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.

6 entries on 1 page. Showing entries 1 - 6.
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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     

Methylation     

Template     

Technique     

Tissue     

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Disease     

ID_report     

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Owner     
+?/. - c.6929C>T r.(?) p.(Thr2310Met) - Unknown - likely pathogenic g.216143995G>A - USH2A(NM_206933.4):c.6929C>T (p.T2310M) - USH2A_001787 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.6929C>T r.(?) p.(Thr2310Met) - Unknown - VUS g.216143995G>A - USH2A(NM_206933.4):c.6929C>T (p.T2310M) - USH2A_001787 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. 36 c.6929C>T r.(?) p.(Thr2310Met) - Unknown - likely pathogenic (recessive) g.216143995G>A - c.6929C>T - USH2A_001787 - PubMed: Colombo-2020 - rs151057466 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
?/. - c.6929C>T r.(?) p.(Thr2310Met) - Parent #1 - VUS g.216143995G>A g.215970653G>A USH2A c.6929C>T, p.Thr2310Met - USH2A_001787 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD17124003 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+?/. 36 c.6929C>T r.(?) p.(Thr2310Met) - Parent #2 ACMG likely pathogenic g.216143995G>A g.215970653G>A USH2A c.6929C>T, p.T2310M - USH2A_001787 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease HSR85 PubMed: Zhu 2021 family 79, patient HSR85 M - China - - - - - 1 LOVD
?/. - c.6929C>T r.(?) p.(Thr2310Met) - Unknown ACMG VUS g.216143995G>A g.215970653G>A - - USH2A_001787 ACMG GN005 criteria: PM2_P PM3_M PubMed: Gao, F. J. et al., 2021; PubMed: Colombo, L. et al., 2022 - rs151057466 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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