Full data view for gene MYO7A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000260.3 transcript reference sequence.

9 entries on 1 page. Showing entries 1 - 9.
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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     
+/+ 18i c.2187+1G>A r.spl p.? - Unknown - pathogenic g.76886511G>A g.77175465G>A - - MYO7A_000156 Heterozygous PubMed: Adato 1997 - rs111033290 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Poland - - - - - 1 Anne-Françoise Roux
+/+ 18i c.2187+1G>A r.spl p.? - Unknown - pathogenic g.76886511G>A g.77175465G>A - - MYO7A_000156 Heterozygous PubMed: Adato 1997 - rs111033290 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Poland - - - - - 1 Anne-Françoise Roux
+/+ 18i c.2187+1G>A r.spl p.? - Unknown - pathogenic g.76886511G>A g.77175465G>A - - MYO7A_000156 Heterozygous PubMed: Adato 1997 - rs111033290 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Poland - - - - - 1 Anne-Françoise Roux
+/+ 18i c.2187+1G>A r.spl p.? - Unknown - pathogenic g.76886511G>A g.77175465G>A - - MYO7A_000156 Heterozygous PubMed: Adato 1997 - rs111033290 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Poland - - - - - 1 Anne-Françoise Roux
+/+ 18i c.2187+1G>A r.spl p.? - Parent #2 - pathogenic g.76886511G>A g.77175465G>A - - MYO7A_000156 Heterozygous PubMed: Jacobson 2009 - rs111033290 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jacobson 2009 Proband M - - - - - - - 1 William J. Kimberling
+/+ 18i c.2187+1G>A r.spl p.? - Parent #1 - pathogenic g.76886511G>A g.77175465G>A - - MYO7A_000156 Heterozygous; mutation PubMed: Jiang 2015 - rs111033290 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/. - c.2187+1G>A r.spl? p.? - Unknown - pathogenic g.76886511G>A g.77175465G>A - - MYO7A_000156 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.2187+1G>A r.spl? p.? - Parent #1 - likely pathogenic g.76886511G>A g.77175465G>A - - MYO7A_000156 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs111033290 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+/. - c.2187+1G>A r.spl p.? - Unknown ACMG pathogenic g.76886511G>A - - - MYO7A_000156 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
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