Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
G |
A |
8: 120,872,380 (GRCm39) |
V103I |
possibly damaging |
Het |
Aatk |
T |
C |
11: 119,902,209 (GRCm39) |
E729G |
possibly damaging |
Het |
Acaa2 |
A |
G |
18: 74,932,230 (GRCm39) |
T290A |
probably benign |
Het |
Acaca |
C |
T |
11: 84,183,842 (GRCm39) |
T1240I |
probably benign |
Het |
Adgre1 |
A |
G |
17: 57,718,083 (GRCm39) |
N365S |
probably benign |
Het |
Adipor1 |
A |
G |
1: 134,352,553 (GRCm39) |
D108G |
probably damaging |
Het |
Aebp2 |
A |
G |
6: 140,593,736 (GRCm39) |
Q462R |
probably damaging |
Het |
Afg2a |
C |
T |
3: 37,505,930 (GRCm39) |
P670S |
probably damaging |
Het |
Arhgef4 |
A |
G |
1: 34,761,745 (GRCm39) |
T334A |
unknown |
Het |
Art5 |
T |
C |
7: 101,746,412 (GRCm39) |
E280G |
probably benign |
Het |
Bloc1s3 |
A |
G |
7: 19,241,457 (GRCm39) |
S24P |
possibly damaging |
Het |
C2 |
T |
A |
17: 35,081,958 (GRCm39) |
N720I |
possibly damaging |
Het |
Caprin2 |
T |
C |
6: 148,744,332 (GRCm39) |
D1031G |
probably damaging |
Het |
Catsper1 |
A |
G |
19: 5,387,785 (GRCm39) |
T355A |
probably benign |
Het |
Cd19 |
T |
A |
7: 126,010,057 (GRCm39) |
E398D |
possibly damaging |
Het |
Cdca8 |
T |
C |
4: 124,830,384 (GRCm39) |
E31G |
probably damaging |
Het |
Ceacam5 |
G |
A |
7: 17,493,520 (GRCm39) |
V848M |
probably damaging |
Het |
Chd8 |
A |
T |
14: 52,457,055 (GRCm39) |
L971Q |
probably damaging |
Het |
Ciao1 |
G |
A |
2: 127,087,684 (GRCm39) |
T217I |
probably damaging |
Het |
Cldn1 |
A |
T |
16: 26,181,924 (GRCm39) |
I95N |
probably damaging |
Het |
Clip2 |
C |
T |
5: 134,533,616 (GRCm39) |
R487Q |
probably benign |
Het |
Cluh |
C |
T |
11: 74,558,772 (GRCm39) |
R1253C |
possibly damaging |
Het |
Cngb3 |
A |
T |
4: 19,505,187 (GRCm39) |
Q640L |
probably benign |
Het |
Cspg4b |
T |
C |
13: 113,456,503 (GRCm39) |
S850P |
|
Het |
Cyp2c40 |
A |
T |
19: 39,766,443 (GRCm39) |
V384D |
probably damaging |
Het |
Cyp2d26 |
T |
A |
15: 82,674,672 (GRCm39) |
M437L |
probably benign |
Het |
D430041D05Rik |
A |
G |
2: 104,087,189 (GRCm39) |
S596P |
probably benign |
Het |
Dagla |
A |
T |
19: 10,233,053 (GRCm39) |
V448D |
probably damaging |
Het |
Ddx59 |
A |
T |
1: 136,344,594 (GRCm39) |
E88D |
probably benign |
Het |
Dock1 |
T |
A |
7: 134,384,141 (GRCm39) |
F671I |
possibly damaging |
Het |
Dtna |
T |
A |
18: 23,764,454 (GRCm39) |
V541D |
probably damaging |
Het |
Eef2k |
T |
C |
7: 120,491,170 (GRCm39) |
F552S |
probably damaging |
Het |
Erbb2 |
T |
C |
11: 98,311,746 (GRCm39) |
V94A |
possibly damaging |
Het |
Etl4 |
A |
T |
2: 20,771,345 (GRCm39) |
I607F |
possibly damaging |
Het |
Ets2 |
G |
T |
16: 95,516,121 (GRCm39) |
E234* |
probably null |
Het |
Fbp1 |
A |
C |
13: 63,019,023 (GRCm39) |
V175G |
probably damaging |
Het |
Fmn2 |
C |
T |
1: 174,436,194 (GRCm39) |
Q722* |
probably null |
Het |
Fnip1 |
G |
T |
11: 54,381,713 (GRCm39) |
R288L |
probably benign |
Het |
Ghr |
G |
A |
15: 3,362,993 (GRCm39) |
P160S |
probably damaging |
Het |
Glipr1 |
A |
G |
10: 111,832,801 (GRCm39) |
S46P |
probably damaging |
Het |
Kif19b |
A |
T |
5: 140,455,461 (GRCm39) |
T356S |
probably benign |
Het |
Kif9 |
G |
A |
9: 110,346,710 (GRCm39) |
R616H |
probably benign |
Het |
Krt87 |
G |
T |
15: 101,336,484 (GRCm39) |
C56* |
probably null |
Het |
Ldlr |
A |
G |
9: 21,646,626 (GRCm39) |
D264G |
probably damaging |
Het |
Lrrk2 |
A |
T |
15: 91,621,420 (GRCm39) |
D998V |
probably benign |
Het |
Mcm5 |
C |
T |
8: 75,844,168 (GRCm39) |
S313F |
probably benign |
Het |
Mrc1 |
A |
G |
2: 14,324,110 (GRCm39) |
N1149S |
probably benign |
Het |
Myo1c |
T |
A |
11: 75,559,899 (GRCm39) |
V661E |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,963,879 (GRCm39) |
S643P |
probably benign |
Het |
Nbl1 |
T |
A |
4: 138,812,608 (GRCm39) |
T75S |
probably benign |
Het |
Ndn |
C |
T |
7: 61,998,337 (GRCm39) |
P61L |
possibly damaging |
Het |
Nqo2 |
T |
A |
13: 34,156,361 (GRCm39) |
V25E |
possibly damaging |
Het |
Oma1 |
G |
T |
4: 103,210,726 (GRCm39) |
V411L |
possibly damaging |
Het |
Or12e13 |
T |
G |
2: 87,663,478 (GRCm39) |
F32V |
probably benign |
Het |
Or5v1 |
T |
A |
17: 37,810,331 (GRCm39) |
I263N |
probably damaging |
Het |
Or8b12i |
A |
G |
9: 20,082,093 (GRCm39) |
V258A |
probably damaging |
Het |
Osgin2 |
G |
T |
4: 15,998,427 (GRCm39) |
H398Q |
probably damaging |
Het |
Pepd |
A |
C |
7: 34,743,218 (GRCm39) |
D419A |
probably benign |
Het |
Pikfyve |
A |
T |
1: 65,303,561 (GRCm39) |
S1694C |
probably benign |
Het |
Pirb |
G |
A |
7: 3,720,617 (GRCm39) |
R294C |
possibly damaging |
Het |
Plec |
A |
T |
15: 76,065,213 (GRCm39) |
L1619Q |
unknown |
Het |
Pphln1-ps1 |
A |
G |
16: 13,495,087 (GRCm39) |
D62G |
probably benign |
Het |
Prkag3 |
T |
G |
1: 74,786,378 (GRCm39) |
Q189P |
probably damaging |
Het |
Prkcg |
A |
T |
7: 3,359,360 (GRCm39) |
M136L |
probably benign |
Het |
Ptprn2 |
T |
C |
12: 117,125,278 (GRCm39) |
L604P |
probably benign |
Het |
Rab6b |
A |
T |
9: 103,017,601 (GRCm39) |
T31S |
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,359,879 (GRCm39) |
N4424S |
|
Het |
Ryr3 |
A |
T |
2: 112,491,966 (GRCm39) |
L3795Q |
probably damaging |
Het |
Scg2 |
A |
G |
1: 79,412,936 (GRCm39) |
Y556H |
probably damaging |
Het |
Serpina3j |
A |
G |
12: 104,286,093 (GRCm39) |
N416S |
probably damaging |
Het |
Sik3 |
T |
A |
9: 46,120,117 (GRCm39) |
H735Q |
probably benign |
Het |
Slain1 |
A |
C |
14: 103,902,112 (GRCm39) |
T60P |
|
Het |
Slc14a1 |
C |
A |
18: 78,152,807 (GRCm39) |
A367S |
probably damaging |
Het |
Slc46a2 |
A |
T |
4: 59,914,056 (GRCm39) |
V289E |
probably damaging |
Het |
Sorcs3 |
A |
T |
19: 48,711,364 (GRCm39) |
Y643F |
probably damaging |
Het |
Sox30 |
A |
G |
11: 45,875,640 (GRCm39) |
N464S |
possibly damaging |
Het |
Spta1 |
A |
G |
1: 174,035,880 (GRCm39) |
Y1062C |
probably damaging |
Het |
Srrm3 |
A |
G |
5: 135,881,105 (GRCm39) |
D135G |
probably damaging |
Het |
Stat5b |
T |
A |
11: 100,699,276 (GRCm39) |
H25L |
possibly damaging |
Het |
Synj2 |
A |
G |
17: 6,063,794 (GRCm39) |
I513V |
probably benign |
Het |
Syt11 |
T |
A |
3: 88,669,325 (GRCm39) |
Q189L |
probably benign |
Het |
Tbc1d1 |
G |
A |
5: 64,443,350 (GRCm39) |
R523Q |
probably damaging |
Het |
Traf3ip2 |
T |
A |
10: 39,521,772 (GRCm39) |
D443E |
probably benign |
Het |
Traf6 |
G |
T |
2: 101,524,625 (GRCm39) |
C235F |
probably damaging |
Het |
Treh |
A |
G |
9: 44,592,416 (GRCm39) |
D47G |
probably damaging |
Het |
Trpc4 |
C |
A |
3: 54,225,550 (GRCm39) |
H966Q |
probably benign |
Het |
Ttbk1 |
A |
T |
17: 46,784,516 (GRCm39) |
D316E |
possibly damaging |
Het |
Txndc16 |
A |
T |
14: 45,442,799 (GRCm39) |
F132Y |
probably damaging |
Het |
Uggt1 |
A |
T |
1: 36,273,886 (GRCm39) |
|
probably null |
Het |
Usp25 |
A |
T |
16: 76,874,046 (GRCm39) |
I541F |
probably damaging |
Het |
Xirp1 |
A |
T |
9: 119,847,274 (GRCm39) |
D536E |
possibly damaging |
Het |
Zfp51 |
A |
G |
17: 21,684,291 (GRCm39) |
E302G |
probably damaging |
Het |
Zfp648 |
A |
T |
1: 154,080,110 (GRCm39) |
T90S |
probably benign |
Het |
Zfp84 |
A |
G |
7: 29,476,264 (GRCm39) |
T319A |
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 |
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 |
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 |
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 |
|
|