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.

21 entries on 1 page. Showing entries 1 - 21.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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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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Re-site     

VIP     

Methylation     

Template     

Technique     

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Disease     

ID_report     

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Remarks     

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Panel size     

Owner     
+/+ 48i c.9570+1G>A r.spl p.? - Parent #2 - pathogenic g.215990338C>T g.215816996C>T - - USH2A_000788 Heterozygous; Mutation PubMed: Huang 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Huang 2013 Proband F - China - - - - - 1 Anne-Françoise Roux
+/+ 48i c.9570+1G>A r.spl p.? - Parent #2 - pathogenic g.215990338C>T g.215816996C>T - - USH2A_000788 Heterozygous; Mutation PubMed: Huang 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Huang 2013 Relative F - China - - - - - 1 Anne-Françoise Roux
+/+ 48i c.9570+1G>A r.spl p.? - Unknown - pathogenic g.215990338C>T g.215816996C>T - - USH2A_000788 Heterozygous; Mutation PubMed: Yang 2013 - - Germline - 0/400 controls - - - DNA SEQ, SEQ-NG-S - - DFN - PubMed: Yang 2013 Proband - age < 6 yrs - - China - - - - - 1 Anne-Françoise Roux
+/+ 48i c.9570+1G>A r.spl p.? - Paternal (confirmed) - pathogenic g.215990338C>T g.215816996C>T - - USH2A_000788 Heterozygous; mutation PubMed: Qu 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Qu 2014 Relative F - China - - - - - 1 Anne-Françoise Roux
+/+ 48i c.9570+1G>A r.spl p.? - Paternal (confirmed) - pathogenic g.215990338C>T g.215816996C>T - - USH2A_000788 Heterozygous; mutation PubMed: Qu 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Qu 2014 Relative M - China - - - - - 1 Anne-Françoise Roux
+/. - c.9570+1G>A r.spl? p.? - Unknown - pathogenic g.215990338C>T g.215816996C>T - - USH2A_000788 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs760225886 Germline - 1/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 1 Yoshito Koyanagi
+/. - c.9570+1G>A r.spl p.? - Parent #2 - pathogenic (recessive) g.215990338C>T g.215816996C>T - - USH2A_000788 - PubMed: Xu 2014 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease RP219 PubMed: Xu 2014 patient M - China - - - - - 1 LOVD
+/. - c.9570+1G>A r.spl? p.? - Unknown - pathogenic g.215990338C>T - USH2A(NM_206933.4):c.9570+1G>A - USH2A_000788 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.9570+1G>A r.spl p.(?) - Unknown - pathogenic g.215990338C>T g.215816996C>T c.9570+1C>T, p.? - USH2A_000788 error in annotation: c.9570+1C>T instead of G>A , compound heterozygous PubMed: Wang 2019 - - Germline yes - - - - DNA SEQ-NG blood panel of 126 genes retinal disease 13623 PubMed: Wang 2019 - M - China - - - - - 1 LOVD
+?/. - c.9570+1G>A r.spl p.? - Both (homozygous) - likely pathogenic g.215990338C>T g.215816996C>T USH2A c.9570 + 1G > A, splicing - USH2A_000788 homozygous, no ACMG classification PubMed: Shen 2021 - - Germline yes - - - - DNA SEQ-NG-I blood whole exome sequencing retinal disease F6‑III PubMed: Shen 2021 - F yes China - - - - - 1 LOVD
+/. - c.9570+1G>A r.spl p.(?) - Unknown ACMG pathogenic g.215990338C>T g.215816996C>T USH2A c.4576G>A(;)9570+1G>A, V1: c.9570+1G>A, - USH2A_000788 alleles in cis or trans; heterozygous PubMed: Chen 2021 - - Unknown ? - - - - DNA SEQ-NG blood 212 inherited retinal disease-related genes retinal disease F295 PubMed: Chen 2021 - ? - Taiwan - - - - - 1 LOVD
+?/. - c.9570+1G>A r.(?) p.(?) - Unknown - likely pathogenic g.215990338C>T g.215816996C>T USH2A c.9570+1G>A, Splicesite - USH2A_000788 heterozygous PubMed: Ng 2019 - - Germline yes - - - - DNA SEQ-NG-I blood Whole exome sequencing USH F2-II:6 PubMed: Ng 2019 proband; pedigree patient numbers differ from table numbers F - China - - - - - 1 LOVD
+?/. - c.9570+1G>A r.(?) p.(?) - Unknown - likely pathogenic g.215990338C>T g.215816996C>T USH2A c.9570+1G>A, Splicesite - USH2A_000788 heterozygous PubMed: Ng 2019 - - Germline yes - - - - DNA SEQ-NG-I blood Whole exome sequencing USH F2-II:5 PubMed: Ng 2019 proband's older sister (5) F - China - - - - - 1 LOVD
+/. - c.9570+1G>A r.spl p.(?) - Parent #2 - pathogenic g.215990338C>T g.215816996C>T USH2A c.9570+1G>A, - - USH2A_000788 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD181026A PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+/. 48i c.9570+1G>A r.spl p.(?) - Parent #1 ACMG pathogenic g.215990338C>T g.215816996C>T USH2A c.9570+1G>A - USH2A_000788 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF2185 PubMed: Zhu 2021 family 100, patient SRF2185 M - China - - - - - 1 LOVD
+/. 48i c.9570+1G>A r.spl p.(?) - Parent #1 ACMG pathogenic g.215990338C>T g.215816996C>T USH2A c.9570+1G>A - USH2A_000788 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 13 PubMed: Zhu 2021 family 122, patient 13 M - China - - - - - 1 LOVD
+/. 48i c.9570+1G>A r.spl p.(?) - Parent #1 ACMG pathogenic g.215990338C>T g.215816996C>T USH2A c.9570+1G>A - USH2A_000788 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 901 PubMed: Zhu 2021 family 233, patient 901 M - China - - - - - 1 LOVD
+/. 48i c.9570+1G>A r.spl p.(?) - Parent #1 ACMG pathogenic g.215990338C>T g.215816996C>T USH2A c.9570+1G>A - USH2A_000788 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 42785585 PubMed: Zhu 2021 family 26, patient 42785585 M - China - - - - - 1 LOVD
+/. 48i c.9570+1G>A r.spl p.(?) - Parent #2 ACMG pathogenic g.215990338C>T g.215816996C>T USH2A c.9570+1G>A - USH2A_000788 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF351 PubMed: Zhu 2021 family 3, patient SRF351 M - China - - - - - 1 LOVD
+/. - c.9570+1G>A r.spl p.? - Unknown - pathogenic g.215990338C>T g.215816996C>T USH2A c.4576G>A(;)9570+1G>A; p.? - USH2A_000788 heterozygous PubMed: Chen 2021 - - Germline/De novo (untested) ? Taiwan Biobank: 0.000659; GnomAD_exome_East: 0.000544; GnomAD_All: 0.0000399 - - - DNA SEQ-NG - targeted 212 IRD-related genes retinal disease F295 PubMed: Chen 2021 - - - Taiwan - - - - - 1 LOVD
+/. - c.9570+1G>A r.spl p.? - Unknown ACMG pathogenic g.215990338C>T g.215816996C>T - - USH2A_000788 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PP1_P PubMed: Gao, F. J. et al., 2021; PubMed: Yang, T. et al., 2013; PubMed: Huang, X. F. et al., 2013 - rs760225886 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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