ClinVar Miner

List of variants in gene KCNJ8 reported as likely benign for Brugada syndrome

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_004982.4(KCNJ8):c.1265C>T (p.Ser422Leu) rs72554071 0.00121
NM_004982.4(KCNJ8):c.1036G>A (p.Val346Ile) rs147316959 0.00032
NM_004982.4(KCNJ8):c.138G>T (p.Ala46=) rs568067955 0.00007
NM_004982.4(KCNJ8):c.144G>A (p.Lys48=) rs368274950 0.00007
NM_004982.4(KCNJ8):c.600C>T (p.Ala200=) rs755870233 0.00006
NM_004982.4(KCNJ8):c.870G>A (p.Leu290=) rs549973587 0.00005
NM_004982.4(KCNJ8):c.807C>T (p.His269=) rs745683723 0.00004
NM_004982.4(KCNJ8):c.1266G>A (p.Ser422=) rs772569559 0.00003
NM_004982.4(KCNJ8):c.588T>C (p.His196=) rs373707000 0.00003
NM_004982.4(KCNJ8):c.189C>T (p.Thr63=) rs375355931 0.00002
NM_004982.4(KCNJ8):c.12A>G (p.Arg4=) rs775249538 0.00001
NM_004982.4(KCNJ8):c.225C>T (p.Ile75=) rs1940806660 0.00001
NM_004982.4(KCNJ8):c.243C>T (p.Leu81=) rs771727850 0.00001
NM_004982.4(KCNJ8):c.352A>G (p.Thr118Ala) rs761526890 0.00001
NM_004982.4(KCNJ8):c.720G>A (p.Val240=) rs876661349 0.00001
NM_004982.4(KCNJ8):c.1066C>A (p.Arg356=) rs778531267
NM_004982.4(KCNJ8):c.1104C>T (p.Thr368=)
NM_004982.4(KCNJ8):c.1122G>A (p.Leu374=)
NM_004982.4(KCNJ8):c.1143G>A (p.Arg381=)
NM_004982.4(KCNJ8):c.1257A>G (p.Gln419=) rs751945188
NM_004982.4(KCNJ8):c.132C>T (p.Asn44=)
NM_004982.4(KCNJ8):c.198C>T (p.Asp66=) rs2137051977
NM_004982.4(KCNJ8):c.306T>C (p.Tyr102=) rs752928813
NM_004982.4(KCNJ8):c.36T>C (p.Tyr12=) rs1482460942
NM_004982.4(KCNJ8):c.374+8T>C
NM_004982.4(KCNJ8):c.45G>A (p.Ala15=) rs1162681542
NM_004982.4(KCNJ8):c.471G>C (p.Thr157=) rs143319002
NM_004982.4(KCNJ8):c.483C>T (p.Leu161=)
NM_004982.4(KCNJ8):c.642C>T (p.Asp214=) rs2137047449
NM_004982.4(KCNJ8):c.648G>A (p.Arg216=) rs2137047441
NM_004982.4(KCNJ8):c.66G>A (p.Leu22=)
NM_004982.4(KCNJ8):c.717G>A (p.Glu239=)
NM_004982.4(KCNJ8):c.735A>G (p.Gln245=)
NM_004982.4(KCNJ8):c.762C>A (p.Ile254=)
NM_004982.4(KCNJ8):c.789C>T (p.Ala263=)
NM_004982.4(KCNJ8):c.819G>A (p.Lys273=) rs1940614320
NM_004982.4(KCNJ8):c.969C>A (p.Arg323=) rs1311193970

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