ClinVar Miner

List of variants in gene combination LOC126806462, SATB2 reported as uncertain significance for syndrome caused by partial chromosomal deletion

Included ClinVar conditions (110):
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Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_001172509.2(SATB2):c.2182G>C (p.Ala728Pro) rs377368865 0.00003
NM_001172509.2(SATB2):c.2047G>A (p.Ala683Thr) rs372032415 0.00001
NM_001172509.2(SATB2):c.2183C>G (p.Ala728Gly) rs140532313 0.00001
NM_001172509.2(SATB2):c.2196G>T (p.Gln732His) rs778160560 0.00001
NM_001172509.2(SATB2):c.1741G>A (p.Val581Ile)
NM_001172509.2(SATB2):c.1751G>A (p.Arg584Lys) rs2105707604
NM_001172509.2(SATB2):c.1754A>G (p.Gln585Arg) rs1692196085
NM_001172509.2(SATB2):c.1774G>A (p.Glu592Lys) rs2105707521
NM_001172509.2(SATB2):c.1795G>A (p.Glu599Lys)
NM_001172509.2(SATB2):c.1808C>T (p.Pro603Leu)
NM_001172509.2(SATB2):c.1843C>A (p.Pro615Thr)
NM_001172509.2(SATB2):c.1852C>T (p.Arg618Cys) rs2105707260
NM_001172509.2(SATB2):c.1865C>T (p.Ser622Phe)
NM_001172509.2(SATB2):c.1918C>T (p.Pro640Ser)
NM_001172509.2(SATB2):c.1940C>A (p.Thr647Asn)
NM_001172509.2(SATB2):c.2000G>T (p.Arg667Leu) rs1559136030
NM_001172509.2(SATB2):c.2015A>G (p.His672Arg)
NM_001172509.2(SATB2):c.2020G>A (p.Gly674Arg)
NM_001172509.2(SATB2):c.2024A>C (p.Lys675Thr)
NM_001172509.2(SATB2):c.2026C>A (p.Leu676Met)
NM_001172509.2(SATB2):c.2038C>G (p.Leu680Val)
NM_001172509.2(SATB2):c.2074G>A (p.Glu692Lys) rs1559135904
NM_001172509.2(SATB2):c.2089G>A (p.Glu697Lys)
NM_001172509.2(SATB2):c.2104G>A (p.Asp702Asn)
NM_001172509.2(SATB2):c.2119T>C (p.Ser707Pro)
NM_001172509.2(SATB2):c.2125G>A (p.Glu709Lys) rs1574458712
NM_001172509.2(SATB2):c.2126A>G (p.Glu709Gly) rs2105706602
NM_001172509.2(SATB2):c.2130G>C (p.Met710Ile) rs1286415699
NM_001172509.2(SATB2):c.2158G>A (p.Ala720Thr) rs531933724
NM_001172509.2(SATB2):c.2164A>C (p.Lys722Gln) rs2105706499
NM_001172509.2(SATB2):c.2167del (p.Ser723fs)
NM_001172509.2(SATB2):c.2174C>T (p.Ala725Val) rs767329844
NM_001172509.2(SATB2):c.2185G>A (p.Glu729Lys) rs1489038642
NM_001172509.2(SATB2):c.2189T>C (p.Ile730Thr) rs373319001

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