Variant #0000533310 (NC_000008.10:g.100874154G>A, NM_017890.3:c.11270G>A (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.100874154G>A
DNA change (hg38) g.99861926G>A
Published as VPS13B(NM_017890.4):c.11270G>A (p.R3757Q, p.(Arg3757Gln)), VPS13B(NM_017890.5):c.11270G>A (p.R3757Q)
ISCN -
DB-ID VPS13B_000338 See all 5 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) 0.00186 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX6C NM_004374.3 -?/. - c.*16355C>T r.(=) p.(=)
VPS13B NM_017890.3 -?/. - c.11270G>A r.(?) p.(Arg3757Gln)
VPS13B NM_152564.4 -?/. - c.11195G>A r.(?) p.(Arg3732Gln)


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