Variant #0000016292 (NC_000008.10:g.100050722_100050723delinsT, NM_017890.3:c.219_220delinsT (VPS13B))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.100050722_100050723delinsT
DNA change (hg38) g.99038494_99038495delinsT
Published as 219_20delACinsT
ISCN -
DB-ID VPS13B_000010 See all 2 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 10:58:05 +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 +/+ 3 c.219_220delinsT r.(219_220delinsu) p.(Lys73Asnfs*8)


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