Variant #0000803358 (NC_000008.10:g.100871569T>C, NM_017890.3:c.10980T>C (VPS13B))

Chromosome 8
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.100871569T>C
DNA change (hg38) -
Published as VPS13B(NM_017890.4):c.10980T>C (p.P3660=), VPS13B(NM_017890.5):c.10980T>C (p.P3660=)
ISCN -
DB-ID COX6C_000085 See all 3 reported entries
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) 0.00077 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.*18940A>G r.(=) p.(=)
VPS13B NM_017890.3 -?/. - c.10980T>C r.(?) p.(Pro3660=)
VPS13B NM_152564.4 -?/. - c.10905T>C r.(?) p.(Pro3635=)


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