Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aaas |
C |
T |
15: 102,247,068 (GRCm39) |
|
probably benign |
Het |
Aadacl4fm5 |
G |
A |
4: 144,504,389 (GRCm39) |
T254I |
possibly damaging |
Het |
Abce1 |
A |
G |
8: 80,412,578 (GRCm39) |
I583T |
probably benign |
Het |
Abtb3 |
T |
C |
10: 85,469,563 (GRCm39) |
L828P |
probably damaging |
Het |
Adcy1 |
A |
T |
11: 7,111,945 (GRCm39) |
T937S |
probably benign |
Het |
Adgra2 |
A |
G |
8: 27,601,196 (GRCm39) |
I279V |
possibly damaging |
Het |
Adgrl4 |
A |
T |
3: 151,216,416 (GRCm39) |
N533I |
possibly damaging |
Het |
Adipor1 |
T |
C |
1: 134,350,771 (GRCm39) |
S7P |
probably benign |
Het |
Amelx |
A |
T |
X: 167,965,153 (GRCm39) |
|
probably null |
Het |
Anks1b |
A |
T |
10: 89,885,792 (GRCm39) |
T163S |
probably damaging |
Het |
Apc |
A |
G |
18: 34,450,388 (GRCm39) |
E2394G |
probably damaging |
Het |
Arhgef39 |
C |
T |
4: 43,499,309 (GRCm39) |
G56E |
probably damaging |
Het |
Arnt |
C |
T |
3: 95,355,704 (GRCm39) |
S16L |
possibly damaging |
Het |
Arsj |
A |
G |
3: 126,232,670 (GRCm39) |
N472S |
probably benign |
Het |
Atg2b |
T |
C |
12: 105,635,677 (GRCm39) |
Y197C |
probably damaging |
Het |
B3gat1 |
A |
T |
9: 26,667,248 (GRCm39) |
D160V |
possibly damaging |
Het |
Bmp7 |
T |
C |
2: 172,781,714 (GRCm39) |
E50G |
probably damaging |
Het |
Bms1 |
T |
C |
6: 118,369,939 (GRCm39) |
E869G |
probably damaging |
Het |
Brd4 |
G |
A |
17: 32,440,340 (GRCm39) |
P332L |
possibly damaging |
Het |
C130074G19Rik |
T |
C |
1: 184,615,095 (GRCm39) |
T32A |
probably benign |
Het |
C1rl |
A |
T |
6: 124,486,021 (GRCm39) |
Y464F |
probably damaging |
Het |
Ccdc150 |
T |
A |
1: 54,303,068 (GRCm39) |
M193K |
probably benign |
Het |
Ccdc7a |
A |
G |
8: 129,706,616 (GRCm39) |
S338P |
probably damaging |
Het |
Cenpu |
T |
C |
8: 47,025,872 (GRCm39) |
|
probably benign |
Het |
Cep170 |
A |
C |
1: 176,597,013 (GRCm39) |
V448G |
probably benign |
Het |
Col27a1 |
G |
T |
4: 63,196,031 (GRCm39) |
A879S |
probably benign |
Het |
Crtac1 |
C |
T |
19: 42,276,383 (GRCm39) |
S515N |
possibly damaging |
Het |
Cstad |
G |
A |
2: 30,498,293 (GRCm39) |
V43M |
unknown |
Het |
Daam1 |
T |
C |
12: 72,029,529 (GRCm39) |
|
probably null |
Het |
Dnmt1 |
C |
T |
9: 20,838,442 (GRCm39) |
R207H |
probably benign |
Het |
Dsg3 |
A |
G |
18: 20,655,162 (GRCm39) |
N153S |
probably damaging |
Het |
Dzip3 |
C |
A |
16: 48,747,956 (GRCm39) |
L1151F |
probably damaging |
Het |
Eml5 |
A |
T |
12: 98,826,220 (GRCm39) |
H644Q |
probably damaging |
Het |
Emsy |
A |
G |
7: 98,297,027 (GRCm39) |
L52P |
probably damaging |
Het |
Eno1 |
T |
A |
4: 150,331,232 (GRCm39) |
|
probably null |
Het |
Epha3 |
T |
A |
16: 63,593,315 (GRCm39) |
T258S |
probably benign |
Het |
Ern1 |
T |
C |
11: 106,317,723 (GRCm39) |
T134A |
probably damaging |
Het |
Fam151b |
G |
T |
13: 92,614,410 (GRCm39) |
T26K |
probably damaging |
Het |
Fam151b |
T |
A |
13: 92,614,411 (GRCm39) |
T26S |
probably damaging |
Het |
Fat1 |
T |
C |
8: 45,493,719 (GRCm39) |
V3955A |
probably damaging |
Het |
Fgr |
A |
G |
4: 132,725,673 (GRCm39) |
M361V |
probably benign |
Het |
Fmo4 |
G |
A |
1: 162,631,259 (GRCm39) |
T236I |
probably benign |
Het |
Fndc7 |
G |
A |
3: 108,790,825 (GRCm39) |
T67I |
probably damaging |
Het |
Fxr2 |
A |
G |
11: 69,534,766 (GRCm39) |
T216A |
probably benign |
Het |
Gdf10 |
G |
A |
14: 33,654,710 (GRCm39) |
A406T |
probably benign |
Het |
Gm42669 |
A |
T |
5: 107,656,738 (GRCm39) |
E355D |
possibly damaging |
Het |
Gm5174 |
A |
T |
10: 86,492,617 (GRCm39) |
|
noncoding transcript |
Het |
Gm5431 |
A |
T |
11: 48,779,224 (GRCm39) |
L844* |
probably null |
Het |
Gm6489 |
T |
C |
1: 31,326,452 (GRCm39) |
|
noncoding transcript |
Het |
Gna11 |
A |
G |
10: 81,366,678 (GRCm39) |
V344A |
probably damaging |
Het |
Gtpbp3 |
A |
G |
8: 71,943,099 (GRCm39) |
E170G |
probably damaging |
Het |
H2az1 |
A |
C |
3: 137,571,275 (GRCm39) |
|
probably benign |
Het |
Heatr1 |
A |
G |
13: 12,411,419 (GRCm39) |
N87D |
probably damaging |
Het |
Iars2 |
T |
C |
1: 185,027,868 (GRCm39) |
K687E |
possibly damaging |
Het |
Ica1 |
T |
C |
6: 8,749,736 (GRCm39) |
D71G |
possibly damaging |
Het |
Ifnlr1 |
T |
C |
4: 135,413,881 (GRCm39) |
L10P |
probably damaging |
Het |
Il1r1 |
T |
A |
1: 40,352,300 (GRCm39) |
L490* |
probably null |
Het |
Ip6k3 |
A |
T |
17: 27,370,142 (GRCm39) |
L92Q |
probably benign |
Het |
Itgbl1 |
T |
A |
14: 124,204,090 (GRCm39) |
F394I |
probably damaging |
Het |
Kat6b |
T |
C |
14: 21,678,947 (GRCm39) |
Y437H |
probably damaging |
Het |
Kcnh5 |
G |
C |
12: 74,944,358 (GRCm39) |
Q964E |
probably benign |
Het |
Krt27 |
A |
T |
11: 99,237,309 (GRCm39) |
|
probably null |
Het |
Mki67 |
A |
T |
7: 135,300,128 (GRCm39) |
D1635E |
probably benign |
Het |
Mmp23 |
G |
T |
4: 155,736,509 (GRCm39) |
H177Q |
possibly damaging |
Het |
Myef2l |
G |
T |
3: 10,154,346 (GRCm39) |
V372F |
probably benign |
Het |
Mylk2 |
C |
A |
2: 152,759,527 (GRCm39) |
Q406K |
possibly damaging |
Het |
Myo1g |
A |
G |
11: 6,462,159 (GRCm39) |
|
probably null |
Het |
Myrf |
T |
C |
19: 10,197,160 (GRCm39) |
T261A |
probably benign |
Het |
Nmt2 |
C |
T |
2: 3,326,419 (GRCm39) |
P486L |
possibly damaging |
Het |
Oard1 |
T |
A |
17: 48,722,304 (GRCm39) |
L100* |
probably null |
Het |
Oca2 |
T |
C |
7: 55,971,246 (GRCm39) |
I391T |
possibly damaging |
Het |
Or51v14 |
T |
A |
7: 103,260,618 (GRCm39) |
*314L |
probably null |
Het |
Or5k17 |
T |
A |
16: 58,746,530 (GRCm39) |
M135L |
probably benign |
Het |
Or5p64 |
A |
C |
7: 107,854,403 (GRCm39) |
L314* |
probably null |
Het |
Or6c68 |
A |
T |
10: 129,157,740 (GRCm39) |
I83F |
possibly damaging |
Het |
Or8b39 |
T |
A |
9: 37,996,419 (GRCm39) |
C96S |
probably damaging |
Het |
Or9k2b |
C |
A |
10: 130,015,847 (GRCm39) |
A301S |
possibly damaging |
Het |
Pabpc4 |
T |
A |
4: 123,180,658 (GRCm39) |
S127T |
probably damaging |
Het |
Pcdhb1 |
A |
G |
18: 37,398,760 (GRCm39) |
D237G |
probably damaging |
Het |
Pdcd6ip |
T |
C |
9: 113,537,090 (GRCm39) |
Y29C |
probably damaging |
Het |
Phf3 |
C |
A |
1: 30,870,601 (GRCm39) |
R95L |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,757,421 (GRCm39) |
V1539D |
probably damaging |
Het |
Plxna1 |
A |
T |
6: 89,308,273 (GRCm39) |
D1271E |
probably damaging |
Het |
Ppp3r2 |
A |
G |
4: 49,681,726 (GRCm39) |
F75L |
probably damaging |
Het |
Pth2r |
C |
A |
1: 65,411,514 (GRCm39) |
D350E |
probably damaging |
Het |
Rabgap1 |
T |
C |
2: 37,373,774 (GRCm39) |
F262S |
possibly damaging |
Het |
Rbbp6 |
T |
C |
7: 122,589,511 (GRCm39) |
S438P |
probably benign |
Het |
Rexo1 |
G |
A |
10: 80,379,200 (GRCm39) |
R1038C |
probably damaging |
Het |
Rnf10 |
A |
G |
5: 115,398,381 (GRCm39) |
|
probably benign |
Het |
Scyl1 |
C |
A |
19: 5,810,132 (GRCm39) |
A565S |
probably benign |
Het |
Septin4 |
A |
G |
11: 87,481,193 (GRCm39) |
T378A |
probably benign |
Het |
Sh3yl1 |
A |
G |
12: 30,992,787 (GRCm39) |
|
probably null |
Het |
Slc1a7 |
G |
T |
4: 107,825,782 (GRCm39) |
D14Y |
probably benign |
Het |
Slc32a1 |
T |
C |
2: 158,455,963 (GRCm39) |
V206A |
probably damaging |
Het |
Smyd5 |
G |
A |
6: 85,415,121 (GRCm39) |
R43Q |
probably benign |
Het |
Snrnp200 |
G |
A |
2: 127,058,095 (GRCm39) |
A286T |
possibly damaging |
Het |
Sp110 |
A |
C |
1: 85,505,050 (GRCm39) |
F434C |
probably benign |
Het |
Srebf2 |
T |
A |
15: 82,079,155 (GRCm39) |
H794Q |
probably benign |
Het |
Ssbp2 |
T |
C |
13: 91,812,303 (GRCm39) |
|
probably benign |
Het |
Sspo |
G |
A |
6: 48,455,207 (GRCm39) |
G3023D |
probably damaging |
Het |
St6galnac5 |
T |
A |
3: 152,552,120 (GRCm39) |
Q149L |
probably benign |
Het |
Stab2 |
A |
G |
10: 86,697,334 (GRCm39) |
Y1985H |
probably benign |
Het |
Suz12 |
A |
G |
11: 79,889,926 (GRCm39) |
M146V |
probably benign |
Het |
Tac2 |
A |
G |
10: 127,564,349 (GRCm39) |
|
probably null |
Het |
Thbd |
T |
C |
2: 148,248,899 (GRCm39) |
E323G |
probably damaging |
Het |
Tnfrsf26 |
T |
A |
7: 143,171,660 (GRCm39) |
T98S |
probably damaging |
Het |
Trim15 |
T |
C |
17: 37,173,215 (GRCm39) |
|
probably benign |
Het |
Trpt1 |
T |
C |
19: 6,975,561 (GRCm39) |
V105A |
possibly damaging |
Het |
Vcam1 |
T |
C |
3: 115,919,606 (GRCm39) |
Y226C |
probably damaging |
Het |
Vmn1r175 |
A |
G |
7: 23,507,808 (GRCm39) |
V273A |
probably benign |
Het |
Vmn2r109 |
A |
G |
17: 20,784,969 (GRCm39) |
V17A |
probably benign |
Het |
Vmn2r84 |
G |
A |
10: 130,226,677 (GRCm39) |
A387V |
probably benign |
Het |
Wdfy4 |
A |
T |
14: 32,693,641 (GRCm39) |
L2728Q |
probably damaging |
Het |
Zfp934 |
T |
A |
13: 62,666,108 (GRCm39) |
T178S |
possibly damaging |
Het |
|
Other mutations in Fbn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Fbn1
|
APN |
2 |
125,166,867 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00159:Fbn1
|
APN |
2 |
125,239,793 (GRCm39) |
missense |
probably benign |
0.14 |
IGL00500:Fbn1
|
APN |
2 |
125,159,436 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00558:Fbn1
|
APN |
2 |
125,171,048 (GRCm39) |
splice site |
probably benign |
|
IGL00645:Fbn1
|
APN |
2 |
125,159,023 (GRCm39) |
splice site |
probably benign |
|
IGL00863:Fbn1
|
APN |
2 |
125,245,139 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00926:Fbn1
|
APN |
2 |
125,160,962 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00935:Fbn1
|
APN |
2 |
125,219,830 (GRCm39) |
nonsense |
probably null |
|
IGL00950:Fbn1
|
APN |
2 |
125,200,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01090:Fbn1
|
APN |
2 |
125,236,696 (GRCm39) |
splice site |
probably benign |
|
IGL01106:Fbn1
|
APN |
2 |
125,193,626 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01486:Fbn1
|
APN |
2 |
125,231,898 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01519:Fbn1
|
APN |
2 |
125,158,939 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01585:Fbn1
|
APN |
2 |
125,202,030 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01730:Fbn1
|
APN |
2 |
125,154,894 (GRCm39) |
splice site |
probably benign |
|
IGL01793:Fbn1
|
APN |
2 |
125,229,213 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01803:Fbn1
|
APN |
2 |
125,192,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01803:Fbn1
|
APN |
2 |
125,143,645 (GRCm39) |
missense |
probably benign |
|
IGL01916:Fbn1
|
APN |
2 |
125,157,366 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02035:Fbn1
|
APN |
2 |
125,177,282 (GRCm39) |
splice site |
probably null |
|
IGL02097:Fbn1
|
APN |
2 |
125,205,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02233:Fbn1
|
APN |
2 |
125,163,530 (GRCm39) |
splice site |
probably benign |
|
IGL02512:Fbn1
|
APN |
2 |
125,180,380 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02552:Fbn1
|
APN |
2 |
125,254,633 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02657:Fbn1
|
APN |
2 |
125,193,945 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02718:Fbn1
|
APN |
2 |
125,211,806 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02863:Fbn1
|
APN |
2 |
125,145,176 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02974:Fbn1
|
APN |
2 |
125,188,250 (GRCm39) |
missense |
probably null |
0.99 |
IGL03058:Fbn1
|
APN |
2 |
125,245,120 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03172:Fbn1
|
APN |
2 |
125,162,888 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03288:Fbn1
|
APN |
2 |
125,145,103 (GRCm39) |
missense |
probably benign |
0.13 |
Carinatum
|
UTSW |
2 |
125,184,750 (GRCm39) |
missense |
possibly damaging |
0.70 |
Elasticity
|
UTSW |
2 |
125,245,052 (GRCm39) |
missense |
possibly damaging |
0.63 |
Excavatum
|
UTSW |
2 |
125,177,407 (GRCm39) |
missense |
probably damaging |
1.00 |
Exceedingly
|
UTSW |
2 |
125,186,015 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Extensor
|
UTSW |
2 |
125,170,078 (GRCm39) |
missense |
probably damaging |
1.00 |
lincoln
|
UTSW |
2 |
125,245,090 (GRCm39) |
missense |
possibly damaging |
0.50 |
Long
|
UTSW |
2 |
125,158,958 (GRCm39) |
missense |
probably damaging |
1.00 |
Pectus
|
UTSW |
2 |
125,163,611 (GRCm39) |
missense |
possibly damaging |
0.82 |
Reach
|
UTSW |
2 |
125,223,954 (GRCm39) |
nonsense |
probably null |
|
reaper
|
UTSW |
2 |
125,157,324 (GRCm39) |
missense |
probably damaging |
0.98 |
Scythe
|
UTSW |
2 |
125,245,148 (GRCm39) |
missense |
possibly damaging |
0.84 |
String_bean
|
UTSW |
2 |
125,221,054 (GRCm39) |
splice site |
probably null |
|
wirey
|
UTSW |
2 |
125,151,415 (GRCm39) |
missense |
probably benign |
|
3-1:Fbn1
|
UTSW |
2 |
125,236,525 (GRCm39) |
splice site |
probably benign |
|
BB004:Fbn1
|
UTSW |
2 |
125,225,656 (GRCm39) |
missense |
possibly damaging |
0.82 |
BB014:Fbn1
|
UTSW |
2 |
125,225,656 (GRCm39) |
missense |
possibly damaging |
0.82 |
P0012:Fbn1
|
UTSW |
2 |
125,211,241 (GRCm39) |
splice site |
probably benign |
|
PIT4403001:Fbn1
|
UTSW |
2 |
125,184,831 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4466001:Fbn1
|
UTSW |
2 |
125,148,421 (GRCm39) |
missense |
possibly damaging |
0.90 |
PIT4472001:Fbn1
|
UTSW |
2 |
125,148,421 (GRCm39) |
missense |
possibly damaging |
0.90 |
PIT4651001:Fbn1
|
UTSW |
2 |
125,205,909 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0226:Fbn1
|
UTSW |
2 |
125,162,830 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0310:Fbn1
|
UTSW |
2 |
125,205,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R0362:Fbn1
|
UTSW |
2 |
125,151,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R0374:Fbn1
|
UTSW |
2 |
125,163,596 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0433:Fbn1
|
UTSW |
2 |
125,190,135 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0441:Fbn1
|
UTSW |
2 |
125,151,675 (GRCm39) |
critical splice donor site |
probably null |
|
R0501:Fbn1
|
UTSW |
2 |
125,143,669 (GRCm39) |
missense |
probably benign |
0.23 |
R0510:Fbn1
|
UTSW |
2 |
125,184,845 (GRCm39) |
splice site |
probably benign |
|
R0573:Fbn1
|
UTSW |
2 |
125,231,169 (GRCm39) |
missense |
probably damaging |
0.99 |
R0622:Fbn1
|
UTSW |
2 |
125,220,944 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0630:Fbn1
|
UTSW |
2 |
125,236,690 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0724:Fbn1
|
UTSW |
2 |
125,193,984 (GRCm39) |
missense |
probably benign |
0.14 |
R0739:Fbn1
|
UTSW |
2 |
125,209,550 (GRCm39) |
missense |
probably benign |
0.18 |
R0744:Fbn1
|
UTSW |
2 |
125,156,734 (GRCm39) |
splice site |
probably benign |
|
R0811:Fbn1
|
UTSW |
2 |
125,245,090 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0812:Fbn1
|
UTSW |
2 |
125,245,090 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0862:Fbn1
|
UTSW |
2 |
125,184,811 (GRCm39) |
nonsense |
probably null |
|
R0864:Fbn1
|
UTSW |
2 |
125,184,811 (GRCm39) |
nonsense |
probably null |
|
R1061:Fbn1
|
UTSW |
2 |
125,187,883 (GRCm39) |
missense |
probably benign |
0.01 |
R1126:Fbn1
|
UTSW |
2 |
125,163,112 (GRCm39) |
splice site |
probably null |
|
R1172:Fbn1
|
UTSW |
2 |
125,236,607 (GRCm39) |
missense |
probably benign |
0.13 |
R1175:Fbn1
|
UTSW |
2 |
125,236,607 (GRCm39) |
missense |
probably benign |
0.13 |
R1183:Fbn1
|
UTSW |
2 |
125,163,537 (GRCm39) |
missense |
probably benign |
0.07 |
R1218:Fbn1
|
UTSW |
2 |
125,254,669 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1241:Fbn1
|
UTSW |
2 |
125,214,447 (GRCm39) |
splice site |
probably benign |
|
R1248:Fbn1
|
UTSW |
2 |
125,143,529 (GRCm39) |
missense |
probably benign |
0.01 |
R1345:Fbn1
|
UTSW |
2 |
125,156,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R1374:Fbn1
|
UTSW |
2 |
125,188,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R1458:Fbn1
|
UTSW |
2 |
125,143,849 (GRCm39) |
missense |
probably benign |
0.01 |
R1474:Fbn1
|
UTSW |
2 |
125,203,185 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1496:Fbn1
|
UTSW |
2 |
125,151,415 (GRCm39) |
missense |
probably benign |
|
R1502:Fbn1
|
UTSW |
2 |
125,205,626 (GRCm39) |
nonsense |
probably null |
|
R1511:Fbn1
|
UTSW |
2 |
125,148,205 (GRCm39) |
missense |
probably benign |
0.00 |
R1588:Fbn1
|
UTSW |
2 |
125,161,034 (GRCm39) |
missense |
probably benign |
0.19 |
R1626:Fbn1
|
UTSW |
2 |
125,183,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R1676:Fbn1
|
UTSW |
2 |
125,151,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R1712:Fbn1
|
UTSW |
2 |
125,188,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R1772:Fbn1
|
UTSW |
2 |
125,245,148 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1776:Fbn1
|
UTSW |
2 |
125,163,654 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1869:Fbn1
|
UTSW |
2 |
125,193,947 (GRCm39) |
missense |
probably benign |
0.00 |
R1894:Fbn1
|
UTSW |
2 |
125,236,541 (GRCm39) |
missense |
probably damaging |
0.96 |
R1925:Fbn1
|
UTSW |
2 |
125,205,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R1995:Fbn1
|
UTSW |
2 |
125,192,293 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2140:Fbn1
|
UTSW |
2 |
125,185,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R2142:Fbn1
|
UTSW |
2 |
125,254,628 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2268:Fbn1
|
UTSW |
2 |
125,163,661 (GRCm39) |
missense |
possibly damaging |
0.49 |
R3409:Fbn1
|
UTSW |
2 |
125,254,585 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3418:Fbn1
|
UTSW |
2 |
125,162,846 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3508:Fbn1
|
UTSW |
2 |
125,148,247 (GRCm39) |
missense |
probably benign |
0.19 |
R3778:Fbn1
|
UTSW |
2 |
125,159,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R3800:Fbn1
|
UTSW |
2 |
125,187,894 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4001:Fbn1
|
UTSW |
2 |
125,319,415 (GRCm39) |
critical splice donor site |
probably null |
|
R4169:Fbn1
|
UTSW |
2 |
125,205,872 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4398:Fbn1
|
UTSW |
2 |
125,239,701 (GRCm39) |
missense |
probably benign |
0.32 |
R4482:Fbn1
|
UTSW |
2 |
125,205,530 (GRCm39) |
critical splice donor site |
probably null |
|
R4559:Fbn1
|
UTSW |
2 |
125,193,634 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4608:Fbn1
|
UTSW |
2 |
125,148,420 (GRCm39) |
missense |
probably benign |
0.05 |
R4634:Fbn1
|
UTSW |
2 |
125,185,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R4706:Fbn1
|
UTSW |
2 |
125,212,069 (GRCm39) |
missense |
probably benign |
0.21 |
R4712:Fbn1
|
UTSW |
2 |
125,183,236 (GRCm39) |
missense |
probably benign |
0.12 |
R4783:Fbn1
|
UTSW |
2 |
125,166,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Fbn1
|
UTSW |
2 |
125,166,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Fbn1
|
UTSW |
2 |
125,166,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R4793:Fbn1
|
UTSW |
2 |
125,163,155 (GRCm39) |
nonsense |
probably null |
|
R4838:Fbn1
|
UTSW |
2 |
125,214,319 (GRCm39) |
missense |
probably benign |
0.01 |
R4864:Fbn1
|
UTSW |
2 |
125,214,317 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4887:Fbn1
|
UTSW |
2 |
125,151,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R4942:Fbn1
|
UTSW |
2 |
125,225,536 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4952:Fbn1
|
UTSW |
2 |
125,159,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Fbn1
|
UTSW |
2 |
125,254,624 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5044:Fbn1
|
UTSW |
2 |
125,171,022 (GRCm39) |
missense |
probably damaging |
0.97 |
R5057:Fbn1
|
UTSW |
2 |
125,308,615 (GRCm39) |
missense |
probably benign |
0.33 |
R5115:Fbn1
|
UTSW |
2 |
125,174,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Fbn1
|
UTSW |
2 |
125,174,253 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5498:Fbn1
|
UTSW |
2 |
125,202,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R5526:Fbn1
|
UTSW |
2 |
125,207,559 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5529:Fbn1
|
UTSW |
2 |
125,215,870 (GRCm39) |
missense |
probably benign |
0.01 |
R5602:Fbn1
|
UTSW |
2 |
125,163,661 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5760:Fbn1
|
UTSW |
2 |
125,203,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R5837:Fbn1
|
UTSW |
2 |
125,221,054 (GRCm39) |
splice site |
probably null |
|
R5955:Fbn1
|
UTSW |
2 |
125,200,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R5980:Fbn1
|
UTSW |
2 |
125,157,324 (GRCm39) |
missense |
probably damaging |
0.98 |
R6039:Fbn1
|
UTSW |
2 |
125,205,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Fbn1
|
UTSW |
2 |
125,205,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R6058:Fbn1
|
UTSW |
2 |
125,308,532 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6089:Fbn1
|
UTSW |
2 |
125,163,145 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6136:Fbn1
|
UTSW |
2 |
125,245,052 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6161:Fbn1
|
UTSW |
2 |
125,211,721 (GRCm39) |
nonsense |
probably null |
|
R6162:Fbn1
|
UTSW |
2 |
125,202,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R6165:Fbn1
|
UTSW |
2 |
125,174,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R6169:Fbn1
|
UTSW |
2 |
125,177,409 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6221:Fbn1
|
UTSW |
2 |
125,162,841 (GRCm39) |
missense |
probably benign |
0.07 |
R6223:Fbn1
|
UTSW |
2 |
125,254,591 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6225:Fbn1
|
UTSW |
2 |
125,172,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R6238:Fbn1
|
UTSW |
2 |
125,166,865 (GRCm39) |
missense |
probably damaging |
0.98 |
R6329:Fbn1
|
UTSW |
2 |
125,150,393 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6401:Fbn1
|
UTSW |
2 |
125,188,370 (GRCm39) |
missense |
probably damaging |
0.98 |
R6480:Fbn1
|
UTSW |
2 |
125,177,338 (GRCm39) |
missense |
probably benign |
0.05 |
R6513:Fbn1
|
UTSW |
2 |
125,225,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R6530:Fbn1
|
UTSW |
2 |
125,231,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R6595:Fbn1
|
UTSW |
2 |
125,184,750 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6781:Fbn1
|
UTSW |
2 |
125,158,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R6849:Fbn1
|
UTSW |
2 |
125,163,611 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6860:Fbn1
|
UTSW |
2 |
125,170,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R6960:Fbn1
|
UTSW |
2 |
125,223,980 (GRCm39) |
missense |
probably benign |
0.16 |
R7134:Fbn1
|
UTSW |
2 |
125,223,969 (GRCm39) |
missense |
probably benign |
0.03 |
R7241:Fbn1
|
UTSW |
2 |
125,148,415 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7295:Fbn1
|
UTSW |
2 |
125,177,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R7312:Fbn1
|
UTSW |
2 |
125,308,594 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7322:Fbn1
|
UTSW |
2 |
125,321,115 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7349:Fbn1
|
UTSW |
2 |
125,157,321 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7365:Fbn1
|
UTSW |
2 |
125,193,969 (GRCm39) |
missense |
probably damaging |
0.97 |
R7392:Fbn1
|
UTSW |
2 |
125,185,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R7442:Fbn1
|
UTSW |
2 |
125,245,132 (GRCm39) |
missense |
possibly damaging |
0.45 |
R7452:Fbn1
|
UTSW |
2 |
125,347,375 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7453:Fbn1
|
UTSW |
2 |
125,162,879 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7457:Fbn1
|
UTSW |
2 |
125,193,667 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7458:Fbn1
|
UTSW |
2 |
125,161,036 (GRCm39) |
missense |
probably benign |
0.14 |
R7549:Fbn1
|
UTSW |
2 |
125,185,947 (GRCm39) |
missense |
probably damaging |
0.99 |
R7570:Fbn1
|
UTSW |
2 |
125,239,772 (GRCm39) |
missense |
probably benign |
0.29 |
R7666:Fbn1
|
UTSW |
2 |
125,148,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R7723:Fbn1
|
UTSW |
2 |
125,223,954 (GRCm39) |
nonsense |
probably null |
|
R7745:Fbn1
|
UTSW |
2 |
125,145,115 (GRCm39) |
missense |
probably benign |
0.06 |
R7754:Fbn1
|
UTSW |
2 |
125,321,200 (GRCm39) |
splice site |
probably null |
|
R7780:Fbn1
|
UTSW |
2 |
125,143,678 (GRCm39) |
missense |
probably benign |
0.15 |
R7849:Fbn1
|
UTSW |
2 |
125,151,405 (GRCm39) |
missense |
probably damaging |
0.98 |
R7927:Fbn1
|
UTSW |
2 |
125,225,656 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7942:Fbn1
|
UTSW |
2 |
125,254,706 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7948:Fbn1
|
UTSW |
2 |
125,183,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R7985:Fbn1
|
UTSW |
2 |
125,143,798 (GRCm39) |
missense |
probably benign |
0.01 |
R8051:Fbn1
|
UTSW |
2 |
125,148,383 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8054:Fbn1
|
UTSW |
2 |
125,187,938 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8058:Fbn1
|
UTSW |
2 |
125,193,889 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8113:Fbn1
|
UTSW |
2 |
125,319,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:Fbn1
|
UTSW |
2 |
125,347,402 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8472:Fbn1
|
UTSW |
2 |
125,151,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R8690:Fbn1
|
UTSW |
2 |
125,186,015 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8724:Fbn1
|
UTSW |
2 |
125,202,066 (GRCm39) |
missense |
probably damaging |
0.98 |
R8856:Fbn1
|
UTSW |
2 |
125,156,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R8916:Fbn1
|
UTSW |
2 |
125,245,149 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8931:Fbn1
|
UTSW |
2 |
125,202,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R8988:Fbn1
|
UTSW |
2 |
125,212,726 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9127:Fbn1
|
UTSW |
2 |
125,223,985 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9161:Fbn1
|
UTSW |
2 |
125,192,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R9495:Fbn1
|
UTSW |
2 |
125,160,984 (GRCm39) |
missense |
probably damaging |
0.96 |
R9515:Fbn1
|
UTSW |
2 |
125,207,551 (GRCm39) |
missense |
probably benign |
0.03 |
R9557:Fbn1
|
UTSW |
2 |
125,180,458 (GRCm39) |
missense |
probably damaging |
0.99 |
R9597:Fbn1
|
UTSW |
2 |
125,187,906 (GRCm39) |
missense |
probably benign |
|
R9680:Fbn1
|
UTSW |
2 |
125,310,484 (GRCm39) |
missense |
probably benign |
0.29 |
R9723:Fbn1
|
UTSW |
2 |
125,202,119 (GRCm39) |
nonsense |
probably null |
|
R9734:Fbn1
|
UTSW |
2 |
125,231,898 (GRCm39) |
missense |
probably benign |
0.03 |
R9796:Fbn1
|
UTSW |
2 |
125,158,941 (GRCm39) |
missense |
probably benign |
0.19 |
X0019:Fbn1
|
UTSW |
2 |
125,225,563 (GRCm39) |
missense |
possibly damaging |
0.82 |
X0020:Fbn1
|
UTSW |
2 |
125,211,260 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Fbn1
|
UTSW |
2 |
125,184,718 (GRCm39) |
critical splice donor site |
probably null |
|
X0067:Fbn1
|
UTSW |
2 |
125,211,834 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1088:Fbn1
|
UTSW |
2 |
125,192,208 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Fbn1
|
UTSW |
2 |
125,229,270 (GRCm39) |
missense |
possibly damaging |
0.51 |
Z1177:Fbn1
|
UTSW |
2 |
125,231,151 (GRCm39) |
missense |
probably damaging |
1.00 |
|