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.

12 entries on 1 page. Showing entries 1 - 12.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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Clinical classification     

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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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Disease     

ID_report     

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Owner     
?/. - c.11389+3A>T r.spl? p.? - Unknown - VUS g.215931934T>A g.215758592T>A - - USH2A_001482 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs753886165 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.11389+3A>T r.(11347_11389del) p.? - Parent #1 - likely pathogenic g.215931934T>A g.215758592T>A - - USH2A_001482 effect on splicing predicted from mini-gene splicing assay PubMed: Soens 2017 - - Germline - - - - - DNA SEQ - - retinal disease SRF_1694 PubMed: Soens 2017 possible duplicate - - - - - - - - 1 LOVD
+?/. - c.11389+3A>T r.(11347_11389del) p.? - Parent #1 - likely pathogenic g.215931934T>A g.215758592T>A - - USH2A_001482 effect on splicing predicted from mini-gene splicing assay PubMed: Soens 2017 - - Germline - - - - - DNA SEQ - - retinal disease SRF_1687 PubMed: Soens 2017 possible duplicate - - - - - - - - 1 LOVD
+/. 58i c.11389+3A>T r.spl? p.? - Both (homozygous) ACMG pathogenic (recessive) g.215931934T>A - - - USH2A_001482 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH Pat42 PubMed: Bahena 2021 - F yes Iran - - - - - 1 Barbara Vona
+?/. - c.11389+3A>T r.spl? p.? - Unknown ACMG VUS g.215931934T>A - - - USH2A_001482 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_GH_0015 - - F - Korea, South (Republic) - - - - - 1 Jinu Han
+?/. - c.11389+3A>T r.spl? p.(?) - Unknown - likely pathogenic g.215931934T>A g.215758592T>A c.1810_1817delGTTTGTGA; c.11389+3A/T(alleles in trans) - USH2A_001482 - PubMed: Hariri 2018 - - Germline ? - - - - DNA SEQ - retrospective analysis retinal disease - PubMed: Hariri 2018 - ? - - - - - - - 1 LOVD
?/. - c.11389+3A>T r.spl? p.(?) - Unknown ACMG VUS g.215931934T>A g.215758592T>A USH2A c.11389+3A>T(;)13339A>G, V2: c.11389+3A>T, - USH2A_001482 alleles in cis or trans; heterozygous PubMed: Chen 2021 - - Unknown ? - - - - DNA SEQ-NG blood 212 inherited retinal disease-related genes retinal disease F060 PubMed: Chen 2021 - ? - Taiwan - - - - - 1 LOVD
+?/. 58i c.11389+3A>T r.spl? p.? - Unknown - likely pathogenic g.215931934T>A g.215758592T>A USH2A c.11389 + 3A  - USH2A_001482 single heterozygous variant in a recessive gene PubMed: He 2020 SCV000579424.1 - Unknown ? - - - - DNA SEQ blood - USH 3 PubMed: He 2020 - F - China - - - - - 1 LOVD
?/. - c.11389+3A>T r.spl? p.? - Unknown - VUS g.215931934T>A g.215758592T>A USH2A c.11389+3A>T(;)13339A>G; p.? - USH2A_001482 heterozygous PubMed: Chen 2021 - - Germline/De novo (untested) ? Taiwan Biobank: 0; GnomAD_exome_East: 0.0000544; GnomAD_All: 0.00000798 - - - DNA SEQ-NG - targeted 212 IRD-related genes retinal disease F060 PubMed: Chen 2021 - - - Taiwan - - - - - 1 LOVD
+?/. 58i c.11389+3A>T r.spl? p.(?) - Parent #2 - likely pathogenic g.215931934T>A - c.11389+3A>T - USH2A_001482 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
?/. - c.11389+3A>T r.spl p.? - Unknown ACMG VUS g.215931934T>A g.215758592T>A - - USH2A_001482 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Bahena, P. et al., 2022 - rs753886165 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.11389+3A>T r.spl p.? - Parent #2 - likely pathogenic g.215931934T>A g.215758592T>A - - USH2A_001482 - PubMed: Moon 2021 - - Germline - - - - - DNA SEQ, SEQ-NG - gene panel retinal disease Pat85 PubMed: Moon 2021 - - - Korea - - - - - 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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