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.

18 entries on 1 page. Showing entries 1 - 18.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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DB-ID     

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ClinVar ID     

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Owner     
+/+ 12i c.2168-1G>C r.2168_2174del p.Leu724Valfs*31 Laminin EGF-like 4 (694-746) Unknown - pathogenic g.216420569C>G g.216247227C>G - - USH2A_000091 Heterozygous; del first 7 nt E13 (Vaché , 2010) PubMed: Baux 2007 - - Germline - - - - - DNA, RNA SEQ - - USH2 - PubMed: Baux 2007 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 12i c.2168-1G>C r.(2168_2174del) p.(Leu724Valfs*31) Laminin EGF-like 4 (694-746) Paternal (confirmed) - pathogenic g.216420569C>G g.216247227C>G - - USH2A_000091 Heterozygous PubMed: Vaché 2012 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Vaché 2012 Proband F - Italy - - - - - 1 Anne-Françoise Roux
+/+ 12i c.2168-1G>C r.(2168_2174del) p.(Leu724Valfs*31) Laminin EGF-like 4 (694-746) Unknown - pathogenic g.216420569C>G g.216247227C>G - - USH2A_000091 Heterozygous PubMed: Sandberg 2008 - - Germline - - - - - DNA SEQ - - ? - PubMed: Sandberg 2008 Proband - USH2 or ARRP - - United States - - - - - 1 Anne-Françoise Roux
+/+ 12i c.2168-1G>C r.(2168_2174del) p.(Leu724Valfs*31) Laminin EGF-like 4 (694-746) Unknown - pathogenic g.216420569C>G g.216247227C>G - - USH2A_000091 Heterozygous; pathogenic mutation PubMed: Pierrottet 2014 - - Germline - - - - - DNA SEQ - - USH2 P44 [F7] PubMed: Pierrottet 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+?/. - c.2168-1G>C r.spl p.? - Parent #1 - likely pathogenic (recessive) g.216420569C>G g.216247227C>G - - USH2A_000091 - PubMed: Eandi 2017 - - Germline - - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam4PatTO5 PubMed: Eandi 2017 - M - Italy - - - - - 1 LOVD
+?/. - c.2168-1G>C r.spl p.? - Both (homozygous) - likely pathogenic g.216420569C>G g.216247227C>G IVS12-1G>C - USH2A_000091 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 585 PubMed: Stone 2017 family, 2 affected F - (United States) - - - - - 2 LOVD
+?/. 12i c.2168-1G>C r.(?) p.(?) - Unknown - likely pathogenic g.216420569C>G g.216247227C>G USH2A Ex.3 c.497A>G p.(Glu166Gly), IVS12 c.2168-1G>C p.(?), ABCA4: Ex.45 c.6148G>A p.(Val2050Leu) - USH2A_000091 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-1370 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. - c.2168-1G>C r.spl p.(?) - Maternal (confirmed) - likely pathogenic g.216420569C>G g.216247227C>G c.2168-1G>C, p.(?) - USH2A_000091 - PubMed: Li 2019 - - Germline yes - - - - DNA SEQ-NG, SEQ blood panel containing 168 deafness genes, low-coverage WGS retinal disease Case 3 PubMed: Li 2019 - M no - - - - - - 1 LOVD
+/. - c.2168-1G>C r.spl p.(?) - Unknown - pathogenic g.216420569C>G g.216247227C>G c.2168-1G>C - USH2A_000091 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, PCRq blood - retinal disease 121-174 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. - c.2168-1G>C r.(?) p.(Leu724ValfsTer31) - Unknown ACMG pathogenic g.216420569C>G - - - USH2A_000091 - PubMed: Mansard et al, 2021 - rs748961218 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.2168-1G>C r.spl p.(?) - Parent #1 - likely pathogenic g.216420569C>G g.216247227C>G USH2A, variant 1: c.2168-1G>C/p.?, variant 2: c.653T>A/p.V218E - USH2A_000091 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 794 PubMed: Weisschuh 2020 Filing key number: 312, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.2168-1G>C r.spl p.(?) - Parent #1 - likely pathogenic g.216420569C>G g.216247227C>G USH2A, variant 1: c.2168-1G>C/p.?, variant 2: c.9056-2A>G/p.? - USH2A_000091 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET5 targeted sequencing panel - see paper retinal disease 903 PubMed: Weisschuh 2020 Filing key number: 380, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+/. - c.2168-1G>C r.spl p.(?) - Maternal (confirmed) - pathogenic g.216420569C>G g.216247227C>G USH2A c.2168-1G>C, p.(?) - USH2A_000091 - PubMed: Niepokoj 2018 - - Germline yes - - - - DNA SEQ-NG-I DNA TruSight One Sequencing kit (targted) retinal disease III:6 PubMed: Niepokoj 2018 index patient M - Poland - - - - - 1 LOVD
+/. - c.2168-1G>C r.spl p.(?) - Maternal (confirmed) - pathogenic g.216420569C>G g.216247227C>G USH2A c.2168-1G>C, p.(?) - USH2A_000091 - PubMed: Niepokoj 2018 - - Germline yes - - - - DNA SEQ DNA - retinal disease III:3 PubMed: Niepokoj 2018 brother of index patient M - Poland - - - - - 1 LOVD
+/. - c.2168-1G>C r.spl p.(?) - Parent #2 - pathogenic g.216420569C>G g.216247227C>G USH2A c.2168-1G>C, - - USH2A_000091 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD17082179 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. 12i c.2168-1G>C r.spl? p.(?) - Parent #1 - pathogenic g.216420569C>G - c.2168-1G>C - USH2A_000091 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+/. 12i c.2168-1G>C r.spl? p.(?) - Parent #1 - pathogenic g.216420569C>G - c.2168-1G>C - USH2A_000091 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
+/. - c.2168-1G>C r.spl p.? - Unknown ACMG pathogenic g.216420569C>G g.216247227C>G - - USH2A_000091 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Gao, F. J. et al., 2021; PubMed: Mansard, L. et al., 2021; PubMed: Weisschuh, N. et al., 2020; PubMed: Eandi, C. M. et al., 2017 - rs748961218 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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