ClinVar Miner

List of variants in gene SLC25A38 studied for X-linked disease

Included ClinVar conditions (313):
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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_017875.4(SLC25A38):c.*304C>T rs113251543
NM_017875.4(SLC25A38):c.*472G>T rs141567816
NM_017875.4(SLC25A38):c.*490G>A rs150889211
NM_017875.4(SLC25A38):c.*642del rs34288981
NM_017875.4(SLC25A38):c.*809C>T rs71325527
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.239C>G (p.Thr80Arg) rs144149294
NM_017875.4(SLC25A38):c.382A>G (p.Met128Val) rs146940902
NM_017875.4(SLC25A38):c.446C>T (p.Thr149Met) rs143865753
NM_017875.4(SLC25A38):c.462G>A (p.Gly154=) rs369980078

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