Full data view for gene VPS13B

Information The variants shown are described using the transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 12 c.1563G>A r.[1563G>A, spl] p.[=, Lys521fs*20] Unknown - pathogenic g.100147961G>A g.99135733G>A c.1563G>A: p.Lys521fsX20, normal transcript in a very low level and abnormal transcript including more than 177 bp of the intron 11, resulting in a new reading frame of 19 codons followed by a stop co - VPS13B_000026 1 German/English COH1 family (com-het); Splice site mutation PubMed: Seifert et al. 2006 - rs180177355 SUMMARY record yes - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.1563G>A r.(?) p.(Lys521=) Parent #1 - likely pathogenic g.100147961G>A g.99135733G>A VPS13B, variant 1: c.1563G>A/p.?, variant 2 :Deletion exon 46-50 - VPS13B_000026 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET7 targeted sequencing panel - see paper retinal disease 107 PubMed: Weisschuh 2020 Filing key number: 49, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
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