ClinVar Miner

List of variants in gene KCNJ10 reported as uncertain significance by Ambry Genetics

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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_002241.5(KCNJ10):c.136G>A (p.Asp46Asn) rs141553756 0.00146
NM_002241.5(KCNJ10):c.530A>G (p.Glu177Gly) rs145947380 0.00043
NM_002241.5(KCNJ10):c.52C>T (p.Arg18Trp) rs138457635 0.00041
NM_002241.5(KCNJ10):c.1043G>A (p.Arg348His) rs146396982 0.00034
NM_002241.5(KCNJ10):c.1061A>G (p.Lys354Arg) rs142596580 0.00029
NM_002241.5(KCNJ10):c.301C>A (p.Pro101Thr) rs375361490 0.00011
NM_002241.5(KCNJ10):c.512G>A (p.Arg171Gln) rs200320916 0.00005
NM_002241.5(KCNJ10):c.1124G>A (p.Arg375His) rs189596680 0.00004
NM_002241.5(KCNJ10):c.10G>A (p.Val4Ile) rs144428351 0.00003
NM_002241.5(KCNJ10):c.506T>C (p.Ile169Thr) rs777546233 0.00003
NM_002241.5(KCNJ10):c.80G>A (p.Arg27Gln) rs776766074 0.00003
NM_002241.5(KCNJ10):c.241C>T (p.Leu81Phe) rs939420346 0.00002
NM_002241.5(KCNJ10):c.541T>C (p.Phe181Leu) rs374746230 0.00002
NM_002241.5(KCNJ10):c.1033A>G (p.Ser345Gly) rs752571720 0.00001
NM_002241.5(KCNJ10):c.115G>A (p.Val39Met) rs1274663711 0.00001
NM_002241.5(KCNJ10):c.133G>A (p.Ala45Thr) rs750246232 0.00001
NM_002241.5(KCNJ10):c.179T>C (p.Ile60Thr) rs759993423 0.00001
NM_002241.5(KCNJ10):c.250G>A (p.Val84Met) rs140646329 0.00001
NM_002241.5(KCNJ10):c.538C>T (p.Arg180Cys) rs557187094 0.00001
NM_002241.5(KCNJ10):c.76C>T (p.Arg26Ter) rs138943405 0.00001
NM_002241.5(KCNJ10):c.1006G>C (p.Val336Leu) rs1085307763
NM_002241.5(KCNJ10):c.130A>G (p.Ile44Val)
NM_002241.5(KCNJ10):c.248G>C (p.Gly83Ala) rs17853258
NM_002241.5(KCNJ10):c.300C>A (p.Asp100Glu) rs139069413
NM_002241.5(KCNJ10):c.629G>A (p.Gly210Asp)
NM_002241.5(KCNJ10):c.62T>C (p.Met21Thr) rs878854483
NM_002241.5(KCNJ10):c.814A>G (p.Ser272Gly)
NM_002241.5(KCNJ10):c.880T>C (p.Cys294Arg) rs2101924693
NM_002241.5(KCNJ10):c.904C>T (p.Pro302Ser)
NM_002241.5(KCNJ10):c.934_935delinsTT (p.Thr312Leu) rs1571265205
NM_002241.5(KCNJ10):c.953C>T (p.Ser318Leu)

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