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)     

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     
+/+ 1 c.143T>C r.(?) p.(Leu48Pro) Ankyrin repeat 1 (31-60) Parent #2 - pathogenic g.72919026A>G g.74922931A>G - - USH1G_000003 heterozygous, {USMAUSH1G:L48P} {MSV3dQ495M9:p.Leu48Pro} PubMed: Weil et al., 2003 - rs104894651 Germline - 0/160 controls - - - DNA SEQ - - USH1 - PubMed: Weil et al., 2003 proband M - Germany - - - - - 1 Anne-Françoise Roux
+/+ 1 c.143T>C r.(?) p.(Leu48Pro) Ankyrin repeat 1 (31-60) Parent #2 - pathogenic g.72919026A>G g.74922931A>G - - USH1G_000003 heterozygous, {USMAUSH1G:L48P} {MSV3dQ495M9:p.Leu48Pro} PubMed: Weil et al., 2003 - rs104894651 Germline - 0/160 controls - - - DNA SEQ - - USH1 - PubMed: Weil et al., 2003 relative M - Germany - - - - - 1 Anne-Françoise Roux
+/+ 1 c.143T>C r.(?) p.(Leu48Pro) Ankyrin repeat 1 (31-60) Unknown - pathogenic g.72919026A>G g.74922931A>G - - USH1G_000003 heterozygous, {USMAUSH1G:L48P} {MSV3dQ495M9:p.Leu48Pro} PubMed: Krawitz et al., 2014 - rs104894651 Germline - - - - - DNA SEQ-NG-S - - USH1 - PubMed: Krawitz et al., 2014 proband F - Germany - - - - - 1 Peter Krawitz
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