Variant #0000289904 (NC_000020.10:g.10654110_10654111delinsC, NM_000214.2:c.68_69delinsG (JAG1))

Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.10654110_10654111delinsC
DNA change (hg38) g.10673462_10673463delinsC
Published as JAG1(NM_000214.3):c.68_69delCCinsG (p.A23Gfs*23)
ISCN -
DB-ID JAG1_000103
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 2020-07-16 15:08:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JAG1 NM_000214.2 +/. - c.68_69delinsG r.(?) p.(Ala23GlyfsTer23)


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