ClinVar Miner

List of variants in gene SLMAP reported as uncertain significance for Brugada syndrome

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_007159.4(SLMAP):c.1063G>A (p.Glu355Lys) rs149548827
NM_007159.4(SLMAP):c.1131_1132delinsCA (p.Leu377_Gln378delinsPheLys)
NM_007159.4(SLMAP):c.1168A>G (p.Thr390Ala) rs746146243
NM_007159.4(SLMAP):c.1182A>G (p.Gln394=)
NM_007159.4(SLMAP):c.1280A>C (p.Glu427Ala) rs901233405
NM_007159.4(SLMAP):c.1330G>A (p.Asp444Asn) rs1016820088
NM_007159.4(SLMAP):c.1522+1G>T rs140490085
NM_007159.4(SLMAP):c.1918+5A>G
NM_007159.4(SLMAP):c.1940A>G (p.Lys647Arg) rs150439110
NM_007159.4(SLMAP):c.2085A>G (p.Gln695=)
NM_007159.4(SLMAP):c.2292G>T (p.Glu764Asp) rs750893840
NM_007159.4(SLMAP):c.2300A>G (p.Gln767Arg) rs142778041
NM_007159.4(SLMAP):c.2329G>C (p.Glu777Gln) rs751083292
NM_007159.4(SLMAP):c.347-1G>T rs1060503190
NM_007159.4(SLMAP):c.407G>A (p.Arg136Gln) rs142516364
NM_007159.4(SLMAP):c.563C>T (p.Thr188Met) rs763740777
NM_007159.4(SLMAP):c.572G>A (p.Arg191Gln)
NM_007159.4(SLMAP):c.646C>T (p.Arg216Trp)
NM_007159.4(SLMAP):c.652G>A (p.Glu218Lys)
NM_007159.4(SLMAP):c.703A>G (p.Ser235Gly)
NM_007159.4(SLMAP):c.722T>C (p.Ile241Thr)
NM_007159.4(SLMAP):c.928G>A (p.Ala310Thr) rs754387957

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