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.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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-?/? 8 c.1346G>A r.(?) p.(Arg449His) Laminin N-terminal (271-517) Paternal (confirmed) ACMG likely benign g.216497020C>T g.216323678C>T - - USH2A_000878 Heterozygous; uncertain pathogenicity PubMed: Mutai 2013, USMA missense analysis, missense variant in MSV3d - - Germline - 5/378 controls - - - DNA SEQ, SEQ-NG-S - - DFN - PubMed: Mutai 2013 Proband F - Japan - - - - - 1 Anne-Françoise Roux
?/. - c.1346G>A r.(?) p.(Arg449His) - Unknown - VUS g.216497020C>T g.216323678C>T - - USH2A_000878 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs766715882 Germline - 8/1203 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1203 retinitis pigmentosa cases - - Japan - - - - - 8 Yoshito Koyanagi
?/. - c.1346G>A r.(?) p.(Arg449His) - Unknown - VUS g.216497020C>T - - - USH2A_000878 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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