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.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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Reference     

ClinVar ID     

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Disease     

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Owner     
+?/? 27 c.3502C>T r.3502c>t p.Arg1168Trp MyTH4 1 (1017-1253) Parent #2 ACMG VUS g.76895759C>T g.77184714C>T - - MYO7A_000264 Heterozygous; No effect on splicing (minigene) PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs554073390 Germline - 0/200 controls +BstXI;-MspI;-HpaII;-BsaWI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 27 c.3502C>T r.3502c>t p.Arg1168Trp MyTH4 1 (1017-1253) Unknown ACMG VUS g.76895759C>T g.77184714C>T - - MYO7A_000264 Heterozygous PubMed: Baux, Vaché 2017; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs554073390 Germline - - +BstXI;-MspI;-HpaII;-BsaWI; - - DNA SEQ, SEQ-NG-S - - DFNB S1692 PubMed: Baux 2017 Proband F - France - - - - - 1 Anne-Françoise Roux
+/. - c.3502C>T r.(?) p.(Arg1168Trp) - Parent #1 - pathogenic (recessive) g.76895759C>T g.77184714C>T - - MYO7A_000264 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4281 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.3502C>T r.(?) p.(Arg1168Trp) - Parent #1 - pathogenic (recessive) g.76895759C>T g.77184714C>T - - MYO7A_000264 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4692 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.3502C>T r.(?) p.(Arg1168Trp) - Both (homozygous) - pathogenic (recessive) g.76895759C>T g.77184714C>T - - MYO7A_000264 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL PKDF628 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.3502C>T r.(?) p.(Arg1168Trp) - Maternal (confirmed) - pathogenic (recessive) g.76895759C>T g.77184714C>T - - MYO7A_000264 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4652 PubMed: Richard 2019 4-generation family, 3 affected sibs (F, 2M) - yes Pakistan - - - - - 3 Johan den Dunnen
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