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.

11 entries on 1 page. Showing entries 1 - 11.
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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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 43 c.5886_5889del r.(?) p.(Phe1962Leufs*7) FERM 2 (1902-2205) Parent #1 - pathogenic g.76919504_76919507del g.77208459_77208462del 5886_5889delCTTT - MYO7A_000089 Heterozygous PubMed: Roux 2011 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 43 c.5886_5889del r.(?) p.(Phe1962Leufs*7) FERM 2 (1902-2205) Parent #1 - pathogenic g.76919504_76919507del g.77208459_77208462del 5886_5889delCTTT - MYO7A_000089 Heterozygous PubMed: Le Guédard-Méreuze 2010 - - Germline - - - - - DNA minigene, SEQ - - USH1B ? PubMed: Le Guédard-Méreuze 2010 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 43 c.5886_5889del r.(?) p.(Phe1962Leufs*7) FERM 2 (1902-2205) Parent #2 - pathogenic g.76919504_76919507del g.77208459_77208462del 5886_5889delCTTT - MYO7A_000089 - PubMed: Gerber 2006 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Gerber 2006 Proband - - France - - - - - 1 Anne-Françoise Roux
+/+ 43 c.5886_5889del r.(?) p.(Phe1962Leufs*7) FERM 2 (1902-2205) Parent #2 - pathogenic g.76919504_76919507del g.77208459_77208462del 5886_5889delCTTT - MYO7A_000089 Heterozygous PubMed: Gerber 2006 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Gerber 2006 Proband - - France - - - - - 1 Anne-Françoise Roux
+/+ 43 c.5886_5889del r.(?) p.(Phe1962Leufs*7) FERM 2 (1902-2205) Paternal (inferred) - pathogenic g.76919504_76919507del g.77208459_77208462del 5886_5889delCTTT - MYO7A_000089 Homozygous; UV4 PubMed: Aparisi 2014 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 43 c.5886_5889del r.(?) p.(Phe1962Leufs*7) FERM 2 (1902-2205) Maternal (inferred) - pathogenic g.76919504_76919507del g.77208459_77208462del 5886_5889delCTTT - MYO7A_000089 Homozygous; UV4 PubMed: Aparisi 2014 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/. 43 c.5886_5889del r.(?) p.(Phe1963Serfs*8) - Both (homozygous) - pathogenic g.76919504_76919507del - c.5886_5889del - MYO7A_000089 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. 43 c.5886_5889del r.(?) p.(Phe1963Serfs*8) - Parent #2 - pathogenic g.76919504_76919507del - c.5886_5889delCTTT - MYO7A_000089 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. - c.5886_5889delCTTT r.(?) p.(Phe1962LeufsTer7) - Paternal (confirmed) ACMG pathogenic g.76919504_76919507del - - - MYO7A_000089 - PubMed: Mansard et al, 2021 - rs1397834886 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.5886_5889delCTTT r.(?) p.(Phe1962LeufsTer7) - Maternal (confirmed) ACMG pathogenic g.76919504_76919507del - - - MYO7A_000089 - PubMed: Mansard et al, 2021 - rs1397834886 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - ? - - - - - - - 1 Anne-Françoise Roux
+/. - c.5886_5889delCTTT r.(?) p.(Phe1962LeufsTer7) - Maternal (confirmed) ACMG pathogenic g.76919504_76919507del - - - MYO7A_000089 - PubMed: Mansard et al, 2021 - rs1397834886 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
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