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.

15 entries on 1 page. Showing entries 1 - 15.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

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Disease     

ID_report     

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+/+ 31 c.6901C>T r.(?) p.(Gln2301*) Calx-beta 16 (2283-2323) Parent #1 - pathogenic g.89986808C>T g.90690991C>T - - GPR98_000003 heterozygous PubMed: Weston 2004 - rs121909762 Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Proband F - - - - - - - 1 David Baux
+/+ 31 c.6901C>T r.(?) p.(Gln2301*) Calx-beta 16 (2283-2323) Paternal (inferred) - pathogenic g.89986808C>T g.90690991C>T - - GPR98_000003 homozygous PubMed: Weston 2004 - rs121909762 Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Proband F - - - - - - - 1 David Baux
+/+ 31 c.6901C>T r.(?) p.(Gln2301*) Calx-beta 16 (2283-2323) Parent #1 - pathogenic g.89986808C>T g.90690991C>T - - GPR98_000003 heterozygous PubMed: Weston 2004 - rs121909762 Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Proband F - - - - - - - 1 David Baux
+/+ 31 c.6901C>T r.(?) p.(Gln2301*) Calx-beta 16 (2283-2323) Parent #1 - pathogenic g.89986808C>T g.90690991C>T - - GPR98_000003 heterozygous PubMed: Weston 2004 - rs121909762 Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Relative F - - - - - - - 1 David Baux
+/+ 31 c.6901C>T r.(?) p.(Gln2301*) Calx-beta 16 (2283-2323) Parent #1 - pathogenic g.89986808C>T g.90690991C>T - - GPR98_000003 heterozygous PubMed: Weston 2004 - rs121909762 Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Relative F - - - - - - - 1 David Baux
+/+ 31 c.6901C>T r.(?) p.(Gln2301*) Calx-beta 16 (2283-2323) Parent #1 - pathogenic g.89986808C>T g.90690991C>T - - GPR98_000003 heterozygous PubMed: Weston 2004 - rs121909762 Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Relative F - - - - - - - 1 David Baux
+/+ 31 c.6901C>T r.(?) p.(Gln2301*) Calx-beta 16 (2283-2323) Maternal (inferred) - pathogenic g.89986808C>T g.90690991C>T - - GPR98_000003 homozygous PubMed: Weston 2004 - rs121909762 Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Proband F - - - - - - - 1 David Baux
+/+ 31 c.6901C>T r.(?) p.(Gln2301*) Calx-beta 16 (2283-2323) Unknown - pathogenic g.89986808C>T g.90690991C>T - - GPR98_000003 heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - rs121909762 Germline - 0/878 controls +DraI;+MseI;-XmnI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/. - c.6901C>T r.(?) p.(Gln2301*) - Unknown - pathogenic (recessive) g.89986808C>T - 5:89986808C>T ENST00000405460.2:c.6901C>T (Gln2301Ter) - GPR98_000003 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G005198 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+/. 31 c.6901C>T r.(?) p.(Gln2301*) - Unknown - pathogenic g.89986808C>T - Q2301X (6901C?T) - GPR98_000003 - PubMed: Jacobson 2008; PubMed: Schwartz 2005 - - Unknown - - - - - DNA SSCA - - retinal disease - PubMed: Jacobson 2008; PubMed: Schwartz 2005 Schwartz:F1 -P6 (27y) F - - - - - - - 1 LOVD
+/. 31 c.6901C>T r.(?) p.(Gln2301*) - Unknown - pathogenic g.89986808C>T - Q2301X (6901C?T) - GPR98_000003 - PubMed: Jacobson 2008; PubMed: Schwartz 2005 - - Unknown - - - - - DNA SSCA - - retinal disease - PubMed: Jacobson 2008; PubMed: Schwartz 2005 Schwartz:F1 -P5 (33y) F - - - - - - - 1 LOVD
+/. 31 c.6901C>T r.(?) p.(Gln2301*) - Unknown - pathogenic g.89986808C>T - Q2301X (6901C?T) - GPR98_000003 - PubMed: Jacobson 2008; PubMed: Schwartz 2005 - - Unknown - - - - - DNA SSCA - - retinal disease - PubMed: Jacobson 2008; PubMed: Schwartz 2005 Schwartz:F1 -P1 (40y) F - - - - - - - 1 LOVD
+/. - c.6901C>T r.(?) p.(Gln2301*) - Unknown - pathogenic g.89986808C>T g.90690991C>T GPR98 c.6901C>T, p.Gln2301Ter - GPR98_000003 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 184-163 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
?/. - c.6901C>T r.(?) p.(Gln2301*) - Unknown - VUS g.89986808C>T g.90690991C>T GPR98 c.6901C>T, p.Gln2301Ter - GPR98_000003 unsolved PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 121-056 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. - c.6901C>T r.(?) p.(Gln2301*) - Unknown - pathogenic g.89986808C>T g.90690991C>T GPR98 c.6901C>T, p.Gln2301Ter - GPR98_000003 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G005198 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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