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.

60 entries on 1 page. Showing entries 1 - 60.
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Effect     

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AscendingDNA change (cDNA)     

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Protein     

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Classification method     

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     

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Methylation     

Template     

Technique     

Tissue     

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Disease     

ID_report     

Reference     

Remarks     

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+/. - c.5581C>T r.(?) p.(Arg1861Ter) - Unknown - pathogenic g.76916607C>T g.77205562C>T MYO7A(NM_000260.4):c.5581C>T (p.R1861*) - MYO7A_000144 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.5581C>T r.(?) p.(Arg1861Ter) - Unknown - pathogenic g.76916607C>T g.77205562C>T MYO7A(NM_000260.4):c.5581C>T (p.R1861*) - MYO7A_000144 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 40 c.5581C>T r.(?) p.(Arg1861*) - Both (homozygous) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 - Sharon, submitted - - Germline - - - - - DNA SEQ - - USH1 - Sharon, submitted - F yes Israel Samaritans - - - - 1 Dror Sharon
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Adato 1997 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Jordan - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Parent #2 - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Heterozygous PubMed: Jaijo 2007 - rs878864531 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jaijo 2007 Proband F - Spain - - - - - 1 Jose Maria Millan
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Jaijo 2010 - rs878864531 Germline - - - - - DNA minigene, RT-PCR, SEQ - - USH1B ? PubMed: Jaijo 2010 Proband - Minigene and Nasal cell studies in Aparisi et al., 2013 - - Spain - - - - - 1 Jose Maria Millan
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous PubMed: Jaijo 2010 - rs878864531 Germline - - - - - DNA minigene, RT-PCR, SEQ - - USH1B ? PubMed: Jaijo 2010 Proband - Minigene and Nasal cell studies in Aparisi et al., 2013 - - Spain - - - - - 1 Jose Maria Millan
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (confirmed) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Heterozygous PubMed: Lenarduzzi 2015 - rs878864531 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Lenarduzzi 2015 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Parent #2 - pathogenic g.76916607C>T g.77205562C>T NM_001127180:C5467T - p.R1823X - MYO7A_000144 Heterozygous; mutation PubMed: Jiang 2015 - rs878864531 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband F - China - - - - - 1 Anne-Françoise Roux
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Parent #2 - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Heterozygous; mutation PubMed: Bonnet 2016 - rs878864531 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous; mutation PubMed: Bonnet 2016 - rs878864531 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Maternal (inferred) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Homozygous; mutation PubMed: Bonnet 2016 - rs878864531 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Parent #1 - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Heterozygous; mutation PubMed: Bonnet 2016 - rs878864531 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+/+ 40 c.5581C>T r.(?) p.(Arg1861*) MyTH4 2 (1747-1896) Paternal (confirmed) - pathogenic g.76916607C>T g.77205562C>T - - MYO7A_000144 Heterozygous PubMed: Baux, Vaché 2017 - rs878864531 Germline - - - - - DNA SEQ, SEQ-NG-S - - DFNB S1741 PubMed: Baux 2017 Proband M - France - - - - - 1 Anne-Françoise Roux
+/. - c.5581C>T r.(?) p.(Arg1861*) - Unknown ACMG pathogenic g.76916607C>T - - - MYO7A_000144 - PubMed: Sharon 2019 - - Germline - 2/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - 2 Global Variome, with Curator vacancy
+/. - c.5581C>T r.(?) p.(Arg1861*) - Unknown ACMG pathogenic g.76916607C>T g.77205562C>T NM_001127180.1:c.5467C>T - MYO7A_000144 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19838 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. 40 c.5581C>T r.(?) p.(Arg1861*) - Unknown ACMG pathogenic g.76916607C>T g.77205562C>T NM_000260.3:c.5581C>T, NP_000251.3:p.(Arg1861Ter), NC_000011.9:g.76916607C>T - MYO7A_000144 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - panel of 441 hereditary eye disease genes including 291 genes related to IRD retinal disease 2016112104 PubMed: Wang 2018 - M ? China Han Chinese - - - - 1 LOVD
+?/. - c.5581C>T r.(?) p.(Arg1861*) - Parent #1 - likely pathogenic g.76916607C>T g.77205562C>T MYO7A c.5581C>T, p.R1861X - MYO7A_000144 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 140 PubMed: Jauregui 2020 - F - (United States) Other - - - - 1 LOVD
+/. - c.5581C>T r.(?) p.(Arg1861Ter) - Both (homozygous) ACMG pathogenic g.76916607C>T - - - MYO7A_000144 - PubMed: Mansard et al, 2021 - rs878864531 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.5581C>T r.(?) p.(Arg1861Ter) - Unknown ACMG pathogenic g.76916607C>T - - - MYO7A_000144 - PubMed: Mansard et al, 2021 - rs878864531 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.5581C>T r.(?) p.(Arg1861*) - Parent #1 - likely pathogenic g.76916607C>T g.77205562C>T MYO7A, variant 1: c.5581C>T/p.R1861*, variant 2: c.5617C>T/p.R1873W - MYO7A_000144 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET6 targeted sequencing panel - see paper retinal disease 86 PubMed: Weisschuh 2020 Filing key number: 43, Usher syndrome type I, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
?/. 40 c.5581C>T r.(?) p.(Gln1861*) - Unknown - VUS g.76916607C>T - c.5581C>T - MYO7A_000144 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Khalaileh-2018 - - yes - Samarian Jew - - - - 1 LOVD
?/. 40 c.5581C>T r.(?) p.(Gln1861*) - Unknown - VUS g.76916607C>T - c.5581C>T - MYO7A_000144 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Khalaileh-2018 - - yes - Samarian Jew - - - - 1 LOVD
+/. 40 c.5581C>T r.(?) p.(Gln1861*) - Unknown - pathogenic g.76916607C>T - c.5581C>T - MYO7A_000144 - PubMed: Colombo-2020 - rs878864531 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+/. 40 c.5581C>T r.(?) p.(Gln1861*) - Unknown - pathogenic g.76916607C>T - c.5581C>T - MYO7A_000144 - PubMed: Colombo-2020 - rs878864531 Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+/. 40 c.5581C>T r.(?) p.(Gln1861*) - Parent #2 - pathogenic g.76916607C>T - c.5581C>T - MYO7A_000144 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. 40 c.5581C>T r.(?) p.(Gln1861*) - Both (homozygous) - pathogenic g.76916607C>T - c.5581C>T - MYO7A_000144 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
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