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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Disease     

ID_report     

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VIP     

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Owner     
+/+ 9 c.1608C>G r.(?) p.(Tyr536*) - Paternal (inferred) - pathogenic g.89925125C>G g.90629308C>G - - GPR98_000528 homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Germany - - - - - 1 Crystel Bonnet
+/+ 9 c.1608C>G r.(?) p.(Tyr536*) - Maternal (inferred) - pathogenic g.89925125C>G g.90629308C>G - - GPR98_000528 homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Germany - - - - - 1 Crystel Bonnet
+/. - c.1608C>G r.(?) p.(Tyr536*) - Both (homozygous) ACMG pathogenic g.89925125C>G - - - GPR98_000528 - - - - Germline - - - - - DNA SEQ-NG - - albinism, USH2C - - - - - - - - - - - 1 Anju Shukla
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