Variant #0000888091 (NC_000008.10:g.100866185A>G, NM_017890.3:c.10643A>G (VPS13B))

Chromosome 8
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.100866185A>G
DNA change (hg38) -
Published as VPS13B(NM_017890.4):c.10643A>G (p.Y3548C), VPS13B(NM_017890.5):c.10643A>G (p.Y3548C)
ISCN -
DB-ID VPS13B_000329 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) 0.00017 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 2022-11-01 13:01:21 +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.*24324T>C r.(=) p.(=)
VPS13B NM_017890.3 ?/. - c.10643A>G r.(?) p.(Tyr3548Cys)
VPS13B NM_152564.4 ?/. - c.10568A>G r.(?) p.(Tyr3523Cys)


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