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     

Gender     

Consanguinity     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. - c.853C>G r.(?) p.(Arg285Gly) - Unknown - VUS g.89923208C>G g.90627391C>G ADGRV1(NM_032119.4):c.853C>G (p.R285G) - GPR98_010033 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.853C>G r.(?) p.(Arg285Gly) - Unknown - VUS g.89923208C>G g.90627391C>G ADGRV1(NM_032119.4):c.853C>G (p.R285G) - GPR98_010033 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.853C>G r.(?) p.(Arg285Gly) - Unknown - VUS g.89923208C>G g.90627391C>G ADGRV1 nucleotide 1, protein 1:c.357+48A>G, p.? nucleotide 2, protein 2:c.853C>G, p.Arg285Gly - GPR98_010033 heterozygous, ACMG unclassified - no access to supplementary table 2 PubMed: Hull 2020 - - Germline ? - - - - DNA ? blood NGS gene panel investigation in 60 families, Sanger sequencing in 27 families, and Asper microarray in 25 families retinal disease 69 PubMed: Hull 2020 - ? - New Zealand white - - - - 1 LOVD
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