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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-?/? 23 c.2886G>C r.(?) p.(Gln962His) - Unknown ACMG likely benign g.76892617G>C g.77181571G>C - - MYO7A_000408 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/878 controls -BssKI;-NlaIV;-StyD4I;-BstNI;-PspGI;-ScrFI; - - DNA SEQ - - USH - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
?/. - c.2886G>C r.(?) p.(Gln962His) - Unknown - VUS g.76892617G>C g.77181571G>C MYO7A(NM_000260.3):c.2886G>C (p.Q962H), MYO7A(NM_000260.4):c.2886G>C (p.Q962H) - MYO7A_000408 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.2886G>C r.(?) p.(Gln962His) - Unknown - VUS g.76892617G>C g.77181571G>C MYO7A(NM_000260.3):c.2886G>C (p.Q962H), MYO7A(NM_000260.4):c.2886G>C (p.Q962H) - MYO7A_000408 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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