Variant #0001033639 (NC_000003.11:g.12647694A>G, NC_000003.11(NM_002880.3):c.680+6T>C (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.12647694A>G
DNA change (hg38) -
Published as RAF1(NM_002880.3):c.680+6T>C (p.(=)), RAF1(NM_002880.4):c.680+6T>C
ISCN -
DB-ID RAF1_000011 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) 0.00015 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.680+6T>C r.(=) p.(=)


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