Variant #0000646565 (NC_000015.9:g.91557186C>T, NC_000015.9(NM_018668.3):c.290-85G>A (VPS33B))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.91557186C>T
DNA change (hg38) g.91013956C>T
Published as -
ISCN -
DB-ID VPS33B_000203
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1972926
Origin Unknown
Segregation -
Frequency 0.193
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Paul Gissen
Database submission license No license selected
Created by Paul Gissen
Date created 2011-08-22 11:16:40 +02:00 (CEST)
Date last edited 2021-09-09 14:41:03 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS33B NM_018668.3 ?/? 4i c.290-85G>A r.(=) p.(=)


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