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     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

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VIP     

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Owner     
+/. - c.490G>T r.(?) p.(Val164Phe) - Unknown - pathogenic g.216592017C>A g.216418675C>A - - USH2A_001553 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs527236123 Germline - 2/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 2 Yoshito Koyanagi
+/. - c.490G>T r.(?) p.(Val164Phe) - Parent #2 - pathogenic g.216592017C>A g.216418675C>A - - USH2A_001553 - PubMed: Maeda 2018 - rs527236123 Germline - - - - - DNA SEQ, SEQ-NG - 39-gene panel retinal disease Pat29 PubMed: Maeda 2018 family F - Japan - - - - - 1 LOVD
+?/. - c.490G>T r.(?) p.(Val164Phe) - Parent #2 - likely pathogenic g.216592017C>A g.216418675C>A - - USH2A_001553 - PubMed: Oishi 2014 - - Germline - - - - - DNA SEQ-NG - 193-gene panel retinal disease K1766 PubMed: Oishi 2014 simplex case - - Japan - - - - - 1 LOVD
+?/. - c.490G>T r.(?) p.(Val164Phe) - Parent #2 - likely pathogenic g.216592017C>A g.216418675C>A - - USH2A_001553 - PubMed: Oishi 2014 - - Germline - - - - - DNA SEQ-NG - 193-gene panel retinal disease K1793 PubMed: Oishi 2014 family - - Japan - - - - - 1 LOVD
-/. 3 c.490G>T r.(?) p.(Val164Phe) - Both (homozygous) - benign g.216592017C>A - c.490G>T - USH2A_001553 - PubMed: Nishiguchi-2013 - - Germline - - - - - DNA SEQ-NG blood - retinal disease - PubMed: Nishiguchi-2013 - F yes - Japanese - - - - 1 Julia Lopez
+?/. - c.490G>T r.(?) p.(Val164Phe) - Unknown - likely pathogenic g.216592017C>A g.216418675C>A USH2A p.(Val164Phe) - USH2A_001553 only protein changes written in the publication; Mutalyzer Back Translator used for coding DNA variant (impossible in case of frameshift mutations); compound heterozygous PubMed: Koyanagi 2020 - - Unknown ? - - - - DNA ? - retrospective study retinal disease N-168 PubMed: Koyanagi 2020 - M - Japan - - - - - 1 LOVD
+/. 3 c.490G>T r.(?) p.(Val164Phe) - Unknown - pathogenic (recessive) g.216592017C>A - c.490G>T:p.V164F - USH2A_001553 - PubMed: Numa-2020 - - Germline - - - - - DNA SEQ, SEQ-NG - - retinal disease - PubMed: Numa 2020 - F - Japan Japanese - - - - 1 LOVD
+?/. - c.490G>T r.(?) p.(Val164Phe) - Parent #1 - likely pathogenic g.216592017C>A g.216418675C>A USH2A c.490G>T, p.(Val164Phe) - USH2A_001553 heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
+?/. - c.490G>T r.(?) p.(Val164Phe) - Parent #1 - likely pathogenic g.216592017C>A g.216418675C>A USH2A c.490G>T, p.(Val164Phe) - USH2A_001553 heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
+?/. - c.490G>T r.(?) p.(Val164Phe) - Parent #1 - likely pathogenic g.216592017C>A g.216418675C>A USH2A c.490G>T, p.(Val164Phe) - USH2A_001553 heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
?/. - c.490G>T r.(?) p.(Val164Phe) - Unknown ACMG VUS g.216592017C>A g.216418675C>A - - USH2A_001553 ACMG GN005 criteria: PM2_P PM3_P PubMed: Inaba, A. et al., 2020; PubMed: Inaba, A. et al., 2020 - rs527236123 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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