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.

6 entries on 1 page. Showing entries 1 - 6.
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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     

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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     

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Panel size     

Owner     
+/+ 2 c.6_9dup r.(?) p.(Leu4Aspfs*39) - Unknown - pathogenic g.76841686_76841689dup g.77130640_77130643dup - - MYO7A_000164 Heterozygous PubMed: Jaijo 2006 - - Germline - - none - - DNA minigene, RT-PCR, SEQ - - USH1B ? PubMed: Jaijo 2006 Proband - Minigene and Nasal cell studies in Aparisi et al., 2013 M - Spain - - - - - 1 Jose Maria Millan
+/+ 2 c.6_9dup r.(?) p.(Leu4Aspfs*39) - Maternal (confirmed) - pathogenic g.76841686_76841689dup g.77130640_77130643dup - - MYO7A_000164 Heterozygous PubMed: Roux 2011 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Besnard, Garcia-Garcia 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 2 c.6_9dup r.(?) p.(Leu4fsAsp*39) - Parent #2 - pathogenic g.76841686_76841689dup g.77130640_77130643dup - - MYO7A_000164 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+?/. - c.6_9dup r.(?) p.(Leu4Aspfs*39) - Unknown - likely pathogenic g.76841686_76841689dup g.77130640_77130643dup , c.6_9dup, p.Leu4AspfsTer39 - MYO7A_000164 - PubMed: Ezquerra-Inchausti 2018 - - Germline yes - - - - DNA SEQ-NG blood - retinal disease II:3 PubMed: Ezquerra-Inchausti 2018 Family RP88, II:3 ? no Spain - - - - - 1 LOVD
+?/. - c.6_9dup r.(?) p.(Leu4Aspfs*39) - Unknown - likely pathogenic g.76841686_76841689dup g.77130640_77130643dup , c.6_9dup, p.Leu4AspfsTer39 - MYO7A_000164 - PubMed: Ezquerra-Inchausti 2018 - - Germline yes - - - - DNA SEQ-NG blood - retinal disease II:5 PubMed: Ezquerra-Inchausti 2018 Family RP88, II:5 ? no Spain - - - - - 1 LOVD
+/. 2 c.6_9dup r.(?) p.(Leu4Aspfs*39) - Parent #2 - pathogenic g.76841686_76841689dup - c.6_9dup(UV4) - MYO7A_000164 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 8 LOVD
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