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.
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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     

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Consanguinity     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 31 c.6856C>T r.(?) p.(Arg2286*) Calx-beta 16 (2283-2323) Unknown - pathogenic g.89986763C>T g.90690946C>T - - GPR98_000062 heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - -BspMI;-BfuAI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/. - c.6856C>T r.(?) p.(Arg2286*) - Unknown - pathogenic g.89986763C>T - - - GPR98_000062 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.6856C>T r.(?) p.(Arg2286Ter) - Unknown ACMG pathogenic (recessive) g.89986763C>T g.90690946C>T - - GPR98_000062 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHII-341 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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