Variant #0000276218 (NC_000017.10:g.19189083_19189096del, NM_014964.4:c.746_759del (EPN2))

Chromosome 17
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.19189083_19189096del
DNA change (hg38) g.19285770_19285783del
Published as EPN2(NM_014964.4):c.746_759delCTTGTGACCGCGCA (p.T249Sfs*20)
ISCN -
DB-ID EPN2_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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-13 10:52:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPN2 NM_014964.4 ?/. - c.746_759del r.(?) p.(Thr249SerfsTer20)


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