Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy3 |
T |
A |
12: 4,260,870 (GRCm39) |
N995K |
probably damaging |
Het |
Aldh4a1 |
T |
C |
4: 139,361,233 (GRCm39) |
M60T |
probably benign |
Het |
Alpk2 |
A |
T |
18: 65,505,809 (GRCm39) |
H70Q |
probably damaging |
Het |
Babam2 |
T |
A |
5: 31,859,207 (GRCm39) |
I5N |
possibly damaging |
Het |
Blm |
T |
C |
7: 80,162,977 (GRCm39) |
T125A |
probably benign |
Het |
Bloc1s1 |
T |
C |
10: 128,759,826 (GRCm39) |
|
probably benign |
Het |
Calcr |
G |
T |
6: 3,714,651 (GRCm39) |
Q160K |
probably benign |
Het |
Ccdc43 |
C |
T |
11: 102,581,058 (GRCm39) |
A131T |
probably damaging |
Het |
Cdh15 |
A |
T |
8: 123,591,839 (GRCm39) |
N575Y |
probably damaging |
Het |
Chd8 |
T |
C |
14: 52,441,611 (GRCm39) |
D827G |
probably damaging |
Het |
Col3a1 |
A |
G |
1: 45,387,059 (GRCm39) |
|
probably null |
Het |
Creb5 |
A |
T |
6: 53,658,002 (GRCm39) |
M255L |
possibly damaging |
Het |
Cst8 |
A |
G |
2: 148,646,503 (GRCm39) |
I78V |
probably benign |
Het |
Cyld |
A |
G |
8: 89,459,664 (GRCm39) |
E440G |
possibly damaging |
Het |
Cyp2b9 |
A |
C |
7: 25,887,167 (GRCm39) |
D192A |
probably damaging |
Het |
Dclre1b |
C |
T |
3: 103,711,290 (GRCm39) |
R207H |
probably damaging |
Het |
Dnah6 |
A |
T |
6: 73,100,838 (GRCm39) |
F1936L |
probably damaging |
Het |
Dpp9 |
A |
C |
17: 56,496,424 (GRCm39) |
Y761* |
probably null |
Het |
Drc1 |
A |
T |
5: 30,513,745 (GRCm39) |
M434L |
probably benign |
Het |
Dtx3l |
A |
T |
16: 35,753,397 (GRCm39) |
I403N |
probably damaging |
Het |
Ecpas |
T |
A |
4: 58,809,401 (GRCm39) |
K1658* |
probably null |
Het |
Efcab9 |
A |
G |
11: 32,477,484 (GRCm39) |
Y13H |
probably damaging |
Het |
Efhb |
T |
A |
17: 53,708,654 (GRCm39) |
N672I |
possibly damaging |
Het |
Eif5b |
T |
C |
1: 38,084,835 (GRCm39) |
V894A |
possibly damaging |
Het |
Elovl3 |
T |
C |
19: 46,123,135 (GRCm39) |
F237S |
probably benign |
Het |
Emc1 |
T |
A |
4: 139,093,802 (GRCm39) |
D637E |
probably damaging |
Het |
Erbb2 |
C |
A |
11: 98,324,238 (GRCm39) |
P742Q |
probably damaging |
Het |
Fam234b |
C |
A |
6: 135,210,355 (GRCm39) |
L584M |
probably damaging |
Het |
Fancd2 |
A |
T |
6: 113,545,673 (GRCm39) |
D14V |
possibly damaging |
Het |
Fat2 |
T |
C |
11: 55,153,646 (GRCm39) |
H3522R |
probably benign |
Het |
Fgfr2 |
T |
C |
7: 129,842,945 (GRCm39) |
N147D |
possibly damaging |
Het |
Gm26657 |
A |
G |
4: 56,741,180 (GRCm39) |
|
probably benign |
Het |
Hcrtr1 |
C |
T |
4: 130,029,518 (GRCm39) |
V188M |
probably benign |
Het |
Herc1 |
T |
C |
9: 66,375,169 (GRCm39) |
V3331A |
probably damaging |
Het |
Hmcn2 |
T |
C |
2: 31,320,453 (GRCm39) |
V3978A |
possibly damaging |
Het |
Invs |
G |
A |
4: 48,385,262 (GRCm39) |
R202K |
probably benign |
Het |
Lgr5 |
C |
T |
10: 115,314,469 (GRCm39) |
S156N |
probably benign |
Het |
Mras |
T |
G |
9: 99,276,669 (GRCm39) |
D67A |
probably damaging |
Het |
Mrpl39 |
A |
G |
16: 84,520,790 (GRCm39) |
L283P |
probably damaging |
Het |
Ncoa6 |
A |
T |
2: 155,275,915 (GRCm39) |
I110N |
probably benign |
Het |
Neb |
T |
C |
2: 52,102,596 (GRCm39) |
D544G |
possibly damaging |
Het |
Nlrc3 |
A |
G |
16: 3,782,617 (GRCm39) |
I264T |
possibly damaging |
Het |
Or10a2 |
T |
A |
7: 106,673,080 (GRCm39) |
M15K |
probably benign |
Het |
Or1j13 |
A |
G |
2: 36,369,309 (GRCm39) |
Y278H |
probably damaging |
Het |
Or5k16 |
T |
C |
16: 58,736,248 (GRCm39) |
Y252C |
possibly damaging |
Het |
Or7g18 |
A |
G |
9: 18,787,442 (GRCm39) |
K273R |
probably benign |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Phf11d |
T |
C |
14: 59,590,120 (GRCm39) |
D234G |
probably null |
Het |
Rasa1 |
A |
T |
13: 85,437,022 (GRCm39) |
|
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Sec23a |
A |
G |
12: 59,053,791 (GRCm39) |
V69A |
probably benign |
Het |
Sipa1 |
A |
G |
19: 5,709,640 (GRCm39) |
I260T |
probably damaging |
Het |
Smarcc1 |
T |
A |
9: 110,020,017 (GRCm39) |
L628H |
probably damaging |
Het |
Snx31 |
A |
G |
15: 36,525,730 (GRCm39) |
V323A |
probably damaging |
Het |
Sun2 |
A |
G |
15: 79,611,723 (GRCm39) |
S565P |
probably damaging |
Het |
Tmem74 |
C |
T |
15: 43,730,564 (GRCm39) |
D160N |
possibly damaging |
Het |
Tnik |
T |
C |
3: 28,648,241 (GRCm39) |
M431T |
probably benign |
Het |
Trp53inp1 |
A |
G |
4: 11,165,305 (GRCm39) |
T110A |
probably benign |
Het |
Ttll9 |
G |
T |
2: 152,826,144 (GRCm39) |
C118F |
probably benign |
Het |
Vps4b |
A |
G |
1: 106,719,422 (GRCm39) |
L42P |
probably benign |
Het |
Xirp2 |
A |
T |
2: 67,342,250 (GRCm39) |
N1497I |
probably damaging |
Het |
Xpo4 |
A |
G |
14: 57,875,764 (GRCm39) |
V123A |
probably damaging |
Het |
Zfhx4 |
A |
T |
3: 5,477,485 (GRCm39) |
T3367S |
probably damaging |
Het |
Zfp236 |
T |
C |
18: 82,615,813 (GRCm39) |
E1782G |
possibly damaging |
Het |
Zfp35 |
T |
A |
18: 24,135,973 (GRCm39) |
C106S |
possibly damaging |
Het |
Zfpm1 |
A |
G |
8: 123,062,812 (GRCm39) |
T624A |
probably benign |
Het |
Zmiz2 |
C |
T |
11: 6,347,519 (GRCm39) |
Q276* |
probably null |
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 |
R1932:Polq
|
UTSW |
16 |
36,882,666 (GRCm39) |
missense |
possibly damaging |
0.92 |
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 |
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 |
|
|