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.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+?/? 6 c.1001G>A r.(?) p.(Arg334Gln) Laminin N-terminal (271-517) Parent #1 ACMG VUS g.216498789C>T g.216325447C>T - - USH2A_000099 Heterozygous PubMed: Baux 2007, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
+/. - c.1001G>A r.(?) p.(Arg334Gln) - Unknown ACMG pathogenic g.216498789C>T - - - USH2A_000099 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+/. - c.1001G>A r.(?) p.(Arg334Gln) - Unknown ACMG pathogenic g.216498789C>T - - - USH2A_000099 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.1001G>A r.(?) p.(Arg334Gln) - Unknown - likely pathogenic g.216498789C>T - - - USH2A_000099 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.1001G>A r.(?) p.(Arg334Gln) - Parent #1 ACMG likely pathogenic (recessive) g.216498789C>T g.216325447C>T - - USH2A_000099 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19891 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
?/. - c.1001G>A r.(?) p.(Arg334Gln) - Unknown ACMG VUS g.216498789C>T g.216325447C>T - - USH2A_000099 ACMG GN005 criteria: PM2_P PM3_M PubMed: Sun, T. et al., 2018 - rs758303489 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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