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.

16 entries on 1 page. Showing entries 1 - 16.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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?/. - c.9259G>A r.(?) p.(Val3087Ile) - Unknown - VUS g.216011445C>T g.215838103C>T USH2A(NM_206933.2):c.9259G>A (p.V3087I) - USH2A_001193 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.9259G>A r.(?) p.(Val3087Ile) - Unknown - VUS g.216011445C>T g.215838103C>T - - USH2A_001193 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs200382994 Germline - 1/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 1 Yoshito Koyanagi
+?/. - c.9259G>A r.(?) p.(Val3087Ile) - Unknown ACMG likely pathogenic (recessive) g.216011445C>T g.215838103C>T - - USH2A_001193 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 28017 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
?/. - c.9259G>A r.(?) p.(Val3087Ile) - Unknown - VUS g.216011445C>T g.215838103C>T - - USH2A_001193 - PubMed: Xu 2014 - rs200382994 Germline - 1/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP274 PubMed: Xu 2014 - - - China - - - - - 1 LOVD
?/. - c.9259G>A r.(?) p.(Val3087Ile) - Unknown - VUS g.216011445C>T - - - USH2A_001193 - PubMed: Guo 2021, Journal: Guo 2021 - - Germline - - - - - DNA SEQ - - HL FamPatIV2 PubMed: Guo 2021, Journal: Guo 2021 daughter of PatIII2 F no China - - - - - 1 Johan den Dunnen
+?/. - c.9259G>A r.(?) p.(Val3087Ile) - Parent #1 - likely pathogenic g.216011445C>T g.215838103C>T - - USH2A_001193 - PubMed: Huang 2015 - - Germline yes - - - - DNA SEQ-NG - 284 gene panel retinal disease W32-1 PubMed: Huang 2015 - M - China - - - - - 1 LOVD
?/. 47 c.9259G>A r.(?) p.(Val3087Ile) - Both (homozygous) - VUS g.216011445C>T - c.9259G>A - USH2A_001193 - PubMed: Chen-2013 - rs200382994 Unknown - - - - - DNA SEQ blood - retinal disease - PubMed: Chen-2013 - - - China Chinese - - - - 1 LOVD
?/. 47 c.9259G>A r.(?) p.(Val3087Ile) - Parent #2 ACMG VUS g.216011445C>T g.215838103C>T USH2A c.9259G>A, p.Val3087Ile - USH2A_001193 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes retinal disease 50 PubMed: Meng 2020 - M - China - - - - - 1 LOVD
+/. - c.9259G>A r.(?) p.(Val3087Ile) - Parent #2 - pathogenic g.216011445C>T g.215838103C>T USH2A c.9259G>A, p.Val3087Ile - USH2A_001193 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease DP19003141 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. 47 c.9259G>A r.(?) p.(Val3087Ile) - Parent #1 ACMG likely pathogenic g.216011445C>T g.215838103C>T USH2A c.9259G>A, p.V3087I - USH2A_001193 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease W32-1 PubMed: Zhu 2021 family 131, patient W32-1 M - China - - - - - 1 LOVD
+?/. 47 c.9259G>A r.(?) p.(Val3087Ile) - Parent #2 ACMG likely pathogenic g.216011445C>T g.215838103C>T USH2A c.9259G>A, p.V3087I - USH2A_001193 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 42630776 PubMed: Zhu 2021 family 148, patient 42630776 M - China - - - - - 1 LOVD
+?/. 47 c.9259G>A r.(?) p.(Val3087Ile) - Parent #2 ACMG likely pathogenic g.216011445C>T g.215838103C>T USH2A c.9259G>A, p.V3087I - USH2A_001193 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF2103 PubMed: Zhu 2021 family 58, patient SRF2103 M - China - - - - - 1 LOVD
+?/. 47 c.9259G>A r.(?) p.(Val3087Ile) - Parent #2 ACMG likely pathogenic g.216011445C>T g.215838103C>T USH2A c.9259G>A, p.V3087I - USH2A_001193 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF361 PubMed: Zhu 2021 family 59, patient SRF361 M - China - - - - - 1 LOVD
+?/. 47 c.9259G>A r.(?) p.(Val3087Ile) - Parent #2 ACMG likely pathogenic g.216011445C>T g.215838103C>T USH2A c.9259G>A, p.V3087I - USH2A_001193 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 42630776_1 PubMed: Zhu 2021 family 148, patient 42630776_ M - China - - - - - 1 LOVD
?/. 47 c.9259G>A r.(?) p.(Val3087Ile) - Parent #2 - VUS g.216011445C>T - c.9259G>A - USH2A_001193 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. - c.9259G>A r.(?) p.(Val3087Ile) - Unknown ACMG VUS g.216011445C>T g.215838103C>T - - USH2A_001193 ACMG GN005 criteria: PM2_P PM3_M BP4_P PubMed: Gao, F. J. et al., 2021; PubMed: Sun, T. et al., 2018; PubMed: Meng, X. et al., 2021; PubMed: Huang, X. F. et al., 2015 - rs200382994 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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