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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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Owner     
+?/? 59 c.11534A>C r.(?) p.(Gln3845Pro) Fibronectin type-III 23 (3768-3862) Parent #1 ACMG VUS g.215916533T>G g.215743191T>G - - USH2A_000259 Heterozygous PubMed: Baux 2007, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 59 c.11534A>C r.(?) p.(Gln3845Pro) Fibronectin type-III 23 (3768-3862) Unknown ACMG VUS g.215916533T>G g.215743191T>G - - USH2A_000259 Heterozygous PubMed: Le Guédard-Méreuze 2010, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA minigene, SEQ - - USH2 - PubMed: Le Guédard-Méreuze 2010 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/? 59 c.11534A>C r.(?) p.(Gln3845Pro) Fibronectin type-III 23 (3768-3862) Unknown ACMG VUS g.215916533T>G g.215743191T>G - - USH2A_000259 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/. - c.11534A>C r.(?) p.(Gln3845Pro) - Unknown ACMG likely pathogenic g.215916533T>G - - - USH2A_000259 - PubMed: Mansard et al, 2021 - rs1553257674 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
?/. - c.11534A>C r.(?) p.(Gln3845Pro) - Unknown ACMG VUS g.215916533T>G g.215743191T>G - - USH2A_000259 ACMG GN005 criteria: PM2_P PM3_P PubMed: Mansard, L. et al., 2021 - rs1553257674 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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