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)     

RNA change     

Protein     

P-domain     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Disease     

ID_report     

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Owner     
+/+ 10-11 c.1644+10004_1972-12164del r.(?) p.(Cys549_Gln657del) Laminin EGF-like 1 (518-574);Laminin EGF-like 2 (575-640);Laminin EGF-like 3 (641-693) Paternal (confirmed) - pathogenic g.216436604_216485221del g.216263262_216311879del - - USH2A_000463 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 10-11 c.1644+10004_1972-12164del r.(?) p.(Cys549_Gln657del) Laminin EGF-like 1 (518-574);Laminin EGF-like 2 (575-640);Laminin EGF-like 3 (641-693) Paternal (inferred) - pathogenic g.216436604_216485221del g.216263262_216311879del - - USH2A_000463 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/. 9i_11i c.1644+10004_1972-12164del r.(1644_1972del) p.(Cys549_Gln657del) - Parent #2 ACMG pathogenic g.216436604_216485221del g.216263262_216311879del - - USH2A_000463 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0862 Journal: Reurink 2021 - - - Poland - - - - - 1 Janine Reurink
+/. - c.1644+10004_1972-12164del r.(?) p.(?) - Parent #1 - pathogenic g.216436604_216485221del g.216263262_216311879del USH2A allele 1: Exon 10-11 deletion, g.216436604_ 216485221 del, allele 2: p.Gly602GlufsX34 - USH2A_000463 breakpoints identical to ClinVar variant PubMed: Austin-Tse 2018 SCV000709744 - 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-3 PubMed: Austin-Tse 2018 Discovery Cohort ? - United States - - - - - 1 LOVD
+/. - c.1644+10004_1972-12164del r.(?) p.(Cys549_Gln657del) - Parent #2 ACMG pathogenic g.216436604_216485221del g.216263262_216311879del USH2A c.1644+10004_1972-12164del, p.(Cys549_Gln657del) - USH2A_000463 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0862 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+?/. - c.1644+10004_1972-12164del r.? p.? - Unknown ACMG likely pathogenic (recessive) g.216436604_216485221del g.216263262_216311879del - - USH2A_000463 ACMG PM2, PVS1 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHII-362-1 PubMed: Weisschuh 2024 family, 3 affected M - Germany - - - - - 3 Johan den Dunnen
+?/. - c.1644+10004_1972-12164del r.? p.? - Unknown ACMG likely pathogenic (recessive) g.216436604_216485221del g.216263262_216311879del - - USH2A_000463 ACMG PM2, PVS1 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHII-362-2 PubMed: Weisschuh 2024 relative M - Germany - - - - - 1 Johan den Dunnen
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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