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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-?/? 53 c.10437G>T r.(?) p.(Trp3479Cys) Fibronectin type-III 19 (3404-3494) Unknown ACMG likely benign g.215956228C>A g.215782886C>A - - USH2A_000428 Heterozygous; unknown PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
?/. - c.10437G>T r.(?) p.(Trp3479Cys) - Unknown - VUS g.215956228C>A g.215782886C>A USH2A c.10437G>T, p.Trp3479Cys - USH2A_000428 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI663_001340 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. 53 c.10437G>T r.(?) p.(Trp3479Cys) - Unknown - likely pathogenic (recessive) g.215956228C>A - c.10437G>T - USH2A_000428 - PubMed: Colombo-2020 - rs1308924086 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+/. - c.10437G>T r.(?) p.(Trp3479Cys) - Parent #1 - pathogenic g.215956228C>A g.215782886C>A USH2A c.10437G>T, p.(Trp3479Cys) - USH2A_000428 heterozygous PubMed: Falsini 2021 - - Germline yes - - - - DNA SEQ-NG-I - retrospective study (warning: duplicates in database possible) retinal disease 8 PubMed: Falsini 2021 - M - Italy - - - - - 1 LOVD
?/. - c.10437G>T r.(?) p.(Trp3479Cys) - Unknown ACMG VUS g.215956228C>A g.215782886C>A - - USH2A_000428 ACMG GN005 criteria: PM2_P PM3_M PubMed: Falsini, B. et al., 2021; PubMed: Colombo, L. et al., 2022 - rs1308924086 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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