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.

14 entries on 1 page. Showing entries 1 - 14.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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Reference     

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+?/? 65 c.14243C>T r.(?) p.(Ser4748Phe) Fibronectin type-III 33 (4732-4825) Unknown ACMG VUS g.215824034G>A g.215650692G>A - - USH2A_000865 Heterozygous; possible pathogenic PubMed: Zhao 2014, USMA missense analysis, missense variant in MSV3d - - Germline - 0/400 controls - - - DNA SEQ - - RPar - PubMed: Zhao 2014 Proband - - Japan - - - - - 1 Anne-Françoise Roux
+/. - c.14243C>T r.(?) p.(Ser4748Phe) - Unknown - pathogenic g.215824034G>A g.215650692G>A - - USH2A_000865 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs527236126 Germline - 6/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 6 Yoshito Koyanagi
+?/. - c.14243C>T r.(?) p.(Ser4748Phe) - Both (homozygous) - likely pathogenic g.215824034G>A g.215650692G>A - - USH2A_000865 - PubMed: Oishi 2014 - - Germline - - - - - DNA SEQ-NG - 193-gene panel retinal disease K6166 PubMed: Oishi 2014 family - - Japan - - - - - 1 LOVD
+?/. - c.14243C>T r.(?) p.(Ser4748Phe) - Unknown ACMG VUS g.215824034G>A - - - USH2A_000865 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_GS_0010 - - F - Korea, South (Republic) - - - - - 1 Jinu Han
+?/. - c.14243C>T r.(?) p.(Ser4748Phe) - Unknown ACMG VUS g.215824034G>A - - - USH2A_000865 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_GS_0063 - - F - Korea, South (Republic) - - - - - 1 Jinu Han
+?/. - c.14243C>T r.(?) p.(Ser4748Phe) - Unknown ACMG VUS g.215824034G>A - - - USH2A_000865 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - USH IR_GH_0065 - - F - Korea, South (Republic) - - - - - 1 Jinu Han
+?/. - c.14243C>T r.(?) p.(Ser4748Phe) - Unknown - likely pathogenic g.215824034G>A g.215650692G>A USH2A p.(Ser4748Phe) - USH2A_000865 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-109 PubMed: Koyanagi 2020 - M - Japan - - - - - 1 LOVD
+?/. - c.14243C>T r.(?) p.(Ser4748Phe) - Unknown - likely pathogenic g.215824034G>A g.215650692G>A USH2A p.(Ser4748Phe) - USH2A_000865 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-208 PubMed: Koyanagi 2020 - F - Japan - - - - - 1 LOVD
?/. 65 c.14243C>T r.(?) p.(Ser4748Phe) - Unknown - VUS g.215824034G>A - c.14243C>T:p.S4748F - USH2A_000865 - PubMed: Numa-2020 - - Unknown - - - - - DNA SEQ, SEQ-NG - - retinal disease - PubMed: Numa 2020 - M - Japan Japanese - - - - 1 LOVD
+?/. - c.14243C>T r.(?) p.(Ser4748Phe) - Both (homozygous) - likely pathogenic g.215824034G>A g.215650692G>A USH2A c.14243C>T, p.(Ser4748Phe) - USH2A_000865 homozygous 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.14243C>T r.(?) p.(Ser4748Phe) - Parent #1 - likely pathogenic g.215824034G>A g.215650692G>A USH2A c.14243C>T, p.(Ser4748Phe) - USH2A_000865 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.14243C>T r.(?) p.(Ser4748Phe) - Parent #2 - likely pathogenic g.215824034G>A g.215650692G>A USH2A c.14243C>T, p.(Ser4748Phe) - USH2A_000865 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
?/. 65 c.14243C>T r.(?) p.(Ser4748Phe) - Parent #2 - VUS g.215824034G>A - c.14243C>T - USH2A_000865 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. - c.14243C>T r.(?) p.(Ser4748Phe) - Unknown ACMG VUS g.215824034G>A g.215650692G>A - - USH2A_000865 ACMG GN005 criteria: PM2_P PM3_M PubMed: Inaba, A. et al., 2020 - rs527236126 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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