Variant #0000325792 (NC_000018.9:g.2906770_2906797del, NC_000018.9(NM_032048.2):c.2360-11_2376del (EMILIN2))

Chromosome 18
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.2906770_2906797del
DNA change (hg38) g.2906772_2906799del
Published as EMILIN2(NM_032048.2):c.2360-16_2371del (p.?)
ISCN -
DB-ID EMILIN2_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-14 16:24:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EMILIN2 NM_032048.2 ?/. - c.2360-11_2376del r.spl? p.?


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