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.

15 entries on 1 page. Showing entries 1 - 15.
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+?/. - c.13465G>A r.(?) p.(Gly4489Ser) - Unknown - likely pathogenic g.215847788C>T g.215674446C>T USH2A(NM_206933.4):c.13465G>A (p.G4489S) - USH2A_001143 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.13465G>A r.(?) p.(Gly4489Ser) - Parent #2 - likely pathogenic g.215847788C>T g.215674446C>T - - USH2A_001143 - PubMed: Huang 2018 - - Germline - - - - - DNA SEQ-NG - 283-gene panel retinal disease RP079 PubMed: Huang 2018 - - - - - - - - - 1 LOVD
+?/. - c.13465G>A r.(?) p.(Gly4489Ser) - Unknown - likely pathogenic g.215847788C>T g.215674446C>T c.13465G>A, p.Gly4489Ser - USH2A_001143 heterozygous PubMed: Gao 2019 - - Germline ? - - - - DNA SEQ-NG - - retinal disease RD17060612 PubMed: Gao 2019 - ? - China - - - - - 1 LOVD
?/. 63 c.13465G>A r.(?) p.(Gly4489Ser) - Unknown ACMG VUS g.215674446C>T g.215674446C>T USH2A c.13465G > A, p.Gly4489Ser, heterozygous - USH2A_001143 - PubMed: Sun 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted NGS with molecular inversion probes: coding exons of 27 genes associated with Joubert syndrome retinal disease 16 PubMed: Sun 2020 - F - China - - - - - 1 LOVD
+?/. 63 c.13465G>A r.(?) p.(Gly4489Ser) - Unknown - likely pathogenic (recessive) g.215847788C>T - c.13465G>A - USH2A_001143 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - F - - - - - - - 1 LOVD
+?/. 63 c.13465G>A r.(?) p.(Gly4489Ser) - Parent #2 ACMG likely pathogenic g.215847788C>T g.215674446C>T USH2A c.13465G>A, p.Gly4489Ser - USH2A_001143 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes USH 16 PubMed: Meng 2020 - F - China - - - - - 1 LOVD
+/. - c.13465G>A r.(?) p.(Gly4489Ser) - Parent #1 - pathogenic g.215847788C>T g.215674446C>T USH2A c.13465G>A, p.Gly4489Ser - USH2A_001143 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease R017100416 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. - c.13465G>A r.(?) p.(Gly4489Ser) - Parent #1 - pathogenic g.215847788C>T g.215674446C>T USH2A c.13465G>A, p.Gly4489Ser - USH2A_001143 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD17094479 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+/. - c.13465G>A r.(?) p.(Gly4489Ser) - Parent #1 - pathogenic g.215847788C>T g.215674446C>T USH2A c.13465G>A, p.Gly4489Ser - USH2A_001143 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD18071422 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. - c.13465G>A r.(?) p.(Gly4489Ser) - Both (homozygous) - pathogenic g.215847788C>T g.215674446C>T USH2A c.13465G>A, p.Gly4489Ser - USH2A_001143 homozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD180727A PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. - c.13465G>A r.(?) p.(Gly4489Ser) - Parent #1 - likely pathogenic g.215847788C>T g.215674446C>T USH2A c.G13465A, p.G4489S - USH2A_001143 heterozygous PubMed: Zhu 2020 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease rpz05-II:1 PubMed: Zhu 2020 - F - China - - - - - 1 LOVD
+?/. 63 c.13465G>A r.(?) p.(Gly4489Ser) - Parent #2 ACMG likely pathogenic g.215847788C>T g.215674446C>T USH2A c.13465G>A, p.G4489S - USH2A_001143 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF454 PubMed: Zhu 2021 family 34, patient SRF454 M - China - - - - - 1 LOVD
+?/. 63 c.13465G>A r.(?) p.(Gly4489Ser) - Unknown ACMG likely pathogenic g.215847788C>T g.215674446C>T M9: USH2A c.13465G>A, G4489S - USH2A_001143 heterozygous PubMed: Chen 2020 - - Germline yes - - - - DNA SEQ-NG-I blood xGen Exome Research Panel retinal disease 5-II:1 PubMed: Chen 2020 - F - China - - - - - 1 LOVD
+?/. - c.13465G>A r.(?) p.(Gly4489Ser) - Unknown - likely pathogenic g.215847788C>T g.215674446C>T USH2A (NM_206933.2):c.13465G>A(p.G4489S)/c.8641_8642insTATT(p.S2881Lfs*9) - USH2A_001143 - PubMed: Sun 2018 - - Germline/De novo (untested) ? 128 - - - DNA SEQ-NG-I blood - ? WHP28 PubMed: Sun 2018 - F - China - - - - - 1 LOVD
?/. - c.13465G>A r.(?) p.(Gly4489Ser) - Unknown ACMG VUS g.215847788C>T g.215674446C>T - - USH2A_001143 ACMG GN005 criteria: PM2_P PM3_S PubMed: Gao, F. J. et al., 2021; PubMed: Zhu, X. et al., 2020; PubMed: Meng, X. et al., 2021; PubMed: Sun, Y. et al., 2020 - rs1293619630 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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