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.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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+/. - c.2653C>T r.(?) p.(His885Tyr) - Unknown - pathogenic g.216420083G>A g.216246741G>A - - USH2A_001537 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs746071929 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.2653C>T r.(?) p.(His885Tyr) - Parent #1 - pathogenic (recessive) g.216420083G>A g.216246741G>A - - USH2A_001537 - PubMed: Xu 2014 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease RP309 PubMed: Xu 2014 patient F - China - - - - - 1 LOVD
+/. - c.2653C>T r.(?) p.(His885Tyr) - Parent #1 - pathogenic (recessive) g.216420083G>A g.216246741G>A - - USH2A_001537 - PubMed: Xu 2014 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease RP202 PubMed: Xu 2014 patient F - China - - - - - 1 LOVD
+/. - c.2653C>T r.(?) p.(His885Tyr) - Parent #2 - pathogenic g.216420083G>A g.216246741G>A USH2A c.2653C>T, p.His885Tyr - USH2A_001537 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD17110186 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+/. - c.2653C>T r.(?) p.(His885Tyr) - Parent #2 - pathogenic g.216420083G>A g.216246741G>A USH2A c.2653C>T, p.His885Tyr - USH2A_001537 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD18043350 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. - c.2653C>T r.(?) p.(His885Tyr) - Parent #1 - likely pathogenic g.216420083G>A g.216246741G>A USH2A c.2653C>T, p.(His885Tyr) - USH2A_001537 these 4 variants were confirmed by segregation analysis; heterozygous PubMed: Inaba 2020 - - Germline yes - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
?/. - c.2653C>T r.(?) p.(His885Tyr) - Unknown ACMG VUS g.216420083G>A g.216246741G>A - - USH2A_001537 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Gao, F. J. et al., 2021; PubMed: Inaba, A. et al., 2020 - rs746071929 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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