Full data view for gene RCBTB1

Information The variants shown are described using the NM_018191.3 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
+/. - c.930G>T r.(?) p.(Trp310Cys) Both (homozygous) - pathogenic (recessive) g.50123709C>A g.49549573C>A - - RCBTB1_000003 - PubMed: Coppieters 2016 - - Germline yes - - - - DNA SEQ, SEQ-NG - - retinal disease 27486781-FamF4 PubMed: Coppieters 2016 3-generation family, 4 affected (F, 3M), unaffected heterozygous carrier parents/relatives F;M - Greece - - - - - 4 Johan den Dunnen
+?/. - c.930G>T r.(?) p.(Trp310Cys) Parent #1 - likely pathogenic g.50123709C>A g.49549573C>A RCBTB1, variant 1: c.930G>T/p.W310C, variant 2: c.930G>T/p.W310C - RCBTB1_000003 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 1121 PubMed: Weisschuh 2020 Filing key number: 765, cone-rod dystrophy, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
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