Full data view for gene ARHGEF18

Information The variants shown are described using the 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     

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ClinVar ID     

dbSNP ID     

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Methylation     

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Disease     

ID_report     

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Owner     
+/. - c.1996C>T r.(?) p.(Arg666*) Maternal (confirmed) - pathogenic (recessive) g.7527145C>T g.7462259C>T - - ARHGEF18_000031 - PubMed: Arno 2017 - - Germline - - - - - DNA SEQ, SEQ-NG - WGS retinal disease FamGC18203Pat1 PubMed: Arno 2017 3-generation family, 1 affeted, unaffected heterozygous carrier parents F - - - - - - - 1 Johan den Dunnen
+?/. - c.1996C>T r.(?) p.(Arg666*) Unknown - likely pathogenic g.7527145C>T g.7462259C>T ARHGEF18 c.1996C>T, p.Arg666Ter - ARHGEF18_000031 heterozygous, different transcript, NM_001130955.1:c.1996C>T, p.Arg666Ter PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G005994 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
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