ClinVar Miner

List of variants in gene PDYN reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_024411.5(PDYN):c.271C>T (p.Pro91Ser) rs147355936 0.00028
NM_024411.5(PDYN):c.268G>A (p.Gly90Arg) rs201585283 0.00015
NM_024411.5(PDYN):c.59C>T (p.Ala20Val) rs146598522 0.00013
NM_024411.5(PDYN):c.490G>A (p.Ala164Thr) rs376124198 0.00004
NM_024411.5(PDYN):c.724G>A (p.Glu242Lys) rs1181111571 0.00002
NM_024411.5(PDYN):c.571G>T (p.Gly191Trp) rs767807436 0.00001
NM_024411.5(PDYN):c.73C>T (p.Arg25Trp) rs1028619685 0.00001
NM_024411.5(PDYN):c.250A>G (p.Ser84Gly)
NM_024411.5(PDYN):c.293T>C (p.Leu98Pro) rs2514337892
NM_024411.5(PDYN):c.352A>C (p.Lys118Gln)
NM_024411.5(PDYN):c.503C>A (p.Pro168His) rs1242938963
NM_024411.5(PDYN):c.509A>T (p.Glu170Val) rs2514335903
NM_024411.5(PDYN):c.529G>A (p.Gly177Ser)
NM_024411.5(PDYN):c.53C>T (p.Thr18Ile) rs1555778420
NM_024411.5(PDYN):c.557G>C (p.Ser186Thr)
NM_024411.5(PDYN):c.566T>C (p.Val189Ala)
NM_024411.5(PDYN):c.568G>T (p.Ala190Ser) rs2122307518
NM_024411.5(PDYN):c.578G>C (p.Gly193Ala)
NM_024411.5(PDYN):c.580G>T (p.Asp194Tyr)
NM_024411.5(PDYN):c.596G>C (p.Gly199Ala) rs949868832
NM_024411.5(PDYN):c.67C>G (p.Leu23Val)
NM_024411.5(PDYN):c.691C>T (p.Arg231Trp) rs201204862
NM_024411.5(PDYN):c.692G>A (p.Arg231Gln)
NM_024411.5(PDYN):c.723G>C (p.Gln241His) rs2514333411
NM_024411.5(PDYN):c.728A>T (p.Asp243Val)
NM_024411.5(PDYN):c.98C>T (p.Thr33Ile)

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.