Variant #0000571425 (NC_000022.10:g.20779975dup, NM_182895.2:c.2289dup (SCARF2))

Chromosome 22
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.20779975dup
DNA change (hg38) g.20425683dup
Published as SCARF2(NM_153334.7):c.2303dupC (p.P769Afs*10), SCARF2(NM_153334.7):c.2307dupC (p.E770Rfs*9)
ISCN -
DB-ID SCARF2_000005 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
SCARF2 NM_182895.2 -?/. - c.2289dup r.(?) p.(Glu764ArgfsTer9)


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