Other mutations in this stock |
Total: 145 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
A |
G |
4: 103,128,057 (GRCm39) |
|
probably benign |
Het |
Adamts6 |
T |
C |
13: 104,563,438 (GRCm39) |
|
probably benign |
Het |
Adamts9 |
T |
A |
6: 92,889,626 (GRCm39) |
Y316F |
probably damaging |
Het |
Agl |
A |
T |
3: 116,580,433 (GRCm39) |
F374I |
probably damaging |
Het |
Akr1c19 |
A |
G |
13: 4,286,250 (GRCm39) |
T83A |
possibly damaging |
Het |
Ankrd36 |
T |
A |
11: 5,579,274 (GRCm39) |
S179R |
probably damaging |
Het |
Appbp2 |
A |
G |
11: 85,082,513 (GRCm39) |
S573P |
probably benign |
Het |
Arid4a |
T |
A |
12: 71,093,988 (GRCm39) |
F254I |
probably damaging |
Het |
Bin3 |
T |
C |
14: 70,361,336 (GRCm39) |
|
probably null |
Het |
Bmi1 |
T |
C |
2: 18,688,883 (GRCm39) |
|
probably null |
Het |
Bmper |
G |
T |
9: 23,317,983 (GRCm39) |
C534F |
probably damaging |
Het |
Bora |
T |
A |
14: 99,299,059 (GRCm39) |
C205* |
probably null |
Het |
Btnl2 |
A |
G |
17: 34,577,091 (GRCm39) |
E82G |
probably benign |
Het |
Ccdc8 |
A |
T |
7: 16,729,939 (GRCm39) |
D476V |
unknown |
Het |
Ccr3 |
C |
A |
9: 123,829,478 (GRCm39) |
T271K |
possibly damaging |
Het |
Cd276 |
A |
G |
9: 58,447,961 (GRCm39) |
L23P |
possibly damaging |
Het |
Cd3e |
T |
C |
9: 44,913,552 (GRCm39) |
Q61R |
probably benign |
Het |
Cep97 |
A |
G |
16: 55,726,142 (GRCm39) |
S582P |
probably benign |
Het |
Chml |
A |
T |
1: 175,514,748 (GRCm39) |
M391K |
probably damaging |
Het |
Chst1 |
A |
G |
2: 92,444,169 (GRCm39) |
N214D |
probably benign |
Het |
Chuk |
T |
C |
19: 44,070,377 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
G |
A |
9: 79,588,750 (GRCm39) |
H1122Y |
possibly damaging |
Het |
Cpne6 |
A |
G |
14: 55,752,059 (GRCm39) |
K272R |
probably damaging |
Het |
Cpsf2 |
T |
A |
12: 101,956,262 (GRCm39) |
L355Q |
probably damaging |
Het |
Cyp2c29 |
T |
A |
19: 39,298,224 (GRCm39) |
D256E |
probably benign |
Het |
Daglb |
G |
A |
5: 143,479,952 (GRCm39) |
V420I |
probably benign |
Het |
Ddx42 |
G |
T |
11: 106,138,675 (GRCm39) |
G825C |
probably benign |
Het |
Dis3 |
T |
C |
14: 99,318,826 (GRCm39) |
|
probably benign |
Het |
Dkk4 |
C |
T |
8: 23,115,359 (GRCm39) |
R70C |
probably damaging |
Het |
Dock6 |
G |
T |
9: 21,713,732 (GRCm39) |
Q1933K |
probably damaging |
Het |
Dpep2 |
T |
G |
8: 106,716,620 (GRCm39) |
Q186H |
probably benign |
Het |
Dzip3 |
A |
C |
16: 48,780,006 (GRCm39) |
|
probably benign |
Het |
Egflam |
T |
A |
15: 7,252,239 (GRCm39) |
I853F |
probably damaging |
Het |
Fastkd5 |
A |
G |
2: 130,457,837 (GRCm39) |
I251T |
probably benign |
Het |
Fem1al |
T |
C |
11: 29,774,990 (GRCm39) |
I156V |
probably damaging |
Het |
Fer1l4 |
C |
A |
2: 155,894,115 (GRCm39) |
V63L |
probably benign |
Het |
Frem1 |
T |
A |
4: 82,830,874 (GRCm39) |
D2062V |
probably benign |
Het |
Galnt6 |
A |
C |
15: 100,594,538 (GRCm39) |
|
probably benign |
Het |
Get3 |
A |
C |
8: 85,745,236 (GRCm39) |
V277G |
probably damaging |
Het |
Gm10972 |
A |
T |
3: 94,550,440 (GRCm39) |
|
probably benign |
Het |
Gm4846 |
G |
A |
1: 166,319,114 (GRCm39) |
T208I |
probably benign |
Het |
Gorab |
A |
G |
1: 163,214,174 (GRCm39) |
L252P |
probably damaging |
Het |
Gtsf2 |
A |
G |
15: 103,352,988 (GRCm39) |
C63R |
probably damaging |
Het |
Hal |
T |
C |
10: 93,325,036 (GRCm39) |
V15A |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,752,170 (GRCm39) |
|
probably benign |
Het |
Hormad2 |
A |
T |
11: 4,358,833 (GRCm39) |
H191Q |
possibly damaging |
Het |
Hspa2 |
A |
T |
12: 76,451,990 (GRCm39) |
D228V |
probably damaging |
Het |
Igfn1 |
A |
T |
1: 135,896,267 (GRCm39) |
M1433K |
probably benign |
Het |
Il18 |
A |
G |
9: 50,486,628 (GRCm39) |
D19G |
probably damaging |
Het |
Il1rl2 |
G |
A |
1: 40,368,216 (GRCm39) |
V129I |
probably benign |
Het |
Inpp5b |
C |
A |
4: 124,676,201 (GRCm39) |
Y352* |
probably null |
Het |
Insrr |
A |
T |
3: 87,720,463 (GRCm39) |
M1034L |
possibly damaging |
Het |
Jmjd1c |
T |
C |
10: 67,061,534 (GRCm39) |
S1296P |
probably damaging |
Het |
Kdm5b |
G |
T |
1: 134,548,761 (GRCm39) |
|
probably null |
Het |
Krba1 |
C |
T |
6: 48,393,188 (GRCm39) |
T998I |
probably benign |
Het |
L3mbtl4 |
A |
G |
17: 69,084,907 (GRCm39) |
N606S |
probably benign |
Het |
Lonrf1 |
T |
A |
8: 36,698,313 (GRCm39) |
N395I |
possibly damaging |
Het |
Lpp |
A |
G |
16: 24,790,720 (GRCm39) |
D393G |
probably damaging |
Het |
Lrrc17 |
A |
G |
5: 21,765,528 (GRCm39) |
I3M |
probably benign |
Het |
Lrrtm4 |
A |
T |
6: 79,999,029 (GRCm39) |
Q147L |
probably damaging |
Het |
Map1a |
A |
G |
2: 121,133,422 (GRCm39) |
M1413V |
probably benign |
Het |
Mapk8ip2 |
A |
G |
15: 89,340,861 (GRCm39) |
E102G |
possibly damaging |
Het |
Marf1 |
C |
T |
16: 13,960,398 (GRCm39) |
A549T |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,698,916 (GRCm39) |
|
probably benign |
Het |
Mfng |
A |
C |
15: 78,641,514 (GRCm39) |
H294Q |
probably benign |
Het |
Mical2 |
T |
A |
7: 111,870,524 (GRCm39) |
N4K |
probably benign |
Het |
Mov10l1 |
T |
A |
15: 88,883,042 (GRCm39) |
V384E |
probably damaging |
Het |
Myo18b |
A |
G |
5: 113,021,442 (GRCm39) |
|
probably benign |
Het |
Nlrp1b |
T |
G |
11: 71,073,241 (GRCm39) |
I201L |
probably damaging |
Het |
Nos2 |
C |
T |
11: 78,830,903 (GRCm39) |
P249L |
probably damaging |
Het |
Notch4 |
A |
G |
17: 34,794,065 (GRCm39) |
T681A |
probably damaging |
Het |
Nr1i3 |
C |
T |
1: 171,044,805 (GRCm39) |
|
probably benign |
Het |
Obscn |
A |
G |
11: 58,899,333 (GRCm39) |
|
probably null |
Het |
Onecut2 |
A |
T |
18: 64,473,820 (GRCm39) |
I124F |
possibly damaging |
Het |
Or10a49 |
C |
T |
7: 108,468,057 (GRCm39) |
M101I |
possibly damaging |
Het |
Or2a14 |
A |
T |
6: 43,130,395 (GRCm39) |
H52L |
probably benign |
Het |
Or2ag1 |
T |
A |
7: 106,313,908 (GRCm39) |
|
probably benign |
Het |
Or2f2 |
C |
T |
6: 42,767,530 (GRCm39) |
R186* |
probably null |
Het |
Or2t47 |
C |
A |
11: 58,442,462 (GRCm39) |
C201F |
probably damaging |
Het |
Or4a75 |
A |
T |
2: 89,448,438 (GRCm39) |
Y33N |
probably damaging |
Het |
Or4c123 |
C |
T |
2: 89,127,083 (GRCm39) |
C177Y |
probably damaging |
Het |
Or52u1 |
C |
T |
7: 104,237,682 (GRCm39) |
R224* |
probably null |
Het |
Or5m12 |
T |
A |
2: 85,735,030 (GRCm39) |
M123L |
possibly damaging |
Het |
Or8b35 |
A |
G |
9: 37,904,438 (GRCm39) |
T217A |
probably benign |
Het |
Otol1 |
G |
A |
3: 69,934,937 (GRCm39) |
G310R |
probably damaging |
Het |
Oxct2b |
T |
A |
4: 123,010,633 (GRCm39) |
S184R |
possibly damaging |
Het |
Oxct2b |
ACTG |
A |
4: 123,010,705 (GRCm39) |
|
probably benign |
Het |
P2rx6 |
A |
G |
16: 17,385,291 (GRCm39) |
|
probably benign |
Het |
Pde4a |
A |
G |
9: 21,115,699 (GRCm39) |
N411S |
probably damaging |
Het |
Phkb |
A |
T |
8: 86,783,153 (GRCm39) |
D983V |
probably benign |
Het |
Piezo2 |
G |
A |
18: 63,157,522 (GRCm39) |
T2396I |
probably damaging |
Het |
Pik3ap1 |
T |
A |
19: 41,275,929 (GRCm39) |
D717V |
probably damaging |
Het |
Plce1 |
T |
A |
19: 38,766,465 (GRCm39) |
|
probably benign |
Het |
Plekhg1 |
A |
G |
10: 3,887,853 (GRCm39) |
I261V |
probably damaging |
Het |
Ppfia4 |
T |
C |
1: 134,251,851 (GRCm39) |
H441R |
probably damaging |
Het |
Prpf8 |
T |
A |
11: 75,392,768 (GRCm39) |
|
probably benign |
Het |
Ptn |
T |
A |
6: 36,718,388 (GRCm39) |
|
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,649,362 (GRCm39) |
Y255C |
possibly damaging |
Het |
Ptpn4 |
A |
G |
1: 119,693,645 (GRCm39) |
Y126H |
probably damaging |
Het |
Ptprc |
T |
C |
1: 138,016,435 (GRCm39) |
N505D |
probably damaging |
Het |
Ptprs |
T |
A |
17: 56,761,220 (GRCm39) |
I116F |
possibly damaging |
Het |
Rab1a |
T |
G |
11: 20,173,169 (GRCm39) |
V90G |
probably damaging |
Het |
Rcor1 |
T |
C |
12: 111,068,102 (GRCm39) |
V267A |
probably benign |
Het |
Reep4 |
A |
G |
14: 70,784,678 (GRCm39) |
|
probably null |
Het |
Rere |
T |
A |
4: 150,699,779 (GRCm39) |
|
probably benign |
Het |
Rin3 |
T |
A |
12: 102,353,823 (GRCm39) |
Y743* |
probably null |
Het |
Rprm |
A |
G |
2: 53,975,067 (GRCm39) |
S84P |
probably damaging |
Het |
Sdhaf2 |
C |
T |
19: 10,494,383 (GRCm39) |
E109K |
probably damaging |
Het |
Sec31b |
G |
T |
19: 44,523,225 (GRCm39) |
Q24K |
probably damaging |
Het |
Sema5a |
T |
C |
15: 32,574,949 (GRCm39) |
|
probably benign |
Het |
Sh3pxd2a |
T |
C |
19: 47,256,186 (GRCm39) |
Y844C |
probably damaging |
Het |
Shmt2 |
A |
C |
10: 127,355,941 (GRCm39) |
N134K |
probably damaging |
Het |
Slc9a8 |
C |
T |
2: 167,266,125 (GRCm39) |
A34V |
probably benign |
Het |
Spidr |
A |
C |
16: 15,957,936 (GRCm39) |
S64A |
possibly damaging |
Het |
Stk10 |
A |
G |
11: 32,567,882 (GRCm39) |
T895A |
probably benign |
Het |
Syne2 |
A |
T |
12: 76,080,365 (GRCm39) |
|
probably benign |
Het |
Szt2 |
T |
C |
4: 118,230,149 (GRCm39) |
|
probably null |
Het |
Tecpr1 |
A |
T |
5: 144,150,899 (GRCm39) |
V303D |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,350,776 (GRCm39) |
Y1048H |
probably damaging |
Het |
Tfb2m |
A |
G |
1: 179,373,396 (GRCm39) |
C101R |
probably damaging |
Het |
Tg |
T |
C |
15: 66,554,253 (GRCm39) |
V556A |
probably damaging |
Het |
Thbs4 |
A |
C |
13: 92,903,692 (GRCm39) |
I441M |
probably benign |
Het |
Thsd7a |
A |
T |
6: 12,379,593 (GRCm39) |
Y944N |
probably damaging |
Het |
Tm9sf3 |
C |
A |
19: 41,236,331 (GRCm39) |
|
probably benign |
Het |
Tmem145 |
T |
C |
7: 25,010,787 (GRCm39) |
F359S |
probably damaging |
Het |
Ttc21b |
C |
T |
2: 66,053,142 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
G |
2: 76,579,880 (GRCm39) |
V23671A |
probably damaging |
Het |
Txnl4b |
T |
C |
8: 110,298,103 (GRCm39) |
I78T |
probably benign |
Het |
Ubr4 |
C |
A |
4: 139,133,889 (GRCm39) |
L762I |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,208,149 (GRCm39) |
|
probably null |
Het |
Ugt1a8 |
C |
T |
1: 88,016,079 (GRCm39) |
P164L |
probably damaging |
Het |
Unc13b |
T |
C |
4: 43,263,559 (GRCm39) |
S1594P |
probably damaging |
Het |
Utrn |
A |
T |
10: 12,278,639 (GRCm39) |
F912I |
probably benign |
Het |
Vat1l |
T |
C |
8: 114,963,319 (GRCm39) |
|
probably benign |
Het |
Vmn1r50 |
T |
A |
6: 90,084,863 (GRCm39) |
S203T |
probably damaging |
Het |
Vmn2r4 |
A |
T |
3: 64,296,784 (GRCm39) |
L667Q |
probably damaging |
Het |
Vmn2r66 |
T |
G |
7: 84,656,023 (GRCm39) |
Q331P |
probably damaging |
Het |
Wdsub1 |
A |
T |
2: 59,708,669 (GRCm39) |
V68D |
possibly damaging |
Het |
Wnk2 |
C |
G |
13: 49,238,870 (GRCm39) |
A564P |
possibly damaging |
Het |
Wnk2 |
T |
A |
13: 49,238,872 (GRCm39) |
K563M |
probably damaging |
Het |
Zan |
T |
A |
5: 137,468,580 (GRCm39) |
H297L |
probably damaging |
Het |
Zfp426 |
A |
T |
9: 20,381,327 (GRCm39) |
H539Q |
probably damaging |
Het |
Zfp488 |
T |
A |
14: 33,692,497 (GRCm39) |
N222I |
probably damaging |
Het |
Zfp536 |
T |
A |
7: 37,268,243 (GRCm39) |
H391L |
probably damaging |
Het |
Zp1 |
T |
A |
19: 10,893,571 (GRCm39) |
N31I |
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 |
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 |
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 |
|