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)     

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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Technique     

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Disease     

ID_report     

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VIP     

Data_av     

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Owner     
+/. - c.10962C>A r.(?) p.(Tyr3654*) - Unknown ACMG pathogenic (recessive) g.215940108G>T g.215766766G>T - - USH2A_001845 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19495 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+?/. 56 c.10962C>A r.(?) p.(Tyr3654*) - Unknown - likely pathogenic (recessive) g.215940108G>T - c.10962C>A - USH2A_001845 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
+/. - c.10962C>A r.(?) p.(Tyr3654*) - Parent #1 - pathogenic g.215940108G>T g.215766766G>T USH2A c.10962C>, p.Tyr3654* - USH2A_001845 error in annotation, mutant nucleotide missing; probably it is c.10962C>A (RCV001208723.2); heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD18110234 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. - c.10962C>A r.(?) p.(Tyr3654Ter) - Unknown ACMG likely pathogenic g.215940108G>T g.215766766G>T - - USH2A_001845 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Sun, T. et al., 2018 - rs1661141590 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.10962C>G r.(?) p.(Tyr3654Ter) - Unknown ACMG likely pathogenic g.215940108G>C g.215766766G>C - - USH2A_001845 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Gao, F. J. et al., 2021 - rs1661141590 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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