ClinVar Miner

List of variants in gene DMXL2 reported as uncertain significance by GeneDx

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_001378457.1(DMXL2):c.7543A>G (p.Met2515Val) rs72729259 0.00054
NM_001378457.1(DMXL2):c.1108A>G (p.Ile370Val) rs185394436 0.00019
NM_001378457.1(DMXL2):c.5974G>A (p.Asp1992Asn) rs144241909 0.00014
NM_001378457.1(DMXL2):c.7214-10C>A rs758539671 0.00014
NM_001378457.1(DMXL2):c.7313C>T (p.Pro2438Leu) rs372032462 0.00011
NM_001378457.1(DMXL2):c.2576T>C (p.Ile859Thr) rs201956343 0.00010
NM_001378457.1(DMXL2):c.1922C>G (p.Ser641Cys) rs113890461 0.00004
NM_001378457.1(DMXL2):c.3421G>A (p.Val1141Ile) rs74839639 0.00004
NM_001378457.1(DMXL2):c.6377G>A (p.Arg2126His) rs781633691 0.00003
NM_001378457.1(DMXL2):c.7709C>G (p.Pro2570Arg) rs200591092 0.00003
NM_001378457.1(DMXL2):c.4244A>G (p.Asp1415Gly) rs770608099 0.00002
NM_001378457.1(DMXL2):c.2161A>G (p.Ile721Val) rs1362531644 0.00001
NM_001378457.1(DMXL2):c.5674C>T (p.His1892Tyr) rs371723512 0.00001
NM_001378457.1(DMXL2):c.7789C>A (p.Pro2597Thr) rs1197826935 0.00001
NM_001378457.1(DMXL2):c.1057A>G (p.Asn353Asp)
NM_001378457.1(DMXL2):c.1061C>G (p.Ala354Gly) rs901349844
NM_001378457.1(DMXL2):c.1631C>T (p.Ser544Phe)
NM_001378457.1(DMXL2):c.1721C>T (p.Ser574Phe) rs536579523
NM_001378457.1(DMXL2):c.1845_1853dup (p.Ile617_Asp618insGluHisIle) rs1469022960
NM_001378457.1(DMXL2):c.1993T>G (p.Leu665Val) rs200046847
NM_001378457.1(DMXL2):c.2881A>G (p.Ile961Val) rs750559484
NM_001378457.1(DMXL2):c.2940A>T (p.Gln980His)
NM_001378457.1(DMXL2):c.299A>T (p.Gln100Leu) rs2141049474
NM_001378457.1(DMXL2):c.3184A>G (p.Ser1062Gly)
NM_001378457.1(DMXL2):c.3694C>T (p.Leu1232Phe) rs2548507896
NM_001378457.1(DMXL2):c.389A>T (p.Asp130Val)
NM_001378457.1(DMXL2):c.4419A>C (p.Gln1473His)
NM_001378457.1(DMXL2):c.5333G>A (p.Gly1778Asp) rs186940430
NM_001378457.1(DMXL2):c.589T>C (p.Trp197Arg) rs2548643163
NM_001378457.1(DMXL2):c.7130T>G (p.Leu2377Ter) rs2140326306
NM_001378457.1(DMXL2):c.7319C>T (p.Pro2440Leu) rs2548416541
NM_001378457.1(DMXL2):c.7708C>A (p.Pro2570Thr)
NM_001378457.1(DMXL2):c.890A>T (p.His297Leu)
NM_001378457.1(DMXL2):c.937C>T (p.His313Tyr) rs2548627837

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