ClinVar Miner

List of variants reported as uncertain significance for cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

Included ClinVar conditions (1):
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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_001042545.2(LTBP4):c.2909C>G (p.Pro970Arg) rs200667255 0.00135
NM_001042545.2(LTBP4):c.2436G>A (p.Val812=) rs371083223 0.00090
NM_001042545.2(LTBP4):c.2681-10C>G rs200914063 0.00084
NM_001042545.2(LTBP4):c.1324C>T (p.Arg442Cys) rs199875504 0.00071
NM_001042545.2(LTBP4):c.1825A>G (p.Thr609Ala) rs201279198 0.00069
NM_001042545.2(LTBP4):c.2235G>A (p.Ser745=) rs374862225 0.00057
NM_001042545.2(LTBP4):c.284T>C (p.Val95Ala) rs200888669 0.00038
NM_001042545.2(LTBP4):c.4604G>A (p.Cys1535Tyr) rs200665923 0.00034
NM_001042545.2(LTBP4):c.*121C>G rs551134075 0.00031
NM_001042545.2(LTBP4):c.2431+11T>C rs370485510 0.00014
NM_001042545.2(LTBP4):c.3478G>A (p.Glu1160Lys) rs778595954 0.00014
NM_001042545.2(LTBP4):c.2176G>C (p.Glu726Gln) rs199691160 0.00013
NM_001042545.2(LTBP4):c.443-14C>T rs375934176 0.00009
NM_001042545.2(LTBP4):c.1217G>A (p.Arg406His) rs574587568 0.00008
NM_001042545.2(LTBP4):c.698C>T (p.Ser233Phe) rs886054445 0.00008
NM_001042545.2(LTBP4):c.2157C>G (p.Asn719Lys) rs770079010 0.00006
NM_001042545.2(LTBP4):c.3446G>C (p.Ser1149Thr) rs375879929 0.00006
NM_001042545.2(LTBP4):c.1041C>G (p.Arg347=) rs1213927843 0.00004
NM_001042545.2(LTBP4):c.1161T>C (p.Gly387=) rs554968375 0.00004
NM_001042545.2(LTBP4):c.2934C>T (p.Gly978=) rs768587659 0.00004
NM_001042545.2(LTBP4):c.3368C>T (p.Pro1123Leu) rs369221693 0.00004
NM_003573.2(LTBP4):c.194G>A (p.Arg65Lys) rs200951126 0.00004
NM_001042545.2(LTBP4):c.2098C>T (p.Arg700Trp) rs758290097 0.00003
NM_001042545.2(LTBP4):c.639C>T (p.Tyr213=) rs746458434 0.00003
NM_001042545.2(LTBP4):c.1020G>A (p.Gly340=) rs543717406 0.00002
NM_003573.2(LTBP4):c.310C>G (p.Pro104Ala) rs886054444 0.00002
NM_001042545.2(LTBP4):c.*25C>T rs1284761820 0.00001
NM_001042545.2(LTBP4):c.1452C>G (p.Arg484=) rs745624027 0.00001
NM_001042545.2(LTBP4):c.1835C>T (p.Pro612Leu) rs886054447 0.00001
NM_001042545.2(LTBP4):c.2739C>T (p.Asn913=) rs2303726 0.00001
NM_001042545.2(LTBP4):c.302G>A (p.Arg101His) rs762286016 0.00001
NM_001042545.2(LTBP4):c.371C>G (p.Ala124Gly) rs562892147 0.00001
NM_001042545.2(LTBP4):c.4019C>T (p.Pro1340Leu) rs531174154 0.00001
NM_001042545.2(LTBP4):c.634G>A (p.Gly212Ser) rs771378692 0.00001
NM_001042545.2(LTBP4):c.864C>T (p.Cys288=) rs758784148 0.00001
NM_001042545.2(LTBP4):c.*125C>T rs569370832
NM_001042545.2(LTBP4):c.*126G>T rs567854760
NM_001042545.2(LTBP4):c.*185_*187del rs558641472
NM_001042545.2(LTBP4):c.*259C>G rs868829972
NM_001042545.2(LTBP4):c.*42G>A rs2081663869
NM_001042545.2(LTBP4):c.*59C>T rs1362204630
NM_001042545.2(LTBP4):c.*97G>T rs1242020458
NM_001042545.2(LTBP4):c.1183G>T (p.Gly395Cys)
NM_001042545.2(LTBP4):c.1549C>A (p.Arg517=) rs770158909
NM_001042545.2(LTBP4):c.1611G>C (p.Glu537Asp)
NM_001042545.2(LTBP4):c.1636G>A (p.Val546Met) rs886054446
NM_001042545.2(LTBP4):c.2029C>T (p.Arg677Ter) rs2146029786
NM_001042545.2(LTBP4):c.2160T>C (p.Thr720=) rs578204135
NM_001042545.2(LTBP4):c.2180-3C>A rs560687578
NM_001042545.2(LTBP4):c.2399G>A (p.Arg800Gln)
NM_001042545.2(LTBP4):c.2419G>C (p.Gly807Arg) rs559350666
NM_001042545.2(LTBP4):c.2835T>C (p.Tyr945=) rs762043638
NM_001042545.2(LTBP4):c.289G>C (p.Val97Leu) rs544671195
NM_001042545.2(LTBP4):c.3329G>A (p.Gly1110Glu) rs886054448
NM_001042545.2(LTBP4):c.4022C>G (p.Pro1341Arg) rs886054449
NM_001042545.2(LTBP4):c.4033C>G (p.Pro1345Ala) rs886054450
NM_001042545.2(LTBP4):c.4169G>A (p.Gly1390Glu) rs886054451
NM_001042545.2(LTBP4):c.534G>A (p.Glu178=) rs2081452931
NM_001042545.2(LTBP4):c.564G>A (p.Ala188=) rs759941927
NM_001042545.2(LTBP4):c.5C>T (p.Ala2Val)
NM_001042545.2(LTBP4):c.637T>C (p.Tyr213His)
NM_001042545.2(LTBP4):c.770G>A (p.Cys257Tyr) rs2146021507
NM_001042545.2(LTBP4):c.832C>G (p.Pro278Ala) rs2081460773
NM_001042545.2(LTBP4):c.999dup (p.Val334fs)
NM_003573.2(LTBP4):c.213C>A (p.Leu71=) rs886054443
NM_003573.2(LTBP4):c.231-14C>G rs2081412659
NM_003573.2(LTBP4):c.239A>G (p.Glu80Gly)
NM_003573.2(LTBP4):c.273G>C (p.Arg91=) rs2081413206
NM_003573.2(LTBP4):c.334G>T (p.Ala112Ser) rs2081414000
NM_003573.2(LTBP4):c.76-2A>G

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