ClinVar Miner

List of variants in gene CALM1 reported as uncertain significance for catecholaminergic polymorphic ventricular tachycardia 4

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006888.6(CALM1):c.4-3T>C rs754359981 0.00001
NC_000014.8:g.(?_90863575)_(90871061_?)del
NC_000014.8:g.(?_90863575)_(90871061_?)dup
NC_000014.8:g.(?_90870713)_(90871071_?)dup
NM_006888.6(CALM1):c.106G>C (p.Val36Leu) rs1887015236
NM_006888.6(CALM1):c.133A>G (p.Thr45Ala)
NM_006888.6(CALM1):c.154A>G (p.Met52Val)
NM_006888.6(CALM1):c.157A>G (p.Ile53Val) rs1555365887
NM_006888.6(CALM1):c.199C>T (p.Pro67Ser)
NM_006888.6(CALM1):c.280G>C (p.Asp94His) rs1887099943
NM_006888.6(CALM1):c.293A>T (p.Asn98Ile)
NM_006888.6(CALM1):c.301A>G (p.Ile101Val) rs1595102592
NM_006888.6(CALM1):c.328A>C (p.Met110Leu) rs2139771638
NM_006888.6(CALM1):c.35-12_35-11delinsCC
NM_006888.6(CALM1):c.35-44_77dup
NM_006888.6(CALM1):c.70G>A (p.Gly24Ser) rs2503454539

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.