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     
+/+ 12 c.2258_2270del r.(?) p.(Gln753Leufs*8) - Parent #1 - pathogenic g.89938470_89938482del g.90642653_90642665del - - GPR98_000008 heterozygous PubMed: Ebermann 2009 - - Germline - 0/50 controls +ScrFI;+BstNI;+PspGI;+StyD4I;+BssKI;-Hpy188III; - - DNA SEQ - - USH2 - PubMed: Ebermann 2009 Proband F - Germany - - - - - 1 David Baux
+/+ 12 c.2258_2270del r.(?) p.(Gln753Leufs*8) - Parent #1 - pathogenic g.89938470_89938482del g.90642653_90642665del - - GPR98_000008 heterozygous PubMed: Ebermann 2009 - - Germline - 0/50 controls +ScrFI;+BstNI;+PspGI;+StyD4I;+BssKI;-Hpy188III; - - DNA SEQ - - USH2 - PubMed: Ebermann 2009 Relative M - Germany - - - - - 1 David Baux
+/+ 12 c.2258_2270del r.(?) p.(Gln753Leufs*8) - Parent #2 - pathogenic g.89938470_89938482del g.90642653_90642665del - - GPR98_000008 heterozygous; Pathogenic PubMed: Bonnet 2011 - - Germline - - +ScrFI;+BstNI;+PspGI;+StyD4I;+BssKI;-Hpy188III; - - DNA SEQ - - USH2 - PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 12 c.2258_2270del r.(?) p.(Gln753Leufs*8) - Parent #1 - pathogenic g.89938470_89938482del g.90642653_90642665del - - GPR98_000008 heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
Legend   How to query  


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