Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
T |
C |
11: 119,909,681 (GRCm39) |
D28G |
probably benign |
Het |
Abcg1 |
T |
A |
17: 31,311,369 (GRCm39) |
S125T |
probably damaging |
Het |
Actbl2 |
T |
C |
13: 111,392,717 (GRCm39) |
S351P |
possibly damaging |
Het |
Ankrd34b |
A |
G |
13: 92,575,569 (GRCm39) |
|
probably null |
Het |
BC051665 |
C |
T |
13: 60,930,468 (GRCm39) |
V295I |
probably benign |
Het |
C1qtnf2 |
A |
G |
11: 43,381,983 (GRCm39) |
N265S |
probably damaging |
Het |
Ccdc14 |
C |
T |
16: 34,542,220 (GRCm39) |
R573* |
probably null |
Het |
Cd55b |
A |
T |
1: 130,337,612 (GRCm39) |
Y247N |
probably damaging |
Het |
Celsr2 |
A |
T |
3: 108,320,907 (GRCm39) |
V635E |
probably benign |
Het |
Clec16a |
T |
C |
16: 10,377,551 (GRCm39) |
|
probably benign |
Het |
Clec4b1 |
A |
G |
6: 123,042,904 (GRCm39) |
Y41C |
probably damaging |
Het |
Cntn5 |
A |
T |
9: 10,172,126 (GRCm39) |
D19E |
probably benign |
Het |
Cop1 |
A |
G |
1: 159,060,375 (GRCm39) |
N53S |
probably damaging |
Het |
Cplane1 |
G |
A |
15: 8,248,700 (GRCm39) |
E1750K |
probably damaging |
Het |
Csad |
A |
T |
15: 102,097,102 (GRCm39) |
M1K |
probably null |
Het |
Cyb5rl |
A |
G |
4: 106,938,142 (GRCm39) |
I200V |
probably benign |
Het |
Cyp26a1 |
A |
G |
19: 37,686,790 (GRCm39) |
T81A |
probably damaging |
Het |
Cyp2d12 |
A |
T |
15: 82,443,237 (GRCm39) |
H433L |
probably benign |
Het |
D7Ertd443e |
T |
A |
7: 133,951,208 (GRCm39) |
|
probably null |
Het |
Dennd1b |
A |
G |
1: 139,097,908 (GRCm39) |
|
probably benign |
Het |
Dmap1 |
G |
T |
4: 117,532,495 (GRCm39) |
T357K |
probably damaging |
Het |
Dzip1 |
G |
T |
14: 119,118,456 (GRCm39) |
T759K |
probably benign |
Het |
Elmo2 |
A |
G |
2: 165,140,607 (GRCm39) |
V300A |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,810,364 (GRCm39) |
D864G |
possibly damaging |
Het |
Ep400 |
A |
G |
5: 110,816,511 (GRCm39) |
V2670A |
probably damaging |
Het |
Epha3 |
T |
A |
16: 63,423,988 (GRCm39) |
I534F |
probably damaging |
Het |
Epha4 |
A |
C |
1: 77,359,628 (GRCm39) |
Y742D |
probably damaging |
Het |
Ergic2 |
A |
G |
6: 148,106,272 (GRCm39) |
|
probably null |
Het |
Ero1a |
A |
T |
14: 45,536,545 (GRCm39) |
|
probably null |
Het |
Fam229a |
A |
G |
4: 129,385,279 (GRCm39) |
D70G |
probably damaging |
Het |
Fbn2 |
C |
T |
18: 58,226,431 (GRCm39) |
R781Q |
probably damaging |
Het |
Fbxo16 |
A |
T |
14: 65,508,163 (GRCm39) |
|
probably benign |
Het |
Fbxo39 |
T |
A |
11: 72,208,111 (GRCm39) |
S154R |
probably benign |
Het |
Fer |
T |
A |
17: 64,298,575 (GRCm39) |
|
probably null |
Het |
Filip1l |
A |
T |
16: 57,391,410 (GRCm39) |
D428V |
probably damaging |
Het |
Filip1l |
A |
G |
16: 57,391,025 (GRCm39) |
I538V |
possibly damaging |
Het |
Fsip2 |
T |
C |
2: 82,809,954 (GRCm39) |
I2091T |
possibly damaging |
Het |
Glyat |
A |
C |
19: 12,628,762 (GRCm39) |
T186P |
possibly damaging |
Het |
Gm10604 |
A |
G |
4: 11,980,083 (GRCm39) |
S74P |
unknown |
Het |
Gm4787 |
T |
G |
12: 81,425,911 (GRCm39) |
K82N |
possibly damaging |
Het |
Hectd4 |
T |
C |
5: 121,358,683 (GRCm39) |
I50T |
unknown |
Het |
Hectd4 |
T |
C |
5: 121,402,030 (GRCm39) |
S373P |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,562,618 (GRCm39) |
C2313* |
probably null |
Het |
Hrob |
T |
C |
11: 102,146,122 (GRCm39) |
Y133H |
possibly damaging |
Het |
Igfn1 |
A |
T |
1: 135,897,054 (GRCm39) |
S1171T |
probably benign |
Het |
Ints8 |
T |
C |
4: 11,241,642 (GRCm39) |
D267G |
probably benign |
Het |
Itln1 |
A |
G |
1: 171,356,727 (GRCm39) |
C251R |
probably damaging |
Het |
Jcad |
C |
T |
18: 4,674,026 (GRCm39) |
T596M |
probably damaging |
Het |
Kcnj16 |
C |
T |
11: 110,916,409 (GRCm39) |
T357M |
probably benign |
Het |
Kif13a |
G |
A |
13: 46,967,676 (GRCm39) |
T346M |
probably damaging |
Het |
Klhl24 |
G |
A |
16: 19,938,917 (GRCm39) |
A491T |
probably benign |
Het |
Kntc1 |
C |
T |
5: 123,916,410 (GRCm39) |
Q748* |
probably null |
Het |
Krt25 |
T |
A |
11: 99,208,122 (GRCm39) |
K369* |
probably null |
Het |
Krt75 |
C |
T |
15: 101,476,466 (GRCm39) |
R433Q |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,793,293 (GRCm39) |
F582L |
unknown |
Het |
Lysmd1 |
G |
A |
3: 95,045,708 (GRCm39) |
V182I |
probably benign |
Het |
Mab21l2 |
T |
A |
3: 86,454,862 (GRCm39) |
E46V |
probably damaging |
Het |
Magi2 |
A |
T |
5: 20,563,934 (GRCm39) |
K355N |
probably damaging |
Het |
Marchf10 |
T |
C |
11: 105,276,398 (GRCm39) |
D630G |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,875,147 (GRCm39) |
I1215N |
probably damaging |
Het |
Nckap1 |
G |
A |
2: 80,360,562 (GRCm39) |
T523I |
probably benign |
Het |
Nexmif |
T |
A |
X: 103,127,999 (GRCm39) |
D1306V |
probably damaging |
Het |
Nfkb1 |
A |
C |
3: 135,295,090 (GRCm39) |
I918R |
possibly damaging |
Het |
Nt5el |
A |
G |
13: 105,246,250 (GRCm39) |
I270M |
probably benign |
Het |
Nup50 |
A |
T |
15: 84,817,859 (GRCm39) |
T93S |
probably benign |
Het |
Nwd2 |
T |
C |
5: 63,961,717 (GRCm39) |
Y434H |
probably benign |
Het |
Or13a28 |
T |
C |
7: 140,218,397 (GRCm39) |
V261A |
probably benign |
Het |
Osbpl1a |
C |
A |
18: 13,038,088 (GRCm39) |
V288L |
probably benign |
Het |
Pan3 |
A |
G |
5: 147,463,846 (GRCm39) |
E562G |
possibly damaging |
Het |
Pappa |
T |
A |
4: 65,099,126 (GRCm39) |
Y548* |
probably null |
Het |
Phf3 |
A |
T |
1: 30,849,870 (GRCm39) |
L1181Q |
probably damaging |
Het |
Phip |
T |
C |
9: 82,797,392 (GRCm39) |
H537R |
possibly damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,348,824 (GRCm39) |
I240T |
probably damaging |
Het |
Pole |
G |
A |
5: 110,438,368 (GRCm39) |
|
probably null |
Het |
Prrt2 |
T |
C |
7: 126,619,396 (GRCm39) |
E23G |
possibly damaging |
Het |
Prss37 |
A |
T |
6: 40,494,760 (GRCm39) |
|
probably null |
Het |
Prune2 |
T |
C |
19: 16,977,400 (GRCm39) |
L45P |
probably damaging |
Het |
Psd |
A |
T |
19: 46,313,352 (GRCm39) |
M6K |
possibly damaging |
Het |
Psmd1 |
A |
G |
1: 86,017,719 (GRCm39) |
E510G |
possibly damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Pxdn |
T |
A |
12: 30,053,405 (GRCm39) |
I1194N |
probably damaging |
Het |
Rbp3 |
C |
T |
14: 33,677,975 (GRCm39) |
T641M |
probably damaging |
Het |
Rgmb |
C |
A |
17: 16,027,909 (GRCm39) |
R270L |
probably benign |
Het |
Rpgrip1l |
A |
G |
8: 92,007,344 (GRCm39) |
|
probably null |
Het |
Rps2 |
G |
A |
17: 24,939,353 (GRCm39) |
|
probably benign |
Het |
Rsbn1l |
G |
T |
5: 21,107,364 (GRCm39) |
A550E |
probably damaging |
Het |
S1pr4 |
C |
T |
10: 81,335,138 (GRCm39) |
R112H |
probably benign |
Het |
Scfd2 |
T |
C |
5: 74,691,838 (GRCm39) |
N148S |
probably damaging |
Het |
Scin |
C |
T |
12: 40,131,705 (GRCm39) |
M276I |
probably benign |
Het |
Sec24d |
T |
C |
3: 123,147,255 (GRCm39) |
I708T |
possibly damaging |
Het |
Skint11 |
T |
A |
4: 114,086,009 (GRCm39) |
F41I |
possibly damaging |
Het |
Slc15a4 |
A |
T |
5: 127,694,303 (GRCm39) |
F44Y |
possibly damaging |
Het |
Slc6a18 |
A |
G |
13: 73,823,925 (GRCm39) |
Y72H |
probably benign |
Het |
Slc7a11 |
A |
T |
3: 50,332,195 (GRCm39) |
|
probably null |
Het |
Slc7a14 |
G |
T |
3: 31,291,650 (GRCm39) |
N209K |
possibly damaging |
Het |
Sstr2 |
T |
C |
11: 113,515,257 (GRCm39) |
C59R |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,884,997 (GRCm39) |
|
probably null |
Het |
Stag1 |
G |
T |
9: 100,748,263 (GRCm39) |
S475I |
probably damaging |
Het |
Stxbp5l |
A |
G |
16: 36,936,029 (GRCm39) |
Y1183H |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,135,628 (GRCm39) |
|
probably null |
Het |
Tm9sf2 |
A |
G |
14: 122,396,096 (GRCm39) |
T653A |
probably benign |
Het |
Tmeff1 |
T |
C |
4: 48,662,059 (GRCm39) |
S366P |
possibly damaging |
Het |
Tnnt2 |
G |
T |
1: 135,779,803 (GRCm39) |
W300L |
probably damaging |
Het |
Traj32 |
A |
G |
14: 54,423,560 (GRCm39) |
|
probably benign |
Het |
Trp53bp2 |
A |
T |
1: 182,269,204 (GRCm39) |
M223L |
probably benign |
Het |
Tsga10 |
G |
A |
1: 37,854,758 (GRCm39) |
T246M |
probably damaging |
Het |
Txn2 |
A |
T |
15: 77,810,870 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
A |
2: 69,768,542 (GRCm39) |
F450I |
probably damaging |
Het |
Usp47 |
T |
C |
7: 111,703,677 (GRCm39) |
|
probably null |
Het |
Vars2 |
C |
T |
17: 35,975,685 (GRCm39) |
R244Q |
probably damaging |
Het |
Xrra1 |
T |
A |
7: 99,546,803 (GRCm39) |
F251L |
probably damaging |
Het |
Zfp804a |
G |
A |
2: 82,087,863 (GRCm39) |
R564Q |
probably benign |
Het |
Zfp983 |
T |
C |
17: 21,877,883 (GRCm39) |
C29R |
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 |
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 |
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 |
|
|