ClinVar Miner

List of variants in gene LTBP4 reported as likely benign for not specified

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_001042545.2(LTBP4):c.3221C>T (p.Thr1074Met) rs10880 0.39072
NM_001042545.2(LTBP4):c.2053G>A (p.Asp685Asn) rs34093919 0.00763
NM_001042545.2(LTBP4):c.1157-17C>G rs181126225 0.00263
NM_001042545.2(LTBP4):c.2681-10C>G rs200914063 0.00084
NM_003573.2(LTBP4):c.16+18C>T rs374791501 0.00016
NM_001042545.2(LTBP4):c.2944+15G>A rs368146894 0.00011
NM_001042545.2(LTBP4):c.1917G>A (p.Ala639=) rs368513626 0.00006
NM_001042545.2(LTBP4):c.3975G>A (p.Ala1325=) rs375560922 0.00006
NM_001042545.2(LTBP4):c.3832+8C>T rs556476928 0.00005
NM_001042545.2(LTBP4):c.2184G>A (p.Val728=) rs540264614 0.00004
NM_001042545.2(LTBP4):c.3066C>T (p.Cys1022=) rs727503154 0.00004
NM_001042545.2(LTBP4):c.4176C>T (p.Phe1392=) rs376464510 0.00004
NM_001042545.2(LTBP4):c.992-11G>C rs367929270 0.00004
NM_001042545.2(LTBP4):c.2179+9G>A rs375581403 0.00003
NM_001042545.2(LTBP4):c.3363G>A (p.Ala1121=) rs750895520 0.00003
NM_001042545.2(LTBP4):c.3699C>T (p.Cys1233=) rs778594212 0.00003
NM_003573.2(LTBP4):c.230+13T>A rs369658361 0.00003
NM_001042545.2(LTBP4):c.1158G>A (p.Glu386=) rs1015435132 0.00002
NM_001042545.2(LTBP4):c.1578C>T (p.Arg526=) rs368999152 0.00001
NM_001042545.2(LTBP4):c.1599C>T (p.Pro533=) rs767751664 0.00001
NM_001042545.2(LTBP4):c.2535A>G (p.Gly845=) rs775848118 0.00001
NM_001042545.2(LTBP4):c.2945-16T>C rs1440291779 0.00001
NM_001042545.2(LTBP4):c.2989G>A (p.Val997Met) rs748078658 0.00001
NM_001042545.2(LTBP4):c.3071-20_3071-19del rs1391593992 0.00001
NM_001042545.2(LTBP4):c.3218-8C>T rs1255065335 0.00001
NM_001042545.2(LTBP4):c.3258C>T (p.Pro1086=) rs727503155 0.00001
NM_001042545.2(LTBP4):c.3832+10C>T rs1440756922 0.00001
NM_001042545.2(LTBP4):c.4425C>T (p.Gly1475=) rs774981506 0.00001
NM_001042545.2(LTBP4):c.607T>C (p.Leu203=) rs754839219 0.00001
NM_003573.2(LTBP4):c.9C>T (p.Asp3=) rs1197222123 0.00001
NM_001042545.2(LTBP4):c.2985C>T (p.His995=) rs566212619
NM_001042545.2(LTBP4):c.3484+7_3484+20delinsTGTCCCC rs1555741788
NM_001042545.2(LTBP4):c.3832+11C>G rs1555742755
NM_001042545.2(LTBP4):c.555G>T (p.Val185=) rs1555730677
NM_001042545.2(LTBP4):c.794-18C>A rs1057524344

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