ClinVar for Gene (Select 115286) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3341697	NM_001379210.1(SLC25A26):c.707+687G>A	SLC25A26	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3319219	NM_001379210.1(SLC25A26):c.487G>A (p.Glu163Lys)	SLC25A26 (E163K +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3319218	NM_001379210.1(SLC25A26):c.604G>A (p.Val202Met)	SLC25A26 (V187M +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3252887	NM_001379210.1(SLC25A26):c.781C>T (p.Arg261Ter)	SLC25A26 (R158* +3 more)	Single nucleotide variant (nonsense +2 more)	not provided	GUncertain significance
Select item 3163662	NM_001379210.1(SLC25A26):c.69A>G (p.Ile23Met)	SLC25A26 (I23M)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 3163661	NM_001379210.1(SLC25A26):c.694C>A (p.Gln232Lys)	SLC25A26 (Q232K +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3163660	NM_001379210.1(SLC25A26):c.650C>A (p.Ala217Asp)	SLC25A26 (A202D +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3163659	NM_001379210.1(SLC25A26):c.401A>T (p.Glu134Val)	SLC25A26 (E134V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3163658	NM_001379210.1(SLC25A26):c.313A>C (p.Ile105Leu)	SLC25A26 (I105L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3163657	NM_001379210.1(SLC25A26):c.108T>A (p.Ser36Arg)	SLC25A26 (S36R)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 3064904	NM_001379210.1(SLC25A26):c.727C>T (p.Pro243Ser)	SLC25A26 (P140S +3 more)	Single nucleotide variant (missense variant +2 more)	Combined oxidative phosphorylation deficiency 28	GUncertain significance
Select item 3054590	NM_001379210.1(SLC25A26):c.156C>T (p.Gly52=)	SLC25A26	Single nucleotide variant (synonymous variant +3 more)	SLC25A26-related disorder	GLikely benign
Select item 3045209	NM_001379210.1(SLC25A26):c.42G>A (p.Gly14=)	SLC25A26	Single nucleotide variant (synonymous variant +3 more)	SLC25A26-related disorder	GLikely benign
Select item 2969745	NM_001379210.1(SLC25A26):c.454-12T>C	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960556	NM_001379210.1(SLC25A26):c.569-13A>G	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2896202	NM_001379210.1(SLC25A26):c.708-8T>C	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2891174	NM_001379210.1(SLC25A26):c.707+7C>T	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2821404	NM_001379210.1(SLC25A26):c.454-4T>C	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2722334	NM_001379210.1(SLC25A26):c.708-7C>T	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2706195	NM_001379210.1(SLC25A26):c.801G>A (p.Leu267=)	SLC25A26	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GLikely benign
Select item 2691394	NC_000003.11:g.(?_66119284)_(66429348_?)dup	LRIG1, SLC25A26	Duplication	not specified	GUncertain significance
Select item 2637851	NM_001379210.1(SLC25A26):c.-13G>A	SLC25A26	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2637850	NM_001379210.1(SLC25A26):c.191-1G>T	SLC25A26	Single nucleotide variant (splice acceptor variant)	Combined oxidative phosphorylation deficiency 28	GLikely pathogenic
Select item 2606065	NM_001379210.1(SLC25A26):c.157G>A (p.Val53Ile)	SLC25A26 (V53I)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2549098	NM_001379210.1(SLC25A26):c.814A>G (p.Lys272Glu)	SLC25A26 (K184E +3 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GLikely benign
Select item 2548379	NM_001379210.1(SLC25A26):c.485G>C (p.Trp162Ser)	SLC25A26 (W162S +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2534004	NM_001379210.1(SLC25A26):c.172A>G (p.Ile58Val)	SLC25A26 (I58V)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GLikely benign
Select item 2521054	NM_001379210.1(SLC25A26):c.689G>A (p.Arg230Gln)	SLC25A26 (R127Q +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2478552	NM_001379210.1(SLC25A26):c.727C>A (p.Pro243Thr)	SLC25A26 (P228T +3 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2472208	NM_001379210.1(SLC25A26):c.148T>C (p.Tyr50His)	SLC25A26 (Y50H)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2471250	NM_001379210.1(SLC25A26):c.88A>G (p.Ile30Val)	SLC25A26 (I30V)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2469606	NM_001379210.1(SLC25A26):c.265A>G (p.Met89Val)	SLC25A26 (M89V +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GLikely benign
Select item 2423906	NC_000003.11:g.(?_65762253)_(66313823_?)dup	MAGI1, SLC25A26	Duplication	not provided	GUncertain significance
Select item 2377618	NM_001379210.1(SLC25A26):c.4G>T (p.Asp2Tyr)	SLC25A26 (D2Y)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2284160	NM_001379210.1(SLC25A26):c.424C>T (p.Arg142Ter)	SLC25A26 (R54* +1 more)	Single nucleotide variant (nonsense +1 more)	Inborn genetic diseases	GPathogenic
Select item 2262733	NM_001379210.1(SLC25A26):c.746G>T (p.Ser249Ile)	SLC25A26 (S234I +3 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2246226	NM_001379210.1(SLC25A26):c.386C>G (p.Ser129Cys)	SLC25A26 (S41C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2238671	NM_001379210.1(SLC25A26):c.196G>A (p.Ala66Thr)	SLC25A26 (A66T)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2231724	NM_001379210.1(SLC25A26):c.155G>A (p.Gly52Asp)	SLC25A26 (G52D)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2231371	NM_001379210.1(SLC25A26):c.425G>A (p.Arg142Gln)	SLC25A26 (R142Q +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2230912	NM_001379210.1(SLC25A26):c.634-3C>A	SLC25A26	Single nucleotide variant (intron variant)	Inborn genetic diseases	GUncertain significance
Select item 2175441	NM_001379210.1(SLC25A26):c.568+6A>C	SLC25A26	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2068282	NM_001379210.1(SLC25A26):c.721G>A (p.Val241Ile)	SLC25A26 (V226I +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign/Likely benign
Select item 2053502	NM_001379210.1(SLC25A26):c.285C>G (p.Ala95=)	SLC25A26	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2049218	NM_001379210.1(SLC25A26):c.367A>G (p.Arg123Gly)	SLC25A26 (R123G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2046990	NM_001379210.1(SLC25A26):c.603C>T (p.Asp201=)	SLC25A26	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2032995	NM_001379210.1(SLC25A26):c.720del (p.Val241fs)	SLC25A26 (V138fs +3 more)	Deletion (frameshift variant +2 more)	not provided	GUncertain significance
Select item 2028324	NM_001379210.1(SLC25A26):c.501C>T (p.Ala167=)	SLC25A26	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2018181	NM_001379210.1(SLC25A26):c.377A>C (p.Gln126Pro)	SLC25A26 (Q38P +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1959661	NM_001379210.1(SLC25A26):c.634-15T>C	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1932321	NM_001379210.1(SLC25A26):c.405+11T>G	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1912327	NM_001379210.1(SLC25A26):c.634-15T>G	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1907004	NM_001379210.1(SLC25A26):c.405+11T>C	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1902306	NM_001379210.1(SLC25A26):c.666C>T (p.Leu222=)	SLC25A26	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1896368	NM_001379210.1(SLC25A26):c.406-19G>A	SLC25A26	Single nucleotide variant (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1723103	NM_001379210.1(SLC25A26):c.287C>G (p.Ser96Cys)	SLC25A26 (S8C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1706542	NM_001379210.1(SLC25A26):c.581C>A (p.Ala194Asp)	SLC25A26 (A106D +3 more)	Single nucleotide variant (missense variant +1 more)	Hypokalemic periodic paralysis, type 1	GUncertain significance
Select item 1703519	NM_001379210.1(SLC25A26):c.554G>A (p.Cys185Tyr)	SLC25A26 (C170Y +3 more)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation deficiency 28	GUncertain significance
Select item 1703515	NM_001379210.1(SLC25A26):c.719G>T (p.Gly240Val)	SLC25A26 (G137V +3 more)	Single nucleotide variant (missense variant +2 more)	Combined oxidative phosphorylation deficiency 28	GUncertain significance
Select item 1700559	NM_001379210.1(SLC25A26):c.431A>G (p.Tyr144Cys)	SLC25A26 (Y144C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1700531	NM_001379210.1(SLC25A26):c.547G>T (p.Ala183Ser)	SLC25A26 (A168S +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1677970	NM_001379210.1(SLC25A26):c.386C>A (p.Ser129Tyr)	SLC25A26 (S129Y +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1631538	NM_001379210.1(SLC25A26):c.406-20C>T	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1602407	NM_001379210.1(SLC25A26):c.707+11G>T	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1446284	NM_001379210.1(SLC25A26):c.818G>C (p.Ser273Thr)	SLC25A26 (S185T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1430019	NM_001379210.1(SLC25A26):c.298G>A (p.Val100Met)	SLC25A26 (V100M +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1424598	NM_001379210.1(SLC25A26):c.370A>G (p.Thr124Ala)	SLC25A26 (T124A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1346874	NM_001379210.1(SLC25A26):c.362C>T (p.Ser121Phe)	SLC25A26 (S33F +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1334372	NM_001379210.1(SLC25A26):c.34-4A>G	SLC25A26	Single nucleotide variant (intron variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1320563	NM_001379210.1(SLC25A26):c.34-220A>G	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1318440	NM_001379210.1(SLC25A26):c.499-81C>G	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1318363	NM_001379210.1(SLC25A26):c.498+308GT[25]	SLC25A26	Microsatellite (intron variant)	not provided	GLikely benign
Select item 1317386	NM_001379210.1(SLC25A26):c.45A>G (p.Val15=)	SLC25A26	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1317015	NM_001379210.1(SLC25A26):c.33+192C>T	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316880	NM_001379210.1(SLC25A26):c.568+153dup	SLC25A26	Duplication (intron variant)	not provided	GLikely benign
Select item 1316865	NM_001379210.1(SLC25A26):c.33+48C>T	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316806	NM_001379210.1(SLC25A26):c.33G>A (p.Val11=)	SLC25A26	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1316778	NM_173471.4(SLC25A26):c.-150G>T	LOC129936986, SLC25A26	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1316753	NM_001379210.1(SLC25A26):c.190+10T>C	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316695	NM_001379210.1(SLC25A26):c.34-271T>G	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316688	NM_001379210.1(SLC25A26):c.569-288T>A	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316216	NM_001379210.1(SLC25A26):c.301-129del	SLC25A26	Deletion (intron variant)	not provided	GLikely benign
Select item 1315924	NM_173471.4(SLC25A26):c.-198C>G	SLC25A26	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 1288427	NM_001379210.1(SLC25A26):c.*3C>A	SLC25A26	Single nucleotide variant (3 prime UTR variant +1 more)	Combined oxidative phosphorylation deficiency 28 +1 more	GBenign
Select item 1287481	NM_001379210.1(SLC25A26):c.568+168del	SLC25A26	Deletion (intron variant)	not provided	GBenign
Select item 1287365	NM_001379210.1(SLC25A26):c.634-91C>T	SLC25A26	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283584	NM_001379210.1(SLC25A26):c.498+308GT[22]	SLC25A26	Microsatellite (intron variant)	not provided	GBenign
Select item 1281588	NM_001379210.1(SLC25A26):c.301-307T>C	SLC25A26	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263240	NM_001379210.1(SLC25A26):c.*51C>T	SLC25A26	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1258372	NM_001379210.1(SLC25A26):c.569-106_569-99del	SLC25A26	Deletion (intron variant)	not provided	GBenign
Select item 1255170	NM_001379210.1(SLC25A26):c.*219G>A	SLC25A26	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1245030	NM_001379210.1(SLC25A26):c.568+168dup	SLC25A26	Duplication (intron variant)	not provided	GBenign
Select item 1241140	NM_001379210.1(SLC25A26):c.569-292T>C	SLC25A26	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225345	NM_173471.4(SLC25A26):c.-223C>A	SLC25A26	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GBenign
Select item 1181217	NM_001379210.1(SLC25A26):c.633+289A>T	SLC25A26	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1174475	NM_001379210.1(SLC25A26):c.498+308GT[24]	SLC25A26	Microsatellite (intron variant)	not provided	GBenign
Select item 1174317	NM_001379210.1(SLC25A26):c.406-156C>A	SLC25A26	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 756061	NM_001379210.1(SLC25A26):c.417G>T (p.Gly139=)	SLC25A26	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 756025	NM_001379210.1(SLC25A26):c.677A>G (p.His226Arg)	SLC25A26 (H138R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 748302	NM_001379210.1(SLC25A26):c.707+7C>G	SLC25A26	Single nucleotide variant (intron variant)	not provided	GLikely benign

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