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.

5 entries on 1 page. Showing entries 1 - 5.
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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     
-/- 38i c.8730+21dup r.(=) p.(=) - Unknown - benign g.90002232dup g.90706415dup - - GPR98_000255 heterozygous; Neutral PubMed: Garcia-Garcia 2013 - rs60522638 Germline - - none - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2013 Proband - - Spain - - - - - 1 Anne-Françoise Roux
-/- 38i c.8730+21dup r.(=) p.(=) - Unknown - benign g.90002232dup g.90706415dup - - GPR98_000255 heterozygous; Neutral PubMed: Garcia-Garcia 2013 - rs60522638 Germline - - none - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2013 Proband - - Spain - - - - - 1 Anne-Françoise Roux
-/- 38i c.8730+21dup r.(=) p.(=) - Unknown - benign g.90002232dup g.90706415dup c.8730+9_+10insT - GPR98_000255 heterozygous; non causative PubMed: Rong 2014 - rs60522638 Germline - - none - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Rong 2014 Proband - variants found in samples of two affected brothers. They carry the same causative mutations in MYO7A, but other variants cannot be discriminated from the publication. M - China - - - - - 1 Anne-Françoise Roux
-/- 38i c.8730+21dup r.(=) p.(=) - Unknown - benign g.90002232dup g.90706415dup c.8730+9_+10insT - GPR98_000255 heterozygous; non causative PubMed: Rong 2014 - rs60522638 Germline - - none - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband F - China - - - - - 1 Anne-Françoise Roux
-/- 38i c.8730+21dup r.(=) p.(=) - Unknown - benign g.90002232dup g.90706415dup c.8730+9_+10insT - GPR98_000255 heterozygous; non causative PubMed: Rong 2014 - rs60522638 Germline - - none - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Rong 2014 Proband M - China - - - - - 1 Anne-Françoise Roux
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