ClinVar Miner

List of variants in gene OAT reported by Natera, Inc.

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_000274.4(OAT):c.1134C>T (p.Asn378=) rs11461 0.34766
NM_000274.4(OAT):c.969C>T (p.Tyr323=) rs138895801 0.00105
NM_000274.4(OAT):c.1224T>C (p.His408=) rs201864147 0.00071
NM_000274.4(OAT):c.48C>T (p.Arg16=) rs143526711 0.00070
NM_000274.4(OAT):c.1311G>T (p.Leu437Phe) rs1800456 0.00054
NM_000274.4(OAT):c.900+9C>A rs372834151 0.00035
NM_000274.4(OAT):c.1015-6A>G rs561800688 0.00028
NM_000274.4(OAT):c.107G>C (p.Gly36Ala) rs140786333 0.00018
NM_000274.4(OAT):c.915G>T (p.Leu305=) rs1249516048 0.00018
NM_000274.4(OAT):c.478G>A (p.Val160Met) rs148433929 0.00013
NM_000274.4(OAT):c.517G>A (p.Ala173Thr) rs372152657 0.00013
NM_000274.4(OAT):c.546G>T (p.Leu182Phe) rs144763058 0.00013
NM_000274.4(OAT):c.1015-5C>T rs764963374 0.00009
NM_000274.4(OAT):c.1291A>G (p.Ile431Val) rs138709143 0.00009
NM_000274.4(OAT):c.1305C>T (p.Thr435=) rs528039246 0.00009
NM_000274.4(OAT):c.283C>T (p.Pro95Ser) rs372105047 0.00008
NM_000274.4(OAT):c.1110C>T (p.Ala370=) rs148325838 0.00007
NM_000274.4(OAT):c.1250C>T (p.Pro417Leu) rs121965044 0.00005
NM_000274.4(OAT):c.582C>T (p.Tyr194=) rs754489812 0.00005
NM_000274.4(OAT):c.1228G>A (p.Asp410Asn) rs745530000 0.00004
NM_000274.4(OAT):c.1187G>A (p.Arg396Gln) rs776819570 0.00003
NM_000274.4(OAT):c.897C>G (p.Tyr299Ter) rs121965057 0.00003
NM_000274.4(OAT):c.1068G>T (p.Leu356Phe) rs768685095 0.00002
NM_000274.4(OAT):c.1255G>C (p.Val419Leu) rs760922693 0.00002
NM_000274.4(OAT):c.202A>G (p.Ile68Val) rs766674632 0.00002
NM_000274.4(OAT):c.785C>A (p.Ala262Asp) rs772762366 0.00002
NM_000274.4(OAT):c.816T>C (p.Thr272=) rs778561122 0.00002
NM_000274.4(OAT):c.1192C>T (p.Arg398Ter) rs200068769 0.00001
NM_000274.4(OAT):c.1286T>C (p.Ile429Thr) rs774831749 0.00001
NM_000274.4(OAT):c.149A>G (p.Tyr50Cys) rs936463102 0.00001
NM_000274.4(OAT):c.303G>A (p.Leu101=) rs569605240 0.00001
NM_000274.4(OAT):c.352A>G (p.Asn118Asp) rs367710098 0.00001
NM_000274.4(OAT):c.416T>G (p.Met139Arg) rs1043163922 0.00001
NM_000274.4(OAT):c.49G>A (p.Gly17Arg) rs760716065 0.00001
NM_000274.4(OAT):c.606G>A (p.Pro202=) rs369806549 0.00001
NM_000274.4(OAT):c.800C>T (p.Thr267Ile) rs386833618 0.00001
NM_000274.4(OAT):c.823T>A (p.Trp275Arg) rs947658691 0.00001
NM_000274.4(OAT):c.952G>A (p.Glu318Lys) rs386833621 0.00001
NM_000274.4(OAT):c.991C>T (p.Arg331Ter) rs386833623 0.00001
NM_000274.4(OAT):c.1138A>G (p.Ile380Val) rs545710763
NM_000274.4(OAT):c.116C>T (p.Thr39Ile) rs754764229
NM_000274.4(OAT):c.1276C>T (p.Arg426Ter) rs121965058
NM_000274.4(OAT):c.159del (p.His53fs) rs386833599
NM_000274.4(OAT):c.192_193del (p.Gly65fs) rs386833600
NM_000274.4(OAT):c.199+5G>A rs1564739598
NM_000274.4(OAT):c.413C>T (p.Pro138Leu) rs1951673489
NM_000274.4(OAT):c.43A>T (p.Ser15Cys) rs1453312313
NM_000274.4(OAT):c.521-6T>G rs369018496
NM_000274.4(OAT):c.614A>G (p.Asp205Gly) rs375157197
NM_000274.4(OAT):c.627T>A (p.Tyr209Ter) rs121965056
NM_000274.4(OAT):c.966A>T (p.Thr322=) rs1951417723

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