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.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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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     
+/+ 62 c.12555_12556del r.(?) p.(Glu4186Glyfs*17) - Unknown - pathogenic g.90073749_90073750del g.90777932_90777933del 12552_12553delGG - GPR98_000020 heterozygous; Pathogenic PubMed: Bonnet 2011 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 62 c.12555_12556del r.(?) p.(Glu4186Glyfs*17) - Parent #1 - pathogenic g.90073749_90073750del g.90777932_90777933del - - GPR98_000020 heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
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