ClinVar Miner

List of variants in gene SMAD4 reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP
NM_005359.5(SMAD4):c.*5637_*5640delACAC rs368759758
NM_005359.6(SMAD4):c.*1179T>C rs10470
NM_005359.6(SMAD4):c.*11C>T rs11663402
NM_005359.6(SMAD4):c.*12G>A rs148687037
NM_005359.6(SMAD4):c.*1659C>A
NM_005359.6(SMAD4):c.*1820T>G rs141309481
NM_005359.6(SMAD4):c.*1864C>A rs561442548
NM_005359.6(SMAD4):c.*1866A>G rs4940037
NM_005359.6(SMAD4):c.*2122A>G rs149424787
NM_005359.6(SMAD4):c.*2353C>T rs550660083
NM_005359.6(SMAD4):c.*2361A>G rs143842829
NM_005359.6(SMAD4):c.*2488T>A rs148190627
NM_005359.6(SMAD4):c.*2796G>T rs4939651
NM_005359.6(SMAD4):c.*2914C>T rs147352474
NM_005359.6(SMAD4):c.*2989A>G rs139526377
NM_005359.6(SMAD4):c.*30A>C rs767288576
NM_005359.6(SMAD4):c.*334C>T rs534790830
NM_005359.6(SMAD4):c.*3398A>G rs182735651
NM_005359.6(SMAD4):c.*3662C>T
NM_005359.6(SMAD4):c.*412A>G rs28403611
NM_005359.6(SMAD4):c.*4378T>G rs540039847
NM_005359.6(SMAD4):c.*4643T>C rs369040052
NM_005359.6(SMAD4):c.*4748C>T rs375580807
NM_005359.6(SMAD4):c.*4862A>G rs139595540
NM_005359.6(SMAD4):c.*5080A>G rs532965680
NM_005359.6(SMAD4):c.*5083G>A rs145596898
NM_005359.6(SMAD4):c.*5131A>G rs12456284
NM_005359.6(SMAD4):c.*5170C>T rs117142232
NM_005359.6(SMAD4):c.*5259A>T rs139414609
NM_005359.6(SMAD4):c.*5419T>C rs146551171
NM_005359.6(SMAD4):c.*5535A>G rs75712226
NM_005359.6(SMAD4):c.*5627G>A rs185010226
NM_005359.6(SMAD4):c.*5691_*5693del rs374306389
NM_005359.6(SMAD4):c.*5801T>C rs577928234
NM_005359.6(SMAD4):c.*5863_*5867del rs78989198
NM_005359.6(SMAD4):c.*5994A>C rs3819122
NM_005359.6(SMAD4):c.*6009G>C rs181250637
NM_005359.6(SMAD4):c.*6423G>C rs2282544
NM_005359.6(SMAD4):c.*6492A>T rs569819237
NM_005359.6(SMAD4):c.*6513C>T rs76020793
NM_005359.6(SMAD4):c.*685A>C rs16952798
NM_005359.6(SMAD4):c.-401C>T
NM_005359.6(SMAD4):c.1086T>C (p.Phe362=) rs1801250
NM_005359.6(SMAD4):c.1140-10T>C rs186332162
NM_005359.6(SMAD4):c.1392C>T (p.Ala464=) rs140487104
NM_005359.6(SMAD4):c.20C>T (p.Thr7Met) rs372316981
NM_005359.6(SMAD4):c.354G>A (p.Ala118=) rs145988618
NM_005359.6(SMAD4):c.424+5G>A rs200772603
NM_005359.6(SMAD4):c.455-6A>G rs181178864

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