Variant #0000249668 (NC_000008.10:g.100832259A>G, NM_017890.3:c.8978A>G (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.100832259A>G
DNA change (hg38) g.99820031A>G
Published as VPS13B(NM_017890.4):c.8978A>G (p.N2993S), VPS13B(NM_017890.5):c.8978A>G (p.N2993S), VPS13B(NM_152564.5):c.8903A>G (p.(Asn2968Ser))
ISCN -
DB-ID VPS13B_000108 See all 8 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) 0.00323 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX6C NM_004374.3 ?/. - c.*58250T>C r.(=) p.(=)
VPS13B NM_017890.3 ?/. - c.8978A>G r.(?) p.(Asn2993Ser)
VPS13B NM_152564.4 ?/. - c.8903A>G r.(?) p.(Asn2968Ser)


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