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.

13 entries on 1 page. Showing entries 1 - 13.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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Reference     

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Disease     

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?/. - c.6998T>C r.(?) p.(Val2333Ala) - Unknown - VUS g.216138781A>G g.215965439A>G USH2A(NM_206933.2):c.6998T>C (p.V2333A, p.(Val2333Ala)) - USH2A_001212 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.6998T>C r.(?) p.(Val2333Ala) - Parent #1 ACMG likely pathogenic (recessive) g.216138781A>G g.215965439A>G - - USH2A_001212 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 19987 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+?/. - c.6998T>C r.(?) p.(Val2333Ala) - Unknown - likely pathogenic g.216138781A>G g.215965439A>G - - USH2A_001212 - PubMed: Huang 2018 - - Germline - - - - - DNA SEQ-NG - 283-gene panel retinal disease RP063 PubMed: Huang 2018 - - - - - - - - - 1 LOVD
+?/. - c.6998T>C r.(?) p.(Val2333Ala) - Unknown - likely pathogenic (recessive) g.216138781A>G g.215965439A>G - - USH2A_001212 - PubMed: Xu 2014 - rs144817385 Germline - 3/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP302 PubMed: Xu 2014 - - - China - - - - - 1 LOVD
+?/. - c.6998T>C r.(?) p.(Val2333Ala) - Unknown - likely pathogenic (recessive) g.216138781A>G g.215965439A>G - - USH2A_001212 - PubMed: Xu 2014 - rs144817385 Germline - 3/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP223 PubMed: Xu 2014 patient M - China - - - - - 1 LOVD
+?/. - c.6998T>C r.(?) p.(Val2333Ala) - Unknown - likely pathogenic (recessive) g.216138781A>G g.215965439A>G - - USH2A_001212 - PubMed: Xu 2014 - rs144817385 Germline - 3/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP100 PubMed: Xu 2014 family F - China - - - - - 1 LOVD
?/. - c.6998T>C r.(?) p.(Val2333Ala) - Unknown - VUS g.216138781A>G g.215965439A>G USH2A c.6998T>C, p.Val2333Ala - USH2A_001212 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD18050819 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. 37 c.6998T>C r.(?) p.(Val2333Ala) - Parent #1 ACMG likely pathogenic g.216138781A>G g.215965439A>G USH2A c.6998T>C, p.V2333A - USH2A_001212 single heterozygous variant in a recessive disesase, no second allele PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_8 PubMed: Zhu 2021 family , patient - - China - - - - - 1 LOVD
+?/. 37 c.6998T>C r.(?) p.(Val2333Ala) - Parent #1 ACMG likely pathogenic g.216138781A>G g.215965439A>G USH2A c.6998T>C, p.V2333A - USH2A_001212 single heterozygous variant in a recessive disesase, no second allele PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_9 PubMed: Zhu 2021 family , patient - - China - - - - - 1 LOVD
+?/. 37 c.6998T>C r.(?) p.(Val2333Ala) - Unknown ACMG likely pathogenic g.216138781A>G g.215965439A>G USH2A c.6998T>C, p.V2333A - USH2A_001212 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 54 PubMed: Zhu 2021 family 123, patient 54 M - China - - - - - 1 LOVD
+?/. 37 c.6998T>C r.(?) p.(Val2333Ala) - Parent #2 ACMG likely pathogenic g.216138781A>G g.215965439A>G USH2A c.6998T>C, p.V2333A - USH2A_001212 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF463 PubMed: Zhu 2021 family 77, patient SRF463 M - China - - - - - 1 LOVD
?/. - c.6998T>C r.(?) p.(Val2333Ala) - Unknown - VUS g.216138781A>G - USH2A(NM_206933.2):c.6998T>C (p.V2333A, p.(Val2333Ala)) - USH2A_001212 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.6998T>C r.(?) p.(Val2333Ala) - Unknown ACMG VUS g.216138781A>G g.215965439A>G - - USH2A_001212 ACMG GN005 criteria: PubMed: Gao, F. J. et al., 2021; PubMed: Sun, T. et al., 2018 - rs144817385 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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