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)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Reference     

ClinVar ID     

dbSNP ID     

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Owner     
+/+ 18 c.3920C>G r.(?) p.(Ser1307*) Fibronectin type-III 3 (1242-1357) Maternal (confirmed) - pathogenic g.216371818G>C g.216198476G>C - - USH2A_000464 Heterozygous PubMed: Baux 2014 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband - - France - - - - - 1 Anne-Françoise Roux
+/+ 18 c.3920C>G r.(?) p.(Ser1307*) Fibronectin type-III 3 (1242-1357) Maternal (confirmed) - pathogenic g.216371818G>C g.216198476G>C - - USH2A_000464 Heterozygous; Pathogenic PubMed: Bonnet 2011 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Bonnet 2011 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 18 c.3920C>G r.(?) p.(Ser1307*) Fibronectin type-III 3 (1242-1357) Maternal (confirmed) - pathogenic g.216371818G>C g.216198476G>C - - USH2A_000464 Heterozygous; Pathogenic PubMed: Bonnet 2011 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Bonnet 2011 Relative F - - - - - - - 1 Anne-Françoise Roux
+?/. 18 c.3920C>G r.(?) p.(Ser1307*) - Unknown - likely pathogenic g.216371818G>C g.216198476G>C USH2A Ex.13 c.2299del p.(Glu767Serfs*21), Ex.18 c.3920C>G (p.Ser1307*) - USH2A_000464 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-2877 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+/. - c.3920C>G r.(?) p.(Ser1307Ter) - Unknown ACMG pathogenic g.216371818G>C g.216198476G>C - - USH2A_000464 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Colombo, L. et al., 2022 - rs756623509 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.3920C>G r.(?) p.(Ser1307Ter) - Unknown ACMG pathogenic (recessive) g.216371818G>C g.216198476G>C - - USH2A_000464 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHII-345 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - 1 Johan den Dunnen
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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