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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Effect     

Exon     

AscendingDNA change (cDNA)     

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?/. - c.2792G>A r.(?) p.(Cys931Tyr) - Unknown - VUS g.216419944C>T g.216246602C>T USH2A(NM_206933.4):c.2792G>A (p.C931Y) - USH2A_001657 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.2792G>A r.(?) p.(Cys931Tyr) - Unknown - likely pathogenic (recessive) g.216419944C>T g.216246602C>T - - USH2A_001657 - PubMed: Xu 2014 - rs145383772 Germline - 1/314 case chromosomes - - - DNA SEQ - - retinal disease RP300 PubMed: Xu 2014 - - - China - - - - - 1 Isabelle Audo
+?/. 13 c.2792G>A r.(?) p.(Cys931Tyr) - Parent #1 ACMG likely pathogenic g.216419944C>T g.216246602C>T USH2A c.2792G>A, p.C931Y - USH2A_001657 single heterozygous variant in a recessive disesase, no second allele PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 42922992 PubMed: Zhu 2021 family 140, patient 42922992 F - China - - - - - 1 LOVD
+?/. 13 c.2792G>A r.(?) p.(Cys931Tyr) - Parent #2 ACMG likely pathogenic g.216419944C>T g.216246602C>T USH2A c.2792G>A, p.C931Y - USH2A_001657 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 43861981 PubMed: Zhu 2021 family 111, patient 43861981 F - China - - - - - 1 LOVD
+/. 13 c.2792G>A r.(?) p.(Cys931Tyr) - Paternal (confirmed) ACMG pathogenic g.216419944C>T g.216246602C>T M1: USH2A c.2792G>A, C931Y - USH2A_001657 heterozygous PubMed: Chen 2020 - - Germline ? - - - - DNA SEQ-NG-I blood xGen Exome Research Panel retinal disease 1-II:2 PubMed: Chen 2020 family 1, proband F - China - - - - - 1 LOVD
+/. 13 c.2792G>A r.(?) p.(Cys931Tyr) - Paternal (confirmed) ACMG pathogenic g.216419944C>T g.216246602C>T M1: USH2A c.2792G>A, C931Y - USH2A_001657 heterozygous PubMed: Chen 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood xGen Exome Research Panel retinal disease 1-II:3 PubMed: Chen 2020 family 1, brother of proband M - China - - - - - 1 LOVD
+?/. - c.6923C>A r.(?) p.(Ala2308Glu) - Unknown - likely pathogenic g.216419944C>T g.216246602C>T c.6923G>T, p.(Ala2308Glu) - USH2A_001657 error in annotation: c.6923G>T instead of C>A, compound heterozygous PubMed: Wang 2019 - - Germline ? - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 13720 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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