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     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/? 27 c.3503G>C r.[3503g>c, 3376_3503del] p.[Arg1168Pro, Val1126Glyfs*59] MyTH4 1 (1017-1253) Parent #2 ACMG likely pathogenic g.76895760G>C g.77184715G>C - - MYO7A_000160 Heterozygous; E27 skipping (Le Guédard-Méreuze , 2010) PubMed: Jaijo 2006 - - Germline - 0/200 controls -BsaWI;-MspI;-HpaII; - - DNA SEQ - - USH1B ? PubMed: Jaijo 2006 Proband M - Spain - - - - - 1 Jose Maria Millan
+/. 27 c.3503G>C r.(?) p.(Arg1168Pro) - Parent #2 - pathogenic g.76895760G>C - c.3503G>C - MYO7A_000160 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. 27 c.3503G>C r.(?) p.(Arg1168Pro) - Parent #2 - pathogenic g.76895760G>C - c.3503G>C - MYO7A_000160 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 8 LOVD
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