Variant #0000991384 (NC_000001.10:g.63064445C>T, NC_000001.10(NM_033407.2):c.1683-12150G>A (DOCK7))

Chromosome 1
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.63064445C>T
DNA change (hg38) -
Published as ANGPTL3(NM_014495.4):c.574C>T (p.Q192*), DOCK7(NM_001367561.1):c.1683-12150G>A
ISCN -
DB-ID ANGPTL3_000119
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) 2.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:07:21 +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.574C>T r.(?) p.(Gln192*)
DOCK7 NM_033407.2 +?/. - c.1683-12150G>A r.(=) p.(=)


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