Full data view for gene USH2A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_206933.2 transcript reference sequence.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Owner     
+/+ 12 c.2135del r.(?) p.(Ser712*) Laminin EGF-like 4 (694-746) Parent #2 - pathogenic g.216424277del g.216250935del 2135delC - USH2A_000197 Heterozygous PubMed: Bernal 2005 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Bernal 2005 Proband M - Spain - - - - - 1 Anne-Françoise Roux
?/. - c.2135del r.(?) p.(Ser712*) - Unknown - VUS g.216424277del g.216250935del - - USH2A_000197 - - ClinVar-000803390 - Germline yes - - - - DNA SEQ-NG-I - WES LCA2 RPCR-XIV-2 - 2 generations- 1(F) and 1(M), both parents are confirmed carriers, this patient was also diagnosed with Ushers syndrome, parents are unknown carriers- no sequencing done for USH2A for parents M no Costa Rica - - - - none 2 Bailey Glen
+/. - c.2135del r.(?) p.(Ser712*) - Parent #1 - pathogenic (recessive) g.216424277del g.216250935del c.2135delC - USH2A_000197 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP2022 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.2135del r.(?) p.(Ser712*) - Unknown - likely pathogenic g.216424277del g.216250935del - - USH2A_000197 - PubMed: Perez-Carro 2018 - - Germline ? - - - - DNA SEQ blood - retinal disease RP-0004 PubMed: Perez-Carro 2018 family RP-0004 M no Spain - - - - - 1 LOVD
+?/. - c.2135del r.(?) p.(Ser712*) - Maternal (confirmed) - likely pathogenic g.216424277del g.216250935del - - USH2A_000197 - PubMed: Perez-Carro 2018 - - Germline yes - - - - DNA arraySNP blood - retinal disease RP-0879 PubMed: Perez-Carro 2018 family RP-0879 F no Spain - - - - - 1 LOVD
+/. - c.2135del r.(?) p.(Ser712Ter) - Unknown ACMG pathogenic g.216424277del g.216250935del 2135delC - USH2A_000197 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Perez-Carro, R. et al., 2018 - rs1238314101 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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