ClinVar Miner

List of variants in gene SLC25A22 reported as likely benign for not specified

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Gene type:
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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_001191061.2(SLC25A22):c.293+27G>A rs79478359 0.08883
NM_001191061.2(SLC25A22):c.705T>C (p.Ala235=) rs142861804 0.00262
NM_001191061.2(SLC25A22):c.151G>A (p.Asp51Asn) rs116134953 0.00210
NM_001191061.2(SLC25A22):c.169G>A (p.Val57Ile) rs150242281 0.00204
NM_001191061.2(SLC25A22):c.570C>T (p.Leu190=) rs145322467 0.00137
NM_001191061.2(SLC25A22):c.618G>A (p.Pro206=) rs150544061 0.00118
NM_001191061.2(SLC25A22):c.495C>T (p.Ala165=) rs374780430 0.00063
NM_001191061.2(SLC25A22):c.876G>A (p.Ala292=) rs146300431 0.00058
NM_001191061.2(SLC25A22):c.742+9A>G rs370309722 0.00014
NM_001191061.2(SLC25A22):c.930C>T (p.Ile310=) rs765908991 0.00014
NM_001191061.2(SLC25A22):c.177C>T (p.Ser59=) rs761165876 0.00009
NM_001191061.2(SLC25A22):c.412+9G>A rs369276282 0.00009
NM_001191061.2(SLC25A22):c.651G>A (p.Pro217=) rs768604742 0.00008
NM_001191061.2(SLC25A22):c.819-15G>A rs546478081 0.00008
NM_001191061.2(SLC25A22):c.743-16C>T rs200493024 0.00007
NM_001191061.2(SLC25A22):c.146+7G>A rs376889561 0.00005
NM_001191061.2(SLC25A22):c.726C>T (p.Ala242=) rs771026197 0.00004
NM_001191061.2(SLC25A22):c.-163-878T>C rs1057522653 0.00003
NM_001191061.2(SLC25A22):c.133G>A (p.Val45Met) rs570016062 0.00003
NM_001191061.2(SLC25A22):c.15G>A (p.Gln5=) rs370880055 0.00003
NM_001191061.2(SLC25A22):c.654G>A (p.Ala218=) rs769899113 0.00003
NM_001191061.2(SLC25A22):c.708G>A (p.Gly236=) rs1246435430 0.00003
NM_001191061.2(SLC25A22):c.742+18C>T rs750077318 0.00003
NM_001191061.2(SLC25A22):c.743-15G>A rs780768183 0.00003
NM_001191061.2(SLC25A22):c.909G>A (p.Gln303=) rs756957992 0.00003
NM_001191061.2(SLC25A22):c.147-15del rs752991536 0.00002
NM_001191061.2(SLC25A22):c.54C>T (p.Ala18=) rs950168213 0.00002
NM_001191061.2(SLC25A22):c.-163-884C>T rs796053243 0.00001
NM_001191061.2(SLC25A22):c.-29C>T rs776639940 0.00001
NM_001191061.2(SLC25A22):c.146+20G>A rs533314464 0.00001
NM_001191061.2(SLC25A22):c.146+9G>A rs1205601942 0.00001
NM_001191061.2(SLC25A22):c.351G>A (p.Gln117=) rs377299330 0.00001
NM_001191061.2(SLC25A22):c.462G>T (p.Gly154=) rs955053926 0.00001
NM_001191061.2(SLC25A22):c.588-8C>T rs778856445 0.00001
NM_001191061.2(SLC25A22):c.609G>A (p.Val203=) rs751993115 0.00001
NM_001191061.2(SLC25A22):c.87C>T (p.Ile29=) rs138185663 0.00001
NM_001191061.2(SLC25A22):c.*20C>A rs796053237
NM_001191061.2(SLC25A22):c.-159G>A rs1554966277
NM_001191061.2(SLC25A22):c.-163-5_-163-4delinsCT rs1554966284
NM_001191061.2(SLC25A22):c.146+20G>T rs533314464
NM_001191061.2(SLC25A22):c.147-17T>C rs1057522785
NM_001191061.2(SLC25A22):c.203-12C>T rs1432924818
NM_001191061.2(SLC25A22):c.412+17G>A rs929871203
NM_001191061.2(SLC25A22):c.412+8C>G rs760438511
NM_001191061.2(SLC25A22):c.413-14C>G rs1554965634
NM_001191061.2(SLC25A22):c.413-7T>C rs969941249
NM_001191061.2(SLC25A22):c.413-8G>A rs376015598
NM_001191061.2(SLC25A22):c.587+17A>G rs1554965494
NM_001191061.2(SLC25A22):c.587+19G>A rs1057520368
NM_001191061.2(SLC25A22):c.587+26dup rs543775528
NM_001191061.2(SLC25A22):c.681G>C (p.Val227=) rs376895051
NM_001191061.2(SLC25A22):c.743-9C>T rs763707732
NM_001191061.2(SLC25A22):c.900C>T (p.Gly300=) rs1057522422

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