Variant #0000690123 (NC_000008.10:g.100866058T>C, NM_017890.3:c.10516T>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.100866058T>C
DNA change (hg38) -
Published as VPS13B(NM_017890.4):c.10516T>C (p.C3506R)
ISCN -
DB-ID COX6C_000122
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) 4.0E-5 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 2020-09-15 15:50:26 +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.*24451A>G r.(=) p.(=)
VPS13B NM_017890.3 -?/. - c.10516T>C r.(?) p.(Cys3506Arg)
VPS13B NM_152564.4 -?/. - c.10441T>C r.(?) p.(Cys3481Arg)


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