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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

Methylation     

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Tissue     

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Disease     

ID_report     

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Owner     
+?/. - c.4147dup r.(?) p.(Gln1383ProfsTer17) Unknown ACMG likely pathogenic g.73677801dup g.73450674dup ALMS1 c.4150dup, p.(Thr1384Asnfs*15) - ALMS1_000702 different transcript: single heterozygous variant (recessive) PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 342 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+/. 8 c.4153dup r.(?) p.(Thr1385AsnfsTer15) Unknown ACMG pathogenic (recessive) g.73677807dup g.73450680dup c.4156dup - ALMS1_000702 ACMG: Class 5 (PVS1, PM3, PS4_SUP, PM2_SUP) PMID: 25706677, 25296579, 23188138, 28432734, ClinVar-000210127 - Germline yes - - - - DNA SEQ-NG-I - - ALMS 176610 - - F - Germany - - - - - 1 Andreas Laner
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