ClinVar Miner

List of variants in gene NR2F1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 132
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HGVS dbSNP gnomAD frequency
NM_005654.6(NR2F1):c.-187G>A rs866080178 0.02747
NM_005654.6(NR2F1):c.-1588T>C rs76981368 0.01884
NM_005654.6(NR2F1):c.463+99C>G rs533917207 0.00374
NM_005654.6(NR2F1):c.237G>C (p.Gln79His) rs199844882 0.00054
NM_005654.6(NR2F1):c.993C>T (p.Asp331=) rs202243427 0.00032
NM_005654.6(NR2F1):c.192C>T (p.Pro64=) rs747522225 0.00026
NM_005654.6(NR2F1):c.708C>T (p.Asn236=) rs372227484 0.00020
NM_005654.6(NR2F1):c.903C>A (p.Ile301=) rs750683610 0.00015
NM_005654.6(NR2F1):c.811C>T (p.Leu271=) rs777533706 0.00012
NM_005654.6(NR2F1):c.1008G>A (p.Ser336=) rs145104274 0.00005
NM_005654.6(NR2F1):c.40G>T (p.Asp14Tyr) rs1193147148 0.00005
NM_005654.6(NR2F1):c.505G>A (p.Gly169Ser) rs370606773 0.00005
NM_005654.6(NR2F1):c.1014G>A (p.Ala338=) rs201229023 0.00004
NM_005654.6(NR2F1):c.464-19C>T rs904035084 0.00004
NM_005654.6(NR2F1):c.48C>T (p.Ala16=) rs780151168 0.00004
NM_005654.6(NR2F1):c.756A>G (p.Leu252=) rs547985564 0.00004
NM_005654.6(NR2F1):c.1050C>T (p.Cys350=) rs530910180 0.00003
NM_005654.6(NR2F1):c.1149C>T (p.Ser383=) rs144876856 0.00003
NM_005654.6(NR2F1):c.183C>T (p.Pro61=) rs1054029785 0.00003
NM_005654.6(NR2F1):c.558C>T (p.Ser186=) rs773102110 0.00003
NM_005654.6(NR2F1):c.1023C>T (p.Ile341=) rs776732958 0.00002
NM_005654.6(NR2F1):c.1212C>T (p.Arg404=) rs761244180 0.00002
NM_005654.6(NR2F1):c.465G>T (p.Ala155=) rs372471207 0.00002
NM_005654.6(NR2F1):c.540C>T (p.Asn180=) rs747863258 0.00002
NM_005654.6(NR2F1):c.63C>A (p.Gly21=) rs1432991015 0.00002
NM_005654.6(NR2F1):c.1170C>T (p.Phe390=) rs1420094450 0.00001
NM_005654.6(NR2F1):c.1219T>C (p.Leu407=) rs750040062 0.00001
NM_005654.6(NR2F1):c.153G>A (p.Thr51=) rs1057522243 0.00001
NM_005654.6(NR2F1):c.204G>A (p.Gly68=) rs1401241589 0.00001
NM_005654.6(NR2F1):c.20G>A (p.Ser7Asn) rs1753203799 0.00001
NM_005654.6(NR2F1):c.276G>A (p.Lys92=) rs906581747 0.00001
NM_005654.6(NR2F1):c.463+5A>G rs747394434 0.00001
NM_005654.6(NR2F1):c.666G>A (p.Leu222=) rs764266826 0.00001
NM_005654.6(NR2F1):c.681C>T (p.Leu227=) rs751683829 0.00001
NM_005654.6(NR2F1):c.765C>G (p.Thr255=) rs778504524 0.00001
NM_005654.6(NR2F1):c.891C>T (p.Asp297=) rs774531602 0.00001
NM_005654.6(NR2F1):c.987G>A (p.Thr329=) rs757861079 0.00001
NM_005654.6(NR2F1):c.-1751CT[11] rs140194624
NM_005654.6(NR2F1):c.-1761A>G
NM_005654.6(NR2F1):c.1017C>G (p.Ala339=)
NM_005654.6(NR2F1):c.1023C>A (p.Ile341=)
NM_005654.6(NR2F1):c.102C>T (p.Gly34=)
NM_005654.6(NR2F1):c.1044G>A (p.Ser348=) rs142689077
NM_005654.6(NR2F1):c.1044G>T (p.Ser348=)
NM_005654.6(NR2F1):c.1065C>T (p.Tyr355=)
NM_005654.6(NR2F1):c.107_115dup (p.Gly36_Gly38dup) rs1414612574
NM_005654.6(NR2F1):c.1086C>T (p.Asn362=)
NM_005654.6(NR2F1):c.1092C>T (p.Pro364=)
NM_005654.6(NR2F1):c.110_115dup (p.Ala37_Gly38dup) rs1159055932
NM_005654.6(NR2F1):c.1111C>T (p.Leu371=)
NM_005654.6(NR2F1):c.111C>G (p.Ala37=) rs1183108440
NM_005654.6(NR2F1):c.112G>T (p.Gly38Cys)
NM_005654.6(NR2F1):c.1134C>A (p.Arg378=) rs755004144
NM_005654.6(NR2F1):c.1134C>T (p.Arg378=)
NM_005654.6(NR2F1):c.1140G>A (p.Val380=)
NM_005654.6(NR2F1):c.1146C>T (p.Ser382=)
NM_005654.6(NR2F1):c.114C>A (p.Gly38=)
NM_005654.6(NR2F1):c.114C>T (p.Gly38=) rs986172152
NM_005654.6(NR2F1):c.1155C>T (p.Ile385=)
NM_005654.6(NR2F1):c.1212C>A (p.Arg404=)
NM_005654.6(NR2F1):c.1231A>G (p.Ser411Gly)
NM_005654.6(NR2F1):c.123G>A (p.Gln41=)
NM_005654.6(NR2F1):c.1262A>C (p.Gln421Pro)
NM_005654.6(NR2F1):c.1263G>A (p.Gln421=)
NM_005654.6(NR2F1):c.138G>C (p.Ser46=)
NM_005654.6(NR2F1):c.14T>C (p.Val5Ala)
NM_005654.6(NR2F1):c.165G>A (p.Pro55=)
NM_005654.6(NR2F1):c.165G>C (p.Pro55=) rs772383390
NM_005654.6(NR2F1):c.174C>A (p.Pro58=) rs1191057648
NM_005654.6(NR2F1):c.189C>T (p.Thr63=) rs1753208796
NM_005654.6(NR2F1):c.198G>A (p.Thr66=)
NM_005654.6(NR2F1):c.231G>C (p.Ser77=) rs1234276128
NM_005654.6(NR2F1):c.246G>A (p.Gln82=)
NM_005654.6(NR2F1):c.279G>T (p.Ser93=) rs774052702
NM_005654.6(NR2F1):c.282C>T (p.Ser94=)
NM_005654.6(NR2F1):c.288G>A (p.Lys96=) rs1580358607
NM_005654.6(NR2F1):c.29A>G (p.Asp10Gly)
NM_005654.6(NR2F1):c.303C>T (p.Phe101=)
NM_005654.6(NR2F1):c.351C>T (p.Asn117=) rs1329040695
NM_005654.6(NR2F1):c.376A>C (p.Arg126=) rs2149941634
NM_005654.6(NR2F1):c.384T>C (p.Cys128=)
NM_005654.6(NR2F1):c.393C>T (p.Asp131=)
NM_005654.6(NR2F1):c.414C>T (p.Cys138=) rs1753212998
NM_005654.6(NR2F1):c.429C>T (p.Leu143=) rs2149941661
NM_005654.6(NR2F1):c.463+13_463+15del
NM_005654.6(NR2F1):c.463+7A>G
NM_005654.6(NR2F1):c.464-11_464-8del rs769788437
NM_005654.6(NR2F1):c.464-20TC[2]
NM_005654.6(NR2F1):c.464-7_464-6del
NM_005654.6(NR2F1):c.464-9_464-6del
NM_005654.6(NR2F1):c.513C>T (p.Tyr171=)
NM_005654.6(NR2F1):c.519C>T (p.Leu173=) rs2149942955
NM_005654.6(NR2F1):c.549C>T (p.Cys183=)
NM_005654.6(NR2F1):c.57C>T (p.Asn19=) rs1197079076
NM_005654.6(NR2F1):c.585C>G (p.Ala195=)
NM_005654.6(NR2F1):c.594C>T (p.Tyr198=)
NM_005654.6(NR2F1):c.601T>A (p.Ser201Thr) rs368008985
NM_005654.6(NR2F1):c.60C>G (p.Pro20=) rs753932507
NM_005654.6(NR2F1):c.60C>T (p.Pro20=)
NM_005654.6(NR2F1):c.639T>A (p.Ile213=)
NM_005654.6(NR2F1):c.645C>G (p.Gly215=)
NM_005654.6(NR2F1):c.651G>A (p.Glu217=)
NM_005654.6(NR2F1):c.66C>T (p.Gly22=) rs971963375
NM_005654.6(NR2F1):c.726T>C (p.Asp242=)
NM_005654.6(NR2F1):c.72C>A (p.Asn24Lys) rs1753205307
NM_005654.6(NR2F1):c.741C>T (p.Asp247=) rs1753265081
NM_005654.6(NR2F1):c.75C>T (p.Pro25=)
NM_005654.6(NR2F1):c.801C>T (p.Cys267=) rs1331078890
NM_005654.6(NR2F1):c.810G>A (p.Pro270=) rs1561524973
NM_005654.6(NR2F1):c.816C>T (p.His272=)
NM_005654.6(NR2F1):c.81G>A (p.Ala27=)
NM_005654.6(NR2F1):c.834C>T (p.Ala278=) rs1019282462
NM_005654.6(NR2F1):c.840C>T (p.Ala280=)
NM_005654.6(NR2F1):c.843C>T (p.Gly281=)
NM_005654.6(NR2F1):c.852C>T (p.Ala284=)
NM_005654.6(NR2F1):c.867C>T (p.Ala289=) rs768598143
NM_005654.6(NR2F1):c.894C>T (p.His298=)
NM_005654.6(NR2F1):c.90C>A (p.Ala30=)
NM_005654.6(NR2F1):c.92GCG[4] (p.Gly35_Gly36del)
NM_005654.6(NR2F1):c.92GCG[5] (p.Gly36del)
NM_005654.6(NR2F1):c.92GCG[7] (p.Gly36dup) rs954495672
NM_005654.6(NR2F1):c.92GCG[9] (p.Gly34_Gly36dup) rs954495672
NM_005654.6(NR2F1):c.945C>T (p.Asp315=)
NM_005654.6(NR2F1):c.975C>T (p.Ile325=)
NM_005654.6(NR2F1):c.981G>A (p.Leu327=)
NM_005654.6(NR2F1):c.991+10C>A rs1554074872
NM_005654.6(NR2F1):c.991+12del rs774050994
NM_005654.6(NR2F1):c.991+17_991+38dup
NM_005654.6(NR2F1):c.991+9G>A
NM_005654.6(NR2F1):c.992-16G>A rs946631304
NM_005654.6(NR2F1):c.992-19C>T
NM_005654.6(NR2F1):c.992-6G>T

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