Variant #0000016299 (NC_000008.10:g.(100115349_100123325)_(100182392_100205103)del, NC_000008.10(NM_017890.3):c.(580+1_581-1)_(2333+1_2334-1)del (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.(100115349_100123325)_(100182392_100205103)del
DNA change (hg38) -
Published as del ex6-16
ISCN -
DB-ID VPS13B_000017 See all 6 reported entries
Variant remarks shared haplotype; 1 Greek COH1 family (hom) and 3 Italian COH1 families (2 com-het, 1 hom)
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 10:03:33 +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 +/+ 5i_16i c.(580+1_581-1)_(2333+1_2334-1)del r.(581_2333del) p.(Ala194Glyfs*9)


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