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.

2 entries on 1 page. Showing entries 1 - 2.
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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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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 2 c.387dup r.(?) p.(Lys130Glnfs*5) Central (127-384) Paternal (inferred) - pathogenic g.72916547dup g.74920452dup 387dupC - USH1G_000054 homozygous PubMed: Bonnet et al., 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bonnet et al., 2016 - M - Germany - - - - - 1 Crystel Bonnet
+/+ 2 c.387dup r.(?) p.(Lys130Glnfs*5) Central (127-384) Maternal (inferred) - pathogenic g.72916547dup g.74920452dup 387dupC - USH1G_000054 homozygous PubMed: Bonnet et al., 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bonnet et al., 2016 - M - Germany - - - - - 1 Crystel Bonnet
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