ClinVar Miner

List of variants in gene SMAD4 reported as uncertain significance by Color

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Gene type:
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Total variants: 82
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HGVS dbSNP
NM_005359.5(SMAD4):c.*14T>C rs989027869
NM_005359.5(SMAD4):c.*14T>G rs989027869
NM_005359.5(SMAD4):c.*1G>A rs1555687622
NM_005359.5(SMAD4):c.*7_*8del rs1176679575
NM_005359.5(SMAD4):c.-3C>G rs886053892
NM_005359.5(SMAD4):c.1046C>T (p.Thr349Ile) rs564408927
NM_005359.5(SMAD4):c.1106A>G (p.Asn369Ser) rs139569694
NM_005359.5(SMAD4):c.1124C>T (p.Ala375Val) rs1555686499
NM_005359.5(SMAD4):c.1148T>C (p.Ile383Thr) rs377767355
NM_005359.5(SMAD4):c.1219G>C (p.Val407Leu) rs147621330
NM_005359.5(SMAD4):c.1258C>T (p.Arg420Cys) rs1367209662
NM_005359.5(SMAD4):c.1280A>G (p.His427Arg) rs1555686619
NM_005359.5(SMAD4):c.1308+4A>T rs1555686626
NM_005359.5(SMAD4):c.1309-5A>G rs1568211170
NM_005359.5(SMAD4):c.1309G>A (p.Val437Ile) rs1568211172
NM_005359.5(SMAD4):c.1326G>C (p.Gln442His) rs1568211178
NM_005359.5(SMAD4):c.1339A>C (p.Met447Leu) rs1568211184
NM_005359.5(SMAD4):c.1393G>A (p.Val465Met) rs786201798
NM_005359.5(SMAD4):c.1438C>T (p.Pro480Ser) rs1555687390
NM_005359.5(SMAD4):c.1487G>A (p.Arg496His) rs876660045
NM_005359.5(SMAD4):c.1525T>G (p.Trp509Gly) rs377767369
NM_005359.5(SMAD4):c.155A>T (p.Asp52Val) rs1057524809
NM_005359.5(SMAD4):c.1635T>G (p.Ile545Met) rs200595795
NM_005359.5(SMAD4):c.16A>G (p.Ile6Val) rs1376500870
NM_005359.5(SMAD4):c.179C>T (p.Ala60Val) rs1555685030
NM_005359.5(SMAD4):c.181A>G (p.Ile61Val) rs1064794204
NM_005359.5(SMAD4):c.209A>C (p.Lys70Thr) rs1555685038
NM_005359.5(SMAD4):c.20C>T (p.Thr7Met) rs372316981
NM_005359.5(SMAD4):c.304C>G (p.Pro102Ala) rs1568203445
NM_005359.5(SMAD4):c.332A>C (p.His111Pro) rs1064794363
NM_005359.5(SMAD4):c.333T>A (p.His111Gln) rs1568203454
NM_005359.5(SMAD4):c.38A>G (p.Asn13Ser) rs281875323
NM_005359.5(SMAD4):c.424+5G>A rs200772603
NM_005359.5(SMAD4):c.424+6T>C rs771456293
NM_005359.5(SMAD4):c.442C>G (p.Leu148Val) rs1568203602
NM_005359.5(SMAD4):c.454+7A>C rs755891338
NM_005359.5(SMAD4):c.466A>T (p.Met156Leu) rs534355764
NM_005359.5(SMAD4):c.471G>A (p.Met157Ile) rs780716382
NM_005359.5(SMAD4):c.521C>A (p.Thr174Asn) rs138800446
NM_005359.5(SMAD4):c.530A>C (p.His177Pro) rs1568205026
NM_005359.5(SMAD4):c.554C>A (p.Pro185Gln) rs770798845
NM_005359.5(SMAD4):c.554C>T (p.Pro185Leu) rs770798845
NM_005359.5(SMAD4):c.55A>G (p.Ile19Val) rs1568202964
NM_005359.5(SMAD4):c.560G>A (p.Ser187Asn) rs927620013
NM_005359.5(SMAD4):c.566G>A (p.Arg189His) rs759288477
NM_005359.5(SMAD4):c.566G>T (p.Arg189Leu) rs759288477
NM_005359.5(SMAD4):c.568G>T (p.Ala190Ser) rs61751988
NM_005359.5(SMAD4):c.575C>T (p.Thr192Ile) rs587780792
NM_005359.5(SMAD4):c.580A>T (p.Thr194Ser) rs1432058632
NM_005359.5(SMAD4):c.58G>T (p.Val20Leu) rs1568202971
NM_005359.5(SMAD4):c.614A>C (p.Glu205Ala) rs748615724
NM_005359.5(SMAD4):c.643C>T (p.Pro215Ser) rs1064793270
NM_005359.5(SMAD4):c.644C>G (p.Pro215Arg) rs777495692
NM_005359.5(SMAD4):c.651T>G (p.Ile217Met) rs997151197
NM_005359.5(SMAD4):c.667+6T>C rs1060500745
NM_005359.5(SMAD4):c.675_676delTGinsCC (p.Ala226Pro) rs1568206030
NM_005359.5(SMAD4):c.677C>T (p.Ala226Val) rs539739051
NM_005359.5(SMAD4):c.679A>G (p.Ser227Gly) rs1443767329
NM_005359.5(SMAD4):c.700A>C (p.Ser234Arg) rs758642067
NM_005359.5(SMAD4):c.700A>G (p.Ser234Gly) rs758642067
NM_005359.5(SMAD4):c.702T>G (p.Ser234Arg) rs1555685911
NM_005359.5(SMAD4):c.715C>G (p.Gln239Glu) rs1163381283
NM_005359.5(SMAD4):c.716A>T (p.Gln239Leu) rs1555685916
NM_005359.5(SMAD4):c.736C>A (p.Pro246Thr) rs876659967
NM_005359.5(SMAD4):c.743A>T (p.Gln248Leu) rs751985298
NM_005359.5(SMAD4):c.746_747delAGinsCC (p.Gln249Pro) rs587782209
NM_005359.5(SMAD4):c.752A>G (p.Asn251Ser) rs1555685926
NM_005359.5(SMAD4):c.779A>C (p.Tyr260Ser) rs1555685937
NM_005359.5(SMAD4):c.788-14G>A rs769943457
NM_005359.5(SMAD4):c.845A>C (p.His282Pro) rs1555685962
NM_005359.5(SMAD4):c.860A>G (p.His287Arg) rs1568206180
NM_005359.5(SMAD4):c.875C>T (p.Pro292Leu) rs786201404
NM_005359.5(SMAD4):c.877C>T (p.Pro293Ser) rs1555685965
NM_005359.5(SMAD4):c.880A>G (p.Met294Val) rs7238500
NM_005359.5(SMAD4):c.884C>T (p.Pro295Leu) rs370176106
NM_005359.5(SMAD4):c.887C>A (p.Pro296His) rs1417632301
NM_005359.5(SMAD4):c.907C>G (p.Pro303Ala) rs1568206575
NM_005359.5(SMAD4):c.917A>G (p.Asn306Ser) rs730881953
NM_005359.5(SMAD4):c.919G>A (p.Glu307Lys) rs1555686079
NM_005359.5(SMAD4):c.940A>G (p.Ile314Val) rs748622028
NM_005359.5(SMAD4):c.947A>G (p.Asn316Ser) rs377119288
NM_005359.5(SMAD4):c.956-3T>C rs748283001

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