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.

13 entries on 1 page. Showing entries 1 - 13.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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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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Template     

Technique     

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Disease     

ID_report     

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Owner     
+/+ 64 c.13822C>T r.(?) p.(Arg4608*) Fibronectin type-III 31 (4529-4627) Parent #1 - pathogenic g.215844625G>A g.215671283G>A - - USH2A_000132 Heterozygous - - - Germline - - - - - DNA SEQ - - RPar - - Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 64 c.13822C>T r.(?) p.(Arg4608*) Fibronectin type-III 31 (4529-4627) Parent #1 - pathogenic g.215844625G>A g.215671283G>A - - USH2A_000132 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Relative M - Spain - - - - - 1 Anne-Françoise Roux
+/+ 64 c.13822C>T r.(?) p.(Arg4608*) Fibronectin type-III 31 (4529-4627) Paternal (confirmed) - pathogenic g.215844625G>A g.215671283G>A - - USH2A_000132 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - Spain - - - - - 1 Anne-Françoise Roux
+/+ 64 c.13822C>T r.(?) p.(Arg4608*) Fibronectin type-III 31 (4529-4627) Unknown - pathogenic g.215844625G>A g.215671283G>A - - USH2A_000132 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA MLPA, SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 64 c.13822C>T r.(?) p.(Arg4608*) Fibronectin type-III 31 (4529-4627) Parent #1 - pathogenic g.215844625G>A g.215671283G>A - - USH2A_000132 Heterozygous; mutation PubMed: Jiang 2015 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 64 c.13822C>T r.(?) p.(Arg4608*) Fibronectin type-III 31 (4529-4627) Parent #2 - pathogenic g.215844625G>A g.215671283G>A - - USH2A_000132 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. - c.13822C>T r.(?) p.(Arg4608*) - Parent #2 - pathogenic (recessive) g.215844625G>A g.215671283G>A - - USH2A_000132 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP2005 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.13822C>T r.(?) p.(Arg4608Ter) - Parent #2 - likely pathogenic g.215844625G>A g.215671283G>A - - USH2A_000132 - PubMed: Bravo-Gil 2017 - - Germline yes - - - - DNA SEQ-NG - 68-gene panel retinal disease Pat17 PubMed: Bravo-Gil 2017 family - - Spain - - - - - 1 Nereida Bravo Gil
+?/. - c.13822C>T r.(?) p.(Arg4608*) - Parent #1 - likely pathogenic g.215844625G>A g.215671283G>A USH2A, variant 1: c.920_923dup/p.H308Qfs*16, variant 2: c.13822C>T/p.R4608* - USH2A_000132 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 784 PubMed: Weisschuh 2020 Filing key number: 303, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. 64 c.13822C>T r.(?) p.(Arg4608*) - Parent #1 ACMG pathogenic g.215844625G>A g.215671283G>A USH2A c.C13822T, p.R4608* - USH2A_000132 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease USHsrf69 PubMed: Zhu 2021 family 217, patient USHsrf69 M - China - - - - - 1 LOVD
+/. 64 c.13822C>T r.(?) p.(Arg4608*) - Parent #2 - pathogenic g.215844625G>A - c.13822C>T - USH2A_000132 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+/. - c.13822C>T r.(?) p.(Arg4608Ter) - Unknown ACMG pathogenic g.215844625G>A g.215671283G>A - - USH2A_000132 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Bonnet, C. et al., 2016; PubMed: Jiang, L. et al., 2015; PubMed: Bravo-Gil, N. et al., 2017 - rs367674026 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.13822C>T r.(?) p.(Arg4608Ter) - Unknown ACMG pathogenic (recessive) g.215844625G>A g.215671283G>A - - USH2A_000132 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHII-304 PubMed: Weisschuh 2024 patient, no family history 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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