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)     

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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 65 c.14222C>T r.(?) p.(Pro4741Leu) - Unknown ACMG likely pathogenic g.215824055G>A g.215650713G>A NM_206933.2:c.14222C>T, NP_996816.2:p.(Pro4741Leu), NC_000001.10:g.215824055G>A - USH2A_002136 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - exome sequencing retinal disease 2016101720 PubMed: Wang 2018 - F ? China Han Chinese - - - - 1 LOVD
+?/. 65 c.14222C>T r.(?) p.(Pro4741Leu) - Unknown - likely pathogenic g.215824055G>A g.215650713G>A USH2A Ex.13 c.2276G>T p.(Cys759Phe), Ex.65 c.14222C>T p.(Pro4741Leu) - USH2A_002136 compound heterozygous PubMed: Martin Merida 2019 - - Germline yes - - - - DNA SEQ-NG-I - - retinal disease RP-2526 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. 65 c.14222C>T r.(?) p.(Pro4741Leu) - Parent #2 ACMG likely pathogenic g.215824055G>A g.215650713G>A USH2A c.14222C>T, p.P4741L - USH2A_002136 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_7 PubMed: Zhu 2021 family 27, patient AXLM_7 M - 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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