Variant #0001033636 (NC_000003.11:g.12626019G>A, NM_002880.3:c.1941C>T (RAF1))

Chromosome 3
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.12626019G>A
DNA change (hg38) -
Published as RAF1(NM_002880.4):c.1941C>T (p.V647=, p.(Val647=))
ISCN -
DB-ID RAF1_000037 See all 2 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) 0.00683 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 2025-05-05 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     
RAF1 NM_002880.3 -?/. - c.1941C>T r.(?) p.(Val647=)
MKRN2 NM_014160.3 -?/. - c.*2267G>A r.(=) p.(=)


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