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     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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-/? 33 c.7229A>G r.(?) p.(Tyr2410Cys) - Unknown ACMG likely benign g.89989802A>G g.90693985A>G - - GPR98_000151 heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033430 Germline - 1/872 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/. - c.7229A>G r.(?) p.(Tyr2410Cys) - Unknown - likely benign g.89989802A>G g.90693985A>G ADGRV1(NM_032119.4):c.7229A>G (p.Y2410C), GPR98(NM_032119.3):c.7229A>G (p.(Tyr2410Cys)) - GPR98_000151 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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