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.

8 entries on 1 page. Showing entries 1 - 8.
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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.6133G>A r.(?) p.(Gly2045Arg) - Unknown - benign g.89979871G>A g.90684054G>A ADGRV1(NM_032119.4):c.6133G>A (p.G2045R) - GPR98_010134 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.6133G>A r.(?) p.(Gly2045Arg) - Unknown - benign g.89979871G>A g.90684054G>A ADGRV1(NM_032119.4):c.6133G>A (p.G2045R) - GPR98_010134 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.6133G>A r.(?) p.(Gly2045Arg) - Unknown - likely benign g.89979871G>A g.90684054G>A ADGRV1(NM_032119.4):c.6133G>A (p.G2045R) - GPR98_010134 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.6133G>A r.(?) p.(Gly2045Arg) - Unknown - likely benign g.89979871G>A g.90684054G>A ADGRV1(NM_032119.4):c.6133G>A (p.G2045R) - GPR98_010134 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.6133G>A r.(?) p.(Gly2045Arg) - Parent #1 - VUS g.89979871G>A g.90684054G>A - - GPR98_010134 conflicting interpretations of pathogenicity; 8 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs41308846 Germline - 8/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 8 Mohammed Faruq
?/. - c.6133G>A r.(?) p.(Gly2045Arg) - Unknown - VUS g.89979871G>A g.90684054G>A - - GPR98_010134 - PubMed: Eandi 2017 - - Germline - - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam6PatTO7 PubMed: Eandi 2017 - F - Italy - - - - - 1 LOVD
?/. - c.6133G>A r.(?) p.(Gly2045Arg) - Unknown - VUS g.89979871G>A g.90684054G>A - - GPR98_010134 - PubMed: Eandi 2017 - - Germline yes - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam13PatTO16 PubMed: Eandi 2017 2-generation family, 2 affected M - Italy - - - - - 2 LOVD
?/. - c.6133G>A r.(?) p.(Gly2045Arg) - Unknown - VUS g.89979871G>A g.90684054G>A - - GPR98_010134 - PubMed: Eandi 2017 - - Germline yes - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam13PatTO17 PubMed: Eandi 2017 brother M - Italy - - - - - 1 LOVD
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