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     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.13040_13062delinsTCAGAAGTCA r.(?) p.(Thr4347Ilefs*22) - Parent #2 ACMG pathogenic (recessive) g.215848191_215848213delinsTGACTTCTGA g.215674849_215674871delinsTGACTTCTGA - - USH2A_001841 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19860 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+?/. 63 c.13040_13062delinsTCAGAAGTCA r.(?) p.(Thr4347Ilefs*22) - Unknown - likely pathogenic g.215848191_215848213delinsTGACTTCTGA - c.13040_13062delinsTCAGAAGTCA,p.T4347IfsX22 - USH2A_001841 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. - c.13040_13062delinsTCAGAAGTCA r.(?) p.(Thr4347Ilefs*22) - Parent #2 - pathogenic g.215848191_215848213delinsTGACTTCTGA g.215674849_215674871delinsTGACTTCTGA USH2A c.13040_13062delinsTCAGAAGTCA, p.Thr4347ifs - USH2A_001841 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH R017060523 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+/. 63 c.13040_13062delinsTCAGAAGTCA r.(?) p.(Thr4347Ilefs*22) - Parent #2 ACMG pathogenic g.215848191_215848213delinsTGACTTCTGA g.215674849_215674871delinsTGACTTCTGA USH2A c.13040_13062delinsTCAGAAGTCA, p.T4347Ifs*22 - USH2A_001841 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 17214119 PubMed: Zhu 2021 family 39, patient 17214119 M - China - - - - - 1 LOVD
+?/. - c.13040_13062delinsTCAGAAGTCA r.(?) p.(Thr4347IlefsTer22) - Unknown ACMG likely pathogenic g.215848191_215848213delinsTGACTTCTGA g.215674849_215674871delinsTGACTTCTGA - - USH2A_001841 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Gao, F. J. et al., 2021; 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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