Variant #0000860988 (NC_000008.10:g.100146946T>G, NM_017890.3:c.1293T>G (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.100146946T>G
DNA change (hg38) -
Published as VPS13B(NM_017890.4):c.1293T>G (p.T431=), VPS13B(NM_152564.5):c.1293T>G (p.(Thr431=))
ISCN -
DB-ID VPS13B_000188 See all 3 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) 0.0032 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +02:00 (CEST)
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.*743563A>C r.(=) p.(=)
VPS13B NM_017890.3 -?/. - c.1293T>G r.(?) p.(Thr431=)
VPS13B NM_152564.4 -?/. - c.1293T>G r.(?) p.(Thr431=)


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