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.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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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     
+/+ 23 c.2766_2779del r.(?) p.(Lys923Alafs*8) Coiled coil (858-935) Parent #2 - pathogenic g.76892497_76892510del g.77181451_77181464del - - MYO7A_000015 Heterozygous PubMed: Vastinsalo 2006 - - Germline - 1/200 controls - - - DNA SEQ - - USH1B ? PubMed: Vastinsalo 2006 Proband F - Finland - - - - - 1 Anne-Françoise Roux
+/+ 23 c.2766_2779del r.(?) p.(Lys923Alafs*8) Coiled coil (858-935) Parent #2 - pathogenic g.76892497_76892510del g.77181451_77181464del - - MYO7A_000015 Heterozygous PubMed: Vastinsalo 2006 - - Germline - 1/200 controls - - - DNA SEQ - - USH1B ? PubMed: Vastinsalo 2006 Proband F - Finland - - - - - 1 Anne-Françoise Roux
+/+ 23 c.2766_2779del r.(?) p.(Lys923Alafs*8) Coiled coil (858-935) Paternal (inferred) - pathogenic g.76892497_76892510del g.77181451_77181464del - - MYO7A_000015 Homozygous PubMed: Malm 2010 - - Germline - 1/200 controls - - - DNA PE, SEQ - APEX USH1B ? PubMed: Malm 2010 Proband - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 23 c.2766_2779del r.(?) p.(Lys923Alafs*8) Coiled coil (858-935) Maternal (inferred) - pathogenic g.76892497_76892510del g.77181451_77181464del - - MYO7A_000015 Homozygous PubMed: Malm 2010 - - Germline - 1/200 controls - - - DNA PE, SEQ - APEX USH1B ? PubMed: Malm 2010 Proband - - Sweden - - - - - 1 Anne-Françoise Roux
+/+ 23 c.2766_2779del r.(?) p.(Lys923Alafs*8) Coiled coil (858-935) Unknown - pathogenic g.76892497_76892510del g.77181451_77181464del - - MYO7A_000015 Heterozygous PubMed: Vastinsalo 2012 - - Germline - - - - - DNA PE, SEQ - APEX USH1B ? PubMed: Vastinsalo 2012 Proband - - Finland - - - - - 1 Anne-Françoise Roux
+/. 23 c.2766_2779del r.(?) p.(Lys923Alafs*8) Coiled coil (858-935) Parent #2 - pathogenic (recessive) g.76892497_76892510del g.77181451_77181464del - - MYO7A_000015 - PubMed: Ivanova 2018 - - Germline - - - - - DNA SEQ-NG-S - - USH1B Pat7 PubMed: Ivanova 2018 Proband F - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+?/. - c.2766_2779del r.(?) p.(Lys923Alafs*8) - Both (homozygous) - likely pathogenic (recessive) g.76892497_76892510del g.77181451_77181464del c.2766_2779del14 - MYO7A_000015 - PubMed: Holtan 2020 - - Germline - 1/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 1 homozygous patient - - Norway - - - - - 1 Global Variome, with Curator vacancy
+/. - c.2766_2779del r.(?) p.(Lys923Alafs*8) - Parent #2 - pathogenic (recessive) g.76892497_76892510del g.77181451_77181464del - - MYO7A_000015 - PubMed: Avela 2018 - - Germline - - - - - DNA SEQ-NG - - retinal disease Pat24 PubMed: Avela 2018 - - - Finland - - - - - 1 LOVD
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