Variant #0000533317 (NC_000008.10:g.100887867_100887870dup, NM_017890.3:c.12042_12045dup (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.100887867_100887870dup
DNA change (hg38) g.99875639_99875642dup
Published as VPS13B(NM_017890.4):c.12038_12039insAAAT (p.(Ala4016Ter)), VPS13B(NM_017890.4):c.12042_12045dupTAAA (p.A4016*)
ISCN -
DB-ID COX6C_000093 See all 2 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.*2642_*2645dup r.(=) p.(=)
VPS13B NM_017890.3 ?/. - c.12042_12045dup r.(?) p.(Ala4016Ter)
VPS13B NM_152564.4 ?/. - c.11967_11970dup r.(?) p.(Ala3991Ter)


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