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.

10 entries on 1 page. Showing entries 1 - 10.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

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Disease     

ID_report     

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Owner     
+/+ 61 c.11754G>A r.(?) p.(Trp3918*) Fibronectin type-III 24 (3863-3960) Maternal (confirmed) - pathogenic g.215901684C>T g.215728342C>T - - USH2A_000466 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband - - France - - - - - 1 Anne-Françoise Roux
+/. - c.11754G>A r.(?) p.(Trp3918Ter) - Unknown - pathogenic g.215901684C>T g.215728342C>T - - USH2A_000466 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 61 c.11754G>A r.(?) p.(Trp3918*) - Unknown ACMG pathogenic g.215901684C>T g.215728342C>T NM_206933.2:c.11754G>A, NP_996816.2:p.(Trp3918Ter), NC_000001.10:g.215901684C>T - USH2A_000466 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - panel of 441 hereditary eye disease genes including 291 genes related to IRD retinal disease 2016103102 PubMed: Wang 2018 - F ? China Han Chinese - - - - 1 LOVD
+?/. - c.11754G>A r.(?) p.(Trp3918*) - Maternal (confirmed) - likely pathogenic g.215901684C>T g.215728342C>T NM_206933, c.11754G>A, p.Trp3918Ter - USH2A_000466 - PubMed: Ezquerra-Inchausti 2018 - - Germline yes - - - - DNA SEQ-NG blood - retinal disease III:2 PubMed: Ezquerra-Inchausti 2018 Family RP91, III:2 ? no Spain - - - - - 1 LOVD
+?/. - c.11754G>A r.(?) p.(Trp3918*) - Parent #2 - likely pathogenic g.215901684C>T g.215728342C>T USH2A c.G11754A, p.W3918X - USH2A_000466 heterozygous PubMed: Zhu 2020 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease rpz05-II:1 PubMed: Zhu 2020 - F - China - - - - - 1 LOVD
+/. 61 c.11754G>A r.(?) p.(Trp3918*) - Parent #2 ACMG pathogenic g.215901684C>T g.215728342C>T USH2A c.11754G>A, p.W3918* - USH2A_000466 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 41554658 PubMed: Zhu 2021 family 166, patient 41554658 F - China - - - - - 1 LOVD
+/. 61 c.11754G>A r.(?) p.(Trp3918*) - Parent #2 ACMG pathogenic g.215901684C>T g.215728342C>T USH2A c.11754G>A, p.W3918* - USH2A_000466 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 41554659 PubMed: Zhu 2021 family 166, patient 41554659 M - China - - - - - 1 LOVD
+/. 61 c.11754G>A r.(?) p.(Trp3918*) - Parent #2 - pathogenic g.215901684C>T - c.11754G>A - USH2A_000466 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
+/. 61 c.11754G>A r.(?) p.(Trp3918*) - Parent #2 - pathogenic g.215901684C>T - c.11754G>A - USH2A_000466 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+?/. - c.11754G>A r.(?) p.(Trp3918Ter) - Unknown ACMG likely pathogenic g.215901684C>T g.215728342C>T - - USH2A_000466 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Zhu, X. et al., 2020 - rs1358947010 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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