Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox1 |
T |
A |
11: 116,065,231 (GRCm39) |
D608V |
probably damaging |
Het |
Actg1 |
A |
T |
11: 120,239,013 (GRCm39) |
C26S |
unknown |
Het |
Ahnak |
T |
A |
19: 8,988,247 (GRCm39) |
V3177E |
possibly damaging |
Het |
Akap11 |
G |
A |
14: 78,750,938 (GRCm39) |
T483I |
|
Het |
Akr1cl |
A |
G |
1: 65,063,830 (GRCm39) |
S120P |
probably benign |
Het |
Ankle2 |
G |
A |
5: 110,400,610 (GRCm39) |
V649M |
possibly damaging |
Het |
Ankrd55 |
A |
T |
13: 112,504,570 (GRCm39) |
I439F |
probably damaging |
Het |
Asb8 |
A |
G |
15: 98,040,635 (GRCm39) |
M9T |
possibly damaging |
Het |
Ascc1 |
A |
T |
10: 59,843,645 (GRCm39) |
Y69F |
probably benign |
Het |
Atp9a |
A |
T |
2: 168,518,060 (GRCm39) |
|
probably null |
Het |
Cd8b1 |
T |
C |
6: 71,306,752 (GRCm39) |
F160L |
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,143,306 (GRCm39) |
A3005V |
possibly damaging |
Het |
Cep250 |
A |
G |
2: 155,818,350 (GRCm39) |
T842A |
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,630,847 (GRCm39) |
K552* |
probably null |
Het |
Cntnap4 |
C |
T |
8: 113,602,600 (GRCm39) |
T1227M |
possibly damaging |
Het |
Cobll1 |
C |
A |
2: 64,981,333 (GRCm39) |
V86F |
probably damaging |
Het |
Dchs2 |
A |
G |
3: 83,255,561 (GRCm39) |
N2419S |
probably damaging |
Het |
Dhx30 |
A |
T |
9: 109,914,494 (GRCm39) |
L1001* |
probably null |
Het |
Diaph1 |
C |
T |
18: 38,024,162 (GRCm39) |
V559M |
unknown |
Het |
Dis3l |
A |
T |
9: 64,217,731 (GRCm39) |
H783Q |
probably benign |
Het |
Dock7 |
T |
G |
4: 98,877,350 (GRCm39) |
T1063P |
unknown |
Het |
Dsc1 |
T |
C |
18: 20,232,214 (GRCm39) |
T265A |
possibly damaging |
Het |
Eif2ak4 |
A |
T |
2: 118,258,393 (GRCm39) |
Q581L |
probably damaging |
Het |
Eprs1 |
A |
T |
1: 185,106,334 (GRCm39) |
D183V |
possibly damaging |
Het |
Fads2 |
G |
C |
19: 10,069,183 (GRCm39) |
D80E |
probably benign |
Het |
Fam167b |
G |
A |
4: 129,470,875 (GRCm39) |
R158C |
probably damaging |
Het |
Flnb |
T |
A |
14: 7,892,976 (GRCm38) |
I682K |
possibly damaging |
Het |
Garin4 |
G |
A |
1: 190,894,900 (GRCm39) |
T581I |
possibly damaging |
Het |
Gpatch2l |
C |
T |
12: 86,291,152 (GRCm39) |
P112S |
probably benign |
Het |
Gpn1 |
T |
A |
5: 31,654,710 (GRCm39) |
H87Q |
unknown |
Het |
Greb1l |
T |
C |
18: 10,499,983 (GRCm39) |
V350A |
probably benign |
Het |
Grm5 |
A |
T |
7: 87,724,024 (GRCm39) |
K771N |
probably damaging |
Het |
Gucy2c |
C |
T |
6: 136,728,045 (GRCm39) |
S319N |
probably benign |
Het |
H2bc8 |
A |
G |
13: 23,755,761 (GRCm39) |
D52G |
probably damaging |
Het |
Hcfc2 |
G |
T |
10: 82,535,041 (GRCm39) |
A22S |
probably benign |
Het |
Hnf4a |
A |
G |
2: 163,393,497 (GRCm39) |
D39G |
probably benign |
Het |
Il6st |
C |
T |
13: 112,635,340 (GRCm39) |
T584M |
probably damaging |
Het |
Irf3 |
T |
A |
7: 44,650,246 (GRCm39) |
V254E |
possibly damaging |
Het |
Iws1 |
G |
A |
18: 32,213,213 (GRCm39) |
E214K |
possibly damaging |
Het |
Kank4 |
T |
A |
4: 98,668,289 (GRCm39) |
K53* |
probably null |
Het |
Kcnj11 |
A |
T |
7: 45,748,176 (GRCm39) |
F382L |
possibly damaging |
Het |
Kcnq3 |
T |
C |
15: 65,867,510 (GRCm39) |
Y711C |
probably damaging |
Het |
Kctd3 |
A |
G |
1: 188,704,636 (GRCm39) |
S712P |
possibly damaging |
Het |
Krt20 |
A |
G |
11: 99,323,087 (GRCm39) |
I245T |
possibly damaging |
Het |
Larp1b |
T |
C |
3: 40,925,039 (GRCm39) |
I219T |
probably damaging |
Het |
Lman2l |
A |
G |
1: 36,478,771 (GRCm39) |
F114L |
probably damaging |
Het |
Loxl2 |
T |
A |
14: 69,929,859 (GRCm39) |
Y746N |
possibly damaging |
Het |
Lrrc43 |
T |
C |
5: 123,646,109 (GRCm39) |
S628P |
probably benign |
Het |
Mroh8 |
A |
C |
2: 157,111,545 (GRCm39) |
D136E |
probably damaging |
Het |
Nek8 |
T |
A |
11: 78,063,342 (GRCm39) |
M141L |
probably benign |
Het |
Nr2e1 |
C |
A |
10: 42,454,268 (GRCm39) |
R22L |
probably damaging |
Het |
Nr6a1 |
C |
T |
2: 38,816,129 (GRCm39) |
|
probably null |
Het |
Onecut2 |
A |
G |
18: 64,473,890 (GRCm39) |
Y147C |
probably damaging |
Het |
Or1ad1 |
T |
A |
11: 50,876,166 (GRCm39) |
C213S |
probably damaging |
Het |
Or1j1 |
T |
A |
2: 36,702,214 (GRCm39) |
M297L |
possibly damaging |
Het |
Or5d37 |
A |
G |
2: 87,924,194 (GRCm39) |
F29L |
probably damaging |
Het |
Or5d39 |
T |
C |
2: 87,979,908 (GRCm39) |
M152V |
probably benign |
Het |
Pcdhac2 |
T |
C |
18: 37,277,316 (GRCm39) |
F99L |
probably benign |
Het |
Pcdhga2 |
T |
G |
18: 37,802,795 (GRCm39) |
V213G |
possibly damaging |
Het |
Pgap1 |
A |
T |
1: 54,519,908 (GRCm39) |
V909E |
probably benign |
Het |
Pik3r4 |
A |
T |
9: 105,547,038 (GRCm39) |
T939S |
probably benign |
Het |
Pip4k2c |
T |
C |
10: 127,035,246 (GRCm39) |
D374G |
possibly damaging |
Het |
Plxdc1 |
A |
T |
11: 97,844,788 (GRCm39) |
D252E |
probably benign |
Het |
Pm20d1 |
A |
C |
1: 131,730,115 (GRCm39) |
D218A |
probably damaging |
Het |
Pram1 |
A |
T |
17: 33,860,131 (GRCm39) |
I233F |
probably benign |
Het |
Prr27 |
C |
A |
5: 87,990,994 (GRCm39) |
P202Q |
probably benign |
Het |
Prss41 |
A |
T |
17: 24,061,361 (GRCm39) |
H143Q |
probably damaging |
Het |
Ptpn21 |
A |
G |
12: 98,655,261 (GRCm39) |
Y569H |
probably damaging |
Het |
Rad17 |
T |
C |
13: 100,773,564 (GRCm39) |
K142E |
probably damaging |
Het |
Rcan3 |
T |
C |
4: 135,152,607 (GRCm39) |
E38G |
probably benign |
Het |
Rgl3 |
C |
A |
9: 21,885,356 (GRCm39) |
R658L |
possibly damaging |
Het |
Rnf125 |
T |
A |
18: 21,116,240 (GRCm39) |
*141K |
probably null |
Het |
Ros1 |
G |
T |
10: 52,019,502 (GRCm39) |
N711K |
probably damaging |
Het |
Rsph10b |
T |
A |
5: 143,896,504 (GRCm39) |
Y421N |
probably benign |
Het |
Ryr1 |
C |
T |
7: 28,776,471 (GRCm39) |
V2222I |
probably damaging |
Het |
Samsn1 |
C |
T |
16: 75,656,449 (GRCm39) |
C333Y |
probably damaging |
Het |
Slc9a2 |
G |
A |
1: 40,794,944 (GRCm39) |
E502K |
probably benign |
Het |
Stard9 |
A |
T |
2: 120,533,500 (GRCm39) |
E3252D |
possibly damaging |
Het |
Syne1 |
C |
A |
10: 5,123,008 (GRCm39) |
R309S |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,172,289 (GRCm39) |
I5051V |
probably benign |
Het |
Syngap1 |
A |
G |
17: 27,183,948 (GRCm39) |
S1241G |
probably damaging |
Het |
Tbpl2 |
T |
C |
2: 23,966,030 (GRCm39) |
K321R |
probably damaging |
Het |
Tnrc18 |
C |
T |
5: 142,717,107 (GRCm39) |
G2449E |
probably damaging |
Het |
Trim25 |
A |
G |
11: 88,901,731 (GRCm39) |
D342G |
probably benign |
Het |
Tssk4 |
T |
A |
14: 55,887,904 (GRCm39) |
H33Q |
probably benign |
Het |
Ttc3 |
G |
A |
16: 94,268,831 (GRCm39) |
G1971D |
possibly damaging |
Het |
Tufm |
C |
T |
7: 126,088,849 (GRCm39) |
Q347* |
probably null |
Het |
Ubxn10 |
G |
A |
4: 138,448,133 (GRCm39) |
S181F |
possibly damaging |
Het |
Ushbp1 |
T |
C |
8: 71,841,539 (GRCm39) |
E430G |
probably benign |
Het |
Vmn1r33 |
T |
C |
6: 66,588,716 (GRCm39) |
I279M |
possibly damaging |
Het |
Vmn2r115 |
T |
C |
17: 23,564,784 (GRCm39) |
F224L |
probably damaging |
Het |
Vmn2r23 |
A |
T |
6: 123,681,323 (GRCm39) |
H77L |
probably benign |
Het |
Vps13a |
T |
C |
19: 16,663,961 (GRCm39) |
I1481V |
probably benign |
Het |
Vps35 |
T |
C |
8: 86,007,898 (GRCm39) |
N294S |
possibly damaging |
Het |
Washc3 |
A |
T |
10: 88,051,916 (GRCm39) |
T102S |
probably benign |
Het |
Zfp27 |
T |
A |
7: 29,595,359 (GRCm39) |
E202V |
possibly damaging |
Het |
Zfp58 |
T |
C |
13: 67,640,035 (GRCm39) |
H152R |
possibly damaging |
Het |
Zfr2 |
T |
C |
10: 81,080,496 (GRCm39) |
V390A |
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 |
|
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 |
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 |
|
|