Variant #0000508132 (NC_000001.10:g.63064450T>C, NC_000001.10(NM_033407.2):c.1683-12155A>G (DOCK7))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.63064450T>C
DNA change (hg38) g.62598779T>C
Published as ANGPTL3(NM_014495.4):c.579T>C (p.H193=), DOCK7(NM_001271999.2):c.1683-12155A>G
ISCN -
DB-ID ANGPTL3_000040
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) 4.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANGPTL3 NM_014495.2 -/. - c.579T>C r.(?) p.(His193=)
DOCK7 NM_033407.2 -/. - c.1683-12155A>G r.(=) p.(=)


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