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.

11 entries on 1 page. Showing entries 1 - 11.
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+/+ 42 c.8522G>A r.(?) p.(Trp2841*) Fibronectin type-III 15 (2821-2920) Parent #1 - pathogenic g.216052142C>T g.215878800C>T - - USH2A_001018 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - Germany - - - - - 1 Crystel Bonnet
+?/. - c.8522G>A r.(?) p.(Trp2841*) - Parent #2 - likely pathogenic g.216052142C>T g.215878800C>T - - USH2A_001018 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 583 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+/. - c.8522G>A r.(?) p.(Trp2841*) - Parent #2 - pathogenic (recessive) g.216052142C>T g.215878800C>T - - USH2A_001018 - PubMed: Tiwari 2016 - - Germline - - - - - DNA SEQ-NG - WES retinal disease Case71749 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - 1 LOVD
+/. - c.8522G>A r.(?) p.(Trp2841*) - Parent #2 - pathogenic g.216052142C>T g.215878800C>T - - USH2A_001018 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ - - USH Pat108 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+?/. 42 c.8522G>A r.(?) p.(Trp2841*) - Unknown - likely pathogenic g.216052142C>T - c.8522G>A - USH2A_001018 - PubMed: Foote-2019 - - Germline - - - - - DNA SEQ-NG blood - retinal disease - PubMed: Foote-2019 - M - United States - - - - - 1 LOVD
+?/. - c.8522G>A r.(?) p.(Trp2841*) - Parent #1 - likely pathogenic g.216052142C>T g.215878800C>T USH2A, variant 1: c.8522G>A/p.W2841*, variant 2: c.9258+1G>A/p.? - USH2A_001018 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET6 targeted sequencing panel - see paper retinal disease 555 PubMed: Weisschuh 2020 Filing key number: 198, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.8522G>A r.(?) p.(Trp2841*) - Parent #1 - likely pathogenic g.216052142C>T g.215878800C>T USH2A, variant 1: c.8522G>A/p.W2841*, variant 2: c.9424G>T/p.G3142* - USH2A_001018 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 566 PubMed: Weisschuh 2020 Filing key number: 203, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.8522G>A r.(?) p.(Trp2841*) - Parent #1 - likely pathogenic g.216052142C>T g.215878800C>T USH2A, variant 1: c.802G>A/p.G268R, variant 2: c.8522G>A/p.W2841* - USH2A_001018 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET7 targeted sequencing panel - see paper retinal disease 28 PubMed: Weisschuh 2020 Filing key number: 14, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.8522G>A r.(?) p.(Trp2841*) - Parent #1 - likely pathogenic g.216052142C>T g.215878800C>T USH2A, variant 1: c.11864G>A/p.W3955*, variant 2: c.8522G>A/p.W2841* - USH2A_001018 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET7 targeted sequencing panel - see paper retinal disease 704 PubMed: Weisschuh 2020 Filing key number: 260, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. - c.8522G>A r.(?) p.(Trp2841Ter) - Unknown ACMG pathogenic g.216052142C>T g.215878800C>T - - USH2A_001018 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Bonnet, C. et al., 2016; PubMed: Weisschuh, N. et al., 2020; PubMed: Sloan-Heggen, C. M. et al., 2016; PubMed: Neuhaus, C. et al., 2017 - rs1064797134 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.8522G>A r.(?) p.(Trp2841Ter) - Unknown ACMG likely pathogenic (recessive) g.216052142C>T g.215878800C>T - - USH2A_001018 ACMG PM2, PVS1 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? SRP-53 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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