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)     

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Owner     
-?/? 25 c.5051C>T r.(?) p.(Pro1684Leu) Laminin G-like 1 (1517-1709) Maternal (confirmed) ACMG likely benign g.216258156G>A g.216084814G>A - - USH2A_000937 Heterozygous; mutation PubMed: Wei 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - DFN - PubMed: Wei 2014 Proband - also carries GJB2:c.235del (het) F - China - - - - - 1 Anne-Françoise Roux
?/. - c.5051C>T r.(?) p.(Pro1684Leu) - Parent #1 - VUS g.216258156G>A g.216084814G>A - - USH2A_000937 - PubMed: Sun 2015 - - Germline - 1/596 chromosomes - - - DNA SEQ-NG - WES retinal disease HM758 PubMed: Sun 2015 proband - - China - - - - - 1 LOVD
?/. - c.5051C>T r.(?) p.(Pro1684Leu) - Unknown - VUS g.216258156G>A g.216084814G>A - - USH2A_000937 - PubMed: Sun 2015 - - Germline - 1/624 control chromosomes - - - DNA SEQ-NG - WES Healthy/Control control PubMed: Sun 2015 healthy control - - China - - - - - 1 LOVD
+?/. 25 c.5051C>T r.(?) p.(Pro1684Leu) - Unknown - likely pathogenic (recessive) g.216258156G>A - c.5051C>T - USH2A_000937 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
+?/. 25 c.5051C>T r.(?) p.(Pro1684Leu) - Parent #2 ACMG likely pathogenic g.216258156G>A g.216084814G>A USH2A c.5051C>T, p.P1684L - USH2A_000937 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_21 PubMed: Zhu 2021 family 85, patient AXLM_21 M - China - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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