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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+/? 12 c.2149T>G r.(?) p.(Cys717Gly) Laminin EGF-like 4 (694-746) Maternal (confirmed) ACMG likely pathogenic g.216424263A>C g.216250921A>C - - USH2A_000347 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/? 12 c.2149T>G r.(?) p.(Cys717Gly) Laminin EGF-like 4 (694-746) Maternal (confirmed) ACMG likely pathogenic g.216424263A>C g.216250921A>C - - USH2A_000347 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/? 12 c.2149T>G r.(?) p.(Cys717Gly) Laminin EGF-like 4 (694-746) Paternal (confirmed) ACMG likely pathogenic g.216424263A>C g.216250921A>C - - USH2A_000347 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA minigene, SEQ, SEQ-NG-S - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/? 12 c.2149T>G r.(?) p.(Cys717Gly) Laminin EGF-like 4 (694-746) Parent #2 ACMG likely pathogenic g.216424263A>C g.216250921A>C - - USH2A_000347 Heterozygous PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. - c.2149T>G r.(?) p.(Cys717Gly) - Unknown ACMG likely pathogenic g.216424263A>C - - - USH2A_000347 - PubMed: Mansard et al, 2021 - rs1304016981 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.2149T>G r.(?) p.(Cys717Gly) - Unknown ACMG likely pathogenic g.216424263A>C - - - USH2A_000347 - PubMed: Mansard et al, 2021 - rs1304016981 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
?/. - c.2149T>G r.(?) p.(Cys717Gly) - Unknown ACMG VUS g.216424263A>C g.216250921A>C - - USH2A_000347 ACMG GN005 criteria: PM2_P PM3_M PP3_P PubMed: Bonnet, C. et al., 2016; PubMed: Mansard, L. et al., 2021 - rs1304016981 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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