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     

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VIP     

Data_av     

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Panel size     

Owner     
+/+ 38 c.8713_8716dup r.(?) p.(Ile2906Lysfs*6) - Parent #2 - pathogenic g.90002194_90002197dup g.90706377_90706380dup - - GPR98_000004 heterozygous PubMed: Weston 2004 - - Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Proband F - - - - - - - 1 David Baux
+/+ 38 c.8713_8716dup r.(?) p.(Ile2906Lysfs*6) - Unknown - pathogenic g.90002194_90002197dup g.90706377_90706380dup - - GPR98_000004 heterozygous PubMed: Weston 2004 - - Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Relative F - - - - - - - 1 David Baux
+/+ 38 c.8713_8716dup r.(?) p.(Ile2906Lysfs*6) - Parent #2 - pathogenic g.90002194_90002197dup g.90706377_90706380dup - - GPR98_000004 heterozygous PubMed: Weston 2004 - - Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Relative F - - - - - - - 1 David Baux
+/+ 38 c.8713_8716dup r.(?) p.(Ile2906Lysfs*6) - Parent #2 - pathogenic g.90002194_90002197dup g.90706377_90706380dup - - GPR98_000004 heterozygous PubMed: Weston 2004 - - Germline - 0/190 controls - - - DNA SEQ - - USH2 - PubMed: Weston 2004 Relative F - - - - - - - 1 David Baux
+/. 38 c.8713_8716dup r.(?) p.(Ile2906Lysfs*6) - Unknown - pathogenic g.90002194_90002197dup - I2906FS (8716insAACA) - GPR98_000004 - PubMed: Jacobson 2008; PubMed: Schwartz 2005 - - Unknown - - - - - DNA SSCA - - retinal disease - PubMed: Jacobson 2008; PubMed: Schwartz 2005 Schwartz:F1 -P6 (27y) F - - - - - - - 1 LOVD
+/. 38 c.8713_8716dup r.(?) p.(Ile2906Lysfs*6) - Unknown - pathogenic g.90002194_90002197dup - I2906FS (8716insAACA) - GPR98_000004 - PubMed: Jacobson 2008; PubMed: Schwartz 2005 - - Unknown - - - - - DNA SSCA - - retinal disease - PubMed: Jacobson 2008; PubMed: Schwartz 2005 Schwartz:F1 -P5 (33y) F - - - - - - - 1 LOVD
+/. 38 c.8713_8716dup r.(?) p.(Ile2906Lysfs*6) - Unknown - pathogenic g.90002194_90002197dup - I2906FS (8716insAACA) - GPR98_000004 - PubMed: Jacobson 2008; PubMed: Schwartz 2005 - - Unknown - - - - - DNA SSCA - - retinal disease - PubMed: Jacobson 2008; PubMed: Schwartz 2005 Schwartz:F1 -P1 (40y) F - - - - - - - 1 LOVD
+?/. - c.8713_8716dup r.(?) p.(Ile2906Lysfs*6) - Unknown - likely pathogenic g.90002194_90002197dup g.90706377_90706380dup c.8713_8716dup, p.Ile2906LysfsTer6 - GPR98_000004 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 184-163 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
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