Full data view for gene B3GALT6

Ehlers Danlos Syndrome Variant Database


Information The variants shown are described using the NM_080605.3 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Predicted     

Type/DNA     

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     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 1 c.536_541dup r.(?) p.(Arg179_Arg180dup) duplication duplication Both (homozygous) - pathogenic g.1168194_1168199dup g.1232814_1232819dup 536_541dupGCCGCC - B3GALT6_000025 - PubMed: Alazami 2016 - - Unknown - - - - - DNA SEQ, SEQ-NG - - EDS, EDSSPD2 Family 9 PubMed: Alazami 2016 The formal ID for this family is 12DG2007.The technique used was whole exome sequencing. - - Saudi Arabia - - - - - 1 Raymond Dalgleish
+/. - c.536_541dup r.(?) p.(Arg179_Arg180dup) - - Both (homozygous) - pathogenic (recessive) g.1168194_1168199dup g.1232814_1232819dup NM_080605.3:c.536_541dupGCCGCC:p.(Arg179_Arg180dup) - B3GALT6_000025 - PubMed: Maddirevula 2018 - - Germline - - - - - DNA SEQ, SEQ-NG - WES skeletal dysplasia 12DG2007 PubMed: Maddirevula 2018 isolated case F yes - Arab - - - - 1 LOVD
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