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.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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Owner     
+?/? 10 c.1729T>C r.(?) p.(Cys577Arg) Laminin EGF-like 2 (575-640) Unknown ACMG VUS g.216465628A>G g.216292286A>G - - USH2A_000657 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - 0/170 controls +HincII;+Hpy166II;-HpyCH4V; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/? 10 c.1729T>C r.(?) p.(Cys577Arg) Laminin EGF-like 2 (575-640) Parent #2 ACMG VUS g.216465628A>G g.216292286A>G - - USH2A_000657 Heterozygous PubMed: Sodi 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - +HincII;+Hpy166II;-HpyCH4V; - - DNA SEQ - - USH2 - PubMed: Sodi 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/. - c.1729T>C r.(?) p.(Cys577Arg) - Unknown - pathogenic g.216465628A>G g.216292286A>G - - USH2A_000657 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - - Germline - 1/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 1 Yoshito Koyanagi
?/. - c.1729T>C r.(?) p.(Cys577Arg) - Unknown ACMG VUS g.216465628A>G g.216292286A>G - - USH2A_000657 ACMG GN005 criteria: PM2_P PP3_P PubMed: Colombo, L. et al., 2022 - rs1553327470 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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