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)     

RNA change     

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DNA change (hg38)     

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+/? 50 c.9844T>C r.(?) p.(Cys3282Arg) Cystein rich (3192-3358) Parent #2 ACMG likely pathogenic g.215972363A>G g.215799021A>G - - USH2A_000083 Heterozygous PubMed: Baux 2007, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
?/. 50 c.9844T>C r.(?) p.(Cys3282Arg) - Parent #2 - VUS g.215972363A>G - c.9844T>C - USH2A_000083 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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