ClinVar Miner

List of variants in gene SLC9A6 reported by Ambry Genetics

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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_001379110.1(SLC9A6):c.1306+8G>A rs6654310 0.05510
NM_001379110.1(SLC9A6):c.1689C>T (p.Ser563=) rs2307131 0.03011
NM_001379110.1(SLC9A6):c.1662-4G>A rs188072063 0.00707
NM_001379110.1(SLC9A6):c.474T>C (p.Ser158=) rs144316388 0.00625
NM_001379110.1(SLC9A6):c.1029A>C (p.Ala343=) rs142049079 0.00390
NM_001379110.1(SLC9A6):c.1460+4A>G rs180727016 0.00236
NM_001379110.1(SLC9A6):c.1637G>A (p.Arg546Gln) rs146263125 0.00166
NM_001379110.1(SLC9A6):c.*8A>T rs200171451 0.00157
NM_001379110.1(SLC9A6):c.*5_*6del rs781795776 0.00149
NM_001379110.1(SLC9A6):c.1083G>A (p.Leu361=) rs151178361 0.00022
NM_001379110.1(SLC9A6):c.852A>T (p.Ala284=) rs371472909 0.00015
NM_001379110.1(SLC9A6):c.-9G>T rs367724979 0.00008
NM_001379110.1(SLC9A6):c.228T>C (p.Asn76=) rs782529317 0.00006
NM_001379110.1(SLC9A6):c.1005A>G (p.Val335=) rs782706500 0.00004
NM_001379110.1(SLC9A6):c.-53G>C rs1382310975 0.00002
NM_001379110.1(SLC9A6):c.1833A>T (p.Thr611=) rs782629258 0.00002
NM_001379110.1(SLC9A6):c.1862C>T (p.Pro621Leu) rs782442071 0.00002
NM_001379110.1(SLC9A6):c.1955T>C (p.Ile652Thr) rs2071568073 0.00002
NM_001379110.1(SLC9A6):c.1385C>T (p.Thr462Met) rs1229345478 0.00001
NM_001379110.1(SLC9A6):c.517G>A (p.Val173Ile) rs782117973 0.00001
NM_001379110.1(SLC9A6):c.548C>T (p.Thr183Met) rs782759179 0.00001
NM_001379110.1(SLC9A6):c.549G>A (p.Thr183=) rs782386487 0.00001
NM_001379110.1(SLC9A6):c.638-5A>G rs1057520615 0.00001
NM_001379110.1(SLC9A6):c.674A>G (p.Asp225Gly) rs1248694142 0.00001
NM_001379110.1(SLC9A6):c.-43C>T rs1569523768
NM_001379110.1(SLC9A6):c.-51G>A rs2089321131
NM_001379110.1(SLC9A6):c.1260AAG[1] (p.Arg421del) rs2521367951
NM_001379110.1(SLC9A6):c.1321A>G (p.Met441Val) rs2521382531
NM_001379110.1(SLC9A6):c.1387C>G (p.Leu463Val) rs2148189943
NM_001379110.1(SLC9A6):c.1394T>C (p.Ile465Thr) rs2521383035
NM_001379110.1(SLC9A6):c.1578C>T (p.His526=) rs782430960
NM_001379110.1(SLC9A6):c.1702A>G (p.Thr568Ala) rs2071481648
NM_001379110.1(SLC9A6):c.1777C>G (p.Gln593Glu) rs2521484199
NM_001379110.1(SLC9A6):c.1938G>A (p.Gly646=) rs2521485929
NM_001379110.1(SLC9A6):c.284del (p.Ser95fs) rs2521144179
NM_001379110.1(SLC9A6):c.370-9_370-5del rs796053290
NM_001379110.1(SLC9A6):c.448-6dup rs375038684
NM_001379110.1(SLC9A6):c.465del (p.Ser158fs) rs2089536867
NM_001379110.1(SLC9A6):c.481G>T (p.Ala161Ser) rs2521183715
NM_001379110.1(SLC9A6):c.506T>A (p.Ile169Asn) rs2521184115
NM_001379110.1(SLC9A6):c.539G>A (p.Gly180Asp) rs2521188381
NM_001379110.1(SLC9A6):c.786C>T (p.Thr262=) rs1393599406

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