ClinVar Miner

List of variants in gene MAGT1 reported as likely benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_001367916.1(MAGT1):c.932T>G (p.Val311Gly) rs145245774 0.00119
NM_032121.5(MAGT1):c.58C>T (p.Arg20Trp) rs370329684 0.00012
NM_001367916.1(MAGT1):c.391-12G>A rs782752973 0.00010
NM_001367916.1(MAGT1):c.880A>G (p.Met294Val) rs374143885 0.00008
NM_001367916.1(MAGT1):c.273-5T>C rs371338746 0.00007
NM_001367916.1(MAGT1):c.449G>A (p.Arg150Gln) rs1032635187 0.00007
NM_001367916.1(MAGT1):c.219C>T (p.Ser73=) rs183592456 0.00002
NM_001367916.1(MAGT1):c.272+18G>A rs782342148 0.00002
NM_001367916.1(MAGT1):c.672+19A>G rs549144446 0.00002
NM_001367916.1(MAGT1):c.753G>A (p.Thr251=) rs374493047 0.00002
NM_032121.5(MAGT1):c.27C>T (p.Cys9=) rs782341239 0.00002
NM_001367916.1(MAGT1):c.510C>T (p.Ile170=) rs1387470785 0.00001
NM_001367916.1(MAGT1):c.870T>C (p.Ala290=) rs1557214380 0.00001
NM_001367916.1(MAGT1):c.103-16A>G
NM_001367916.1(MAGT1):c.103-19C>G
NM_001367916.1(MAGT1):c.216C>T (p.Tyr72=)
NM_001367916.1(MAGT1):c.220G>A (p.Val74Ile)
NM_001367916.1(MAGT1):c.272+17C>T
NM_001367916.1(MAGT1):c.273-18G>T
NM_001367916.1(MAGT1):c.279T>C (p.Ala93=)
NM_001367916.1(MAGT1):c.387G>A (p.Gln129=)
NM_001367916.1(MAGT1):c.391-12G>C rs782752973
NM_001367916.1(MAGT1):c.405A>G (p.Ser135=)
NM_001367916.1(MAGT1):c.411A>G (p.Pro137=)
NM_001367916.1(MAGT1):c.426T>C (p.Phe142=)
NM_001367916.1(MAGT1):c.476G>A (p.Arg159Gln)
NM_001367916.1(MAGT1):c.480T>C (p.Gly160=) rs1603361797
NM_001367916.1(MAGT1):c.513C>T (p.Ala171=)
NM_001367916.1(MAGT1):c.530A>G (p.Asn177Ser)
NM_001367916.1(MAGT1):c.531+16A>T rs2149018390
NM_001367916.1(MAGT1):c.531+20A>C rs2149018388
NM_001367916.1(MAGT1):c.532-20T>G
NM_001367916.1(MAGT1):c.628A>G (p.Met210Val)
NM_001367916.1(MAGT1):c.633A>G (p.Glu211=)
NM_001367916.1(MAGT1):c.673-10T>C rs2076979441
NM_001367916.1(MAGT1):c.756A>G (p.Gly252=)
NM_001367916.1(MAGT1):c.762+16G>A
NM_001367916.1(MAGT1):c.763-18_763-17del
NM_001367916.1(MAGT1):c.771C>A (p.Ile257=) rs782533209
NM_001367916.1(MAGT1):c.816T>C (p.Val272=)
NM_001367916.1(MAGT1):c.826+18G>A
NM_001367916.1(MAGT1):c.827-7T>G rs782176437
NM_001367916.1(MAGT1):c.888T>C (p.Ile296=)
NM_001367916.1(MAGT1):c.901+11T>G
NM_001367916.1(MAGT1):c.901+8A>G
NM_001367916.1(MAGT1):c.945T>C (p.Ser315=)
NM_032121.5(MAGT1):c.58C>A (p.Arg20=) rs370329684
NM_032121.5(MAGT1):c.65_66del (p.Lys22fs) rs782474570

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