Variant #0000923826 (NC_000003.11:g.12645007C>T, NC_000003.11(NM_002880.3):c.834+628G>A (RAF1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.12645007C>T
DNA change (hg38) -
Published as RAF1(NM_001354689.3):c.864G>A (p.A288=), RAF1(NM_002880.4):c.834+628G>A
ISCN -
DB-ID RAF1_000010 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-04-16 21:50:28 +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.834+628G>A r.(=) p.(=)


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