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.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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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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Disease     

ID_report     

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VIP     

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Owner     
+/+ 2 c.1373A>T r.(?) p.(Asp458Val) - Both (homozygous) - pathogenic g.72915558T>A g.74919463T>A - - USH1G_000006 homozygous, {USMAUSH1G:D458V} {MSV3dQ495M9:p.Asp458Val} PubMed: Kalay et al., 2005 - - Germline - 1/498 controls - - - DNA SEQ - - USH - PubMed: Kalay et al., 2005 proband F - Turkey - - - - - 1 Anne-Françoise Roux
+/+ 2 c.1373A>T r.(?) p.(Asp458Val) - Both (homozygous) - pathogenic g.72915558T>A g.74919463T>A - - USH1G_000006 homozygous, {USMAUSH1G:D458V} {MSV3dQ495M9:p.Asp458Val} PubMed: Kalay et al., 2005 - - Germline - 1/498 controls - - - DNA SEQ - - USH - PubMed: Kalay et al., 2005 relative M - Turkey - - - - - 1 Anne-Françoise Roux
+/+ 2 c.1373A>T r.(?) p.(Asp458Val) - Both (homozygous) - pathogenic g.72915558T>A g.74919463T>A - - USH1G_000006 homozygous, {USMAUSH1G:D458V} {MSV3dQ495M9:p.Asp458Val} PubMed: Kalay et al., 2005 - - Germline - 1/498 controls - - - DNA SEQ - - USH - PubMed: Kalay et al., 2005 relative F - Turkey - - - - - 1 Anne-Françoise Roux
+/+ 2 c.1373A>T r.(?) p.(Asp458Val) - Both (homozygous) - pathogenic g.72915558T>A g.74919463T>A - - USH1G_000006 homozygous, {USMAUSH1G:D458V} {MSV3dQ495M9:p.Asp458Val} PubMed: Kalay et al., 2005 - - Germline - 1/498 controls - - - DNA SEQ - - USH - PubMed: Kalay et al., 2005 relative F - Turkey - - - - - 1 Anne-Françoise Roux
+/+ 2 c.1373A>T r.(?) p.(Asp458Val) - Both (homozygous) - pathogenic g.72915558T>A g.74919463T>A - - USH1G_000006 homozygous, {USMAUSH1G:D458V} {MSV3dQ495M9:p.Asp458Val} PubMed: Kalay et al., 2005 - - Germline - 1/498 controls - - - DNA SEQ - - USH - PubMed: Kalay et al., 2005 relative F - Turkey - - - - - 1 Anne-Françoise Roux
+/+ 2 c.1373A>T r.(?) p.(Asp458Val) - Both (homozygous) - pathogenic g.72915558T>A g.74919463T>A - - USH1G_000006 homozygous, {USMAUSH1G:D458V} {MSV3dQ495M9:p.Asp458Val} PubMed: Kalay et al., 2005 - - Germline - 1/498 controls - - - DNA SEQ - - USH - PubMed: Kalay et al., 2005 relative M - Turkey - - - - - 1 Anne-Françoise Roux
+/. - c.1373A>T r.(?) p.(Asp458Val) - Both (homozygous) - pathogenic g.72915558T>A g.74919463T>A - - USH1G_000006 - PubMed: Neuhaus 2017 - rs397517925 Germline - - - - - DNA arraySNP, SEQ - locus‐specific polymorphic microsatellite marker USH PatDEM74 PubMed: Neuhaus 2017 - - yes Pakistan - - - - - 1 LOVD
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