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.

9 entries on 1 page. Showing entries 1 - 9.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Owner     
+/+ 82 c.17668_17669del r.(?) p.(Met5890Valfs*10) GPS (5853-5902) Paternal (confirmed) - pathogenic g.90151631_90151632del g.90855814_90855815del - - GPR98_000017 heterozygous; Pathogenic PubMed: Bonnet 2011 - rs757696771 Germline - - +HpyCH4IV;+BmgBI;+AleI;-NspI;-FatI;-NlaIII; - - DNA SEQ - - USH2 - PubMed: Bonnet 2011 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 82 c.17668_17669del r.(?) p.(Met5890Valfs*10) GPS (5853-5902) Unknown - pathogenic g.90151631_90151632del g.90855814_90855815del - - GPR98_000017 heterozygous; Pathogenic PubMed: Besnard 2012 - rs757696771 Germline - - +HpyCH4IV;+BmgBI;+AleI;-NspI;-FatI;-NlaIII; - - DNA arrayCGH, SEQ - - USH2 - PubMed: Besnard 2012 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 82 c.17668_17669del r.(?) p.(Met5890Valfs*10) GPS (5853-5902) Paternal (inferred) - pathogenic g.90151631_90151632del g.90855814_90855815del - - GPR98_000017 homozygous; mutation PubMed: Bonnet 2016 - rs757696771 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/+ 82 c.17668_17669del r.(?) p.(Met5890Valfs*10) GPS (5853-5902) Maternal (inferred) - pathogenic g.90151631_90151632del g.90855814_90855815del - - GPR98_000017 homozygous; mutation PubMed: Bonnet 2016 - rs757696771 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/+ 82 c.17668_17669del r.(?) p.(Met5890Valfs*10) GPS (5853-5902) Paternal (inferred) - pathogenic g.90151631_90151632del g.90855814_90855815del - - GPR98_000017 heterozygous PubMed: Baux, Vaché 2017 - rs757696771 Germline - - +HpyCH4IV;+BmgBI;+AleI;-NspI;-FatI;-NlaIII; - - DNA SEQ, SEQ-NG-S - - DFN S1601 PubMed: Baux 2017 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/. - c.17668_17669del r.(?) p.(Met5890Valfs*10) - Parent #2 - likely pathogenic (recessive) g.90151631_90151632del g.90855814_90855815del - - GPR98_000017 - PubMed: Bryant 2018 - rs757696771 Germline - - - - - DNA SEQ-NG - WES retinal disease JB324 PubMed: Bryant 2018 - - - United States - - - - - 1 LOVD
+/. - c.17668_17669del r.(?) p.(Met5890ValfsTer10) - Parent #2 - pathogenic (recessive) g.90151631_90151632del g.90855814_90855815del 17668_17669delAT - GPR98_000017 - PubMed: Consugar 2015 - - Germline yes - - - - DNA SEQ-NG - 238-gene panel retinal disease OGI-277-591 PubMed: Consugar 2015 - - - United States - - - - - 1 LOVD
+/. - c.17668_17669del r.(?) p.(Met5890Valfs*10) - Unknown - pathogenic g.90151631_90151632del g.90855814_90855815del GPR98 c.17668_17669del, p.Met5890ValfsTer10 - GPR98_000017 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 003-005 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. - c.17668_17669del r.(?) p.(Met5890ValfsTer10) - Unknown - pathogenic g.90151631_90151632del - ADGRV1(NM_032119.4):c.17668_17669delAT (p.M5890Vfs*10) - GPR98_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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