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     

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     
?/. 7 c.769G>A r.(?) p.(Gly257Arg) - Unknown - VUS g.89923124G>A - c.769G>A (p.Glu257Lys) - GPR98_010783 - PubMed: SkorczykWerner-2020 - - Germline - - - - - DNA arraySNP, SEQ-NG - - retinal disease - PubMed: SkorczykWerner 2020 - F - - Polish - - - - 1 LOVD
?/. 7 c.769G>A r.(?) p.(Gly257Arg) - Unknown - VUS g.89923124G>A - c.769G>A (p.Glu257Lys) - GPR98_010783 - PubMed: SkorczykWerner-2020 - - Germline - - - - - DNA SEQ-NG - - retinal disease - PubMed: SkorczykWerner 2020 - M - - Polish - - - - 1 LOVD
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