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.

16 entries on 1 page. Showing entries 1 - 16.
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?/. - c.2296T>C r.(?) p.(Cys766Arg) - Unknown - VUS g.216420440A>G g.216247098A>G - - USH2A_000129 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/? 13 c.2296T>C r.(?) p.(Cys766Arg) Laminin EGF-like 5 (747-794) Unknown ACMG VUS g.216420440A>G g.216247098A>G - - USH2A_000129 Heterozygous USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - RPar - - Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 13 c.2296T>C r.(?) p.(Cys766Arg) Laminin EGF-like 5 (747-794) Unknown ACMG VUS g.216420440A>G g.216247098A>G - - USH2A_000129 Heterozygous; likely pathogenic PubMed: Glöckle 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Glöckle 2014 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/? 13 c.2296T>C r.(?) p.(Cys766Arg) Laminin EGF-like 5 (747-794) Unknown ACMG VUS g.216420440A>G g.216247098A>G - - USH2A_000129 Heterozygous; UV3 PubMed: Aparisi 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+?/? 13 c.2296T>C r.(?) p.(Cys766Arg) Laminin EGF-like 5 (747-794) Parent #2 ACMG VUS g.216420440A>G g.216247098A>G - - USH2A_000129 Heterozygous PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. - c.2296T>C r.(?) p.(Cys766Arg) - Both (homozygous) - pathogenic (recessive) g.216420440A>G g.216247098A>G - - USH2A_000129 - PubMed: Karali 2019, Journal: Karali 2019 - - Germline - - - - - DNA SEQ-NG - - retinal disease Fam26P30 PubMed: Karali 2019, Journal: Karali 2019 - - - Italy - - - - - 1 Sandro Banfi
+?/. - c.2296T>C r.(?) p.(Cys766Arg) - Unknown ACMG likely pathogenic g.216420440A>G - - - USH2A_000129 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+/. 13 c.2296T>C r.(?) p.(Cys766Arg) - Parent #1 - pathogenic g.216420440A>G g.216247098A>G - - USH2A_000129 - PubMed: Bernardis 2016 - - Germline - - - - - DNA SEQ-NG - 72-gene panel retinal disease IRD023 PubMed: Bernardis 2016 familial case - - Italy - - - - - 1 LOVD
+/. 13 c.2296T>C r.(?) p.(Cys766Arg) - Parent #1 - pathogenic g.216420440A>G g.216247098A>G - - USH2A_000129 - PubMed: Bernardis 2016 - - Germline - - - - - DNA SEQ-NG - 72-gene panel retinal disease IRD024 PubMed: Bernardis 2016 - - - Italy - - - - - 1 LOVD
+/. 13 c.2296T>C r.(?) p.(Cys766Arg) - Parent #1 - pathogenic g.216420440A>G g.216247098A>G - - USH2A_000129 - PubMed: Bernardis 2016 - - Germline - - - - - DNA SEQ-NG - 72-gene panel retinal disease IRD038 PubMed: Bernardis 2016 - - Italy - - - - - 1 LOVD
+/. 13 c.2296T>C r.(?) p.(Cys766Arg) - Unknown - pathogenic g.216420440A>G - c.2296T>C - USH2A_000129 - PubMed: Foote-2019 - - Germline - - - - - DNA SEQ-NG blood - retinal disease - PubMed: Foote-2019 - M - United States - - - - - 1 LOVD
+?/. - c.2296T>C r.(?) p.(Cys766Arg) - Parent #1 - likely pathogenic g.216420440A>G g.216247098A>G USH2A, variant 1: c.2296T>C/p.C766R, variant 2: c.11864G>A/p.W3955* - USH2A_000129 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET2 targeted sequencing panel - see paper retinal disease 522 PubMed: Weisschuh 2020 Filing key number: 174, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.2296T>C r.(?) p.(Cys766Arg) - Parent #1 - likely pathogenic g.216420440A>G g.216247098A>G USH2A, variant 1: c.908G>A/p.R303H, variant 2: c.2296T>C/p.C766R - USH2A_000129 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET7 targeted sequencing panel - see paper retinal disease 1190 PubMed: Weisschuh 2020 Filing key number: 880, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
?/. 13 c.2296T>C r.(?) p.(Cys766Arg) - Unknown - VUS g.216420440A>G - c.2296T>C - USH2A_000129 - PubMed: Colombo-2020 - rs368687374 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
?/. 13 c.2296T>C r.(?) p.(Cys766Arg) - Unknown - VUS g.216420440A>G - c.2296T>C - USH2A_000129 - PubMed: Colombo-2020 - rs368687374 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+/. - c.2296T>C r.(?) p.(Cys766Arg) - Unknown ACMG pathogenic g.216420440A>G g.216247098A>G - - USH2A_000129 ACMG GN005 criteria: PM2_P PM3_VS PP3_P PubMed: Bonnet, C. et al., 2016; PubMed: Glockle, N. et al., 2014; PubMed: Colombo, L. et al., 2022; PubMed: Karali, M. et al., 2019; PubMed: Weisschuh, N. et al., 2020; PubMed: Colombo, L. et al., 2021; PubMed: Aparisi, M. J. et al., 2014 - rs368687374 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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