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.

8 entries on 1 page. Showing entries 1 - 8.
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+?/? 2 c.232T>G r.(?) p.(Phe78Val) - Parent #2 ACMG VUS g.216595447A>C g.216422105A>C - - USH2A_000979 Heterozygous; mutation PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - rs775094277 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+?/? 2 c.232T>G r.(?) p.(Phe78Val) - Parent #2 ACMG VUS g.216595447A>C g.216422105A>C - - USH2A_000979 Heterozygous; mutation PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - rs775094277 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
?/. 2 c.232T>G r.(?) p.(Phe78Val) - Unknown - VUS g.216595447A>C - c.232T>G - USH2A_000979 - PubMed: Colombo-2020 - rs775094277 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
?/. 2 c.232T>G r.(?) p.(Phe78Val) - Unknown - VUS g.216595447A>C - c.232T>G - USH2A_000979 - PubMed: Colombo-2020 - rs775094277 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
?/. 2 c.232T>G r.(?) p.(Phe78Val) - Parent #1 - VUS g.216595447A>C - c.232T>G - USH2A_000979 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
?/. 2 c.232T>G r.(?) p.(Phe78Val) - Parent #1 - VUS g.216595447A>C - c.232T>G - USH2A_000979 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+?/. - c.232T>G r.(?) p.(Phe78Val) - Unknown ACMG likely pathogenic g.216595447A>C g.216422105A>C - - USH2A_000979 ACMG GN005 criteria: PM2_P PM3_S PP3_P PubMed: Bonnet, C. et al., 2016; PubMed: Colombo, L. et al., 2021 - rs775094277 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.232T>G r.(?) p.(Phe78Val) - Unknown - VUS g.216595447A>C - USH2A(NM_206933.4):c.232T>G (p.(Phe78Val)) - USH2A_000979 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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