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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P-domain     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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Reference     

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Disease     

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Owner     
+?/? 54 c.10724G>A r.(?) p.(Cys3575Tyr) Fibronectin type-III 20 (3499-3585) Paternal (confirmed) ACMG VUS g.215955400C>T g.215782058C>T - - USH2A_000581 Heterozygous; UV4 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - rs111033265 Germline - 0/878 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 54 c.10724G>A r.(?) p.(Cys3575Tyr) Fibronectin type-III 20 (3499-3585) Unknown ACMG VUS g.215955400C>T g.215782058C>T - - USH2A_000581 Heterozygous PubMed: Lenassi 2015, USMA missense analysis, missense variant in MSV3d - rs111033265 Germline - - none - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Lenassi 2015 Proband - - Canada - - - - - 1 Eva Lenassi
?/. - c.10724G>A r.(?) p.(Cys3575Tyr) - Unknown ACMG VUS g.215955400C>T g.215782058C>T - - USH2A_000581 ACMG GN005 criteria: PM2_P PubMed: Lenassi, E. et al., 2015; PubMed: Le Quesne Stabej, P. et al., 2012 - rs111033265 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.10724G>A r.(?) p.(Cys3575Tyr) - Unknown ACMG likely pathogenic (recessive) g.215955400C>T g.215782058C>T - - USH2A_000581 ACMG PM2, PM1_SUPPORTING, PP5_STRONG PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHII-304 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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