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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P-domain     

Allele     

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DNA change (hg38)     

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ISCN     

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Reference     

ClinVar ID     

dbSNP ID     

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VIP     

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Disease     

ID_report     

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Owner     
+/+ 64i c.14134-3169A>G r.(14133_14134ins14134-3221_14134-3168) p.(Gln14711_Val4712delinsEKPTH*) Fibronectin type-III 32 (4633-4730) Paternal (confirmed) ACMG likely pathogenic g.215827312T>C g.215653970T>C Val4711Glufs*6 - USH2A_001080 effect on splicing predicted from minigene splicing assay PubMed: Baux, Vaché 2017 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - DFN S1679 PubMed: Baux 2017 Proband - Age 14 at the time of the study - possible USH2 F - France - - - - - 1 Anne-Françoise Roux
+?/. - c.14134-3169A>G r.(?) p.(Val4711GlufsTer6) - Unknown ACMG likely pathogenic g.215827312T>C - - - USH2A_001080 - PubMed: Mansard et al, 2021 - rs998302546 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
?/. - c.14134-3169A>G r.(?) p.(Val4711GlufsTer6) - Unknown ACMG VUS g.215827312T>C g.215653970T>C - - USH2A_001080 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Mansard, L. et al., 2021 - rs998302546 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.14134-3169A>G r.(?) p.(?) - Unknown - pathogenic g.215827312T>C - - - USH2A_001080 - - - rs998302546 Unknown - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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