Variant #0000570130 (NC_000020.10:g.57897449dup, NM_000114.2:c.565dup (EDN3))

Chromosome 20
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.57897449dup
DNA change (hg38) g.59322394dup
Published as EDN3(NM_207032.2):c.565dupA (p.T189Nfs*63)
ISCN -
DB-ID EDN3_000011 See all 4 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EDN3 NM_000114.2 ?/. 4 c.565dup r.(?) p.(Thr189AsnfsTer10)
EDN3 NM_207034.1 ?/. - c.565dup r.(?) p.(Thr189AsnfsTer10)


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