Variant #0000016294 (NC_000008.10:g.100115179A>G, NC_000008.10(NM_017890.3):c.413-2A>G (VPS13B))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.100115179A>G
DNA change (hg38) g.99102951A>G
Published as IVS4-2A>G
ISCN -
DB-ID VPS13B_000012 See all 3 reported entries
Variant remarks 1 COH1 family (com-het)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2012-11-14 13:00:16 +01:00 (CET)
Date last edited 2019-03-08 11:03:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS13B NM_017890.3 +/+? 4i c.413-2A>G r.spl p.?


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