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.

17 entries on 1 page. Showing entries 1 - 17.
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Effect     

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AscendingDNA change (cDNA)     

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Owner     
+?/? 48 c.6557T>C r.(?) p.(Leu2186Pro) FERM 2 (1902-2205) Parent #1 ACMG VUS g.76925023T>C g.77213978T>C - - MYO7A_000137 Heterozygous PubMed: Gerber 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls +SgrAI;+MspI;+HpaII;+BsaWI;-BsrI;-TspRI; - - DNA SEQ - - USH1B ? PubMed: Gerber 2006 Proband - - France - - - - - 1 Anne-Françoise Roux
+?/- 48 c.6557T>C r.(?) p.(Leu2186Pro) FERM 2 (1902-2205) Unknown ACMG VUS g.76925023T>C g.77213978T>C - - MYO7A_000137 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +SgrAI;+MspI;+HpaII;+BsaWI;-BsrI;-TspRI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/? 48 c.6557T>C r.(?) p.(Leu2186Pro) FERM 2 (1902-2205) Unknown ACMG VUS g.76925023T>C g.77213978T>C - - MYO7A_000137 Heterozygous PubMed: Bonnet 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/666 controls +SgrAI;+MspI;+HpaII;+BsaWI;-BsrI;-TspRI; - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/+ 48 c.6557T>C r.(?) p.(Leu2186Pro) FERM2 (1902-2205) Unknown ACMG VUS g.76925023T>C g.77213978T>C - - MYO7A_000137 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+?/? 48 c.6557T>C r.(?) p.(Leu2186Pro) FERM2 (1902-2205) Maternal (inferred) ACMG VUS g.76925023T>C g.77213978T>C - - MYO7A_000137 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+?/+ 48 c.6557T>C r.(?) p.(Leu2186Pro) FERM2 (1902-2205) Maternal (confirmed) ACMG VUS g.76925023T>C g.77213978T>C - - MYO7A_000137 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/? 48 c.6557T>C r.(?) p.(Leu2186Pro) FERM2 (1902-2205) Paternal (confirmed) ACMG VUS g.76925023T>C g.77213978T>C - - MYO7A_000137 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/+ 48 c.6557T>C r.(?) p.(Leu2186Pro) FERM2 (1902-2205) Parent #1 ACMG VUS g.76925023T>C g.77213978T>C - - MYO7A_000137 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+?/? 48 c.6557T>C r.(?) p.(Leu2186Pro) FERM 2 (1902-2205) Paternal (confirmed) ACMG VUS g.76925023T>C g.77213978T>C - - MYO7A_000137 Heterozygous PubMed: Baux, Vaché 2017; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +SgrAI;+MspI;+HpaII;+BsaWI;-BsrI;-TspRI; - - DNA SEQ, SEQ-NG-S - - DFNB S1799 PubMed: Baux 2017 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/. - c.6557T>C r.(?) p.(Leu2186Pro) - Maternal (confirmed) ACMG likely pathogenic g.76925023T>C - - - MYO7A_000137 - PubMed: Mansard et al, 2021 - rs876657417 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.6557T>C r.(?) p.(Leu2186Pro) - Both (homozygous) ACMG likely pathogenic g.76925023T>C - - - MYO7A_000137 - PubMed: Mansard et al, 2021 - rs876657417 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.6557T>C r.(?) p.(Leu2186Pro) - Paternal (confirmed) ACMG likely pathogenic g.76925023T>C - - - MYO7A_000137 - PubMed: Mansard et al, 2021 - rs876657417 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.6557T>C r.(?) p.(Leu2186Pro) - Unknown ACMG likely pathogenic g.76925023T>C - - - MYO7A_000137 - PubMed: Mansard et al, 2021 - rs876657417 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.6557T>C r.(?) p.(Leu2186Pro) - Paternal (confirmed) ACMG likely pathogenic g.76925023T>C - - - MYO7A_000137 - PubMed: Mansard et al, 2021 - rs876657417 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - ? - - - - - - - 1 Anne-Françoise Roux
+?/. - c.6557T>C r.(?) p.(Leu2186Pro) - Maternal (confirmed) ACMG likely pathogenic g.76925023T>C - - - MYO7A_000137 - PubMed: Mansard et al, 2021 - rs876657417 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.6557T>C r.(?) p.(Leu2186Pro) - Unknown ACMG pathogenic g.76925023T>C - - - MYO7A_000137 - PubMed: Mansard et al, 2021 - rs876657417 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. 48 c.6557T>C r.(?) p.(Leu2186Pro) - Both (homozygous) - likely pathogenic (recessive) g.76925023T>C - c.6557T>C p.Leu2186Pro - MYO7A_000137 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC03222 PubMed: Khateb 2020 simplex case F - - French - - - - 1 LOVD
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