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.

7 entries on 1 page. Showing entries 1 - 7.
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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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ISCN     

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Variant remarks     

Reference     

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Owner     
+/. - c.1397G>T r.(?) p.(Gly466Val) - Parent #1 - pathogenic (recessive) g.216496969C>A g.216323627C>A - - USH2A_002069 - PubMed: Xu 2014 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease RP296 PubMed: Xu 2014 family M - China - - - - - 1 LOVD
+/. 8 c.1397G>T r.(?) p.(Gly466Val) - Unknown ACMG pathogenic g.216496969C>A g.216323627C>A NM_206933.2:c.1397G>T, NP_996816.2:p.(Gly466Val), NC_000001.10:g.216496969C>A - USH2A_002069 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - exome sequencing retinal disease 2016092605 PubMed: Wang 2018 - M ? China Han Chinese - - - - 1 LOVD
+?/. 8 c.1397G>T r.(?) p.(Gly466Val) - Both (homozygous) ACMG likely pathogenic g.216496969C>A g.216323627C>A USH2A c.1397G>T, p.(Gly466Val) - USH2A_002069 homozygous PubMed: Dan 2020 - - Germline ? - - - - DNA SEQ-NG blood Panel 1 containing 70 genes retinal disease 37 PubMed: Dan 2020 - F ? China - - - - - 1 LOVD
+?/. 8 c.1397G>T r.(?) p.(Gly466Val) - Unknown - likely pathogenic (recessive) g.216496969C>A - c.1397G>T - USH2A_002069 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - WES retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
+?/. 8 c.1397G>T r.(?) p.(Gly466Val) - Parent #1 ACMG likely pathogenic g.216496969C>A g.216323627C>A USH2A c.1397G>T, p.G466V - USH2A_002069 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 1249 PubMed: Zhu 2021 family 130, patient 1249 F - China - - - - - 1 LOVD
+?/. 8 c.1397G>T r.(?) p.(Gly466Val) - Parent #2 ACMG likely pathogenic g.216496969C>A g.216323627C>A USH2A c.1397G>T, p.G466V - USH2A_002069 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF_1357 PubMed: Zhu 2021 family 18, patient SRF_1357 F - China - - - - - 1 LOVD
?/. - c.1397G>T r.(?) p.(Gly466Val) - Unknown ACMG VUS g.216496969C>A g.216323627C>A - - USH2A_002069 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Dan, H. et al., 2020 - rs1553250627 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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