Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
A |
G |
6: 91,905,707 (GRCm39) |
T493A |
probably damaging |
Het |
Aars1 |
A |
G |
8: 111,776,493 (GRCm39) |
K650E |
probably benign |
Het |
Abcb1b |
C |
T |
5: 8,882,258 (GRCm39) |
S793F |
probably benign |
Het |
Adamts18 |
T |
A |
8: 114,501,908 (GRCm39) |
I318F |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,571,322 (GRCm39) |
I1137T |
probably damaging |
Het |
Ambra1 |
T |
A |
2: 91,603,838 (GRCm39) |
F607L |
probably benign |
Het |
Ankrd46 |
A |
T |
15: 36,479,566 (GRCm39) |
V175D |
possibly damaging |
Het |
Arhgap28 |
C |
A |
17: 68,208,277 (GRCm39) |
E114* |
probably null |
Het |
Arrdc1 |
C |
T |
2: 24,816,158 (GRCm39) |
G282S |
probably damaging |
Het |
Atp1a3 |
A |
T |
7: 24,681,216 (GRCm39) |
L790Q |
probably damaging |
Het |
Bend5 |
T |
A |
4: 111,272,406 (GRCm39) |
V12D |
probably damaging |
Het |
Cdc123 |
T |
A |
2: 5,808,775 (GRCm39) |
I234L |
probably benign |
Het |
Cep126 |
T |
G |
9: 8,120,749 (GRCm39) |
E91D |
probably damaging |
Het |
Cep89 |
T |
A |
7: 35,113,570 (GRCm39) |
D199E |
possibly damaging |
Het |
Ces1d |
T |
C |
8: 93,897,765 (GRCm39) |
T442A |
probably benign |
Het |
Chsy3 |
C |
T |
18: 59,542,299 (GRCm39) |
A479V |
probably benign |
Het |
Clcn4 |
C |
A |
7: 7,296,060 (GRCm39) |
G261C |
probably damaging |
Het |
Clhc1 |
A |
T |
11: 29,507,651 (GRCm39) |
|
probably null |
Het |
Cnot3 |
T |
A |
7: 3,658,565 (GRCm39) |
|
probably null |
Het |
Col9a1 |
C |
A |
1: 24,276,261 (GRCm39) |
P723H |
probably damaging |
Het |
Crybg3 |
A |
T |
16: 59,375,605 (GRCm39) |
M169K |
probably benign |
Het |
Cxxc4 |
A |
G |
3: 133,963,814 (GRCm39) |
R353G |
probably benign |
Het |
Dennd3 |
A |
T |
15: 73,412,657 (GRCm39) |
I440F |
probably damaging |
Het |
Dnai3 |
A |
G |
3: 145,772,675 (GRCm39) |
L457P |
probably damaging |
Het |
Elmo3 |
G |
T |
8: 106,035,649 (GRCm39) |
S553I |
probably damaging |
Het |
Elovl2 |
A |
G |
13: 41,340,943 (GRCm39) |
Y198H |
probably benign |
Het |
Epm2aip1 |
A |
G |
9: 111,101,105 (GRCm39) |
Y26C |
probably damaging |
Het |
Ext1 |
A |
C |
15: 52,953,335 (GRCm39) |
C510G |
possibly damaging |
Het |
Extl3 |
A |
T |
14: 65,314,938 (GRCm39) |
D81E |
probably benign |
Het |
Fbxl5 |
T |
A |
5: 43,916,018 (GRCm39) |
T465S |
probably benign |
Het |
Fbxo31 |
G |
A |
8: 122,291,384 (GRCm39) |
|
probably null |
Het |
Gabrr2 |
A |
T |
4: 33,081,470 (GRCm39) |
K169* |
probably null |
Het |
Haus4 |
A |
G |
14: 54,779,602 (GRCm39) |
Y341H |
probably damaging |
Het |
Itgae |
A |
T |
11: 73,011,099 (GRCm39) |
|
probably null |
Het |
Jmjd7 |
C |
T |
2: 119,860,996 (GRCm39) |
H149Y |
possibly damaging |
Het |
Kcnh2 |
C |
T |
5: 24,529,561 (GRCm39) |
C725Y |
probably damaging |
Het |
Mroh1 |
C |
T |
15: 76,331,532 (GRCm39) |
P1252L |
probably benign |
Het |
Ms4a14 |
A |
G |
19: 11,280,308 (GRCm39) |
F750S |
probably benign |
Het |
Naf1 |
T |
A |
8: 67,313,165 (GRCm39) |
D49E |
unknown |
Het |
Notch3 |
T |
C |
17: 32,341,747 (GRCm39) |
T2002A |
possibly damaging |
Het |
Or10q12 |
T |
A |
19: 13,745,716 (GRCm39) |
D3E |
probably benign |
Het |
Or14c44 |
A |
G |
7: 86,057,119 (GRCm39) |
|
probably benign |
Het |
Or1e33 |
A |
T |
11: 73,738,333 (GRCm39) |
I206N |
probably benign |
Het |
Or2d3c |
A |
T |
7: 106,525,777 (GRCm39) |
D296E |
probably benign |
Het |
Or2l13b |
A |
T |
16: 19,349,167 (GRCm39) |
C168S |
probably damaging |
Het |
Or7e175 |
A |
T |
9: 20,048,871 (GRCm39) |
N153I |
probably benign |
Het |
Or9s23 |
G |
A |
1: 92,501,810 (GRCm39) |
D306N |
probably benign |
Het |
Pck1 |
A |
G |
2: 172,997,743 (GRCm39) |
T271A |
possibly damaging |
Het |
Penk |
A |
G |
4: 4,133,976 (GRCm39) |
W224R |
possibly damaging |
Het |
Per2 |
C |
A |
1: 91,372,481 (GRCm39) |
V198F |
probably damaging |
Het |
Phf11d |
A |
G |
14: 59,599,280 (GRCm39) |
M23T |
probably damaging |
Het |
Pla2g4d |
A |
G |
2: 120,097,211 (GRCm39) |
V796A |
probably benign |
Het |
Pramel51 |
A |
T |
12: 88,143,122 (GRCm39) |
N360K |
possibly damaging |
Het |
Prdx6 |
A |
T |
1: 161,069,428 (GRCm39) |
|
probably null |
Het |
Prep |
A |
T |
10: 44,967,108 (GRCm39) |
N47I |
probably damaging |
Het |
Prodh2 |
A |
T |
7: 30,212,064 (GRCm39) |
|
probably null |
Het |
Prss38 |
G |
T |
11: 59,265,996 (GRCm39) |
H96N |
probably damaging |
Het |
Rab11a |
C |
A |
9: 64,635,613 (GRCm39) |
E47* |
probably null |
Het |
Rad18 |
C |
T |
6: 112,626,798 (GRCm39) |
G369D |
probably benign |
Het |
Rragc |
T |
C |
4: 123,823,717 (GRCm39) |
V330A |
probably damaging |
Het |
Serpina9 |
A |
T |
12: 103,967,680 (GRCm39) |
H238Q |
probably benign |
Het |
Serpinb3b |
T |
A |
1: 107,085,467 (GRCm39) |
K91N |
probably damaging |
Het |
Slc16a12 |
T |
G |
19: 34,652,730 (GRCm39) |
S139R |
probably benign |
Het |
Slc22a27 |
T |
A |
19: 7,887,472 (GRCm39) |
|
probably null |
Het |
Slc25a11 |
A |
G |
11: 70,536,005 (GRCm39) |
V243A |
probably benign |
Het |
Slc38a9 |
A |
T |
13: 112,868,148 (GRCm39) |
I545F |
probably benign |
Het |
Slc39a8 |
A |
T |
3: 135,590,157 (GRCm39) |
H349L |
probably damaging |
Het |
Slk |
C |
T |
19: 47,630,510 (GRCm39) |
T1227I |
possibly damaging |
Het |
Spdye4b |
A |
G |
5: 143,180,609 (GRCm39) |
E25G |
possibly damaging |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
St3gal1 |
A |
G |
15: 66,983,114 (GRCm39) |
V214A |
probably benign |
Het |
St7l |
T |
A |
3: 104,833,893 (GRCm39) |
M550K |
probably benign |
Het |
Tbk1 |
A |
C |
10: 121,388,151 (GRCm39) |
F638C |
possibly damaging |
Het |
Tex101 |
A |
T |
7: 24,369,190 (GRCm39) |
C114S |
probably damaging |
Het |
Ttll13 |
A |
G |
7: 79,905,135 (GRCm39) |
M384V |
probably benign |
Het |
Ugt2b37 |
A |
T |
5: 87,402,189 (GRCm39) |
D147E |
probably damaging |
Het |
Vmn1r10 |
A |
T |
6: 57,090,686 (GRCm39) |
T93S |
probably benign |
Het |
Wasl |
G |
A |
6: 24,619,396 (GRCm39) |
P375S |
unknown |
Het |
Zfp236 |
C |
A |
18: 82,692,481 (GRCm39) |
E165* |
probably null |
Het |
Zfp839 |
A |
T |
12: 110,822,060 (GRCm39) |
R291S |
probably damaging |
Het |
|
Other mutations in Bod1l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00944:Bod1l
|
APN |
5 |
41,974,166 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00990:Bod1l
|
APN |
5 |
41,986,208 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01021:Bod1l
|
APN |
5 |
41,995,516 (GRCm39) |
splice site |
probably benign |
|
IGL01022:Bod1l
|
APN |
5 |
41,951,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01303:Bod1l
|
APN |
5 |
41,974,942 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01654:Bod1l
|
APN |
5 |
41,975,519 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01748:Bod1l
|
APN |
5 |
41,974,304 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01758:Bod1l
|
APN |
5 |
41,983,953 (GRCm39) |
splice site |
probably benign |
|
IGL01783:Bod1l
|
APN |
5 |
41,966,055 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01790:Bod1l
|
APN |
5 |
41,989,593 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01803:Bod1l
|
APN |
5 |
41,974,732 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01829:Bod1l
|
APN |
5 |
41,977,811 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01952:Bod1l
|
APN |
5 |
41,974,297 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02005:Bod1l
|
APN |
5 |
41,973,682 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02110:Bod1l
|
APN |
5 |
41,973,796 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02129:Bod1l
|
APN |
5 |
41,979,193 (GRCm39) |
missense |
probably benign |
0.36 |
IGL02572:Bod1l
|
APN |
5 |
41,978,573 (GRCm39) |
nonsense |
probably null |
|
IGL02583:Bod1l
|
APN |
5 |
41,973,550 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02643:Bod1l
|
APN |
5 |
41,976,148 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02714:Bod1l
|
APN |
5 |
41,973,682 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02728:Bod1l
|
APN |
5 |
41,983,846 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02752:Bod1l
|
APN |
5 |
41,973,806 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02822:Bod1l
|
APN |
5 |
41,951,688 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03032:Bod1l
|
APN |
5 |
41,988,927 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03372:Bod1l
|
APN |
5 |
41,962,578 (GRCm39) |
splice site |
probably benign |
|
capacitance
|
UTSW |
5 |
41,949,156 (GRCm39) |
missense |
possibly damaging |
0.91 |
gauss
|
UTSW |
5 |
41,974,210 (GRCm39) |
missense |
probably benign |
0.01 |
Tesla
|
UTSW |
5 |
41,952,411 (GRCm39) |
critical splice donor site |
probably null |
|
R0102:Bod1l
|
UTSW |
5 |
41,974,612 (GRCm39) |
missense |
probably benign |
0.36 |
R0147:Bod1l
|
UTSW |
5 |
41,976,040 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0148:Bod1l
|
UTSW |
5 |
41,976,040 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0490:Bod1l
|
UTSW |
5 |
41,979,235 (GRCm39) |
missense |
probably damaging |
0.96 |
R0577:Bod1l
|
UTSW |
5 |
41,952,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R0587:Bod1l
|
UTSW |
5 |
41,978,980 (GRCm39) |
missense |
probably benign |
0.16 |
R0620:Bod1l
|
UTSW |
5 |
41,958,576 (GRCm39) |
missense |
probably benign |
0.16 |
R0626:Bod1l
|
UTSW |
5 |
41,988,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R0785:Bod1l
|
UTSW |
5 |
41,977,359 (GRCm39) |
missense |
probably benign |
0.00 |
R1139:Bod1l
|
UTSW |
5 |
41,988,814 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1165:Bod1l
|
UTSW |
5 |
41,978,396 (GRCm39) |
missense |
probably benign |
0.02 |
R1418:Bod1l
|
UTSW |
5 |
41,976,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1509:Bod1l
|
UTSW |
5 |
41,976,883 (GRCm39) |
missense |
probably damaging |
0.99 |
R1533:Bod1l
|
UTSW |
5 |
41,979,498 (GRCm39) |
nonsense |
probably null |
|
R1538:Bod1l
|
UTSW |
5 |
41,973,772 (GRCm39) |
missense |
probably benign |
0.00 |
R1591:Bod1l
|
UTSW |
5 |
41,976,563 (GRCm39) |
missense |
probably benign |
0.06 |
R1616:Bod1l
|
UTSW |
5 |
41,966,058 (GRCm39) |
missense |
probably benign |
|
R1628:Bod1l
|
UTSW |
5 |
41,974,325 (GRCm39) |
missense |
probably benign |
0.01 |
R1667:Bod1l
|
UTSW |
5 |
41,974,118 (GRCm39) |
missense |
probably benign |
0.01 |
R1869:Bod1l
|
UTSW |
5 |
41,991,018 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1870:Bod1l
|
UTSW |
5 |
41,991,018 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1993:Bod1l
|
UTSW |
5 |
41,974,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Bod1l
|
UTSW |
5 |
41,966,085 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2066:Bod1l
|
UTSW |
5 |
41,962,499 (GRCm39) |
missense |
probably damaging |
0.99 |
R2067:Bod1l
|
UTSW |
5 |
41,974,429 (GRCm39) |
missense |
probably benign |
0.11 |
R2073:Bod1l
|
UTSW |
5 |
41,976,532 (GRCm39) |
missense |
probably benign |
0.19 |
R2092:Bod1l
|
UTSW |
5 |
41,988,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R2105:Bod1l
|
UTSW |
5 |
41,989,622 (GRCm39) |
missense |
probably benign |
0.00 |
R2243:Bod1l
|
UTSW |
5 |
41,978,888 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2322:Bod1l
|
UTSW |
5 |
41,984,463 (GRCm39) |
missense |
probably benign |
0.09 |
R2849:Bod1l
|
UTSW |
5 |
41,995,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R2883:Bod1l
|
UTSW |
5 |
41,989,602 (GRCm39) |
missense |
probably benign |
0.03 |
R3037:Bod1l
|
UTSW |
5 |
41,979,380 (GRCm39) |
missense |
probably damaging |
0.99 |
R3910:Bod1l
|
UTSW |
5 |
41,974,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R3911:Bod1l
|
UTSW |
5 |
41,974,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R3962:Bod1l
|
UTSW |
5 |
41,966,064 (GRCm39) |
missense |
probably benign |
0.07 |
R4235:Bod1l
|
UTSW |
5 |
41,978,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R4308:Bod1l
|
UTSW |
5 |
41,949,156 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4414:Bod1l
|
UTSW |
5 |
41,977,870 (GRCm39) |
missense |
probably benign |
0.04 |
R4535:Bod1l
|
UTSW |
5 |
41,989,574 (GRCm39) |
missense |
probably benign |
0.06 |
R4631:Bod1l
|
UTSW |
5 |
41,975,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R4657:Bod1l
|
UTSW |
5 |
41,975,955 (GRCm39) |
missense |
probably benign |
0.00 |
R4782:Bod1l
|
UTSW |
5 |
41,991,006 (GRCm39) |
missense |
probably benign |
0.06 |
R4786:Bod1l
|
UTSW |
5 |
41,976,781 (GRCm39) |
missense |
probably benign |
0.43 |
R4840:Bod1l
|
UTSW |
5 |
41,975,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R4877:Bod1l
|
UTSW |
5 |
41,977,337 (GRCm39) |
missense |
probably benign |
0.00 |
R4982:Bod1l
|
UTSW |
5 |
41,977,816 (GRCm39) |
missense |
probably benign |
0.00 |
R5152:Bod1l
|
UTSW |
5 |
41,973,886 (GRCm39) |
missense |
probably benign |
0.04 |
R5284:Bod1l
|
UTSW |
5 |
41,977,810 (GRCm39) |
missense |
probably benign |
0.05 |
R5354:Bod1l
|
UTSW |
5 |
41,988,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R5369:Bod1l
|
UTSW |
5 |
41,984,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R5486:Bod1l
|
UTSW |
5 |
41,964,524 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5541:Bod1l
|
UTSW |
5 |
41,949,276 (GRCm39) |
missense |
probably benign |
0.06 |
R5610:Bod1l
|
UTSW |
5 |
41,979,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Bod1l
|
UTSW |
5 |
41,974,387 (GRCm39) |
missense |
probably benign |
0.06 |
R5705:Bod1l
|
UTSW |
5 |
41,974,345 (GRCm39) |
missense |
probably benign |
0.01 |
R5819:Bod1l
|
UTSW |
5 |
41,989,948 (GRCm39) |
missense |
probably benign |
0.27 |
R5890:Bod1l
|
UTSW |
5 |
41,977,921 (GRCm39) |
missense |
probably benign |
0.43 |
R5923:Bod1l
|
UTSW |
5 |
41,974,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5991:Bod1l
|
UTSW |
5 |
41,974,206 (GRCm39) |
nonsense |
probably null |
|
R6017:Bod1l
|
UTSW |
5 |
41,976,103 (GRCm39) |
missense |
probably benign |
0.01 |
R6253:Bod1l
|
UTSW |
5 |
41,983,881 (GRCm39) |
missense |
probably damaging |
0.96 |
R6284:Bod1l
|
UTSW |
5 |
41,976,130 (GRCm39) |
missense |
probably benign |
0.35 |
R6483:Bod1l
|
UTSW |
5 |
41,978,425 (GRCm39) |
missense |
probably benign |
0.03 |
R6485:Bod1l
|
UTSW |
5 |
41,974,459 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6575:Bod1l
|
UTSW |
5 |
41,995,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R6679:Bod1l
|
UTSW |
5 |
41,974,009 (GRCm39) |
missense |
probably damaging |
0.97 |
R6788:Bod1l
|
UTSW |
5 |
41,979,216 (GRCm39) |
nonsense |
probably null |
|
R7006:Bod1l
|
UTSW |
5 |
41,989,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R7095:Bod1l
|
UTSW |
5 |
41,952,411 (GRCm39) |
critical splice donor site |
probably null |
|
R7111:Bod1l
|
UTSW |
5 |
41,970,463 (GRCm39) |
critical splice donor site |
probably null |
|
R7190:Bod1l
|
UTSW |
5 |
41,977,281 (GRCm39) |
missense |
probably benign |
0.14 |
R7311:Bod1l
|
UTSW |
5 |
41,951,676 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7336:Bod1l
|
UTSW |
5 |
41,978,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R7341:Bod1l
|
UTSW |
5 |
41,946,200 (GRCm39) |
missense |
probably benign |
0.00 |
R7396:Bod1l
|
UTSW |
5 |
41,988,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R7431:Bod1l
|
UTSW |
5 |
41,970,463 (GRCm39) |
critical splice donor site |
probably null |
|
R7442:Bod1l
|
UTSW |
5 |
41,964,522 (GRCm39) |
missense |
probably damaging |
0.96 |
R7539:Bod1l
|
UTSW |
5 |
41,975,203 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7583:Bod1l
|
UTSW |
5 |
41,991,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Bod1l
|
UTSW |
5 |
41,977,986 (GRCm39) |
frame shift |
probably null |
|
R7748:Bod1l
|
UTSW |
5 |
41,989,683 (GRCm39) |
missense |
probably damaging |
0.97 |
R7767:Bod1l
|
UTSW |
5 |
41,974,099 (GRCm39) |
missense |
probably benign |
0.01 |
R7773:Bod1l
|
UTSW |
5 |
41,990,055 (GRCm39) |
missense |
probably benign |
0.14 |
R7782:Bod1l
|
UTSW |
5 |
41,975,286 (GRCm39) |
missense |
probably benign |
0.01 |
R7975:Bod1l
|
UTSW |
5 |
41,973,620 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7977:Bod1l
|
UTSW |
5 |
41,952,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7987:Bod1l
|
UTSW |
5 |
41,952,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R8104:Bod1l
|
UTSW |
5 |
41,991,075 (GRCm39) |
nonsense |
probably null |
|
R8217:Bod1l
|
UTSW |
5 |
41,988,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R8307:Bod1l
|
UTSW |
5 |
41,978,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R8469:Bod1l
|
UTSW |
5 |
41,978,834 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8506:Bod1l
|
UTSW |
5 |
41,976,398 (GRCm39) |
nonsense |
probably null |
|
R8934:Bod1l
|
UTSW |
5 |
41,976,944 (GRCm39) |
missense |
probably benign |
0.11 |
R8984:Bod1l
|
UTSW |
5 |
41,946,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R8989:Bod1l
|
UTSW |
5 |
41,979,025 (GRCm39) |
missense |
probably benign |
0.00 |
R8993:Bod1l
|
UTSW |
5 |
41,974,210 (GRCm39) |
missense |
probably benign |
0.01 |
R9128:Bod1l
|
UTSW |
5 |
41,946,266 (GRCm39) |
missense |
probably benign |
0.22 |
R9129:Bod1l
|
UTSW |
5 |
41,976,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R9198:Bod1l
|
UTSW |
5 |
41,957,129 (GRCm39) |
missense |
probably benign |
0.08 |
R9254:Bod1l
|
UTSW |
5 |
41,979,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R9445:Bod1l
|
UTSW |
5 |
41,974,619 (GRCm39) |
missense |
probably benign |
0.04 |
R9457:Bod1l
|
UTSW |
5 |
41,979,310 (GRCm39) |
missense |
probably damaging |
0.99 |
R9470:Bod1l
|
UTSW |
5 |
41,974,439 (GRCm39) |
missense |
probably damaging |
0.99 |
R9536:Bod1l
|
UTSW |
5 |
41,974,305 (GRCm39) |
missense |
probably benign |
0.01 |
R9654:Bod1l
|
UTSW |
5 |
41,975,707 (GRCm39) |
missense |
probably benign |
0.02 |
R9734:Bod1l
|
UTSW |
5 |
41,962,573 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9771:Bod1l
|
UTSW |
5 |
41,949,206 (GRCm39) |
missense |
probably damaging |
0.96 |
X0027:Bod1l
|
UTSW |
5 |
41,990,012 (GRCm39) |
missense |
probably benign |
0.20 |
X0058:Bod1l
|
UTSW |
5 |
41,981,361 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Bod1l
|
UTSW |
5 |
41,966,107 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1088:Bod1l
|
UTSW |
5 |
41,978,489 (GRCm39) |
missense |
probably damaging |
1.00 |
|