Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
T |
C |
11: 109,679,547 (GRCm39) |
|
probably benign |
Het |
6430571L13Rik |
T |
A |
9: 107,219,707 (GRCm39) |
D53E |
possibly damaging |
Het |
A2ml1 |
T |
A |
6: 128,527,736 (GRCm39) |
N1018I |
probably damaging |
Het |
Abi3 |
C |
A |
11: 95,727,937 (GRCm39) |
A85S |
probably benign |
Het |
Acsl5 |
A |
T |
19: 55,272,904 (GRCm39) |
M340L |
probably benign |
Het |
Adam29 |
T |
A |
8: 56,324,612 (GRCm39) |
H614L |
probably benign |
Het |
Adgrg6 |
A |
T |
10: 14,312,628 (GRCm39) |
S720T |
probably damaging |
Het |
Adrb2 |
G |
T |
18: 62,312,441 (GRCm39) |
A128E |
probably damaging |
Het |
Afap1l1 |
T |
C |
18: 61,872,291 (GRCm39) |
E510G |
probably benign |
Het |
Angel1 |
A |
G |
12: 86,764,487 (GRCm39) |
|
probably null |
Het |
Aox3 |
T |
G |
1: 58,211,458 (GRCm39) |
I1005S |
possibly damaging |
Het |
Apc |
C |
A |
18: 34,451,507 (GRCm39) |
P2767Q |
probably damaging |
Het |
Apob |
T |
G |
12: 8,066,193 (GRCm39) |
D4387E |
probably benign |
Het |
Apobr |
T |
C |
7: 126,185,827 (GRCm39) |
V446A |
possibly damaging |
Het |
Arhgap28 |
A |
T |
17: 68,203,108 (GRCm39) |
|
probably null |
Het |
Aspm |
G |
T |
1: 139,419,339 (GRCm39) |
K3001N |
probably damaging |
Het |
Asxl3 |
G |
T |
18: 22,655,937 (GRCm39) |
V1316F |
probably benign |
Het |
Atp2a1 |
T |
A |
7: 126,046,162 (GRCm39) |
|
probably null |
Het |
Bach1 |
A |
G |
16: 87,526,359 (GRCm39) |
D607G |
possibly damaging |
Het |
Batf3 |
A |
G |
1: 190,832,935 (GRCm39) |
D27G |
probably damaging |
Het |
Baz1a |
G |
T |
12: 55,022,055 (GRCm39) |
Q76K |
probably damaging |
Het |
Bdnf |
G |
A |
2: 109,553,883 (GRCm39) |
V86M |
probably benign |
Het |
Birc7 |
A |
G |
2: 180,573,098 (GRCm39) |
I172V |
probably benign |
Het |
Cacna1e |
T |
A |
1: 154,364,563 (GRCm39) |
E337V |
probably damaging |
Het |
Cacna1h |
A |
G |
17: 25,612,520 (GRCm39) |
F287L |
possibly damaging |
Het |
Ces1e |
A |
G |
8: 93,950,671 (GRCm39) |
Y37H |
probably benign |
Het |
Clasrp |
A |
T |
7: 19,318,418 (GRCm39) |
|
probably benign |
Het |
Clec2d |
T |
A |
6: 129,160,090 (GRCm39) |
S35T |
probably damaging |
Het |
Cntn4 |
T |
A |
6: 106,639,539 (GRCm39) |
D556E |
probably benign |
Het |
Cntnap5c |
A |
T |
17: 58,349,422 (GRCm39) |
D245V |
probably benign |
Het |
Col5a1 |
T |
A |
2: 27,818,255 (GRCm39) |
L160* |
probably null |
Het |
Col6a6 |
T |
C |
9: 105,654,943 (GRCm39) |
E926G |
probably benign |
Het |
Cpsf2 |
T |
A |
12: 101,951,490 (GRCm39) |
H142Q |
probably benign |
Het |
Cr2 |
A |
C |
1: 194,853,419 (GRCm39) |
S20A |
possibly damaging |
Het |
Ct45a |
G |
A |
X: 55,590,399 (GRCm39) |
P134L |
probably benign |
Het |
Cyp2j5 |
A |
T |
4: 96,547,749 (GRCm39) |
H164Q |
probably benign |
Het |
D430041D05Rik |
G |
C |
2: 103,998,295 (GRCm39) |
P1836R |
probably damaging |
Het |
Dmbt1 |
G |
A |
7: 130,703,811 (GRCm39) |
V1124M |
probably damaging |
Het |
Dmxl2 |
T |
C |
9: 54,323,838 (GRCm39) |
H1182R |
probably damaging |
Het |
Dnah2 |
A |
T |
11: 69,368,509 (GRCm39) |
S1709T |
probably benign |
Het |
Dop1b |
T |
C |
16: 93,560,844 (GRCm39) |
V776A |
probably damaging |
Het |
Emc3 |
T |
C |
6: 113,492,992 (GRCm39) |
T220A |
probably benign |
Het |
Entpd1 |
A |
C |
19: 40,715,769 (GRCm39) |
N312T |
probably benign |
Het |
Fam8a1 |
A |
T |
13: 46,824,699 (GRCm39) |
I229F |
probably damaging |
Het |
Fancc |
G |
A |
13: 63,465,205 (GRCm39) |
P501S |
probably damaging |
Het |
Fasn |
T |
C |
11: 120,702,751 (GRCm39) |
R1704G |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,819,302 (GRCm39) |
I5012V |
probably benign |
Het |
Glce |
T |
C |
9: 61,968,282 (GRCm39) |
T290A |
probably benign |
Het |
Gns |
G |
A |
10: 121,219,349 (GRCm39) |
|
probably null |
Het |
Gsdma2 |
A |
G |
11: 98,542,810 (GRCm39) |
N190S |
probably damaging |
Het |
Hectd4 |
T |
A |
5: 121,415,887 (GRCm39) |
S563T |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,674,470 (GRCm39) |
|
probably null |
Het |
Jup |
A |
T |
11: 100,267,589 (GRCm39) |
M578K |
probably benign |
Het |
Kir3dl1 |
G |
A |
X: 135,434,594 (GRCm39) |
|
probably null |
Het |
Krt75 |
A |
G |
15: 101,482,025 (GRCm39) |
F81S |
probably benign |
Het |
Lrp1 |
G |
T |
10: 127,403,233 (GRCm39) |
D2113E |
probably damaging |
Het |
Maged2 |
T |
A |
X: 149,594,830 (GRCm39) |
N176Y |
probably damaging |
Het |
Mrc1 |
T |
A |
2: 14,333,382 (GRCm39) |
C1354* |
probably null |
Het |
Mup7 |
A |
C |
4: 60,069,742 (GRCm39) |
V74G |
possibly damaging |
Het |
Naca |
A |
G |
10: 127,877,031 (GRCm39) |
|
probably benign |
Het |
Nav3 |
T |
G |
10: 109,659,325 (GRCm39) |
Y764S |
probably damaging |
Het |
Nkpd1 |
A |
T |
7: 19,257,099 (GRCm39) |
T293S |
probably benign |
Het |
Numb |
A |
G |
12: 83,842,614 (GRCm39) |
Y510H |
probably damaging |
Het |
Nynrin |
T |
G |
14: 56,105,492 (GRCm39) |
L834R |
probably damaging |
Het |
Or11g27 |
T |
C |
14: 50,771,159 (GRCm39) |
S97P |
possibly damaging |
Het |
Or2ak5 |
G |
T |
11: 58,611,347 (GRCm39) |
H176N |
probably benign |
Het |
Or8g18 |
T |
A |
9: 39,149,162 (GRCm39) |
N186I |
possibly damaging |
Het |
Otog |
T |
C |
7: 45,920,797 (GRCm39) |
V1000A |
possibly damaging |
Het |
Pafah1b3 |
A |
G |
7: 24,996,554 (GRCm39) |
V43A |
possibly damaging |
Het |
Pcnx1 |
A |
G |
12: 82,030,450 (GRCm39) |
Y1775C |
possibly damaging |
Het |
Phka1 |
G |
A |
X: 101,564,437 (GRCm39) |
R1074C |
probably damaging |
Het |
Pi4ka |
T |
A |
16: 17,111,765 (GRCm39) |
Y1570F |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,152,329 (GRCm39) |
K2588E |
probably damaging |
Het |
Pkd1 |
A |
G |
17: 24,794,549 (GRCm39) |
T2079A |
probably damaging |
Het |
Plekhd1 |
G |
T |
12: 80,764,075 (GRCm39) |
Q212H |
probably damaging |
Het |
Plekhh1 |
C |
T |
12: 79,087,359 (GRCm39) |
R16* |
probably null |
Het |
Polm |
C |
A |
11: 5,786,207 (GRCm39) |
R120L |
probably damaging |
Het |
Ptpn22 |
T |
C |
3: 103,767,721 (GRCm39) |
M1T |
probably null |
Het |
Ptprh |
G |
A |
7: 4,567,271 (GRCm39) |
L534F |
probably benign |
Het |
Rabl6 |
C |
T |
2: 25,482,778 (GRCm39) |
|
probably null |
Het |
Rap2a |
A |
G |
14: 120,716,403 (GRCm39) |
S89G |
probably damaging |
Het |
Rara |
A |
T |
11: 98,862,406 (GRCm39) |
|
probably null |
Het |
Reck |
A |
G |
4: 43,930,295 (GRCm39) |
D623G |
probably benign |
Het |
Relt |
A |
T |
7: 100,498,023 (GRCm39) |
L237Q |
probably damaging |
Het |
Rngtt |
A |
G |
4: 33,329,598 (GRCm39) |
|
probably null |
Het |
Rtn4rl2 |
T |
G |
2: 84,710,763 (GRCm39) |
Y167S |
probably damaging |
Het |
Sec24c |
C |
T |
14: 20,738,505 (GRCm39) |
R353C |
probably damaging |
Het |
Slc35g2 |
T |
C |
9: 100,435,495 (GRCm39) |
S59G |
probably benign |
Het |
Smarcd2 |
A |
T |
11: 106,158,241 (GRCm39) |
M107K |
probably benign |
Het |
Smg1 |
T |
C |
7: 117,781,606 (GRCm39) |
N1227S |
possibly damaging |
Het |
Snrnp200 |
A |
G |
2: 127,063,734 (GRCm39) |
N638D |
possibly damaging |
Het |
Sntb1 |
A |
G |
15: 55,506,179 (GRCm39) |
S465P |
probably benign |
Het |
Sp4 |
A |
G |
12: 118,263,314 (GRCm39) |
L244P |
probably damaging |
Het |
Sulf1 |
A |
G |
1: 12,887,716 (GRCm39) |
|
probably null |
Het |
Tbc1d17 |
T |
C |
7: 44,492,509 (GRCm39) |
T385A |
probably benign |
Het |
Tbx10 |
C |
A |
19: 4,047,873 (GRCm39) |
D206E |
probably benign |
Het |
Tcea2 |
C |
T |
2: 181,329,431 (GRCm39) |
P275S |
probably damaging |
Het |
Tns3 |
C |
A |
11: 8,443,121 (GRCm39) |
R414L |
probably benign |
Het |
Trip11 |
T |
C |
12: 101,852,235 (GRCm39) |
R610G |
possibly damaging |
Het |
Ugt2b1 |
T |
C |
5: 87,073,720 (GRCm39) |
K213R |
probably null |
Het |
Unc80 |
A |
G |
1: 66,647,601 (GRCm39) |
S1514G |
probably benign |
Het |
Usp7 |
G |
T |
16: 8,511,778 (GRCm39) |
Q867K |
possibly damaging |
Het |
Vim |
T |
C |
2: 13,579,463 (GRCm39) |
V74A |
probably benign |
Het |
Vmn1r234 |
A |
G |
17: 21,450,007 (GRCm39) |
Y307C |
probably benign |
Het |
Vmn2r74 |
A |
T |
7: 85,610,517 (GRCm39) |
Y58* |
probably null |
Het |
Wdr36 |
C |
A |
18: 32,983,584 (GRCm39) |
A445E |
probably damaging |
Het |
Xpo5 |
T |
A |
17: 46,532,359 (GRCm39) |
W465R |
probably damaging |
Het |
Zscan4d |
T |
A |
7: 10,898,946 (GRCm39) |
R110S |
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 |
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 |
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 |
|