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     
+/. - c.1196_1202del r.(?) p.(Thr399LysfsTer11) Unknown - pathogenic g.73651989_73651995del g.73424861_73424867del 1196_1202delCACAGGA - ALMS1_000438 - - - - Unknown - - - - - DNA SEQ - - ? - - - ? - (Germany) - - - - - 1 IMGAG
+/. - c.1196_1202del r.(?) p.(Thr399LysfsTer11) Unknown ACMG pathogenic g.73651989_73651995del g.73424861_73424867del ALMS1 c.1199_1205del, p.(Thr400Lysfs*11) - ALMS1_000438 compound heterozygous, probably causal PubMed: Zhu 2022 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG, SEQ saliva panel-based next generation sequencing retinal disease 1_1 PubMed: Zhu 2022 family 1, individual 1 M - - - - - - - 1 LOVD
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