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.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+?/+ 29 c.3728C>T r.(?) p.(Pro1243Leu) MyTH4 1 (1017-1253) Parent #2 ACMG VUS g.76901162C>T g.77190117C>T - - MYO7A_000566 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs750358148 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. - c.3728C>T r.(?) p.(Pro1243Leu) - Unknown - likely pathogenic g.76901162C>T g.77190117C>T - - MYO7A_000566 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.3728C>T r.(?) p.(Pro1243Leu) - Unknown - pathogenic (recessive) g.76901162C>T - 11:76901162C>T ENST00000409709.3:c.3728C>T (Pro1243Leu) - MYO7A_000566 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G001030 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+?/. - c.3728C>T r.(?) p.(Pro1243Leu) - Unknown - likely pathogenic g.76901162C>T g.77190117C>T MYO7A c.3728C>T, p.Pro1243Leu - MYO7A_000566 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G001030 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.3728C>T r.(?) p.(Pro1243Leu) - Unknown - likely pathogenic g.76901162C>T g.77190117C>T MYO7A c.3728C>T, p.Pro1243Leu - MYO7A_000566 - PubMed: Georgiou 2021 - - Unknown ? - - - - DNA SEQ-NG blood retrospective study retinal disease P7 PubMed: Georgiou 2021 pedigree ID: 20699, genetic ID: 31899 F - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. 29 c.3728C>T r.(?) p.(Pro1243Leu) - Unknown - likely pathogenic g.76901162C>T - p.P1243L - MYO7A_000566 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 29 c.3728C>T r.(?) p.(Pro1243Leu) - Parent #2 - likely pathogenic (recessive) g.76901162C>T - c.3728C>T p.Pro1243Leu - MYO7A_000566 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC06833 PubMed: Khateb 2020 simplex case M - - Father French and mother Algerian - - - - 1 LOVD
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