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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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Reference     

ClinVar ID     

dbSNP ID     

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VIP     

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Disease     

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Owner     
+?/. - c.3718C>T r.(?) p.(Arg1240Trp) - Unknown - likely pathogenic g.76901152C>T g.77190107C>T - - MYO7A_000152 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/? 29 c.3718C>T r.(?) p.(Arg1240Trp) MyTH4 1 (1017-1253) Unknown ACMG VUS g.76901152C>T g.77190107C>T - - MYO7A_000152 Heterozygous; UV3 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/192 controls +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 29 c.3718C>T r.(?) p.(Arg1240Trp) MyTH4 1 (1017-1253) Unknown ACMG VUS g.76901152C>T g.77190107C>T - - MYO7A_000152 Heterozygous PubMed: Pennings 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Pennings 2004 Proband - - Netherlands - - - - - 1 Anne-Françoise Roux
+?/. - c.3718C>T r.(?) p.(Arg1240Trp) - Unknown - likely pathogenic g.76901152C>T - - - MYO7A_000152 - - - rs371374104 CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.3718C>T r.(?) p.(Arg1240Trp) - Parent #1 - pathogenic g.76901152C>T g.77190107C>T - - MYO7A_000152 - PubMed: Neuhaus 2017 - - Germline yes - - - - DNA SEQ - - USH Pat10 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
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