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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Reference     

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?/. - c.15355C>T r.(?) p.(Arg5119Trp) - Unknown - VUS g.215802320G>A g.215628978G>A - - USH2A_001454 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs767137840 Germline - 10/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 10 Yoshito Koyanagi
?/. 71 c.15355C>T r.(?) p.(Arg5119Trp) - Unknown - VUS g.215802320G>A - c.15355C>T:p.R5119W - USH2A_001454 - PubMed: Numa-2020 - - Unknown - - - - - DNA SEQ, SEQ-NG - - retinal disease - PubMed: Numa 2020 - M - Japan Japanese - - - - 1 LOVD
+?/. - c.15355C>T r.(?) p.(Arg5119Trp) - Parent #2 - likely pathogenic g.215802320G>A g.215628978G>A USH2A c.15355C>T, p.(Arg5119Trp) - USH2A_001454 novel variant whose pathogenicity are suggested by in silico analysis; heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
?/. 71 c.15355C>T r.(?) p.(Arg5119Trp) - Parent #2 - VUS g.215802320G>A - c.15355C>T - USH2A_001454 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. - c.15355C>T r.(?) p.(Arg5119Trp) - Unknown ACMG VUS g.215802320G>A g.215628978G>A - - USH2A_001454 ACMG GN005 criteria: PM2_P BP4_P PubMed: Inaba, A. et al., 2020 - rs767137840 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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