Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530084C06Rik |
G |
T |
13: 31,742,978 (GRCm39) |
R92S |
unknown |
Het |
Adam1b |
A |
G |
5: 121,639,981 (GRCm39) |
C355R |
probably damaging |
Het |
Adamtsl3 |
T |
C |
7: 82,223,117 (GRCm39) |
L966P |
probably damaging |
Het |
Aldh18a1 |
A |
G |
19: 40,553,291 (GRCm39) |
C486R |
probably damaging |
Het |
Aqp11 |
C |
A |
7: 97,387,284 (GRCm39) |
|
probably benign |
Het |
Arhgap28 |
A |
G |
17: 68,178,961 (GRCm39) |
L350P |
probably damaging |
Het |
Art3 |
A |
G |
5: 92,551,514 (GRCm39) |
Q291R |
probably benign |
Het |
Asb15 |
A |
G |
6: 24,559,029 (GRCm39) |
|
probably null |
Het |
Bmp8b |
T |
C |
4: 122,999,448 (GRCm39) |
I102T |
possibly damaging |
Het |
Bsn |
T |
C |
9: 107,992,014 (GRCm39) |
D1246G |
probably benign |
Het |
Cass4 |
G |
A |
2: 172,268,718 (GRCm39) |
G267S |
probably benign |
Het |
Cass4 |
G |
T |
2: 172,268,719 (GRCm39) |
G267V |
probably benign |
Het |
Ccr7 |
T |
C |
11: 99,036,727 (GRCm39) |
Y65C |
probably damaging |
Het |
Clstn2 |
A |
C |
9: 97,464,597 (GRCm39) |
I186S |
probably benign |
Het |
Cyp2r1 |
A |
G |
7: 114,153,879 (GRCm39) |
I105T |
possibly damaging |
Het |
Efr3a |
T |
A |
15: 65,687,262 (GRCm39) |
|
probably null |
Het |
Erg |
A |
C |
16: 95,170,179 (GRCm39) |
|
probably null |
Het |
Eya4 |
A |
T |
10: 22,987,557 (GRCm39) |
V524E |
probably damaging |
Het |
Farp1 |
C |
A |
14: 121,472,589 (GRCm39) |
N241K |
possibly damaging |
Het |
Fat1 |
A |
T |
8: 45,442,031 (GRCm39) |
Y1111F |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,185,947 (GRCm39) |
E1607G |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,824,337 (GRCm39) |
D6690V |
probably damaging |
Het |
Fzd4 |
T |
C |
7: 89,056,346 (GRCm39) |
V131A |
possibly damaging |
Het |
Gfral |
T |
A |
9: 76,106,257 (GRCm39) |
N110I |
probably benign |
Het |
Glce |
T |
C |
9: 61,968,275 (GRCm39) |
D292G |
probably damaging |
Het |
Gm19410 |
T |
A |
8: 36,266,500 (GRCm39) |
I1051K |
probably benign |
Het |
Gm5773 |
A |
T |
3: 93,680,323 (GRCm39) |
|
probably benign |
Het |
Hcn3 |
A |
T |
3: 89,057,307 (GRCm39) |
H430Q |
probably null |
Het |
Hspa8 |
T |
A |
9: 40,714,255 (GRCm39) |
|
probably null |
Het |
Ifna7 |
A |
T |
4: 88,734,664 (GRCm39) |
D67V |
possibly damaging |
Het |
Kif5c |
T |
A |
2: 49,591,105 (GRCm39) |
M319K |
probably benign |
Het |
Klk7 |
G |
T |
7: 43,462,197 (GRCm39) |
|
probably null |
Het |
Kmt2c |
T |
C |
5: 25,619,968 (GRCm39) |
K102E |
possibly damaging |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Lrp1b |
C |
T |
2: 40,765,134 (GRCm39) |
M2897I |
|
Het |
Lysmd2 |
T |
C |
9: 75,544,519 (GRCm39) |
S211P |
probably damaging |
Het |
Magi1 |
T |
G |
6: 93,685,095 (GRCm39) |
E761A |
probably benign |
Het |
Mbd5 |
T |
A |
2: 49,141,355 (GRCm39) |
I106N |
probably damaging |
Het |
Mdc1 |
G |
A |
17: 36,159,749 (GRCm39) |
A669T |
probably null |
Het |
Mmp1b |
A |
G |
9: 7,384,753 (GRCm39) |
I265T |
probably benign |
Het |
Mmp2 |
T |
A |
8: 93,563,594 (GRCm39) |
L356Q |
probably null |
Het |
Mroh8 |
A |
G |
2: 157,111,492 (GRCm39) |
L154P |
probably benign |
Het |
Muc13 |
T |
C |
16: 33,619,806 (GRCm39) |
S185P |
unknown |
Het |
Nuak1 |
T |
A |
10: 84,210,403 (GRCm39) |
I562F |
probably benign |
Het |
Obscn |
C |
A |
11: 58,933,664 (GRCm39) |
|
probably null |
Het |
Or51t4 |
T |
C |
7: 102,597,798 (GRCm39) |
I42T |
possibly damaging |
Het |
Or5w14 |
A |
T |
2: 87,542,115 (GRCm39) |
M45K |
probably damaging |
Het |
Or9k7 |
T |
C |
10: 130,046,853 (GRCm39) |
M49V |
probably benign |
Het |
Pex3 |
T |
C |
10: 13,418,414 (GRCm39) |
M81V |
probably benign |
Het |
Pex5l |
T |
A |
3: 33,136,184 (GRCm39) |
I12F |
probably benign |
Het |
Phf3 |
G |
T |
1: 30,870,556 (GRCm39) |
T164N |
probably benign |
Het |
Phpt1 |
G |
T |
2: 25,464,844 (GRCm39) |
A3E |
probably benign |
Het |
Pja2 |
A |
T |
17: 64,616,410 (GRCm39) |
L162M |
probably damaging |
Het |
Pkdrej |
T |
A |
15: 85,703,994 (GRCm39) |
K647N |
probably damaging |
Het |
Ppp2r1a |
T |
C |
17: 21,182,944 (GRCm39) |
S543P |
possibly damaging |
Het |
Prdm13 |
C |
A |
4: 21,679,072 (GRCm39) |
D473Y |
probably damaging |
Het |
Prl6a1 |
A |
T |
13: 27,502,954 (GRCm39) |
E183D |
probably damaging |
Het |
Psmd3 |
C |
T |
11: 98,581,787 (GRCm39) |
T304M |
probably benign |
Het |
Ptpn5 |
C |
T |
7: 46,735,874 (GRCm39) |
|
probably null |
Het |
Rassf6 |
T |
G |
5: 90,754,661 (GRCm39) |
I206L |
probably damaging |
Het |
Rif1 |
A |
G |
2: 51,968,519 (GRCm39) |
H234R |
possibly damaging |
Het |
Rint1 |
T |
C |
5: 24,020,702 (GRCm39) |
V575A |
probably benign |
Het |
Ros1 |
G |
A |
10: 52,021,930 (GRCm39) |
T639I |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,752,871 (GRCm39) |
F1817L |
probably benign |
Het |
Ska1 |
T |
C |
18: 74,333,088 (GRCm39) |
D110G |
probably benign |
Het |
Slc25a41 |
G |
A |
17: 57,340,791 (GRCm39) |
T227I |
probably damaging |
Het |
Slc6a15 |
T |
C |
10: 103,224,998 (GRCm39) |
S29P |
probably benign |
Het |
Slc8a3 |
A |
T |
12: 81,361,544 (GRCm39) |
I425K |
probably benign |
Het |
Sox8 |
T |
A |
17: 25,786,935 (GRCm39) |
Q256L |
probably damaging |
Het |
Tars3 |
T |
C |
7: 65,297,341 (GRCm39) |
V152A |
probably damaging |
Het |
Tbx10 |
A |
T |
19: 4,046,651 (GRCm39) |
T44S |
probably benign |
Het |
Terb1 |
T |
A |
8: 105,224,716 (GRCm39) |
I52F |
possibly damaging |
Het |
Tes |
AGCCGGCC |
AGCC |
6: 17,099,740 (GRCm39) |
|
probably null |
Het |
Tgm1 |
A |
G |
14: 55,943,360 (GRCm39) |
V527A |
probably benign |
Het |
Tmed10 |
G |
T |
12: 85,391,036 (GRCm39) |
Y167* |
probably null |
Het |
Tmem165 |
T |
G |
5: 76,356,415 (GRCm39) |
S318R |
possibly damaging |
Het |
Trim9 |
G |
T |
12: 70,393,715 (GRCm39) |
S76R |
probably damaging |
Het |
Tti1 |
A |
G |
2: 157,849,088 (GRCm39) |
V717A |
probably damaging |
Het |
Vmn2r86 |
T |
A |
10: 130,282,697 (GRCm39) |
I640F |
probably damaging |
Het |
Vwf |
A |
G |
6: 125,603,230 (GRCm39) |
N860S |
|
Het |
Xirp2 |
A |
G |
2: 67,339,241 (GRCm39) |
K494R |
possibly damaging |
Het |
Zkscan4 |
G |
A |
13: 21,668,419 (GRCm39) |
S319N |
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 |
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 |
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 |
|