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.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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ClinVar ID     

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VIP     

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Disease     

ID_report     

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Owner     
+?/? 7 c.929G>A r.(?) p.(Gly310Glu) - Parent #2 ACMG VUS g.89923284G>A g.90627467G>A - - GPR98_000294 heterozygous; mutation PubMed: Jiang 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs766790920 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/. 7 c.929G>A r.(?) p.(Gly310Glu) - Unknown ACMG pathogenic g.89923284G>A g.90627467G>A NM_032119.3:c.929G>A, NP_115495.3:p.(Gly310Glu), NC_000005.9:g.89923284G>A - GPR98_000294 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - panel of 441 hereditary eye disease genes including 291 genes related to IRD retinal disease 2016121919 PubMed: Wang 2018 - M ? China Han Chinese - - - - 1 LOVD
?/. - c.929G>A r.(?) p.(Gly310Glu) - Unknown ACMG VUS g.89923284G>A g.90627467G>A ADGRV1 c.G929A, p.G310E - GPR98_000294 marked as possibly causative, single heterozygous change in a recessive gene, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 142 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
+?/. 7 c.929G>A r.(?) p.(Gly310Glu) - Unknown - likely pathogenic (recessive) g.89923284G>A - ADGRV1:c.929G>A - GPR98_000294 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
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