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     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.12086dup r.(?) p.(His4029GlnfsTer70) - Unknown ACMG pathogenic g.215853699dup g.215680357dup 12086dupA - USH2A_002521 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Zhu, X. et al., 2020 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.12086dupA r.(?) p.(His4029Glnfs*70) - Unknown - likely pathogenic g.215853699dup g.215680357dup USH2A c.12086dupA, p.H4029Qfs*68 - USH2A_002521 heterozygous PubMed: Ng 2019 - - Germline yes - - - - DNA SEQ-NG-I blood Whole exome sequencing USH F1-II:5 PubMed: Ng 2019 proband; pedigree patient numbers differ from table numbers F - China - - - - - 1 LOVD
+?/. - c.12086dupA r.(?) p.(His4029Glnfs*70) - Unknown - likely pathogenic g.215853699dup g.215680357dup USH2A c.12086dupA, p.H4029Qfs*68 - USH2A_002521 heterozygous PubMed: Ng 2019 - - Germline yes - - - - DNA SEQ-NG-I blood Whole exome sequencing USH F1-II:1 PubMed: Ng 2019 proband's eldest sister (1) F - China - - - - - 1 LOVD
+?/. - c.12086dupA r.(?) p.(His4029Glnfs*70) - Unknown - likely pathogenic g.215853699dup g.215680357dup USH2A c.12086dupA, p.H4029Qfs*68 - USH2A_002521 heterozygous PubMed: Ng 2019 - - Germline yes - - - - DNA SEQ-NG-I blood Whole exome sequencing USH F1-II:3 PubMed: Ng 2019 proband's older sister (3) F - China - - - - - 1 LOVD
+?/. - c.12086dupA r.(?) p.(His4029Glnfs*70) - Paternal (confirmed) - likely pathogenic g.215853699dup g.215680357dup USH2A c.12086dupA, p.H4029fs - USH2A_002521 heterozygous PubMed: Zhu 2020 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease 2150-II:1 PubMed: Zhu 2020 - F - China - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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