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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+?/? 62 c.12268C>A r.(?) p.(Pro4090Thr) - Paternal (confirmed) ACMG VUS g.215853517G>T g.215680175G>T - - USH2A_000768 Heterozygous; likely pathogenic PubMed: Glöckle 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Glöckle 2014 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/. - c.12268C>A r.(?) p.(Pro4090Thr) - Unknown ACMG likely pathogenic g.215853517G>T - - - USH2A_000768 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.12268C>A r.(?) p.(Pro4090Thr) - Parent #1 - likely pathogenic g.215853517G>T g.215680175G>T USH2A, variant 1: c.12268C>A/p.P4090T, variant 2: c.11864G>A/p.W3955* - USH2A_000768 possibly solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET5 targeted sequencing panel - see paper retinal disease 1079 PubMed: Weisschuh 2020 Filing key number: 705, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.12268C>A r.(?) p.(Pro4090Thr) - Parent #1 - likely pathogenic g.215853517G>T g.215680175G>T USH2A, variant 1: c.2299del/p.E767Sfs*21, variant 2: c.12268C>A/p.P4090T - USH2A_000768 possibly solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET2 targeted sequencing panel - see paper retinal disease 1037 PubMed: Weisschuh 2020 Filing key number: 603, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.12268C>A r.(?) p.(Pro4090Thr) - Unknown - likely pathogenic g.215853517G>T g.215680175G>T USH2A c.12268C>A, p.Pro4090Thr - USH2A_000768 only novel variants described in detail in the paper; original cohort contained over 750 patients from over 520 pedigrees, no c.DNA annotation in paper for this variant, c. extrapolated from protein; missense mutations had to show segregation in pedigrees of at least 3 members, two of whom had to be affected. PubMed: Dockery 2017 - - Germline yes - - - - DNA SEQ-NG-I blood panel of 254 genes implicated in retinopathies retinal disease 2 PubMed: Dockery 2017 no patient numbers in the paper, consecutive numbers given ? - Ireland - - - - - 1 LOVD
+?/. - c.12268C>A r.(?) p.(Pro4090Thr) - Unknown ACMG likely pathogenic g.215853517G>T g.215680175G>T - - USH2A_000768 ACMG GN005 criteria: PM2_P PM3_S PP3_P PubMed: Glockle, N. et al., 2014; PubMed: Weisschuh, N. et al., 2020 - rs780893919 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.12268C>A r.(?) p.(Pro4090Thr) - Unknown ACMG likely pathogenic (recessive) g.215853517G>T g.215680175G>T - - USH2A_000768 ACMG PP3, PM2, PP5_STRONG PubMed: Weisschuh 2024 550401 - Germline - - - - - DNA SEQ-NG - WGS ? SRP-1048 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
+?/. - c.12268C>A r.(?) p.(Pro4090Thr) - Unknown - likely pathogenic g.215853517G>T - USH2A(NM_206933.4):c.12268C>A (p.(Pro4090Thr)) - USH2A_000768 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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