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.

5 entries on 1 page. Showing entries 1 - 5.
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     
+?/. 27 c.3476G>T r.(?) p.(Gly1159Val) - Parent #1 - likely pathogenic g.76895733G>T g.77184688G>T - - MYO7A_000263 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - Germline - - - - - DNA SEQ-NG - - deafness - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - 1 Mieke Wesdorp
+/. - c.3476G>T r.(?) p.(Gly1159Val) - Unknown - pathogenic g.76895733G>T g.77184688G>T MYO7A(NM_000260.3):c.3476G>T (p.G1159V) - MYO7A_000263 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/? 27 c.3476G>T r.(?) p.(Gly1159Val) MyTH4 1 (1017-1253) Parent #1 ACMG VUS g.76895733G>T g.77184688G>T - - MYO7A_000263 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/180 controls -BsrDI - - DNA SEQ - - DFNB ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/. - c.3476G>T r.(?) p.(Gly1159Val) - Unknown - likely pathogenic g.76895733G>T g.77184688G>T MYO7A(NM_000260.3):c.3476G>T (p.G1159V) - MYO7A_000263 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.3476G>T r.(?) p.(Gly1159Val) - Unknown - likely pathogenic g.76895733G>T g.77184688G>T MYO7A c.3476G>T, p.Gly1159Val - MYO7A_000263 - PubMed: Georgiou 2021 - - Unknown ? - - - - DNA SEQ-NG blood retrospective study retinal disease P7 PubMed: Georgiou 2021 pedigree ID: 20699, genetic ID: 31899 F - (United Kingdom (Great Britain)) - - - - - 1 LOVD
Legend   How to query  


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