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 (hg38)     

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ISCN     

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Owner     
+?/? 4 c.769G>A r.(?) p.(Gly257Arg) - Unknown ACMG VUS g.216538310C>T g.216364968C>T - - USH2A_000636 Heterozygous; UV2 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 0/96 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/. - c.769G>A r.(?) p.(Gly257Arg) - Parent #1 - pathogenic g.216538310C>T g.216364968C>T - - USH2A_000636 - PubMed: Zhao 2015 - - Germline - - - - - DNA SEQ-NG - 86-gene panel retinal disease Rp55 PubMed: Zhao 2015 family - - Northern Ireland - - - - - 1 LOVD
?/. - c.769G>A r.(?) p.(Gly257Arg) - Parent #2 - VUS g.216538310C>T g.216364968C>T USH2A c.769G>A, p.Gly257Arg - USH2A_000636 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD18041215 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
?/. - c.769G>A r.(?) p.(Gly257Arg) - Unknown ACMG VUS g.216538310C>T g.216364968C>T - - USH2A_000636 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Gao, F. J. et al., 2021; PubMed: Le Quesne Stabej, P. et al., 2012 - rs2102708440 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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