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.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+/? 29 c.3652G>A r.spl p.(Gly1218Arg) MyTH4 1 (1017-1253) Parent #2 ACMG likely pathogenic g.76901086G>A g.77190041G>A - - MYO7A_000171 Heterozygous; shown in Aparisi , 2013 to affect splicing (p.(Asn443_Glu450del)) PubMed: Jaijo 2007; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033195 Germline - 0/100 controls - - - DNA minigene, SEQ - - USH1B ? PubMed: Jaijo 2007 Proband - Minigene studies in Aparisi et al., 2013 - - Italy - - - - - 1 Jose Maria Millan
+/? 29 c.3652G>A r.spl p.(Gly1218Arg) MyTH4 1 (1017-1253) Maternal (confirmed) ACMG likely pathogenic g.76901086G>A g.77190041G>A - - MYO7A_000171 Heterozygous; shown in Aparisi , 2013 to affect splicing (p.(Asn443_Glu450del)) PubMed: Baux, Vaché 2017; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033195 Germline - - - - - DNA SEQ, SEQ-NG-S - - DFNB S1741 PubMed: Baux 2017 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/. - c.3652G>A r.(?) p.(Gly1218Arg) - Unknown ACMG likely pathogenic g.76901086G>A - - - MYO7A_000171 - PubMed: Mansard et al, 2021 - rs111033195 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. - c.3652G>A r.(?) p.(Gly1218Arg) - Unknown ACMG likely pathogenic g.76901086G>A - - - MYO7A_000171 - PubMed: Mansard et al, 2021 - rs111033195 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
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