ClinVar Miner

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

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Gene type:
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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_001172509.2(SATB2):c.1543-218A>C rs114467079 0.00959
NM_001172509.2(SATB2):c.1740+126A>C rs114301127 0.00763
NM_001172509.2(SATB2):c.701-208T>C rs79248084 0.00687
NM_001172509.2(SATB2):c.1173+278C>G rs150912592 0.00615
NM_001172509.2(SATB2):c.210C>T (p.Asp70=) rs34311963 0.00070
NM_001172509.2(SATB2):c.1071C>T (p.Ser357=) rs148055910 0.00035
NM_001172509.2(SATB2):c.333G>C (p.Ala111=) rs140116634 0.00024
NM_001172509.2(SATB2):c.1035C>A (p.Ile345=) rs150824088 0.00019
NM_001172509.2(SATB2):c.1572G>A (p.Lys524=) rs376557576 0.00015
NM_001172509.2(SATB2):c.585C>T (p.Cys195=) rs376383948 0.00014
NM_001172509.2(SATB2):c.1173+6A>G rs747745210 0.00012
NM_001172509.2(SATB2):c.862G>A (p.Ala288Thr) rs142825652 0.00012
NM_001172509.2(SATB2):c.1173+5A>G rs569655648 0.00010
NM_001172509.2(SATB2):c.787T>C (p.Ser263Pro) rs12619995 0.00006
NM_001172509.2(SATB2):c.1467C>T (p.Asp489=) rs370291268 0.00004
NM_001172509.2(SATB2):c.42C>G (p.Pro14=) rs773072163 0.00004
NM_001172509.2(SATB2):c.1398G>A (p.Ser466=) rs377059710 0.00003
NM_001172509.2(SATB2):c.1551G>T (p.Leu517=) rs760937399 0.00003
NM_001172509.2(SATB2):c.163G>C (p.Val55Leu) rs748892556 0.00003
NM_001172509.2(SATB2):c.1239A>G (p.Val413=) rs148608261 0.00002
NM_001172509.2(SATB2):c.756A>G (p.Pro252=) rs375364851 0.00002
NM_001172509.2(SATB2):c.846C>T (p.Ile282=) rs373578751 0.00002
NM_001172509.2(SATB2):c.170-8C>T rs771945626 0.00001
NM_001172509.2(SATB2):c.531T>C (p.Asn177=) rs768204353 0.00001
NM_001172509.2(SATB2):c.1085C>A (p.Pro362Gln) rs2105822933
NM_001172509.2(SATB2):c.1542+294_1542+295insTATATGTGTGTGTG rs372830951
NM_001172509.2(SATB2):c.201G>A (p.Glu67=) rs924915744
NM_001172509.2(SATB2):c.246C>T (p.Ala82=) rs146889022
NM_001172509.2(SATB2):c.300G>A (p.Ala100=)
NM_001172509.2(SATB2):c.46C>A (p.Arg16=) rs937799874
NM_001172509.2(SATB2):c.594C>A (p.Ser198=) rs747345430
NM_001172509.2(SATB2):c.978C>A (p.Leu326=)

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