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     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Segregation     

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Re-site     

VIP     

Methylation     

Template     

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Tissue     

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Disease     

ID_report     

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VIP     

Data_av     

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Panel size     

Owner     
+?/. - c.1190T>A r.(?) p.(Ile397Lys) - Parent #1 ACMG likely pathogenic (recessive) g.216497648A>T g.216324306A>T - - USH2A_001880 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 19198 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+?/. - c.1190T>A r.(?) p.(Ile397Lys) - Parent #1 ACMG likely pathogenic (recessive) g.216497648A>T g.216324306A>T - - USH2A_001880 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19674 PubMed: Sun 2018 family - no China - - - - - 1 LOVD
+?/. - c.1190T>A r.(?) p.(Ile397Lys) - Unknown ACMG VUS g.216497648A>T - - - USH2A_001880 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_GS_0157 - - F - Korea, South (Republic) - - - - - 1 Jinu Han
?/. - c.1190T>A r.(?) p.(Ile397Lys) - Unknown ACMG VUS g.216497648A>T g.216324306A>T - - USH2A_001880 ACMG GN005 criteria: PM2_P PM3_M PP3_P PubMed: Sun, T. et al., 2018; PubMed: Kim, Y. N. et al., 2021 - rs2037684112 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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