Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
G |
A |
7: 119,815,561 (GRCm39) |
A270T |
probably benign |
Het |
Abcb7 |
A |
T |
X: 103,386,142 (GRCm39) |
H97Q |
probably damaging |
Het |
Adat3 |
T |
C |
10: 80,442,249 (GRCm39) |
L29P |
probably damaging |
Het |
AI987944 |
A |
T |
7: 41,024,020 (GRCm39) |
C320S |
probably damaging |
Het |
Asic4 |
C |
T |
1: 75,446,126 (GRCm39) |
R285W |
probably damaging |
Het |
Asic5 |
A |
T |
3: 81,928,293 (GRCm39) |
I419L |
probably damaging |
Het |
Batf |
A |
G |
12: 85,736,102 (GRCm39) |
K42E |
probably damaging |
Het |
Bcar3 |
A |
G |
3: 122,301,785 (GRCm39) |
N160S |
probably benign |
Het |
Bco2 |
C |
A |
9: 50,461,863 (GRCm39) |
G47V |
probably damaging |
Het |
Bicc1 |
T |
G |
10: 70,794,614 (GRCm39) |
K181T |
probably damaging |
Het |
Brinp2 |
A |
G |
1: 158,082,542 (GRCm39) |
|
probably null |
Het |
Cacng8 |
A |
G |
7: 3,463,568 (GRCm39) |
D240G |
possibly damaging |
Het |
Calca |
A |
G |
7: 114,232,962 (GRCm39) |
Y96H |
probably damaging |
Het |
Cdh1 |
A |
T |
8: 107,390,882 (GRCm39) |
K666I |
possibly damaging |
Het |
Cdh16 |
A |
T |
8: 105,344,631 (GRCm39) |
I500N |
possibly damaging |
Het |
Chst14 |
A |
G |
2: 118,757,830 (GRCm39) |
Y208C |
probably damaging |
Het |
Chst9 |
T |
C |
18: 15,586,017 (GRCm39) |
H182R |
probably damaging |
Het |
Clk2 |
A |
G |
3: 89,082,502 (GRCm39) |
I367M |
possibly damaging |
Het |
Cobl |
G |
C |
11: 12,203,258 (GRCm39) |
S1066W |
probably damaging |
Het |
Ctcfl |
A |
G |
2: 172,960,478 (GRCm39) |
V35A |
probably benign |
Het |
Dchs1 |
G |
T |
7: 105,413,363 (GRCm39) |
H1151N |
probably benign |
Het |
Dennd1c |
T |
C |
17: 57,374,083 (GRCm39) |
T529A |
probably benign |
Het |
Dnah11 |
A |
T |
12: 118,070,209 (GRCm39) |
V1532D |
possibly damaging |
Het |
Dync1h1 |
A |
G |
12: 110,612,738 (GRCm39) |
Y2871C |
probably damaging |
Het |
Dytn |
T |
C |
1: 63,716,420 (GRCm39) |
E51G |
probably benign |
Het |
Esd |
C |
T |
14: 74,987,113 (GRCm39) |
A266V |
probably damaging |
Het |
Gli1 |
T |
C |
10: 127,165,975 (GRCm39) |
M1093V |
possibly damaging |
Het |
Gm15446 |
A |
G |
5: 110,091,253 (GRCm39) |
K502E |
probably damaging |
Het |
Gm4076 |
T |
A |
13: 85,275,447 (GRCm39) |
|
noncoding transcript |
Het |
Gm9830 |
A |
G |
9: 44,375,825 (GRCm39) |
|
noncoding transcript |
Het |
Gm9938 |
G |
A |
19: 23,701,955 (GRCm39) |
|
probably benign |
Het |
Grhl1 |
G |
A |
12: 24,634,909 (GRCm39) |
R245H |
probably damaging |
Het |
Hnrnpul1 |
A |
T |
7: 25,426,191 (GRCm39) |
D553E |
probably benign |
Het |
Hpn |
G |
A |
7: 30,798,468 (GRCm39) |
Q415* |
probably null |
Het |
Hsd11b1 |
T |
G |
1: 192,906,068 (GRCm39) |
M175L |
probably benign |
Het |
Htra1 |
G |
A |
7: 130,586,799 (GRCm39) |
V461I |
possibly damaging |
Het |
Il1rl2 |
A |
G |
1: 40,366,694 (GRCm39) |
H76R |
probably damaging |
Het |
Insrr |
G |
A |
3: 87,721,184 (GRCm39) |
V1112M |
probably damaging |
Het |
Ints9 |
T |
C |
14: 65,257,872 (GRCm39) |
S351P |
probably benign |
Het |
Itgav |
T |
A |
2: 83,601,680 (GRCm39) |
N350K |
probably damaging |
Het |
Kdm4d |
C |
A |
9: 14,375,613 (GRCm39) |
V82L |
probably benign |
Het |
Klc1 |
T |
C |
12: 111,748,261 (GRCm39) |
|
probably null |
Het |
Kmt5c |
T |
A |
7: 4,745,714 (GRCm39) |
C69* |
probably null |
Het |
Lgals3 |
T |
G |
14: 47,622,164 (GRCm39) |
N193K |
possibly damaging |
Het |
Morc2b |
T |
A |
17: 33,354,748 (GRCm39) |
D1008V |
probably damaging |
Het |
Mpg |
C |
T |
11: 32,181,720 (GRCm39) |
Q243* |
probably null |
Het |
Muc15 |
C |
T |
2: 110,567,697 (GRCm39) |
R281* |
probably null |
Het |
Ncstn |
CAGCTCCACGAAG |
CAG |
1: 171,899,038 (GRCm39) |
|
probably null |
Het |
Nek5 |
A |
G |
8: 22,597,745 (GRCm39) |
M278T |
probably benign |
Het |
Npas2 |
A |
G |
1: 39,384,503 (GRCm39) |
T599A |
probably benign |
Het |
Nrf1 |
A |
G |
6: 30,144,787 (GRCm39) |
D519G |
probably null |
Het |
Nup43 |
A |
G |
10: 7,549,373 (GRCm39) |
H176R |
probably damaging |
Het |
Nxpe2 |
T |
C |
9: 48,237,914 (GRCm39) |
T114A |
probably damaging |
Het |
Or10j3 |
T |
C |
1: 173,031,795 (GRCm39) |
Y291H |
probably damaging |
Het |
Or5p72 |
A |
T |
7: 108,022,147 (GRCm39) |
Y123F |
possibly damaging |
Het |
Or6c75 |
A |
C |
10: 129,336,902 (GRCm39) |
I50L |
probably benign |
Het |
Perm1 |
C |
T |
4: 156,302,340 (GRCm39) |
R295C |
probably benign |
Het |
Pik3ip1 |
G |
T |
11: 3,283,304 (GRCm39) |
A135S |
probably damaging |
Het |
Pira13 |
A |
C |
7: 3,827,573 (GRCm39) |
C195G |
probably benign |
Het |
Ppp4c |
A |
G |
7: 126,385,452 (GRCm39) |
V119A |
probably damaging |
Het |
Prepl |
A |
G |
17: 85,395,878 (GRCm39) |
Y35H |
possibly damaging |
Het |
Ptpn13 |
A |
G |
5: 103,649,545 (GRCm39) |
Y316C |
possibly damaging |
Het |
Pxk |
C |
T |
14: 8,151,507 (GRCm38) |
R441* |
probably null |
Het |
Ranbp2 |
T |
C |
10: 58,299,921 (GRCm39) |
V491A |
probably benign |
Het |
Ranbp9 |
C |
A |
13: 43,569,933 (GRCm39) |
C495F |
possibly damaging |
Het |
Rfx8 |
A |
T |
1: 39,709,746 (GRCm39) |
|
probably null |
Het |
Rnf111 |
T |
A |
9: 70,383,656 (GRCm39) |
K92N |
probably damaging |
Het |
Rtn1 |
A |
G |
12: 72,259,337 (GRCm39) |
I772T |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,673,844 (GRCm39) |
K72* |
probably null |
Het |
Sergef |
A |
T |
7: 46,264,040 (GRCm39) |
|
probably null |
Het |
Sez6l |
T |
C |
5: 112,620,665 (GRCm39) |
N305S |
probably damaging |
Het |
Slc40a1 |
A |
T |
1: 45,950,302 (GRCm39) |
C383* |
probably null |
Het |
Stard9 |
A |
G |
2: 120,524,189 (GRCm39) |
T795A |
probably benign |
Het |
Stk31 |
T |
C |
6: 49,415,408 (GRCm39) |
I536T |
probably damaging |
Het |
Stox1 |
T |
A |
10: 62,501,178 (GRCm39) |
T461S |
possibly damaging |
Het |
Suv39h2 |
T |
C |
2: 3,460,805 (GRCm39) |
Y219C |
probably damaging |
Het |
Tap1 |
T |
G |
17: 34,413,915 (GRCm39) |
D643E |
probably damaging |
Het |
Tbc1d2b |
T |
A |
9: 90,100,996 (GRCm39) |
I665F |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,935,696 (GRCm39) |
N1784S |
probably benign |
Het |
Tmem14c |
T |
C |
13: 41,174,633 (GRCm39) |
F81L |
possibly damaging |
Het |
Tnrc6c |
A |
G |
11: 117,605,188 (GRCm39) |
N108D |
probably benign |
Het |
Tox3 |
A |
T |
8: 90,996,869 (GRCm39) |
N131K |
probably benign |
Het |
Tspear |
T |
A |
10: 77,706,308 (GRCm39) |
D359E |
probably benign |
Het |
Ttc9 |
A |
G |
12: 81,678,551 (GRCm39) |
I125V |
probably benign |
Het |
Ttn |
A |
T |
2: 76,728,531 (GRCm39) |
|
probably benign |
Het |
Ubn2 |
C |
T |
6: 38,468,226 (GRCm39) |
S980F |
probably damaging |
Het |
Vcf1 |
G |
T |
11: 113,554,212 (GRCm39) |
P161H |
probably damaging |
Het |
Zfp362 |
T |
A |
4: 128,684,057 (GRCm39) |
T30S |
probably benign |
Het |
Zfp385c |
A |
C |
11: 100,528,630 (GRCm39) |
H32Q |
probably damaging |
Het |
Zfp870 |
A |
T |
17: 33,102,863 (GRCm39) |
H156Q |
possibly damaging |
Het |
Zfp873 |
T |
C |
10: 81,897,080 (GRCm39) |
C641R |
probably damaging |
Het |
Zfp950 |
A |
T |
19: 61,107,549 (GRCm39) |
H511Q |
probably benign |
Het |
|
Other mutations in Stab2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Stab2
|
APN |
10 |
86,705,070 (GRCm39) |
splice site |
probably null |
|
IGL00809:Stab2
|
APN |
10 |
86,684,038 (GRCm39) |
splice site |
probably benign |
|
IGL00911:Stab2
|
APN |
10 |
86,805,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01347:Stab2
|
APN |
10 |
86,737,567 (GRCm39) |
splice site |
probably null |
|
IGL01411:Stab2
|
APN |
10 |
86,815,872 (GRCm39) |
splice site |
probably benign |
|
IGL01503:Stab2
|
APN |
10 |
86,776,477 (GRCm39) |
splice site |
probably benign |
|
IGL01599:Stab2
|
APN |
10 |
86,758,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01635:Stab2
|
APN |
10 |
86,816,992 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01640:Stab2
|
APN |
10 |
86,790,035 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01671:Stab2
|
APN |
10 |
86,805,141 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02023:Stab2
|
APN |
10 |
86,707,695 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02075:Stab2
|
APN |
10 |
86,803,514 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02174:Stab2
|
APN |
10 |
86,695,606 (GRCm39) |
splice site |
probably null |
|
IGL02600:Stab2
|
APN |
10 |
86,790,123 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Stab2
|
APN |
10 |
86,686,766 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02668:Stab2
|
APN |
10 |
86,682,027 (GRCm39) |
splice site |
probably benign |
|
IGL02709:Stab2
|
APN |
10 |
86,682,029 (GRCm39) |
splice site |
probably benign |
|
IGL02728:Stab2
|
APN |
10 |
86,692,420 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02803:Stab2
|
APN |
10 |
86,786,133 (GRCm39) |
splice site |
probably benign |
|
IGL02938:Stab2
|
APN |
10 |
86,707,785 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03033:Stab2
|
APN |
10 |
86,832,667 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03238:Stab2
|
APN |
10 |
86,690,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03402:Stab2
|
APN |
10 |
86,805,165 (GRCm39) |
missense |
probably benign |
0.03 |
prospector
|
UTSW |
10 |
86,737,431 (GRCm39) |
splice site |
probably null |
|
songbird
|
UTSW |
10 |
86,694,016 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Stab2
|
UTSW |
10 |
86,705,041 (GRCm39) |
missense |
probably damaging |
0.96 |
F6893:Stab2
|
UTSW |
10 |
86,691,035 (GRCm39) |
missense |
probably damaging |
1.00 |
K7371:Stab2
|
UTSW |
10 |
86,779,153 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4142001:Stab2
|
UTSW |
10 |
86,703,039 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4362001:Stab2
|
UTSW |
10 |
86,697,299 (GRCm39) |
nonsense |
probably null |
|
R0015:Stab2
|
UTSW |
10 |
86,679,481 (GRCm39) |
missense |
probably benign |
|
R0254:Stab2
|
UTSW |
10 |
86,733,824 (GRCm39) |
missense |
probably benign |
|
R0310:Stab2
|
UTSW |
10 |
86,803,477 (GRCm39) |
splice site |
probably benign |
|
R0333:Stab2
|
UTSW |
10 |
86,677,491 (GRCm39) |
missense |
probably benign |
|
R0391:Stab2
|
UTSW |
10 |
86,783,008 (GRCm39) |
missense |
probably benign |
0.27 |
R0400:Stab2
|
UTSW |
10 |
86,708,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Stab2
|
UTSW |
10 |
86,679,355 (GRCm39) |
splice site |
probably benign |
|
R0440:Stab2
|
UTSW |
10 |
86,785,792 (GRCm39) |
missense |
probably benign |
0.23 |
R0743:Stab2
|
UTSW |
10 |
86,723,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R0847:Stab2
|
UTSW |
10 |
86,805,735 (GRCm39) |
missense |
probably benign |
0.00 |
R0883:Stab2
|
UTSW |
10 |
86,760,314 (GRCm39) |
splice site |
probably benign |
|
R1078:Stab2
|
UTSW |
10 |
86,742,997 (GRCm39) |
splice site |
probably null |
|
R1118:Stab2
|
UTSW |
10 |
86,721,582 (GRCm39) |
splice site |
probably null |
|
R1119:Stab2
|
UTSW |
10 |
86,695,619 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1179:Stab2
|
UTSW |
10 |
86,786,165 (GRCm39) |
missense |
probably damaging |
0.98 |
R1440:Stab2
|
UTSW |
10 |
86,697,231 (GRCm39) |
splice site |
probably null |
|
R1550:Stab2
|
UTSW |
10 |
86,714,790 (GRCm39) |
missense |
probably benign |
0.01 |
R1616:Stab2
|
UTSW |
10 |
86,721,582 (GRCm39) |
splice site |
probably null |
|
R1728:Stab2
|
UTSW |
10 |
86,773,903 (GRCm39) |
missense |
probably benign |
0.41 |
R1768:Stab2
|
UTSW |
10 |
86,838,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R1772:Stab2
|
UTSW |
10 |
86,790,098 (GRCm39) |
missense |
probably benign |
0.06 |
R1776:Stab2
|
UTSW |
10 |
86,793,680 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1784:Stab2
|
UTSW |
10 |
86,773,903 (GRCm39) |
missense |
probably benign |
0.41 |
R1957:Stab2
|
UTSW |
10 |
86,697,334 (GRCm39) |
missense |
probably benign |
0.13 |
R1972:Stab2
|
UTSW |
10 |
86,796,180 (GRCm39) |
missense |
probably damaging |
0.99 |
R1975:Stab2
|
UTSW |
10 |
86,732,360 (GRCm39) |
critical splice donor site |
probably null |
|
R1976:Stab2
|
UTSW |
10 |
86,732,360 (GRCm39) |
critical splice donor site |
probably null |
|
R1996:Stab2
|
UTSW |
10 |
86,838,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R2085:Stab2
|
UTSW |
10 |
86,790,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Stab2
|
UTSW |
10 |
86,700,904 (GRCm39) |
nonsense |
probably null |
|
R2169:Stab2
|
UTSW |
10 |
86,723,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Stab2
|
UTSW |
10 |
86,776,503 (GRCm39) |
missense |
probably benign |
0.22 |
R2296:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2297:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2298:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2326:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2434:Stab2
|
UTSW |
10 |
86,805,183 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2519:Stab2
|
UTSW |
10 |
86,770,704 (GRCm39) |
splice site |
probably benign |
|
R2696:Stab2
|
UTSW |
10 |
86,697,363 (GRCm39) |
missense |
probably benign |
0.45 |
R2883:Stab2
|
UTSW |
10 |
86,803,550 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2923:Stab2
|
UTSW |
10 |
86,697,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R3711:Stab2
|
UTSW |
10 |
86,702,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Stab2
|
UTSW |
10 |
86,805,141 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3834:Stab2
|
UTSW |
10 |
86,785,776 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3970:Stab2
|
UTSW |
10 |
86,714,750 (GRCm39) |
missense |
probably damaging |
0.97 |
R3979:Stab2
|
UTSW |
10 |
86,699,320 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4003:Stab2
|
UTSW |
10 |
86,693,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Stab2
|
UTSW |
10 |
86,758,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R4151:Stab2
|
UTSW |
10 |
86,838,847 (GRCm39) |
missense |
probably benign |
0.12 |
R4190:Stab2
|
UTSW |
10 |
86,714,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R4556:Stab2
|
UTSW |
10 |
86,803,543 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4773:Stab2
|
UTSW |
10 |
86,743,235 (GRCm39) |
nonsense |
probably null |
|
R4825:Stab2
|
UTSW |
10 |
86,783,011 (GRCm39) |
missense |
probably benign |
0.08 |
R4865:Stab2
|
UTSW |
10 |
86,679,364 (GRCm39) |
splice site |
probably null |
|
R4871:Stab2
|
UTSW |
10 |
86,778,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R4943:Stab2
|
UTSW |
10 |
86,790,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R4981:Stab2
|
UTSW |
10 |
86,796,087 (GRCm39) |
missense |
probably benign |
|
R4994:Stab2
|
UTSW |
10 |
86,785,771 (GRCm39) |
missense |
probably benign |
|
R4999:Stab2
|
UTSW |
10 |
86,773,773 (GRCm39) |
missense |
probably damaging |
0.97 |
R5061:Stab2
|
UTSW |
10 |
86,743,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Stab2
|
UTSW |
10 |
86,699,422 (GRCm39) |
missense |
probably benign |
0.23 |
R5073:Stab2
|
UTSW |
10 |
86,699,422 (GRCm39) |
missense |
probably benign |
0.23 |
R5074:Stab2
|
UTSW |
10 |
86,699,422 (GRCm39) |
missense |
probably benign |
0.23 |
R5134:Stab2
|
UTSW |
10 |
86,707,674 (GRCm39) |
splice site |
probably null |
|
R5213:Stab2
|
UTSW |
10 |
86,743,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R5508:Stab2
|
UTSW |
10 |
86,796,143 (GRCm39) |
missense |
probably benign |
0.01 |
R5530:Stab2
|
UTSW |
10 |
86,783,026 (GRCm39) |
missense |
probably benign |
0.04 |
R5540:Stab2
|
UTSW |
10 |
86,683,989 (GRCm39) |
missense |
probably benign |
0.30 |
R5839:Stab2
|
UTSW |
10 |
86,708,555 (GRCm39) |
missense |
probably damaging |
0.97 |
R5949:Stab2
|
UTSW |
10 |
86,805,713 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6015:Stab2
|
UTSW |
10 |
86,773,906 (GRCm39) |
missense |
probably damaging |
0.99 |
R6019:Stab2
|
UTSW |
10 |
86,838,886 (GRCm39) |
missense |
probably benign |
0.00 |
R6116:Stab2
|
UTSW |
10 |
86,743,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6131:Stab2
|
UTSW |
10 |
86,719,642 (GRCm39) |
splice site |
probably null |
|
R6209:Stab2
|
UTSW |
10 |
86,758,867 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6243:Stab2
|
UTSW |
10 |
86,743,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R6433:Stab2
|
UTSW |
10 |
86,737,431 (GRCm39) |
splice site |
probably null |
|
R6787:Stab2
|
UTSW |
10 |
86,754,948 (GRCm39) |
missense |
probably benign |
0.07 |
R6841:Stab2
|
UTSW |
10 |
86,778,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6873:Stab2
|
UTSW |
10 |
86,697,230 (GRCm39) |
critical splice donor site |
probably null |
|
R7025:Stab2
|
UTSW |
10 |
86,686,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R7043:Stab2
|
UTSW |
10 |
86,706,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R7047:Stab2
|
UTSW |
10 |
86,694,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R7107:Stab2
|
UTSW |
10 |
86,741,456 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7214:Stab2
|
UTSW |
10 |
86,735,705 (GRCm39) |
missense |
probably damaging |
0.99 |
R7271:Stab2
|
UTSW |
10 |
86,838,972 (GRCm39) |
splice site |
probably null |
|
R7291:Stab2
|
UTSW |
10 |
86,782,084 (GRCm39) |
missense |
probably damaging |
0.96 |
R7336:Stab2
|
UTSW |
10 |
86,805,049 (GRCm39) |
nonsense |
probably null |
|
R7432:Stab2
|
UTSW |
10 |
86,721,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R7580:Stab2
|
UTSW |
10 |
86,705,028 (GRCm39) |
missense |
probably benign |
0.00 |
R7622:Stab2
|
UTSW |
10 |
86,709,766 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7629:Stab2
|
UTSW |
10 |
86,719,646 (GRCm39) |
critical splice donor site |
probably null |
|
R7658:Stab2
|
UTSW |
10 |
86,816,999 (GRCm39) |
missense |
probably benign |
0.12 |
R7798:Stab2
|
UTSW |
10 |
86,793,776 (GRCm39) |
missense |
probably damaging |
0.98 |
R7835:Stab2
|
UTSW |
10 |
86,708,483 (GRCm39) |
missense |
probably benign |
0.06 |
R7845:Stab2
|
UTSW |
10 |
86,832,758 (GRCm39) |
missense |
probably benign |
0.09 |
R7863:Stab2
|
UTSW |
10 |
86,808,745 (GRCm39) |
missense |
probably benign |
0.30 |
R7885:Stab2
|
UTSW |
10 |
86,714,776 (GRCm39) |
missense |
probably benign |
0.03 |
R7904:Stab2
|
UTSW |
10 |
86,790,056 (GRCm39) |
nonsense |
probably null |
|
R7947:Stab2
|
UTSW |
10 |
86,681,897 (GRCm39) |
missense |
probably benign |
0.31 |
R7963:Stab2
|
UTSW |
10 |
86,683,887 (GRCm39) |
critical splice donor site |
probably null |
|
R8014:Stab2
|
UTSW |
10 |
86,686,767 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8021:Stab2
|
UTSW |
10 |
86,741,403 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8024:Stab2
|
UTSW |
10 |
86,681,916 (GRCm39) |
missense |
probably benign |
0.34 |
R8097:Stab2
|
UTSW |
10 |
86,704,959 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8281:Stab2
|
UTSW |
10 |
86,709,728 (GRCm39) |
missense |
probably damaging |
0.98 |
R8462:Stab2
|
UTSW |
10 |
86,803,598 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8670:Stab2
|
UTSW |
10 |
86,776,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R8692:Stab2
|
UTSW |
10 |
86,808,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R8744:Stab2
|
UTSW |
10 |
86,805,213 (GRCm39) |
missense |
probably benign |
0.32 |
R8745:Stab2
|
UTSW |
10 |
86,805,213 (GRCm39) |
missense |
probably benign |
0.32 |
R8782:Stab2
|
UTSW |
10 |
86,735,685 (GRCm39) |
missense |
probably benign |
0.00 |
R8875:Stab2
|
UTSW |
10 |
86,832,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R8978:Stab2
|
UTSW |
10 |
86,785,782 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9141:Stab2
|
UTSW |
10 |
86,704,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R9248:Stab2
|
UTSW |
10 |
86,727,481 (GRCm39) |
missense |
probably damaging |
0.98 |
R9326:Stab2
|
UTSW |
10 |
86,791,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R9426:Stab2
|
UTSW |
10 |
86,704,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R9568:Stab2
|
UTSW |
10 |
86,699,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R9627:Stab2
|
UTSW |
10 |
86,793,704 (GRCm39) |
missense |
probably damaging |
0.98 |
R9635:Stab2
|
UTSW |
10 |
86,686,651 (GRCm39) |
nonsense |
probably null |
|
R9648:Stab2
|
UTSW |
10 |
86,692,561 (GRCm39) |
frame shift |
probably null |
|
R9649:Stab2
|
UTSW |
10 |
86,692,561 (GRCm39) |
frame shift |
probably null |
|
R9650:Stab2
|
UTSW |
10 |
86,692,561 (GRCm39) |
frame shift |
probably null |
|
R9726:Stab2
|
UTSW |
10 |
86,790,095 (GRCm39) |
missense |
probably benign |
0.00 |
R9756:Stab2
|
UTSW |
10 |
86,803,553 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9786:Stab2
|
UTSW |
10 |
86,757,997 (GRCm39) |
missense |
probably benign |
0.03 |
RF061:Stab2
|
UTSW |
10 |
86,702,622 (GRCm39) |
critical splice acceptor site |
probably benign |
|
X0023:Stab2
|
UTSW |
10 |
86,758,062 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0025:Stab2
|
UTSW |
10 |
86,723,680 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Stab2
|
UTSW |
10 |
86,785,778 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Stab2
|
UTSW |
10 |
86,732,460 (GRCm39) |
missense |
probably damaging |
1.00 |
|