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.

2 entries on 1 page. Showing entries 1 - 2.
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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     

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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     

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Panel size     

Owner     
+/+ 89 c.18646del r.(?) p.(Ala6216Hisfs*13) Cytoplasmic 4 (6155-6306) Parent #2 - pathogenic g.90449059del g.91153242del - - GPR98_000007 heterozygous PubMed: Ebermann 2009 - - Germline - 0/50 controls - - - DNA SEQ - - USH2 - PubMed: Ebermann 2009 Proband M - Canada - - - - - 1 David Baux
+?/. - c.18646del r.(?) p.(Ala6216Hisfs*13) - Unknown - likely pathogenic g.90449059del g.91153242del c.18646del, p.Ala6216HisfsTer13 - GPR98_000007 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 184-031 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
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