Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1600012H06Rik |
A |
T |
17: 15,164,001 (GRCm39) |
I43L |
possibly damaging |
Het |
4930449A18Rik |
T |
A |
3: 59,749,153 (GRCm39) |
|
noncoding transcript |
Het |
Abcc8 |
T |
C |
7: 45,800,252 (GRCm39) |
K510R |
probably damaging |
Het |
Adamtsl3 |
C |
T |
7: 82,178,069 (GRCm39) |
R511C |
probably damaging |
Het |
Arhgap11a |
T |
C |
2: 113,670,107 (GRCm39) |
S339G |
probably damaging |
Het |
C2cd3 |
A |
G |
7: 100,065,397 (GRCm39) |
T728A |
probably benign |
Het |
Cand1 |
C |
A |
10: 119,049,451 (GRCm39) |
|
probably null |
Het |
Catspere1 |
A |
T |
1: 177,699,624 (GRCm39) |
|
noncoding transcript |
Het |
Ccdc121rt2 |
A |
T |
5: 112,598,106 (GRCm39) |
K218* |
probably null |
Het |
Cd209c |
G |
T |
8: 3,995,905 (GRCm39) |
R2S |
probably benign |
Het |
Cdc16 |
A |
G |
8: 13,831,644 (GRCm39) |
|
probably benign |
Het |
Ces1g |
C |
T |
8: 94,060,323 (GRCm39) |
E99K |
probably benign |
Het |
Chrna7 |
A |
C |
7: 62,862,196 (GRCm39) |
L10R |
probably benign |
Het |
Clnk |
C |
T |
5: 38,870,412 (GRCm39) |
|
probably null |
Het |
Cntrob |
C |
G |
11: 69,206,220 (GRCm39) |
L315F |
possibly damaging |
Het |
Ctdp1 |
A |
G |
18: 80,451,941 (GRCm39) |
S145P |
unknown |
Het |
Dennd2a |
T |
C |
6: 39,474,044 (GRCm39) |
D430G |
probably damaging |
Het |
Dnajc16 |
A |
G |
4: 141,501,936 (GRCm39) |
F298S |
probably damaging |
Het |
Dock5 |
T |
C |
14: 68,055,012 (GRCm39) |
D618G |
probably damaging |
Het |
Drc3 |
G |
A |
11: 60,261,361 (GRCm39) |
A171T |
probably benign |
Het |
Ecel1 |
A |
T |
1: 87,081,023 (GRCm39) |
N322K |
probably damaging |
Het |
Eftud2 |
A |
G |
11: 102,745,640 (GRCm39) |
F362L |
probably damaging |
Het |
Egfr |
C |
T |
11: 16,861,607 (GRCm39) |
H1129Y |
probably benign |
Het |
Eif2b1 |
A |
G |
5: 124,714,971 (GRCm39) |
S102P |
probably damaging |
Het |
Erich3 |
T |
A |
3: 154,410,480 (GRCm39) |
F112I |
possibly damaging |
Het |
Fam107b |
T |
C |
2: 3,779,580 (GRCm39) |
L261S |
probably damaging |
Het |
Fat3 |
A |
C |
9: 15,908,883 (GRCm39) |
V2373G |
probably damaging |
Het |
Fcgbpl1 |
T |
A |
7: 27,850,147 (GRCm39) |
C1198S |
probably damaging |
Het |
Gadd45a |
A |
T |
6: 67,013,873 (GRCm39) |
L58Q |
probably damaging |
Het |
Gask1b |
G |
A |
3: 79,843,912 (GRCm39) |
R377H |
probably damaging |
Het |
Gipr |
C |
T |
7: 18,896,601 (GRCm39) |
R165H |
probably damaging |
Het |
Gje1 |
C |
T |
10: 14,593,082 (GRCm39) |
G45R |
probably null |
Het |
Gldc |
T |
A |
19: 30,111,132 (GRCm39) |
N548I |
possibly damaging |
Het |
Gm13035 |
A |
G |
4: 146,009,993 (GRCm39) |
|
noncoding transcript |
Het |
Gm27013 |
T |
A |
6: 130,497,700 (GRCm39) |
|
noncoding transcript |
Het |
Gm5436 |
A |
T |
12: 84,305,584 (GRCm39) |
|
noncoding transcript |
Het |
Grik3 |
C |
A |
4: 125,584,969 (GRCm39) |
N612K |
probably damaging |
Het |
H2bc13 |
C |
T |
13: 21,900,234 (GRCm39) |
|
probably benign |
Het |
Hfm1 |
C |
A |
5: 107,040,617 (GRCm39) |
W716L |
probably damaging |
Het |
Il5ra |
T |
C |
6: 106,715,336 (GRCm39) |
Y166C |
probably damaging |
Het |
Iqcb1 |
A |
G |
16: 36,655,952 (GRCm39) |
E113G |
probably benign |
Het |
Kcnk10 |
A |
T |
12: 98,401,175 (GRCm39) |
M486K |
probably benign |
Het |
Kcnv2 |
A |
G |
19: 27,301,190 (GRCm39) |
D347G |
probably damaging |
Het |
Kif21b |
C |
A |
1: 136,072,958 (GRCm39) |
H119N |
probably damaging |
Het |
Lamb1 |
C |
T |
12: 31,337,432 (GRCm39) |
H388Y |
probably damaging |
Het |
Leng9 |
T |
C |
7: 4,152,385 (GRCm39) |
D97G |
probably damaging |
Het |
Lmbr1 |
G |
A |
5: 29,492,424 (GRCm39) |
T55I |
probably damaging |
Het |
Lrp1 |
G |
T |
10: 127,419,805 (GRCm39) |
R935S |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,299,755 (GRCm39) |
V3099E |
probably benign |
Het |
Lrrcc1 |
C |
A |
3: 14,627,571 (GRCm39) |
D503E |
probably benign |
Het |
Map1a |
T |
A |
2: 121,132,567 (GRCm39) |
S890T |
probably damaging |
Het |
Msh2 |
C |
A |
17: 88,030,841 (GRCm39) |
A906E |
probably benign |
Het |
Mybph |
A |
T |
1: 134,126,233 (GRCm39) |
E349V |
probably damaging |
Het |
Myh7b |
C |
A |
2: 155,475,909 (GRCm39) |
L1935M |
probably benign |
Het |
Myh9 |
T |
C |
15: 77,653,453 (GRCm39) |
E1348G |
probably damaging |
Het |
Myzap |
A |
G |
9: 71,456,037 (GRCm39) |
S328P |
probably damaging |
Het |
Nbeal1 |
T |
C |
1: 60,292,534 (GRCm39) |
L1062P |
probably damaging |
Het |
Nepro |
G |
A |
16: 44,555,160 (GRCm39) |
S412N |
probably null |
Het |
Nr1h3 |
A |
G |
2: 91,020,563 (GRCm39) |
F257L |
probably benign |
Het |
Nudt5 |
T |
C |
2: 5,869,239 (GRCm39) |
V155A |
probably benign |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Or13a25 |
A |
T |
7: 140,247,502 (GRCm39) |
I94F |
probably damaging |
Het |
Or52d3 |
A |
T |
7: 104,229,422 (GRCm39) |
I190L |
probably benign |
Het |
Or6ae1 |
A |
G |
7: 139,742,602 (GRCm39) |
L87P |
possibly damaging |
Het |
Pde1a |
T |
A |
2: 79,959,181 (GRCm39) |
|
probably benign |
Het |
Pde4dip |
T |
A |
3: 97,700,844 (GRCm39) |
H220L |
probably damaging |
Het |
Pde9a |
T |
A |
17: 31,662,135 (GRCm39) |
|
probably null |
Het |
Pnkp |
C |
A |
7: 44,511,070 (GRCm39) |
|
probably null |
Het |
Pnpla7 |
A |
G |
2: 24,870,064 (GRCm39) |
T15A |
probably benign |
Het |
Ppfia2 |
C |
T |
10: 106,690,818 (GRCm39) |
T553I |
probably benign |
Het |
Ptk6 |
T |
G |
2: 180,838,784 (GRCm39) |
N323T |
possibly damaging |
Het |
Rhox3c |
G |
A |
X: 36,652,077 (GRCm39) |
A60T |
probably damaging |
Het |
Rnf4 |
T |
A |
5: 34,506,053 (GRCm39) |
V61E |
probably damaging |
Het |
Rnf5 |
A |
G |
17: 34,820,977 (GRCm39) |
|
probably benign |
Het |
Sardh |
A |
G |
2: 27,081,967 (GRCm39) |
V853A |
probably benign |
Het |
Scfd1 |
T |
C |
12: 51,436,109 (GRCm39) |
V86A |
probably damaging |
Het |
Scube3 |
G |
A |
17: 28,383,097 (GRCm39) |
C425Y |
probably damaging |
Het |
Sema5a |
C |
T |
15: 32,609,563 (GRCm39) |
H490Y |
probably benign |
Het |
Sfta2 |
T |
C |
17: 35,960,773 (GRCm39) |
|
probably benign |
Het |
Sh3d19 |
T |
C |
3: 86,031,049 (GRCm39) |
Y738H |
probably damaging |
Het |
Shc2 |
T |
C |
10: 79,458,295 (GRCm39) |
R463G |
probably damaging |
Het |
Socs7 |
T |
A |
11: 97,267,829 (GRCm39) |
I320N |
possibly damaging |
Het |
Speer2 |
A |
T |
16: 69,654,988 (GRCm39) |
M159K |
probably benign |
Het |
Sppl2c |
A |
C |
11: 104,078,478 (GRCm39) |
H426P |
probably benign |
Het |
Stag3 |
T |
G |
5: 138,307,627 (GRCm39) |
|
probably null |
Het |
Stxbp5 |
C |
A |
10: 9,638,635 (GRCm39) |
V1055L |
probably benign |
Het |
Synpo |
A |
T |
18: 60,736,684 (GRCm39) |
S421T |
probably damaging |
Het |
Taf6l |
A |
G |
19: 8,759,770 (GRCm39) |
V135A |
possibly damaging |
Het |
Tas2r116 |
G |
A |
6: 132,832,660 (GRCm39) |
S87N |
probably benign |
Het |
Tomm6 |
T |
C |
17: 47,998,994 (GRCm39) |
|
probably benign |
Het |
Trabd |
T |
C |
15: 88,966,915 (GRCm39) |
M113T |
probably benign |
Het |
Trim58 |
G |
A |
11: 58,542,150 (GRCm39) |
G370E |
probably damaging |
Het |
Ttc41 |
C |
T |
10: 86,566,989 (GRCm39) |
R552C |
probably benign |
Het |
Vit |
T |
C |
17: 78,909,308 (GRCm39) |
S252P |
probably benign |
Het |
Vma21-ps |
T |
A |
4: 52,496,943 (GRCm39) |
D101V |
probably damaging |
Het |
Vmn1r173 |
A |
T |
7: 23,402,361 (GRCm39) |
I199F |
probably damaging |
Het |
Vmn2r114 |
T |
A |
17: 23,529,336 (GRCm39) |
R255S |
probably benign |
Het |
Vmn2r17 |
A |
G |
5: 109,582,246 (GRCm39) |
N545S |
probably damaging |
Het |
Zfp865 |
A |
G |
7: 5,034,640 (GRCm39) |
Y875C |
probably 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 |
|
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 |
|
|