ClinVar Miner

List of variants in gene TGFB3 reported as likely benign for not provided

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Gene type:
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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_003239.5(TGFB3):c.926+188G>A rs3917202 0.02072
NM_003239.5(TGFB3):c.754+293T>A rs3917193 0.01979
NM_003239.5(TGFB3):c.*820G>A rs3917218 0.01459
NM_003239.5(TGFB3):c.*682G>A rs4252349 0.00758
NM_003239.5(TGFB3):c.*255C>T rs4252347 0.00653
NM_003239.5(TGFB3):c.352+115G>C rs112619396 0.00563
NM_003239.5(TGFB3):c.*824T>C rs116586110 0.00502
NM_003239.5(TGFB3):c.1080+163T>C rs115411167 0.00502
NM_003239.5(TGFB3):c.755-307A>C rs11466436 0.00456
NM_003239.5(TGFB3):c.1081-146G>A rs4252344 0.00385
NM_003239.5(TGFB3):c.516+37G>A rs74723274 0.00289
NM_003239.5(TGFB3):c.744C>A (p.Ile248=) rs45477900 0.00123
NM_003239.5(TGFB3):c.164G>A (p.Ser55Asn) rs143229915 0.00100
NM_003239.5(TGFB3):c.34C>T (p.Leu12=) rs143612445 0.00096
NM_003239.5(TGFB3):c.293C>T (p.Ser98Leu) rs142047577 0.00092
NM_003239.5(TGFB3):c.179C>T (p.Thr60Met) rs4252315 0.00066
NM_003239.5(TGFB3):c.*496G>A rs3917217 0.00058
NM_003239.5(TGFB3):c.354C>T (p.Asn118=) rs145051522 0.00029
NM_003239.5(TGFB3):c.193G>A (p.Val65Ile) rs201059075 0.00023
NM_003239.5(TGFB3):c.412T>G (p.Ser138Ala) rs201453600 0.00018
NM_003239.5(TGFB3):c.88T>C (p.Leu30=) rs3917145 0.00013
NM_003239.5(TGFB3):c.873G>A (p.Pro291=) rs370006165 0.00010
NM_003239.5(TGFB3):c.558C>T (p.Ile186=) rs138389291 0.00009
NM_003239.5(TGFB3):c.101A>G (p.His34Arg) rs199791687 0.00008
NM_003239.5(TGFB3):c.504C>T (p.Ile168=) rs148029842 0.00006
NM_003239.5(TGFB3):c.*8C>T rs3917215 0.00004
NM_003239.5(TGFB3):c.192C>T (p.His64=) rs374423962 0.00004
NM_003239.5(TGFB3):c.288C>T (p.Thr96=) rs201047560 0.00004
NM_003239.5(TGFB3):c.519C>T (p.Ile173=) rs754898843 0.00004
NM_003239.5(TGFB3):c.792G>A (p.Leu264=) rs375034484 0.00004
NM_003239.5(TGFB3):c.*13G>A rs375846390 0.00003
NM_003239.5(TGFB3):c.591C>T (p.Ala197=) rs375090568 0.00003
NM_003239.5(TGFB3):c.948T>C (p.Cys316=) rs1364994786 0.00003
NM_003239.5(TGFB3):c.324C>T (p.Phe108=) rs779502039 0.00002
NM_003239.5(TGFB3):c.294G>A (p.Ser98=) rs778214495 0.00001
NM_003239.5(TGFB3):c.357A>G (p.Glu119=) rs748598952 0.00001
NM_003239.5(TGFB3):c.471C>G (p.Pro157=) rs768917005 0.00001
NM_003239.5(TGFB3):c.755-5T>C rs768188445 0.00001
NM_003239.5(TGFB3):c.798C>T (p.Arg266=) rs772654040 0.00001
NM_003239.5(TGFB3):c.927-19T>C rs199714510 0.00001
NM_003239.5(TGFB3):c.-1048GGAGAG[2] rs151325226
NM_003239.5(TGFB3):c.1080+13C>T rs1242820215
NM_003239.5(TGFB3):c.1146C>T (p.Asp382=) rs1595336694
NM_003239.5(TGFB3):c.352+331G>A rs111897020
NM_003239.5(TGFB3):c.441C>T (p.Phe147=) rs560468476
NM_003239.5(TGFB3):c.600G>T (p.Leu200=) rs1594787709
NM_003239.5(TGFB3):c.661C>T (p.Leu221=) rs1595340555
NM_003239.5(TGFB3):c.69T>C (p.Ser23=) rs1167977988
NM_003239.5(TGFB3):c.711T>C (p.Asp237=) rs1206735679
NM_003239.5(TGFB3):c.754+5C>T rs754211381
NM_003239.5(TGFB3):c.754+6_754+10del rs1414628117
NM_003239.5(TGFB3):c.926+147_926+148del rs199778146

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