Variant #0000911112 (NC_000001.10:g.63063720A>G, NC_000001.10(NM_033407.2):c.1683-11425T>C (DOCK7))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.63063720A>G
DNA change (hg38) -
Published as ANGPTL3(NM_014495.4):c.483A>G (p.V161=), DOCK7(NM_001367561.1):c.1683-11425T>C
ISCN -
DB-ID ANGPTL3_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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.483A>G r.(?) p.(Val161=)
DOCK7 NM_033407.2 -?/. - c.1683-11425T>C r.(=) p.(=)


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