Variant #0000332257 (NC_000008.10:g.100874030G>A, NM_017890.3:c.11146G>A (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.100874030G>A
DNA change (hg38) g.99861802G>A
Published as VPS13B(NM_017890.4):c.11146G>A (p.A3716T, p.(Ala3716Thr)), VPS13B(NM_017890.5):c.11146G>A (p.A3716T)
ISCN -
DB-ID VPS13B_000161 See all 6 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) 0.00241 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.*16479C>T r.(=) p.(=)
VPS13B NM_017890.3 -?/. - c.11146G>A r.(?) p.(Ala3716Thr)
VPS13B NM_152564.4 -?/. - c.11071G>A r.(?) p.(Ala3691Thr)


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