Variant #0000655948 (NC_000008.10:g.100587947C>T, NM_017890.3:c.5086C>T (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.100587947C>T
DNA change (hg38) g.99575719C>T
Published as -
ISCN -
DB-ID VPS13B_000049 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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX6C NM_004374.3 +/. - c.*302562G>A r.(=) p.(=)
VPS13B NM_017890.3 +/. - c.5086C>T r.(?) p.(Arg1696Ter)
VPS13B NM_152564.4 +/. - c.5011C>T r.(?) p.(Arg1671Ter)


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