Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
T |
A |
9: 44,190,691 (GRCm39) |
Q278H |
probably benign |
Het |
Ace3 |
T |
C |
11: 105,895,436 (GRCm39) |
|
probably null |
Het |
Aco1 |
T |
C |
4: 40,176,499 (GRCm39) |
V221A |
probably damaging |
Het |
Adamts20 |
T |
A |
15: 94,301,891 (GRCm39) |
H27L |
probably benign |
Het |
Adamts8 |
A |
G |
9: 30,867,808 (GRCm39) |
D544G |
probably benign |
Het |
Angptl4 |
C |
A |
17: 34,000,249 (GRCm39) |
E40* |
probably null |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atf7ip2 |
T |
A |
16: 10,059,567 (GRCm39) |
I369N |
possibly damaging |
Het |
Atp6ap1l |
T |
A |
13: 91,031,806 (GRCm39) |
Y292F |
probably damaging |
Het |
Atp6v1b2 |
A |
T |
8: 69,555,459 (GRCm39) |
K217* |
probably null |
Het |
Bid |
C |
T |
6: 120,874,216 (GRCm39) |
A110T |
possibly damaging |
Het |
Blvra |
T |
A |
2: 126,937,068 (GRCm39) |
W174R |
probably damaging |
Het |
Catsperg1 |
C |
T |
7: 28,897,568 (GRCm39) |
G239R |
probably damaging |
Het |
Ccdc157 |
G |
T |
11: 4,096,549 (GRCm39) |
A400D |
probably damaging |
Het |
Chd2 |
G |
T |
7: 73,104,193 (GRCm39) |
P1298T |
probably damaging |
Het |
CK137956 |
G |
A |
4: 127,840,651 (GRCm39) |
L352F |
possibly damaging |
Het |
Col22a1 |
G |
A |
15: 71,741,989 (GRCm39) |
P503S |
unknown |
Het |
Cox15 |
C |
T |
19: 43,735,224 (GRCm39) |
R181H |
probably benign |
Het |
Crem |
C |
T |
18: 3,299,284 (GRCm39) |
G47R |
probably benign |
Het |
Crygs |
T |
A |
16: 22,625,304 (GRCm39) |
T46S |
probably benign |
Het |
Cts8 |
T |
A |
13: 61,401,429 (GRCm39) |
H62L |
probably damaging |
Het |
Cyp4a32 |
T |
A |
4: 115,468,474 (GRCm39) |
F319I |
possibly damaging |
Het |
Dchs1 |
T |
C |
7: 105,415,109 (GRCm39) |
S692G |
probably damaging |
Het |
Ddx23 |
G |
A |
15: 98,548,599 (GRCm39) |
R370W |
possibly damaging |
Het |
Defa29 |
A |
T |
8: 21,816,865 (GRCm39) |
S43T |
probably damaging |
Het |
Dnajc14 |
A |
G |
10: 128,652,661 (GRCm39) |
D573G |
probably damaging |
Het |
Drd5 |
A |
G |
5: 38,477,319 (GRCm39) |
Y104C |
probably benign |
Het |
Efcab7 |
C |
T |
4: 99,768,215 (GRCm39) |
P102L |
probably damaging |
Het |
Efhc1 |
A |
G |
1: 21,037,624 (GRCm39) |
Y267C |
probably damaging |
Het |
Eif2ak4 |
T |
C |
2: 118,278,967 (GRCm39) |
Y243H |
probably damaging |
Het |
Gfm2 |
T |
A |
13: 97,278,475 (GRCm39) |
I7N |
probably damaging |
Het |
Gmds |
A |
G |
13: 32,311,980 (GRCm39) |
F150L |
possibly damaging |
Het |
Gp2 |
T |
C |
7: 119,053,455 (GRCm39) |
T169A |
possibly damaging |
Het |
Grb14 |
A |
G |
2: 64,743,146 (GRCm39) |
F508L |
probably damaging |
Het |
Hdac5 |
T |
A |
11: 102,086,698 (GRCm39) |
|
probably benign |
Het |
Heatr1 |
T |
A |
13: 12,450,066 (GRCm39) |
M620K |
probably damaging |
Het |
Herc3 |
A |
G |
6: 58,853,778 (GRCm39) |
E608G |
probably damaging |
Het |
Hoxb4 |
T |
C |
11: 96,210,867 (GRCm39) |
Y156H |
probably damaging |
Het |
Ifi205 |
T |
A |
1: 173,855,980 (GRCm39) |
I17F |
possibly damaging |
Het |
Il2rb |
A |
T |
15: 78,375,977 (GRCm39) |
S25T |
possibly damaging |
Het |
Kansl1 |
T |
C |
11: 104,225,923 (GRCm39) |
T998A |
probably damaging |
Het |
Kcna6 |
G |
T |
6: 126,715,451 (GRCm39) |
H479Q |
probably benign |
Het |
Kif2a |
T |
C |
13: 107,114,599 (GRCm39) |
K350R |
probably benign |
Het |
Lct |
G |
T |
1: 128,221,898 (GRCm39) |
A1547E |
probably damaging |
Het |
Lhx9 |
T |
A |
1: 138,769,747 (GRCm39) |
|
probably benign |
Het |
Lingo1 |
T |
A |
9: 56,526,934 (GRCm39) |
I552F |
possibly damaging |
Het |
Lrp4 |
G |
A |
2: 91,327,700 (GRCm39) |
W1516* |
probably null |
Het |
Lrp5 |
C |
T |
19: 3,660,131 (GRCm39) |
V978I |
probably benign |
Het |
Ltbp1 |
T |
A |
17: 75,620,029 (GRCm39) |
D719E |
probably benign |
Het |
Ltbp4 |
A |
G |
7: 27,007,191 (GRCm39) |
|
probably null |
Het |
Macf1 |
A |
G |
4: 123,345,830 (GRCm39) |
I1326T |
probably damaging |
Het |
Manba |
T |
C |
3: 135,250,501 (GRCm39) |
F376S |
probably benign |
Het |
Mink1 |
T |
C |
11: 70,499,254 (GRCm39) |
|
probably null |
Het |
Nfatc2ip |
C |
T |
7: 125,984,164 (GRCm39) |
V410I |
probably damaging |
Het |
Nlrp1b |
A |
T |
11: 71,072,964 (GRCm39) |
I293N |
probably damaging |
Het |
Or10aa3 |
T |
C |
1: 173,878,244 (GRCm39) |
Y102H |
probably damaging |
Het |
Otol1 |
A |
C |
3: 69,935,437 (GRCm39) |
E476D |
probably benign |
Het |
Pcdhb4 |
C |
T |
18: 37,442,594 (GRCm39) |
P635S |
probably benign |
Het |
Pfkfb4 |
T |
A |
9: 108,828,237 (GRCm39) |
F91I |
probably damaging |
Het |
Polr3c |
A |
T |
3: 96,626,614 (GRCm39) |
L270H |
probably damaging |
Het |
Ppp1r15b |
C |
T |
1: 133,059,363 (GRCm39) |
|
probably benign |
Het |
Prkca |
T |
G |
11: 108,082,975 (GRCm39) |
D90A |
probably benign |
Het |
Sall3 |
T |
C |
18: 81,012,968 (GRCm39) |
D1156G |
probably benign |
Het |
Scn7a |
A |
T |
2: 66,506,446 (GRCm39) |
L1481H |
probably damaging |
Het |
Selenon |
A |
T |
4: 134,271,929 (GRCm39) |
I292N |
probably damaging |
Het |
Sema6d |
T |
A |
2: 124,501,806 (GRCm39) |
|
probably null |
Het |
Sgpp1 |
G |
T |
12: 75,762,953 (GRCm39) |
Y409* |
probably null |
Het |
Sh3pxd2a |
A |
G |
19: 47,255,947 (GRCm39) |
S924P |
probably benign |
Het |
Slc25a13 |
A |
G |
6: 6,042,264 (GRCm39) |
V638A |
probably benign |
Het |
Snhg11 |
T |
C |
2: 158,218,746 (GRCm39) |
|
probably benign |
Het |
Sorbs2 |
A |
G |
8: 46,249,389 (GRCm39) |
Q800R |
probably benign |
Het |
Srf |
C |
A |
17: 46,860,912 (GRCm39) |
G401C |
probably damaging |
Het |
Stradb |
A |
C |
1: 59,030,264 (GRCm39) |
N173H |
probably benign |
Het |
Swap70 |
C |
T |
7: 109,878,470 (GRCm39) |
A480V |
possibly damaging |
Het |
Sycp2 |
A |
G |
2: 178,023,750 (GRCm39) |
V422A |
probably damaging |
Het |
Taf4 |
G |
A |
2: 179,573,822 (GRCm39) |
T682M |
probably damaging |
Het |
Tet3 |
T |
C |
6: 83,381,361 (GRCm39) |
N269S |
possibly damaging |
Het |
Thap12 |
A |
T |
7: 98,366,045 (GRCm39) |
I738F |
possibly damaging |
Het |
Tiam2 |
C |
T |
17: 3,565,000 (GRCm39) |
R1413C |
possibly damaging |
Het |
Tmem229a |
A |
T |
6: 24,955,010 (GRCm39) |
F248Y |
probably damaging |
Het |
Tmprss7 |
G |
A |
16: 45,504,956 (GRCm39) |
Q145* |
probably null |
Het |
Tnc |
A |
T |
4: 63,911,262 (GRCm39) |
|
probably null |
Het |
Tonsl |
A |
T |
15: 76,508,797 (GRCm39) |
Y21N |
probably damaging |
Het |
Tpr |
A |
G |
1: 150,297,414 (GRCm39) |
D1009G |
probably benign |
Het |
Trpm2 |
G |
A |
10: 77,776,992 (GRCm39) |
A435V |
probably damaging |
Het |
Ubr3 |
T |
A |
2: 69,783,820 (GRCm39) |
|
probably null |
Het |
Vcan |
T |
C |
13: 89,853,653 (GRCm39) |
N436D |
possibly damaging |
Het |
Vmn2r104 |
T |
A |
17: 20,261,031 (GRCm39) |
Y464F |
probably damaging |
Het |
Vmn2r44 |
T |
A |
7: 8,370,981 (GRCm39) |
R688S |
probably benign |
Het |
Wdr74 |
G |
T |
19: 8,715,311 (GRCm39) |
V157L |
probably benign |
Het |
Wnt7a |
T |
A |
6: 91,371,530 (GRCm39) |
D144V |
probably benign |
Het |
Zfp106 |
C |
T |
2: 120,362,162 (GRCm39) |
A986T |
possibly damaging |
Het |
|
Other mutations in Polq |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Polq
|
APN |
16 |
36,885,609 (GRCm39) |
splice site |
probably benign |
|
IGL00539:Polq
|
APN |
16 |
36,880,931 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00960:Polq
|
APN |
16 |
36,880,874 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01100:Polq
|
APN |
16 |
36,881,474 (GRCm39) |
missense |
probably benign |
|
IGL01112:Polq
|
APN |
16 |
36,837,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01138:Polq
|
APN |
16 |
36,866,231 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01432:Polq
|
APN |
16 |
36,892,184 (GRCm39) |
splice site |
probably benign |
|
IGL01522:Polq
|
APN |
16 |
36,848,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01565:Polq
|
APN |
16 |
36,833,475 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01592:Polq
|
APN |
16 |
36,855,212 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01690:Polq
|
APN |
16 |
36,883,200 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01943:Polq
|
APN |
16 |
36,881,805 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02531:Polq
|
APN |
16 |
36,882,736 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02553:Polq
|
APN |
16 |
36,862,130 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02623:Polq
|
APN |
16 |
36,880,737 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02692:Polq
|
APN |
16 |
36,880,989 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02717:Polq
|
APN |
16 |
36,843,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02937:Polq
|
APN |
16 |
36,833,471 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02959:Polq
|
APN |
16 |
36,906,928 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03086:Polq
|
APN |
16 |
36,911,411 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03141:Polq
|
APN |
16 |
36,837,720 (GRCm39) |
splice site |
probably benign |
|
IGL03302:Polq
|
APN |
16 |
36,892,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03393:Polq
|
APN |
16 |
36,865,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013_Polq_667
|
UTSW |
16 |
36,882,201 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4238_Polq_233
|
UTSW |
16 |
36,833,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R4280_polq_867
|
UTSW |
16 |
36,902,419 (GRCm39) |
missense |
probably damaging |
1.00 |
G1Funyon:Polq
|
UTSW |
16 |
36,882,181 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4403001:Polq
|
UTSW |
16 |
36,880,949 (GRCm39) |
missense |
probably benign |
0.00 |
R0013:Polq
|
UTSW |
16 |
36,882,201 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0082:Polq
|
UTSW |
16 |
36,837,619 (GRCm39) |
missense |
probably benign |
0.01 |
R0212:Polq
|
UTSW |
16 |
36,887,216 (GRCm39) |
missense |
probably damaging |
0.99 |
R0387:Polq
|
UTSW |
16 |
36,909,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Polq
|
UTSW |
16 |
36,849,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R0427:Polq
|
UTSW |
16 |
36,882,355 (GRCm39) |
nonsense |
probably null |
|
R0454:Polq
|
UTSW |
16 |
36,855,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R0513:Polq
|
UTSW |
16 |
36,914,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0622:Polq
|
UTSW |
16 |
36,881,355 (GRCm39) |
missense |
probably benign |
0.02 |
R0848:Polq
|
UTSW |
16 |
36,882,492 (GRCm39) |
missense |
probably benign |
0.08 |
R1142:Polq
|
UTSW |
16 |
36,833,579 (GRCm39) |
missense |
probably damaging |
0.98 |
R1218:Polq
|
UTSW |
16 |
36,849,808 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1331:Polq
|
UTSW |
16 |
36,862,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R1398:Polq
|
UTSW |
16 |
36,882,857 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1424:Polq
|
UTSW |
16 |
36,906,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R1644:Polq
|
UTSW |
16 |
36,880,626 (GRCm39) |
missense |
probably damaging |
0.96 |
R1777:Polq
|
UTSW |
16 |
36,880,586 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1820:Polq
|
UTSW |
16 |
36,849,780 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1854:Polq
|
UTSW |
16 |
36,882,471 (GRCm39) |
missense |
probably benign |
0.01 |
R1880:Polq
|
UTSW |
16 |
36,906,954 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2008:Polq
|
UTSW |
16 |
36,882,844 (GRCm39) |
missense |
probably damaging |
0.96 |
R2014:Polq
|
UTSW |
16 |
36,898,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R2026:Polq
|
UTSW |
16 |
36,883,107 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2178:Polq
|
UTSW |
16 |
36,883,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R2259:Polq
|
UTSW |
16 |
36,882,459 (GRCm39) |
missense |
probably benign |
0.03 |
R2266:Polq
|
UTSW |
16 |
36,882,515 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2305:Polq
|
UTSW |
16 |
36,882,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R2370:Polq
|
UTSW |
16 |
36,894,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Polq
|
UTSW |
16 |
36,832,304 (GRCm39) |
missense |
unknown |
|
R2517:Polq
|
UTSW |
16 |
36,909,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R2697:Polq
|
UTSW |
16 |
36,862,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R2858:Polq
|
UTSW |
16 |
36,883,115 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3436:Polq
|
UTSW |
16 |
36,882,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R3437:Polq
|
UTSW |
16 |
36,882,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R3699:Polq
|
UTSW |
16 |
36,862,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R3838:Polq
|
UTSW |
16 |
36,898,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R3875:Polq
|
UTSW |
16 |
36,894,389 (GRCm39) |
missense |
probably damaging |
0.99 |
R4050:Polq
|
UTSW |
16 |
36,913,182 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4172:Polq
|
UTSW |
16 |
36,881,120 (GRCm39) |
missense |
probably benign |
0.02 |
R4238:Polq
|
UTSW |
16 |
36,833,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R4240:Polq
|
UTSW |
16 |
36,833,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R4280:Polq
|
UTSW |
16 |
36,902,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R4296:Polq
|
UTSW |
16 |
36,881,663 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4360:Polq
|
UTSW |
16 |
36,880,701 (GRCm39) |
missense |
probably benign |
0.00 |
R4373:Polq
|
UTSW |
16 |
36,833,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R4375:Polq
|
UTSW |
16 |
36,833,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R4376:Polq
|
UTSW |
16 |
36,833,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R4509:Polq
|
UTSW |
16 |
36,868,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Polq
|
UTSW |
16 |
36,868,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R4511:Polq
|
UTSW |
16 |
36,868,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R4543:Polq
|
UTSW |
16 |
36,881,147 (GRCm39) |
missense |
probably benign |
0.43 |
R4633:Polq
|
UTSW |
16 |
36,868,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R4739:Polq
|
UTSW |
16 |
36,862,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Polq
|
UTSW |
16 |
36,848,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R4841:Polq
|
UTSW |
16 |
36,869,145 (GRCm39) |
critical splice donor site |
probably null |
|
R4842:Polq
|
UTSW |
16 |
36,869,145 (GRCm39) |
critical splice donor site |
probably null |
|
R4937:Polq
|
UTSW |
16 |
36,848,274 (GRCm39) |
missense |
probably benign |
0.01 |
R4955:Polq
|
UTSW |
16 |
36,881,444 (GRCm39) |
missense |
probably benign |
0.32 |
R4992:Polq
|
UTSW |
16 |
36,881,524 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5008:Polq
|
UTSW |
16 |
36,882,749 (GRCm39) |
missense |
probably benign |
|
R5221:Polq
|
UTSW |
16 |
36,862,540 (GRCm39) |
missense |
probably damaging |
0.98 |
R5254:Polq
|
UTSW |
16 |
36,909,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R5292:Polq
|
UTSW |
16 |
36,881,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R5375:Polq
|
UTSW |
16 |
36,903,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R5480:Polq
|
UTSW |
16 |
36,833,652 (GRCm39) |
splice site |
probably benign |
|
R5552:Polq
|
UTSW |
16 |
36,914,872 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5591:Polq
|
UTSW |
16 |
36,832,247 (GRCm39) |
utr 5 prime |
probably benign |
|
R5653:Polq
|
UTSW |
16 |
36,860,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R5708:Polq
|
UTSW |
16 |
36,881,380 (GRCm39) |
missense |
probably damaging |
0.98 |
R5754:Polq
|
UTSW |
16 |
36,837,625 (GRCm39) |
missense |
probably benign |
|
R5757:Polq
|
UTSW |
16 |
36,907,043 (GRCm39) |
missense |
probably benign |
0.01 |
R5764:Polq
|
UTSW |
16 |
36,837,706 (GRCm39) |
missense |
probably damaging |
0.97 |
R6019:Polq
|
UTSW |
16 |
36,882,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Polq
|
UTSW |
16 |
36,866,174 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6177:Polq
|
UTSW |
16 |
36,892,071 (GRCm39) |
missense |
probably damaging |
0.98 |
R6307:Polq
|
UTSW |
16 |
36,837,718 (GRCm39) |
critical splice donor site |
probably null |
|
R6499:Polq
|
UTSW |
16 |
36,881,189 (GRCm39) |
missense |
probably benign |
0.03 |
R6520:Polq
|
UTSW |
16 |
36,880,739 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6598:Polq
|
UTSW |
16 |
36,881,993 (GRCm39) |
missense |
probably benign |
0.39 |
R6694:Polq
|
UTSW |
16 |
36,835,535 (GRCm39) |
missense |
probably null |
0.99 |
R6788:Polq
|
UTSW |
16 |
36,897,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R7104:Polq
|
UTSW |
16 |
36,909,715 (GRCm39) |
nonsense |
probably null |
|
R7159:Polq
|
UTSW |
16 |
36,883,215 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7222:Polq
|
UTSW |
16 |
36,906,995 (GRCm39) |
nonsense |
probably null |
|
R7340:Polq
|
UTSW |
16 |
36,881,288 (GRCm39) |
missense |
probably benign |
0.00 |
R7361:Polq
|
UTSW |
16 |
36,880,790 (GRCm39) |
missense |
probably benign |
0.00 |
R7384:Polq
|
UTSW |
16 |
36,849,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R7509:Polq
|
UTSW |
16 |
36,880,706 (GRCm39) |
missense |
probably benign |
0.00 |
R7509:Polq
|
UTSW |
16 |
36,880,705 (GRCm39) |
missense |
probably benign |
|
R7575:Polq
|
UTSW |
16 |
36,911,496 (GRCm39) |
missense |
probably benign |
0.00 |
R7785:Polq
|
UTSW |
16 |
36,848,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R7787:Polq
|
UTSW |
16 |
36,837,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R7891:Polq
|
UTSW |
16 |
36,848,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R7898:Polq
|
UTSW |
16 |
36,865,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R7917:Polq
|
UTSW |
16 |
36,885,650 (GRCm39) |
missense |
probably benign |
0.08 |
R7940:Polq
|
UTSW |
16 |
36,881,004 (GRCm39) |
missense |
probably benign |
0.27 |
R8028:Polq
|
UTSW |
16 |
36,881,678 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8114:Polq
|
UTSW |
16 |
36,862,577 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8144:Polq
|
UTSW |
16 |
36,849,846 (GRCm39) |
missense |
probably benign |
0.01 |
R8288:Polq
|
UTSW |
16 |
36,848,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R8301:Polq
|
UTSW |
16 |
36,882,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R8341:Polq
|
UTSW |
16 |
36,892,133 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8348:Polq
|
UTSW |
16 |
36,837,559 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8448:Polq
|
UTSW |
16 |
36,837,559 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8815:Polq
|
UTSW |
16 |
36,853,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R8843:Polq
|
UTSW |
16 |
36,832,280 (GRCm39) |
missense |
unknown |
|
R8878:Polq
|
UTSW |
16 |
36,860,869 (GRCm39) |
missense |
probably benign |
0.02 |
R9016:Polq
|
UTSW |
16 |
36,843,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R9189:Polq
|
UTSW |
16 |
36,865,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Polq
|
UTSW |
16 |
36,869,011 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9352:Polq
|
UTSW |
16 |
36,862,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R9398:Polq
|
UTSW |
16 |
36,881,394 (GRCm39) |
missense |
probably benign |
0.02 |
R9403:Polq
|
UTSW |
16 |
36,882,215 (GRCm39) |
missense |
probably benign |
0.00 |
R9489:Polq
|
UTSW |
16 |
36,843,173 (GRCm39) |
missense |
probably benign |
0.00 |
R9605:Polq
|
UTSW |
16 |
36,843,173 (GRCm39) |
missense |
probably benign |
0.00 |
R9664:Polq
|
UTSW |
16 |
36,848,176 (GRCm39) |
missense |
probably damaging |
0.98 |
R9801:Polq
|
UTSW |
16 |
36,913,190 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:Polq
|
UTSW |
16 |
36,837,599 (GRCm39) |
nonsense |
probably null |
|
Z1176:Polq
|
UTSW |
16 |
36,862,619 (GRCm39) |
critical splice donor site |
probably null |
|
|