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 (hg38)     

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ISCN     

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Reference     

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-?/. - c.8342C>T r.(?) p.(Thr2781Ile) - Unknown - likely benign g.216052322G>A g.215878980G>A USH2A(NM_206933.2):c.8342C>T (p.T2781I) - USH2A_000792 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/? 42 c.8342C>T r.(?) p.(Thr2781Ile) Fibronectin type-III 14 (2724-2812) Unknown ACMG VUS g.216052322G>A g.215878980G>A - - USH2A_000792 Heterozygous; Mutation PubMed: Yang 2013, USMA missense analysis, missense variant in MSV3d - rs143240767 Germline - 0/400 controls - - - DNA SEQ, SEQ-NG-S - - DFN - PubMed: Yang 2013 Proband - age < 6 yrs - - China - - - - - 1 Anne-Françoise Roux
?/. - c.8342C>T r.(?) p.(Thr2781Ile) - Unknown - VUS g.216052322G>A g.215878980G>A - - USH2A_000792 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs143240767 Germline - 18/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 18 Yoshito Koyanagi
?/. 42 c.8342C>T r.(?) p.(Thr2781Ile) - Parent #1 - VUS g.216052322G>A - c.8342C>T - USH2A_000792 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. - c.8342C>T r.(?) p.(Thr2781Ile) - Unknown ACMG VUS g.216052322G>A g.215878980G>A - - USH2A_000792 ACMG GN005 criteria: PubMed: Yang, T. et al., 2013 - rs143240767 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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