Variant #0000016589 (NC_000015.9:g.40710439_40710459del, IVD(NM_002225.3):c.(1258_1278del))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.40710439_40710459del
DNA change (hg38) g.40418240_40418260del
Published as DEL7
ISCN -
DB-ID IVD_000015
Variant remarks No IVD activity found
Reference PubMed: Volchenboum et al (2000)
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ivo F.A.C. Fokkema
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2012-11-27 22:56:15 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IVD NM_002225.3 +/+? 12 c.(1258_1278del) r.(1258_1278del) p.(Ala420*)