Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
T |
A |
9: 44,279,394 (GRCm38) |
Q278H |
probably benign |
Het |
Ace3 |
T |
C |
11: 106,004,610 (GRCm38) |
|
probably null |
Het |
Aco1 |
T |
C |
4: 40,176,499 (GRCm38) |
V221A |
probably damaging |
Het |
Adamts20 |
T |
A |
15: 94,404,010 (GRCm38) |
H27L |
probably benign |
Het |
Adamts8 |
A |
G |
9: 30,956,512 (GRCm38) |
D544G |
probably benign |
Het |
Angptl4 |
C |
A |
17: 33,781,275 (GRCm38) |
E40* |
probably null |
Het |
Arsi |
G |
A |
18: 60,916,651 (GRCm38) |
G202E |
probably benign |
Het |
Atf7ip2 |
T |
A |
16: 10,241,703 (GRCm38) |
I369N |
possibly damaging |
Het |
Atp6ap1l |
T |
A |
13: 90,883,687 (GRCm38) |
Y292F |
probably damaging |
Het |
Atp6v1b2 |
A |
T |
8: 69,102,807 (GRCm38) |
K217* |
probably null |
Het |
Bid |
C |
T |
6: 120,897,255 (GRCm38) |
A110T |
possibly damaging |
Het |
Blvra |
T |
A |
2: 127,095,148 (GRCm38) |
W174R |
probably damaging |
Het |
Catsperg1 |
C |
T |
7: 29,198,143 (GRCm38) |
G239R |
probably damaging |
Het |
Ccdc157 |
G |
T |
11: 4,146,549 (GRCm38) |
A400D |
probably damaging |
Het |
Chd2 |
G |
T |
7: 73,454,445 (GRCm38) |
P1298T |
probably damaging |
Het |
CK137956 |
G |
A |
4: 127,946,858 (GRCm38) |
L352F |
possibly damaging |
Het |
Col22a1 |
G |
A |
15: 71,870,140 (GRCm38) |
P503S |
unknown |
Het |
Cox15 |
C |
T |
19: 43,746,785 (GRCm38) |
R181H |
probably benign |
Het |
Crem |
C |
T |
18: 3,299,284 (GRCm38) |
G47R |
probably benign |
Het |
Crygs |
T |
A |
16: 22,806,554 (GRCm38) |
T46S |
probably benign |
Het |
Cts8 |
T |
A |
13: 61,253,615 (GRCm38) |
H62L |
probably damaging |
Het |
Cyp4a32 |
T |
A |
4: 115,611,277 (GRCm38) |
F319I |
possibly damaging |
Het |
Dchs1 |
T |
C |
7: 105,765,902 (GRCm38) |
S692G |
probably damaging |
Het |
Ddx23 |
G |
A |
15: 98,650,718 (GRCm38) |
R370W |
possibly damaging |
Het |
Defa29 |
A |
T |
8: 21,326,849 (GRCm38) |
S43T |
probably damaging |
Het |
Dnajc14 |
A |
G |
10: 128,816,792 (GRCm38) |
D573G |
probably damaging |
Het |
Drd5 |
A |
G |
5: 38,319,976 (GRCm38) |
Y104C |
probably benign |
Het |
Efcab7 |
C |
T |
4: 99,911,018 (GRCm38) |
P102L |
probably damaging |
Het |
Efhc1 |
A |
G |
1: 20,967,400 (GRCm38) |
Y267C |
probably damaging |
Het |
Eif2ak4 |
T |
C |
2: 118,448,486 (GRCm38) |
Y243H |
probably damaging |
Het |
Gfm2 |
T |
A |
13: 97,141,967 (GRCm38) |
I7N |
probably damaging |
Het |
Gmds |
A |
G |
13: 32,127,997 (GRCm38) |
F150L |
possibly damaging |
Het |
Gp2 |
T |
C |
7: 119,454,232 (GRCm38) |
T169A |
possibly damaging |
Het |
Grb14 |
A |
G |
2: 64,912,802 (GRCm38) |
F508L |
probably damaging |
Het |
Hdac5 |
T |
A |
11: 102,195,872 (GRCm38) |
|
probably benign |
Het |
Heatr1 |
T |
A |
13: 12,435,185 (GRCm38) |
M620K |
probably damaging |
Het |
Herc3 |
A |
G |
6: 58,876,793 (GRCm38) |
E608G |
probably damaging |
Het |
Hoxb4 |
T |
C |
11: 96,320,041 (GRCm38) |
Y156H |
probably damaging |
Het |
Ifi205 |
T |
A |
1: 174,028,414 (GRCm38) |
I17F |
possibly damaging |
Het |
Il2rb |
A |
T |
15: 78,491,777 (GRCm38) |
S25T |
possibly damaging |
Het |
Kansl1 |
T |
C |
11: 104,335,097 (GRCm38) |
T998A |
probably damaging |
Het |
Kcna6 |
G |
T |
6: 126,738,488 (GRCm38) |
H479Q |
probably benign |
Het |
Kif2a |
T |
C |
13: 106,978,091 (GRCm38) |
K350R |
probably benign |
Het |
Lct |
G |
T |
1: 128,294,161 (GRCm38) |
A1547E |
probably damaging |
Het |
Lhx9 |
T |
A |
1: 138,842,009 (GRCm38) |
|
probably benign |
Het |
Lingo1 |
T |
A |
9: 56,619,650 (GRCm38) |
I552F |
possibly damaging |
Het |
Lrp4 |
G |
A |
2: 91,497,355 (GRCm38) |
W1516* |
probably null |
Het |
Lrp5 |
C |
T |
19: 3,610,131 (GRCm38) |
V978I |
probably benign |
Het |
Ltbp1 |
T |
A |
17: 75,313,034 (GRCm38) |
D719E |
probably benign |
Het |
Ltbp4 |
A |
G |
7: 27,307,766 (GRCm38) |
|
probably null |
Het |
Macf1 |
A |
G |
4: 123,452,037 (GRCm38) |
I1326T |
probably damaging |
Het |
Manba |
T |
C |
3: 135,544,740 (GRCm38) |
F376S |
probably benign |
Het |
Mink1 |
T |
C |
11: 70,608,428 (GRCm38) |
|
probably null |
Het |
Nfatc2ip |
C |
T |
7: 126,384,992 (GRCm38) |
V410I |
probably damaging |
Het |
Nlrp1b |
A |
T |
11: 71,182,138 (GRCm38) |
I293N |
probably damaging |
Het |
Olfr432 |
T |
C |
1: 174,050,678 (GRCm38) |
Y102H |
probably damaging |
Het |
Otol1 |
A |
C |
3: 70,028,104 (GRCm38) |
E476D |
probably benign |
Het |
Pcdhb4 |
C |
T |
18: 37,309,541 (GRCm38) |
P635S |
probably benign |
Het |
Pfkfb4 |
T |
A |
9: 108,999,169 (GRCm38) |
F91I |
probably damaging |
Het |
Polr3c |
A |
T |
3: 96,719,298 (GRCm38) |
L270H |
probably damaging |
Het |
Ppp1r15b |
C |
T |
1: 133,131,625 (GRCm38) |
|
probably benign |
Het |
Prkca |
T |
G |
11: 108,192,149 (GRCm38) |
D90A |
probably benign |
Het |
Sall3 |
T |
C |
18: 80,969,753 (GRCm38) |
D1156G |
probably benign |
Het |
Scn7a |
A |
T |
2: 66,676,102 (GRCm38) |
L1481H |
probably damaging |
Het |
Selenon |
A |
T |
4: 134,544,618 (GRCm38) |
I292N |
probably damaging |
Het |
Sema6d |
T |
A |
2: 124,659,886 (GRCm38) |
|
probably null |
Het |
Sgpp1 |
G |
T |
12: 75,716,179 (GRCm38) |
Y409* |
probably null |
Het |
Sh3pxd2a |
A |
G |
19: 47,267,508 (GRCm38) |
S924P |
probably benign |
Het |
Slc25a13 |
A |
G |
6: 6,042,264 (GRCm38) |
V638A |
probably benign |
Het |
Snhg11 |
T |
C |
2: 158,376,826 (GRCm38) |
|
probably benign |
Het |
Sorbs2 |
A |
G |
8: 45,796,352 (GRCm38) |
Q800R |
probably benign |
Het |
Srf |
C |
A |
17: 46,549,986 (GRCm38) |
G401C |
probably damaging |
Het |
Stradb |
A |
C |
1: 58,991,105 (GRCm38) |
N173H |
probably benign |
Het |
Swap70 |
C |
T |
7: 110,279,263 (GRCm38) |
A480V |
possibly damaging |
Het |
Sycp2 |
A |
G |
2: 178,381,957 (GRCm38) |
V422A |
probably damaging |
Het |
Taf4 |
G |
A |
2: 179,932,029 (GRCm38) |
T682M |
probably damaging |
Het |
Tet3 |
T |
C |
6: 83,404,379 (GRCm38) |
N269S |
possibly damaging |
Het |
Thap12 |
A |
T |
7: 98,716,838 (GRCm38) |
I738F |
possibly damaging |
Het |
Tiam2 |
C |
T |
17: 3,514,725 (GRCm38) |
R1413C |
possibly damaging |
Het |
Tmem229a |
A |
T |
6: 24,955,011 (GRCm38) |
F248Y |
probably damaging |
Het |
Tmprss7 |
G |
A |
16: 45,684,593 (GRCm38) |
Q145* |
probably null |
Het |
Tnc |
A |
T |
4: 63,993,025 (GRCm38) |
|
probably null |
Het |
Tonsl |
A |
T |
15: 76,624,597 (GRCm38) |
Y21N |
probably damaging |
Het |
Tpr |
A |
G |
1: 150,421,663 (GRCm38) |
D1009G |
probably benign |
Het |
Trpm2 |
G |
A |
10: 77,941,158 (GRCm38) |
A435V |
probably damaging |
Het |
Ubr3 |
T |
A |
2: 69,953,476 (GRCm38) |
|
probably null |
Het |
Vcan |
T |
C |
13: 89,705,534 (GRCm38) |
N436D |
possibly damaging |
Het |
Vmn2r104 |
T |
A |
17: 20,040,769 (GRCm38) |
Y464F |
probably damaging |
Het |
Vmn2r44 |
T |
A |
7: 8,367,982 (GRCm38) |
R688S |
probably benign |
Het |
Wdr74 |
G |
T |
19: 8,737,947 (GRCm38) |
V157L |
probably benign |
Het |
Wnt7a |
T |
A |
6: 91,394,548 (GRCm38) |
D144V |
probably benign |
Het |
Zfp106 |
C |
T |
2: 120,531,681 (GRCm38) |
A986T |
possibly damaging |
Het |
|
Other mutations in Polq |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Polq
|
APN |
16 |
37,065,247 (GRCm38) |
splice site |
probably benign |
|
IGL00539:Polq
|
APN |
16 |
37,060,569 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL00960:Polq
|
APN |
16 |
37,060,512 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL01100:Polq
|
APN |
16 |
37,061,112 (GRCm38) |
missense |
probably benign |
|
IGL01112:Polq
|
APN |
16 |
37,017,309 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01138:Polq
|
APN |
16 |
37,045,869 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL01432:Polq
|
APN |
16 |
37,071,822 (GRCm38) |
splice site |
probably benign |
|
IGL01522:Polq
|
APN |
16 |
37,027,903 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01565:Polq
|
APN |
16 |
37,013,113 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01592:Polq
|
APN |
16 |
37,034,850 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01690:Polq
|
APN |
16 |
37,062,838 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL01943:Polq
|
APN |
16 |
37,061,443 (GRCm38) |
missense |
possibly damaging |
0.47 |
IGL02531:Polq
|
APN |
16 |
37,062,374 (GRCm38) |
missense |
possibly damaging |
0.75 |
IGL02553:Polq
|
APN |
16 |
37,041,768 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02623:Polq
|
APN |
16 |
37,060,375 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02692:Polq
|
APN |
16 |
37,060,627 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02717:Polq
|
APN |
16 |
37,022,740 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02937:Polq
|
APN |
16 |
37,013,109 (GRCm38) |
missense |
probably benign |
0.14 |
IGL02959:Polq
|
APN |
16 |
37,086,566 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03086:Polq
|
APN |
16 |
37,091,049 (GRCm38) |
missense |
probably benign |
0.02 |
IGL03141:Polq
|
APN |
16 |
37,017,358 (GRCm38) |
splice site |
probably benign |
|
IGL03302:Polq
|
APN |
16 |
37,071,772 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03393:Polq
|
APN |
16 |
37,044,794 (GRCm38) |
missense |
probably damaging |
1.00 |
R0013_Polq_667
|
UTSW |
16 |
37,061,839 (GRCm38) |
missense |
possibly damaging |
0.56 |
R4238_Polq_233
|
UTSW |
16 |
37,013,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R4280_polq_867
|
UTSW |
16 |
37,082,057 (GRCm38) |
missense |
probably damaging |
1.00 |
G1Funyon:Polq
|
UTSW |
16 |
37,061,819 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4403001:Polq
|
UTSW |
16 |
37,060,587 (GRCm38) |
missense |
probably benign |
0.00 |
R0013:Polq
|
UTSW |
16 |
37,061,839 (GRCm38) |
missense |
possibly damaging |
0.56 |
R0082:Polq
|
UTSW |
16 |
37,017,257 (GRCm38) |
missense |
probably benign |
0.01 |
R0212:Polq
|
UTSW |
16 |
37,066,854 (GRCm38) |
missense |
probably damaging |
0.99 |
R0387:Polq
|
UTSW |
16 |
37,089,317 (GRCm38) |
missense |
probably damaging |
1.00 |
R0387:Polq
|
UTSW |
16 |
37,029,430 (GRCm38) |
missense |
probably damaging |
1.00 |
R0427:Polq
|
UTSW |
16 |
37,061,993 (GRCm38) |
nonsense |
probably null |
|
R0454:Polq
|
UTSW |
16 |
37,034,890 (GRCm38) |
missense |
probably damaging |
0.98 |
R0513:Polq
|
UTSW |
16 |
37,094,502 (GRCm38) |
missense |
probably damaging |
1.00 |
R0622:Polq
|
UTSW |
16 |
37,060,993 (GRCm38) |
missense |
probably benign |
0.02 |
R0848:Polq
|
UTSW |
16 |
37,062,130 (GRCm38) |
missense |
probably benign |
0.08 |
R1142:Polq
|
UTSW |
16 |
37,013,217 (GRCm38) |
missense |
probably damaging |
0.98 |
R1218:Polq
|
UTSW |
16 |
37,029,446 (GRCm38) |
missense |
possibly damaging |
0.93 |
R1331:Polq
|
UTSW |
16 |
37,041,747 (GRCm38) |
missense |
probably damaging |
1.00 |
R1398:Polq
|
UTSW |
16 |
37,062,495 (GRCm38) |
missense |
possibly damaging |
0.87 |
R1424:Polq
|
UTSW |
16 |
37,086,528 (GRCm38) |
missense |
probably damaging |
1.00 |
R1644:Polq
|
UTSW |
16 |
37,060,264 (GRCm38) |
missense |
probably damaging |
0.96 |
R1777:Polq
|
UTSW |
16 |
37,060,224 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1820:Polq
|
UTSW |
16 |
37,029,418 (GRCm38) |
missense |
possibly damaging |
0.48 |
R1854:Polq
|
UTSW |
16 |
37,062,109 (GRCm38) |
missense |
probably benign |
0.01 |
R1880:Polq
|
UTSW |
16 |
37,086,592 (GRCm38) |
missense |
possibly damaging |
0.90 |
R2008:Polq
|
UTSW |
16 |
37,062,482 (GRCm38) |
missense |
probably damaging |
0.96 |
R2014:Polq
|
UTSW |
16 |
37,078,366 (GRCm38) |
missense |
probably damaging |
1.00 |
R2026:Polq
|
UTSW |
16 |
37,062,745 (GRCm38) |
missense |
possibly damaging |
0.93 |
R2178:Polq
|
UTSW |
16 |
37,062,829 (GRCm38) |
missense |
probably damaging |
1.00 |
R2259:Polq
|
UTSW |
16 |
37,062,097 (GRCm38) |
missense |
probably benign |
0.03 |
R2266:Polq
|
UTSW |
16 |
37,062,153 (GRCm38) |
missense |
possibly damaging |
0.59 |
R2305:Polq
|
UTSW |
16 |
37,062,337 (GRCm38) |
missense |
probably damaging |
0.99 |
R2370:Polq
|
UTSW |
16 |
37,073,939 (GRCm38) |
missense |
probably damaging |
1.00 |
R2504:Polq
|
UTSW |
16 |
37,011,942 (GRCm38) |
missense |
unknown |
|
R2517:Polq
|
UTSW |
16 |
37,089,325 (GRCm38) |
missense |
probably damaging |
1.00 |
R2697:Polq
|
UTSW |
16 |
37,042,153 (GRCm38) |
missense |
probably damaging |
1.00 |
R2858:Polq
|
UTSW |
16 |
37,062,753 (GRCm38) |
missense |
possibly damaging |
0.88 |
R3436:Polq
|
UTSW |
16 |
37,062,337 (GRCm38) |
missense |
probably damaging |
0.99 |
R3437:Polq
|
UTSW |
16 |
37,062,337 (GRCm38) |
missense |
probably damaging |
0.99 |
R3699:Polq
|
UTSW |
16 |
37,042,156 (GRCm38) |
missense |
probably damaging |
1.00 |
R3838:Polq
|
UTSW |
16 |
37,078,349 (GRCm38) |
missense |
probably damaging |
1.00 |
R3875:Polq
|
UTSW |
16 |
37,074,027 (GRCm38) |
missense |
probably damaging |
0.99 |
R4050:Polq
|
UTSW |
16 |
37,092,820 (GRCm38) |
critical splice acceptor site |
probably null |
|
R4172:Polq
|
UTSW |
16 |
37,060,758 (GRCm38) |
missense |
probably benign |
0.02 |
R4238:Polq
|
UTSW |
16 |
37,013,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R4240:Polq
|
UTSW |
16 |
37,013,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R4280:Polq
|
UTSW |
16 |
37,082,057 (GRCm38) |
missense |
probably damaging |
1.00 |
R4296:Polq
|
UTSW |
16 |
37,061,301 (GRCm38) |
missense |
possibly damaging |
0.94 |
R4360:Polq
|
UTSW |
16 |
37,060,339 (GRCm38) |
missense |
probably benign |
0.00 |
R4373:Polq
|
UTSW |
16 |
37,013,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R4375:Polq
|
UTSW |
16 |
37,013,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R4376:Polq
|
UTSW |
16 |
37,013,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R4509:Polq
|
UTSW |
16 |
37,048,563 (GRCm38) |
missense |
probably damaging |
1.00 |
R4510:Polq
|
UTSW |
16 |
37,048,563 (GRCm38) |
missense |
probably damaging |
1.00 |
R4511:Polq
|
UTSW |
16 |
37,048,563 (GRCm38) |
missense |
probably damaging |
1.00 |
R4543:Polq
|
UTSW |
16 |
37,060,785 (GRCm38) |
missense |
probably benign |
0.43 |
R4633:Polq
|
UTSW |
16 |
37,048,542 (GRCm38) |
missense |
probably damaging |
1.00 |
R4739:Polq
|
UTSW |
16 |
37,041,747 (GRCm38) |
missense |
probably damaging |
1.00 |
R4834:Polq
|
UTSW |
16 |
37,027,814 (GRCm38) |
missense |
probably damaging |
1.00 |
R4841:Polq
|
UTSW |
16 |
37,048,783 (GRCm38) |
critical splice donor site |
probably null |
|
R4842:Polq
|
UTSW |
16 |
37,048,783 (GRCm38) |
critical splice donor site |
probably null |
|
R4937:Polq
|
UTSW |
16 |
37,027,912 (GRCm38) |
missense |
probably benign |
0.01 |
R4955:Polq
|
UTSW |
16 |
37,061,082 (GRCm38) |
missense |
probably benign |
0.32 |
R4992:Polq
|
UTSW |
16 |
37,061,162 (GRCm38) |
missense |
possibly damaging |
0.59 |
R5008:Polq
|
UTSW |
16 |
37,062,387 (GRCm38) |
missense |
probably benign |
|
R5221:Polq
|
UTSW |
16 |
37,042,178 (GRCm38) |
missense |
probably damaging |
0.98 |
R5254:Polq
|
UTSW |
16 |
37,089,319 (GRCm38) |
missense |
probably damaging |
1.00 |
R5292:Polq
|
UTSW |
16 |
37,061,383 (GRCm38) |
missense |
probably damaging |
1.00 |
R5375:Polq
|
UTSW |
16 |
37,082,784 (GRCm38) |
missense |
probably damaging |
1.00 |
R5480:Polq
|
UTSW |
16 |
37,013,290 (GRCm38) |
splice site |
probably benign |
|
R5552:Polq
|
UTSW |
16 |
37,094,510 (GRCm38) |
missense |
possibly damaging |
0.93 |
R5591:Polq
|
UTSW |
16 |
37,011,885 (GRCm38) |
utr 5 prime |
probably benign |
|
R5653:Polq
|
UTSW |
16 |
37,040,534 (GRCm38) |
missense |
probably damaging |
1.00 |
R5708:Polq
|
UTSW |
16 |
37,061,018 (GRCm38) |
missense |
probably damaging |
0.98 |
R5754:Polq
|
UTSW |
16 |
37,017,263 (GRCm38) |
missense |
probably benign |
|
R5757:Polq
|
UTSW |
16 |
37,086,681 (GRCm38) |
missense |
probably benign |
0.01 |
R5764:Polq
|
UTSW |
16 |
37,017,344 (GRCm38) |
missense |
probably damaging |
0.97 |
R6019:Polq
|
UTSW |
16 |
37,061,764 (GRCm38) |
missense |
probably damaging |
1.00 |
R6170:Polq
|
UTSW |
16 |
37,045,812 (GRCm38) |
missense |
possibly damaging |
0.82 |
R6177:Polq
|
UTSW |
16 |
37,071,709 (GRCm38) |
missense |
probably damaging |
0.98 |
R6307:Polq
|
UTSW |
16 |
37,017,356 (GRCm38) |
critical splice donor site |
probably null |
|
R6499:Polq
|
UTSW |
16 |
37,060,827 (GRCm38) |
missense |
probably benign |
0.03 |
R6520:Polq
|
UTSW |
16 |
37,060,377 (GRCm38) |
missense |
possibly damaging |
0.88 |
R6598:Polq
|
UTSW |
16 |
37,061,631 (GRCm38) |
missense |
probably benign |
0.39 |
R6694:Polq
|
UTSW |
16 |
37,015,173 (GRCm38) |
missense |
probably null |
0.99 |
R6788:Polq
|
UTSW |
16 |
37,077,148 (GRCm38) |
missense |
probably damaging |
1.00 |
R7104:Polq
|
UTSW |
16 |
37,089,353 (GRCm38) |
nonsense |
probably null |
|
R7159:Polq
|
UTSW |
16 |
37,062,853 (GRCm38) |
missense |
possibly damaging |
0.87 |
R7222:Polq
|
UTSW |
16 |
37,086,633 (GRCm38) |
nonsense |
probably null |
|
R7340:Polq
|
UTSW |
16 |
37,060,926 (GRCm38) |
missense |
probably benign |
0.00 |
R7361:Polq
|
UTSW |
16 |
37,060,428 (GRCm38) |
missense |
probably benign |
0.00 |
R7384:Polq
|
UTSW |
16 |
37,029,418 (GRCm38) |
missense |
probably damaging |
1.00 |
R7509:Polq
|
UTSW |
16 |
37,060,344 (GRCm38) |
missense |
probably benign |
0.00 |
R7509:Polq
|
UTSW |
16 |
37,060,343 (GRCm38) |
missense |
probably benign |
|
R7575:Polq
|
UTSW |
16 |
37,091,134 (GRCm38) |
missense |
probably benign |
0.00 |
R7785:Polq
|
UTSW |
16 |
37,027,877 (GRCm38) |
missense |
probably damaging |
1.00 |
R7787:Polq
|
UTSW |
16 |
37,017,309 (GRCm38) |
missense |
probably damaging |
1.00 |
R7891:Polq
|
UTSW |
16 |
37,027,882 (GRCm38) |
missense |
probably damaging |
1.00 |
R7898:Polq
|
UTSW |
16 |
37,044,883 (GRCm38) |
missense |
probably damaging |
0.98 |
R7917:Polq
|
UTSW |
16 |
37,065,288 (GRCm38) |
missense |
probably benign |
0.08 |
R7940:Polq
|
UTSW |
16 |
37,060,642 (GRCm38) |
missense |
probably benign |
0.27 |
R8028:Polq
|
UTSW |
16 |
37,061,316 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8114:Polq
|
UTSW |
16 |
37,042,215 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8144:Polq
|
UTSW |
16 |
37,029,484 (GRCm38) |
missense |
probably benign |
0.01 |
R8288:Polq
|
UTSW |
16 |
37,027,910 (GRCm38) |
missense |
probably damaging |
1.00 |
R8301:Polq
|
UTSW |
16 |
37,061,819 (GRCm38) |
missense |
probably damaging |
1.00 |
R8341:Polq
|
UTSW |
16 |
37,071,771 (GRCm38) |
missense |
possibly damaging |
0.96 |
R8348:Polq
|
UTSW |
16 |
37,017,197 (GRCm38) |
critical splice acceptor site |
probably null |
|
R8448:Polq
|
UTSW |
16 |
37,017,197 (GRCm38) |
critical splice acceptor site |
probably null |
|
R8815:Polq
|
UTSW |
16 |
37,033,531 (GRCm38) |
missense |
probably damaging |
1.00 |
R8843:Polq
|
UTSW |
16 |
37,011,918 (GRCm38) |
missense |
unknown |
|
R8878:Polq
|
UTSW |
16 |
37,040,507 (GRCm38) |
missense |
probably benign |
0.02 |
R9016:Polq
|
UTSW |
16 |
37,022,797 (GRCm38) |
missense |
probably damaging |
1.00 |
R9189:Polq
|
UTSW |
16 |
37,044,903 (GRCm38) |
missense |
probably damaging |
1.00 |
R9209:Polq
|
UTSW |
16 |
37,048,649 (GRCm38) |
missense |
possibly damaging |
0.94 |
R9352:Polq
|
UTSW |
16 |
37,041,890 (GRCm38) |
missense |
probably damaging |
0.98 |
R9398:Polq
|
UTSW |
16 |
37,061,032 (GRCm38) |
missense |
probably benign |
0.02 |
R9403:Polq
|
UTSW |
16 |
37,061,853 (GRCm38) |
missense |
probably benign |
0.00 |
R9489:Polq
|
UTSW |
16 |
37,022,811 (GRCm38) |
missense |
probably benign |
0.00 |
R9605:Polq
|
UTSW |
16 |
37,022,811 (GRCm38) |
missense |
probably benign |
0.00 |
R9664:Polq
|
UTSW |
16 |
37,027,814 (GRCm38) |
missense |
probably damaging |
0.98 |
R9801:Polq
|
UTSW |
16 |
37,092,828 (GRCm38) |
missense |
probably damaging |
1.00 |
X0060:Polq
|
UTSW |
16 |
37,017,237 (GRCm38) |
nonsense |
probably null |
|
Z1176:Polq
|
UTSW |
16 |
37,042,257 (GRCm38) |
critical splice donor site |
probably null |
|
|