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.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+?/. 22 c.2617C>T r.(?) p.(Arg873Trp) - Parent #1 - likely pathogenic g.76891450C>T g.77180404C>T - - MYO7A_000426 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - Germline - - - - - DNA SEQ-NG - - deafness - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - 1 Mieke Wesdorp
-?/? 22 c.2617C>T r.(?) p.(Arg873Trp) - Unknown ACMG likely benign g.76891450C>T g.77180404C>T - - MYO7A_000426 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 1/874 controls -Fnu4HI;-AciI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/? 22 c.2617C>T r.(?) p.(Arg873Trp) - Paternal (confirmed) ACMG likely benign g.76891450C>T g.77180404C>T - - MYO7A_000426 Heterozygous; mutation PubMed: Vastinsalo 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/150 controls -Fnu4HI;-AciI; - - DNA PE, SEQ - APEX USH2 ? PubMed: Vastinsalo 2012 Proband F - Finland - - - - - 1 Anne-Françoise Roux
-?/? 22 c.2617C>T r.(?) p.(Arg873Trp) - Unknown ACMG likely benign g.76891450C>T g.77180404C>T - - MYO7A_000426 Heterozygous; mutation PubMed: Vastinsalo 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/150 controls -Fnu4HI;-AciI; - - DNA PE, SEQ - APEX USH2 ? PubMed: Vastinsalo 2012 Proband - - Finland - - - - - 1 Anne-Françoise Roux
-?/. - c.2617C>T r.(?) p.(Arg873Trp) - Unknown - likely benign g.76891450C>T g.77180404C>T MYO7A(NM_000260.3):c.2617C>T (p.R873W), MYO7A(NM_000260.4):c.2617C>T (p.R873W) - MYO7A_000426 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.2617C>T r.(?) p.(Arg873Trp) - Unknown - VUS g.76891450C>T - MYO7A(NM_000260.3):c.2617C>T (p.R873W), MYO7A(NM_000260.4):c.2617C>T (p.R873W) - MYO7A_000426 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.2617C>T r.(?) p.(Arg873Trp) - Unknown - VUS g.76891450C>T - MYO7A(NM_000260.3):c.2617C>T (p.R873W), MYO7A(NM_000260.4):c.2617C>T (p.R873W) - MYO7A_000426 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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