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     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.977_986dup r.(?) p.(Gly330Alafs*29) - Both (homozygous) - pathogenic (recessive) g.72915945_72915954dup g.74919850_74919859dup 977_986dupTCAGCGTCCC - USH1G_000063 - PubMed: Alzahrani 2020, Journal: Alzahrani 2020 - - Germline yes - - - - DNA SEQ, SEQ-NG - - ?, USH 10DF10800_a PubMed: Alzahrani 2020, Journal: Alzahrani 2020 2-generation family, affected sister/brother, unaffected heterozygous carrier parents F yes Saudi Arabia - - - - - 2 Johan den Dunnen
+/. - c.977_986dup r.(?) p.(Gly330Alafs*29) - Both (homozygous) - pathogenic (recessive) g.72915945_72915954dup g.74919850_74919859dup 977_986dupTCAGCGTCCC - USH1G_000063 - PubMed: Alzahrani 2020, Journal: Alzahrani 2020 - - Germline yes - - - - DNA SEQ, SEQ-NG - - ?, USH 10DF10800_b PubMed: Alzahrani 2020, Journal: Alzahrani 2020 brother M yes Saudi Arabia - - - - - 1 Johan den Dunnen
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