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.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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ISCN     

DB-ID     

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ClinVar ID     

dbSNP ID     

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Disease     

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Panel size     

Owner     
+/. - c.5299-932_5573-1099delinsAGGTAACTTTCCCAAGGTCACATGGCTAGTAAGCAGATAGCAAGACACTAAGTCTCTCAGGCAGCCTGTTATAAAG r.spl p.(Met1767Valfs*6) - Paternal (confirmed) - pathogenic g.216247745_216252636delinsATAACAGGCTGCCTGAGAGACTTAGTGTCTTGCTATCTGCTTACTAGCCATGTGACCTTGGGAAAGTTACCT g.216074403_216079294delinsATAACAGGCTGCCTGAGAGACTTAGTGTCTTGCTATCTGCTTACTAGCCATGTGACCTTGGGAAAGTTACCT USH2A exon 27 deleted c.[5299-932_5572+1023del; 5572+1100_5573-1099del], p.(Met1767Valfs*6) - USH2A_002494 error in annotation, a delins is marked as two independent deletions; should be c.5299-932_5573-1099delinsAGGTAACTTTCCCAAGGTCACATGGCTAGTAAGCAGATAGCAAGACACTAAGTCTCTCAGGCAGCCTGTTATAAAG PubMed: Steele-Stallard 2013 - - Germline yes - - - - DNA MLPA, arrayCGH, PCR, SEQ - - retinal disease 148_II:1 PubMed: Steele-Stallard 2013 proband of family 148_II:1 M - United Kingdom (Great Britain) white - - - - 1 LOVD
+/. - c.5299-932_5573-1099delinsAGGTAACTTTCCCAAGGTCACATGGCTAGTAAGCAGATAGCAAGACACTAAGTCTCTCAGGCAGCCTGTTATAAAG r.(?) p.(?) - Parent #1 - pathogenic g.216247745_216252636delinsATAACAGGCTGCCTGAGAGACTTAGTGTCTTGCTATCTGCTTACTAGCCATGTGACCTTGGGAAAGTTACCT g.216074403_216079294delinsATAACAGGCTGCCTGAGAGACTTAGTGTCTTGCTATCTGCTTACTAGCCATGTGACCTTGGGAAAGTTACCT USH2A allele 1: Exon 27 deletion, g.[216250408_216252636del;216247741_216250331del], allele 2: p.Gln1063SerfsX15 - USH2A_002494 error in annotation, a delins is marked as two independent deletions; should be g.216247745_216252636delinsATAACAGGCTGCCTGAGAGACTTAGTGTCTTGCTATCTGCTTACTAGCCATGTGACCTTGGGAAAGTTACCT PubMed: Austin-Tse 2018 SCV000205712 - Germline yes - - - - DNA SEQ-NG-I, MLPA - sequenced by dideoxy sequencing or hearing loss gene panel by either microarray-based resequencing or oligonucleotide-based target capture followed by next generation sequencing using Illumina HiSeq2000 or MiSeq instrument USH D-6 PubMed: Austin-Tse 2018 Discovery Cohort ? - United States - - - - - 1 LOVD
+/. - c.5299-932_5573-1099delinsAGGTAACTTTCCCAAGGTCACATGGCTAGTAAGCAGATAGCAAGACACTAAGTCTCTCAGGCAGCCTGTTATAAAG r.(?) p.(?) - Parent #1 - pathogenic g.216247745_216252636delinsATAACAGGCTGCCTGAGAGACTTAGTGTCTTGCTATCTGCTTACTAGCCATGTGACCTTGGGAAAGTTACCT g.216074403_216079294delinsATAACAGGCTGCCTGAGAGACTTAGTGTCTTGCTATCTGCTTACTAGCCATGTGACCTTGGGAAAGTTACCT USH2A allele 1: Exon 27 deletion, g.[216250408_216252636del;216247741_216250331del], allele 2: p.Arg317Arg - USH2A_002494 error in annotation, a delins is marked as two independent deletions; should be g.216247745_216252636delinsATAACAGGCTGCCTGAGAGACTTAGTGTCTTGCTATCTGCTTACTAGCCATGTGACCTTGGGAAAGTTACCT PubMed: Austin-Tse 2018 SCV000205712 - Germline yes - - - - DNA SEQ-NG-I, PCRdd - sequenced by dideoxy sequencing or hearing loss gene panel by either microarray-based resequencing or oligonucleotide-based target capture followed by next generation sequencing using Illumina HiSeq2000 or MiSeq instrument SNHL R-5 PubMed: Austin-Tse 2018 Retrospective Cohort ? - United States - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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