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.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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ClinVar ID     

dbSNP ID     

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VIP     

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Owner     
+?/+ 19 c.2210A>G r.(?) p.(Glu737Gly) - Unknown ACMG VUS g.76888617A>G g.77177571A>G - - MYO7A_000552 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs782595324 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
?/. - c.2210A>G r.(?) p.(Glu737Gly) - Unknown ACMG VUS g.76888617A>G g.77177571A>G - - MYO7A_000552 ACMG PP3, PM2 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHI-3 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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