Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,773,874 (GRCm39) |
K1021R |
probably damaging |
Het |
2610528J11Rik |
G |
A |
4: 118,386,762 (GRCm39) |
V36M |
probably damaging |
Het |
4930402F06Rik |
T |
A |
2: 35,265,795 (GRCm39) |
R292* |
probably null |
Het |
Abcb4 |
T |
C |
5: 8,959,194 (GRCm39) |
F207S |
probably damaging |
Het |
Adcy4 |
A |
C |
14: 56,008,990 (GRCm39) |
N812K |
probably benign |
Het |
Afap1l2 |
G |
T |
19: 56,916,872 (GRCm39) |
|
probably benign |
Het |
Arfgef2 |
A |
T |
2: 166,687,385 (GRCm39) |
H203L |
probably benign |
Het |
Avl9 |
G |
T |
6: 56,713,468 (GRCm39) |
R242L |
probably benign |
Het |
Cfi |
A |
C |
3: 129,642,416 (GRCm39) |
H90P |
probably damaging |
Het |
Cyp2d10 |
C |
T |
15: 82,288,794 (GRCm39) |
M229I |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,245,897 (GRCm39) |
|
probably benign |
Het |
Dnttip2 |
G |
T |
3: 122,069,452 (GRCm39) |
M222I |
probably benign |
Het |
Dync1li2 |
A |
T |
8: 105,154,757 (GRCm39) |
Y284N |
probably benign |
Het |
Ebf1 |
T |
C |
11: 44,882,282 (GRCm39) |
Y413H |
probably benign |
Het |
Exog |
A |
G |
9: 119,281,319 (GRCm39) |
T186A |
possibly damaging |
Het |
Fam171a2 |
T |
C |
11: 102,334,939 (GRCm39) |
N66S |
possibly damaging |
Het |
Gprc5a |
A |
T |
6: 135,056,033 (GRCm39) |
N160I |
probably damaging |
Het |
Haus3 |
A |
G |
5: 34,323,258 (GRCm39) |
|
probably null |
Het |
Klhl20 |
A |
T |
1: 160,918,015 (GRCm39) |
C90* |
probably null |
Het |
Krt84 |
T |
A |
15: 101,437,138 (GRCm39) |
I342L |
probably damaging |
Het |
Lifr |
G |
A |
15: 7,208,373 (GRCm39) |
D584N |
probably damaging |
Het |
Lmbrd2 |
G |
A |
15: 9,184,039 (GRCm39) |
R551K |
probably damaging |
Het |
Lrtm1 |
T |
A |
14: 28,744,184 (GRCm39) |
|
probably benign |
Het |
Mat1a |
T |
A |
14: 40,842,187 (GRCm39) |
|
probably benign |
Het |
Mest |
A |
G |
6: 30,746,269 (GRCm39) |
I279V |
probably damaging |
Het |
Mroh5 |
A |
T |
15: 73,691,199 (GRCm39) |
D155E |
probably benign |
Het |
Naa25 |
A |
G |
5: 121,573,632 (GRCm39) |
D787G |
possibly damaging |
Het |
Naaladl1 |
C |
T |
19: 6,162,534 (GRCm39) |
P465S |
probably damaging |
Het |
Necab3 |
G |
A |
2: 154,387,232 (GRCm39) |
R302C |
probably damaging |
Het |
Nsg1 |
A |
T |
5: 38,316,254 (GRCm39) |
D32E |
probably damaging |
Het |
Ntrk2 |
T |
C |
13: 58,956,607 (GRCm39) |
V22A |
probably benign |
Het |
Nuggc |
A |
G |
14: 65,851,000 (GRCm39) |
D290G |
probably null |
Het |
Nup205 |
A |
T |
6: 35,202,715 (GRCm39) |
|
probably benign |
Het |
Or2t35 |
C |
T |
14: 14,407,876 (GRCm38) |
S218F |
probably damaging |
Het |
Or4f57 |
G |
C |
2: 111,790,942 (GRCm39) |
Q159E |
probably damaging |
Het |
Pde4b |
T |
A |
4: 102,447,375 (GRCm39) |
S9T |
probably benign |
Het |
Phip |
A |
T |
9: 82,787,845 (GRCm39) |
|
probably null |
Het |
Pitpnm3 |
C |
T |
11: 71,947,072 (GRCm39) |
V776M |
probably damaging |
Het |
Pon2 |
A |
G |
6: 5,289,091 (GRCm39) |
|
probably benign |
Het |
Ppp1r12b |
T |
A |
1: 134,763,637 (GRCm39) |
|
probably null |
Het |
Ppp1r15b |
A |
G |
1: 133,060,908 (GRCm39) |
N475S |
probably damaging |
Het |
Prorp |
A |
G |
12: 55,429,082 (GRCm39) |
D535G |
probably benign |
Het |
Prrt3 |
A |
T |
6: 113,474,790 (GRCm39) |
L144H |
probably damaging |
Het |
Psmb7 |
A |
G |
2: 38,533,377 (GRCm39) |
V50A |
possibly damaging |
Het |
Sacs |
T |
A |
14: 61,442,017 (GRCm39) |
S1354R |
probably damaging |
Het |
Sdcbp2 |
A |
G |
2: 151,425,884 (GRCm39) |
T29A |
probably benign |
Het |
Shbg |
T |
A |
11: 69,508,415 (GRCm39) |
|
probably benign |
Het |
Shcbp1 |
A |
G |
8: 4,794,452 (GRCm39) |
I447T |
probably damaging |
Het |
Spata31h1 |
T |
A |
10: 82,119,390 (GRCm39) |
K4540M |
probably damaging |
Het |
Spata31h2 |
T |
A |
5: 23,542,489 (GRCm39) |
|
noncoding transcript |
Het |
Thbd |
A |
T |
2: 148,248,903 (GRCm39) |
C322S |
probably damaging |
Het |
Tnfrsf21 |
C |
T |
17: 43,349,104 (GRCm39) |
H239Y |
probably benign |
Het |
Trappc12 |
A |
T |
12: 28,796,751 (GRCm39) |
F260L |
probably damaging |
Het |
Trgv4 |
T |
G |
13: 19,369,370 (GRCm39) |
F38C |
possibly damaging |
Het |
Trim10 |
C |
A |
17: 37,181,074 (GRCm39) |
H102N |
probably damaging |
Het |
Ube2u |
A |
G |
4: 100,407,122 (GRCm39) |
T215A |
possibly damaging |
Het |
Vcan |
T |
G |
13: 89,851,787 (GRCm39) |
T1058P |
probably benign |
Het |
Vwa3b |
A |
C |
1: 37,174,595 (GRCm39) |
E670A |
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 |
|
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 |
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 |
|