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.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

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AscendingDNA change (cDNA)     

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+?/. - c.3221G>A r.(?) p.(Trp1074*) - Parent #1 - likely pathogenic g.216380710C>T g.216207368C>T USH2A, variant 1: c.908G>A/p.R303H, variant 2: c.3221G>A/p.W1074* - USH2A_002400 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 757 PubMed: Weisschuh 2020 Filing key number: 292, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. - c.3221G>A r.(?) p.(Trp1074Ter) - Unknown ACMG pathogenic g.216380710C>T g.216207368C>T - - USH2A_002400 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Weisschuh, N. et al., 2020 - rs1064797138 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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