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     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Disease     

ID_report     

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Data_av     

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Owner     
?/. 35 c.6661T>C r.(?) p.(Cys2221Arg) - Parent #1 ACMG VUS g.216166506A>G g.215993164A>G USH2A c.6661T>C, p.Cys2221Arg - USH2A_002557 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes USH 12 PubMed: Meng 2020 - F - China - - - - - 1 LOVD
?/. - c.6661T>C r.(?) p.(Cys2221Arg) - Parent #2 - VUS g.216166506A>G g.215993164A>G USH2A c.6661T>C, p.Cys2221Arg - USH2A_002557 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD17124002 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
?/. - c.6661T>C r.(?) p.(Cys2221Arg) - Parent #2 - VUS g.216166506A>G g.215993164A>G USH2A c.6661T>C, p.Cys2221Arg - USH2A_002557 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD17124989 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
?/. - c.6661T>C r.(?) p.(Cys2221Arg) - Unknown ACMG VUS g.216166506A>G g.215993164A>G - - USH2A_002557 ACMG GN005 criteria: PM2_P PM3_P PP1_P PubMed: Gao, F. J. et al., 2021 - rs1668046327 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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