Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
G |
11: 9,242,080 (GRCm39) |
D1314E |
probably benign |
Het |
Abcb1a |
A |
T |
5: 8,724,707 (GRCm39) |
R47W |
probably benign |
Het |
Abcc6 |
T |
C |
7: 45,629,184 (GRCm39) |
N1354S |
probably damaging |
Het |
Abracl |
T |
C |
10: 17,887,444 (GRCm39) |
Y61C |
probably damaging |
Het |
Adamtsl1 |
A |
G |
4: 86,208,027 (GRCm39) |
T633A |
probably benign |
Het |
Agap3 |
G |
A |
5: 24,681,439 (GRCm39) |
|
probably benign |
Het |
Ago4 |
A |
T |
4: 126,400,904 (GRCm39) |
M647K |
probably damaging |
Het |
Akap7 |
G |
T |
10: 25,155,676 (GRCm39) |
S72R |
unknown |
Het |
Arhgef12 |
A |
G |
9: 42,885,870 (GRCm39) |
L1251S |
possibly damaging |
Het |
Astn2 |
A |
T |
4: 66,322,164 (GRCm39) |
V145E |
unknown |
Het |
Atxn2l |
A |
T |
7: 126,097,393 (GRCm39) |
S304R |
probably damaging |
Het |
Cd226 |
A |
T |
18: 89,287,155 (GRCm39) |
I318F |
probably damaging |
Het |
Cep250 |
C |
T |
2: 155,812,042 (GRCm39) |
A446V |
unknown |
Het |
Cfap65 |
A |
T |
1: 74,958,510 (GRCm39) |
|
probably benign |
Het |
Cfap96 |
T |
G |
8: 46,415,403 (GRCm39) |
D201A |
probably benign |
Het |
Chtf8 |
A |
G |
8: 107,613,640 (GRCm39) |
V18A |
probably benign |
Het |
Cit |
G |
T |
5: 116,074,896 (GRCm39) |
E683* |
probably null |
Het |
Ckmt2 |
T |
C |
13: 92,007,337 (GRCm39) |
R286G |
probably damaging |
Het |
Clec4a2 |
T |
A |
6: 123,116,218 (GRCm39) |
W128R |
probably damaging |
Het |
Clec4n |
T |
G |
6: 123,212,447 (GRCm39) |
S88A |
probably damaging |
Het |
Cndp2 |
G |
A |
18: 84,699,121 (GRCm39) |
A48V |
probably benign |
Het |
Csmd1 |
T |
C |
8: 16,273,286 (GRCm39) |
T849A |
probably benign |
Het |
Cts3 |
A |
T |
13: 61,715,235 (GRCm39) |
Y199* |
probably null |
Het |
Dag1 |
A |
T |
9: 108,085,734 (GRCm39) |
L469* |
probably null |
Het |
Dclre1c |
T |
C |
2: 3,439,125 (GRCm39) |
V225A |
|
Het |
Dedd |
A |
G |
1: 171,166,409 (GRCm39) |
D115G |
probably damaging |
Het |
Efcab3 |
T |
A |
11: 104,741,407 (GRCm39) |
V2166D |
probably benign |
Het |
Eif2ak3 |
T |
A |
6: 70,860,704 (GRCm39) |
W427R |
probably damaging |
Het |
Fbln2 |
T |
A |
6: 91,210,473 (GRCm39) |
V139D |
probably damaging |
Het |
Gm17019 |
A |
T |
5: 15,081,113 (GRCm39) |
Y109* |
probably null |
Het |
Gm32742 |
T |
A |
9: 51,056,015 (GRCm39) |
N1255Y |
probably damaging |
Het |
Gm5431 |
T |
A |
11: 48,779,600 (GRCm39) |
K441* |
probably null |
Het |
Golga2 |
A |
G |
2: 32,196,079 (GRCm39) |
D898G |
|
Het |
Gramd4 |
G |
A |
15: 85,975,525 (GRCm39) |
R39H |
probably benign |
Het |
Gucy1a2 |
A |
G |
9: 3,634,553 (GRCm39) |
N199S |
probably damaging |
Het |
Heyl |
G |
A |
4: 123,139,885 (GRCm39) |
R148H |
probably damaging |
Het |
Ifi208 |
A |
T |
1: 173,523,400 (GRCm39) |
M557L |
probably benign |
Het |
Igf2r |
A |
G |
17: 12,958,238 (GRCm39) |
V145A |
probably damaging |
Het |
Ighv1-4 |
A |
T |
12: 114,450,879 (GRCm39) |
Y76* |
probably null |
Het |
Ikzf4 |
T |
C |
10: 128,468,487 (GRCm39) |
D664G |
unknown |
Het |
Il1a |
T |
A |
2: 129,146,715 (GRCm39) |
Y126F |
possibly damaging |
Het |
Lmf2 |
C |
A |
15: 89,239,771 (GRCm39) |
|
probably benign |
Het |
Lyst |
T |
C |
13: 13,808,827 (GRCm39) |
S166P |
probably damaging |
Het |
Mgat5 |
A |
C |
1: 127,294,197 (GRCm39) |
T180P |
probably benign |
Het |
Mical2 |
A |
C |
7: 111,870,589 (GRCm39) |
K26T |
possibly damaging |
Het |
Mov10 |
G |
T |
3: 104,711,659 (GRCm39) |
Y209* |
probably null |
Het |
Nol8 |
T |
C |
13: 49,815,475 (GRCm39) |
Y528H |
probably benign |
Het |
Numa1 |
T |
A |
7: 101,641,869 (GRCm39) |
S106T |
possibly damaging |
Het |
Or1e1d-ps1 |
A |
T |
11: 73,819,167 (GRCm39) |
E39V |
probably damaging |
Het |
Or4c124 |
G |
A |
2: 89,156,474 (GRCm39) |
Q17* |
probably null |
Het |
Or5b107 |
A |
G |
19: 13,142,396 (GRCm39) |
N6S |
probably damaging |
Het |
Or7g27 |
A |
G |
9: 19,250,026 (GRCm39) |
H90R |
probably benign |
Het |
Pcdhb14 |
A |
G |
18: 37,582,091 (GRCm39) |
N399S |
probably damaging |
Het |
Plcl2 |
T |
A |
17: 50,918,032 (GRCm39) |
S944T |
probably benign |
Het |
Pml |
A |
T |
9: 58,127,660 (GRCm39) |
I695N |
probably benign |
Het |
Ppard |
G |
T |
17: 28,505,349 (GRCm39) |
R12L |
unknown |
Het |
Ppip5k1 |
C |
T |
2: 121,158,125 (GRCm39) |
|
probably null |
Het |
Ppp1r3g |
T |
C |
13: 36,152,621 (GRCm39) |
S14P |
probably benign |
Het |
Pramel55 |
A |
G |
5: 95,951,623 (GRCm39) |
Y470C |
probably damaging |
Het |
Prrc2b |
C |
A |
2: 32,103,764 (GRCm39) |
R1081S |
probably damaging |
Het |
Rasgrp2 |
A |
T |
19: 6,454,438 (GRCm39) |
E160D |
possibly damaging |
Het |
Rb1cc1 |
G |
A |
1: 6,333,073 (GRCm39) |
V1331I |
probably damaging |
Het |
Rnd3 |
A |
T |
2: 51,022,413 (GRCm39) |
S210T |
probably benign |
Het |
Scaf11 |
T |
C |
15: 96,312,764 (GRCm39) |
T1426A |
probably benign |
Het |
Sin3b |
C |
T |
8: 73,460,034 (GRCm39) |
T207I |
possibly damaging |
Het |
Slc26a7 |
A |
T |
4: 14,593,873 (GRCm39) |
Y81N |
probably damaging |
Het |
Slc28a3 |
C |
T |
13: 58,724,581 (GRCm39) |
M224I |
probably benign |
Het |
Slc30a1 |
T |
C |
1: 191,639,342 (GRCm39) |
I75T |
probably damaging |
Het |
Slc6a21 |
T |
A |
7: 44,929,674 (GRCm39) |
|
probably benign |
Het |
Slco2a1 |
T |
A |
9: 102,945,243 (GRCm39) |
L206Q |
probably damaging |
Het |
Spata31d1e |
A |
G |
13: 59,890,828 (GRCm39) |
S331P |
probably benign |
Het |
Sptbn1 |
A |
G |
11: 30,104,356 (GRCm39) |
V116A |
probably damaging |
Het |
Syngap1 |
G |
A |
17: 27,181,095 (GRCm39) |
D1008N |
probably damaging |
Het |
Syt11 |
T |
C |
3: 88,669,643 (GRCm39) |
D83G |
probably benign |
Het |
Syt14 |
G |
A |
1: 192,584,131 (GRCm39) |
T428I |
probably damaging |
Het |
Taf15 |
T |
A |
11: 83,395,085 (GRCm39) |
Y338* |
probably null |
Het |
Tfap4 |
A |
T |
16: 4,365,183 (GRCm39) |
M253K |
possibly damaging |
Het |
Tnr |
T |
C |
1: 159,713,680 (GRCm39) |
S703P |
possibly damaging |
Het |
Trrap |
G |
A |
5: 144,767,830 (GRCm39) |
D2577N |
probably benign |
Het |
Uqcc6 |
A |
T |
10: 82,458,588 (GRCm39) |
M21K |
probably benign |
Het |
Wdr20 |
C |
T |
12: 110,759,597 (GRCm39) |
S161L |
possibly damaging |
Het |
Zfp503 |
C |
A |
14: 22,037,418 (GRCm39) |
V62L |
probably benign |
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 |
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 |
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 |
|