ClinVar Miner

List of variants in gene SLC12A5 reported as likely benign for not provided

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Gene type:
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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_020708.5(SLC12A5):c.1189A>T (p.Thr397Ser) rs34058554 0.00540
NM_020708.5(SLC12A5):c.96C>T (p.Thr32=) rs143969641 0.00212
NM_020708.5(SLC12A5):c.1695C>T (p.Phe565=) rs41282784 0.00044
NM_020708.5(SLC12A5):c.2376T>C (p.Ile792=) rs201525976 0.00032
NM_020708.5(SLC12A5):c.1989G>C (p.Gly663=) rs373648545 0.00029
NM_020708.5(SLC12A5):c.936G>A (p.Thr312=) rs150595305 0.00026
NM_020708.5(SLC12A5):c.942C>T (p.Thr314=) rs143072268 0.00026
NM_020708.5(SLC12A5):c.2499C>T (p.His833=) rs371925559 0.00011
NM_020708.5(SLC12A5):c.2430C>T (p.Asn810=) rs540937956 0.00010
NM_020708.5(SLC12A5):c.2259C>T (p.Gly753=) rs764791575 0.00002
NM_020708.5(SLC12A5):c.1740G>A (p.Thr580=) rs200135706 0.00001
NM_001134771.2(SLC12A5):c.121+1058GGA[16]
NM_020708.5(SLC12A5):c.*1031G>A rs2084720068
NM_020708.5(SLC12A5):c.*1040C>T
NM_020708.5(SLC12A5):c.*2010G>C rs150067894
NM_020708.5(SLC12A5):c.*989G>A
NM_020708.5(SLC12A5):c.1204C>T (p.Leu402=) rs1600597195
NM_020708.5(SLC12A5):c.1260C>A (p.Arg420=) rs1210104106
NM_020708.5(SLC12A5):c.1488T>C (p.Cys496=) rs1600598684
NM_020708.5(SLC12A5):c.1497G>A (p.Gly499=) rs1471957997
NM_020708.5(SLC12A5):c.1611C>T (p.Ala537=)
NM_020708.5(SLC12A5):c.1836C>T (p.Ile612=)
NM_020708.5(SLC12A5):c.2265C>A (p.Ser755=)
NM_020708.5(SLC12A5):c.2907G>A (p.Glu969=)
NM_020708.5(SLC12A5):c.3159C>T (p.Ala1053=)
NM_020708.5(SLC12A5):c.531G>C (p.Gly177=) rs1600592327

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