ClinVar Miner

List of variants in gene SATB2 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_001172509.2(SATB2):c.170-76T>C rs7596597 0.93948
NM_001172509.2(SATB2):c.1543-4A>C rs10153730 0.93908
NM_001172509.2(SATB2):c.1740+171A>G rs3748904 0.78410
NM_001172509.2(SATB2):c.474-35G>C rs1348813 0.63041
NM_001172509.2(SATB2):c.473+99G>A rs2305262 0.27757
NM_001172509.2(SATB2):c.1542+295G>A rs2011269 0.17979
NM_001172509.2(SATB2):c.-59-231C>T rs13014796 0.13657
NM_001172509.2(SATB2):c.347-200A>G rs79303419 0.03310
NM_001172509.2(SATB2):c.1173+260G>C rs13387985 0.03231
NM_001172509.2(SATB2):c.597+170T>C rs72931316 0.03209
NM_001172509.2(SATB2):c.1543-119G>A rs16831258 0.01845
NM_001172509.2(SATB2):c.1740+197G>A rs78338033 0.01578
NM_001172509.2(SATB2):c.1434C>T (p.Gly478=) rs149056216 0.00109
NM_001172509.2(SATB2):c.210C>T (p.Asp70=) rs34311963 0.00070
NM_001172509.2(SATB2):c.195C>T (p.Val65=) rs147613731 0.00065
NM_001172509.2(SATB2):c.1071C>T (p.Ser357=) rs148055910 0.00035
NM_001172509.2(SATB2):c.1257G>A (p.Gln419=) rs367947535 0.00029
NM_001172509.2(SATB2):c.405C>T (p.Pro135=) rs150990155 0.00014
NM_001172509.2(SATB2):c.306G>A (p.Leu102=) rs201405384 0.00008
NM_001172509.2(SATB2):c.894T>A (p.Leu298=) rs199530574 0.00001
NM_001172509.2(SATB2):c.1173+301G>C rs10153573
NM_001172509.2(SATB2):c.1542+294_1542+295insTATATGTGTGTG rs372830951
NM_001172509.2(SATB2):c.1542+294_1542+295insTATG rs372830951
NM_001172509.2(SATB2):c.1542+294_1542+295insTATGTG rs372830951
NM_001172509.2(SATB2):c.1542+294_1542+295insTATGTGTG rs372830951
NM_001172509.2(SATB2):c.701-12A>C rs116585116

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