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     

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Consanguinity     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/? 70 c.15188T>G r.(=) p.(Leu5063Arg) Transmembrane (5043-5063) Maternal (confirmed) ACMG VUS g.215807910A>C g.215634568A>C - - USH2A_000857 Heterozygous; pathogenic PubMed: Méndez-Vidal 2013, USMA missense analysis, missense variant in MSV3d - rs376816523 Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Méndez-Vidal 2013 Proband F - Spain - - - - - 1 Anne-Françoise Roux
+?/? 70 c.15188T>G r.(=) p.(Leu5063Arg) Transmembrane (5043-5063) Maternal (confirmed) ACMG VUS g.215807910A>C g.215634568A>C - - USH2A_000857 Heterozygous; pathogenic PubMed: Méndez-Vidal 2013, USMA missense analysis, missense variant in MSV3d - rs376816523 Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Méndez-Vidal 2013 Relative M - Spain - - - - - 1 Anne-Françoise Roux
+?/? 70 c.15188T>G r.(=) p.(Leu5063Arg) Transmembrane (5043-5063) Maternal (confirmed) ACMG VUS g.215807910A>C g.215634568A>C - - USH2A_000857 Heterozygous; pathogenic PubMed: Méndez-Vidal 2013, USMA missense analysis, missense variant in MSV3d - rs376816523 Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Méndez-Vidal 2013 Relative F - Spain - - - - - 1 Anne-Françoise Roux
+?/? 70 c.15188T>G r.(=) p.(Leu5063Arg) Transmembrane (5043-5063) Maternal (confirmed) ACMG VUS g.215807910A>C g.215634568A>C - - USH2A_000857 Heterozygous; pathogenic PubMed: Méndez-Vidal 2013, USMA missense analysis, missense variant in MSV3d - rs376816523 Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Méndez-Vidal 2013 Relative M - Spain - - - - - 1 Anne-Françoise Roux
+?/? 70 c.15188T>G r.(=) p.(Leu5063Arg) Transmembrane (5043-5063) Maternal (confirmed) ACMG VUS g.215807910A>C g.215634568A>C - - USH2A_000857 Heterozygous; pathogenic PubMed: Méndez-Vidal 2013, USMA missense analysis, missense variant in MSV3d - rs376816523 Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Méndez-Vidal 2013 Relative F - Spain - - - - - 1 Anne-Françoise Roux
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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