Variant #0000533314 (NC_000008.10:g.100883872A>C, NM_017890.3:c.11767A>C (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.100883872A>C
DNA change (hg38) g.99871644A>C
Published as VPS13B(NM_017890.4):c.11767A>C (p.N3923H)
ISCN -
DB-ID COX6C_000090
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.*6637T>G r.(=) p.(=)
VPS13B NM_017890.3 -?/. - c.11767A>C r.(?) p.(Asn3923His)
VPS13B NM_152564.4 -?/. - c.11692A>C r.(?) p.(Asn3898His)


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