Full data view for gene ALMS1

This database is one of the "Eye disease" gene variant databases and the EURO-WABB
project
, the EU registry for Wolfram syndrome, Alström syndrome, Bardet-Biedl syndrome
and other rare diabetes syndromes.
Information The variants shown are described using the NM_001378454.1 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     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 8 c.2819T>A r.(?) p.(Leu940Ter) Unknown - pathogenic g.73676473T>A g.73449346T>A c.2816T>A(p.L939*) - ALMS1_000774 - PubMed: Wang 2016 - - Germline - - - - - DNA SEQ-NG, arrayCGH, SEQ blood - retinal disease 4 PubMed: Wang 2016 - M - United States - - - - - 1 LOVD
?/. - c.2819T>A r.(?) p.(Leu940Ter) Unknown - VUS g.73676473T>A g.73449346T>A ALMS1 nucleotide 1, protein 1:c.2822T>A, p.Leu941* nucleotide 2, protein 2:c.10483C>T, p.Gln3495* - ALMS1_000774 heterozygous, ACMG unclassified - no access to supplementary table 2 PubMed: Hull 2020 - - Germline ? - - - - DNA ? blood NGS gene panel investigation in 60 families, Sanger sequencing in 27 families, and Asper microarray in 25 families retinal disease 45 PubMed: Hull 2020 - ? - New Zealand white - - - - 1 LOVD
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