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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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?/. - c.13478G>A r.(?) p.(Arg4493His) - Unknown - VUS g.215847775C>T g.215674433C>T USH2A(NM_206933.2):c.13478G>A (p.R4493H) - USH2A_001142 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.13478G>A r.(?) p.(Arg4493His) - Unknown - benign g.215847775C>T g.215674433C>T - - USH2A_001142 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs138879998 Germline - 41/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 41 Yoshito Koyanagi
-/. - c.13478G>A r.(?) p.(Arg4493His) - Both (homozygous) - benign g.215847775C>T g.215674433C>T - - USH2A_001142 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs138879998 Germline - 2/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 2 Yoshito Koyanagi
?/. - c.13478G>A r.(?) p.(Arg4493His) - Unknown - VUS g.215847775C>T g.215674433C>T - - USH2A_001142 - PubMed: Xu 2014 - rs138879998 Germline - 1/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP391 PubMed: Xu 2014 - - - China - - - - - 1 LOVD
-?/. - c.13478G>A r.(?) p.(Arg4493His) - Unknown ACMG likely benign g.215847775C>T g.215674433C>T - - USH2A_001142 ACMG GN005 criteria: BS2_S BP4_P PubMed: Huang, L. et al., 2018 - rs138879998 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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