Variant #0000888095 (NC_000008.10:g.100887815_100887816insG, NM_152564.4:c.11915_11916insG (VPS13B))

Chromosome 8
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.100887815_100887816insG
DNA change (hg38) -
Published as -
ISCN -
DB-ID COX6C_000219
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX6C NM_004374.3 +/. - c.*2693_*2694insC r.(=) p.(=)
VPS13B NM_152564.4 +/. - c.11915_11916insG r.(?) p.(Asp3973*)


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