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.

12 entries on 1 page. Showing entries 1 - 12.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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?/. - c.6628C>G r.(?) p.(Pro2210Ala) - Unknown - VUS g.216172258G>C g.215998916G>C USH2A(NM_206933.2):c.6628C>G (p.P2210A), USH2A(NM_206933.4):c.6628C>G (p.P2210A) - USH2A_001221 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.6628C>G r.(?) p.(Pro2210Ala) - Unknown - VUS g.216172258G>C g.215998916G>C - - USH2A_001221 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs192115090 Germline - 24/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 24 Yoshito Koyanagi
+?/. - c.6628C>G r.(?) p.(Pro2210Ala) - Parent #1 ACMG likely pathogenic (recessive) g.216172258G>C g.215998916G>C - - USH2A_001221 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19433 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+?/. - c.6628C>G r.(?) p.(Pro2210Ala) - Unknown - likely pathogenic (recessive) g.216172258G>C g.215998916G>C - - USH2A_001221 - PubMed: Xu 2014 - rs192115090 Germline - 5/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP202 PubMed: Xu 2014 patient F - China - - - - - 1 LOVD
+?/. - c.6628C>G r.(?) p.(Pro2210Ala) - Unknown - likely pathogenic (recessive) g.216172258G>C g.215998916G>C - - USH2A_001221 - PubMed: Xu 2014 - rs192115090 Germline - 5/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP372 PubMed: Xu 2014 - - - China - - - - - 1 LOVD
+?/. - c.6628C>G r.(?) p.(Pro2210Ala) - Unknown - likely pathogenic (recessive) g.216172258G>C g.215998916G>C - - USH2A_001221 - PubMed: Xu 2014 - rs192115090 Germline - 5/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP193 PubMed: Xu 2014 patient F - China - - - - - 1 LOVD
+?/. - c.6628C>G r.(?) p.(Pro2210Ala) - Unknown - likely pathogenic (recessive) g.216172258G>C g.215998916G>C - - USH2A_001221 - PubMed: Xu 2014 - rs192115090 Germline - 5/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP245 PubMed: Xu 2014 family M - China - - - - - 1 LOVD
+?/. - c.6628C>G r.(?) p.(Pro2210Ala) - Unknown - likely pathogenic (recessive) g.216172258G>C g.215998916G>C - - USH2A_001221 - PubMed: Xu 2014 - rs192115090 Germline - 5/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP319 PubMed: Xu 2014 - - - China - - - - - 1 LOVD
+/. 34 c.6628C>G r.(?) p.(Pro2210Ala) - Paternal (confirmed) - pathogenic g.216172258G>C g.215998916G>C USH2A c.6628C>G, p.P2210A - USH2A_001221 heterozygous PubMed: Qu 2020 - - Germline yes - - - - DNA SEQ-NG, SEQ blood 103 known RD genes panel retinal disease RP F5-II-2 PubMed: Qu 2020 - M - - - - - - - 1 LOVD
+?/. 34 c.6628C>G r.(?) p.(Pro2210Ala) - Parent #2 ACMG likely pathogenic g.216172258G>C g.215998916G>C USH2A c.6628C>G, p.P2210A - USH2A_001221 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF486 PubMed: Zhu 2021 family 79, patient SRF486 F - China - - - - - 1 LOVD
-?/. - c.6628C>G r.(?) p.(Pro2210Ala) - Unknown - likely benign g.216172258G>C - USH2A(NM_206933.2):c.6628C>G (p.P2210A), USH2A(NM_206933.4):c.6628C>G (p.P2210A) - USH2A_001221 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.6628C>G r.(?) p.(Pro2210Ala) - Unknown ACMG VUS g.216172258G>C g.215998916G>C - - USH2A_001221 ACMG GN005 criteria: PubMed: Qu, L. H. et al., 2020; PubMed: Sun, T. et al., 2018 - rs192115090 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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