Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
T |
C |
5: 8,763,229 (GRCm39) |
S586P |
probably damaging |
Het |
Abcc3 |
G |
A |
11: 94,266,028 (GRCm39) |
|
probably benign |
Het |
Ap5z1 |
G |
A |
5: 142,461,546 (GRCm39) |
R583H |
probably benign |
Het |
Arrb1 |
G |
T |
7: 99,247,708 (GRCm39) |
V346L |
probably benign |
Het |
Atrnl1 |
T |
A |
19: 57,661,573 (GRCm39) |
F518I |
probably benign |
Het |
Bank1 |
T |
A |
3: 135,799,127 (GRCm39) |
I405F |
probably damaging |
Het |
Cacna1c |
A |
G |
6: 118,607,224 (GRCm39) |
C1227R |
probably benign |
Het |
Cacna1h |
A |
G |
17: 25,607,602 (GRCm39) |
L905P |
probably damaging |
Het |
Cc2d1a |
A |
G |
8: 84,860,465 (GRCm39) |
Y826H |
probably benign |
Het |
Cenpo |
A |
G |
12: 4,266,643 (GRCm39) |
V155A |
probably benign |
Het |
Cnmd |
A |
G |
14: 79,898,863 (GRCm39) |
F63S |
probably damaging |
Het |
Cnn3 |
G |
A |
3: 121,248,600 (GRCm39) |
G72D |
probably damaging |
Het |
Cox10 |
A |
G |
11: 63,962,539 (GRCm39) |
S101P |
probably benign |
Het |
Ctdsp1 |
T |
C |
1: 74,433,806 (GRCm39) |
V129A |
probably damaging |
Het |
Cyp2d34 |
A |
T |
15: 82,502,807 (GRCm39) |
S140T |
probably benign |
Het |
Dennd5a |
G |
A |
7: 109,532,820 (GRCm39) |
H317Y |
possibly damaging |
Het |
Dnaaf9 |
A |
G |
2: 130,555,334 (GRCm39) |
F858S |
probably damaging |
Het |
Eef2 |
C |
CN |
10: 81,014,603 (GRCm39) |
|
probably null |
Het |
Enox1 |
T |
A |
14: 77,819,876 (GRCm39) |
D210E |
probably damaging |
Het |
Fam171a1 |
A |
G |
2: 3,198,464 (GRCm39) |
N190S |
probably damaging |
Het |
Fat2 |
T |
A |
11: 55,144,459 (GRCm39) |
K4138N |
possibly damaging |
Het |
Fat4 |
A |
T |
3: 39,011,623 (GRCm39) |
D2241V |
probably damaging |
Het |
Foxf2 |
T |
A |
13: 31,811,188 (GRCm39) |
Y376N |
probably damaging |
Het |
Fras1 |
T |
A |
5: 96,900,857 (GRCm39) |
S3025R |
probably benign |
Het |
Gba1 |
T |
C |
3: 89,111,307 (GRCm39) |
I24T |
probably benign |
Het |
Gdpd5 |
A |
G |
7: 99,087,540 (GRCm39) |
D68G |
probably damaging |
Het |
Grid1 |
G |
A |
14: 34,544,576 (GRCm39) |
S49N |
probably benign |
Het |
Grtp1 |
T |
C |
8: 13,229,639 (GRCm39) |
T250A |
possibly damaging |
Het |
Gucy1b1 |
T |
C |
3: 81,945,295 (GRCm39) |
N448D |
probably benign |
Het |
H2-Ob |
A |
G |
17: 34,463,100 (GRCm39) |
|
probably benign |
Het |
Hcn4 |
A |
G |
9: 58,730,795 (GRCm39) |
M1V |
probably null |
Het |
Hmcn2 |
G |
A |
2: 31,310,383 (GRCm39) |
A3326T |
probably damaging |
Het |
Impg2 |
TACCACCACCACCACCACCACCACCA |
TACCACCACCACCACCACCACCA |
16: 56,078,302 (GRCm39) |
|
probably benign |
Het |
Ippk |
C |
A |
13: 49,596,947 (GRCm39) |
Q254K |
probably damaging |
Het |
Itga2 |
A |
T |
13: 115,007,150 (GRCm39) |
L393I |
possibly damaging |
Het |
Kcna10 |
A |
T |
3: 107,102,575 (GRCm39) |
E402V |
possibly damaging |
Het |
Kcnab1 |
G |
A |
3: 65,205,141 (GRCm39) |
D119N |
probably damaging |
Het |
Kcnip4 |
T |
A |
5: 48,567,202 (GRCm39) |
T122S |
probably benign |
Het |
Kcnma1 |
G |
A |
14: 23,350,086 (GRCm39) |
P1151L |
probably damaging |
Het |
Klhl22 |
T |
A |
16: 17,610,453 (GRCm39) |
M568K |
probably benign |
Het |
Krt6a |
C |
T |
15: 101,601,183 (GRCm39) |
V257M |
probably damaging |
Het |
Ksr2 |
A |
C |
5: 117,693,290 (GRCm39) |
H246P |
probably damaging |
Het |
Lca5 |
T |
C |
9: 83,281,806 (GRCm39) |
D326G |
possibly damaging |
Het |
Lcp1 |
A |
G |
14: 75,451,928 (GRCm39) |
E393G |
probably benign |
Het |
Leo1 |
G |
A |
9: 75,352,831 (GRCm39) |
E125K |
probably benign |
Het |
Lipt1 |
T |
A |
1: 37,914,382 (GRCm39) |
V146E |
probably damaging |
Het |
Mael |
A |
T |
1: 166,062,968 (GRCm39) |
|
probably null |
Het |
Mga |
C |
T |
2: 119,778,442 (GRCm39) |
L1996F |
probably damaging |
Het |
Mllt6 |
A |
G |
11: 97,569,387 (GRCm39) |
N913S |
probably damaging |
Het |
Mphosph9 |
A |
C |
5: 124,436,822 (GRCm39) |
D507E |
probably damaging |
Het |
Mvp |
G |
A |
7: 126,586,728 (GRCm39) |
A801V |
probably benign |
Het |
Ndrg2 |
A |
G |
14: 52,146,119 (GRCm39) |
|
probably benign |
Het |
Neb |
T |
C |
2: 52,182,707 (GRCm39) |
D1053G |
possibly damaging |
Het |
Nubp1 |
C |
A |
16: 10,231,585 (GRCm39) |
L79I |
probably benign |
Het |
Or1e1f |
G |
A |
11: 73,856,246 (GRCm39) |
E271K |
probably benign |
Het |
Or1o2 |
A |
C |
17: 37,543,223 (GRCm39) |
L13V |
probably benign |
Het |
Or8d2 |
G |
A |
9: 38,759,805 (GRCm39) |
V132I |
probably benign |
Het |
Pnpla8 |
G |
A |
12: 44,330,188 (GRCm39) |
V29M |
probably benign |
Het |
Psmb2 |
T |
A |
4: 126,601,350 (GRCm39) |
I151N |
possibly damaging |
Het |
Ptgs2 |
C |
T |
1: 149,977,105 (GRCm39) |
T104I |
probably benign |
Het |
Ptpro |
A |
G |
6: 137,345,077 (GRCm39) |
T28A |
probably benign |
Het |
Raf1 |
A |
G |
6: 115,603,671 (GRCm39) |
|
probably null |
Het |
Ranbp2 |
T |
C |
10: 58,301,351 (GRCm39) |
M668T |
probably benign |
Het |
Rbm48 |
A |
T |
5: 3,641,760 (GRCm39) |
|
probably null |
Het |
Rhag |
A |
T |
17: 41,142,469 (GRCm39) |
T225S |
possibly damaging |
Het |
Rhof |
A |
C |
5: 123,269,950 (GRCm39) |
L69R |
probably damaging |
Het |
Slc24a5 |
T |
C |
2: 124,910,724 (GRCm39) |
S52P |
probably damaging |
Het |
Slc8a2 |
T |
C |
7: 15,875,039 (GRCm39) |
V429A |
probably damaging |
Het |
Slfn10-ps |
G |
A |
11: 82,926,388 (GRCm39) |
|
noncoding transcript |
Het |
Spam1 |
G |
A |
6: 24,796,886 (GRCm39) |
R279H |
probably damaging |
Het |
Srfbp1 |
A |
G |
18: 52,620,588 (GRCm39) |
D102G |
probably damaging |
Het |
Srrm3 |
A |
C |
5: 135,902,136 (GRCm39) |
|
probably benign |
Het |
Tk1 |
T |
C |
11: 117,712,933 (GRCm39) |
E98G |
probably damaging |
Het |
Trim13 |
G |
A |
14: 61,843,149 (GRCm39) |
V389I |
probably benign |
Het |
Ttc28 |
A |
T |
5: 111,383,366 (GRCm39) |
Y1289F |
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Ugt1a10 |
T |
A |
1: 87,983,904 (GRCm39) |
V234D |
probably benign |
Het |
Vmn2r18 |
C |
A |
5: 151,496,395 (GRCm39) |
|
probably benign |
Het |
Vmn2r75 |
C |
T |
7: 85,814,575 (GRCm39) |
G306E |
probably benign |
Het |
Vmn2r86 |
C |
T |
10: 130,289,497 (GRCm39) |
V133I |
probably benign |
Het |
Vps13c |
C |
A |
9: 67,841,758 (GRCm39) |
Q1927K |
probably benign |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zfp219 |
T |
A |
14: 52,244,395 (GRCm39) |
T550S |
probably benign |
Het |
Zfp329 |
T |
A |
7: 12,545,395 (GRCm39) |
N43I |
probably benign |
Het |
Zfp507 |
G |
A |
7: 35,502,048 (GRCm39) |
|
probably benign |
Het |
Zfp97 |
T |
A |
17: 17,365,552 (GRCm39) |
F350L |
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 |
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 |
R1957:Fbn1
|
UTSW |
2 |
125,209,574 (GRCm39) |
missense |
possibly damaging |
0.93 |
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 |
|