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 (hg38)     

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Owner     
+/+ 63 c.13621C>T r.(?) p.(Gln4541*) Fibronectin type-III 31 (4529-4627) Unknown - pathogenic g.215847632G>A g.215674290G>A - - USH2A_000560 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls -HpyCH4V;-Cac8I; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 63 c.13621C>T r.(?) p.(Gln4541*) Fibronectin type-III 31 (4529-4627) Paternal (inferred) - pathogenic g.215847632G>A g.215674290G>A - - USH2A_000560 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls -HpyCH4V;-Cac8I; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 63 c.13621C>T r.(?) p.(Gln4541*) Fibronectin type-III 31 (4529-4627) Paternal (inferred) - pathogenic g.215847632G>A g.215674290G>A - - USH2A_000560 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls -HpyCH4V;-Cac8I; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. - c.13621C>T r.(?) p.(Gln4541*) - Parent #1 - likely pathogenic g.215847632G>A g.215674290G>A - - USH2A_000560 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 103 PubMed: Stone 2017 1 affected M - (United States) - - - - - 1 LOVD
+?/. - c.13621C>T r.(?) p.(Gln4541*) - Parent #1 - likely pathogenic g.215847632G>A g.215674290G>A - - USH2A_000560 - PubMed: Huang 2017 - - Germline - - - - - DNA SEQ-NG - WES retinal disease RP-116 PubMed: Huang 2017 family - - China - - - - - 1 LOVD
+?/. - c.13621C>T r.(?) p.(Gln4541*) - Unknown - likely pathogenic g.215847632G>A g.215674290G>A - - USH2A_000560 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 13005697 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+/. - c.13621C>T r.(?) p.(Gln4541Ter) - Unknown ACMG pathogenic g.215847632G>A g.215674290G>A - - USH2A_000560 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Le Quesne Stabej, P. et al., 2012 - rs765476745 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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