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)     

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-/? 85 c.18040T>C r.(?) p.(Phe6014Leu) Transmembrane 4 (6011-6031) Maternal (confirmed) ACMG likely benign g.90281227T>C g.90985410T>C - - GPR98_000059 heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/878 controls none - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
?/. - c.18040T>C r.(?) p.(Phe6014Leu) - Unknown - VUS g.90281227T>C - ADGRV1(NM_032119.4):c.18040T>C (p.F6014L) - GPR98_000059 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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