ClinVar Miner

List of variants in gene SLC22A5 reported as benign for not provided

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Gene type:
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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_003060.4(SLC22A5):c.1451-250A>C rs274549 0.74695
NM_003060.4(SLC22A5):c.285T>C (p.Leu95=) rs2631365 0.42203
NM_003060.4(SLC22A5):c.951+108C>T rs274555 0.41680
NM_003060.4(SLC22A5):c.807A>G (p.Leu269=) rs274558 0.39440
NM_003060.4(SLC22A5):c.652+77A>G rs274559 0.39418
NM_003060.4(SLC22A5):c.824+13T>C rs274557 0.39418
NM_003060.4(SLC22A5):c.497+236C>T rs274567 0.36490
NM_003060.4(SLC22A5):c.497+172_497+174dup rs3841486 0.27402
NM_003060.4(SLC22A5):c.652+270A>G rs635620 0.27334
NM_003060.4(SLC22A5):c.652+272G>A rs635619 0.27319
NM_003060.4(SLC22A5):c.*47C>T rs1045020 0.09512
NM_003060.4(SLC22A5):c.951+222C>T rs17689550 0.09253
NM_003060.4(SLC22A5):c.498-150G>T rs71583486 0.07751
NM_003060.4(SLC22A5):c.394-296C>T rs2073642 0.07739
NM_003060.4(SLC22A5):c.498-143C>G rs78399358 0.07340
NM_003060.4(SLC22A5):c.393+314C>T rs3788988 0.06992
NM_003060.4(SLC22A5):c.1052+101A>G rs2073645 0.06948
NM_003060.4(SLC22A5):c.1268-217G>C rs35295663 0.04956
NM_003060.4(SLC22A5):c.824+88C>G rs75999741 0.02893
NM_003060.4(SLC22A5):c.497+325G>A rs77123396 0.02888
NM_003060.4(SLC22A5):c.394-376C>G rs76127816 0.02453
NM_003060.4(SLC22A5):c.393+118C>A rs116370664 0.02359
NM_003060.4(SLC22A5):c.430C>T (p.Leu144Phe) rs10040427 0.02340
NM_003060.4(SLC22A5):c.1249A>G (p.Met417Val) rs139775414 0.00365
NM_003060.4(SLC22A5):c.59T>A (p.Leu20His) rs144020613 0.00362
NM_003060.4(SLC22A5):c.1368A>G (p.Thr456=) rs142355575 0.00335
NM_003060.4(SLC22A5):c.1590G>T (p.Met530Ile) rs148233131 0.00335
NM_003060.4(SLC22A5):c.414C>T (p.Asp138=) rs150705788 0.00059
NM_003060.4(SLC22A5):c.*92del rs142209594
NM_003060.4(SLC22A5):c.1052+237T>C rs274554
NM_003060.4(SLC22A5):c.1053-144C>T rs75495463
NM_003060.4(SLC22A5):c.393+232G>A rs3788987
NM_003060.4(SLC22A5):c.652+6= rs4551059

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