ClinVar Miner

List of variants in gene TGFB2 reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
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.357G>A (p.Pro119=) rs138514914 0.00054
NM_003238.6(TGFB2):c.356C>T (p.Pro119Leu) rs149533093 0.00047
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.555C>T (p.Ile185=) rs760740958 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.330C>T (p.Pro110=) rs150348450 0.00003
NM_003238.6(TGFB2):c.745A>C (p.Arg249=) rs201845761 0.00003
NM_003238.6(TGFB2):c.456T>C (p.Phe152=) rs372071268 0.00002
NM_003238.6(TGFB2):c.798T>A (p.Thr266=) rs376354795 0.00002
NM_003238.6(TGFB2):c.1098A>G (p.Leu366=) rs931960431 0.00001
NM_003238.6(TGFB2):c.1122A>T (p.Ala374=) rs1316829320 0.00001
NM_003238.6(TGFB2):c.261C>T (p.Ala87=) rs746416777 0.00001
NM_003238.6(TGFB2):c.369C>T (p.Tyr123=) rs368157039 0.00001
NM_003238.6(TGFB2):c.40C>T (p.Leu14=) rs1407180803 0.00001
NM_003238.6(TGFB2):c.501G>A (p.Glu167=) rs550789732 0.00001
NM_003238.6(TGFB2):c.612T>C (p.Thr204=) rs960874816 0.00001
NM_003238.6(TGFB2):c.942G>A (p.Gln314=) rs188801474 0.00001
NM_003238.6(TGFB2):c.957A>C (p.Leu319=) rs755474865 0.00001
NM_003238.6(TGFB2):c.1038T>C (p.Cys346=)
NM_003238.6(TGFB2):c.106A>C (p.Arg36=)
NM_003238.6(TGFB2):c.1083C>T (p.Ser361=)
NM_003238.6(TGFB2):c.1134T>C (p.Pro378=)
NM_003238.6(TGFB2):c.1162C>T (p.Leu388=)
NM_003238.6(TGFB2):c.1179C>T (p.Tyr393=)
NM_003238.6(TGFB2):c.117G>C (p.Ala39=) rs1430240541
NM_003238.6(TGFB2):c.147G>A (p.Lys49=)
NM_003238.6(TGFB2):c.156T>C (p.Ser52=)
NM_003238.6(TGFB2):c.162A>G (p.Pro54=)
NM_003238.6(TGFB2):c.189C>A (p.Val63=)
NM_003238.6(TGFB2):c.189C>T (p.Val63=) rs774030175
NM_003238.6(TGFB2):c.252G>A (p.Arg84=)
NM_003238.6(TGFB2):c.277A>C (p.Arg93=)
NM_003238.6(TGFB2):c.291G>A (p.Glu97=)
NM_003238.6(TGFB2):c.31A>C (p.Ile11Leu)
NM_003238.6(TGFB2):c.393A>G (p.Arg131=)
NM_003238.6(TGFB2):c.468C>T (p.Asn156=)
NM_003238.6(TGFB2):c.54G>C (p.Ala18=)
NM_003238.6(TGFB2):c.555C>A (p.Ile185=)
NM_003238.6(TGFB2):c.597C>T (p.Leu199=)
NM_003238.6(TGFB2):c.600C>G (p.Ser200=)
NM_003238.6(TGFB2):c.675C>T (p.His225=)
NM_003238.6(TGFB2):c.720A>G (p.Pro240=)
NM_003238.6(TGFB2):c.723T>C (p.Asn241=)
NM_003238.6(TGFB2):c.78A>G (p.Thr26=)
NM_003238.6(TGFB2):c.84T>C (p.Asp28=)
NM_003238.6(TGFB2):c.882A>G (p.Gln294=)
NM_003238.6(TGFB2):c.936T>C (p.Asn312=)

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