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     

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AscendingDNA change (cDNA)     

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Owner     
+/+ 27 c.5399G>A r.(?) p.(Trp1800*) Laminin G-like 2 (1714-1891) Unknown - pathogenic g.216251604C>T g.216078262C>T - - USH2A_000728 Heterozygous PubMed: Baux 2014 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 27 c.5399G>A r.(?) p.(Trp1800*) Laminin G-like 2 (1714-1891) Maternal (confirmed) - pathogenic g.216251604C>T g.216078262C>T - - USH2A_000728 Heterozygous; Pathogenic PubMed: Lenarduzzi 2015 - - Germline - - none - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Lenarduzzi 2015 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/. - c.5399G>A r.(?) p.(Trp1800Ter) - Paternal (confirmed) ACMG pathogenic g.216251604C>T - - - USH2A_000728 - PubMed: Mansard et al, 2021 - rs1553299079 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.5399G>A r.(?) p.(Trp1800*) - Parent #1 - likely pathogenic g.216251604C>T g.216078262C>T USH2A, variant 1: c.9056-2A>G/p.?, variant 2: c.5399G>A/p.W1800* - USH2A_000728 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 1245 PubMed: Weisschuh 2020 Filing key number: 1016, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. 27 c.5399G>A r.(?) p.(Trp1800*) - Parent #2 - pathogenic g.216251604C>T - c.5399G>A - USH2A_000728 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
+/. - c.5399G>A r.(?) p.(Trp1800Ter) - Unknown ACMG pathogenic g.216251604C>T g.216078262C>T - - USH2A_000728 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Mansard, L. et al., 2021 - rs1553299079 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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