Full data view for gene BBS1

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_024649.4 transcript reference sequence.

15 entries on 1 page. Showing entries 1 - 15.
Legend   How to query  

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.436C>T r.(?) p.(Arg146Ter) Unknown - likely pathogenic g.66283014C>T - BBS1(NM_024649.5):c.436C>T (p.R146*) - BBS1_000116 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. 7 c.436C>T r.(?) p.(Arg146*) Both (homozygous) - likely pathogenic g.66283014C>T - c.436C>T - BBS1_000116 - PubMed: Muller-2010, Beales 2003 - - Germline - - - - - DNA ? blood ASPER microarray retinal disease - PubMed: Muller-2010, Beales 2003 - - - - North Africa - - - - 2 LOVD
+?/. 7 c.436C>T r.(?) p.(Arg146*) Parent #1 - likely pathogenic g.66283014C>T - c.436C>T - BBS1_000116 - PubMed: Muller-2010, Beales 2003 - - Germline - - - - - DNA SEQ blood Direct digestion retinal disease - PubMed: Muller-2010, Beales 2003 - - - - white - - - - 1 LOVD
+?/. 7 c.436C>T r.(?) p.(Arg146*) Parent #1 - likely pathogenic g.66283014C>T - c.436C>T - BBS1_000116 - PubMed: Muller-2010, Katsanis 2000 - - Germline - - - - - DNA ? blood ASPER microarray retinal disease - PubMed: Muller-2010, Katsanis 2000 - - - - white - - - - 1 LOVD
+/. 7 c.436C>T r.(?) p.(Arg146*) Unknown - pathogenic g.66283014C>T - 436C>T - BBS1_000116 - PubMed: Fauser-2003, Beales 2003 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Fauser-2003, Beales 2003 - - no - European - - - - 1 LOVD
+?/. 7 c.436C>T r.(?) p.(Arg146*) Unknown - likely pathogenic g.66283014C>T - c.436C>T - BBS1_000116 - PubMed: Feuillan-2011 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Feuillan-2011 - - - - - - - - - 1 LOVD
+/. 7 c.436C>T r.(?) p.? Both (homozygous) - pathogenic g.66283014C>T - c.[436C>T];[436C>T] - BBS1_000116 - PubMed: Redin-2012 - - Germline yes - - - - DNA arrayCNV, SEQ blood - retinal disease - PubMed: Redin-2012 - - - Tunisia - - - - - 1 LOVD
+/. 7 c.436C>T r.(?) p.(Arg146*) Unknown - pathogenic g.66283014C>T - c.436C>T(h) - BBS1_000116 Family AR122 (A2831) has previously been published for linkage to the BBS1 locus by Katsanis et al. 1999 PubMed: Janssen-2011 - - Germline - 0.015 - - - DNA SEQ, HD - SEQ or HD retinal disease AR122(A2831)-4 PubMed: Janssen-2011 - - - - Northern-Europe - - - - 1 LOVD
+/. 7 c.436C>T r.(?) p.(Arg146*) Unknown - pathogenic g.66283014C>T - c.436C>T(h) - BBS1_000116 - PubMed: Janssen-2011 - - Germline - 0.009 - - - DNA SEQ, HD - SEQ or HD retinal disease AR603(A2858)-3 PubMed: Janssen-2011 - - - - Northern-Europe - - - - 1 LOVD
+/. 7 c.436C>T r.(?) p.(Arg146*) Unknown - pathogenic g.66283014C>T - c.436C>T(h) - BBS1_000116 - PubMed: Janssen-2011 - - Germline - 0.009 - - - DNA SEQ, HD - SEQ or HD retinal disease AR603(A2858)-3 PubMed: Janssen-2011 - - - - Northern-Europe - - - - 1 LOVD
+?/. 7 c.436C>T r.(?) p.(Arg146*) Unknown - likely pathogenic g.66283014C>T - p.(Arg146*) - BBS1_000116 - PubMed: Castro Sanchez 2015 - - Germline - - - - - DNA SEQ blood - retinal disease - PubMed: Castro Sanchez 2015 - M - Spain Spanish - - - - 1 LOVD
+?/. - c.436C>T r.(?) p.(Arg146*) Parent #1 - likely pathogenic g.66283014C>T g.66515543C>T BBS1, variant 1: c.436C>T/p.R146*, variant 2: c.1169T>G/p.M390R - BBS1_000116 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET2 targeted sequencing panel - see paper retinal disease 32 PubMed: Weisschuh 2020 Filing key number: 18, Bardet-Biedl syndrome, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. 7 c.436C>T r.(?) p.(Arg146*) Parent #2 - pathogenic (recessive) g.66283014C>T - c.[592-?_830+?del];[436C>T] - BBS1_000116 - PubMed: Mary-2019 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Mary 2019 Fetus: term at 19 gestation weeks F - France - - - - - 1 LOVD
+/. 7 c.436C>T r.(?) p.(Arg146*) Parent #2 - pathogenic (recessive) g.66283014C>T - c.[592-?_830+?del];[436C>T] - BBS1_000116 - PubMed: Mary-2019 - - Germline - - - - - DNA SEQ - - retinal disease - PubMed: Mary 2019 Fetus: term at 12 gestation weeks F - France - - - - - 1 LOVD
+/. - c.436C>T r.(?) p.(Arg146*) Both (homozygous) - pathogenic (recessive) g.66283014C>T - 448C>T (Arg146Stop) - BBS1_000116 - PubMed: Smaoui 2006 - - Germline - - - - - DNA SEQ - - BBS Fam57007 PubMed: Smaoui 2006 - - yes Tunisia - - - - - 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.