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.

8 entries on 1 page. Showing entries 1 - 8.
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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)     

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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/- 37 c.8538T>G r.(=) p.(=) - Unknown - benign g.90001368T>G g.90705551T>G - - GPR98_000194 heterozygous PubMed: Besnard 2012 - rs6880570 Germline - - +PvuII;+MspA1I; - - DNA SEQ - - USH2 - PubMed: Besnard 2012 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 37 c.8538T>G r.(=) p.(=) - Unknown - benign g.90001368T>G g.90705551T>G - - GPR98_000194 heterozygous PubMed: Besnard 2012 - rs6880570 Germline - - +PvuII;+MspA1I; - - DNA SEQ - - USH2 - PubMed: Besnard 2012 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 37 c.8538T>G r.(=) p.(=) - Unknown - benign g.90001368T>G g.90705551T>G - - GPR98_000194 heterozygous PubMed: Besnard 2012 - rs6880570 Germline - - +PvuII;+MspA1I; - - DNA arrayCGH, SEQ - - USH2 - PubMed: Besnard 2012 Proband M - - - - - - - 1 Anne-Françoise Roux
-/- 37 c.8538T>G r.(=) p.(=) - Unknown - benign g.90001368T>G g.90705551T>G - - GPR98_000194 heterozygous PubMed: Besnard 2012 - rs6880570 Germline - - +PvuII;+MspA1I; - - DNA SEQ - - USH2 - PubMed: Besnard 2012 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 37 c.8538T>G r.(=) p.(=) - Paternal (inferred) - benign g.90001368T>G g.90705551T>G - - GPR98_000194 homozygous PubMed: Garcia-Garcia 2013 - rs6880570 Germline - - +PvuII;+MspA1I; - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2013 Proband - - Spain - - - - - 1 Anne-Françoise Roux
-/- 37 c.8538T>G r.(=) p.(=) - Maternal (inferred) - benign g.90001368T>G g.90705551T>G - - GPR98_000194 homozygous PubMed: Garcia-Garcia 2013 - rs6880570 Germline - - +PvuII;+MspA1I; - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2013 Proband - - Spain - - - - - 1 Anne-Françoise Roux
-/- 37 c.8538T>G r.(=) p.(=) - Unknown - benign g.90001368T>G g.90705551T>G - - GPR98_000194 heterozygous PubMed: Garcia-Garcia 2013 - rs6880570 Germline - - +PvuII;+MspA1I; - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2013 Proband - - Spain - - - - - 1 Anne-Françoise Roux
-/. - c.8538T>G r.(?) p.(Leu2846=) - Unknown - benign g.90001368T>G g.90705551T>G ADGRV1(NM_032119.4):c.8538T>G (p.L2846=) - GPR98_000194 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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