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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Owner     
-?/? 89 c.18746T>G r.(?) p.(Leu6249Arg) Cytoplasmic 4 (6155-6306) Unknown ACMG likely benign g.90449159T>G g.91153342T>G - - GPR98_000113 heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs41311625 Germline - 0/878 controls -TspRI - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/. - c.18746T>G r.(?) p.(Leu6249Arg) - Unknown - likely benign g.90449159T>G g.91153342T>G ADGRV1(NM_032119.4):c.18746T>G (p.L6249R) - GPR98_000113 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.18746T>G r.(?) p.(Leu6249Arg) - Unknown - VUS g.90449159T>G g.91153342T>G ADGRV1(NM_032119.4):c.18746T>G (p.L6249R) - GPR98_000113 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.18746T>G r.(?) p.(Leu6249Arg) - Both (homozygous) - likely benign g.90449159T>G g.91153342T>G - - GPR98_000113 - PubMed: Gariballa 2017 - rs41311625 Germline - - - - - DNA, RNA RT-PCR, SEQ, SEQ-NG - WES ODCD - PubMed: Gariballa 2017 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F yes United Arab Emirates - - - - - 1 Johan den Dunnen
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