Full data view for gene MYO15A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_016239.3 transcript reference sequence.

6 entries on 1 page. Showing entries 1 - 6.
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     
?/-? 57 c.9478C>T r.(?) p.(Leu3160Phe) MyTH4 2 (3050-3204) Both (homozygous) ACMG likely benign g.18064722C>T g.18161408C>T - - MYO15A_000018 homozygous, {MSV3dQ9UKN7:p.Leu3160Phe} PubMed: Nal et al., 2007 - rs140029076 Germline - 1/266 controls +MboII;-MnlI - - DNA SEQ - - DFNB - PubMed: Nal et al., 2007 proband - - Pakistan - - - - - 1 Anne-Françoise Roux
?/-? 57 c.9478C>T r.(?) p.(Leu3160Phe) MyTH4 2 (3050-3204) Unknown ACMG likely benign g.18064722C>T g.18161408C>T - - MYO15A_000018 heterozygous, {MSV3dQ9UKN7:p.Leu3160Phe} PubMed: Besnard, Garcia-Garcia et al., 2014 - rs140029076 Germline - - +MboII;-MnlI - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Besnard, Garcia-Garcia et al., 2014 proband M - France - - - - - 1 Anne-Françoise Roux
-?/-? 57 c.9478C>T r.(?) p.(Leu3160Phe) MyTH4 2 (3050-3204) Unknown ACMG likely benign g.18064722C>T g.18161408C>T - - MYO15A_000018 heterozygous, {MSV3dQ9UKN7:p.Leu3160Phe} PubMed: Ebermann et al., 2010 - rs140029076 Germline - - +MboII;-MnlI - - DNA SEQ - - USH2 - PubMed: Ebermann et al., 2010 proband M - France - - - - - 1 Anne-Françoise Roux
?/-? 57 c.9478C>T r.(?) p.(Leu3160Phe) MyTH4 2 (3050-3204) Maternal (confirmed) ACMG likely benign g.18064722C>T g.18161408C>T - - MYO15A_000018 heterozygous, {MSV3dQ9UKN7:p.Leu3160Phe} PubMed: Miyagawa et al., 2013 - rs140029076 Germline - - - - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Miyagawa et al., 2013 proband M - Japan - - - - - 1 Anne-Françoise Roux
?/-? 57 c.9478C>T r.(?) p.(Leu3160Phe) MyTH4 2 (3050-3204) Maternal (confirmed) ACMG likely benign g.18064722C>T g.18161408C>T - - MYO15A_000018 heterozygous, {MSV3dQ9UKN7:p.Leu3160Phe} PubMed: Miyagawa et al., 2013 - rs140029076 Germline - - - - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Miyagawa et al., 2013 relative M - Japan - - - - - 1 Anne-Françoise Roux
?/-? 57 c.9478C>T r.(?) p.(Leu3160Phe) MyTH4 2 (3050-3204) Maternal (confirmed) ACMG likely benign g.18064722C>T g.18161408C>T - - MYO15A_000018 heterozygous, {MSV3dQ9UKN7:p.Leu3160Phe} PubMed: Miyagawa et al., 2013 - rs140029076 Germline - 0/144 controls +MboII;-MnlI - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Miyagawa et al., 2013 proband M - Japan - - - - - 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.