Variant #0000608282 (NC_000003.11:g.12626612_12626613del, NC_000003.11(NM_002880.3):c.1668+10_1668+11del (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.12626612_12626613del
DNA change (hg38) g.12585113_12585114del
Published as RAF1(NM_002880.3):c.1668+10_1668+11delTG, RAF1(NM_002880.4):c.1668+10_1668+11delTG
ISCN -
DB-ID RAF1_000004 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAF1 NM_002880.3 -?/. - c.1668+10_1668+11del r.(=) p.(=)
MKRN2 NM_014160.3 -?/. - c.*2860_*2861del r.(=) p.(=)


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