Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acbd5 |
A |
T |
2: 22,984,356 (GRCm39) |
D294V |
probably damaging |
Het |
Actn2 |
A |
T |
13: 12,355,320 (GRCm39) |
I21N |
probably benign |
Het |
Adamts2 |
C |
A |
11: 50,558,942 (GRCm39) |
P219H |
possibly damaging |
Het |
Atg16l2 |
A |
G |
7: 100,939,113 (GRCm39) |
F584L |
probably benign |
Het |
Ccdc81 |
C |
T |
7: 89,535,390 (GRCm39) |
R282Q |
probably benign |
Het |
Ccn4 |
G |
T |
15: 66,763,448 (GRCm39) |
V12L |
possibly damaging |
Het |
Cd200r3 |
G |
A |
16: 44,771,811 (GRCm39) |
C25Y |
possibly damaging |
Het |
Cdkl4 |
C |
T |
17: 80,863,731 (GRCm39) |
|
probably null |
Het |
Chrne |
T |
C |
11: 70,509,254 (GRCm39) |
E109G |
possibly damaging |
Het |
Clmp |
A |
G |
9: 40,693,856 (GRCm39) |
T358A |
probably benign |
Het |
Cmtr1 |
G |
T |
17: 29,906,021 (GRCm39) |
|
probably null |
Het |
Col25a1 |
A |
G |
3: 130,343,699 (GRCm39) |
E389G |
probably damaging |
Het |
Ctc1 |
C |
T |
11: 68,911,968 (GRCm39) |
T49M |
probably damaging |
Het |
Cyth3 |
T |
A |
5: 143,687,127 (GRCm39) |
M120K |
probably damaging |
Het |
D430041D05Rik |
T |
A |
2: 103,983,308 (GRCm39) |
E1996V |
probably damaging |
Het |
Dnah9 |
T |
C |
11: 65,928,463 (GRCm39) |
M2069V |
probably damaging |
Het |
Dsg1c |
T |
C |
18: 20,408,234 (GRCm39) |
Y428H |
probably damaging |
Het |
Exosc8 |
T |
A |
3: 54,641,752 (GRCm39) |
T7S |
probably damaging |
Het |
F5 |
A |
G |
1: 164,023,191 (GRCm39) |
Y1583C |
probably damaging |
Het |
Fam178b |
A |
G |
1: 36,683,405 (GRCm39) |
I105T |
probably damaging |
Het |
Fam181a |
T |
A |
12: 103,282,591 (GRCm39) |
Y165* |
probably null |
Het |
Gbgt1 |
A |
T |
2: 28,394,988 (GRCm39) |
M209L |
probably benign |
Het |
Gkn2 |
C |
A |
6: 87,355,152 (GRCm39) |
Y120* |
probably null |
Het |
Gm14295 |
T |
A |
2: 176,499,157 (GRCm39) |
D1E |
probably damaging |
Het |
Gpr141 |
A |
T |
13: 19,936,082 (GRCm39) |
|
probably null |
Het |
Gramd2b |
C |
A |
18: 56,565,423 (GRCm39) |
P26Q |
probably benign |
Het |
Greb1 |
A |
G |
12: 16,724,771 (GRCm39) |
I1801T |
probably damaging |
Het |
Gstm3 |
T |
A |
3: 107,875,151 (GRCm39) |
I64F |
possibly damaging |
Het |
Gtse1 |
A |
G |
15: 85,751,779 (GRCm39) |
Y324C |
probably benign |
Het |
Hal |
C |
G |
10: 93,352,159 (GRCm39) |
T650R |
probably benign |
Het |
Hdac7 |
G |
A |
15: 97,706,285 (GRCm39) |
Q293* |
probably null |
Het |
Hdlbp |
A |
T |
1: 93,351,591 (GRCm39) |
N437K |
probably damaging |
Het |
Hif1an |
A |
G |
19: 44,557,862 (GRCm39) |
D248G |
probably damaging |
Het |
Hivep3 |
T |
C |
4: 119,952,901 (GRCm39) |
S406P |
possibly damaging |
Het |
Hmcn2 |
A |
T |
2: 31,348,051 (GRCm39) |
D4899V |
possibly damaging |
Het |
Ikzf3 |
C |
T |
11: 98,381,157 (GRCm39) |
|
probably null |
Het |
Inka2 |
G |
A |
3: 105,624,136 (GRCm39) |
G151D |
probably damaging |
Het |
Itgb4 |
C |
A |
11: 115,882,142 (GRCm39) |
Y819* |
probably null |
Het |
Itpripl1 |
T |
C |
2: 126,983,555 (GRCm39) |
D189G |
possibly damaging |
Het |
Kmt2e |
A |
G |
5: 23,687,500 (GRCm39) |
Y450C |
probably damaging |
Het |
Mc4r |
A |
G |
18: 66,993,068 (GRCm39) |
L15P |
probably benign |
Het |
Mical1 |
T |
G |
10: 41,357,389 (GRCm39) |
|
probably null |
Het |
Mical3 |
C |
T |
6: 121,001,768 (GRCm39) |
V575M |
probably damaging |
Het |
Mki67 |
A |
T |
7: 135,310,547 (GRCm39) |
|
probably null |
Het |
Mocs2 |
G |
A |
13: 114,961,158 (GRCm39) |
E52K |
probably benign |
Het |
Myo7b |
T |
C |
18: 32,133,104 (GRCm39) |
N415S |
probably damaging |
Het |
Notch1 |
G |
A |
2: 26,368,624 (GRCm39) |
T555I |
possibly damaging |
Het |
Notch3 |
T |
C |
17: 32,358,165 (GRCm39) |
D1686G |
probably benign |
Het |
Oit3 |
A |
G |
10: 59,264,061 (GRCm39) |
F358L |
probably damaging |
Het |
Or10x1 |
A |
C |
1: 174,196,515 (GRCm39) |
I11L |
probably benign |
Het |
Or6k4 |
A |
T |
1: 173,964,883 (GRCm39) |
D191V |
probably damaging |
Het |
Orai1 |
T |
A |
5: 123,167,265 (GRCm39) |
I146N |
probably damaging |
Het |
Pck1 |
A |
G |
2: 172,996,511 (GRCm39) |
I142V |
probably benign |
Het |
Pdap1 |
C |
T |
5: 145,069,739 (GRCm39) |
V89M |
possibly damaging |
Het |
Phf11a |
T |
C |
14: 59,525,000 (GRCm39) |
D68G |
possibly damaging |
Het |
Pilrb2 |
T |
C |
5: 137,869,510 (GRCm39) |
N30S |
probably damaging |
Het |
Pkd1 |
G |
A |
17: 24,797,243 (GRCm39) |
V2551I |
probably damaging |
Het |
Pnpla7 |
T |
C |
2: 24,942,611 (GRCm39) |
V132A |
probably damaging |
Het |
Prr35 |
G |
A |
17: 26,166,508 (GRCm39) |
P343L |
probably benign |
Het |
Rad18 |
C |
T |
6: 112,605,480 (GRCm39) |
S398N |
probably damaging |
Het |
Rdh16f1 |
C |
A |
10: 127,626,722 (GRCm39) |
N258K |
probably benign |
Het |
Riox2 |
A |
G |
16: 59,303,405 (GRCm39) |
H240R |
probably damaging |
Het |
Ruvbl1 |
C |
T |
6: 88,462,752 (GRCm39) |
A292V |
probably damaging |
Het |
Ryr1 |
C |
T |
7: 28,794,915 (GRCm39) |
G1151S |
probably damaging |
Het |
Serpinb9b |
T |
C |
13: 33,213,548 (GRCm39) |
I35T |
possibly damaging |
Het |
Slc1a1 |
T |
A |
19: 28,882,122 (GRCm39) |
M328K |
probably benign |
Het |
Slc7a13 |
A |
T |
4: 19,824,031 (GRCm39) |
T267S |
possibly damaging |
Het |
Speer3 |
G |
T |
5: 13,846,335 (GRCm39) |
M218I |
probably benign |
Het |
Sptan1 |
A |
G |
2: 29,876,432 (GRCm39) |
I271V |
probably damaging |
Het |
Swap70 |
A |
G |
7: 109,863,255 (GRCm39) |
T195A |
probably benign |
Het |
Tgs1 |
T |
A |
4: 3,585,964 (GRCm39) |
N280K |
probably benign |
Het |
Tonsl |
A |
G |
15: 76,522,709 (GRCm39) |
C181R |
probably damaging |
Het |
Trdn |
A |
G |
10: 33,134,098 (GRCm39) |
K333R |
possibly damaging |
Het |
Trpc4 |
T |
A |
3: 54,206,600 (GRCm39) |
M600K |
probably damaging |
Het |
Ubr3 |
C |
T |
2: 69,808,067 (GRCm39) |
Q1183* |
probably null |
Het |
Ubxn4 |
T |
A |
1: 128,200,588 (GRCm39) |
L360I |
possibly damaging |
Het |
Ugt2b1 |
T |
A |
5: 87,074,267 (GRCm39) |
T31S |
probably benign |
Het |
Uspl1 |
T |
C |
5: 149,152,009 (GRCm39) |
S1056P |
probably damaging |
Het |
Vmn2r60 |
A |
T |
7: 41,785,279 (GRCm39) |
K164* |
probably null |
Het |
Vwce |
T |
A |
19: 10,624,108 (GRCm39) |
L333* |
probably null |
Het |
Wdr95 |
T |
A |
5: 149,497,581 (GRCm39) |
L253Q |
probably damaging |
Het |
Zfp113 |
T |
C |
5: 138,143,930 (GRCm39) |
M107V |
probably benign |
Het |
Zfp142 |
T |
C |
1: 74,610,934 (GRCm39) |
T851A |
possibly damaging |
Het |
|
Other mutations in Fbn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00694:Fbn2
|
APN |
18 |
58,170,881 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00780:Fbn2
|
APN |
18 |
58,229,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00923:Fbn2
|
APN |
18 |
58,145,397 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01011:Fbn2
|
APN |
18 |
58,228,312 (GRCm39) |
splice site |
probably benign |
|
IGL01123:Fbn2
|
APN |
18 |
58,237,153 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01304:Fbn2
|
APN |
18 |
58,194,817 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01339:Fbn2
|
APN |
18 |
58,246,442 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01465:Fbn2
|
APN |
18 |
58,336,905 (GRCm39) |
missense |
probably null |
0.67 |
IGL01608:Fbn2
|
APN |
18 |
58,186,776 (GRCm39) |
nonsense |
probably null |
|
IGL01682:Fbn2
|
APN |
18 |
58,205,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01752:Fbn2
|
APN |
18 |
58,209,049 (GRCm39) |
splice site |
probably null |
|
IGL01764:Fbn2
|
APN |
18 |
58,178,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02002:Fbn2
|
APN |
18 |
58,247,625 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02010:Fbn2
|
APN |
18 |
58,170,794 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02029:Fbn2
|
APN |
18 |
58,342,675 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02037:Fbn2
|
APN |
18 |
58,229,087 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02350:Fbn2
|
APN |
18 |
58,237,067 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02357:Fbn2
|
APN |
18 |
58,237,067 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02653:Fbn2
|
APN |
18 |
58,209,777 (GRCm39) |
missense |
probably benign |
|
IGL03233:Fbn2
|
APN |
18 |
58,235,449 (GRCm39) |
missense |
probably benign |
0.39 |
IGL03347:Fbn2
|
APN |
18 |
58,146,737 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03410:Fbn2
|
APN |
18 |
58,183,315 (GRCm39) |
missense |
possibly damaging |
0.95 |
pinch
|
UTSW |
18 |
58,202,256 (GRCm39) |
missense |
probably damaging |
1.00 |
stick
|
UTSW |
18 |
58,204,891 (GRCm39) |
missense |
possibly damaging |
0.94 |
tweak
|
UTSW |
18 |
58,191,461 (GRCm39) |
missense |
probably damaging |
1.00 |
BB009:Fbn2
|
UTSW |
18 |
58,153,555 (GRCm39) |
missense |
possibly damaging |
0.61 |
BB019:Fbn2
|
UTSW |
18 |
58,153,555 (GRCm39) |
missense |
possibly damaging |
0.61 |
PIT4434001:Fbn2
|
UTSW |
18 |
58,229,134 (GRCm39) |
missense |
probably damaging |
0.99 |
R0020:Fbn2
|
UTSW |
18 |
58,238,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R0069:Fbn2
|
UTSW |
18 |
58,202,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Fbn2
|
UTSW |
18 |
58,189,275 (GRCm39) |
missense |
probably benign |
0.00 |
R0116:Fbn2
|
UTSW |
18 |
58,235,445 (GRCm39) |
nonsense |
probably null |
|
R0277:Fbn2
|
UTSW |
18 |
58,178,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R0284:Fbn2
|
UTSW |
18 |
58,183,362 (GRCm39) |
splice site |
probably benign |
|
R0316:Fbn2
|
UTSW |
18 |
58,246,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R0323:Fbn2
|
UTSW |
18 |
58,178,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R0421:Fbn2
|
UTSW |
18 |
58,160,876 (GRCm39) |
splice site |
probably benign |
|
R0455:Fbn2
|
UTSW |
18 |
58,168,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Fbn2
|
UTSW |
18 |
58,172,532 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0520:Fbn2
|
UTSW |
18 |
58,146,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R0632:Fbn2
|
UTSW |
18 |
58,170,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R0638:Fbn2
|
UTSW |
18 |
58,178,446 (GRCm39) |
missense |
probably damaging |
0.98 |
R0645:Fbn2
|
UTSW |
18 |
58,191,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R1051:Fbn2
|
UTSW |
18 |
58,145,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R1209:Fbn2
|
UTSW |
18 |
58,203,088 (GRCm39) |
missense |
probably benign |
0.00 |
R1319:Fbn2
|
UTSW |
18 |
58,333,682 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1400:Fbn2
|
UTSW |
18 |
58,213,265 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1437:Fbn2
|
UTSW |
18 |
58,186,731 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1463:Fbn2
|
UTSW |
18 |
58,143,452 (GRCm39) |
missense |
probably benign |
|
R1612:Fbn2
|
UTSW |
18 |
58,194,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R1629:Fbn2
|
UTSW |
18 |
58,159,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R1639:Fbn2
|
UTSW |
18 |
58,191,534 (GRCm39) |
missense |
probably benign |
0.41 |
R1722:Fbn2
|
UTSW |
18 |
58,181,124 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1749:Fbn2
|
UTSW |
18 |
58,183,348 (GRCm39) |
missense |
probably benign |
0.35 |
R1802:Fbn2
|
UTSW |
18 |
58,186,048 (GRCm39) |
nonsense |
probably null |
|
R1850:Fbn2
|
UTSW |
18 |
58,172,377 (GRCm39) |
splice site |
probably benign |
|
R1913:Fbn2
|
UTSW |
18 |
58,194,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Fbn2
|
UTSW |
18 |
58,223,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Fbn2
|
UTSW |
18 |
58,181,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R2143:Fbn2
|
UTSW |
18 |
58,186,065 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2144:Fbn2
|
UTSW |
18 |
58,186,065 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2149:Fbn2
|
UTSW |
18 |
58,235,397 (GRCm39) |
splice site |
probably null |
|
R2207:Fbn2
|
UTSW |
18 |
58,214,471 (GRCm39) |
nonsense |
probably null |
|
R2219:Fbn2
|
UTSW |
18 |
58,186,035 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2263:Fbn2
|
UTSW |
18 |
58,228,248 (GRCm39) |
splice site |
probably benign |
|
R2375:Fbn2
|
UTSW |
18 |
58,169,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R2424:Fbn2
|
UTSW |
18 |
58,336,859 (GRCm39) |
missense |
probably damaging |
0.99 |
R2504:Fbn2
|
UTSW |
18 |
58,226,431 (GRCm39) |
missense |
probably damaging |
0.99 |
R2879:Fbn2
|
UTSW |
18 |
58,202,314 (GRCm39) |
missense |
probably damaging |
0.97 |
R3040:Fbn2
|
UTSW |
18 |
58,226,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R3080:Fbn2
|
UTSW |
18 |
58,282,122 (GRCm39) |
missense |
probably damaging |
0.97 |
R3625:Fbn2
|
UTSW |
18 |
58,194,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R3901:Fbn2
|
UTSW |
18 |
58,199,083 (GRCm39) |
missense |
probably damaging |
0.97 |
R4089:Fbn2
|
UTSW |
18 |
58,186,841 (GRCm39) |
missense |
probably benign |
0.01 |
R4133:Fbn2
|
UTSW |
18 |
58,229,034 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4155:Fbn2
|
UTSW |
18 |
58,156,359 (GRCm39) |
nonsense |
probably null |
|
R4288:Fbn2
|
UTSW |
18 |
58,168,411 (GRCm39) |
missense |
probably damaging |
0.98 |
R4289:Fbn2
|
UTSW |
18 |
58,168,411 (GRCm39) |
missense |
probably damaging |
0.98 |
R4363:Fbn2
|
UTSW |
18 |
58,282,122 (GRCm39) |
missense |
probably damaging |
0.97 |
R4559:Fbn2
|
UTSW |
18 |
58,209,146 (GRCm39) |
missense |
probably benign |
0.00 |
R4601:Fbn2
|
UTSW |
18 |
58,186,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R4609:Fbn2
|
UTSW |
18 |
58,323,341 (GRCm39) |
nonsense |
probably null |
|
R4626:Fbn2
|
UTSW |
18 |
58,146,819 (GRCm39) |
nonsense |
probably null |
|
R4638:Fbn2
|
UTSW |
18 |
58,143,376 (GRCm39) |
missense |
probably benign |
0.01 |
R4675:Fbn2
|
UTSW |
18 |
58,173,265 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4707:Fbn2
|
UTSW |
18 |
58,189,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Fbn2
|
UTSW |
18 |
58,159,458 (GRCm39) |
missense |
probably benign |
0.00 |
R4945:Fbn2
|
UTSW |
18 |
58,183,325 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4955:Fbn2
|
UTSW |
18 |
58,191,455 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4980:Fbn2
|
UTSW |
18 |
58,143,703 (GRCm39) |
missense |
probably benign |
0.05 |
R4998:Fbn2
|
UTSW |
18 |
58,205,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Fbn2
|
UTSW |
18 |
58,172,412 (GRCm39) |
missense |
probably damaging |
0.99 |
R5322:Fbn2
|
UTSW |
18 |
58,172,387 (GRCm39) |
missense |
probably benign |
0.00 |
R5414:Fbn2
|
UTSW |
18 |
58,226,477 (GRCm39) |
missense |
probably damaging |
0.96 |
R5538:Fbn2
|
UTSW |
18 |
58,204,973 (GRCm39) |
missense |
probably benign |
0.22 |
R5557:Fbn2
|
UTSW |
18 |
58,248,731 (GRCm39) |
missense |
probably benign |
0.00 |
R5754:Fbn2
|
UTSW |
18 |
58,257,383 (GRCm39) |
missense |
probably benign |
0.04 |
R5769:Fbn2
|
UTSW |
18 |
58,238,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R5790:Fbn2
|
UTSW |
18 |
58,209,768 (GRCm39) |
missense |
probably benign |
0.34 |
R5830:Fbn2
|
UTSW |
18 |
58,247,541 (GRCm39) |
missense |
probably benign |
0.01 |
R5845:Fbn2
|
UTSW |
18 |
58,186,840 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5880:Fbn2
|
UTSW |
18 |
58,156,354 (GRCm39) |
nonsense |
probably null |
|
R5907:Fbn2
|
UTSW |
18 |
58,178,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R5948:Fbn2
|
UTSW |
18 |
58,170,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R5955:Fbn2
|
UTSW |
18 |
58,177,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R5974:Fbn2
|
UTSW |
18 |
58,181,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Fbn2
|
UTSW |
18 |
58,202,596 (GRCm39) |
missense |
probably benign |
0.31 |
R6024:Fbn2
|
UTSW |
18 |
58,209,908 (GRCm39) |
missense |
probably benign |
0.03 |
R6037:Fbn2
|
UTSW |
18 |
58,177,295 (GRCm39) |
missense |
probably benign |
0.05 |
R6037:Fbn2
|
UTSW |
18 |
58,177,295 (GRCm39) |
missense |
probably benign |
0.05 |
R6315:Fbn2
|
UTSW |
18 |
58,188,025 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6437:Fbn2
|
UTSW |
18 |
58,246,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R6519:Fbn2
|
UTSW |
18 |
58,196,647 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6520:Fbn2
|
UTSW |
18 |
58,235,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R6734:Fbn2
|
UTSW |
18 |
58,169,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R6755:Fbn2
|
UTSW |
18 |
58,246,405 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6789:Fbn2
|
UTSW |
18 |
58,143,686 (GRCm39) |
missense |
probably benign |
0.00 |
R6801:Fbn2
|
UTSW |
18 |
58,246,420 (GRCm39) |
missense |
probably benign |
0.04 |
R6862:Fbn2
|
UTSW |
18 |
58,257,393 (GRCm39) |
missense |
probably benign |
0.04 |
R6900:Fbn2
|
UTSW |
18 |
58,209,903 (GRCm39) |
missense |
probably benign |
|
R6906:Fbn2
|
UTSW |
18 |
58,204,891 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6919:Fbn2
|
UTSW |
18 |
58,257,259 (GRCm39) |
splice site |
probably null |
|
R6950:Fbn2
|
UTSW |
18 |
58,168,993 (GRCm39) |
missense |
probably null |
0.21 |
R6985:Fbn2
|
UTSW |
18 |
58,201,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R7056:Fbn2
|
UTSW |
18 |
58,209,798 (GRCm39) |
missense |
probably benign |
|
R7199:Fbn2
|
UTSW |
18 |
58,186,833 (GRCm39) |
nonsense |
probably null |
|
R7219:Fbn2
|
UTSW |
18 |
58,186,099 (GRCm39) |
missense |
probably benign |
0.04 |
R7226:Fbn2
|
UTSW |
18 |
58,170,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Fbn2
|
UTSW |
18 |
58,199,188 (GRCm39) |
missense |
probably benign |
0.14 |
R7414:Fbn2
|
UTSW |
18 |
58,229,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Fbn2
|
UTSW |
18 |
58,204,912 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7523:Fbn2
|
UTSW |
18 |
58,199,152 (GRCm39) |
missense |
probably benign |
0.01 |
R7549:Fbn2
|
UTSW |
18 |
58,153,536 (GRCm39) |
nonsense |
probably null |
|
R7619:Fbn2
|
UTSW |
18 |
58,213,299 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7638:Fbn2
|
UTSW |
18 |
58,238,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R7789:Fbn2
|
UTSW |
18 |
58,172,385 (GRCm39) |
missense |
probably benign |
0.22 |
R7932:Fbn2
|
UTSW |
18 |
58,153,555 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8013:Fbn2
|
UTSW |
18 |
58,237,153 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8076:Fbn2
|
UTSW |
18 |
58,159,496 (GRCm39) |
nonsense |
probably null |
|
R8300:Fbn2
|
UTSW |
18 |
58,342,687 (GRCm39) |
missense |
probably benign |
|
R8345:Fbn2
|
UTSW |
18 |
58,191,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R8487:Fbn2
|
UTSW |
18 |
58,153,462 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8520:Fbn2
|
UTSW |
18 |
58,171,270 (GRCm39) |
critical splice donor site |
probably null |
|
R8781:Fbn2
|
UTSW |
18 |
58,194,719 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8801:Fbn2
|
UTSW |
18 |
58,287,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R8857:Fbn2
|
UTSW |
18 |
58,286,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R8878:Fbn2
|
UTSW |
18 |
58,257,318 (GRCm39) |
missense |
probably benign |
0.30 |
R8909:Fbn2
|
UTSW |
18 |
58,192,508 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8973:Fbn2
|
UTSW |
18 |
58,286,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R8975:Fbn2
|
UTSW |
18 |
58,286,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R8979:Fbn2
|
UTSW |
18 |
58,286,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R8991:Fbn2
|
UTSW |
18 |
58,239,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R9003:Fbn2
|
UTSW |
18 |
58,176,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R9205:Fbn2
|
UTSW |
18 |
58,192,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R9215:Fbn2
|
UTSW |
18 |
58,209,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R9263:Fbn2
|
UTSW |
18 |
58,257,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R9307:Fbn2
|
UTSW |
18 |
58,342,856 (GRCm39) |
missense |
probably benign |
|
R9337:Fbn2
|
UTSW |
18 |
58,342,723 (GRCm39) |
missense |
probably benign |
|
R9403:Fbn2
|
UTSW |
18 |
58,199,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R9501:Fbn2
|
UTSW |
18 |
58,209,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R9503:Fbn2
|
UTSW |
18 |
58,171,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R9509:Fbn2
|
UTSW |
18 |
58,247,550 (GRCm39) |
missense |
probably benign |
0.22 |
R9561:Fbn2
|
UTSW |
18 |
58,181,611 (GRCm39) |
nonsense |
probably null |
|
R9565:Fbn2
|
UTSW |
18 |
58,228,298 (GRCm39) |
missense |
probably benign |
0.20 |
R9652:Fbn2
|
UTSW |
18 |
58,146,722 (GRCm39) |
critical splice donor site |
probably null |
|
R9659:Fbn2
|
UTSW |
18 |
58,342,654 (GRCm39) |
missense |
probably damaging |
0.98 |
R9679:Fbn2
|
UTSW |
18 |
58,201,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R9683:Fbn2
|
UTSW |
18 |
58,186,099 (GRCm39) |
missense |
probably benign |
0.04 |
R9773:Fbn2
|
UTSW |
18 |
58,143,481 (GRCm39) |
missense |
probably benign |
|
X0062:Fbn2
|
UTSW |
18 |
58,189,285 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fbn2
|
UTSW |
18 |
58,202,262 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fbn2
|
UTSW |
18 |
58,188,554 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Fbn2
|
UTSW |
18 |
58,143,451 (GRCm39) |
missense |
probably benign |
0.00 |
|