Screening #0000046479

Individual ID 00046374
Template DNA
Technique SEQ
Tissue -
Remarks -
Variants found? 1
Owner name Martine van Belzen


Genes screened


AscendingSymbol     

Gene     

Chr     

Band

Transcripts     

Variants     

Unique variants     

Last updated     

Associated with diseases
B3GLCT beta 3-glucosyltransferase 13 q12.3 1 113 42 2018-06-03 Peters-plus syndrome



Variants found

1 entry on 1 page. Showing entry 1.
Legend  

Chr     

Allele     

AscendingDNA 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     

Owner     

Gene     

Effect     

Codon change     

IDbase Accession Number     

VariO/DNA     

VariO/Protein     

VariO/RNA     

Exon     

DNA change (cDNA)     

Haplotype     

ClassClinical     

Published as     

RNA change     

Protein     

P-domain     

Exon_old     

DNA/Legacy     

Function/GVS     

Effect in vitro     

Protein/Legacy     

CodonNr     

Method     

Predict/AGVGD     

Predict/Grantham     

Predict/MutationTaster     

Predict/PolyPhen     

Predict/PolyPhenScore     

Predict/SIFT     

Predicted     

FunctionalAnalysis/Result     

FunctionalAnalysis/Technique     

Type/DNA     

Conservation     

CpG     

Enzyme activity     

FunctionalPrediction     

mRNA level     

Predict/CADD     

Predict/Splice     

Protein/Stain     

Protein level     
13 Both (homozygous) g.31843415G>A g.31269278G>A 1020+1G>A - B3GLCT_000002 - PubMed: Lesnik Oberstein 2006 - - Unknown - - - 0 - Martine van Belzen B3GLCT ?/? - - - - - 8i NM_194318.3:c.660+1G>A - - - r.spl? p.? - - - - - - - - - - - - - - - - - - - - - - - - - - -
Legend