ClinVar Miner

List of variants in gene TGFB2 reported as uncertain significance by GeneDx

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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_003238.6(TGFB2):c.199G>A (p.Val67Met) rs201761868 0.00015
NM_003238.6(TGFB2):c.194C>T (p.Pro65Leu) rs750324465 0.00006
NM_003238.6(TGFB2):c.386T>C (p.Ile129Thr) rs752823052 0.00005
NM_003238.6(TGFB2):c.518A>G (p.Lys173Arg) rs749692412 0.00004
NM_003238.6(TGFB2):c.400G>A (p.Val134Ile) rs757551766 0.00003
NM_003238.6(TGFB2):c.251G>A (p.Arg84Gln) rs781392453 0.00002
NM_003238.6(TGFB2):c.1102A>G (p.Asn368Asp) rs1417916795 0.00001
NM_003238.6(TGFB2):c.1141G>A (p.Val381Met) rs376159002 0.00001
NM_003238.6(TGFB2):c.1181T>C (p.Ile394Thr) rs886045980 0.00001
NM_003238.6(TGFB2):c.181G>A (p.Glu61Lys) rs763228811 0.00001
NM_003238.6(TGFB2):c.236A>G (p.Gln79Arg) rs371241859 0.00001
NM_003238.6(TGFB2):c.338C>T (p.Pro113Leu) rs1057524627 0.00001
NM_003238.6(TGFB2):c.362C>G (p.Thr121Ser) rs1300823855 0.00001
NM_003238.6(TGFB2):c.371G>A (p.Arg124Lys) rs863223789 0.00001
NM_003238.6(TGFB2):c.474A>T (p.Lys158Asn) rs775251473 0.00001
NM_003238.6(TGFB2):c.493C>T (p.Arg165Trp) rs773820426 0.00001
NM_003238.6(TGFB2):c.548G>A (p.Arg183His) rs773177511 0.00001
NM_003238.6(TGFB2):c.645C>G (p.Asp215Glu) rs1342706944 0.00001
NM_003238.6(TGFB2):c.686G>T (p.Cys229Phe) rs1185241582 0.00001
NM_003238.6(TGFB2):c.742G>A (p.Ala248Thr) rs778265133 0.00001
NM_003238.6(TGFB2):c.773C>T (p.Thr258Ile) rs373352179 0.00001
NM_003238.6(TGFB2):c.826G>A (p.Gly276Arg) rs1169804851 0.00001
NM_003238.6(TGFB2):c.893G>A (p.Arg298Gln) rs762561484 0.00001
NM_003238.6(TGFB2):c.910T>G (p.Leu304Val) rs1478901182 0.00001
NM_003238.6(TGFB2):c.101G>A (p.Arg34His) rs1064796462
NM_003238.6(TGFB2):c.1033T>C (p.Phe345Leu) rs748732392
NM_003238.6(TGFB2):c.1037G>T (p.Cys346Phe) rs2102630125
NM_003238.6(TGFB2):c.1049G>A (p.Cys350Tyr) rs1558264109
NM_003238.6(TGFB2):c.1078C>T (p.His360Tyr) rs2102630186
NM_003238.6(TGFB2):c.1134_1135insA (p.Cys379fs) rs2102634374
NM_003238.6(TGFB2):c.1136G>T (p.Cys379Phe) rs1660141597
NM_003238.6(TGFB2):c.119T>A (p.Ile40Asn) rs2102527486
NM_003238.6(TGFB2):c.1229C>G (p.Ser410Cys)
NM_003238.6(TGFB2):c.1233C>G (p.Cys411Trp) rs2102634511
NM_003238.6(TGFB2):c.1236dup (p.Cys413fs)
NM_003238.6(TGFB2):c.154A>G (p.Ser52Gly) rs771351240
NM_003238.6(TGFB2):c.286G>A (p.Glu96Lys)
NM_003238.6(TGFB2):c.302AGG[1] (p.Glu102del) rs1656708526
NM_003238.6(TGFB2):c.482T>G (p.Val161Gly)
NM_003238.6(TGFB2):c.519G>T (p.Lys173Asn) rs769193722
NM_003238.6(TGFB2):c.611C>G (p.Thr204Ser) rs1659896577
NM_003238.6(TGFB2):c.637C>T (p.His213Tyr)
NM_003238.6(TGFB2):c.663A>T (p.Lys221Asn) rs863223791
NM_003238.6(TGFB2):c.666A>G (p.Ile222Met) rs1659904233
NM_003238.6(TGFB2):c.688A>G (p.Thr230Ala)
NM_003238.6(TGFB2):c.715A>T (p.Ile239Phe) rs1131691445
NM_003238.6(TGFB2):c.716T>G (p.Ile239Ser) rs2102626827
NM_003238.6(TGFB2):c.839_841del (p.His280del) rs2102628559
NM_003238.6(TGFB2):c.863C>G (p.Ser288Cys) rs2102628591
NM_003238.6(TGFB2):c.964C>T (p.Leu322Phe) rs2102630024
NM_003238.6(TGFB2):c.967T>C (p.Tyr323His) rs752807885
NM_003238.6(TGFB2):c.981G>T (p.Lys327Asn) rs1085307561

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