ClinVar Miner

List of variants in gene SLC25A22 reported as uncertain significance by GeneDx

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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_001191061.2(SLC25A22):c.64G>A (p.Gly22Ser) rs757575372 0.00028
NM_001191061.2(SLC25A22):c.267C>G (p.Phe89Leu) rs143064022 0.00024
NM_001191061.2(SLC25A22):c.464G>C (p.Gly155Ala) rs200992080 0.00016
NM_001191061.2(SLC25A22):c.653C>T (p.Ala218Val) rs150645806 0.00014
NM_001191061.2(SLC25A22):c.647G>A (p.Arg216His) rs201932343 0.00012
NM_001191061.2(SLC25A22):c.506C>T (p.Thr169Met) rs533726078 0.00011
NM_001191061.2(SLC25A22):c.146+6T>C rs369906148 0.00008
NM_001191061.2(SLC25A22):c.124G>A (p.Gly42Ser) rs535927522 0.00007
NM_001191061.2(SLC25A22):c.551C>G (p.Ala184Gly) rs755147242 0.00006
NM_001191061.2(SLC25A22):c.493G>A (p.Ala165Thr) rs763227728 0.00005
NM_001191061.2(SLC25A22):c.130C>T (p.Arg44Cys) rs576145791 0.00004
NM_001191061.2(SLC25A22):c.541C>T (p.Arg181Cys) rs374216522 0.00004
NM_001191061.2(SLC25A22):c.553G>A (p.Gly185Ser) rs761249044 0.00004
NM_001191061.2(SLC25A22):c.562A>G (p.Lys188Glu) rs767949941 0.00004
NM_001191061.2(SLC25A22):c.-163-875C>T rs559971351 0.00003
NM_001191061.2(SLC25A22):c.292G>A (p.Gly98Arg) rs781514122 0.00003
NM_001191061.2(SLC25A22):c.658G>A (p.Glu220Lys) rs781132225 0.00003
NM_001191061.2(SLC25A22):c.871C>T (p.Arg291Cys) rs762897089 0.00003
NM_001191061.2(SLC25A22):c.190G>A (p.Gly64Ser) rs774766308 0.00002
NM_001191061.2(SLC25A22):c.452C>T (p.Ser151Leu) rs750386693 0.00002
NM_001191061.2(SLC25A22):c.731A>G (p.Asn244Ser) rs778299128 0.00002
NM_001191061.2(SLC25A22):c.784G>A (p.Glu262Lys) rs199612664 0.00002
NM_001191061.2(SLC25A22):c.173G>A (p.Arg58His) rs754048758 0.00001
NM_001191061.2(SLC25A22):c.178G>A (p.Glu60Lys) rs193920962 0.00001
NM_001191061.2(SLC25A22):c.251T>G (p.Leu84Arg) rs772950759 0.00001
NM_001191061.2(SLC25A22):c.284C>G (p.Ser95Cys) rs369735050 0.00001
NM_001191061.2(SLC25A22):c.307C>G (p.Leu103Val) rs370392070 0.00001
NM_001191061.2(SLC25A22):c.340G>A (p.Gly114Ser) rs905293556 0.00001
NM_001191061.2(SLC25A22):c.548T>C (p.Ile183Thr) rs765513862 0.00001
NM_001191061.2(SLC25A22):c.725C>T (p.Ala242Val) rs781424186 0.00001
NM_001191061.2(SLC25A22):c.735_736del (p.Pro245_Cys246insTer) rs796053242 0.00001
NM_001191061.2(SLC25A22):c.874G>A (p.Ala292Thr) rs369729483 0.00001
NM_001191061.2(SLC25A22):c.128A>G (p.Gln43Arg) rs1554966124
NM_001191061.2(SLC25A22):c.226G>A (p.Val76Ile)
NM_001191061.2(SLC25A22):c.316G>A (p.Glu106Lys) rs1162879084
NM_001191061.2(SLC25A22):c.391C>A (p.Leu131Met) rs796053239
NM_001191061.2(SLC25A22):c.421A>G (p.Arg141Gly) rs1332758149
NM_001191061.2(SLC25A22):c.488C>T (p.Pro163Leu)
NM_001191061.2(SLC25A22):c.524G>A (p.Arg175His) rs769329043
NM_001191061.2(SLC25A22):c.524G>T (p.Arg175Leu) rs769329043
NM_001191061.2(SLC25A22):c.55G>A (p.Gly19Arg) rs780652429
NM_001191061.2(SLC25A22):c.600C>G (p.Phe200Leu)
NM_001191061.2(SLC25A22):c.704C>T (p.Ala235Val) rs796053240

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