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.

9 entries on 1 page. Showing entries 1 - 9.
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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     

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Disease     

ID_report     

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Owner     
?/. - c.9340C>T r.(?) p.(Pro3114Ser) - Unknown - VUS g.216011364G>A g.215838022G>A - - USH2A_001497 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs201071654 Germline - 46/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 46 Yoshito Koyanagi
-?/. - c.9340C>T r.(?) p.(Pro3114Ser) - Unknown - likely benign g.216011364G>A g.215838022G>A USH2A(NM_206933.2):c.9340C>T (p.P3114S) - USH2A_001497 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.9340C>T r.(?) p.(Pro3114Ser) - Unknown - likely pathogenic (recessive) g.216011364G>A g.215838022G>A - - USH2A_001497 - PubMed: Xu 2014 - rs201071654 Germline - 3/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP202 PubMed: Xu 2014 patient F - China - - - - - 1 LOVD
?/. - c.9340C>T r.(?) p.(Pro3114Ser) - Unknown - VUS g.216011364G>A g.215838022G>A - - USH2A_001497 - PubMed: Xu 2014 - rs201071654 Germline - 3/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP021 PubMed: Xu 2014 family M - China - - - - - 1 LOVD
?/. - c.9340C>T r.(?) p.(Pro3114Ser) - Unknown - VUS g.216011364G>A g.215838022G>A - - USH2A_001497 - PubMed: Xu 2014 - rs201071654 Germline - 3/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP056 PubMed: Xu 2014 patient M - China - - - - - 1 LOVD
-/. 47 c.9340C>T r.(?) p.(Pro3114Ser) - Both (homozygous) - benign g.216011364G>A - c.9340C>T - USH2A_001497 - PubMed: Nishiguchi-2013 - - Germline - - - - - DNA SEQ-NG blood - retinal disease - PubMed: Nishiguchi-2013 - F yes - Japanese - - - - 1 Julia Lopez
-?/. 47 c.9340C>T r.(?) p.(Pro3114Ser) - Parent #2 ACMG likely benign g.216011364G>A g.215838022G>A USH2A c.9340C>T, p.Pro3114Ser - USH2A_001497 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes retinal disease 55 PubMed: Meng 2020 - M - China - - - - - 1 LOVD
+?/. - c.9340C>T r.(?) p.(Pro3114Ser) - Parent #2 - likely pathogenic g.216011364G>A g.215838022G>A USH2A c.9340C>T, p.Pro3114Ser - USH2A_001497 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease DTP190123 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
-/. - c.9340C>T r.(?) p.(Pro3114Ser) - Unknown ACMG benign g.216011364G>A g.215838022G>A - - USH2A_001497 ACMG GN005 criteria: BS1_P BS2_S BP4_P PubMed: Gao, F. J. et al., 2021; PubMed: Meng, X. et al., 2021 - rs201071654 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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