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.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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Reference     

ClinVar ID     

dbSNP ID     

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VIP     

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-/. - c.6077A>G r.(?) p.(Lys2026Arg) - Unknown - benign g.216221962T>C g.216048620T>C USH2A(NM_206933.2):c.6077A>G (p.K2026R), USH2A(NM_206933.4):c.6077A>G (p.K2026R) - USH2A_000505 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/? 31 c.6077A>G r.(?) p.(Lys2026Arg) Fibronectin type-III 6 (1954-2051) Paternal (confirmed) ACMG likely benign g.216221962T>C g.216048620T>C - - USH2A_000505 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs115039883 Germline - - +AcuI;+Hpy188I; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
?/. - c.6077A>G r.(?) p.(Lys2026Arg) - Unknown - VUS g.216221962T>C g.216048620T>C - - USH2A_000505 - PubMed: Wang 2014 - rs115039883 Germline - - - - - DNA SEQ-NG - 66-gene panel retinal disease 60 PubMed: Wang 2014 - F - United States - - - - - 1 LOVD
-?/. - c.6077A>G r.(?) p.(Lys2026Arg) - Unknown - likely benign g.216221962T>C - USH2A(NM_206933.2):c.6077A>G (p.K2026R), USH2A(NM_206933.4):c.6077A>G (p.K2026R) - USH2A_000505 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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