ClinVar Miner

List of variants in gene SLC25A38 studied for anemia (disease)

Included ClinVar conditions (262):
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Gene type:
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Total variants: 38
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HGVS dbSNP
NM_017875.4(SLC25A38):c.*304C>T rs113251543
NM_017875.4(SLC25A38):c.*310A>T rs12991
NM_017875.4(SLC25A38):c.*370C>T rs886058472
NM_017875.4(SLC25A38):c.*404G>A rs886058473
NM_017875.4(SLC25A38):c.*431G>A rs73058292
NM_017875.4(SLC25A38):c.*472G>T rs141567816
NM_017875.4(SLC25A38):c.*490G>A rs150889211
NM_017875.4(SLC25A38):c.*588T>A rs6890
NM_017875.4(SLC25A38):c.*642del rs34288981
NM_017875.4(SLC25A38):c.*809C>T rs71325527
NM_017875.4(SLC25A38):c.-161G>A rs528990278
NM_017875.4(SLC25A38):c.-209A>G rs143903497
NM_017875.4(SLC25A38):c.-219T>C rs886058469
NM_017875.4(SLC25A38):c.-225G>A rs370977005
NM_017875.4(SLC25A38):c.-227G>A rs886058468
NM_017875.4(SLC25A38):c.-237G>A rs527536267
NM_017875.4(SLC25A38):c.-292G>A rs142441701
NM_017875.4(SLC25A38):c.-303A>C rs114422738
NM_017875.4(SLC25A38):c.-325G>C rs886058467
NM_017875.4(SLC25A38):c.-69C>T rs886058470
NM_017875.4(SLC25A38):c.12C>T (p.Asn4=) rs142420345
NM_017875.4(SLC25A38):c.161G>A (p.Arg54His) rs144319567
NM_017875.4(SLC25A38):c.165G>A (p.Leu55=) rs2270770
NM_017875.4(SLC25A38):c.239C>G (p.Thr80Arg) rs144149294
NM_017875.4(SLC25A38):c.277-1G>A rs869312029
NM_017875.4(SLC25A38):c.288A>G (p.Arg96=) rs765578993
NM_017875.4(SLC25A38):c.320_321CT[2] (p.Tyr109fs) rs869320719
NM_017875.4(SLC25A38):c.349C>T (p.Arg117Ter) rs121918330
NM_017875.4(SLC25A38):c.382A>G (p.Met128Val) rs146940902
NM_017875.4(SLC25A38):c.400C>T (p.Arg134Cys) rs1293528130
NM_017875.4(SLC25A38):c.446C>T (p.Thr149Met) rs143865753
NM_017875.4(SLC25A38):c.462G>A (p.Gly154=) rs369980078
NM_017875.4(SLC25A38):c.560G>C (p.Arg187Pro) rs121918331
NM_017875.4(SLC25A38):c.570C>A (p.Pro190=) rs886058471
NM_017875.4(SLC25A38):c.625G>C (p.Asp209His) rs146864395
NM_017875.4(SLC25A38):c.652A>T (p.Ile218Phe) rs764125735
NM_017875.4(SLC25A38):c.70-2A>C rs1233124208
NM_017875.4(SLC25A38):c.790A>T (p.Lys264Ter) rs121918332

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