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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/? 19 c.3482C>G r.(?) p.(Ser1161Cys) - Paternal (confirmed) - VUS g.89948228C>G g.90652411C>G - - GPR98_010006 - - - - Germline no - - - - DNA SEQ, SEQ-NG-I - - EE - - - M yes - - - - - - 1 Lab Zuffardi
-/. - c.3482C>G r.(?) p.(Ser1161Cys) - Unknown - benign g.89948228C>G g.90652411C>G ADGRV1(NM_032119.4):c.3482C>G (p.S1161C) - GPR98_010006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.3482C>G r.(?) p.(Ser1161Cys) - Unknown - likely benign g.89948228C>G g.90652411C>G ADGRV1(NM_032119.4):c.3482C>G (p.S1161C) - GPR98_010006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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