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)     

RNA change     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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VIP     

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Disease     

ID_report     

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Owner     
-?/. - c.1007G>A r.(?) p.(Arg336His) - Unknown - likely benign g.76870496G>A g.77159450G>A MYO7A(NM_000260.3):c.1007G>A (p.R336H), MYO7A(NM_000260.4):c.1007G>A (p.R336H) - MYO7A_000186 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 10 c.1007G>A r.(?) p.(Arg336His) Motor domain (1-729) Unknown ACMG likely benign g.76870496G>A g.77159450G>A - - MYO7A_000186 Heterozygous; polymorphism PubMed: Luijendijk 2004; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs45629132 Germline - - - - - DNA SEQ - - DFNA1 ? PubMed: Luijendijk 2004 Proband F - Netherlands - - - - - 1 Anne-Françoise Roux
-/? 10 c.1007G>A r.(?) p.(Arg336His) Motor domain (1-729) Parent #2 ACMG likely benign g.76870496G>A g.77159450G>A - - MYO7A_000186 Heterozygous PubMed: Jaijo 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs45629132 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jaijo 2006 Proband F - Spain - - - - - 1 Jose Maria Millan
-?/. - c.1007G>A r.(?) p.(Arg336His) - Unknown - likely benign g.76870496G>A g.77159450G>A MYO7A(NM_000260.3):c.1007G>A (p.R336H), MYO7A(NM_000260.4):c.1007G>A (p.R336H) - MYO7A_000186 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.1007G>A r.(?) p.(Arg336His) - Parent #1 - VUS g.76870496G>A g.77159450G>A - - MYO7A_000186 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs45629132 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
?/. - c.1007G>A r.(?) p.(Arg336His) - Unknown - VUS g.76870496G>A - MYO7A(NM_000260.3):c.1007G>A (p.R336H), MYO7A(NM_000260.4):c.1007G>A (p.R336H) - MYO7A_000186 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. 10 c.1007G>A r.(?) p.(Arg336His) - Both (homozygous) - VUS g.76870496G>A - c.1007G>A, p.(Arg336His) - MYO7A_000186 - PubMed: Maia-2020 - - Germline yes - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Maia-2020 - M yes - - - - - - 1 LOVD
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