ClinVar Miner

List of variants in gene TGFB2 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 18
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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.356C>T (p.Pro119Leu) rs149533093 0.00047
NM_003238.6(TGFB2):c.747A>G (p.Arg249=) rs147960792 0.00032
NM_003238.6(TGFB2):c.1008C>T (p.His336=) rs886038528 0.00005
NM_003238.6(TGFB2):c.745A>C (p.Arg249=) rs201845761 0.00003
NM_003238.6(TGFB2):c.1095C>T (p.Ser365=) rs748818194 0.00001
NM_003238.6(TGFB2):c.37C>A (p.His13Asn) rs763918203 0.00001
NM_003238.6(TGFB2):c.942G>A (p.Gln314=) rs188801474 0.00001
NM_003238.6(TGFB2):c.108G>A (p.Arg36=)
NM_003238.6(TGFB2):c.174T>G (p.Pro58=)
NM_003238.6(TGFB2):c.468C>T (p.Asn156=)
NM_003238.6(TGFB2):c.758T>C (p.Ile253Thr)
NM_003238.6(TGFB2):c.816A>C (p.Lys272Asn)
NM_003238.6(TGFB2):c.833C>T (p.Thr278Ile)
NM_003238.6(TGFB2):c.895C>T (p.Arg299Trp) rs863223792

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