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.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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+/. - c.4616C>T r.(?) p.(Thr1539Ile) - Unknown - pathogenic g.216348605G>A g.216175263G>A - - USH2A_001531 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs758095361 Germline - 5/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 5 Yoshito Koyanagi
+/. - c.4616C>T r.(?) p.(Thr1539Ile) - Parent #1 ACMG pathogenic (recessive) g.216348605G>A g.216175263G>A - - USH2A_001531 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19891 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
?/. 21 c.4616C>T r.(?) p.(Thr1539Ile) - Unknown - VUS g.216348605G>A g.216175263G>A C4616T - USH2A_001531 - PubMed: Katagiri 2014 - - Germline - - - - - DNA SEQ-NG - WES retinal disease RP#008 PubMed: Katagiri 2014 family - - Japan - - - - - 1 LOVD
+?/. 21 c.4616C>T r.(?) p.(Thr1539Ile) - Unknown ACMG likely pathogenic g.216348605G>A g.216175263G>A NM_206933.2:c.4616C>T, NP_996816.2:p.(Thr1539Ile), NC_000001.10:g.216348605G>A - USH2A_001531 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - panel of 441 hereditary eye disease genes including 291 genes related to IRD retinal disease 2016060109 PubMed: Wang 2018 - F ? China Han Chinese - - - - 1 LOVD
?/. 21 c.4616C>T r.(?) p.(Thr1539Ile) - Unknown - VUS g.216348605G>A - c.4616C>T - USH2A_001531 - PubMed: Chen-2013 - - Unknown - - - - - DNA SEQ blood - retinal disease - PubMed: Chen-2013 - - - China Chinese - - - - 1 LOVD
?/. 21 c.4616C>T r.(?) p.(Thr1539Ile) - Unknown ACMG VUS g.216348605G>A g.216175263G>A USH2A c.4616C>T, p.(Thr1539Ile) - USH2A_001531 heterozygous PubMed: Dan 2020 - - Germline/De novo (untested) yes - - - - DNA SEQ-NG blood Panel 5 containing 429 genes retinal disease 113 PubMed: Dan 2020 - F ? China - - - - - 1 LOVD
+/. - c.4616C>T r.(?) p.(Thr1539Ile) - Both (homozygous) - pathogenic g.216348605G>A g.216175263G>A USH2A c.4616C>T, p.Thr1539Ile - USH2A_001531 homozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD18125290 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
?/. - c.4616C>T r.(?) p.(Thr1539Ile) - Unknown ACMG VUS g.216348605G>A g.216175263G>A - - USH2A_001531 ACMG GN005 criteria: PM2_P PM3_M PubMed: Gao, F. J. et al., 2021; PubMed: Sun, T. et al., 2018 - rs758095361 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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