ClinVar Miner

List of variants in gene TGFB2 reported as likely benign for not provided

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_003238.6(TGFB2):c.-1302A>G rs10482718 0.03064
NM_003238.6(TGFB2):c.346+198T>G rs1106569 0.03058
NM_003238.6(TGFB2):c.*39G>A rs11466412 0.02204
NM_003238.6(TGFB2):c.511-127C>A rs10482808 0.01735
NM_003238.6(TGFB2):c.643+7A>C rs7531245 0.01418
NM_003238.6(TGFB2):c.*1128G>A rs56271792 0.01172
NM_003238.6(TGFB2):c.754+58A>G rs10482811 0.01102
NM_003238.6(TGFB2):c.511-73G>C rs10482809 0.01100
NM_003238.6(TGFB2):c.-620G>A rs886045971 0.01029
NM_003238.6(TGFB2):c.-1230G>A rs11466363 0.00928
NM_003238.6(TGFB2):c.755-206C>A rs10482816 0.00919
NM_003238.6(TGFB2):c.-288A>T rs116531760 0.00572
NM_003238.6(TGFB2):c.346+16454G>A rs11466375 0.00455
NM_003238.6(TGFB2):c.1239C>T (p.Cys413=) rs141225367 0.00359
NM_003238.6(TGFB2):c.619G>C (p.Val207Leu) rs10482810 0.00359
NM_003238.6(TGFB2):c.272G>A (p.Arg91His) rs10482721 0.00297
NM_003238.6(TGFB2):c.114G>A (p.Glu38=) rs149215818 0.00087
NM_003238.6(TGFB2):c.303G>A (p.Lys101=) rs147052890 0.00072
NM_003238.6(TGFB2):c.823A>G (p.Ser275Gly) rs139825195 0.00062
NM_003238.6(TGFB2):c.357G>A (p.Pro119=) rs138514914 0.00054
NM_003238.6(TGFB2):c.356C>T (p.Pro119Leu) rs149533093 0.00047
NM_003238.6(TGFB2):c.588C>T (p.Gly196=) rs192335285 0.00038
NM_003238.6(TGFB2):c.347-14C>G rs371982231 0.00014
NM_003238.6(TGFB2):c.648G>A (p.Arg216=) rs767503001 0.00012
NM_003238.6(TGFB2):c.644-4C>T rs11466408 0.00006
NM_003238.6(TGFB2):c.1008C>T (p.His336=) rs886038528 0.00005
NM_003238.6(TGFB2):c.1053G>A (p.Pro351=) rs142741166 0.00004
NM_003238.6(TGFB2):c.555C>T (p.Ile185=) rs760740958 0.00004
NM_003238.6(TGFB2):c.798T>A (p.Thr266=) rs376354795 0.00002
NM_003238.6(TGFB2):c.501G>A (p.Glu167=) rs550789732 0.00001
NM_003238.6(TGFB2):c.942G>A (p.Gln314=) rs188801474 0.00001
NM_003238.6(TGFB2):c.-4A>C rs1571820524
NM_003238.6(TGFB2):c.1011A>G (p.Glu337=) rs1571904243
NM_003238.6(TGFB2):c.375C>G (p.Pro125=) rs1658868131
NM_003238.6(TGFB2):c.510+12TTG[11] rs10482769
NM_003238.6(TGFB2):c.510+53CT[10] rs142802402
NM_003238.6(TGFB2):c.511-10del rs376560786
NM_003238.6(TGFB2):c.644-18T>A rs1553302992
NM_003238.6(TGFB2):c.933-6del rs11285412

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