/. - c.35G>T r.(?) p.(Gly12Val)
CSDE1 NM_007158.5 +/. - c.*2043G>T r.(=) p.(=)


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