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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Re-site     

VIP     

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Tissue     

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Disease     

ID_report     

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VIP     

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Owner     
?/. - c.83C>T r.(?) p.(Pro28Leu) - Unknown - VUS g.72919086G>A g.74922991G>A USH1G(NM_173477.4):c.83C>T (p.P28L) - USH1G_000022 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/-? 1 c.83C>T r.(?) p.(Pro28Leu) - Unknown ACMG likely benign g.72919086G>A g.74922991G>A - - USH1G_000022 heterozygous, {USMAUSH1G:P28L} {MSV3dQ495M9:p.Pro28Leu} PubMed: Le Quesne Stabej et al., 2012 - rs145448362 Germline - 0/96 controls +MnlI;+EcoNI;+TaqI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej et al., 2012 proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
?/. - c.83C>T r.(?) p.(Pro28Leu) - Unknown - VUS g.72919086G>A - USH1G(NM_173477.4):c.83C>T (p.P28L) - USH1G_000022 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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