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.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Disease     

ID_report     

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Owner     
+?/. 55 c.10830G>C r.(?) p.(Trp3610Cys) - Unknown ACMG likely pathogenic g.215953294C>G g.215779952C>G NM_206933.2:c.10830G>C, NP_996816.2:p.(Trp3610Cys), NC_000001.10:g.215953294C>G - USH2A_002141 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - panel of 441 hereditary eye disease genes including 291 genes related to IRD retinal disease 2016121911 PubMed: Wang 2018 - M ? China Han Chinese - - - - 1 LOVD
?/. 55 c.10830G>C r.(?) p.(Trp3610Cys) - Unknown ACMG VUS g.215779952C>G g.215671166C>G USH2A c.10830G > C, p.Trp3610Cys, heterozygous - USH2A_002141 - PubMed: Sun 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted NGS with molecular inversion probes: coding exons of 27 genes associated with Joubert syndrome retinal disease 11 PubMed: Sun 2020 - F - 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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