Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430550D23Rik |
T |
C |
2: 155,845,150 (GRCm39) |
H113R |
possibly damaging |
Het |
Adgrf3 |
A |
T |
5: 30,402,531 (GRCm39) |
M499K |
probably benign |
Het |
Adgrv1 |
G |
A |
13: 81,255,050 (GRCm39) |
T211I |
probably damaging |
Het |
Adss2 |
C |
T |
1: 177,604,395 (GRCm39) |
E153K |
probably benign |
Het |
Ago4 |
C |
A |
4: 126,405,280 (GRCm39) |
G431V |
possibly damaging |
Het |
Araf |
G |
T |
X: 20,726,339 (GRCm39) |
R601L |
probably damaging |
Homo |
Atp2b4 |
T |
A |
1: 133,654,299 (GRCm39) |
I769F |
probably damaging |
Het |
Atp9a |
T |
C |
2: 168,531,272 (GRCm39) |
|
probably null |
Het |
Bltp1 |
T |
C |
3: 37,011,148 (GRCm39) |
V1782A |
probably benign |
Het |
Brap |
C |
A |
5: 121,803,372 (GRCm39) |
D173E |
probably benign |
Het |
Brca2 |
G |
T |
5: 150,490,443 (GRCm39) |
R3035L |
probably benign |
Het |
Ccdc8 |
C |
A |
7: 16,730,176 (GRCm39) |
P555Q |
probably benign |
Het |
Ccser2 |
A |
G |
14: 36,662,675 (GRCm39) |
S170P |
probably benign |
Het |
Celsr2 |
T |
C |
3: 108,300,444 (GRCm39) |
H860R |
probably damaging |
Het |
Cenpc1 |
C |
A |
5: 86,194,244 (GRCm39) |
R174M |
probably damaging |
Het |
Cfap57 |
T |
G |
4: 118,436,607 (GRCm39) |
I930L |
probably damaging |
Het |
Cx3cr1 |
C |
T |
9: 119,880,760 (GRCm39) |
R214H |
probably damaging |
Het |
Cyp4f14 |
T |
A |
17: 33,125,291 (GRCm39) |
H429L |
probably benign |
Het |
D5Ertd579e |
A |
G |
5: 36,772,620 (GRCm39) |
F592L |
probably damaging |
Het |
Ddb1 |
A |
G |
19: 10,603,287 (GRCm39) |
E865G |
probably damaging |
Het |
Ddx50 |
A |
T |
10: 62,457,345 (GRCm39) |
|
probably null |
Het |
Dpp6 |
A |
G |
5: 27,254,626 (GRCm39) |
T14A |
probably damaging |
Het |
Echs1 |
C |
A |
7: 139,692,982 (GRCm39) |
Q51H |
possibly damaging |
Het |
Ecm2 |
A |
T |
13: 49,683,783 (GRCm39) |
D587V |
probably damaging |
Het |
Ect2l |
A |
T |
10: 18,016,145 (GRCm39) |
Y666N |
possibly damaging |
Het |
Epha2 |
G |
A |
4: 141,044,223 (GRCm39) |
G342S |
probably benign |
Het |
Fbxo33 |
C |
A |
12: 59,252,865 (GRCm39) |
K211N |
probably benign |
Het |
Fchsd2 |
A |
G |
7: 100,908,983 (GRCm39) |
|
probably null |
Het |
Fen1 |
A |
G |
19: 10,178,051 (GRCm39) |
V131A |
probably damaging |
Het |
Fetub |
C |
T |
16: 22,751,081 (GRCm39) |
R143C |
probably damaging |
Het |
Foxd3 |
A |
G |
4: 99,545,477 (GRCm39) |
T206A |
possibly damaging |
Het |
Fut1 |
A |
G |
7: 45,268,730 (GRCm39) |
E228G |
possibly damaging |
Het |
Galnt13 |
T |
C |
2: 54,823,560 (GRCm39) |
F379L |
probably damaging |
Het |
Gcnt2 |
A |
C |
13: 41,014,717 (GRCm39) |
E296A |
probably damaging |
Het |
Gm7145 |
T |
A |
1: 117,913,870 (GRCm39) |
C251S |
probably damaging |
Het |
Gpam |
G |
A |
19: 55,059,417 (GRCm39) |
P810L |
probably damaging |
Het |
Il1rl2 |
T |
A |
1: 40,366,726 (GRCm39) |
L87M |
possibly damaging |
Het |
Itgae |
A |
G |
11: 73,036,427 (GRCm39) |
S1122G |
probably damaging |
Het |
Kcnh7 |
T |
A |
2: 63,012,570 (GRCm39) |
D46V |
probably damaging |
Het |
Kcnn3 |
T |
G |
3: 89,552,830 (GRCm39) |
Y511* |
probably null |
Het |
Kdm3b |
T |
A |
18: 34,926,058 (GRCm39) |
I66N |
probably damaging |
Het |
Klk1b27 |
A |
T |
7: 43,703,974 (GRCm39) |
H39L |
probably benign |
Het |
Kmo |
C |
T |
1: 175,487,261 (GRCm39) |
T404I |
possibly damaging |
Het |
Krt222 |
C |
T |
11: 99,125,884 (GRCm39) |
|
probably null |
Het |
Magi3 |
G |
C |
3: 103,923,013 (GRCm39) |
H1235D |
probably benign |
Het |
Mapk8ip1 |
C |
A |
2: 92,219,589 (GRCm39) |
G81C |
probably damaging |
Het |
Med15 |
G |
A |
16: 17,470,609 (GRCm39) |
Q583* |
probably null |
Het |
Mroh2a |
T |
C |
1: 88,184,476 (GRCm39) |
V1453A |
probably benign |
Het |
Myh13 |
A |
G |
11: 67,253,327 (GRCm39) |
M1488V |
probably benign |
Het |
Naip2 |
A |
T |
13: 100,288,645 (GRCm39) |
F1193L |
probably damaging |
Het |
Nop58 |
T |
A |
1: 59,742,014 (GRCm39) |
M181K |
probably damaging |
Het |
Npepps |
A |
T |
11: 97,104,616 (GRCm39) |
V796D |
probably damaging |
Het |
Nr1d1 |
A |
G |
11: 98,661,363 (GRCm39) |
F301S |
probably damaging |
Het |
Nynrin |
G |
A |
14: 56,105,485 (GRCm39) |
V832I |
probably damaging |
Het |
Or13a28 |
C |
A |
7: 140,218,346 (GRCm39) |
S244Y |
probably damaging |
Het |
Or1j14 |
T |
A |
2: 36,418,353 (GRCm39) |
C310S |
probably benign |
Het |
Or2ak7 |
A |
T |
11: 58,574,830 (GRCm39) |
T44S |
possibly damaging |
Het |
Or4e1 |
T |
A |
14: 52,701,352 (GRCm39) |
Y38F |
probably damaging |
Het |
Or8k1 |
T |
A |
2: 86,047,566 (GRCm39) |
T163S |
possibly damaging |
Het |
Phrf1 |
T |
A |
7: 140,817,586 (GRCm39) |
C132S |
probably damaging |
Het |
Plekhn1 |
T |
C |
4: 156,315,015 (GRCm39) |
|
probably null |
Het |
Polr2a |
G |
A |
11: 69,635,052 (GRCm39) |
T569M |
probably damaging |
Het |
Prr29 |
A |
G |
11: 106,267,458 (GRCm39) |
|
probably null |
Het |
Rsf1 |
CG |
CGACGGCGGAG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Homo |
Sc5d |
T |
C |
9: 42,166,717 (GRCm39) |
E274G |
probably benign |
Het |
Serpina1d |
A |
T |
12: 103,731,087 (GRCm39) |
|
probably null |
Het |
Serpinb11 |
T |
A |
1: 107,299,972 (GRCm39) |
I106N |
probably damaging |
Het |
Setd2 |
G |
A |
9: 110,377,733 (GRCm39) |
R516K |
probably damaging |
Het |
Sirt2 |
G |
T |
7: 28,487,222 (GRCm39) |
C291F |
probably damaging |
Het |
Stac3 |
T |
C |
10: 127,344,044 (GRCm39) |
V314A |
probably damaging |
Het |
Stat6 |
C |
T |
10: 127,493,581 (GRCm39) |
|
probably null |
Het |
Strn3 |
A |
G |
12: 51,656,890 (GRCm39) |
V712A |
probably damaging |
Het |
Tmc5 |
G |
T |
7: 118,233,437 (GRCm39) |
G84C |
possibly damaging |
Het |
Tnik |
C |
A |
3: 28,704,328 (GRCm39) |
L996I |
probably damaging |
Het |
Trim30d |
G |
T |
7: 104,136,817 (GRCm39) |
T129K |
probably damaging |
Het |
Triml1 |
G |
T |
8: 43,591,793 (GRCm39) |
Y188* |
probably null |
Het |
Trpc7 |
A |
G |
13: 56,921,705 (GRCm39) |
Y760H |
probably damaging |
Het |
Uaca |
G |
A |
9: 60,777,326 (GRCm39) |
R571Q |
probably damaging |
Het |
Ubash3a |
A |
T |
17: 31,458,246 (GRCm39) |
Q575L |
possibly damaging |
Het |
Usp49 |
T |
A |
17: 47,983,827 (GRCm39) |
C61* |
probably null |
Het |
Vmn2r18 |
A |
T |
5: 151,508,116 (GRCm39) |
V336E |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,324,102 (GRCm39) |
V1135A |
probably benign |
Het |
Zcchc4 |
T |
C |
5: 52,940,503 (GRCm39) |
V24A |
probably benign |
Het |
Zfp354c |
A |
G |
11: 50,705,798 (GRCm39) |
Y426H |
probably benign |
Het |
|
Other mutations in Flnb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01017:Flnb
|
APN |
14 |
7,917,390 (GRCm38) |
splice site |
probably benign |
|
IGL01063:Flnb
|
APN |
14 |
7,926,518 (GRCm38) |
splice site |
probably benign |
|
IGL01135:Flnb
|
APN |
14 |
7,909,736 (GRCm38) |
missense |
probably benign |
|
IGL01139:Flnb
|
APN |
14 |
7,945,989 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01364:Flnb
|
APN |
14 |
7,934,562 (GRCm38) |
critical splice acceptor site |
probably null |
|
IGL01417:Flnb
|
APN |
14 |
7,905,513 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01505:Flnb
|
APN |
14 |
7,902,003 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01560:Flnb
|
APN |
14 |
7,893,829 (GRCm38) |
missense |
probably benign |
0.07 |
IGL01621:Flnb
|
APN |
14 |
7,950,470 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01656:Flnb
|
APN |
14 |
7,902,010 (GRCm38) |
splice site |
probably benign |
|
IGL01889:Flnb
|
APN |
14 |
7,935,967 (GRCm38) |
missense |
possibly damaging |
0.85 |
IGL01987:Flnb
|
APN |
14 |
7,922,748 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02322:Flnb
|
APN |
14 |
7,894,676 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02496:Flnb
|
APN |
14 |
7,930,919 (GRCm38) |
splice site |
probably benign |
|
IGL02752:Flnb
|
APN |
14 |
7,917,338 (GRCm38) |
missense |
probably benign |
|
IGL03001:Flnb
|
APN |
14 |
7,934,680 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03076:Flnb
|
APN |
14 |
7,901,988 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03085:Flnb
|
APN |
14 |
7,882,211 (GRCm38) |
missense |
probably benign |
|
IGL03170:Flnb
|
APN |
14 |
7,818,261 (GRCm38) |
missense |
possibly damaging |
0.90 |
IGL03373:Flnb
|
APN |
14 |
7,890,867 (GRCm38) |
critical splice donor site |
probably null |
|
Boomerang
|
UTSW |
14 |
7,901,945 (GRCm38) |
missense |
probably damaging |
1.00 |
Queensland
|
UTSW |
14 |
7,927,352 (GRCm38) |
missense |
probably damaging |
1.00 |
R3437_Flnb_252
|
UTSW |
14 |
7,942,057 (GRCm38) |
missense |
probably damaging |
0.97 |
R8441_Flnb_221
|
UTSW |
14 |
7,896,488 (GRCm38) |
missense |
probably benign |
0.15 |
Rhodelinda
|
UTSW |
14 |
7,887,682 (GRCm38) |
splice site |
probably benign |
|
saul
|
UTSW |
14 |
7,889,183 (GRCm38) |
missense |
probably damaging |
0.99 |
Xerxes
|
UTSW |
14 |
7,867,551 (GRCm38) |
missense |
probably damaging |
1.00 |
R0068:Flnb
|
UTSW |
14 |
7,915,290 (GRCm38) |
missense |
possibly damaging |
0.49 |
R0068:Flnb
|
UTSW |
14 |
7,915,290 (GRCm38) |
missense |
possibly damaging |
0.49 |
R0084:Flnb
|
UTSW |
14 |
7,935,979 (GRCm38) |
missense |
probably benign |
|
R0128:Flnb
|
UTSW |
14 |
7,901,951 (GRCm38) |
missense |
probably damaging |
0.99 |
R0130:Flnb
|
UTSW |
14 |
7,901,951 (GRCm38) |
missense |
probably damaging |
0.99 |
R0148:Flnb
|
UTSW |
14 |
7,939,077 (GRCm38) |
missense |
probably benign |
0.01 |
R0166:Flnb
|
UTSW |
14 |
7,896,115 (GRCm38) |
missense |
probably damaging |
1.00 |
R0376:Flnb
|
UTSW |
14 |
7,946,014 (GRCm38) |
critical splice donor site |
probably null |
|
R0547:Flnb
|
UTSW |
14 |
7,912,943 (GRCm38) |
splice site |
probably null |
|
R0612:Flnb
|
UTSW |
14 |
7,887,682 (GRCm38) |
splice site |
probably benign |
|
R0656:Flnb
|
UTSW |
14 |
7,927,352 (GRCm38) |
missense |
probably damaging |
1.00 |
R0691:Flnb
|
UTSW |
14 |
7,890,810 (GRCm38) |
missense |
probably benign |
0.16 |
R1241:Flnb
|
UTSW |
14 |
7,896,503 (GRCm38) |
missense |
probably benign |
0.06 |
R1572:Flnb
|
UTSW |
14 |
7,883,908 (GRCm38) |
missense |
probably damaging |
0.97 |
R1682:Flnb
|
UTSW |
14 |
7,913,121 (GRCm38) |
missense |
probably benign |
0.04 |
R1807:Flnb
|
UTSW |
14 |
7,934,645 (GRCm38) |
missense |
probably benign |
0.26 |
R1848:Flnb
|
UTSW |
14 |
7,892,113 (GRCm38) |
missense |
probably damaging |
1.00 |
R1959:Flnb
|
UTSW |
14 |
7,884,735 (GRCm38) |
nonsense |
probably null |
|
R2078:Flnb
|
UTSW |
14 |
7,927,466 (GRCm38) |
missense |
probably damaging |
1.00 |
R2132:Flnb
|
UTSW |
14 |
7,873,376 (GRCm38) |
missense |
probably benign |
0.04 |
R2209:Flnb
|
UTSW |
14 |
7,905,507 (GRCm38) |
nonsense |
probably null |
|
R2212:Flnb
|
UTSW |
14 |
7,881,652 (GRCm38) |
small deletion |
probably benign |
|
R2213:Flnb
|
UTSW |
14 |
7,881,652 (GRCm38) |
small deletion |
probably benign |
|
R2363:Flnb
|
UTSW |
14 |
7,945,950 (GRCm38) |
missense |
possibly damaging |
0.95 |
R2415:Flnb
|
UTSW |
14 |
7,929,932 (GRCm38) |
missense |
probably benign |
0.07 |
R2983:Flnb
|
UTSW |
14 |
7,882,250 (GRCm38) |
missense |
probably damaging |
1.00 |
R3001:Flnb
|
UTSW |
14 |
7,907,162 (GRCm38) |
missense |
probably benign |
0.22 |
R3002:Flnb
|
UTSW |
14 |
7,907,162 (GRCm38) |
missense |
probably benign |
0.22 |
R3436:Flnb
|
UTSW |
14 |
7,942,057 (GRCm38) |
missense |
probably damaging |
0.97 |
R3437:Flnb
|
UTSW |
14 |
7,942,057 (GRCm38) |
missense |
probably damaging |
0.97 |
R3778:Flnb
|
UTSW |
14 |
7,915,353 (GRCm38) |
missense |
probably benign |
0.06 |
R3783:Flnb
|
UTSW |
14 |
7,889,236 (GRCm38) |
missense |
probably benign |
0.04 |
R4162:Flnb
|
UTSW |
14 |
7,915,374 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4163:Flnb
|
UTSW |
14 |
7,915,374 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4164:Flnb
|
UTSW |
14 |
7,915,374 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4356:Flnb
|
UTSW |
14 |
7,922,700 (GRCm38) |
missense |
probably benign |
|
R4369:Flnb
|
UTSW |
14 |
7,942,216 (GRCm38) |
missense |
probably benign |
|
R4783:Flnb
|
UTSW |
14 |
7,905,701 (GRCm38) |
missense |
probably benign |
0.12 |
R4785:Flnb
|
UTSW |
14 |
7,905,701 (GRCm38) |
missense |
probably benign |
0.12 |
R4790:Flnb
|
UTSW |
14 |
7,905,661 (GRCm38) |
missense |
probably benign |
0.34 |
R4828:Flnb
|
UTSW |
14 |
7,919,238 (GRCm38) |
missense |
probably benign |
0.13 |
R4882:Flnb
|
UTSW |
14 |
7,929,936 (GRCm38) |
missense |
possibly damaging |
0.56 |
R5002:Flnb
|
UTSW |
14 |
7,945,882 (GRCm38) |
missense |
probably damaging |
1.00 |
R5058:Flnb
|
UTSW |
14 |
7,924,262 (GRCm38) |
nonsense |
probably null |
|
R5184:Flnb
|
UTSW |
14 |
7,901,945 (GRCm38) |
missense |
probably damaging |
1.00 |
R5186:Flnb
|
UTSW |
14 |
7,909,748 (GRCm38) |
missense |
probably damaging |
1.00 |
R5395:Flnb
|
UTSW |
14 |
7,883,881 (GRCm38) |
missense |
probably benign |
0.02 |
R5421:Flnb
|
UTSW |
14 |
7,926,494 (GRCm38) |
missense |
probably damaging |
1.00 |
R5667:Flnb
|
UTSW |
14 |
7,890,843 (GRCm38) |
missense |
probably benign |
0.00 |
R5671:Flnb
|
UTSW |
14 |
7,890,843 (GRCm38) |
missense |
probably benign |
0.00 |
R5714:Flnb
|
UTSW |
14 |
7,929,073 (GRCm38) |
missense |
probably damaging |
1.00 |
R5860:Flnb
|
UTSW |
14 |
7,931,135 (GRCm38) |
missense |
probably damaging |
1.00 |
R5892:Flnb
|
UTSW |
14 |
7,907,183 (GRCm38) |
missense |
probably damaging |
1.00 |
R5924:Flnb
|
UTSW |
14 |
7,890,765 (GRCm38) |
missense |
probably benign |
0.00 |
R6131:Flnb
|
UTSW |
14 |
7,894,635 (GRCm38) |
missense |
possibly damaging |
0.79 |
R6489:Flnb
|
UTSW |
14 |
7,867,551 (GRCm38) |
missense |
probably damaging |
1.00 |
R6582:Flnb
|
UTSW |
14 |
7,892,275 (GRCm38) |
critical splice donor site |
probably null |
|
R6586:Flnb
|
UTSW |
14 |
7,929,138 (GRCm38) |
missense |
possibly damaging |
0.93 |
R6611:Flnb
|
UTSW |
14 |
7,915,318 (GRCm38) |
missense |
probably damaging |
1.00 |
R6626:Flnb
|
UTSW |
14 |
7,929,012 (GRCm38) |
missense |
probably damaging |
1.00 |
R6700:Flnb
|
UTSW |
14 |
7,892,189 (GRCm38) |
missense |
probably damaging |
0.99 |
R6738:Flnb
|
UTSW |
14 |
7,904,536 (GRCm38) |
missense |
probably benign |
0.01 |
R6864:Flnb
|
UTSW |
14 |
7,905,640 (GRCm38) |
missense |
possibly damaging |
0.84 |
R6916:Flnb
|
UTSW |
14 |
7,907,171 (GRCm38) |
missense |
probably damaging |
0.99 |
R7117:Flnb
|
UTSW |
14 |
7,894,214 (GRCm38) |
missense |
probably benign |
0.02 |
R7164:Flnb
|
UTSW |
14 |
7,915,944 (GRCm38) |
splice site |
probably null |
|
R7328:Flnb
|
UTSW |
14 |
7,894,660 (GRCm38) |
nonsense |
probably null |
|
R7328:Flnb
|
UTSW |
14 |
7,883,788 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7687:Flnb
|
UTSW |
14 |
7,924,224 (GRCm38) |
missense |
probably damaging |
1.00 |
R7716:Flnb
|
UTSW |
14 |
7,917,274 (GRCm38) |
missense |
possibly damaging |
0.64 |
R7763:Flnb
|
UTSW |
14 |
7,926,478 (GRCm38) |
missense |
probably benign |
0.00 |
R7821:Flnb
|
UTSW |
14 |
7,939,113 (GRCm38) |
missense |
probably benign |
0.00 |
R7921:Flnb
|
UTSW |
14 |
7,933,800 (GRCm38) |
missense |
possibly damaging |
0.57 |
R8008:Flnb
|
UTSW |
14 |
7,892,155 (GRCm38) |
missense |
probably damaging |
1.00 |
R8075:Flnb
|
UTSW |
14 |
7,913,048 (GRCm38) |
missense |
probably benign |
0.00 |
R8084:Flnb
|
UTSW |
14 |
7,907,243 (GRCm38) |
missense |
probably benign |
0.00 |
R8259:Flnb
|
UTSW |
14 |
7,889,183 (GRCm38) |
missense |
probably damaging |
0.99 |
R8441:Flnb
|
UTSW |
14 |
7,896,488 (GRCm38) |
missense |
probably benign |
0.15 |
R8493:Flnb
|
UTSW |
14 |
7,869,822 (GRCm38) |
missense |
probably damaging |
0.97 |
R8508:Flnb
|
UTSW |
14 |
7,950,394 (GRCm38) |
missense |
probably damaging |
0.98 |
R8531:Flnb
|
UTSW |
14 |
7,929,939 (GRCm38) |
missense |
probably damaging |
1.00 |
R8812:Flnb
|
UTSW |
14 |
7,887,624 (GRCm38) |
missense |
probably benign |
0.06 |
R8814:Flnb
|
UTSW |
14 |
7,927,409 (GRCm38) |
missense |
probably damaging |
1.00 |
R8825:Flnb
|
UTSW |
14 |
7,887,566 (GRCm38) |
missense |
probably damaging |
1.00 |
R8868:Flnb
|
UTSW |
14 |
7,908,671 (GRCm38) |
missense |
probably benign |
0.02 |
R8955:Flnb
|
UTSW |
14 |
7,904,688 (GRCm38) |
nonsense |
probably null |
|
R8955:Flnb
|
UTSW |
14 |
7,892,874 (GRCm38) |
missense |
probably damaging |
1.00 |
R8976:Flnb
|
UTSW |
14 |
7,901,882 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9055:Flnb
|
UTSW |
14 |
7,908,553 (GRCm38) |
missense |
probably benign |
0.00 |
R9148:Flnb
|
UTSW |
14 |
7,817,996 (GRCm38) |
start gained |
probably benign |
|
R9179:Flnb
|
UTSW |
14 |
7,887,541 (GRCm38) |
nonsense |
probably null |
|
R9180:Flnb
|
UTSW |
14 |
7,818,219 (GRCm38) |
missense |
probably damaging |
1.00 |
R9189:Flnb
|
UTSW |
14 |
7,892,976 (GRCm38) |
missense |
possibly damaging |
0.90 |
R9286:Flnb
|
UTSW |
14 |
7,873,414 (GRCm38) |
missense |
probably damaging |
0.98 |
R9288:Flnb
|
UTSW |
14 |
7,904,498 (GRCm38) |
missense |
probably benign |
0.43 |
R9354:Flnb
|
UTSW |
14 |
7,818,411 (GRCm38) |
missense |
probably benign |
0.13 |
R9484:Flnb
|
UTSW |
14 |
7,929,004 (GRCm38) |
missense |
probably benign |
0.06 |
R9505:Flnb
|
UTSW |
14 |
7,904,665 (GRCm38) |
missense |
probably benign |
|
R9525:Flnb
|
UTSW |
14 |
7,905,481 (GRCm38) |
missense |
probably damaging |
1.00 |
R9621:Flnb
|
UTSW |
14 |
7,926,421 (GRCm38) |
missense |
probably damaging |
0.99 |
R9630:Flnb
|
UTSW |
14 |
7,926,438 (GRCm38) |
nonsense |
probably null |
|
R9739:Flnb
|
UTSW |
14 |
7,935,954 (GRCm38) |
nonsense |
probably null |
|
R9760:Flnb
|
UTSW |
14 |
7,929,846 (GRCm38) |
missense |
probably damaging |
0.98 |
X0066:Flnb
|
UTSW |
14 |
7,908,636 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1088:Flnb
|
UTSW |
14 |
7,905,871 (GRCm38) |
missense |
probably benign |
0.04 |
Z1176:Flnb
|
UTSW |
14 |
7,942,066 (GRCm38) |
missense |
probably benign |
0.25 |
|