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     

Allele     

Classification method     

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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Segregation     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
+/. - c.8769del r.(?) p.(Leu2924Phefs*20) - Unknown ACMG pathogenic (recessive) g.216040425del g.215867083del c.8769delT - USH2A_001851 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19674 PubMed: Sun 2018 family - no China - - - - - 1 LOVD
+?/. - c.8769del r.(?) p.(Leu2924PhefsTer20) - Unknown ACMG likely pathogenic g.216040425del g.215867083del 8769delT - USH2A_001851 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Sun, T. et al., 2018 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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