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     

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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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Disease     

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Owner     
-/- 29 c.6289C>T r.(?) p.(Arg2097Cys) - Paternal (confirmed) - benign g.89981611C>T g.90685794C>T - - GPR98_000099 heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs16868974 Germline - 10/842 controls +FatI;+NlaIII;+CviAII;-HpyCH4IV;-BmgBI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 29 c.6289C>T r.(?) p.(Arg2097Cys) - Paternal (inferred) - benign g.89981611C>T g.90685794C>T - - GPR98_000099 heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs16868974 Germline - 10/842 controls +FatI;+NlaIII;+CviAII;-HpyCH4IV;-BmgBI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 29 c.6289C>T r.(?) p.(Arg2097Cys) - Paternal (confirmed) - benign g.89981611C>T g.90685794C>T - - GPR98_000099 heterozygous; Neutral PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs16868974 Germline - 10/842 controls +FatI;+NlaIII;+CviAII;-HpyCH4IV;-BmgBI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/. - c.6289C>T r.(?) p.(Arg2097Cys) - Parent #1 - benign g.89981611C>T g.90685794C>T - - GPR98_000099 54 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs16868974 Germline - 54/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 54 Mohammed Faruq
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