Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atr |
T |
A |
9: 95,744,916 (GRCm39) |
S78T |
probably damaging |
Het |
B2m |
T |
C |
2: 121,981,465 (GRCm39) |
L60P |
probably damaging |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Cep350 |
A |
C |
1: 155,724,373 (GRCm39) |
I3075S |
probably damaging |
Het |
Cep97 |
A |
G |
16: 55,725,935 (GRCm39) |
S651P |
probably damaging |
Het |
Chrna5 |
C |
T |
9: 54,888,985 (GRCm39) |
|
probably benign |
Het |
Cog5 |
T |
C |
12: 31,715,468 (GRCm39) |
V80A |
possibly damaging |
Het |
Col9a2 |
G |
A |
4: 120,906,913 (GRCm39) |
|
probably null |
Het |
Cop1 |
C |
T |
1: 159,077,647 (GRCm39) |
L161F |
probably damaging |
Het |
Cyp4f17 |
A |
T |
17: 32,746,846 (GRCm39) |
M383L |
possibly damaging |
Het |
Dennd4a |
A |
G |
9: 64,814,205 (GRCm39) |
D1474G |
possibly damaging |
Het |
Dgkb |
A |
C |
12: 38,150,492 (GRCm39) |
S100R |
probably benign |
Het |
Dnah17 |
A |
G |
11: 118,016,212 (GRCm39) |
V309A |
probably benign |
Het |
Dner |
C |
A |
1: 84,558,457 (GRCm39) |
R169L |
possibly damaging |
Het |
Dus1l |
T |
C |
11: 120,682,120 (GRCm39) |
E362G |
probably benign |
Het |
Eed |
A |
T |
7: 89,619,564 (GRCm39) |
S168T |
possibly damaging |
Het |
Eif3a |
T |
A |
19: 60,751,500 (GRCm39) |
|
probably null |
Het |
Fam234b |
A |
G |
6: 135,205,450 (GRCm39) |
S472G |
probably benign |
Het |
Fbxw16 |
A |
G |
9: 109,265,352 (GRCm39) |
V393A |
possibly damaging |
Het |
Fig4 |
A |
T |
10: 41,096,928 (GRCm39) |
L838Q |
probably benign |
Het |
Gm13941 |
T |
G |
2: 110,927,147 (GRCm39) |
S137R |
unknown |
Het |
Gm9938 |
T |
G |
19: 23,701,981 (GRCm39) |
|
probably benign |
Het |
Igsf10 |
T |
G |
3: 59,238,501 (GRCm39) |
D560A |
probably damaging |
Het |
Lrrk2 |
T |
A |
15: 91,659,198 (GRCm39) |
L1870* |
probably null |
Het |
Mep1b |
T |
A |
18: 21,224,247 (GRCm39) |
Y347N |
probably damaging |
Het |
Mepce |
T |
C |
5: 137,780,968 (GRCm39) |
N613D |
probably damaging |
Het |
Mgat3 |
T |
G |
15: 80,096,097 (GRCm39) |
L308R |
probably damaging |
Het |
Morc2a |
A |
G |
11: 3,625,925 (GRCm39) |
Y175C |
probably damaging |
Het |
Necab2 |
A |
G |
8: 120,178,878 (GRCm39) |
N98S |
probably benign |
Het |
Net1 |
T |
C |
13: 3,934,845 (GRCm39) |
M394V |
probably benign |
Het |
Nfat5 |
G |
A |
8: 108,094,738 (GRCm39) |
G993D |
probably damaging |
Het |
Obscn |
C |
A |
11: 58,887,122 (GRCm39) |
|
probably benign |
Het |
Olr1 |
T |
C |
6: 129,465,904 (GRCm39) |
H34R |
probably damaging |
Het |
Or2ab1 |
A |
G |
11: 58,489,044 (GRCm39) |
Y274C |
probably damaging |
Het |
Or4f60 |
T |
C |
2: 111,902,662 (GRCm39) |
N89D |
probably benign |
Het |
Pmm2 |
T |
A |
16: 8,460,628 (GRCm39) |
F27L |
probably damaging |
Het |
Ptpdc1 |
C |
A |
13: 48,740,466 (GRCm39) |
V261F |
possibly damaging |
Het |
Pyroxd1 |
G |
T |
6: 142,304,808 (GRCm39) |
R345L |
probably benign |
Het |
Radil |
A |
T |
5: 142,480,109 (GRCm39) |
C670* |
probably null |
Het |
Rasgrf2 |
C |
T |
13: 92,167,203 (GRCm39) |
S290N |
probably damaging |
Het |
Rbm33 |
T |
C |
5: 28,599,001 (GRCm39) |
|
probably benign |
Het |
Rnf111 |
A |
T |
9: 70,360,957 (GRCm39) |
S501R |
possibly damaging |
Het |
Sel1l2 |
T |
A |
2: 140,087,334 (GRCm39) |
I446F |
probably benign |
Het |
Sh3pxd2b |
T |
C |
11: 32,372,737 (GRCm39) |
S635P |
probably benign |
Het |
Slc30a2 |
G |
A |
4: 134,074,726 (GRCm39) |
R161Q |
probably damaging |
Het |
Smg1 |
T |
C |
7: 117,745,623 (GRCm39) |
|
probably benign |
Het |
Sorcs2 |
C |
A |
5: 36,225,474 (GRCm39) |
D132Y |
probably damaging |
Het |
Sox18 |
T |
C |
2: 181,313,280 (GRCm39) |
D12G |
probably damaging |
Het |
Srsf4 |
G |
T |
4: 131,628,004 (GRCm39) |
|
probably benign |
Het |
Susd4 |
C |
A |
1: 182,660,721 (GRCm39) |
T81N |
probably benign |
Het |
Tmem256 |
G |
T |
11: 69,729,416 (GRCm39) |
|
probably benign |
Het |
Tor4a |
T |
C |
2: 25,084,853 (GRCm39) |
H350R |
probably benign |
Het |
Ugt2a3 |
T |
A |
5: 87,484,953 (GRCm39) |
S24C |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r77 |
C |
T |
7: 86,451,023 (GRCm39) |
T303I |
probably benign |
Het |
Wdr70 |
T |
A |
15: 7,913,877 (GRCm39) |
I591F |
possibly damaging |
Het |
Wdr93 |
T |
C |
7: 79,399,088 (GRCm39) |
I74T |
probably damaging |
Het |
Zfp292 |
A |
T |
4: 34,809,784 (GRCm39) |
C1087S |
probably damaging |
Het |
Zfp592 |
T |
A |
7: 80,673,067 (GRCm39) |
D10E |
probably damaging |
Het |
Zfp69 |
A |
G |
4: 120,788,295 (GRCm39) |
V340A |
probably benign |
Het |
Zswim2 |
C |
T |
2: 83,751,092 (GRCm39) |
|
probably null |
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 |
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 |
|