Full data view for gene GPR98


This database is one of the ”Retinal and hearing impairment genetic variant databases”. NOTE: gene symbol was recently changed from GPR98 to ADGRV1.
Information The variants shown are described using the NM_032119.3 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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     

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Disease     

ID_report     

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VIP     

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Owner     
+/+ 32 c.6962_6963del r.(?) p.(Val2321Alafs*4) Calx-beta 16 (2283-2323) Unknown - pathogenic g.89988432_89988433del g.90692615_90692616del - - GPR98_000122 heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - -HpyCH4V - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. - c.6962_6963del r.(?) p.(Val2321Alafs*4) - Unknown - likely pathogenic g.89988432_89988433del g.90692615_90692616del ADGRV1(GPR98);NM_032119.3;c.[9748+2T>C];;[6962_6963del];p.[?];[(Val2321Alafs*4)] - GPR98_000122 compound heterozygous PubMed: Jiman 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 176 genes panel retinal disease 20 PubMed: Jiman 2020 - F - (United Kingdom (Great Britain)) - - - - - 1 LOVD
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