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.

16 entries on 1 page. Showing entries 1 - 16.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/? 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Paternal (confirmed) - benign g.89985882A>G g.90690065A>G - - GPR98_000142 heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Unknown - benign g.89985882A>G g.90690065A>G - - GPR98_000142 heterozygous PubMed: Besnard 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA arrayCGH, SEQ - - USH2 - PubMed: Besnard 2012 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Unknown - benign g.89985882A>G g.90690065A>G - - GPR98_000142 heterozygous PubMed: Besnard 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ - - USH2 - PubMed: Besnard 2012 Proband F - - - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Unknown - benign g.89985882A>G g.90690065A>G - - GPR98_000142 heterozygous PubMed: Besnard 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ - - USH2 - PubMed: Besnard 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Unknown - benign g.89985882A>G g.90690065A>G - - GPR98_000142 heterozygous PubMed: Besnard 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA arrayCGH, SEQ - - USH2 - PubMed: Besnard 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Paternal (inferred) - benign g.89985882A>G g.90690065A>G - - GPR98_000142 homozygous PubMed: Besnard 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ - - USH2 - PubMed: Besnard 2012 Proband F - Turkey - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Maternal (inferred) - benign g.89985882A>G g.90690065A>G - - GPR98_000142 homozygous PubMed: Besnard 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ - - USH2 - PubMed: Besnard 2012 Proband F - Turkey - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Unknown - benign g.89985882A>G g.90690065A>G - - GPR98_000142 heterozygous PubMed: Besnard 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ - - USH2 - PubMed: Besnard 2012 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Paternal (inferred) - benign g.89985882A>G g.90690065A>G - - GPR98_000142 homozygous PubMed: Garcia-Garcia 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2013 Proband - - Spain - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Maternal (inferred) - benign g.89985882A>G g.90690065A>G - - GPR98_000142 homozygous PubMed: Garcia-Garcia 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2013 Proband - - Spain - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Unknown - benign g.89985882A>G g.90690065A>G - - GPR98_000142 heterozygous PubMed: Garcia-Garcia 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2013 Proband - - Spain - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Unknown - benign g.89985882A>G g.90690065A>G - - GPR98_000142 heterozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Rong 2014 Proband - variants found in samples of two affected brothers. They carry the same causative mutations in MYO7A, but other variants cannot be discriminated from the publication. M - China - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Paternal (inferred) - benign g.89985882A>G g.90690065A>G - - GPR98_000142 homozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband F - China - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Maternal (inferred) - benign g.89985882A>G g.90690065A>G - - GPR98_000142 homozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband F - China - - - - - 1 Anne-Françoise Roux
-/- 30 c.6695A>G r.(?) p.(Tyr2232Cys) - Unknown - benign g.89985882A>G g.90690065A>G - - GPR98_000142 heterozygous; non causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs10037067 Germline - - none - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband M - China - - - - - 1 Anne-Françoise Roux
-/. - c.6695A>G r.(?) p.(Tyr2232Cys) - Unknown - benign g.89985882A>G - - - GPR98_000142 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.