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.

7 entries on 1 page. Showing entries 1 - 7.
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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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Reference     

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?/. - c.6590C>T r.(?) p.(Thr2197Ile) - Unknown - VUS g.216172296G>A g.215998954G>A USH2A(NM_206933.2):c.6590C>T (p.T2197I), USH2A(NM_206933.4):c.6590C>T (p.T2197I) - USH2A_001224 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. 34 c.6590C>T r.(6590c>u) p.(Thr2197Ile) - Unknown - VUS g.216172296G>A g.215998954G>A - - USH2A_001224 - - - rs140487302 Unknown ? - - - - DNA SEQ-NG-I - Gene Panel (79 IRD genes) retinal disease IRD4.0_#21 Manuscript under review (González-del Pozo et al., 2018) - - ? Spain - ? - - - 1 María González-del Pozo
?/. - c.6590C>T r.(?) p.(Thr2197Ile) - Unknown - VUS g.216172296G>A g.215998954G>A USH2A(NM_206933.2):c.6590C>T (p.T2197I), USH2A(NM_206933.4):c.6590C>T (p.T2197I) - USH2A_001224 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.6590C>T r.(?) p.(Thr2197Ile) - Unknown - VUS g.216172296G>A g.215998954G>A USH2A(NM_206933.2):c.6590C>T (p.T2197I), USH2A(NM_206933.4):c.6590C>T (p.T2197I) - USH2A_001224 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.6590C>T r.(?) p.(Thr2197Ile) - Unknown - likely pathogenic (recessive) g.216172296G>A - 1:216172296G>A ENST00000307340.3:c.6590C>T (Thr2197Ile) - USH2A_001224 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease W000193 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+?/. - c.6590C>T r.(?) p.(Thr2197Ile) - Unknown - likely pathogenic g.216172296G>A g.215998954G>A m10: c.6590 C > T; p.Thr2197Ile - USH2A_001224 - PubMed: Gonzalez del Pozo 2018 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG blood solved retinal disease E (II:4) PubMed: Gonzalez del Pozo 2018 - ? no Spain - - - - - 1 LOVD
?/. - c.6590C>T r.(?) p.(Thr2197Ile) - Unknown ACMG VUS g.216172296G>A g.215998954G>A - - USH2A_001224 ACMG GN005 criteria: PubMed: Gonzalez-Del Pozo, M. et al., 2018 - rs140487302 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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