Variant #0000615068 (NC_000014.8:g.70990738_70990748del, NM_003814.4:c.882_892del (ADAM20))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.70990738_70990748del
DNA change (hg38) g.70524021_70524031del
Published as ADAM20(NM_003814.5):c.732_742delCTATCATCCTT (p.Y245Gfs*3)
ISCN -
DB-ID ADAM20_000001
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 15:24:38 +01:00 (CET)
Date last edited 2020-07-05 15:20:20 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAM20 NM_003814.4 ?/. - c.882_892del r.(?) p.(Tyr295GlyfsTer3)


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