Variant #0000319668 (NC_000008.10:g.100871721G>A, NC_000008.10(NM_017890.3):c.11119+13G>A (VPS13B))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100871721G>A
DNA change (hg38) g.99859493G>A
Published as VPS13B(NM_017890.4):c.11119+13G>A
ISCN -
DB-ID VPS13B_000335 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) 0.00238 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.*18788C>T r.(=) p.(=)
VPS13B NM_017890.3 -/. - c.11119+13G>A r.(=) p.(=)
VPS13B NM_152564.4 -/. - c.11044+13G>A r.(=) p.(=)


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