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.

4 entries on 1 page. Showing entries 1 - 4.
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     
+/+ 48 c.10088_10091del r.(?) p.(Val3363Aspfs*11) EAR 3 (3347-3393) Parent #1 - pathogenic g.90021400_90021403del g.90725583_90725586del - - GPR98_000006 heterozygous PubMed: Ebermann 2009 - - Germline - 0/50 controls - - - DNA SEQ - - USH2 - PubMed: Ebermann 2009 Proband M - Canada - - - - - 1 David Baux
+/+ 48 c.10088_10091del r.(?) p.(Val3363Aspfs*11) EAR 3 (3347-3393) Unknown - pathogenic g.90021400_90021403del g.90725583_90725586del - - GPR98_000006 heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - +Hpy188III - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 48 c.10088_10091del r.(?) p.(Val3363Aspfs*11) EAR 3 (3347-3393) Unknown - pathogenic g.90021400_90021403del g.90725583_90725586del - - GPR98_000006 heterozygous; Mutation PubMed: Yang 2013 - - Germline - 0/400 controls - - - DNA SEQ, SEQ-NG-S - - DFN - PubMed: Yang 2013 Proband - no ophtalmological details - - China - - - - - 1 Anne-Françoise Roux
+/. 48 c.10088_10091del r.(?) p.(Val3363Aspfs*11) - Unknown ACMG pathogenic (recessive) g.90021400_90021403del - - - GPR98_000006 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH Pat36 PubMed: Bahena 2021 - M ? Iran - - - - - 1 Barbara Vona
Legend   How to query  


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