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.

3 entries on 1 page. Showing entries 1 - 3.
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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     

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Template     

Technique     

Tissue     

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Disease     

ID_report     

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VIP     

Data_av     

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Panel size     

Owner     
+?/? 63 c.13156A>T r.(?) p.(Ile4386Phe) Fibronectin type-III 29 (4356-4439) Maternal (confirmed) ACMG VUS g.215848097T>A g.215674755T>A - - USH2A_000952 Heterozygous; mutation PubMed: Shu 2015, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Shu 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+?/. 63 c.13156A>T r.(?) p.(Ile4386Phe) - Parent #2 ACMG likely pathogenic g.215848097T>A g.215674755T>A USH2A c.13156A>T, p.I4386F - USH2A_000952 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 901 PubMed: Zhu 2021 family 233, patient 901 M - China - - - - - 1 LOVD
?/. - c.13156A>T r.(?) p.(Ile4386Phe) - Unknown ACMG VUS g.215848097T>A g.215674755T>A - - USH2A_000952 ACMG GN005 criteria: PM2_P PM3_M PubMed: Shu, H. R. et al., 2015 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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