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.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

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AscendingDNA change (cDNA)     

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Owner     
-/? 50 c.9915G>C r.(?) p.(Glu3305Asp) Cystein rich (3192-3358) Unknown ACMG likely benign g.215972292C>G g.215798950C>G - - USH2A_000780 Heterozygous; polymorphism PubMed: Glöckle 2014, USMA missense analysis, missense variant in MSV3d - rs145278250 Germline - - +HpyCH4III - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Glöckle 2014 Proband - - - - - - - - 1 Anne-Françoise Roux
?/. - c.9915G>C r.(?) p.(Glu3305Asp) - Unknown - VUS g.215972292C>G g.215798950C>G - - USH2A_000780 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs145278250 Germline - 21/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 21 Yoshito Koyanagi
-?/. - c.9915G>C r.(?) p.(Glu3305Asp) - Unknown - likely benign g.215972292C>G g.215798950C>G USH2A(NM_206933.2):c.9915G>C (p.E3305D) - USH2A_000780 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.9915G>C r.(?) p.(Glu3305Asp) - Unknown - likely pathogenic (recessive) g.215972292C>G g.215798950C>G - - USH2A_000780 - PubMed: Xu 2014 - rs145278250 Germline - 2/314 case chromosomes - - - DNA SEQ - - retinal disease RP191 PubMed: Xu 2014 - - - China - - - - - 1 Isabelle Audo
+?/. - c.9915G>C r.(?) p.(Glu3305Asp) - Unknown - likely pathogenic (recessive) g.215972292C>G g.215798950C>G - - USH2A_000780 - PubMed: Xu 2014 - - Germline - 2/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP341 PubMed: Xu 2014 - - - China - - - - - 1 LOVD
?/. 50 c.9915G>C r.(?) p.(Glu3305Asp) - Unknown - VUS g.215972292C>G - c.9915G>C - USH2A_000780 - PubMed: Chen-2013 - rs145278250 Unknown - - - - - DNA SEQ blood - retinal disease - PubMed: Chen-2013 - - - China Chinese - - - - 1 LOVD
?/. 50 c.9915G>C r.(?) p.(Glu3305Asp) - Unknown - VUS g.215972292C>G - c.9915G>C - USH2A_000780 unknown variant 2nd chromosome PubMed: Chen-2013 - rs145278250 Unknown - - - - - DNA SEQ blood - retinal disease - PubMed: Chen-2013 - - - China Chinese - - - - 1 LOVD
?/. - c.9915G>C r.(?) p.(Glu3305Asp) - Parent #1 - VUS g.215972292C>G g.215798950C>G USH2A c.9915G>C, p.Glu3305Asp - USH2A_000780 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD17120980 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. 50 c.9915G>C r.(?) p.(Glu3305Asp) - Parent #1 ACMG likely pathogenic g.215972292C>G g.215798950C>G USH2A c.9915G>C, p.E3305D - USH2A_000780 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 97 PubMed: Zhu 2021 family 125, patient 97 M - China - - - - - 1 LOVD
+?/. 50 c.9915G>C r.(?) p.(Glu3305Asp) - Parent #1 ACMG likely pathogenic g.215972292C>G g.215798950C>G USH2A c.9915G>C, p.E3305D - USH2A_000780 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_6 PubMed: Zhu 2021 family 21, patient AXLM_6 F - China - - - - - 1 LOVD
-/. - c.9915G>C r.(?) p.(Glu3305Asp) - Unknown ACMG benign g.215972292C>G g.215798950C>G - - USH2A_000780 ACMG GN005 criteria: BS2_S BP4_P PubMed: Gao, F. J. et al., 2021 - rs145278250 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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