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.

8 entries on 1 page. Showing entries 1 - 8.
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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     
+/+ 1 c.113G>A r.(?) p.(Trp38*) Ankyrin repeat 1 (31-60) Both (homozygous) - pathogenic g.72919056C>T g.74922961C>T - - USH1G_000007 homozygous PubMed: Ouyang et al., 2005 - rs104894652 Germline - - +BfaI;-PflMI;-BslI; - - DNA SEQ - - USH1 - PubMed: Ouyang et al., 2005 proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.113G>A r.(?) p.(Trp38*) Ankyrin repeat 1 (31-60) Both (homozygous) - pathogenic g.72919056C>T g.74922961C>T - - USH1G_000007 homozygous PubMed: Ouyang et al., 2005 - rs104894652 Germline - - +BfaI;-PflMI;-BslI; - - DNA SEQ - - USH1 - PubMed: Ouyang et al., 2005 proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.113G>A r.(?) p.(Trp38*) Ankyrin repeat 1 (31-60) Unknown - pathogenic g.72919056C>T g.74922961C>T - - USH1G_000007 Heterozygous PubMed: Bonnet et al., 2011 - rs104894652 Germline - - +BfaI;-PflMI;-BslI; - - DNA SEQ - - USH1 - PubMed: Bonnet et al., 2011 proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 1 c.113G>A r.(?) p.(Trp38*) Ankyrin repeat 1 (31-60) Both (homozygous) - pathogenic g.72919056C>T g.74922961C>T - - USH1G_000007 homozygous PubMed: Bujakowska et al., 2014 - rs104894652 Germline - - +BfaI;-PflMI;-BslI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bujakowska et al., 2014 proband M - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.113G>A r.(?) p.(Trp38*) Ankyrin repeat 1 (31-60) Both (homozygous) - pathogenic g.72919056C>T g.74922961C>T - - USH1G_000007 homozygous PubMed: Bujakowska et al., 2014 - rs104894652 Germline - - +BfaI;-PflMI;-BslI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bujakowska et al., 2014 relative M - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.113G>A r.(?) p.(Trp38*) Ankyrin repeat 1 (31-60) Both (homozygous) - pathogenic g.72919056C>T g.74922961C>T - - USH1G_000007 homozygous PubMed: Bujakowska et al., 2014 - rs104894652 Germline - - +BfaI;-PflMI;-BslI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bujakowska et al., 2014 relative F - United States - - - - - 1 Anne-Françoise Roux
+/+ 1 c.113G>A r.(?) p.(Trp38*) Ankyrin repeat 1 (31-60) Parent #1 - pathogenic g.72919056C>T g.74922961C>T - - USH1G_000007 Heterozygous PubMed: Bonnet et al., 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq - - USH1 - PubMed: Bonnet et al., 2016 - M - France - - - - - 1 Crystel Bonnet
+?/. 1 c.113G>A r.(?) p.(Trp38*) - Both (homozygous) - likely pathogenic g.72919056C>T - USH1G:c.113G>A,p.W38X - USH1G_000007 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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