Variant #0001056752 (NC_000019.9:g.50143287dup, NM_021228.2:c.-2219dup (SCAF1))

Chromosome 19
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.50143287dup
DNA change (hg38) -
Published as RRAS(NM_006270.5):c.74dup (p.(Pro26Alafs*32))
ISCN -
DB-ID RRAS_000020
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 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     
RRAS NM_006270.3 ?/. - c.74dup r.(?) p.(Pro26Alafs*32)
SCAF1 NM_021228.2 ?/. - c.-2219dup r.(?) p.(=)


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