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.

9 entries on 1 page. Showing entries 1 - 9.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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Owner     
+?/? 63 c.12505A>C r.(?) p.(Thr4169Pro) Fibronectin type-III 27 (4154-4258) Paternal (confirmed) ACMG VUS g.215848748T>G g.215675406T>G - - USH2A_000727 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - +BmrI;+BsmFI;-CspCI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/. - c.12505A>C r.(?) p.(Thr4169Pro) - Unknown ACMG likely pathogenic g.215848748T>G - - - USH2A_000727 - PubMed: Mansard et al, 2021 - rs113107803 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.12505A>C r.(?) p.(Thr4169Pro) - Unknown ACMG likely pathogenic g.215848748T>G - - - USH2A_000727 - PubMed: Mansard et al, 2021 - rs113107803 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.12505A>C r.(?) p.(Thr4169Pro) - Unknown ACMG likely pathogenic g.215848748T>G - - - USH2A_000727 - PubMed: Mansard et al, 2021 - rs113107803 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.12505A>C r.(?) p.(Thr4169Pro) - Both (homozygous) ACMG likely pathogenic g.215848748T>G - - - USH2A_000727 - PubMed: Mansard et al, 2021 - rs113107803 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.12505A>C r.(?) p.(Thr4169Pro) - Unknown ACMG likely pathogenic g.215848748T>G - - - USH2A_000727 - PubMed: Mansard et al, 2021 - rs113107803 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.12505A>C r.(?) p.(Thr4169Pro) - Unknown ACMG likely pathogenic g.215848748T>G - - - USH2A_000727 - PubMed: Mansard et al, 2021 - rs113107803 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
?/. 63 c.12505A>C r.(?) p.(Thr4169Pro) - Parent #2 - VUS g.215848748T>G - c.12505A>C - USH2A_000727 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. - c.12505A>C r.(?) p.(Thr4169Pro) - Unknown ACMG VUS g.215848748T>G g.215675406T>G - - USH2A_000727 ACMG GN005 criteria: PM2_P PM3_P PubMed: Mansard, L. et al., 2021 - rs113107803 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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