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)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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?/. - c.1391G>A r.(?) p.(Arg464His) - Unknown - VUS g.216496975C>T g.216323633C>T - - USH2A_001548 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs771000800 Germline - 4/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 4 Yoshito Koyanagi
+?/. - c.1391G>A r.(?) p.(Arg464His) - Parent #1 - likely pathogenic g.216496975C>T g.216323633C>T - - USH2A_001548 - PubMed: Bravo-Gil 2017 - - Germline yes - - - - DNA SEQ-NG - 68-gene panel retinal disease Pat17 PubMed: Bravo-Gil 2017 family - - Spain - - - - - 1 Nereida Bravo Gil
+?/. - c.1391G>A r.(?) p.(Arg464His) - Unknown ACMG likely pathogenic g.216496975C>T g.216323633C>T USH2A c.1391G>A, p.(Arg464His), c.13576C>T, p.(Arg4526*), $ - USH2A_001548 - PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 292 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+?/. - c.1391G>A r.(?) p.(Arg464His) - Parent #2 - likely pathogenic g.216496975C>T g.216323633C>T USH2A c.1391G>A - USH2A_001548 no protein annotation written; heterozygous PubMed: Charng 2020 - - Germline yes - - - - DNA SEQ-NG-I blood NGS SmartPanel (version 4 or 7, 183 or 233 genes) retinal disease 13 PubMed: Charng 2020 - M - Australia - - - - - 1 LOVD
+/. 8 c.1391G>A r.(?) p.(Arg464His) - Parent #2 - pathogenic g.216496975C>T - c.1391G>A - USH2A_001548 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
?/. - c.1391G>A r.(?) p.(Arg464His) - Unknown ACMG VUS g.216496975C>T g.216323633C>T - - USH2A_001548 ACMG GN005 criteria: PM2_P PM3_M PP1_P PubMed: Bravo-Gil, N. et al., 2017 - rs771000800 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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