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.

10 entries on 1 page. Showing entries 1 - 10.
Legend   How to query  

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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 22 c.2663dup r.(?) p.(Ala889Glyfs*19) Coiled coil (858-935) Paternal (inferred) - pathogenic g.76891496dup g.77180450dup - - MYO7A_000142 Homozygous PubMed: Kumar 2004 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Kumar 2004 Proband M - India - - - - - 1 Anne-Françoise Roux
+/+ 22 c.2663dup r.(?) p.(Ala889Glyfs*19) Coiled coil (858-935) Maternal (inferred) - pathogenic g.76891496dup g.77180450dup - - MYO7A_000142 Homozygous PubMed: Kumar 2004 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Kumar 2004 Proband M - India - - - - - 1 Anne-Françoise Roux
+/+ 22 c.2663dup r.(?) p.(Ala889Glyfs*19) Coiled coil (858-935) Paternal (inferred) - pathogenic g.76891496dup g.77180450dup - - MYO7A_000142 Homozygous PubMed: Kumar 2004 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Kumar 2004 Relative F - India - - - - - 1 Anne-Françoise Roux
+/+ 22 c.2663dup r.(?) p.(Ala889Glyfs*19) Coiled coil (858-935) Maternal (inferred) - pathogenic g.76891496dup g.77180450dup - - MYO7A_000142 Homozygous PubMed: Kumar 2004 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Kumar 2004 Relative F - India - - - - - 1 Anne-Françoise Roux
+/+ 22 c.2663dup r.(?) p.(Ala889Glyfs*19) Coiled coil (858-935) Paternal (inferred) - pathogenic g.76891496dup g.77180450dup - - MYO7A_000142 Homozygous PubMed: Kumar 2004 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Kumar 2004 Relative F - India - - - - - 1 Anne-Françoise Roux
+/+ 22 c.2663dup r.(?) p.(Ala889Glyfs*19) Coiled coil (858-935) Maternal (inferred) - pathogenic g.76891496dup g.77180450dup - - MYO7A_000142 Homozygous PubMed: Kumar 2004 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Kumar 2004 Relative F - India - - - - - 1 Anne-Françoise Roux
+/+ 22 c.2663dup r.(?) p.(Ala889Glyfs*19) Coiled coil (858-935) Paternal (inferred) - pathogenic g.76891496dup g.77180450dup - - MYO7A_000142 Homozygous PubMed: Kumar 2004 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Kumar 2004 Relative M - India - - - - - 1 Anne-Françoise Roux
+/+ 22 c.2663dup r.(?) p.(Ala889Glyfs*19) Coiled coil (858-935) Maternal (inferred) - pathogenic g.76891496dup g.77180450dup - - MYO7A_000142 Homozygous PubMed: Kumar 2004 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Kumar 2004 Relative M - India - - - - - 1 Anne-Françoise Roux
+/+ 22 c.2663dup r.(?) p.(Ala889Glyfs*19) Coiled coil (858-935) Paternal (inferred) - pathogenic g.76891496dup g.77180450dup - - MYO7A_000142 Homozygous PubMed: Kumar 2004 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Kumar 2004 Relative F - India - - - - - 1 Anne-Françoise Roux
+/+ 22 c.2663dup r.(?) p.(Ala889Glyfs*19) Coiled coil (858-935) Maternal (inferred) - pathogenic g.76891496dup g.77180450dup - - MYO7A_000142 Homozygous PubMed: Kumar 2004 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Kumar 2004 Relative F - India - - - - - 1 Anne-Françoise Roux
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.