ClinVar Miner

List of variants in gene TGFB2 reported as uncertain significance by Ambry Genetics

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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_003238.6(TGFB2):c.823A>G (p.Ser275Gly) rs139825195 0.00062
NM_003238.6(TGFB2):c.588C>T (p.Gly196=) rs192335285 0.00038
NM_003238.6(TGFB2):c.199G>A (p.Val67Met) rs201761868 0.00015
NM_003238.6(TGFB2):c.556G>A (p.Asp186Asn) rs766536496 0.00008
NM_003238.6(TGFB2):c.194C>T (p.Pro65Leu) rs750324465 0.00006
NM_003238.6(TGFB2):c.518A>G (p.Lys173Arg) rs749692412 0.00004
NM_003238.6(TGFB2):c.1186A>C (p.Lys396Gln) rs751650226 0.00002
NM_003238.6(TGFB2):c.1052C>T (p.Pro351Leu) rs773943154 0.00001
NM_003238.6(TGFB2):c.1057T>G (p.Leu353Val) rs777045186 0.00001
NM_003238.6(TGFB2):c.1141G>A (p.Val381Met) rs376159002 0.00001
NM_003238.6(TGFB2):c.209T>C (p.Ile70Thr) rs1027195424 0.00001
NM_003238.6(TGFB2):c.236A>G (p.Gln79Arg) rs371241859 0.00001
NM_003238.6(TGFB2):c.362C>G (p.Thr121Ser) rs1300823855 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.526G>A (p.Asp176Asn) rs1571901046 0.00001
NM_003238.6(TGFB2):c.548G>A (p.Arg183His) rs773177511 0.00001
NM_003238.6(TGFB2):c.589G>A (p.Glu197Lys) rs764028978 0.00001
NM_003238.6(TGFB2):c.742G>A (p.Ala248Thr) rs778265133 0.00001
NM_003238.6(TGFB2):c.764G>A (p.Gly255Asp) rs781514831 0.00001
NM_003238.6(TGFB2):c.773C>T (p.Thr258Ile) rs373352179 0.00001
NM_003238.6(TGFB2):c.775T>G (p.Tyr259Asp) rs1212341043 0.00001
NM_003238.6(TGFB2):c.1009G>A (p.Glu337Lys) rs1476361240
NM_003238.6(TGFB2):c.1012C>T (p.Pro338Ser)
NM_003238.6(TGFB2):c.1033T>C (p.Phe345Leu) rs748732392
NM_003238.6(TGFB2):c.1045G>A (p.Ala349Thr)
NM_003238.6(TGFB2):c.1086G>A (p.Arg362=)
NM_003238.6(TGFB2):c.1126G>A (p.Ala376Thr)
NM_003238.6(TGFB2):c.112G>A (p.Glu38Lys)
NM_003238.6(TGFB2):c.1213A>C (p.Asn405His)
NM_003238.6(TGFB2):c.143T>G (p.Leu48Arg) rs1553292088
NM_003238.6(TGFB2):c.173C>T (p.Pro58Leu)
NM_003238.6(TGFB2):c.176A>G (p.Glu59Gly)
NM_003238.6(TGFB2):c.191C>T (p.Pro64Leu)
NM_003238.6(TGFB2):c.193C>T (p.Pro65Ser) rs747128130
NM_003238.6(TGFB2):c.262G>C (p.Ala88Pro)
NM_003238.6(TGFB2):c.285C>A (p.Asp95Glu) rs767393318
NM_003238.6(TGFB2):c.286G>C (p.Glu96Gln)
NM_003238.6(TGFB2):c.298G>C (p.Ala100Pro)
NM_003238.6(TGFB2):c.331T>G (p.Phe111Val)
NM_003238.6(TGFB2):c.336C>G (p.Phe112Leu)
NM_003238.6(TGFB2):c.346+5G>A rs886042712
NM_003238.6(TGFB2):c.392G>A (p.Arg131Gln) rs758366080
NM_003238.6(TGFB2):c.406G>A (p.Ala136Thr)
NM_003238.6(TGFB2):c.410T>C (p.Met137Thr) rs1264824521
NM_003238.6(TGFB2):c.440_442del (p.Ala147del)
NM_003238.6(TGFB2):c.472A>G (p.Lys158Glu)
NM_003238.6(TGFB2):c.475G>A (p.Ala159Thr)
NM_003238.6(TGFB2):c.494G>A (p.Arg165Gln)
NM_003238.6(TGFB2):c.514C>A (p.Leu172Ile)
NM_003238.6(TGFB2):c.53C>T (p.Ala18Val)
NM_003238.6(TGFB2):c.559A>G (p.Ser187Gly) rs759729701
NM_003238.6(TGFB2):c.595C>T (p.Leu199Phe)
NM_003238.6(TGFB2):c.611C>T (p.Thr204Ile) rs1659896577
NM_003238.6(TGFB2):c.625G>A (p.Glu209Lys)
NM_003238.6(TGFB2):c.668G>T (p.Ser223Ile) rs957164399
NM_003238.6(TGFB2):c.73A>C (p.Ser25Arg)
NM_003238.6(TGFB2):c.755G>A (p.Gly252Asp)
NM_003238.6(TGFB2):c.793A>G (p.Lys265Glu) rs886038965
NM_003238.6(TGFB2):c.812G>A (p.Arg271Lys)
NM_003238.6(TGFB2):c.818A>G (p.Lys273Arg)
NM_003238.6(TGFB2):c.829A>G (p.Lys277Glu)
NM_003238.6(TGFB2):c.877T>G (p.Ser293Ala)
NM_003238.6(TGFB2):c.892C>T (p.Arg298Trp)
NM_003238.6(TGFB2):c.917C>T (p.Ala306Val)
NM_003238.6(TGFB2):c.923A>C (p.Tyr308Ser)
NM_003238.6(TGFB2):c.937G>C (p.Val313Leu)
NM_003238.6(TGFB2):c.961C>A (p.Pro321Thr)
NM_003238.6(TGFB2):c.983G>C (p.Arg328Thr)

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