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.

5 entries on 1 page. Showing entries 1 - 5.
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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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Owner     
+/+ 37 c.5101C>T r.(?) p.(Arg1701*) - Maternal (confirmed) - pathogenic g.76913402C>T g.77202357C>T - - MYO7A_000139 Heterozygous PubMed: Le Quesne Stabej 2012 - rs111033182 Germline - 0/878 controls +Hpy166II - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 37 c.5101C>T r.(?) p.(Arg1701*) - Parent #2 - pathogenic g.76913402C>T g.77202357C>T - - MYO7A_000139 Heterozygous PubMed: Gerber 2006 - rs111033182 Germline - - +Hpy166II - - DNA SEQ - - USH1B ? PubMed: Gerber 2006 Proband - - France - - - - - 1 Anne-Françoise Roux
+/+ 37 c.5101C>T r.(?) p.(Arg1701*) - Unknown - pathogenic g.76913402C>T g.77202357C>T - - MYO7A_000139 Heterozygous PubMed: Roux 2011 - rs111033182 Germline - - +Hpy166II - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/. - c.5101C>T r.(?) p.(Arg1701*) - Unknown - likely pathogenic g.76913402C>T g.77202357C>T c.5101C>T p.(Arg1701*) - MYO7A_000139 single heterozygous variant in a recessive disease PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 054t PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
?/. 37 c.5101C>T r.(?) p.(Arg1701*) - Unknown - VUS g.76913402C>T - c.5101C>T - MYO7A_000139 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
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