ClinVar Miner

List of variants in gene F9 reported as likely benign for coagulation protein disease

Included ClinVar conditions (78):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 201
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HGVS dbSNP gnomAD frequency
NM_000133.4(F9):c.278-27A>G rs3134809 0.01152
NM_000133.4(F9):c.1095A>G (p.Ser365=) rs112057482 0.01021
NM_000133.4(F9):c.967G>A (p.Glu323Lys) rs150351950 0.00294
NM_000133.4(F9):c.*1048G>A rs752396182 0.00125
NM_000133.4(F9):c.696T>C (p.Asp232=) rs140835723 0.00113
NM_000133.4(F9):c.819T>C (p.Val273=) rs1800455 0.00110
NM_000133.4(F9):c.19A>T (p.Ile7Phe) rs150190385 0.00086
NM_000133.4(F9):c.907C>T (p.His303Tyr) rs1801202 0.00044
NM_000133.4(F9):c.8G>A (p.Arg3His) rs148060786 0.00042
NM_000133.4(F9):c.1029C>T (p.Asn343=) rs145026483 0.00017
NM_000133.4(F9):c.250A>G (p.Thr84Ala) rs201120367 0.00013
NM_000133.4(F9):c.768C>T (p.Ile256=) rs758909063 0.00012
NM_000133.4(F9):c.1143A>G (p.Thr381=) rs761784613 0.00011
NM_000133.4(F9):c.114C>T (p.Asn38=) rs745353370 0.00011
NM_000133.4(F9):c.769G>A (p.Val257Ile) rs200608775 0.00010
NM_000133.4(F9):c.1048T>G (p.Ser350Ala) rs147567879 0.00005
NM_000133.4(F9):c.315C>T (p.Gly105=) rs757434127 0.00005
NM_000133.4(F9):c.523C>T (p.Pro175Ser) rs762986355 0.00005
NM_000133.4(F9):c.991G>A (p.Val331Ile) rs776509489 0.00005
NM_000133.4(F9):c.*10G>C rs186616567 0.00004
NM_000133.4(F9):c.108C>T (p.Asn36=) rs184837275 0.00004
NM_000133.4(F9):c.423C>T (p.Cys141=) rs150041781 0.00004
NM_000133.4(F9):c.483T>C (p.Tyr161=) rs1047289457 0.00004
NM_000133.4(F9):c.582T>G (p.Thr194=) rs754155651 0.00004
NM_000133.4(F9):c.658T>A (p.Ser220Thr) rs777361659 0.00004
NM_000133.4(F9):c.730T>C (p.Leu244=) rs765470577 0.00004
NM_000133.4(F9):c.834C>T (p.Val278=) rs199844858 0.00004
NM_000133.4(F9):c.1218A>G (p.Ser406=) rs916632342 0.00003
NM_000133.4(F9):c.333C>T (p.Asp111=) rs139289585 0.00003
NM_000133.4(F9):c.391+4A>G rs749754992 0.00003
NM_000133.4(F9):c.966C>T (p.Asp322=) rs373107855 0.00003
NM_000133.4(F9):c.1284T>C (p.Ile428=) rs1300185736 0.00002
NM_000133.4(F9):c.130C>T (p.Pro44Ser) rs776894974 0.00002
NM_000133.4(F9):c.456G>A (p.Lys152=) rs780347965 0.00002
NM_000133.4(F9):c.465C>T (p.Cys155=) rs375658633 0.00002
NM_000133.4(F9):c.48C>A (p.Thr16=) rs768833956 0.00002
NM_000133.4(F9):c.54C>T (p.Cys18=) rs1337284408 0.00002
NM_000133.4(F9):c.724-4A>G rs755261990 0.00002
NM_000133.4(F9):c.774T>C (p.Asn258=) rs752173947 0.00002
NM_000133.4(F9):c.844C>T (p.His282Tyr) rs763399530 0.00002
NM_000133.4(F9):c.1026G>A (p.Thr342=) rs954954812 0.00001
NM_000133.4(F9):c.106A>G (p.Asn36Asp) rs1169714103 0.00001
NM_000133.4(F9):c.1074A>G (p.Arg358=) rs751992311 0.00001
NM_000133.4(F9):c.1134C>T (p.Asp378=) rs1485359328 0.00001
NM_000133.4(F9):c.116A>G (p.Lys39Arg) rs200505648 0.00001
NM_000133.4(F9):c.1170C>T (p.Ile390=) rs1436679699 0.00001
NM_000133.4(F9):c.1191T>C (p.Ala397=) rs777757344 0.00001
NM_000133.4(F9):c.1209T>C (p.Gly403=) rs900302000 0.00001
NM_000133.4(F9):c.1269T>C (p.Ser423=) rs774786079 0.00001
NM_000133.4(F9):c.1365G>A (p.Lys455=) rs1928133934 0.00001
NM_000133.4(F9):c.154T>C (p.Leu52=) rs1470729875 0.00001
NM_000133.4(F9):c.192T>C (p.Cys64=) rs1261374056 0.00001
NM_000133.4(F9):c.273T>C (p.Tyr91=) rs142980421 0.00001
NM_000133.4(F9):c.384T>C (p.Cys128=) rs780435919 0.00001
NM_000133.4(F9):c.392-10C>T rs1027316695 0.00001
NM_000133.4(F9):c.392-7C>A rs757272947 0.00001
NM_000133.4(F9):c.399A>G (p.Thr133=) rs1296392687 0.00001
NM_000133.4(F9):c.516A>T (p.Pro172=) rs1462862045 0.00001
NM_000133.4(F9):c.520+9C>A rs1453342028 0.00001
NM_000133.4(F9):c.60A>G (p.Leu20=) rs762082146 0.00001
NM_000133.4(F9):c.714C>T (p.Phe238=) rs769442375 0.00001
NM_000133.4(F9):c.723+7T>C rs970573926 0.00001
NM_000133.4(F9):c.894A>C (p.Arg298=) rs780516722 0.00001
NM_000133.4(F9):c.936C>T (p.Tyr312=) rs748996457 0.00001
NM_000133.4(F9):c.972C>T (p.Pro324=) rs1475170749 0.00001
NM_000133.4(F9):c.990C>T (p.Tyr330=) rs1928109999 0.00001
NM_000133.4(F9):c.9C>T (p.Arg3=) rs1335753805 0.00001
NM_000133.4(F9):c.1002T>A (p.Ile334=)
NM_000133.4(F9):c.102T>C (p.His34=)
NM_000133.4(F9):c.1062T>C (p.Ser354=) rs2148367882
NM_000133.4(F9):c.1077C>A (p.Val359=) rs2148367918
NM_000133.4(F9):c.1090A>C (p.Arg364=) rs2148367924
NM_000133.4(F9):c.1107T>A (p.Leu369=) rs750955240
NM_000133.4(F9):c.1119A>G (p.Arg373=)
NM_000133.4(F9):c.1128T>G (p.Leu376=)
NM_000133.4(F9):c.1164C>T (p.Phe388=) rs2148368027
NM_000133.4(F9):c.1185C>T (p.Phe395=)
NM_000133.4(F9):c.1206A>T (p.Gly402=)
NM_000133.4(F9):c.1230T>C (p.Asp410=)
NM_000133.4(F9):c.1233T>C (p.Ser411=)
NM_000133.4(F9):c.1242C>T (p.Pro414=)
NM_000133.4(F9):c.1251T>C (p.Thr417=)
NM_000133.4(F9):c.1257G>A (p.Val419=)
NM_000133.4(F9):c.1281A>G (p.Gly427=) rs2148368224
NM_000133.4(F9):c.1290C>T (p.Ser430=)
NM_000133.4(F9):c.1296T>C (p.Gly432=)
NM_000133.4(F9):c.1296T>G (p.Gly432=) rs2148368246
NM_000133.4(F9):c.129G>A (p.Arg43=) rs2148356042
NM_000133.4(F9):c.1302G>A (p.Glu434=) rs2148368257
NM_000133.4(F9):c.1305T>C (p.Cys435=) rs2148368264
NM_000133.4(F9):c.1332T>C (p.Tyr444=) rs1928132545
NM_000133.4(F9):c.1344C>T (p.Ser448=) rs2148368307
NM_000133.4(F9):c.1345C>A (p.Arg449=)
NM_000133.4(F9):c.1347G>A (p.Arg449=) rs1433326581
NM_000133.4(F9):c.1347G>T (p.Arg449=)
NM_000133.4(F9):c.135G>A (p.Lys45=)
NM_000133.4(F9):c.1377G>A (p.Lys459=)
NM_000133.4(F9):c.1380C>T (p.Leu460=) rs2148368357
NM_000133.4(F9):c.141T>C (p.Tyr47=) rs1556435929
NM_000133.4(F9):c.15C>T (p.Asn5=)
NM_000133.4(F9):c.177C>T (p.Asn59=)
NM_000133.4(F9):c.201A>G (p.Glu67=)
NM_000133.4(F9):c.231T>G (p.Val77=)
NM_000133.4(F9):c.252+12C>T
NM_000133.4(F9):c.252+14C>T
NM_000133.4(F9):c.252+15A>G
NM_000133.4(F9):c.252+16T>C
NM_000133.4(F9):c.252+18A>G
NM_000133.4(F9):c.252+20A>G
NM_000133.4(F9):c.253-12T>C
NM_000133.4(F9):c.253-8C>T
NM_000133.4(F9):c.267G>A (p.Lys89=) rs1927507472
NM_000133.4(F9):c.277+14T>C
NM_000133.4(F9):c.277+19C>T
NM_000133.4(F9):c.277+7A>G
NM_000133.4(F9):c.278-12C>T
NM_000133.4(F9):c.278-13A>C
NM_000133.4(F9):c.278-4A>G
NM_000133.4(F9):c.27A>C (p.Ala9=)
NM_000133.4(F9):c.294G>A (p.Glu98=)
NM_000133.4(F9):c.303A>G (p.Pro101=)
NM_000133.4(F9):c.324C>T (p.Cys108=)
NM_000133.4(F9):c.336T>C (p.Ile112=) rs2148357946
NM_000133.4(F9):c.339T>C (p.Asn113=)
NM_000133.4(F9):c.342C>T (p.Ser114=) rs2148357955
NM_000133.4(F9):c.36A>G (p.Pro12=)
NM_000133.4(F9):c.391+11A>G
NM_000133.4(F9):c.391+9C>G
NM_000133.4(F9):c.392-20G>A
NM_000133.4(F9):c.392-20_392-17del
NM_000133.4(F9):c.402T>C (p.Cys134=)
NM_000133.4(F9):c.426G>A (p.Glu142=) rs2148361169
NM_000133.4(F9):c.444T>C (p.Ser148=)
NM_000133.4(F9):c.471T>C (p.Cys157=) rs1603265493
NM_000133.4(F9):c.504G>A (p.Lys168=)
NM_000133.4(F9):c.507C>G (p.Ser169=) rs565055999
NM_000133.4(F9):c.520+10T>C rs1289621854
NM_000133.4(F9):c.520+19T>C
NM_000133.4(F9):c.521-10A>G rs1603265768
NM_000133.4(F9):c.521-11T>C
NM_000133.4(F9):c.521-12C>T
NM_000133.4(F9):c.521-13T>C
NM_000133.4(F9):c.521-17T>C
NM_000133.4(F9):c.521-5del rs1320990506
NM_000133.4(F9):c.521-7T>C
NM_000133.4(F9):c.522G>A (p.Val174=) rs2148362379
NM_000133.4(F9):c.555A>G (p.Gln185=)
NM_000133.4(F9):c.558T>G (p.Thr186=)
NM_000133.4(F9):c.570C>G (p.Thr190=) rs2148362421
NM_000133.4(F9):c.573T>A (p.Arg191=) rs2148362436
NM_000133.4(F9):c.579G>A (p.Glu193=)
NM_000133.4(F9):c.582T>C (p.Thr194=)
NM_000133.4(F9):c.584T>G (p.Val195Gly)
NM_000133.4(F9):c.589C>T (p.Pro197Ser)
NM_000133.4(F9):c.603T>C (p.Tyr201=)
NM_000133.4(F9):c.615T>C (p.Thr205=) rs2148362491
NM_000133.4(F9):c.621T>C (p.Ala207=) rs1307382807
NM_000133.4(F9):c.676C>A (p.Arg226=)
NM_000133.4(F9):c.699C>T (p.Ala233=)
NM_000133.4(F9):c.723+11C>T
NM_000133.4(F9):c.723+14A>T
NM_000133.4(F9):c.723+15T>C
NM_000133.4(F9):c.732G>A (p.Leu244=)
NM_000133.4(F9):c.735T>C (p.Asn245=)
NM_000133.4(F9):c.738T>C (p.Gly246=)
NM_000133.4(F9):c.744T>A (p.Val248=)
NM_000133.4(F9):c.747T>C (p.Asp249=) rs2148367218
NM_000133.4(F9):c.750A>T (p.Ala250=)
NM_000133.4(F9):c.762C>G (p.Gly254=)
NM_000133.4(F9):c.780A>G (p.Lys260=)
NM_000133.4(F9):c.792T>G (p.Thr264=)
NM_000133.4(F9):c.7C>A (p.Arg3Ser)
NM_000133.4(F9):c.7C>T (p.Arg3Cys) rs766259893
NM_000133.4(F9):c.801C>T (p.His267=)
NM_000133.4(F9):c.838+17A>C
NM_000133.4(F9):c.838+18A>G
NM_000133.4(F9):c.839-16A>G
NM_000133.4(F9):c.840T>C (p.Gly280=) rs2148367615
NM_000133.4(F9):c.861A>T (p.Thr287=) rs2148367626
NM_000133.4(F9):c.879G>A (p.Lys293=)
NM_000133.4(F9):c.88+10C>G rs1603263402
NM_000133.4(F9):c.88+10_88+11del rs2148353026
NM_000133.4(F9):c.88+16T>A
NM_000133.4(F9):c.88+20A>T
NM_000133.4(F9):c.88+8T>C
NM_000133.4(F9):c.885T>C (p.Asn295=)
NM_000133.4(F9):c.888G>A (p.Val296=) rs2148367656
NM_000133.4(F9):c.89-14C>A
NM_000133.4(F9):c.89-15del
NM_000133.4(F9):c.89-19T>A
NM_000133.4(F9):c.89-20A>G
NM_000133.4(F9):c.89-7A>G rs1603264192
NM_000133.4(F9):c.89-9A>G
NM_000133.4(F9):c.894A>G (p.Arg298=)
NM_000133.4(F9):c.906C>T (p.His302=) rs2148367678
NM_000133.4(F9):c.909C>T (p.His303=) rs2148367681
NM_000133.4(F9):c.945C>T (p.Asp315=) rs2148367722
NM_000133.4(F9):c.948T>C (p.Ile316=)
NM_000133.4(F9):c.963G>T (p.Leu321=)
NM_000133.4(F9):c.969A>G (p.Glu323=)
NM_000133.4(F9):c.9C>G (p.Arg3=) rs1335753805

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