ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=) rs45560242
NM_000257.4(MYH7):c.4332G>A (p.Lys1444=) rs1064797183
NM_000257.4(MYH7):c.4343A>T (p.Asn1448Ile) rs753484341
NM_000257.4(MYH7):c.4348G>A (p.Asp1450Asn) rs397516211
NM_000257.4(MYH7):c.4353+6C>T rs765398896
NM_000257.4(MYH7):c.4577T>C (p.Leu1526Pro)
NM_000257.4(MYH7):c.4717G>A (p.Glu1573Lys) rs750987717
NM_000257.4(MYH7):c.5191G>A (p.Asp1731Asn) rs876657885
NM_000257.4(MYH7):c.5203T>A (p.Ser1735Thr) rs144066768

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.