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.

4 entries on 1 page. Showing entries 1 - 4.
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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     
+/+ 50 c.10458G>A r.(?) p.(Trp3486*) EAR 5 (3440-3488) Unknown - pathogenic g.90025490G>A g.90729673G>A - - GPR98_000261 heterozygous PubMed: Besnard, Garcia-Garcia 2014 - - Germline - - + BspCNI;+DdeI;+Hpy188I; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Besnard, Garcia-Garcia 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 50 c.10458G>A r.(?) p.(Trp3486*) EAR 5 (3440-3488) Parent #1 - pathogenic g.90025490G>A g.90729673G>A - - GPR98_000261 heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/+ 50 c.10458G>A r.(?) p.(Trp3486*) EAR 5 (3440-3488) Parent #1 - pathogenic g.90025490G>A g.90729673G>A - - GPR98_000261 heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq, arrayCGH - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. - c.10458G>A r.(?) p.(Trp3486Ter) - Unknown ACMG pathogenic (recessive) g.90025490G>A g.90729673G>A - - GPR98_000261 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHII-179 PubMed: Weisschuh 2024 patient F - Germany - - - - - 1 Johan den Dunnen
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