Variant #0001043105 (NC_000019.9:g.50143259C>G, NM_021228.2:c.-2247C>G (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.50143259C>G
DNA change (hg38) -
Published as RRAS(NM_006270.5):c.97G>C (p.(Val33Leu))
ISCN -
DB-ID RRAS_000018
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 2025-05-05 21:14:00 +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     
RRAS NM_006270.3 ?/. - c.97G>C r.(?) p.(Val33Leu)
SCAF1 NM_021228.2 ?/. - c.-2247C>G r.(?) p.(=)


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