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.

18 entries on 1 page. Showing entries 1 - 18.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Disease     

ID_report     

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Owner     
+/+ 62 c.12234_12235del r.(?) p.(Asn4079Trpfs*19) Fibronectin type-III 26 (4066-4150) Unknown - pathogenic g.215853553_215853554del g.215680211_215680212del 12234_12235delGA - USH2A_000066 Heterozygous PubMed: Baux 2007 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 62 c.12234_12235del r.(?) p.(Asn4079Trpfs*19) Fibronectin type-III 26 (4066-4150) Maternal (confirmed) - pathogenic g.215853553_215853554del g.215680211_215680212del 12234_12235delGA - USH2A_000066 Heterozygous; likely pathogenic PubMed: Glöckle 2014 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Glöckle 2014 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 62 c.12234_12235del r.(?) p.(Asn4079Trpfs*19) Fibronectin type-III 26 (4066-4150) Paternal (inferred) - pathogenic g.215853553_215853554del g.215680211_215680212del 12234_12235delGA - USH2A_000066 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/+ 62 c.12234_12235del r.(?) p.(Asn4079Trpfs*19) Fibronectin type-III 26 (4066-4150) Maternal (inferred) - pathogenic g.215853553_215853554del g.215680211_215680212del 12234_12235delGA - USH2A_000066 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/+ 62 c.12234_12235del r.(?) p.(Asn4079Trpfs*19) Fibronectin type-III 26 (4066-4150) Parent #2 - pathogenic g.215853553_215853554del g.215680211_215680212del 12234_12235delGA - USH2A_000066 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/+ 62 c.12234_12235del r.(?) p.(Asn4079Trpfs*19) Fibronectin type-III 26 (4066-4150) Parent #1 - pathogenic g.215853553_215853554del g.215680211_215680212del 12234_12235delGA - USH2A_000066 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+?/. - c.12234_12235del r.(?) p.(Asn4079Trpfs*19) - Parent #2 - likely pathogenic g.215853553_215853554del g.215680211_215680212del 12231_12232delAG - USH2A_000066 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 575 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+/. - c.12234_12235del r.(?) p.(Asn4079Trpfs*19) - Parent #2 - pathogenic g.215853553_215853554del g.215680211_215680212del 12234_12235delGA - USH2A_000066 - PubMed: Neuhaus 2017 - rs398124618 Germline - - - - - DNA SEQ - - USH Pat115 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+/. - c.12234_12235del r.(?) p.(Asn4079Trpfs*19) - Parent #2 - pathogenic g.215853553_215853554del g.215680211_215680212del 12234_12235delGA - USH2A_000066 - PubMed: Neuhaus 2017 - rs398124618 Germline yes - - - - DNA SEQ - - USH Pat111 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+/. 62 c.12234_12235del r.(12234_12235del) p.(Asn4079Trpfs*19) - Parent #2 ACMG pathogenic g.215853553_215853554del g.215680211_215680212del - - USH2A_000066 - Journal: Reurink 2021 - - Germline yes - - - - DNA SEQ-NG - gene panel retinal disease W19-0859 Journal: Reurink 2021 - - - Poland - - - - - 1 Janine Reurink
+/. - c.12234_12235del r.(?) p.(Asn4079Trpfs*19) - Unknown - pathogenic g.215853553_215853554del g.215680211_215680212del USH2A c.12234_12235del, p.Asn4079TrpfsTer19 - USH2A_000066 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 121-606 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.12234_12235del r.(?) p.(Asn4079Trpfs*19) - Parent #1 - likely pathogenic g.215853553_215853554del g.215680211_215680212del USH2A, variant 1: c.12234_12235del/p.N4079Wfs*19, variant 2: c.10421A>G/p.Y3474C - USH2A_000066 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET6 targeted sequencing panel - see paper retinal disease 307 PubMed: Weisschuh 2020 Filing key number: 102, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+?/. - c.12234_12235del r.(?) p.(Asn4079Trpfs*19) - Parent #1 - likely pathogenic g.215853553_215853554del g.215680211_215680212del USH2A, variant 1: c.8682-9A>G/p.?, variant 2: c.12234_12235del/ p.N4079Wfs*19 - USH2A_000066 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET2 targeted sequencing panel - see paper retinal disease 489 PubMed: Weisschuh 2020 Filing key number: 161, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.12234_12235del r.(?) p.(Asn4079Trpfs*19) - Both (homozygous) - likely pathogenic g.215853553_215853554del g.215680211_215680212del USH2A c.12234_12235del - USH2A_000066 no protein annotation written; homozygous PubMed: Charng 2020 - - Germline yes - - - - DNA SEQ-NG-I blood NGS SmartPanel (version 4 or 7, 183 or 233 genes) retinal disease 18 PubMed: Charng 2020 - M - Australia - - - - - 1 LOVD
+/. - c.12234_12235del r.(?) p.(Asn4079Trpfs*19) - Parent #2 ACMG pathogenic g.215853553_215853554del g.215680211_215680212del USH2A c.12234_12235del, p.(Asn4079Trpfs*19) - USH2A_000066 heterozygous PubMed: Reurink 2021 - - Germline yes - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0859 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. - c.12234_12235del r.(?) p.(Asn4079TrpfsTer19) - Unknown ACMG pathogenic g.215853553_215853554del g.215680211_215680212del 12234_12235delGA - USH2A_000066 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Reurink, J. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Glockle, N. et al., 2014; PubMed: Wafa, T. T. et al., 2021; PubMed: Weisschuh, N. et al., 2020; PubMed: Neuhaus, C. et al., 2017 - rs398124618 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.12234_12235del r.(?) p.(Asn4079TrpfsTer19) - Unknown ACMG pathogenic (recessive) g.215853553_215853554del g.215680211_215680212del - - USH2A_000066 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 96665 - Germline - - - - - DNA SEQ-NG - WGS ? USHII-362-1 PubMed: Weisschuh 2024 family, 3 affected M - Germany - - - - - 3 Johan den Dunnen
+/. - c.12234_12235del r.(?) p.(Asn4079TrpfsTer19) - Unknown ACMG pathogenic (recessive) g.215853553_215853554del g.215680211_215680212del - - USH2A_000066 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 96665 - 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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