Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb2 |
C |
T |
4: 129,912,862 (GRCm39) |
A1329V |
probably benign |
Het |
Aida |
A |
G |
1: 183,099,809 (GRCm39) |
T215A |
probably benign |
Het |
Alpk2 |
A |
G |
18: 65,440,023 (GRCm39) |
S457P |
probably benign |
Het |
Ap4b1 |
G |
A |
3: 103,719,474 (GRCm39) |
V63I |
probably damaging |
Het |
Apaf1 |
A |
G |
10: 90,903,108 (GRCm39) |
V182A |
probably damaging |
Het |
B4galnt4 |
G |
A |
7: 140,646,916 (GRCm39) |
|
probably null |
Het |
Bltp2 |
G |
T |
11: 78,159,583 (GRCm39) |
R544L |
probably damaging |
Het |
Cacna1a |
T |
G |
8: 85,260,031 (GRCm39) |
D331E |
probably damaging |
Het |
Carmil2 |
A |
G |
8: 106,419,423 (GRCm39) |
|
probably null |
Het |
Cdkn1b |
A |
T |
6: 134,898,280 (GRCm39) |
Q133L |
probably benign |
Het |
Cep192 |
G |
C |
18: 67,967,874 (GRCm39) |
S786T |
possibly damaging |
Het |
Cfap418 |
T |
A |
4: 10,881,834 (GRCm39) |
C94S |
probably benign |
Het |
Cfap97 |
G |
A |
8: 46,645,733 (GRCm39) |
R537H |
probably benign |
Het |
Clpx |
C |
G |
9: 65,231,529 (GRCm39) |
A552G |
possibly damaging |
Het |
Cryl1 |
G |
A |
14: 57,523,842 (GRCm39) |
T240I |
probably damaging |
Het |
Ddx60 |
C |
A |
8: 62,411,612 (GRCm39) |
T488K |
probably benign |
Het |
Dennd4b |
A |
G |
3: 90,181,259 (GRCm39) |
H805R |
probably benign |
Het |
Dnmbp |
T |
C |
19: 43,878,996 (GRCm39) |
D25G |
unknown |
Het |
Dysf |
A |
C |
6: 84,126,664 (GRCm39) |
D1293A |
probably benign |
Het |
Efl1 |
T |
C |
7: 82,347,121 (GRCm39) |
L549P |
probably damaging |
Het |
Eif5 |
T |
C |
12: 111,506,697 (GRCm39) |
|
probably benign |
Het |
Eva1c |
A |
G |
16: 90,666,544 (GRCm39) |
K156E |
probably damaging |
Het |
Fbxw10 |
T |
G |
11: 62,767,606 (GRCm39) |
V814G |
possibly damaging |
Het |
Gfap |
C |
T |
11: 102,785,358 (GRCm39) |
R206Q |
probably benign |
Het |
Gjb6 |
A |
T |
14: 57,361,610 (GRCm39) |
L217* |
probably null |
Het |
Gpatch11 |
T |
A |
17: 79,146,595 (GRCm39) |
L80Q |
probably damaging |
Het |
Gramd1b |
T |
C |
9: 40,238,727 (GRCm39) |
Q225R |
probably damaging |
Het |
Gsdmc2 |
A |
G |
15: 63,705,195 (GRCm39) |
S173P |
possibly damaging |
Het |
Hars1 |
C |
G |
18: 36,903,166 (GRCm39) |
R388P |
probably damaging |
Het |
Ighm |
C |
T |
12: 113,385,852 (GRCm39) |
R129H |
|
Het |
Igsf9 |
A |
G |
1: 172,322,841 (GRCm39) |
I602V |
probably benign |
Het |
Inpp4b |
T |
G |
8: 82,679,314 (GRCm39) |
|
probably null |
Het |
Itch |
C |
A |
2: 155,041,302 (GRCm39) |
T450K |
probably damaging |
Het |
Kcnq1 |
T |
C |
7: 142,663,152 (GRCm39) |
F20L |
unknown |
Het |
Kmt2d |
G |
T |
15: 98,753,235 (GRCm39) |
A153E |
probably damaging |
Het |
Macf1 |
T |
A |
4: 123,398,263 (GRCm39) |
N750I |
probably damaging |
Het |
Marveld2 |
T |
A |
13: 100,747,984 (GRCm39) |
H365L |
probably damaging |
Het |
Med13l |
T |
A |
5: 118,892,386 (GRCm39) |
D1936E |
probably benign |
Het |
Mettl8 |
A |
T |
2: 70,803,687 (GRCm39) |
V200E |
probably damaging |
Het |
Mrgbp |
T |
G |
2: 180,227,135 (GRCm39) |
S157A |
possibly damaging |
Het |
Mrps35 |
A |
G |
6: 146,957,481 (GRCm39) |
T169A |
possibly damaging |
Het |
Mycbp2 |
A |
T |
14: 103,526,180 (GRCm39) |
Y551N |
probably damaging |
Het |
Myo18b |
T |
C |
5: 113,021,971 (GRCm39) |
R474G |
probably benign |
Het |
Nfx1 |
T |
A |
4: 41,021,830 (GRCm39) |
S979R |
possibly damaging |
Het |
Nlrp1a |
T |
C |
11: 71,013,634 (GRCm39) |
T539A |
probably benign |
Het |
Oca2 |
T |
A |
7: 56,064,145 (GRCm39) |
D713E |
probably benign |
Het |
Omt2b |
A |
C |
9: 78,235,894 (GRCm39) |
Y73S |
probably benign |
Het |
Or10aa1 |
T |
A |
1: 173,870,099 (GRCm39) |
H194Q |
probably benign |
Het |
Or13a27 |
C |
T |
7: 139,925,318 (GRCm39) |
V195I |
probably benign |
Het |
Or6c38 |
A |
G |
10: 128,929,081 (GRCm39) |
I254T |
probably damaging |
Het |
Or6c69 |
A |
T |
10: 129,748,120 (GRCm39) |
V9D |
possibly damaging |
Het |
Pde11a |
G |
T |
2: 75,836,328 (GRCm39) |
Q20K |
|
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Phrf1 |
C |
A |
7: 140,839,205 (GRCm39) |
T800K |
unknown |
Het |
Polr1f |
T |
G |
12: 33,486,988 (GRCm39) |
C150W |
possibly damaging |
Het |
Pramel4 |
T |
C |
4: 143,795,061 (GRCm39) |
S486P |
probably benign |
Het |
Proc |
T |
C |
18: 32,260,513 (GRCm39) |
D204G |
probably benign |
Het |
Rasgrp3 |
T |
A |
17: 75,823,411 (GRCm39) |
I494N |
possibly damaging |
Het |
Samm50 |
A |
G |
15: 84,081,231 (GRCm39) |
D53G |
probably benign |
Het |
Satb1 |
T |
C |
17: 52,116,217 (GRCm39) |
D22G |
possibly damaging |
Het |
Scarf2 |
T |
C |
16: 17,624,918 (GRCm39) |
S658P |
probably damaging |
Het |
Sfta2 |
T |
A |
17: 35,925,410 (GRCm39) |
I29K |
unknown |
Het |
Slc15a4 |
A |
T |
5: 127,681,742 (GRCm39) |
S292T |
probably benign |
Het |
Slc37a1 |
C |
T |
17: 31,559,237 (GRCm39) |
T439I |
probably damaging |
Het |
Slc4a9 |
C |
A |
18: 36,663,858 (GRCm39) |
P294Q |
probably damaging |
Het |
Slc52a3 |
T |
C |
2: 151,846,086 (GRCm39) |
S16P |
probably damaging |
Het |
Slc6a15 |
A |
G |
10: 103,244,163 (GRCm39) |
I468V |
probably benign |
Het |
Ssbp4 |
T |
C |
8: 71,050,617 (GRCm39) |
R269G |
unknown |
Het |
Tbl1xr1 |
A |
G |
3: 22,257,354 (GRCm39) |
T406A |
possibly damaging |
Het |
Tep1 |
A |
T |
14: 51,104,312 (GRCm39) |
V194D |
possibly damaging |
Het |
Thbs4 |
A |
T |
13: 92,909,767 (GRCm39) |
C343* |
probably null |
Het |
Tmed10 |
A |
T |
12: 85,391,065 (GRCm39) |
S158T |
possibly damaging |
Het |
Trbv3 |
T |
A |
6: 41,025,524 (GRCm39) |
V38E |
probably damaging |
Het |
Ttc6 |
T |
C |
12: 57,743,772 (GRCm39) |
M1258T |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,589,320 (GRCm39) |
D21281G |
probably damaging |
Het |
Usp54 |
T |
C |
14: 20,602,313 (GRCm39) |
R1346G |
probably damaging |
Het |
Vmn2r8 |
C |
A |
5: 108,956,449 (GRCm39) |
E58* |
probably null |
Het |
Vps13d |
C |
T |
4: 144,867,824 (GRCm39) |
E2009K |
|
Het |
Vps33b |
T |
C |
7: 79,935,017 (GRCm39) |
I320T |
probably damaging |
Het |
Vwa8 |
A |
C |
14: 79,219,674 (GRCm39) |
|
probably null |
Het |
Ythdf1 |
T |
C |
2: 180,553,786 (GRCm39) |
Y143C |
probably damaging |
Het |
Zfp213 |
C |
T |
17: 23,778,603 (GRCm39) |
|
probably null |
Het |
Zfp219 |
A |
T |
14: 52,244,570 (GRCm39) |
Y536* |
probably null |
Het |
|
Other mutations in Spag17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01096:Spag17
|
APN |
3 |
99,970,691 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01143:Spag17
|
APN |
3 |
99,846,614 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01329:Spag17
|
APN |
3 |
100,002,865 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01393:Spag17
|
APN |
3 |
99,934,926 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01617:Spag17
|
APN |
3 |
100,016,824 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01705:Spag17
|
APN |
3 |
99,930,046 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01928:Spag17
|
APN |
3 |
99,847,390 (GRCm39) |
splice site |
probably benign |
|
IGL01981:Spag17
|
APN |
3 |
99,966,149 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02435:Spag17
|
APN |
3 |
99,889,760 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02452:Spag17
|
APN |
3 |
99,934,707 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02465:Spag17
|
APN |
3 |
99,983,187 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02615:Spag17
|
APN |
3 |
99,979,401 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02751:Spag17
|
APN |
3 |
99,918,110 (GRCm39) |
nonsense |
probably null |
|
IGL02803:Spag17
|
APN |
3 |
100,016,713 (GRCm39) |
missense |
probably benign |
|
IGL02898:Spag17
|
APN |
3 |
100,008,702 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03037:Spag17
|
APN |
3 |
99,979,486 (GRCm39) |
splice site |
probably null |
|
IGL03068:Spag17
|
APN |
3 |
99,987,521 (GRCm39) |
missense |
probably benign |
0.35 |
IGL03131:Spag17
|
APN |
3 |
99,918,075 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03224:Spag17
|
APN |
3 |
99,918,156 (GRCm39) |
missense |
possibly damaging |
0.53 |
FR4342:Spag17
|
UTSW |
3 |
99,963,568 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Spag17
|
UTSW |
3 |
99,963,565 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Spag17
|
UTSW |
3 |
99,963,570 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Spag17
|
UTSW |
3 |
99,963,574 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Spag17
|
UTSW |
3 |
99,963,561 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Spag17
|
UTSW |
3 |
99,963,573 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Spag17
|
UTSW |
3 |
99,963,571 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Spag17
|
UTSW |
3 |
99,963,570 (GRCm39) |
small insertion |
probably benign |
|
N/A:Spag17
|
UTSW |
3 |
99,889,570 (GRCm39) |
splice site |
probably benign |
|
PIT4504001:Spag17
|
UTSW |
3 |
100,010,426 (GRCm39) |
critical splice acceptor site |
probably null |
|
PIT4514001:Spag17
|
UTSW |
3 |
99,920,527 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0107:Spag17
|
UTSW |
3 |
99,958,103 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0230:Spag17
|
UTSW |
3 |
100,014,143 (GRCm39) |
missense |
probably benign |
0.08 |
R0243:Spag17
|
UTSW |
3 |
99,992,684 (GRCm39) |
missense |
probably benign |
0.04 |
R0321:Spag17
|
UTSW |
3 |
100,008,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R0375:Spag17
|
UTSW |
3 |
99,934,906 (GRCm39) |
missense |
probably benign |
|
R0417:Spag17
|
UTSW |
3 |
99,972,870 (GRCm39) |
missense |
probably benign |
0.11 |
R0490:Spag17
|
UTSW |
3 |
99,889,727 (GRCm39) |
missense |
probably damaging |
0.97 |
R0537:Spag17
|
UTSW |
3 |
100,032,618 (GRCm39) |
missense |
probably damaging |
0.98 |
R0714:Spag17
|
UTSW |
3 |
99,987,472 (GRCm39) |
missense |
probably damaging |
0.97 |
R0844:Spag17
|
UTSW |
3 |
99,912,101 (GRCm39) |
missense |
probably benign |
|
R0919:Spag17
|
UTSW |
3 |
99,979,259 (GRCm39) |
splice site |
probably benign |
|
R0926:Spag17
|
UTSW |
3 |
99,979,432 (GRCm39) |
missense |
probably benign |
|
R1037:Spag17
|
UTSW |
3 |
100,010,433 (GRCm39) |
missense |
probably benign |
0.01 |
R1075:Spag17
|
UTSW |
3 |
100,000,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R1109:Spag17
|
UTSW |
3 |
99,934,667 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1213:Spag17
|
UTSW |
3 |
100,002,954 (GRCm39) |
missense |
probably benign |
0.01 |
R1221:Spag17
|
UTSW |
3 |
99,889,584 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1576:Spag17
|
UTSW |
3 |
99,846,679 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1586:Spag17
|
UTSW |
3 |
99,929,068 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1768:Spag17
|
UTSW |
3 |
99,934,668 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1782:Spag17
|
UTSW |
3 |
99,918,070 (GRCm39) |
missense |
probably benign |
0.02 |
R1789:Spag17
|
UTSW |
3 |
99,846,672 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1945:Spag17
|
UTSW |
3 |
99,847,298 (GRCm39) |
missense |
probably benign |
|
R2065:Spag17
|
UTSW |
3 |
99,920,524 (GRCm39) |
missense |
probably benign |
0.03 |
R2118:Spag17
|
UTSW |
3 |
99,956,556 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2265:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2266:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2267:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2268:Spag17
|
UTSW |
3 |
99,969,182 (GRCm39) |
splice site |
probably null |
|
R2271:Spag17
|
UTSW |
3 |
100,014,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R2389:Spag17
|
UTSW |
3 |
100,014,153 (GRCm39) |
missense |
probably benign |
0.27 |
R2420:Spag17
|
UTSW |
3 |
99,934,935 (GRCm39) |
missense |
probably benign |
|
R2422:Spag17
|
UTSW |
3 |
99,934,935 (GRCm39) |
missense |
probably benign |
|
R2423:Spag17
|
UTSW |
3 |
100,010,772 (GRCm39) |
missense |
probably benign |
|
R3407:Spag17
|
UTSW |
3 |
99,992,615 (GRCm39) |
missense |
probably benign |
0.09 |
R3801:Spag17
|
UTSW |
3 |
99,961,169 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3856:Spag17
|
UTSW |
3 |
100,014,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R4021:Spag17
|
UTSW |
3 |
99,956,546 (GRCm39) |
missense |
probably benign |
0.00 |
R4022:Spag17
|
UTSW |
3 |
99,956,546 (GRCm39) |
missense |
probably benign |
0.00 |
R4408:Spag17
|
UTSW |
3 |
100,010,694 (GRCm39) |
missense |
probably benign |
|
R4468:Spag17
|
UTSW |
3 |
99,992,682 (GRCm39) |
missense |
probably damaging |
0.98 |
R4540:Spag17
|
UTSW |
3 |
99,995,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Spag17
|
UTSW |
3 |
100,010,559 (GRCm39) |
missense |
probably benign |
0.08 |
R4622:Spag17
|
UTSW |
3 |
100,010,559 (GRCm39) |
missense |
probably benign |
0.08 |
R4756:Spag17
|
UTSW |
3 |
100,010,701 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4797:Spag17
|
UTSW |
3 |
99,891,795 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4855:Spag17
|
UTSW |
3 |
99,970,649 (GRCm39) |
missense |
probably benign |
0.02 |
R4887:Spag17
|
UTSW |
3 |
99,958,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Spag17
|
UTSW |
3 |
99,934,939 (GRCm39) |
missense |
probably benign |
|
R5030:Spag17
|
UTSW |
3 |
99,992,657 (GRCm39) |
nonsense |
probably null |
|
R5042:Spag17
|
UTSW |
3 |
99,979,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Spag17
|
UTSW |
3 |
99,987,434 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5195:Spag17
|
UTSW |
3 |
100,008,704 (GRCm39) |
missense |
probably benign |
0.16 |
R5200:Spag17
|
UTSW |
3 |
99,970,787 (GRCm39) |
nonsense |
probably null |
|
R5267:Spag17
|
UTSW |
3 |
99,969,264 (GRCm39) |
missense |
probably damaging |
0.98 |
R5360:Spag17
|
UTSW |
3 |
100,016,726 (GRCm39) |
missense |
probably benign |
0.00 |
R5444:Spag17
|
UTSW |
3 |
99,963,468 (GRCm39) |
missense |
probably benign |
0.06 |
R5498:Spag17
|
UTSW |
3 |
100,010,661 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5503:Spag17
|
UTSW |
3 |
99,934,560 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5540:Spag17
|
UTSW |
3 |
99,963,588 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5547:Spag17
|
UTSW |
3 |
99,963,468 (GRCm39) |
missense |
probably benign |
0.06 |
R5575:Spag17
|
UTSW |
3 |
99,961,138 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5629:Spag17
|
UTSW |
3 |
99,987,435 (GRCm39) |
missense |
probably benign |
0.33 |
R5639:Spag17
|
UTSW |
3 |
99,963,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R5842:Spag17
|
UTSW |
3 |
99,846,566 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5976:Spag17
|
UTSW |
3 |
100,003,107 (GRCm39) |
nonsense |
probably null |
|
R6082:Spag17
|
UTSW |
3 |
100,031,501 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6228:Spag17
|
UTSW |
3 |
99,929,918 (GRCm39) |
missense |
probably benign |
0.33 |
R6254:Spag17
|
UTSW |
3 |
99,972,901 (GRCm39) |
missense |
probably benign |
0.03 |
R6321:Spag17
|
UTSW |
3 |
99,995,743 (GRCm39) |
missense |
probably benign |
0.05 |
R6446:Spag17
|
UTSW |
3 |
100,010,448 (GRCm39) |
missense |
probably benign |
|
R6687:Spag17
|
UTSW |
3 |
100,000,266 (GRCm39) |
missense |
probably benign |
0.07 |
R6853:Spag17
|
UTSW |
3 |
99,920,551 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6946:Spag17
|
UTSW |
3 |
99,911,999 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6953:Spag17
|
UTSW |
3 |
99,942,291 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7038:Spag17
|
UTSW |
3 |
99,891,925 (GRCm39) |
missense |
probably benign |
0.00 |
R7084:Spag17
|
UTSW |
3 |
99,846,586 (GRCm39) |
missense |
probably benign |
0.18 |
R7126:Spag17
|
UTSW |
3 |
100,008,751 (GRCm39) |
missense |
probably benign |
0.00 |
R7144:Spag17
|
UTSW |
3 |
99,934,717 (GRCm39) |
splice site |
probably null |
|
R7198:Spag17
|
UTSW |
3 |
100,002,888 (GRCm39) |
missense |
probably benign |
0.02 |
R7318:Spag17
|
UTSW |
3 |
99,847,299 (GRCm39) |
missense |
probably benign |
0.00 |
R7403:Spag17
|
UTSW |
3 |
99,846,691 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7409:Spag17
|
UTSW |
3 |
99,941,475 (GRCm39) |
missense |
probably benign |
0.00 |
R7537:Spag17
|
UTSW |
3 |
99,846,563 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7609:Spag17
|
UTSW |
3 |
100,002,911 (GRCm39) |
nonsense |
probably null |
|
R7772:Spag17
|
UTSW |
3 |
99,987,434 (GRCm39) |
missense |
probably damaging |
0.98 |
R7842:Spag17
|
UTSW |
3 |
99,961,174 (GRCm39) |
missense |
probably benign |
0.18 |
R7963:Spag17
|
UTSW |
3 |
99,929,954 (GRCm39) |
missense |
probably benign |
0.02 |
R8168:Spag17
|
UTSW |
3 |
99,942,300 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8291:Spag17
|
UTSW |
3 |
99,968,166 (GRCm39) |
missense |
probably benign |
|
R8347:Spag17
|
UTSW |
3 |
99,934,957 (GRCm39) |
missense |
probably benign |
|
R8383:Spag17
|
UTSW |
3 |
99,992,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R8474:Spag17
|
UTSW |
3 |
99,934,586 (GRCm39) |
missense |
probably benign |
0.00 |
R8528:Spag17
|
UTSW |
3 |
100,031,501 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8804:Spag17
|
UTSW |
3 |
99,874,506 (GRCm39) |
missense |
probably benign |
|
R8809:Spag17
|
UTSW |
3 |
99,889,738 (GRCm39) |
missense |
probably benign |
0.33 |
R8818:Spag17
|
UTSW |
3 |
99,920,543 (GRCm39) |
missense |
probably benign |
0.02 |
R8830:Spag17
|
UTSW |
3 |
100,032,751 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8890:Spag17
|
UTSW |
3 |
99,911,994 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9008:Spag17
|
UTSW |
3 |
99,934,942 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9095:Spag17
|
UTSW |
3 |
99,912,092 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9143:Spag17
|
UTSW |
3 |
99,934,906 (GRCm39) |
missense |
probably benign |
|
R9182:Spag17
|
UTSW |
3 |
99,966,158 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9211:Spag17
|
UTSW |
3 |
100,032,614 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9344:Spag17
|
UTSW |
3 |
100,010,793 (GRCm39) |
missense |
probably benign |
0.01 |
R9354:Spag17
|
UTSW |
3 |
99,934,905 (GRCm39) |
missense |
probably benign |
|
R9527:Spag17
|
UTSW |
3 |
99,970,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R9658:Spag17
|
UTSW |
3 |
99,934,932 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9738:Spag17
|
UTSW |
3 |
99,934,526 (GRCm39) |
missense |
possibly damaging |
0.53 |
X0025:Spag17
|
UTSW |
3 |
100,008,767 (GRCm39) |
missense |
probably benign |
0.31 |
Z1088:Spag17
|
UTSW |
3 |
100,002,946 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Spag17
|
UTSW |
3 |
99,920,309 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Spag17
|
UTSW |
3 |
99,995,715 (GRCm39) |
missense |
probably damaging |
1.00 |
|