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.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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P-domain     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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Disease     

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Owner     
+?/? 40 c.5510T>C r.(?) p.(Leu1837Pro) MyTH4 2 (1747-1896) Parent #2 ACMG VUS g.76916536T>C g.77205491T>C - - MYO7A_000548 Heterozygous; mutation PubMed: Jiang 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+?/. - c.5510T>C r.(?) p.(Leu1837Pro) - Parent #2 ACMG likely pathogenic g.76916536T>C g.77205491T>C NM_001127180.1:c.5396T>C - MYO7A_000548 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL 19856 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+?/. 40 c.5510T>C r.(?) p.(Leu1837Pro) - Parent #1 ACMG likely pathogenic (recessive) g.76916536T>C - - - MYO7A_000548 - - - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH Pat13 PubMed: Bahena 2021 - M no Mexico - - - - - 2 Barbara Vona
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