Variant #0000319673 (NC_000008.10:g.100883717C>A, NM_017890.3:c.11612C>A (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.100883717C>A
DNA change (hg38) g.99871489C>A
Published as VPS13B(NM_017890.4):c.11612C>A (p.A3871D)
ISCN -
DB-ID VPS13B_000342
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +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.*6792G>T r.(=) p.(=)
VPS13B NM_017890.3 ?/. - c.11612C>A r.(?) p.(Ala3871Asp)
VPS13B NM_152564.4 ?/. - c.11537C>A r.(?) p.(Ala3846Asp)


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