Variant #0000029465 (NC_000008.10:g.100874030G>A, NM_017890.3:c.11146G>A (VPS13B))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100874030G>A
DNA change (hg38) g.99861802G>A
Published as NM_152564:c.11071G>A
ISCN -
DB-ID VPS13B_000161 See all 6 reported entries
Variant remarks 1 patient (com-het) with autism and COH1 like features
Reference PubMed: Yu al. 2013
ClinVar ID -
dbSNP ID rs142476821
Origin SUMMARY record
Segregation yes
Frequency 1000g 0.230
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00241 View details
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2014-02-04 13:50:04 +01:00 (CET)
Date last edited 2017-05-05 18:33:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS13B NM_017890.3 +?/+? 61 c.11146G>A r.(?) p.(Ala3716Thr)


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