Full data view for gene USH1G


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_173477.2 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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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
-/- 2 c.388A>G r.(?) p.(Lys130Glu) Central (127-384) Unknown ACMG likely benign g.72916543T>C g.74920448T>C 387G>A (Lys130Glu) - USH1G_000015 heterozygous, {USMAUSH1G:K130E} {MSV3dQ495M9:p.Lys130Glu} PubMed: Aparisi et al., 2014 - rs111033465 Germline - - +BsoBI;+AvaI;-BstXI; - - DNA SEQ - - USH1 - PubMed: Jaijo et al., 2010 proband - - Spain - - - - - 1 Jose Maria Millan
-/- 2 c.388A>G r.(?) p.(Lys130Glu) Central (127-384) Unknown ACMG likely benign g.72916543T>C g.74920448T>C - - USH1G_000015 heterozygous, {USMAUSH1G:K130E} {MSV3dQ495M9:p.Lys130Glu} PubMed: Le Quesne Stabej et al., 2012 - rs111033465 Germline - 0/878 controls +BsoBI;+AvaI;-BstXI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej et al., 2012 proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 2 c.388A>G r.(?) p.(Lys130Glu) Central (127-384) Unknown ACMG likely benign g.72916543T>C g.74920448T>C - - USH1G_000015 heterozygous, {USMAUSH1G:K130E} {MSV3dQ495M9:p.Lys130Glu} PubMed: Le Quesne Stabej et al., 2012 - rs111033465 Germline - 0/878 controls +BsoBI;+AvaI;-BstXI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej et al., 2012 proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
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