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     
+/+ 7 c.652_657del r.(?) p.(Asp218_Ile219del) Motor domain (1-729) Parent #2 - pathogenic g.76867967_76867972del g.77156921_77156926del - - MYO7A_000128 Heterozygous PubMed: Levy 1997 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Levy 1997 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 7 c.652_657del r.(?) p.(Asp218_Ile219del) Motor domain (1-729) Unknown - pathogenic g.76867967_76867972del g.77156921_77156926del - - MYO7A_000128 Heterozygous PubMed: Levy 1997 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Levy 1997 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/+? 07 c.652_657del r.(?) p.(Asp218_Ile219del) Myosin motor (65 - 741) Unknown ACMG likely pathogenic g.76867967_76867972del g.77156921_77156926del - - MYO7A_000128 PM2_P, PM3_P, PM4_M, PP1_P, PP4_P, following ClinGen GN005 - - rs1555062984 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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