Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700086D15Rik |
A |
G |
11: 65,043,356 (GRCm39) |
|
probably benign |
Het |
6430548M08Rik |
T |
C |
8: 120,872,221 (GRCm39) |
S50P |
probably damaging |
Het |
Aacs |
A |
G |
5: 125,583,227 (GRCm39) |
D261G |
probably benign |
Het |
Abcc4 |
T |
A |
14: 118,832,306 (GRCm39) |
T775S |
probably benign |
Het |
Acsl6 |
A |
G |
11: 54,232,582 (GRCm39) |
|
probably null |
Het |
Agbl5 |
T |
A |
5: 31,062,061 (GRCm39) |
F196I |
probably benign |
Het |
Ahnak2 |
T |
C |
12: 112,741,118 (GRCm39) |
T985A |
possibly damaging |
Het |
Ak1 |
A |
T |
2: 32,521,134 (GRCm39) |
D101V |
possibly damaging |
Het |
Alx1 |
A |
G |
10: 102,861,061 (GRCm39) |
Y156H |
probably damaging |
Het |
Angptl7 |
T |
A |
4: 148,584,488 (GRCm39) |
S87C |
probably benign |
Het |
Ankrd36 |
A |
G |
11: 5,579,299 (GRCm39) |
T188A |
probably benign |
Het |
Arhgap11a |
A |
C |
2: 113,670,054 (GRCm39) |
S356R |
possibly damaging |
Het |
Ascc3 |
G |
T |
10: 50,521,849 (GRCm39) |
E455* |
probably null |
Het |
Atp6v0a2 |
G |
A |
5: 124,789,225 (GRCm39) |
|
probably null |
Het |
B3gnt7 |
T |
C |
1: 86,233,416 (GRCm39) |
W104R |
probably damaging |
Het |
Bbs9 |
G |
A |
9: 22,723,840 (GRCm39) |
|
probably null |
Het |
Cc2d2a |
T |
A |
5: 43,860,557 (GRCm39) |
D544E |
probably benign |
Het |
Cic |
C |
T |
7: 24,971,202 (GRCm39) |
T311I |
probably benign |
Het |
Cngb1 |
T |
A |
8: 95,975,003 (GRCm39) |
R1157W |
probably null |
Het |
Cntln |
A |
G |
4: 85,033,605 (GRCm39) |
H1310R |
probably benign |
Het |
Cntnap5c |
A |
T |
17: 58,600,948 (GRCm39) |
I764F |
probably benign |
Het |
Col26a1 |
T |
C |
5: 136,773,088 (GRCm39) |
Q362R |
possibly damaging |
Het |
Cyp2c29 |
G |
A |
19: 39,279,585 (GRCm39) |
R100K |
probably benign |
Het |
D17H6S53E |
C |
G |
17: 35,346,222 (GRCm39) |
D44E |
probably damaging |
Het |
Dap3 |
A |
G |
3: 88,838,296 (GRCm39) |
V65A |
probably damaging |
Het |
Dna2 |
A |
T |
10: 62,792,782 (GRCm39) |
I266F |
probably damaging |
Het |
Dnah14 |
G |
A |
1: 181,412,631 (GRCm39) |
G57E |
probably benign |
Het |
Dock9 |
A |
T |
14: 121,880,564 (GRCm39) |
V333E |
probably benign |
Het |
Dpm1 |
A |
G |
2: 168,072,195 (GRCm39) |
Y27H |
probably damaging |
Het |
Dsp |
A |
T |
13: 38,351,631 (GRCm39) |
Y150F |
possibly damaging |
Het |
Emilin3 |
A |
T |
2: 160,750,018 (GRCm39) |
I577N |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,819,552 (GRCm39) |
T189A |
probably benign |
Het |
Fat2 |
A |
G |
11: 55,173,597 (GRCm39) |
I2372T |
possibly damaging |
Het |
Gnl1 |
A |
T |
17: 36,298,425 (GRCm39) |
R390* |
probably null |
Het |
Hivep1 |
A |
G |
13: 42,336,928 (GRCm39) |
I2336V |
probably benign |
Het |
Il17rb |
C |
G |
14: 29,726,228 (GRCm39) |
|
probably null |
Het |
Itga9 |
T |
C |
9: 118,716,883 (GRCm39) |
W396R |
probably damaging |
Het |
Katnal2 |
A |
G |
18: 77,098,734 (GRCm39) |
V152A |
probably benign |
Het |
Kcnk3 |
A |
G |
5: 30,779,744 (GRCm39) |
T265A |
probably benign |
Het |
Klhl1 |
T |
C |
14: 96,374,030 (GRCm39) |
Y672C |
probably benign |
Het |
Leng8 |
C |
A |
7: 4,146,625 (GRCm39) |
N412K |
possibly damaging |
Het |
Lrrc9 |
T |
A |
12: 72,553,167 (GRCm39) |
F1356L |
probably benign |
Het |
Map7 |
A |
G |
10: 20,046,828 (GRCm39) |
|
probably benign |
Het |
Mei1 |
T |
C |
15: 81,966,131 (GRCm39) |
F251S |
probably damaging |
Het |
Mia2 |
A |
G |
12: 59,176,681 (GRCm39) |
E9G |
possibly damaging |
Het |
Ms4a13 |
C |
A |
19: 11,149,249 (GRCm39) |
W182C |
probably benign |
Het |
Muc16 |
C |
T |
9: 18,571,595 (GRCm39) |
R308K |
unknown |
Het |
Or4c103 |
G |
A |
2: 88,514,028 (GRCm39) |
T16I |
possibly damaging |
Het |
Or8g22 |
A |
G |
9: 38,958,827 (GRCm39) |
|
probably benign |
Het |
Pcnt |
A |
G |
10: 76,221,632 (GRCm39) |
V1998A |
probably benign |
Het |
Pgm2 |
A |
T |
5: 64,254,368 (GRCm39) |
N51I |
probably benign |
Het |
Piezo1 |
T |
A |
8: 123,217,020 (GRCm39) |
H1333L |
probably damaging |
Het |
Prg2 |
G |
A |
2: 84,813,600 (GRCm39) |
V199M |
probably damaging |
Het |
Prss51 |
T |
C |
14: 64,334,937 (GRCm39) |
V182A |
probably damaging |
Het |
Psmb9 |
A |
T |
17: 34,402,199 (GRCm39) |
Y132* |
probably null |
Het |
Ralyl |
T |
C |
3: 13,842,091 (GRCm39) |
Y76H |
probably damaging |
Het |
Rnaset2a |
A |
T |
17: 8,349,114 (GRCm39) |
D174E |
probably benign |
Het |
Rnft1 |
G |
A |
11: 86,386,156 (GRCm39) |
|
probably null |
Het |
Robo2 |
T |
C |
16: 73,758,755 (GRCm39) |
Y676C |
probably damaging |
Het |
Samd9l |
T |
G |
6: 3,376,313 (GRCm39) |
Y316S |
possibly damaging |
Het |
Siah3 |
T |
A |
14: 75,693,578 (GRCm39) |
F28Y |
possibly damaging |
Het |
Slc28a3 |
C |
T |
13: 58,721,257 (GRCm39) |
|
probably null |
Het |
Slc8a1 |
A |
G |
17: 81,696,301 (GRCm39) |
F911S |
probably damaging |
Het |
Spata31e2 |
T |
C |
1: 26,722,015 (GRCm39) |
Y1055C |
probably benign |
Het |
Speg |
T |
A |
1: 75,364,552 (GRCm39) |
L156* |
probably null |
Het |
Spopl |
T |
G |
2: 23,407,873 (GRCm39) |
M269L |
probably benign |
Het |
Tacr1 |
C |
T |
6: 82,534,054 (GRCm39) |
T360I |
probably benign |
Het |
Tasor |
T |
A |
14: 27,171,758 (GRCm39) |
L397* |
probably null |
Het |
Tmem262 |
A |
G |
19: 6,130,767 (GRCm39) |
E95G |
probably benign |
Het |
Tmem68 |
G |
T |
4: 3,569,669 (GRCm39) |
T7N |
possibly damaging |
Het |
Top3a |
T |
A |
11: 60,640,319 (GRCm39) |
I460F |
probably damaging |
Het |
Trafd1 |
G |
A |
5: 121,522,137 (GRCm39) |
R5* |
probably null |
Het |
Trim16 |
T |
A |
11: 62,731,695 (GRCm39) |
V435D |
possibly damaging |
Het |
Tspan17 |
A |
G |
13: 54,943,846 (GRCm39) |
D236G |
probably damaging |
Het |
Tssk2 |
A |
T |
16: 17,717,565 (GRCm39) |
M323L |
probably benign |
Het |
Ubqln5 |
A |
G |
7: 103,778,215 (GRCm39) |
V203A |
probably benign |
Het |
Utrn |
A |
T |
10: 12,569,214 (GRCm39) |
L1134* |
probably null |
Het |
Vmn1r37 |
C |
T |
6: 66,708,704 (GRCm39) |
S73F |
possibly damaging |
Het |
Vps13c |
A |
G |
9: 67,834,734 (GRCm39) |
K1688E |
probably damaging |
Het |
Zbtb39 |
A |
G |
10: 127,577,711 (GRCm39) |
D95G |
probably damaging |
Het |
Zfhx3 |
T |
A |
8: 109,527,160 (GRCm39) |
I1019N |
probably damaging |
Het |
Zfp207 |
C |
T |
11: 80,286,329 (GRCm39) |
|
probably benign |
Het |
Zmiz1 |
C |
T |
14: 25,644,062 (GRCm39) |
T169M |
probably 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 |
R1623:Fbn2
|
UTSW |
18 |
58,181,620 (GRCm39) |
missense |
possibly damaging |
0.61 |
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 |
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 |
|