Variant #0000617609 (NC_000019.9:g.39997876_39997892dup, NM_016941.3:c.1291_1307dup (DLL3))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.39997876_39997892dup
DNA change (hg38) g.39507236_39507252dup
Published as DLL3(NM_016941.3):c.1284_1285insCGCGCGGACCCGTGCGC (p.(Pro437ThrfsTer117)), DLL3(NM_016941.3):c.1291_1307dupGACCCGTGCGCCGCGCG (p.P437Tfs*117)
ISCN -
DB-ID DLL3_000024 See all 2 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-15 18:08:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLL3 NM_016941.3 +?/. - c.1291_1307dup r.(?) p.(Pro437ThrfsTer117)


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