Variant #0000799475 (NC_000001.10:g.63063501A>C, NC_000001.10(NM_033407.2):c.1683-11206T>G (DOCK7))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.63063501A>C
DNA change (hg38) -
Published as ANGPTL3(NM_014495.4):c.264A>C (p.Q88H), DOCK7(NM_001367561.1):c.1683-11206T>G
ISCN -
DB-ID ANGPTL3_000083
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANGPTL3 NM_014495.2 ?/. - c.264A>C r.(?) p.(Gln88His)
DOCK7 NM_033407.2 ?/. - c.1683-11206T>G r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.