Variant #0001050198 (NC_000001.10:g.115260809T>G, NM_002524.4:c.-1548A>C (NRAS))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.115260809T>G
DNA change (hg38) -
Published as CSDE1(NM_001007553.3):c.2378A>C (p.(Gln793Pro))
ISCN -
DB-ID CSDE1_000023
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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.-1548A>C r.(?) p.(=)
CSDE1 NM_007158.5 -?/. - c.2285A>C r.(?) p.(Gln762Pro)


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