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.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

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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Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

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Disease     

ID_report     

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Owner     
+/. - c.9676C>T r.(?) p.(Arg3226Ter) - Unknown - pathogenic g.215987141G>A g.215813799G>A - - USH2A_001600 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.9676C>T r.(?) p.(Arg3226*) - Parent #1 - pathogenic g.215987141G>A g.215813799G>A - - USH2A_001600 - PubMed: Neuhaus 2017 - - Germline yes - - - - DNA SEQ - - USH Pat64 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+?/. 49 c.9676C>T r.(?) p.(Arg3226Ter) - Unknown - likely pathogenic g.215987141G>A g.215813799G>A C9676T - USH2A_001600 - PubMed: Katagiri 2014 - - Germline - - - - - DNA SEQ-NG - WES retinal disease RP#023 PubMed: Katagiri 2014 family - - Japan - - - - - 1 LOVD
+?/. - c.9676C>T r.(?) p.(Arg3226*) - Parent #1 - likely pathogenic g.215987141G>A g.215813799G>A USH2A c.9676C>T, p.R3226X - USH2A_001600 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 116 PubMed: Jauregui 2020 - F - (United States) white - - - - 1 LOVD
+/. 49 c.9676C>T r.(?) p.(Arg3226*) - Unknown - pathogenic (recessive) g.215987141G>A - c.9676C>T - USH2A_001600 - PubMed: Colombo-2020 - rs760858249 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+?/. 49 c.9676C>T r.(?) p.(Arg3226*) - Parent #2 ACMG likely pathogenic g.215987141G>A g.215813799G>A USH2A c.9676C>T, p.Arg3226* - USH2A_001600 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes retinal disease 53 PubMed: Meng 2020 - M - China - - - - - 1 LOVD
+?/. - c.9676C>T r.(?) p.(Arg3226*) - Unknown - likely pathogenic g.215987141G>A g.215813799G>A USH2A c.9676C>T, p.Arg3226* - USH2A_001600 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD18093274 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+?/. - c.9676C>T r.(?) p.(Arg3226*) - Unknown - likely pathogenic g.215987141G>A g.215813799G>A USH2A c.9676C>T, p.Arg3226* - USH2A_001600 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD18100638 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. - c.9676C>T r.(?) p.(Arg3226*) - Unknown - likely pathogenic g.215987141G>A g.215813799G>A USH2A c.9676C>T, p.Arg3226* - USH2A_001600 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD18100639 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+/. 49 c.9676C>T r.(?) p.(Arg3226*) - Parent #2 ACMG pathogenic g.215987141G>A g.215813799G>A USH2A c.9676C>T, p.R3226* - USH2A_001600 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF_1361 PubMed: Zhu 2021 family 68, patient SRF_1361 F - China - - - - - 1 LOVD
+/. - c.9676C>T r.(?) p.(Arg3226Ter) - Unknown ACMG pathogenic g.215987141G>A g.215813799G>A - - USH2A_001600 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PP1_M PubMed: Gao, F. J. et al., 2021; PubMed: Meng, X. et al., 2021; PubMed: Colombo, L. et al., 2022; PubMed: Jauregui, R. et al., 2020; PubMed: Neuhaus, C. et al., 2017 - rs760858249 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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