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.

6 entries on 1 page. Showing entries 1 - 6.
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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     

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Segregation     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
-/- 33 c.7176C>T r.(?) p.(=) - Unknown - benign g.89989749C>T g.90693932C>T - - GPR98_000032 heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs111033452 Germline - 2/844 controls -MmeI - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 33 c.7176C>T r.(?) p.(=) - Paternal (confirmed) - benign g.89989749C>T g.90693932C>T - - GPR98_000032 heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs111033452 Germline - 2/846 controls -MmeI - - DNA SEQ - - USH3 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 33 c.7176C>T r.(?) p.(=) - Unknown - benign g.89989749C>T g.90693932C>T - - GPR98_000032 heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs111033452 Germline - 2/846 controls -MmeI - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/. - c.7176C>T r.(?) p.(Ser2392=) - Unknown - benign g.89989749C>T g.90693932C>T ADGRV1(NM_032119.4):c.7176C>T (p.S2392=) - GPR98_000032 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.7176C>T r.(?) p.(Ser2392=) - Unknown - likely benign g.89989749C>T g.90693932C>T ADGRV1(NM_032119.4):c.7176C>T (p.S2392=) - GPR98_000032 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.7176C>T r.(?) p.(Ser2392=) - Parent #2 - likely pathogenic g.89989749C>T g.90693932C>T - - GPR98_000032 - PubMed: Bravo-Gil 2017 - - Germline - - - - - DNA SEQ-NG - 68-gene panel retinal disease Pat115 PubMed: Bravo-Gil 2017 patient - - Spain - - - - - 1 Nereida Bravo Gil
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