ClinVar Miner

List of variants in gene FMN2 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 188
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020066.5(FMN2):c.2855C>G (p.Ala952Gly) rs200503778 0.00593
NM_020066.5(FMN2):c.2886A>G (p.Ala962=) rs199866405 0.00564
NM_020066.5(FMN2):c.2657T>G (p.Met886Arg) rs146874723 0.00562
NM_020066.5(FMN2):c.696T>C (p.Pro232=) rs11583501 0.00376
NM_020066.5(FMN2):c.1259A>C (p.Lys420Thr) rs146681532 0.00336
NM_020066.5(FMN2):c.5136T>G (p.Ser1712=) rs143796494 0.00330
NM_020066.5(FMN2):c.531G>A (p.Ser177=) rs148480631 0.00307
NM_020066.5(FMN2):c.1352T>A (p.Leu451Gln) rs145379416 0.00297
NM_020066.5(FMN2):c.4619C>T (p.Ser1540Leu) rs150801382 0.00221
NM_020066.5(FMN2):c.1358G>A (p.Arg453Gln) rs147961923 0.00134
NM_020066.5(FMN2):c.2835G>A (p.Pro945=) rs1186257105 0.00127
NM_020066.5(FMN2):c.2928T>C (p.Pro976=) rs200418654 0.00124
NM_020066.5(FMN2):c.893G>A (p.Gly298Asp) rs556876873 0.00093
NM_020066.5(FMN2):c.1896C>T (p.Pro632=) rs141897898 0.00091
NM_020066.5(FMN2):c.2572C>A (p.Pro858Thr) rs140315493 0.00085
NM_020066.5(FMN2):c.1653G>A (p.Glu551=) rs149514160 0.00084
NM_020066.5(FMN2):c.3174T>A (p.Leu1058=) rs200287374 0.00081
NM_020066.5(FMN2):c.3405T>A (p.Leu1135=) rs369474345 0.00077
NM_020066.5(FMN2):c.2910T>A (p.Leu970=) rs1176366601 0.00059
NM_020066.5(FMN2):c.2823A>C (p.Gly941=) rs188083977 0.00055
NM_020066.5(FMN2):c.3600T>A (p.Pro1200=) rs138448278 0.00055
NM_020066.5(FMN2):c.2917G>A (p.Ala973Thr) rs138468405 0.00053
NM_020066.5(FMN2):c.3171T>A (p.Pro1057=) rs201761863 0.00043
NM_020066.5(FMN2):c.1869A>G (p.Pro623=) rs147945249 0.00041
NM_020066.5(FMN2):c.1689C>A (p.Ser563=) rs141488751 0.00039
NM_020066.5(FMN2):c.4236C>T (p.Leu1412=) rs374165127 0.00022
NM_020066.5(FMN2):c.3324T>C (p.Pro1108=) rs773602444 0.00019
NM_020066.5(FMN2):c.1656C>T (p.Asn552=) rs773871472 0.00009
NM_020066.5(FMN2):c.3390C>T (p.Pro1130=) rs200984130 0.00009
NM_020066.5(FMN2):c.3264T>A (p.Pro1088=) rs548950268 0.00008
NM_020066.5(FMN2):c.4926G>A (p.Thr1642=) rs368475818 0.00007
NM_020066.5(FMN2):c.1632G>A (p.Glu544=) rs372095380 0.00006
NM_020066.5(FMN2):c.3078C>T (p.Pro1026=) rs201810089 0.00006
NM_020066.5(FMN2):c.1884A>G (p.Pro628=) rs369120788 0.00005
NM_020066.5(FMN2):c.4884A>G (p.Glu1628=) rs1036137349 0.00005
NM_020066.5(FMN2):c.1200C>T (p.Ser400=) rs760802198 0.00004
NM_020066.5(FMN2):c.3555T>C (p.Pro1185=) rs769857934 0.00004
NM_020066.5(FMN2):c.4154-7T>C rs922670089 0.00004
NM_020066.5(FMN2):c.4677G>C (p.Leu1559=) rs146444036 0.00004
NM_020066.5(FMN2):c.1380C>T (p.Ala460=) rs771349783 0.00003
NM_020066.5(FMN2):c.2787A>G (p.Ala929=) rs776163265 0.00003
NM_020066.5(FMN2):c.3413C>T (p.Ala1138Val) rs199570117 0.00003
NM_020066.5(FMN2):c.4154-5C>T rs751736487 0.00003
NM_020066.5(FMN2):c.5073C>T (p.Ala1691=) rs757125774 0.00003
NM_020066.5(FMN2):c.699A>C (p.Ala233=) rs1198518631 0.00002
NM_020066.5(FMN2):c.1615+10C>G rs780352289 0.00001
NM_020066.5(FMN2):c.270C>T (p.Ala90=) rs1278261031 0.00001
NM_020066.5(FMN2):c.468C>T (p.Gly156=) rs370945971 0.00001
NM_020066.5(FMN2):c.84G>A (p.Gly28=) rs757156181 0.00001
NM_020066.5(FMN2):c.1014C>T (p.Pro338=) rs541790538
NM_020066.5(FMN2):c.1077G>A (p.Arg359=) rs761094036
NM_020066.5(FMN2):c.1485G>T (p.Arg495=)
NM_020066.5(FMN2):c.162C>G (p.Gly54=)
NM_020066.5(FMN2):c.177G>T (p.Gly59=)
NM_020066.5(FMN2):c.2112G>C (p.Val704=)
NM_020066.5(FMN2):c.2223G>A (p.Ala741=)
NM_020066.5(FMN2):c.2256C>T (p.Gly752=)
NM_020066.5(FMN2):c.2274T>C (p.Pro758=)
NM_020066.5(FMN2):c.2328A>T (p.Gly776=)
NM_020066.5(FMN2):c.2652T>A (p.Pro884=)
NM_020066.5(FMN2):c.2673G>A (p.Leu891=)
NM_020066.5(FMN2):c.2742T>A (p.Pro914=)
NM_020066.5(FMN2):c.2769G>A (p.Pro923=)
NM_020066.5(FMN2):c.2772G>C (p.Pro924=)
NM_020066.5(FMN2):c.2772_2837del (p.Gly930_Ala951del)
NM_020066.5(FMN2):c.2778A>T (p.Leu926=)
NM_020066.5(FMN2):c.2790C>A (p.Gly930=)
NM_020066.5(FMN2):c.2796C>T (p.Leu932=)
NM_020066.5(FMN2):c.2802G>T (p.Leu934=)
NM_020066.5(FMN2):c.2811A>T (p.Leu937=)
NM_020066.5(FMN2):c.2817A>G (p.Gly939=)
NM_020066.5(FMN2):c.2838C>G (p.Pro946=)
NM_020066.5(FMN2):c.2841T>A (p.Pro947=)
NM_020066.5(FMN2):c.2844_2876del (p.Ala952_Ala962del) rs758726356
NM_020066.5(FMN2):c.2856A>C (p.Ala952=)
NM_020066.5(FMN2):c.2874T>A (p.Pro958=)
NM_020066.5(FMN2):c.2886A>T (p.Ala962=)
NM_020066.5(FMN2):c.2889C>A (p.Gly963=)
NM_020066.5(FMN2):c.2895C>T (p.Pro965=)
NM_020066.5(FMN2):c.2901T>G (p.Pro967=)
NM_020066.5(FMN2):c.2934A>G (p.Pro978=)
NM_020066.5(FMN2):c.2934A>T (p.Pro978=) rs201199944
NM_020066.5(FMN2):c.2937C>G (p.Pro979=)
NM_020066.5(FMN2):c.2940T>A (p.Pro980=)
NM_020066.5(FMN2):c.2943A>T (p.Leu981=)
NM_020066.5(FMN2):c.2952G>A (p.Ala984=)
NM_020066.5(FMN2):c.2955C>A (p.Gly985=)
NM_020066.5(FMN2):c.2961C>T (p.Pro987=)
NM_020066.5(FMN2):c.2967T>A (p.Pro989=)
NM_020066.5(FMN2):c.2967T>C (p.Pro989=)
NM_020066.5(FMN2):c.2967T>G (p.Pro989=)
NM_020066.5(FMN2):c.2976T>A (p.Leu992=)
NM_020066.5(FMN2):c.2979C>T (p.Pro993=)
NM_020066.5(FMN2):c.2982A>G (p.Gly994=)
NM_020066.5(FMN2):c.3003C>G (p.Pro1001=)
NM_020066.5(FMN2):c.3012C>A (p.Pro1004=)
NM_020066.5(FMN2):c.3015A>G (p.Gly1005=)
NM_020066.5(FMN2):c.3018G>A (p.Ala1006=)
NM_020066.5(FMN2):c.3021C>A (p.Gly1007=)
NM_020066.5(FMN2):c.3033T>G (p.Pro1011=)
NM_020066.5(FMN2):c.3036C>G (p.Pro1012=)
NM_020066.5(FMN2):c.3060T>C (p.Pro1020=)
NM_020066.5(FMN2):c.3066A>G (p.Pro1022=)
NM_020066.5(FMN2):c.3072T>A (p.Pro1024=)
NM_020066.5(FMN2):c.3073C>T (p.Leu1025=)
NM_020066.5(FMN2):c.3075A>T (p.Leu1025=)
NM_020066.5(FMN2):c.3087C>A (p.Gly1029=)
NM_020066.5(FMN2):c.3099G>A (p.Pro1033=)
NM_020066.5(FMN2):c.3108T>A (p.Leu1036=)
NM_020066.5(FMN2):c.3126C>T (p.Pro1042=)
NM_020066.5(FMN2):c.3129T>A (p.Pro1043=)
NM_020066.5(FMN2):c.3132G>A (p.Pro1044=)
NM_020066.5(FMN2):c.3132G>T (p.Pro1044=)
NM_020066.5(FMN2):c.3138A>C (p.Pro1046=)
NM_020066.5(FMN2):c.3138A>T (p.Pro1046=)
NM_020066.5(FMN2):c.3159C>T (p.Pro1053=)
NM_020066.5(FMN2):c.3162T>A (p.Pro1054=)
NM_020066.5(FMN2):c.3165T>G (p.Pro1055=)
NM_020066.5(FMN2):c.3168C>G (p.Pro1056=)
NM_020066.5(FMN2):c.3180A>G (p.Gly1060=)
NM_020066.5(FMN2):c.3183G>A (p.Ala1061=) rs1349785596
NM_020066.5(FMN2):c.3186C>A (p.Gly1062=) rs1228832309
NM_020066.5(FMN2):c.3192T>C (p.Pro1064=)
NM_020066.5(FMN2):c.3198A>T (p.Pro1066=)
NM_020066.5(FMN2):c.3204T>A (p.Pro1068=)
NM_020066.5(FMN2):c.3205C>T (p.Leu1069=)
NM_020066.5(FMN2):c.3207A>T (p.Leu1069=)
NM_020066.5(FMN2):c.3210C>T (p.Pro1070=)
NM_020066.5(FMN2):c.3231G>A (p.Pro1077=)
NM_020066.5(FMN2):c.3231G>T (p.Pro1077=)
NM_020066.5(FMN2):c.3240T>A (p.Leu1080=)
NM_020066.5(FMN2):c.3258C>T (p.Pro1086=)
NM_020066.5(FMN2):c.3264T>G (p.Pro1088=)
NM_020066.5(FMN2):c.3267C>G (p.Pro1089=)
NM_020066.5(FMN2):c.3270T>A (p.Pro1090=)
NM_020066.5(FMN2):c.3273A>T (p.Leu1091=)
NM_020066.5(FMN2):c.3276C>T (p.Pro1092=)
NM_020066.5(FMN2):c.3282G>A (p.Ala1094=)
NM_020066.5(FMN2):c.3294T>A (p.Pro1098=)
NM_020066.5(FMN2):c.3297G>A (p.Pro1099=)
NM_020066.5(FMN2):c.3297G>T (p.Pro1099=) rs373533409
NM_020066.5(FMN2):c.3306A>T (p.Leu1102=)
NM_020066.5(FMN2):c.3315G>A (p.Val1105=)
NM_020066.5(FMN2):c.3324TCC[1] (p.Pro1112del) rs780903069
NM_020066.5(FMN2):c.3330G>A (p.Pro1110=)
NM_020066.5(FMN2):c.3339ACCCGGAGCGGGCATACCCCCTCCTCCCCCTCT[1] (p.1115GAGIPPPPPLP[2])
NM_020066.5(FMN2):c.3350G>T (p.Gly1117Val)
NM_020066.5(FMN2):c.3351C>A (p.Gly1117=)
NM_020066.5(FMN2):c.3369T>A (p.Pro1123=)
NM_020066.5(FMN2):c.3372A>T (p.Leu1124=)
NM_020066.5(FMN2):c.3375C>T (p.Pro1125=)
NM_020066.5(FMN2):c.3378A>G (p.Gly1126=)
NM_020066.5(FMN2):c.3393T>A (p.Pro1131=)
NM_020066.5(FMN2):c.3396T>A (p.Pro1132=) rs201646328
NM_020066.5(FMN2):c.3396T>G (p.Pro1132=)
NM_020066.5(FMN2):c.339C>T (p.Ser113=)
NM_020066.5(FMN2):c.3402T>A (p.Pro1134=)
NM_020066.5(FMN2):c.3414G>A (p.Ala1138=)
NM_020066.5(FMN2):c.3417C>A (p.Gly1139=)
NM_020066.5(FMN2):c.3423T>C (p.Pro1141=)
NM_020066.5(FMN2):c.3429A>T (p.Pro1143=)
NM_020066.5(FMN2):c.3456C>T (p.Pro1152=)
NM_020066.5(FMN2):c.3461C>T (p.Pro1154Leu)
NM_020066.5(FMN2):c.3462G>A (p.Pro1154=)
NM_020066.5(FMN2):c.3462G>T (p.Pro1154=)
NM_020066.5(FMN2):c.3468A>T (p.Pro1156=)
NM_020066.5(FMN2):c.3474C>T (p.Pro1158=)
NM_020066.5(FMN2):c.3489C>T (p.Pro1163=)
NM_020066.5(FMN2):c.3495T>A (p.Pro1165=)
NM_020066.5(FMN2):c.3495T>G (p.Pro1165=)
NM_020066.5(FMN2):c.3504A>T (p.Leu1168=)
NM_020066.5(FMN2):c.3507C>T (p.Pro1169=)
NM_020066.5(FMN2):c.3516C>A (p.Gly1172=)
NM_020066.5(FMN2):c.3522C>T (p.Pro1174=)
NM_020066.5(FMN2):c.3528G>A (p.Pro1176=)
NM_020066.5(FMN2):c.3528G>T (p.Pro1176=)
NM_020066.5(FMN2):c.3549A>C (p.Gly1183=)
NM_020066.5(FMN2):c.3561G>A (p.Pro1187=)
NM_020066.5(FMN2):c.3573T>C (p.Pro1191=)
NM_020066.5(FMN2):c.3582A>C (p.Gly1194=)
NM_020066.5(FMN2):c.384C>T (p.Ala128=) rs200157875
NM_020066.5(FMN2):c.4065+7A>G rs749567608
NM_020066.5(FMN2):c.4800C>A (p.Val1600=)
NM_020066.5(FMN2):c.4875G>A (p.Glu1625=)
NM_020066.5(FMN2):c.525C>A (p.Thr175=) rs1572736839
NM_020066.5(FMN2):c.708C>G (p.Pro236=) rs771814202
NM_020066.5(FMN2):c.903C>T (p.Val301=)
NM_020066.5(FMN2):c.924G>C (p.Pro308=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.