Variant #0000923223 (NC_000001.10:g.63063675dup, NC_000001.10(NM_033407.2):c.1683-11380dup (DOCK7))

Chromosome 1
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.63063675dup
DNA change (hg38) -
Published as ANGPTL3(NM_014495.4):c.438dupT (p.N147*), DOCK7(NM_001367561.1):c.1683-11380dupA
ISCN -
DB-ID ANGPTL3_000107
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANGPTL3 NM_014495.2 +/. - c.438dup r.(?) p.(Asn147*)
DOCK7 NM_033407.2 +/. - c.1683-11380dup r.(=) p.(=)


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