ClinVar Miner

List of variants in gene TGFB2 studied for not specified

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_003238.6(TGFB2):c.643+7A>C rs7531245 0.01418
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.-5A>T rs200702935 0.00060
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.747A>G (p.Arg249=) rs147960792 0.00032
NM_003238.6(TGFB2):c.199G>A (p.Val67Met) rs201761868 0.00015
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.297C>T (p.Tyr99=) rs760759052 0.00011
NM_003238.6(TGFB2):c.1140C>T (p.Cys380=) rs201129153 0.00006
NM_003238.6(TGFB2):c.1008C>T (p.His336=) rs886038528 0.00005
NM_003238.6(TGFB2):c.-6T>A rs772514115 0.00004
NM_003238.6(TGFB2):c.1053G>A (p.Pro351=) rs142741166 0.00004
NM_003238.6(TGFB2):c.603C>T (p.Phe201=) rs377264861 0.00004
NM_003238.6(TGFB2):c.984G>A (p.Arg328=) rs147678881 0.00004
NM_003238.6(TGFB2):c.-16T>C rs779785854 0.00003
NM_003238.6(TGFB2):c.*15T>C rs1057520937 0.00001
NM_003238.6(TGFB2):c.*9G>A rs1057521805 0.00001
NM_003238.6(TGFB2):c.-45dup rs200186989
NM_003238.6(TGFB2):c.1086+19T>C rs1553303372
NM_003238.6(TGFB2):c.1087-14C>T rs1341545472
NM_003238.6(TGFB2):c.1129T>C (p.Ser377Pro)
NM_003238.6(TGFB2):c.1167C>G (p.Thr389=) rs1660142912
NM_003238.6(TGFB2):c.346+16375G>A
NM_003238.6(TGFB2):c.346+8C>T rs1553292149
NM_003238.6(TGFB2):c.355C>T (p.Pro119Ser)
NM_003238.6(TGFB2):c.387T>G (p.Ile129Met)
NM_003238.6(TGFB2):c.417G>A (p.Lys139=)
NM_003238.6(TGFB2):c.510+12TTG[12] rs10482769
NM_003238.6(TGFB2):c.597C>G (p.Leu199=)
NM_003238.6(TGFB2):c.59G>C (p.Ser20Thr)
NM_003238.6(TGFB2):c.739G>A (p.Glu247Lys) rs1558262454
NM_003238.6(TGFB2):c.754+10dup rs1553303016
NM_003238.6(TGFB2):c.754+4A>G
NM_003238.6(TGFB2):c.821dup (p.Asn274fs) rs863223796
NM_003238.6(TGFB2):c.837A>G (p.Pro279=) rs1553303186
NM_003238.6(TGFB2):c.870A>G (p.Arg290=) rs1057521201
NM_003238.6(TGFB2):c.917C>T (p.Ala306Val)
NM_003238.6(TGFB2):c.933-6del rs11285412
NM_003238.6(TGFB2):c.933-7_933-6del rs11285412
NM_003238.6(TGFB2):c.933-8_933-6del rs11285412

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