Variant #0000313034 (NC_000015.9:g.91561061G>T, NM_018668.3:c.151C>A (VPS33B))

Chromosome 15
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.91561061G>T
DNA change (hg38) g.91017831G>T
Published as VPS33B(NM_018668.4):c.151C>A (p.R51=), VPS33B(NM_018668.5):c.151C>A (p.R51=)
ISCN -
DB-ID VPS33B_000035 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) 0.08496 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS33B NM_018668.3 -?/. - c.151C>A r.(?) p.(Arg51=)


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