ClinVar Miner

List of variants in gene SLC9A6 reported as uncertain significance by GeneDx

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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_001379110.1(SLC9A6):c.1734C>T (p.Ile578=) rs375760367 0.00008
NM_001379110.1(SLC9A6):c.1119C>T (p.Ile373=) rs140158476 0.00005
NM_001379110.1(SLC9A6):c.15C>G (p.Ile5Met) rs782296172 0.00004
NM_001379110.1(SLC9A6):c.262A>G (p.Thr88Ala) rs372003999 0.00004
NM_001379110.1(SLC9A6):c.1599A>C (p.Glu533Asp) rs781949645 0.00002
NM_001379110.1(SLC9A6):c.-35G>A rs782774568 0.00001
NM_001379110.1(SLC9A6):c.-56-34A>G rs796053277 0.00001
NM_001379110.1(SLC9A6):c.1140A>G (p.Thr380=) rs138074772 0.00001
NM_001379110.1(SLC9A6):c.1588C>A (p.Pro530Thr) rs782145804 0.00001
NM_001379110.1(SLC9A6):c.1738A>T (p.Arg580Trp) rs144661402 0.00001
NM_001379110.1(SLC9A6):c.448A>G (p.Arg150Gly) rs796053280 0.00001
NM_001379110.1(SLC9A6):c.475A>G (p.Ile159Val) rs1395246172 0.00001
NM_001379110.1(SLC9A6):c.-20G>A rs782736274
NM_001379110.1(SLC9A6):c.-25CGG[5] rs796053292
NM_001379110.1(SLC9A6):c.-27G>A
NM_001379110.1(SLC9A6):c.-53G>C
NM_001379110.1(SLC9A6):c.-56-19C>T
NM_001379110.1(SLC9A6):c.-56-31C>T rs2148129457
NM_001379110.1(SLC9A6):c.1042A>C (p.Asn348His)
NM_001379110.1(SLC9A6):c.1070G>C (p.Arg357Thr) rs796053286
NM_001379110.1(SLC9A6):c.1150T>C (p.Phe384Leu) rs2148179151
NM_001379110.1(SLC9A6):c.1313G>A (p.Arg438His) rs2148189865
NM_001379110.1(SLC9A6):c.1378A>G (p.Ser460Gly)
NM_001379110.1(SLC9A6):c.1387C>T (p.Leu463Phe) rs2148189943
NM_001379110.1(SLC9A6):c.1438A>C (p.Met480Leu) rs2148190021
NM_001379110.1(SLC9A6):c.1551-5T>C rs2148196761
NM_001379110.1(SLC9A6):c.1658A>G (p.His553Arg)
NM_001379110.1(SLC9A6):c.1735G>A (p.Ala579Thr)
NM_001379110.1(SLC9A6):c.1751G>A (p.Ser584Asn) rs796053288
NM_001379110.1(SLC9A6):c.1768-9T>G rs2148216706
NM_001379110.1(SLC9A6):c.1777C>G (p.Gln593Glu)
NM_001379110.1(SLC9A6):c.1849G>A (p.Val617Met) rs2148216878
NM_001379110.1(SLC9A6):c.1939G>A (p.Asp647Asn) rs2148217048
NM_001379110.1(SLC9A6):c.1966C>T (p.Arg656Cys)
NM_001379110.1(SLC9A6):c.370-9_370-5del rs796053290
NM_001379110.1(SLC9A6):c.420A>G (p.Ile140Met) rs1556616830
NM_001379110.1(SLC9A6):c.425A>G (p.Tyr142Cys) rs1556616834
NM_001379110.1(SLC9A6):c.512G>A (p.Cys171Tyr)
NM_001379110.1(SLC9A6):c.525-13_525-10del rs2148151047
NM_001379110.1(SLC9A6):c.539G>A (p.Gly180Asp)
NM_001379110.1(SLC9A6):c.563C>T (p.Thr188Met) rs372747388
NM_001379110.1(SLC9A6):c.574G>T (p.Ala192Ser) rs2089542923
NM_001379110.1(SLC9A6):c.586T>C (p.Tyr196His)
NM_001379110.1(SLC9A6):c.634C>G (p.Pro212Ala) rs2148151197
NM_001379110.1(SLC9A6):c.679G>A (p.Glu227Lys)
NM_001379110.1(SLC9A6):c.731T>G (p.Ile244Arg) rs1556617452
NM_001379110.1(SLC9A6):c.746C>T (p.Ser249Leu)
NM_001379110.1(SLC9A6):c.803T>A (p.Met268Lys) rs2148169885
NM_001379110.1(SLC9A6):c.885+5C>T rs2070901186
NM_001379110.1(SLC9A6):c.886-8A>G rs2148173826
NM_001379110.1(SLC9A6):c.921G>C (p.Leu307Phe) rs1556618846

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