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.

18 entries on 1 page. Showing entries 1 - 18.
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     
+/+ 5 c.397dup r.(?) p.(His133Profs*7) Motor domain (1-729) Paternal (inferred) - pathogenic g.76867064dup g.77156018dup 397dupC - MYO7A_000364 Homozygous PubMed: Bonnet 2011 - rs111033187 Germline - - none - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 5 c.397dup r.(?) p.(His133Profs*7) Motor domain (1-729) Maternal (inferred) - pathogenic g.76867064dup g.77156018dup 397dupC - MYO7A_000364 Homozygous PubMed: Bonnet 2011 - rs111033187 Germline - - none - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 5 c.397dup r.(?) p.(His133Profs*7) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76867064dup g.77156018dup 390_391insC - MYO7A_000364 Heterozygous PubMed: Wei 2012 - - Germline - 0/200 controls none - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Wei 2012 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 5 c.397dup r.(?) p.(His133Profs*7) Motor domain (1-729) Parent #2 - pathogenic g.76867064dup g.77156018dup 390_391insC - p.M130fs - MYO7A_000364 Heterozygous; mutation PubMed: Jiang 2015 - rs111033187 Germline - - none - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 5 c.397dup r.(?) p.(His133Profs*7) Motor domain (1-729) Parent #2 - pathogenic g.76867064dup g.77156018dup 397dupC - MYO7A_000364 Heterozygous; mutation PubMed: Bonnet 2016 - rs111033187 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+?/. - c.397dup r.(?) p.(His133ProfsTer7) - Unknown - likely pathogenic g.76867064dup g.77156018dup MYO7A(NM_000260.4):c.397dupC (p.H133Pfs*7) - MYO7A_000364 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.397dup r.(?) p.(His133Profs*7) - Parent #1 ACMG pathogenic g.76867064dup g.77156018dup c.390_391insC - MYO7A_000364 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19942 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. - c.397dup r.(?) p.(His133Profs*7) - Parent #1 ACMG pathogenic g.76867064dup g.77156018dup c.390_391insC - MYO7A_000364 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 19050 PubMed: Sun 2018 sporadic case - no China - - - - - 1 LOVD
+/. 5 c.397dup r.(?) p.(His133Profs*7) - Both (homozygous) ACMG pathogenic (recessive) g.76867064dup - - - MYO7A_000364 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH1B Pat5 PubMed: Bahena 2021 - M - Iran - - - - - 1 Barbara Vona
+/+ 5 c.397dup r.(?) p.(His133Profs*7) - Parent #1 ACMG pathogenic (recessive) g.76867064dup - - - MYO7A_000364 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH1 Pat7 PubMed: Bahena 2021 - F no Iran - - - - - 1 Barbara Vona
+?/. - c.397dup r.(?) p.(His133Profs*7) - Both (homozygous) - likely pathogenic g.76867064dup g.77156018dup 397dupC - MYO7A_000364 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH PatDEM289 PubMed: Neuhaus 2017 - - yes Pakistan - - - - - 1 LOVD
+?/. - c.397dup r.(?) p.(His133Profs*7) - Both (homozygous) - likely pathogenic g.76867064dup g.77156018dup 397dupC - MYO7A_000364 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH PatDEM318 PubMed: Neuhaus 2017 - - yes Pakistan - - - - - 1 LOVD
+/. 5 c.397dup r.(?) p.(His133Profs*7) - Maternal (confirmed) - pathogenic (recessive) g.76867064dup - c.390-391insC - MYO7A_000364 - PubMed: Ma 2016 - - Germline yes 0/120 healthy controls - - - DNA SEQ-NG, SEQ blood - retinal disease II:1 PubMed: Ma 2016 sister of II:2 F - China chinese - - - - 1 LOVD
+/. 5 c.397dup r.(?) p.(His133Profs*7) - Maternal (confirmed) - pathogenic (recessive) g.76867064dup - c.390-391insC - MYO7A_000364 - PubMed: Ma 2016 - - Germline yes 0/120 healthy controls - - - DNA SEQ-NG, SEQ blood - retinal disease II:2 PubMed: Ma 2016 brother of II:1 M - China chinese - - - - 1 LOVD
+/. - c.397dup r.(?) p.(His133ProfsTer7) - Parent #1 - pathogenic (recessive) g.76867064dup g.77156018dup 397dupC - MYO7A_000364 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL PKDF312 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.397dupC r.(?) p.(His133ProfsTer7) - Both (homozygous) ACMG pathogenic g.76867064dup - - - MYO7A_000364 - PubMed: Mansard et al, 2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. - c.397dupC r.(?) p.(His133ProfsTer7) - Unknown ACMG pathogenic g.76867064dup - - - MYO7A_000364 - PubMed: Mansard et al, 2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. - c.397dupC r.(?) p.(His133ProfsTer7) - Maternal (confirmed) ACMG pathogenic g.76867064dup - - - MYO7A_000364 - PubMed: Mansard et al, 2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 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.