Variant #0001012929 (NC_000003.11:g.12645688G>C, NM_002880.3:c.781C>G (RAF1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.12645688G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID RAF1_000024 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121434594
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-10-28 16:59:01 +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     
RAF1 NM_002880.3 +?/. - c.781C>G r.(?) p.(Pro261Ala)


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