Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
T |
13: 81,545,570 (GRCm39) |
V5572I |
probably benign |
Het |
Agap1 |
C |
T |
1: 89,770,818 (GRCm39) |
T656I |
probably damaging |
Het |
Als2cl |
C |
T |
9: 110,716,432 (GRCm39) |
R247W |
probably damaging |
Het |
Ankfy1 |
A |
T |
11: 72,603,071 (GRCm39) |
R33S |
probably benign |
Het |
Ano5 |
T |
C |
7: 51,235,079 (GRCm39) |
F671L |
probably damaging |
Het |
Arhgap26 |
A |
G |
18: 39,283,145 (GRCm39) |
M361V |
probably damaging |
Het |
Bckdk |
A |
G |
7: 127,505,145 (GRCm39) |
E175G |
probably damaging |
Het |
Bptf |
G |
T |
11: 106,964,022 (GRCm39) |
T1724K |
probably damaging |
Het |
Btn2a2 |
T |
A |
13: 23,670,398 (GRCm39) |
I112F |
probably damaging |
Het |
Cln8 |
T |
A |
8: 14,946,621 (GRCm39) |
W212R |
probably damaging |
Het |
Cnbd1 |
T |
C |
4: 18,886,119 (GRCm39) |
E300G |
probably benign |
Het |
Cnksr3 |
T |
C |
10: 7,092,993 (GRCm39) |
I173V |
probably benign |
Het |
Cntn2 |
T |
A |
1: 132,451,170 (GRCm39) |
D484V |
probably damaging |
Het |
Cyp4a14 |
C |
A |
4: 115,348,607 (GRCm39) |
G319V |
probably damaging |
Het |
Cyp4f37 |
G |
A |
17: 32,848,957 (GRCm39) |
R275Q |
possibly damaging |
Het |
Def8 |
C |
T |
8: 124,186,809 (GRCm39) |
|
probably benign |
Het |
Dnaaf4 |
T |
C |
9: 72,879,280 (GRCm39) |
V356A |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,868,855 (GRCm39) |
|
probably null |
Het |
Dock6 |
A |
G |
9: 21,735,712 (GRCm39) |
V1012A |
probably benign |
Het |
Dus3l |
T |
A |
17: 57,076,579 (GRCm39) |
N586K |
probably damaging |
Het |
Dyrk2 |
T |
A |
10: 118,696,173 (GRCm39) |
I362F |
probably damaging |
Het |
Eeig2 |
A |
T |
3: 108,887,468 (GRCm39) |
S265R |
probably benign |
Het |
Erc2 |
T |
A |
14: 27,498,815 (GRCm39) |
D230E |
probably damaging |
Het |
Fbxo44 |
A |
G |
4: 148,241,052 (GRCm39) |
F179S |
probably damaging |
Het |
Fech |
A |
G |
18: 64,611,720 (GRCm39) |
|
probably null |
Het |
Fer1l5 |
T |
A |
1: 36,424,254 (GRCm39) |
C289* |
probably null |
Het |
Fhl5 |
T |
A |
4: 25,214,756 (GRCm39) |
D7V |
probably benign |
Het |
Flvcr1 |
G |
T |
1: 190,741,748 (GRCm39) |
T514K |
probably damaging |
Het |
Fmo1 |
A |
T |
1: 162,667,185 (GRCm39) |
|
probably null |
Het |
Gabra6 |
G |
A |
11: 42,198,268 (GRCm39) |
T384M |
probably benign |
Het |
Gli3 |
A |
G |
13: 15,723,210 (GRCm39) |
Y117C |
probably damaging |
Het |
Gnao1 |
A |
G |
8: 94,622,873 (GRCm39) |
D59G |
probably benign |
Het |
Gria2 |
T |
C |
3: 80,614,556 (GRCm39) |
I495V |
possibly damaging |
Het |
Hnf1b |
C |
A |
11: 83,754,811 (GRCm39) |
H161Q |
probably benign |
Het |
Itga8 |
T |
A |
2: 12,235,019 (GRCm39) |
D413V |
possibly damaging |
Het |
Itpr3 |
A |
T |
17: 27,329,895 (GRCm39) |
Q1563L |
possibly damaging |
Het |
Kctd16 |
A |
G |
18: 40,663,882 (GRCm39) |
N337S |
probably benign |
Het |
Klra4 |
C |
T |
6: 130,030,016 (GRCm39) |
V190M |
possibly damaging |
Het |
Krtap4-9 |
T |
A |
11: 99,676,462 (GRCm39) |
|
probably benign |
Het |
L3mbtl1 |
GGCCG |
GG |
2: 162,809,256 (GRCm39) |
|
probably benign |
Het |
Mchr1 |
T |
C |
15: 81,122,044 (GRCm39) |
F265L |
probably damaging |
Het |
Megf8 |
T |
A |
7: 25,025,866 (GRCm39) |
Y83* |
probably null |
Het |
Mettl18 |
A |
G |
1: 163,824,746 (GRCm39) |
M356V |
probably null |
Het |
Mrm1 |
G |
A |
11: 84,710,018 (GRCm39) |
R61W |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,570,523 (GRCm39) |
T528S |
probably benign |
Het |
Myef2 |
A |
T |
2: 124,937,651 (GRCm39) |
L530* |
probably null |
Het |
Nhlrc4 |
T |
C |
17: 26,162,693 (GRCm39) |
E18G |
probably benign |
Het |
Nisch |
C |
T |
14: 30,895,102 (GRCm39) |
V1065I |
probably benign |
Het |
Nlgn2 |
C |
T |
11: 69,724,975 (GRCm39) |
R97H |
probably damaging |
Het |
Nos2 |
T |
C |
11: 78,828,741 (GRCm39) |
L321S |
probably damaging |
Het |
Oaz3 |
T |
C |
3: 94,343,717 (GRCm39) |
M49V |
possibly damaging |
Het |
Olfm5 |
A |
G |
7: 103,803,362 (GRCm39) |
V367A |
probably damaging |
Het |
Omd |
C |
T |
13: 49,743,112 (GRCm39) |
P54L |
possibly damaging |
Het |
Or10ak12 |
C |
T |
4: 118,666,575 (GRCm39) |
R162H |
probably benign |
Het |
Or11g26 |
C |
A |
14: 50,753,249 (GRCm39) |
A196D |
probably benign |
Het |
Or2g7 |
C |
A |
17: 38,378,641 (GRCm39) |
A193D |
probably benign |
Het |
Or51f23 |
A |
T |
7: 102,453,481 (GRCm39) |
R265S |
probably damaging |
Het |
Or7d10 |
A |
G |
9: 19,832,206 (GRCm39) |
K234E |
probably damaging |
Het |
Pard3b |
T |
A |
1: 61,807,289 (GRCm39) |
|
probably benign |
Het |
Pcdhb18 |
A |
C |
18: 37,624,988 (GRCm39) |
I773L |
possibly damaging |
Het |
Pde11a |
T |
C |
2: 75,970,175 (GRCm39) |
|
probably null |
Het |
Pfkfb4 |
A |
C |
9: 108,859,462 (GRCm39) |
|
probably benign |
Het |
Phb2 |
T |
G |
6: 124,692,612 (GRCm39) |
I260S |
probably damaging |
Het |
Pkd1l1 |
G |
A |
11: 8,908,969 (GRCm39) |
T345I |
unknown |
Het |
Pla2g6 |
T |
C |
15: 79,187,728 (GRCm39) |
|
probably benign |
Het |
Pou4f2 |
G |
A |
8: 79,163,020 (GRCm39) |
S5F |
unknown |
Het |
Ppp1r9a |
A |
T |
6: 5,157,002 (GRCm39) |
|
probably null |
Het |
Pramel5 |
A |
G |
4: 143,999,553 (GRCm39) |
I178T |
probably benign |
Het |
Prom2 |
C |
T |
2: 127,372,053 (GRCm39) |
W745* |
probably null |
Het |
Pros1 |
T |
A |
16: 62,748,424 (GRCm39) |
N632K |
probably damaging |
Het |
Rab4b |
A |
G |
7: 26,873,927 (GRCm39) |
I117T |
probably benign |
Het |
Rbm25 |
T |
A |
12: 83,724,640 (GRCm39) |
H796Q |
possibly damaging |
Het |
Rnf151 |
A |
T |
17: 24,937,004 (GRCm39) |
|
probably null |
Het |
Rps6ka1 |
A |
T |
4: 133,598,882 (GRCm39) |
L97I |
probably damaging |
Het |
Scart1 |
C |
T |
7: 139,810,359 (GRCm39) |
P984S |
probably benign |
Het |
Semp2l2a |
T |
A |
8: 13,887,263 (GRCm39) |
D276V |
probably benign |
Het |
Sergef |
T |
A |
7: 46,092,888 (GRCm39) |
T374S |
probably benign |
Het |
Sh3rf3 |
G |
T |
10: 58,966,808 (GRCm39) |
G717C |
probably damaging |
Het |
Slc29a4 |
C |
T |
5: 142,707,157 (GRCm39) |
T500I |
possibly damaging |
Het |
Smc1b |
T |
A |
15: 84,970,322 (GRCm39) |
D977V |
probably damaging |
Het |
Spata31d1d |
C |
T |
13: 59,874,829 (GRCm39) |
C902Y |
probably benign |
Het |
St14 |
A |
T |
9: 31,015,056 (GRCm39) |
V314D |
probably damaging |
Het |
Stat3 |
A |
T |
11: 100,784,496 (GRCm39) |
I602N |
possibly damaging |
Het |
Stx4a |
T |
A |
7: 127,445,661 (GRCm39) |
I189N |
probably damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,215 (GRCm39) |
S338P |
probably benign |
Het |
Tcirg1 |
T |
A |
19: 3,952,424 (GRCm39) |
T315S |
possibly damaging |
Het |
Tenm4 |
A |
T |
7: 96,503,926 (GRCm39) |
N1295I |
probably damaging |
Het |
Tm7sf3 |
T |
C |
6: 146,505,409 (GRCm39) |
K516E |
possibly damaging |
Het |
Tmem198b |
T |
C |
10: 128,637,323 (GRCm39) |
E272G |
possibly damaging |
Het |
Tnip3 |
A |
G |
6: 65,582,937 (GRCm39) |
Q237R |
probably damaging |
Het |
Trim15 |
C |
T |
17: 37,173,252 (GRCm39) |
|
probably null |
Het |
Trim30a |
T |
A |
7: 104,070,657 (GRCm39) |
N252I |
possibly damaging |
Het |
Ttc39a |
A |
G |
4: 109,288,075 (GRCm39) |
E227G |
probably benign |
Het |
Ttll13 |
A |
G |
7: 79,902,914 (GRCm39) |
E194G |
probably damaging |
Het |
Upf1 |
G |
A |
8: 70,796,912 (GRCm39) |
T107I |
probably benign |
Het |
Vac14 |
A |
G |
8: 111,436,981 (GRCm39) |
I565V |
probably damaging |
Het |
Zcchc14 |
A |
T |
8: 122,338,097 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Fat1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Fat1
|
APN |
8 |
45,477,639 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00157:Fat1
|
APN |
8 |
45,404,707 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL00481:Fat1
|
APN |
8 |
45,503,977 (GRCm39) |
missense |
probably benign |
0.18 |
IGL00983:Fat1
|
APN |
8 |
45,486,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01089:Fat1
|
APN |
8 |
45,470,894 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01135:Fat1
|
APN |
8 |
45,477,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01143:Fat1
|
APN |
8 |
45,488,569 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL01155:Fat1
|
APN |
8 |
45,476,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01376:Fat1
|
APN |
8 |
45,479,878 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01411:Fat1
|
APN |
8 |
45,479,837 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01443:Fat1
|
APN |
8 |
45,493,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01453:Fat1
|
APN |
8 |
45,504,307 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01606:Fat1
|
APN |
8 |
45,476,086 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01622:Fat1
|
APN |
8 |
45,482,592 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01623:Fat1
|
APN |
8 |
45,482,592 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01672:Fat1
|
APN |
8 |
45,493,737 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01735:Fat1
|
APN |
8 |
45,489,276 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01793:Fat1
|
APN |
8 |
45,442,149 (GRCm39) |
missense |
probably benign |
|
IGL01820:Fat1
|
APN |
8 |
45,463,539 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01969:Fat1
|
APN |
8 |
45,405,636 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02012:Fat1
|
APN |
8 |
45,480,577 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02227:Fat1
|
APN |
8 |
45,476,696 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02256:Fat1
|
APN |
8 |
45,403,369 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02273:Fat1
|
APN |
8 |
45,403,368 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02317:Fat1
|
APN |
8 |
45,478,855 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02324:Fat1
|
APN |
8 |
45,493,593 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02336:Fat1
|
APN |
8 |
45,404,620 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02442:Fat1
|
APN |
8 |
45,403,360 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02486:Fat1
|
APN |
8 |
45,478,109 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02551:Fat1
|
APN |
8 |
45,504,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02617:Fat1
|
APN |
8 |
45,488,628 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02698:Fat1
|
APN |
8 |
45,476,201 (GRCm39) |
missense |
probably benign |
|
IGL02885:Fat1
|
APN |
8 |
45,442,204 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02904:Fat1
|
APN |
8 |
45,493,719 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02953:Fat1
|
APN |
8 |
45,477,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03108:Fat1
|
APN |
8 |
45,476,651 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03153:Fat1
|
APN |
8 |
45,483,160 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03183:Fat1
|
APN |
8 |
45,403,623 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03327:Fat1
|
APN |
8 |
45,403,505 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03405:Fat1
|
APN |
8 |
45,478,278 (GRCm39) |
missense |
probably damaging |
1.00 |
Laggardly
|
UTSW |
8 |
45,497,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2257_fat1_465
|
UTSW |
8 |
45,403,408 (GRCm39) |
missense |
probably damaging |
1.00 |
Shrinkage
|
UTSW |
8 |
45,471,074 (GRCm39) |
missense |
probably damaging |
1.00 |
F5493:Fat1
|
UTSW |
8 |
45,478,517 (GRCm39) |
missense |
probably damaging |
0.99 |
G1citation:Fat1
|
UTSW |
8 |
45,479,441 (GRCm39) |
missense |
probably damaging |
1.00 |
I2289:Fat1
|
UTSW |
8 |
45,478,033 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02837:Fat1
|
UTSW |
8 |
45,470,471 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4283001:Fat1
|
UTSW |
8 |
45,490,244 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4283001:Fat1
|
UTSW |
8 |
45,482,577 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4576001:Fat1
|
UTSW |
8 |
45,477,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Fat1
|
UTSW |
8 |
45,479,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Fat1
|
UTSW |
8 |
45,479,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0078:Fat1
|
UTSW |
8 |
45,406,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R0197:Fat1
|
UTSW |
8 |
45,479,590 (GRCm39) |
missense |
probably benign |
0.00 |
R0328:Fat1
|
UTSW |
8 |
45,476,827 (GRCm39) |
missense |
probably benign |
0.35 |
R0367:Fat1
|
UTSW |
8 |
45,477,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R0371:Fat1
|
UTSW |
8 |
45,404,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R0380:Fat1
|
UTSW |
8 |
45,463,160 (GRCm39) |
missense |
probably damaging |
0.97 |
R0389:Fat1
|
UTSW |
8 |
45,403,385 (GRCm39) |
missense |
probably benign |
0.00 |
R0433:Fat1
|
UTSW |
8 |
45,477,686 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0456:Fat1
|
UTSW |
8 |
45,482,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Fat1
|
UTSW |
8 |
45,403,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Fat1
|
UTSW |
8 |
45,475,988 (GRCm39) |
missense |
probably damaging |
0.99 |
R0512:Fat1
|
UTSW |
8 |
45,404,369 (GRCm39) |
nonsense |
probably null |
|
R0624:Fat1
|
UTSW |
8 |
45,504,205 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0701:Fat1
|
UTSW |
8 |
45,479,590 (GRCm39) |
missense |
probably benign |
0.00 |
R0723:Fat1
|
UTSW |
8 |
45,479,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R0787:Fat1
|
UTSW |
8 |
45,493,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0788:Fat1
|
UTSW |
8 |
45,477,020 (GRCm39) |
missense |
probably benign |
0.27 |
R0862:Fat1
|
UTSW |
8 |
45,471,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R0864:Fat1
|
UTSW |
8 |
45,471,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R0907:Fat1
|
UTSW |
8 |
45,479,635 (GRCm39) |
missense |
probably benign |
0.08 |
R0962:Fat1
|
UTSW |
8 |
45,486,363 (GRCm39) |
splice site |
probably benign |
|
R1051:Fat1
|
UTSW |
8 |
45,497,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1156:Fat1
|
UTSW |
8 |
45,492,927 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1237:Fat1
|
UTSW |
8 |
45,497,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Fat1
|
UTSW |
8 |
45,463,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Fat1
|
UTSW |
8 |
45,463,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R1478:Fat1
|
UTSW |
8 |
45,478,659 (GRCm39) |
missense |
probably damaging |
0.99 |
R1482:Fat1
|
UTSW |
8 |
45,406,281 (GRCm39) |
missense |
probably benign |
0.04 |
R1496:Fat1
|
UTSW |
8 |
45,486,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R1498:Fat1
|
UTSW |
8 |
45,478,521 (GRCm39) |
nonsense |
probably null |
|
R1508:Fat1
|
UTSW |
8 |
45,479,899 (GRCm39) |
missense |
probably benign |
0.01 |
R1577:Fat1
|
UTSW |
8 |
45,476,420 (GRCm39) |
missense |
probably benign |
0.30 |
R1646:Fat1
|
UTSW |
8 |
45,471,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R1652:Fat1
|
UTSW |
8 |
45,478,215 (GRCm39) |
nonsense |
probably null |
|
R1656:Fat1
|
UTSW |
8 |
45,478,567 (GRCm39) |
nonsense |
probably null |
|
R1662:Fat1
|
UTSW |
8 |
45,406,201 (GRCm39) |
missense |
probably benign |
0.20 |
R1672:Fat1
|
UTSW |
8 |
45,489,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R1704:Fat1
|
UTSW |
8 |
45,478,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1708:Fat1
|
UTSW |
8 |
45,477,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R1710:Fat1
|
UTSW |
8 |
45,463,519 (GRCm39) |
missense |
probably benign |
0.00 |
R1812:Fat1
|
UTSW |
8 |
45,489,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Fat1
|
UTSW |
8 |
45,491,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Fat1
|
UTSW |
8 |
45,406,341 (GRCm39) |
missense |
probably benign |
0.01 |
R1883:Fat1
|
UTSW |
8 |
45,504,184 (GRCm39) |
missense |
probably benign |
0.17 |
R1893:Fat1
|
UTSW |
8 |
45,476,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R1930:Fat1
|
UTSW |
8 |
45,497,265 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1931:Fat1
|
UTSW |
8 |
45,497,265 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1952:Fat1
|
UTSW |
8 |
45,486,963 (GRCm39) |
missense |
probably benign |
0.00 |
R1957:Fat1
|
UTSW |
8 |
45,493,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R1999:Fat1
|
UTSW |
8 |
45,405,430 (GRCm39) |
missense |
probably damaging |
0.96 |
R2019:Fat1
|
UTSW |
8 |
45,476,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Fat1
|
UTSW |
8 |
45,479,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Fat1
|
UTSW |
8 |
45,477,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Fat1
|
UTSW |
8 |
45,490,500 (GRCm39) |
missense |
probably benign |
0.33 |
R2196:Fat1
|
UTSW |
8 |
45,477,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R2204:Fat1
|
UTSW |
8 |
45,476,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Fat1
|
UTSW |
8 |
45,403,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R2257:Fat1
|
UTSW |
8 |
45,403,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R2409:Fat1
|
UTSW |
8 |
45,493,567 (GRCm39) |
splice site |
probably benign |
|
R2416:Fat1
|
UTSW |
8 |
45,479,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R3021:Fat1
|
UTSW |
8 |
45,497,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R3108:Fat1
|
UTSW |
8 |
45,498,210 (GRCm39) |
splice site |
probably null |
|
R3109:Fat1
|
UTSW |
8 |
45,498,210 (GRCm39) |
splice site |
probably null |
|
R3196:Fat1
|
UTSW |
8 |
45,404,905 (GRCm39) |
missense |
probably benign |
0.00 |
R3683:Fat1
|
UTSW |
8 |
45,470,975 (GRCm39) |
missense |
probably benign |
|
R3732:Fat1
|
UTSW |
8 |
45,406,306 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3732:Fat1
|
UTSW |
8 |
45,406,306 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3733:Fat1
|
UTSW |
8 |
45,406,306 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3753:Fat1
|
UTSW |
8 |
45,478,516 (GRCm39) |
missense |
probably damaging |
0.97 |
R3905:Fat1
|
UTSW |
8 |
45,476,072 (GRCm39) |
missense |
probably benign |
0.00 |
R3907:Fat1
|
UTSW |
8 |
45,476,072 (GRCm39) |
missense |
probably benign |
0.00 |
R3908:Fat1
|
UTSW |
8 |
45,476,072 (GRCm39) |
missense |
probably benign |
0.00 |
R4060:Fat1
|
UTSW |
8 |
45,478,518 (GRCm39) |
missense |
probably benign |
0.09 |
R4061:Fat1
|
UTSW |
8 |
45,478,518 (GRCm39) |
missense |
probably benign |
0.09 |
R4062:Fat1
|
UTSW |
8 |
45,478,518 (GRCm39) |
missense |
probably benign |
0.09 |
R4063:Fat1
|
UTSW |
8 |
45,478,518 (GRCm39) |
missense |
probably benign |
0.09 |
R4078:Fat1
|
UTSW |
8 |
45,442,159 (GRCm39) |
missense |
probably damaging |
0.99 |
R4105:Fat1
|
UTSW |
8 |
45,489,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R4118:Fat1
|
UTSW |
8 |
45,503,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R4118:Fat1
|
UTSW |
8 |
45,463,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R4161:Fat1
|
UTSW |
8 |
45,489,824 (GRCm39) |
missense |
probably benign |
0.00 |
R4364:Fat1
|
UTSW |
8 |
45,405,999 (GRCm39) |
missense |
probably benign |
0.01 |
R4394:Fat1
|
UTSW |
8 |
45,405,383 (GRCm39) |
missense |
probably damaging |
0.98 |
R4395:Fat1
|
UTSW |
8 |
45,405,383 (GRCm39) |
missense |
probably damaging |
0.98 |
R4396:Fat1
|
UTSW |
8 |
45,405,383 (GRCm39) |
missense |
probably damaging |
0.98 |
R4412:Fat1
|
UTSW |
8 |
45,476,636 (GRCm39) |
missense |
probably damaging |
0.99 |
R4542:Fat1
|
UTSW |
8 |
45,494,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R4591:Fat1
|
UTSW |
8 |
45,479,279 (GRCm39) |
missense |
probably benign |
|
R4606:Fat1
|
UTSW |
8 |
45,403,720 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4612:Fat1
|
UTSW |
8 |
45,478,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R4730:Fat1
|
UTSW |
8 |
45,486,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R4778:Fat1
|
UTSW |
8 |
45,491,363 (GRCm39) |
missense |
probably benign |
0.04 |
R4824:Fat1
|
UTSW |
8 |
45,442,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Fat1
|
UTSW |
8 |
45,489,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R4832:Fat1
|
UTSW |
8 |
45,466,102 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4849:Fat1
|
UTSW |
8 |
45,466,007 (GRCm39) |
missense |
probably benign |
0.15 |
R4896:Fat1
|
UTSW |
8 |
45,404,317 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4927:Fat1
|
UTSW |
8 |
45,476,000 (GRCm39) |
missense |
probably damaging |
0.96 |
R4941:Fat1
|
UTSW |
8 |
45,489,312 (GRCm39) |
missense |
probably benign |
0.00 |
R5011:Fat1
|
UTSW |
8 |
45,484,300 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5040:Fat1
|
UTSW |
8 |
45,476,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Fat1
|
UTSW |
8 |
45,477,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Fat1
|
UTSW |
8 |
45,404,851 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5161:Fat1
|
UTSW |
8 |
45,405,549 (GRCm39) |
missense |
probably benign |
0.00 |
R5162:Fat1
|
UTSW |
8 |
45,478,846 (GRCm39) |
missense |
probably benign |
0.02 |
R5353:Fat1
|
UTSW |
8 |
45,489,168 (GRCm39) |
missense |
probably benign |
0.13 |
R5425:Fat1
|
UTSW |
8 |
45,478,922 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5458:Fat1
|
UTSW |
8 |
45,466,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R5479:Fat1
|
UTSW |
8 |
45,489,912 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5543:Fat1
|
UTSW |
8 |
45,476,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R5569:Fat1
|
UTSW |
8 |
45,492,873 (GRCm39) |
missense |
probably damaging |
0.98 |
R5610:Fat1
|
UTSW |
8 |
45,406,109 (GRCm39) |
nonsense |
probably null |
|
R5734:Fat1
|
UTSW |
8 |
45,504,246 (GRCm39) |
missense |
probably damaging |
0.99 |
R5832:Fat1
|
UTSW |
8 |
45,470,460 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5860:Fat1
|
UTSW |
8 |
45,504,166 (GRCm39) |
missense |
probably benign |
|
R5886:Fat1
|
UTSW |
8 |
45,486,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R5886:Fat1
|
UTSW |
8 |
45,480,718 (GRCm39) |
critical splice donor site |
probably null |
|
R5919:Fat1
|
UTSW |
8 |
45,479,910 (GRCm39) |
critical splice donor site |
probably null |
|
R5960:Fat1
|
UTSW |
8 |
45,486,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:Fat1
|
UTSW |
8 |
45,482,493 (GRCm39) |
missense |
probably benign |
0.00 |
R6166:Fat1
|
UTSW |
8 |
45,405,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R6184:Fat1
|
UTSW |
8 |
45,406,429 (GRCm39) |
missense |
probably benign |
0.00 |
R6208:Fat1
|
UTSW |
8 |
45,480,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R6351:Fat1
|
UTSW |
8 |
45,486,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R6391:Fat1
|
UTSW |
8 |
45,405,379 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6701:Fat1
|
UTSW |
8 |
45,403,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R6702:Fat1
|
UTSW |
8 |
45,406,083 (GRCm39) |
missense |
probably benign |
0.28 |
R6703:Fat1
|
UTSW |
8 |
45,406,083 (GRCm39) |
missense |
probably benign |
0.28 |
R6704:Fat1
|
UTSW |
8 |
45,477,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R6822:Fat1
|
UTSW |
8 |
45,479,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R6852:Fat1
|
UTSW |
8 |
45,488,635 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6863:Fat1
|
UTSW |
8 |
45,497,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R6885:Fat1
|
UTSW |
8 |
45,405,489 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6912:Fat1
|
UTSW |
8 |
45,504,060 (GRCm39) |
missense |
probably benign |
0.00 |
R6927:Fat1
|
UTSW |
8 |
45,477,532 (GRCm39) |
missense |
probably benign |
0.41 |
R6964:Fat1
|
UTSW |
8 |
45,496,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R7010:Fat1
|
UTSW |
8 |
45,406,386 (GRCm39) |
nonsense |
probably null |
|
R7062:Fat1
|
UTSW |
8 |
45,403,253 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R7063:Fat1
|
UTSW |
8 |
45,493,812 (GRCm39) |
missense |
probably benign |
0.09 |
R7071:Fat1
|
UTSW |
8 |
45,442,145 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7117:Fat1
|
UTSW |
8 |
45,484,505 (GRCm39) |
missense |
probably damaging |
0.98 |
R7146:Fat1
|
UTSW |
8 |
45,403,962 (GRCm39) |
missense |
probably benign |
|
R7210:Fat1
|
UTSW |
8 |
45,476,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R7227:Fat1
|
UTSW |
8 |
45,463,646 (GRCm39) |
missense |
probably benign |
0.08 |
R7270:Fat1
|
UTSW |
8 |
45,490,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R7373:Fat1
|
UTSW |
8 |
45,479,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R7390:Fat1
|
UTSW |
8 |
45,405,511 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7465:Fat1
|
UTSW |
8 |
45,497,189 (GRCm39) |
missense |
probably benign |
0.35 |
R7476:Fat1
|
UTSW |
8 |
45,484,311 (GRCm39) |
missense |
probably benign |
0.01 |
R7483:Fat1
|
UTSW |
8 |
45,476,197 (GRCm39) |
missense |
probably benign |
0.13 |
R7484:Fat1
|
UTSW |
8 |
45,489,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R7526:Fat1
|
UTSW |
8 |
45,476,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Fat1
|
UTSW |
8 |
45,442,031 (GRCm39) |
missense |
probably benign |
0.01 |
R7554:Fat1
|
UTSW |
8 |
45,490,202 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7620:Fat1
|
UTSW |
8 |
45,462,887 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7652:Fat1
|
UTSW |
8 |
45,406,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R7694:Fat1
|
UTSW |
8 |
45,441,967 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7746:Fat1
|
UTSW |
8 |
45,404,670 (GRCm39) |
missense |
probably damaging |
0.96 |
R7762:Fat1
|
UTSW |
8 |
45,490,374 (GRCm39) |
missense |
probably damaging |
0.99 |
R7762:Fat1
|
UTSW |
8 |
45,476,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R7782:Fat1
|
UTSW |
8 |
45,403,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R7801:Fat1
|
UTSW |
8 |
45,495,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R7807:Fat1
|
UTSW |
8 |
45,495,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R7821:Fat1
|
UTSW |
8 |
45,403,261 (GRCm39) |
missense |
probably benign |
|
R7869:Fat1
|
UTSW |
8 |
45,504,259 (GRCm39) |
missense |
probably benign |
0.02 |
R8034:Fat1
|
UTSW |
8 |
45,404,728 (GRCm39) |
missense |
probably benign |
0.28 |
R8094:Fat1
|
UTSW |
8 |
45,405,739 (GRCm39) |
missense |
probably damaging |
0.98 |
R8111:Fat1
|
UTSW |
8 |
45,479,095 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8220:Fat1
|
UTSW |
8 |
45,492,993 (GRCm39) |
missense |
probably null |
|
R8221:Fat1
|
UTSW |
8 |
45,406,390 (GRCm39) |
missense |
|
|
R8233:Fat1
|
UTSW |
8 |
45,405,055 (GRCm39) |
missense |
|
|
R8250:Fat1
|
UTSW |
8 |
45,406,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R8279:Fat1
|
UTSW |
8 |
45,483,384 (GRCm39) |
critical splice donor site |
probably null |
|
R8726:Fat1
|
UTSW |
8 |
45,477,206 (GRCm39) |
missense |
probably benign |
0.23 |
R8875:Fat1
|
UTSW |
8 |
45,493,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R8937:Fat1
|
UTSW |
8 |
45,483,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Fat1
|
UTSW |
8 |
45,476,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R8971:Fat1
|
UTSW |
8 |
45,495,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R8976:Fat1
|
UTSW |
8 |
45,484,332 (GRCm39) |
missense |
probably benign |
0.02 |
R9000:Fat1
|
UTSW |
8 |
45,497,587 (GRCm39) |
nonsense |
probably null |
|
R9032:Fat1
|
UTSW |
8 |
45,492,894 (GRCm39) |
missense |
probably benign |
0.01 |
R9076:Fat1
|
UTSW |
8 |
45,492,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Fat1
|
UTSW |
8 |
45,491,336 (GRCm39) |
missense |
probably benign |
0.00 |
R9083:Fat1
|
UTSW |
8 |
45,466,127 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9103:Fat1
|
UTSW |
8 |
45,404,850 (GRCm39) |
missense |
probably benign |
0.38 |
R9124:Fat1
|
UTSW |
8 |
45,478,064 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9124:Fat1
|
UTSW |
8 |
45,403,363 (GRCm39) |
missense |
probably benign |
|
R9128:Fat1
|
UTSW |
8 |
45,462,878 (GRCm39) |
missense |
probably benign |
0.14 |
R9148:Fat1
|
UTSW |
8 |
45,405,682 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9162:Fat1
|
UTSW |
8 |
45,404,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Fat1
|
UTSW |
8 |
45,404,791 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9276:Fat1
|
UTSW |
8 |
45,488,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R9303:Fat1
|
UTSW |
8 |
45,463,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R9319:Fat1
|
UTSW |
8 |
45,406,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R9392:Fat1
|
UTSW |
8 |
45,476,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R9616:Fat1
|
UTSW |
8 |
45,406,075 (GRCm39) |
missense |
probably damaging |
0.99 |
R9712:Fat1
|
UTSW |
8 |
45,470,417 (GRCm39) |
missense |
probably benign |
0.05 |
R9756:Fat1
|
UTSW |
8 |
45,496,974 (GRCm39) |
missense |
probably damaging |
0.96 |
RF001:Fat1
|
UTSW |
8 |
45,442,003 (GRCm39) |
missense |
probably benign |
0.00 |
X0064:Fat1
|
UTSW |
8 |
45,478,771 (GRCm39) |
missense |
possibly damaging |
0.58 |
Z1088:Fat1
|
UTSW |
8 |
45,476,844 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1176:Fat1
|
UTSW |
8 |
45,489,875 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fat1
|
UTSW |
8 |
45,476,633 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1176:Fat1
|
UTSW |
8 |
45,403,635 (GRCm39) |
missense |
probably benign |
|
|