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.

10 entries on 1 page. Showing entries 1 - 10.
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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.12845T>C r.(?) p.(Leu4282Pro) Fibronectin type-III 28 (4265-4351) Parent #1 ACMG VUS g.215848408A>G g.215675066A>G - - USH2A_000315 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
+?/? 63 c.12845T>C r.(?) p.(Leu4282Pro) Fibronectin type-III 28 (4265-4351) Parent #1 ACMG VUS g.215848408A>G g.215675066A>G - - USH2A_000315 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Relative M - France - - - - - 1 Anne-Françoise Roux
+?/? 63 c.12845T>C r.(?) p.(Leu4282Pro) Fibronectin type-III 28 (4265-4351) Paternal (confirmed) ACMG VUS g.215848408A>G g.215675066A>G - - USH2A_000315 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 63 c.12845T>C r.(?) p.(Leu4282Pro) Fibronectin type-III 28 (4265-4351) Paternal (inferred) ACMG VUS g.215848408A>G g.215675066A>G - - USH2A_000315 Homozygous; mutation PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+?/? 63 c.12845T>C r.(?) p.(Leu4282Pro) Fibronectin type-III 28 (4265-4351) Maternal (inferred) ACMG VUS g.215848408A>G g.215675066A>G - - USH2A_000315 Homozygous; mutation PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+?/? 63 c.12845T>C r.(?) p.(Leu4282Pro) Fibronectin type-III 28 (4265-4351) Parent #1 ACMG VUS g.215848408A>G g.215675066A>G - - USH2A_000315 Heterozygous; mutation PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. - c.12845T>C r.(?) p.(Leu4282Pro) - Unknown ACMG likely pathogenic g.215848408A>G - - - USH2A_000315 - PubMed: Mansard et al, 2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/+? 63 c.12845T>C r.(?) p.(Leu4282Pro) Fibronectin type-III 28 (4262 - 4357) Unknown ACMG likely pathogenic g.215848408A>G g.215675066A>G - - USH2A_000315 PM2_Sup PM3_St PP1_Sup following GN005 - - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.12845T>C r.(?) p.(Leu4282Pro) - Unknown ACMG VUS g.215848408A>G g.215675066A>G - - USH2A_000315 ACMG GN005 criteria: PM2_P PM3_P PubMed: Bonnet, C. et al., 2016 - rs1657968255 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.12845T>C r.(?) p.(Leu4282Pro) - Unknown ACMG VUS g.215848408A>G g.215675066A>G - - USH2A_000315 ACMG GN005 criteria: PM2_P PM3_P PubMed: Mansard, L. et al., 2021 - rs1657968255 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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