Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
9530002B09Rik |
T |
A |
4: 122,583,115 (GRCm39) |
|
probably benign |
Het |
Acadl |
C |
T |
1: 66,880,905 (GRCm39) |
|
probably null |
Het |
Acss1 |
G |
A |
2: 150,510,051 (GRCm39) |
Q23* |
probably null |
Het |
Afap1l1 |
A |
T |
18: 61,872,193 (GRCm39) |
|
probably null |
Het |
Akt3 |
A |
G |
1: 176,930,551 (GRCm39) |
S136P |
possibly damaging |
Het |
Amy2a1 |
T |
C |
3: 113,324,217 (GRCm39) |
I108V |
probably benign |
Het |
Ano5 |
T |
G |
7: 51,235,134 (GRCm39) |
L639R |
probably damaging |
Het |
Arhgap26 |
T |
C |
18: 39,439,781 (GRCm39) |
S71P |
probably damaging |
Het |
B3gnt2 |
A |
G |
11: 22,786,735 (GRCm39) |
L151P |
probably damaging |
Het |
Bach1 |
A |
T |
16: 87,526,513 (GRCm39) |
K658N |
probably damaging |
Het |
Bdnf |
C |
A |
2: 109,554,247 (GRCm39) |
T207K |
probably damaging |
Het |
Brwd1 |
A |
G |
16: 95,847,665 (GRCm39) |
S652P |
probably benign |
Het |
Ccnt1 |
A |
T |
15: 98,449,823 (GRCm39) |
H156Q |
probably benign |
Het |
Clasp2 |
T |
A |
9: 113,735,225 (GRCm39) |
I1021N |
possibly damaging |
Het |
Cnep1r1 |
G |
T |
8: 88,845,445 (GRCm39) |
|
probably benign |
Het |
Cntn6 |
C |
T |
6: 104,838,783 (GRCm39) |
R946* |
probably null |
Het |
Dnaaf3 |
T |
C |
7: 4,526,798 (GRCm39) |
I426M |
possibly damaging |
Het |
Dnajc13 |
A |
T |
9: 104,098,640 (GRCm39) |
I471N |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Emx2 |
A |
G |
19: 59,450,130 (GRCm39) |
N149S |
probably benign |
Het |
Fbln7 |
G |
T |
2: 128,719,386 (GRCm39) |
R61L |
probably damaging |
Het |
Fgb |
C |
A |
3: 82,956,996 (GRCm39) |
D25Y |
probably benign |
Het |
Filip1 |
A |
G |
9: 79,727,498 (GRCm39) |
S374P |
probably damaging |
Het |
Fry |
T |
A |
5: 150,293,584 (GRCm39) |
|
probably benign |
Het |
Gm12695 |
T |
C |
4: 96,657,963 (GRCm39) |
T69A |
probably benign |
Het |
Gm2959 |
A |
G |
14: 42,235,658 (GRCm39) |
|
noncoding transcript |
Het |
Gm9912 |
T |
C |
3: 148,890,795 (GRCm39) |
T113A |
unknown |
Het |
Hdlbp |
A |
G |
1: 93,349,602 (GRCm39) |
|
probably benign |
Het |
Hunk |
G |
A |
16: 90,278,133 (GRCm39) |
|
probably null |
Het |
Ifnb1 |
T |
A |
4: 88,440,996 (GRCm39) |
I6F |
possibly damaging |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Ints1 |
A |
G |
5: 139,753,251 (GRCm39) |
V720A |
probably benign |
Het |
Invs |
T |
A |
4: 48,396,287 (GRCm39) |
L320Q |
probably damaging |
Het |
Jpt2 |
G |
A |
17: 25,167,713 (GRCm39) |
Q79* |
probably null |
Het |
Lingo2 |
A |
G |
4: 35,709,179 (GRCm39) |
L267P |
probably benign |
Het |
Lonp2 |
A |
G |
8: 87,392,403 (GRCm39) |
T490A |
probably damaging |
Het |
Meiob |
G |
T |
17: 25,037,290 (GRCm39) |
R56L |
probably damaging |
Het |
Mindy3 |
A |
T |
2: 12,424,060 (GRCm39) |
S2T |
probably damaging |
Het |
Mrm3 |
A |
T |
11: 76,141,147 (GRCm39) |
D385V |
probably damaging |
Het |
Mrto4 |
T |
C |
4: 139,076,334 (GRCm39) |
K86E |
probably benign |
Het |
Naf1 |
A |
G |
8: 67,340,432 (GRCm39) |
D414G |
probably damaging |
Het |
Nav1 |
C |
T |
1: 135,376,742 (GRCm39) |
R1694Q |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,875,567 (GRCm39) |
V1701A |
probably damaging |
Het |
Nipal4 |
T |
G |
11: 46,047,622 (GRCm39) |
D104A |
probably damaging |
Het |
Npas4 |
A |
G |
19: 5,037,442 (GRCm39) |
V284A |
probably damaging |
Het |
Nup133 |
C |
A |
8: 124,641,314 (GRCm39) |
D869Y |
probably damaging |
Het |
Obscn |
G |
A |
11: 59,026,558 (GRCm39) |
A215V |
possibly damaging |
Het |
Or4c113 |
A |
G |
2: 88,885,243 (GRCm39) |
Y176H |
probably damaging |
Het |
Or8b12i |
G |
T |
9: 20,082,850 (GRCm39) |
Q6K |
probably benign |
Het |
Or8g24 |
T |
C |
9: 38,989,510 (GRCm39) |
Y177C |
probably damaging |
Het |
Pgs1 |
G |
A |
11: 117,905,396 (GRCm39) |
|
probably benign |
Het |
Phc2 |
T |
C |
4: 128,640,929 (GRCm39) |
F672S |
probably damaging |
Het |
Phldb2 |
A |
T |
16: 45,591,121 (GRCm39) |
L970Q |
probably damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Ppip5k1 |
A |
G |
2: 121,173,352 (GRCm39) |
|
probably benign |
Het |
Prune2 |
A |
G |
19: 17,098,042 (GRCm39) |
D1182G |
possibly damaging |
Het |
Psg25 |
G |
A |
7: 18,263,487 (GRCm39) |
T112I |
probably damaging |
Het |
Sec61g |
T |
C |
11: 16,458,124 (GRCm39) |
T24A |
probably benign |
Het |
Skint1 |
T |
A |
4: 111,882,730 (GRCm39) |
V258D |
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,353,472 (GRCm39) |
|
probably null |
Het |
Sox2 |
C |
A |
3: 34,705,456 (GRCm39) |
Q298K |
possibly damaging |
Het |
Spatc1 |
T |
A |
15: 76,167,737 (GRCm39) |
|
probably null |
Het |
Szt2 |
T |
C |
4: 118,231,177 (GRCm39) |
M2529V |
unknown |
Het |
Thrap3 |
T |
C |
4: 126,069,189 (GRCm39) |
Y654C |
possibly damaging |
Het |
Tpp2 |
T |
G |
1: 44,017,598 (GRCm39) |
I734S |
possibly damaging |
Het |
Troap |
T |
C |
15: 98,980,344 (GRCm39) |
L508P |
probably benign |
Het |
Ttc28 |
C |
A |
5: 111,373,799 (GRCm39) |
F1078L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,544,717 (GRCm39) |
N32795S |
probably damaging |
Het |
Ubap2 |
C |
T |
4: 41,199,872 (GRCm39) |
A752T |
probably benign |
Het |
Ugt2b36 |
T |
C |
5: 87,240,100 (GRCm39) |
E95G |
probably benign |
Het |
Vmn1r55 |
A |
G |
7: 5,150,048 (GRCm39) |
V125A |
possibly damaging |
Het |
Vstm2a |
A |
T |
11: 16,211,483 (GRCm39) |
I98F |
probably benign |
Het |
Zdhhc13 |
T |
A |
7: 48,466,175 (GRCm39) |
V284D |
probably benign |
Het |
Zfp668 |
C |
A |
7: 127,466,203 (GRCm39) |
R327L |
probably damaging |
Het |
Zgrf1 |
T |
C |
3: 127,406,999 (GRCm39) |
C1589R |
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 |
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 |
R7860:Bod1l
|
UTSW |
5 |
41,976,608 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|