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.

3 entries on 1 page. Showing entries 1 - 3.
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     
+?/? 21 c.4400G>A r.(?) p.(Gly1467Glu) - Paternal (inferred) ACMG VUS g.89953743G>A g.90657926G>A - - GPR98_000271 homozygous; likely pathogenic PubMed: Glöcke 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH - PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/? 21 c.4400G>A r.(?) p.(Gly1467Glu) - Maternal (inferred) ACMG VUS g.89953743G>A g.90657926G>A - - GPR98_000271 homozygous; likely pathogenic PubMed: Glöcke 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH - PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/. - c.4400G>A r.(?) p.(Gly1467Glu) - Parent #1 - likely pathogenic g.89953743G>A g.90657926G>A ADGRV1, variant 1: c.4400G>A/p.G1467E, variant 2: c.4400G>A/p.G1467E - GPR98_000271 possibly solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET2 targeted sequencing panel - see paper retinal disease 462 PubMed: Weisschuh 2020 Filing key number: 149, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
Legend   How to query  


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