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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+?/? 27 c.5528C>T r.(?) p.(Pro1843Leu) Laminin G-like 2 (1714-1891) Maternal (confirmed) ACMG VUS g.216251475G>A g.216078133G>A - - USH2A_000717 Heterozygous PubMed: Besnard, Garcia-Garcia 2014, USMA missense analysis, missense variant in MSV3d - rs200209833 Germline - - +SfcI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Besnard, Garcia-Garcia 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 27 c.5528C>T r.(?) p.(Pro1843Leu) Laminin G-like 2 (1714-1891) Unknown ACMG VUS g.216251475G>A g.216078133G>A - - USH2A_000717 Heterozygous; Mutation PubMed: Huang 2013, USMA missense analysis, missense variant in MSV3d - rs200209833 Germline - - +SfcI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Huang 2013 Proband F - China - - - - - 1 Anne-Françoise Roux
+?/? 27 c.5528C>T r.(?) p.(Pro1843Leu) Laminin G-like 2 (1714-1891) Unknown ACMG VUS g.216251475G>A g.216078133G>A - - USH2A_000717 Heterozygous PubMed: Huang 2013, USMA missense analysis, missense variant in MSV3d - rs200209833 Germline - - +SfcI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Huang 2013 Relative F - China - - - - - 1 Anne-Françoise Roux
+?/? 27 c.5528C>T r.(?) p.(Pro1843Leu) Laminin G-like 2 (1714-1891) Parent #2 ACMG VUS g.216251475G>A g.216078133G>A - - USH2A_000717 Heterozygous PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - rs200209833 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
?/. - c.5528C>T r.(?) p.(Pro1843Leu) - Unknown - VUS g.216251475G>A g.216078133G>A - - USH2A_000717 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/+? 27 c.5528C>T r.(?) p.(Pro1843Leu) Laminin G-like 2 (1714 - 1891) Unknown ACMG likely pathogenic g.216251475G>A g.216078133G>A - - USH2A_000717 PM2_P, PM3_S, PP1_P following ClinGen GN005 - - rs200209833 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.5528C>T r.(?) p.(Pro1843Leu) - Unknown ACMG VUS g.216251475G>A g.216078133G>A - - USH2A_000717 ACMG GN005 criteria: PM2_P PM3_P PP1_P PubMed: Bonnet, C. et al., 2016; PubMed: Huang, X. F. et al., 2013 - rs200209833 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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