Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
T |
A |
10: 28,857,575 (GRCm39) |
Q194L |
probably damaging |
Het |
Acsf2 |
T |
A |
11: 94,449,699 (GRCm39) |
K574* |
probably null |
Het |
Adam22 |
T |
C |
5: 8,171,108 (GRCm39) |
E614G |
probably damaging |
Het |
Ap4e1 |
T |
C |
2: 126,889,083 (GRCm39) |
|
probably null |
Het |
Arid3c |
T |
A |
4: 41,724,744 (GRCm39) |
I364F |
probably damaging |
Het |
Bcan |
T |
A |
3: 87,900,401 (GRCm39) |
S611C |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,909,966 (GRCm39) |
V1453A |
probably benign |
Het |
Carnmt1 |
T |
C |
19: 18,680,734 (GRCm39) |
L336P |
probably damaging |
Het |
Ccdc146 |
C |
A |
5: 21,604,719 (GRCm39) |
D40Y |
probably benign |
Het |
Ccdc83 |
C |
T |
7: 89,873,285 (GRCm39) |
V357I |
probably damaging |
Het |
Cdh22 |
A |
T |
2: 164,985,767 (GRCm39) |
|
probably null |
Het |
Cdk5rap2 |
A |
C |
4: 70,184,915 (GRCm39) |
S1178R |
probably benign |
Het |
Cdkl3 |
T |
C |
11: 51,923,322 (GRCm39) |
V45A |
probably benign |
Het |
Chd7 |
A |
G |
4: 8,785,532 (GRCm39) |
D612G |
probably damaging |
Het |
Chst11 |
T |
C |
10: 83,027,004 (GRCm39) |
Y144H |
probably damaging |
Het |
Cops6 |
A |
T |
5: 138,159,403 (GRCm39) |
N10I |
probably benign |
Het |
Cyfip1 |
G |
T |
7: 55,549,705 (GRCm39) |
R624L |
probably null |
Het |
Cyp27a1 |
A |
G |
1: 74,775,846 (GRCm39) |
N344D |
probably damaging |
Het |
Des |
T |
G |
1: 75,340,137 (GRCm39) |
M348R |
probably damaging |
Het |
Dis3l |
T |
A |
9: 64,238,165 (GRCm39) |
D109V |
probably damaging |
Het |
Disp3 |
C |
T |
4: 148,356,059 (GRCm39) |
R267Q |
possibly damaging |
Het |
Dnah3 |
T |
A |
7: 119,574,352 (GRCm39) |
I2136F |
probably benign |
Het |
Dnah9 |
T |
C |
11: 66,003,188 (GRCm39) |
D872G |
probably benign |
Het |
Dnajb14 |
G |
A |
3: 137,591,141 (GRCm39) |
G31S |
probably benign |
Het |
Dop1a |
T |
G |
9: 86,376,471 (GRCm39) |
V235G |
probably damaging |
Het |
Efcab6 |
T |
A |
15: 83,831,200 (GRCm39) |
R571S |
probably benign |
Het |
Emsy |
T |
G |
7: 98,275,830 (GRCm39) |
K352N |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,238,047 (GRCm39) |
N814S |
probably damaging |
Het |
Fgfbp1 |
T |
A |
5: 44,136,672 (GRCm39) |
M207L |
probably benign |
Het |
Filip1 |
T |
C |
9: 79,727,212 (GRCm39) |
E469G |
probably damaging |
Het |
Garem2 |
T |
G |
5: 30,321,972 (GRCm39) |
L777R |
probably damaging |
Het |
Garin5b |
T |
A |
7: 4,761,186 (GRCm39) |
T509S |
probably benign |
Het |
Hkdc1 |
T |
C |
10: 62,253,677 (GRCm39) |
T35A |
probably benign |
Het |
Hps6 |
C |
T |
19: 45,994,121 (GRCm39) |
A686V |
possibly damaging |
Het |
Irs1 |
T |
C |
1: 82,266,180 (GRCm39) |
S679G |
probably benign |
Het |
Ism1 |
T |
A |
2: 139,599,293 (GRCm39) |
I415N |
probably damaging |
Het |
Kdm1b |
TCATTGTCC |
TCATTGTCCATTGTCC |
13: 47,217,564 (GRCm39) |
|
probably null |
Het |
Kpna1 |
G |
A |
16: 35,851,591 (GRCm39) |
A392T |
probably damaging |
Het |
Lipa |
T |
A |
19: 34,488,290 (GRCm39) |
R119* |
probably null |
Het |
Lrrc37 |
T |
C |
11: 103,505,033 (GRCm39) |
T2312A |
possibly damaging |
Het |
Mocs1 |
A |
T |
17: 49,756,137 (GRCm39) |
K198M |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Msh5 |
A |
G |
17: 35,263,366 (GRCm39) |
I154T |
probably benign |
Het |
Muc6 |
T |
A |
7: 141,217,423 (GRCm39) |
T2417S |
possibly damaging |
Het |
Ncbp2 |
T |
C |
16: 31,775,769 (GRCm39) |
Y138H |
probably damaging |
Het |
Ndufv1 |
C |
A |
19: 4,058,347 (GRCm39) |
R359L |
probably benign |
Het |
Neu3 |
G |
C |
7: 99,462,650 (GRCm39) |
R358G |
probably benign |
Het |
Ntrk3 |
A |
C |
7: 78,166,471 (GRCm39) |
|
probably null |
Het |
Or1n1 |
G |
A |
2: 36,749,637 (GRCm39) |
S241F |
probably damaging |
Het |
Or8b12i |
T |
A |
9: 20,082,705 (GRCm39) |
H54L |
possibly damaging |
Het |
Or8j3 |
A |
G |
2: 86,028,161 (GRCm39) |
F312L |
probably benign |
Het |
Pik3c2b |
T |
C |
1: 133,031,166 (GRCm39) |
S1491P |
probably benign |
Het |
Plb1 |
G |
T |
5: 32,450,586 (GRCm39) |
D376Y |
probably damaging |
Het |
Plch1 |
T |
A |
3: 63,651,956 (GRCm39) |
K378N |
probably damaging |
Het |
Plekhm1 |
C |
T |
11: 103,277,948 (GRCm39) |
E383K |
probably benign |
Het |
Plxnb1 |
T |
C |
9: 108,931,776 (GRCm39) |
|
probably null |
Het |
Prkdc |
A |
G |
16: 15,472,681 (GRCm39) |
|
probably null |
Het |
Prpf8 |
T |
A |
11: 75,386,189 (GRCm39) |
V946E |
probably damaging |
Het |
Psma5-ps |
A |
G |
10: 85,149,595 (GRCm39) |
|
noncoding transcript |
Het |
Ptprh |
C |
A |
7: 4,606,132 (GRCm39) |
|
probably benign |
Het |
Rngtt |
T |
A |
4: 33,500,302 (GRCm39) |
C565* |
probably null |
Het |
Sacs |
A |
G |
14: 61,442,109 (GRCm39) |
H1385R |
probably benign |
Het |
Sec24a |
A |
G |
11: 51,607,277 (GRCm39) |
S656P |
possibly damaging |
Het |
Serpinb13 |
A |
T |
1: 106,926,756 (GRCm39) |
I251L |
possibly damaging |
Het |
Shc1 |
G |
A |
3: 89,330,849 (GRCm39) |
G91S |
probably damaging |
Het |
Sin3b |
T |
A |
8: 73,460,047 (GRCm39) |
N211K |
probably benign |
Het |
Slc22a2 |
A |
T |
17: 12,805,692 (GRCm39) |
M148L |
probably benign |
Het |
Slc3a1 |
G |
A |
17: 85,371,220 (GRCm39) |
V591I |
probably benign |
Het |
Slc47a2 |
A |
T |
11: 61,219,352 (GRCm39) |
|
probably null |
Het |
Specc1l |
C |
T |
10: 75,081,438 (GRCm39) |
S278F |
probably damaging |
Het |
Sphkap |
T |
A |
1: 83,234,942 (GRCm39) |
D1628V |
probably damaging |
Het |
Themis3 |
C |
T |
17: 66,862,699 (GRCm39) |
V420I |
possibly damaging |
Het |
Ttc39d |
A |
G |
17: 80,524,675 (GRCm39) |
K445E |
probably damaging |
Het |
U2surp |
T |
C |
9: 95,373,473 (GRCm39) |
E232G |
possibly damaging |
Het |
Usp25 |
T |
A |
16: 76,873,317 (GRCm39) |
F458L |
probably damaging |
Het |
Usp7 |
T |
C |
16: 8,516,333 (GRCm39) |
S649G |
probably benign |
Het |
Vmn1r10 |
A |
G |
6: 57,091,088 (GRCm39) |
T227A |
probably damaging |
Het |
Zcchc12 |
C |
T |
X: 35,462,118 (GRCm39) |
T345M |
possibly damaging |
Het |
Zfp444 |
T |
C |
7: 6,192,554 (GRCm39) |
C191R |
probably damaging |
Het |
Zfp729b |
A |
T |
13: 67,740,352 (GRCm39) |
C648S |
probably damaging |
Het |
Zfp799 |
A |
G |
17: 33,040,777 (GRCm39) |
Y58H |
probably damaging |
Het |
Zfp938 |
C |
T |
10: 82,061,381 (GRCm39) |
G413D |
probably damaging |
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 |
|
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 |
99,934,547 (GRCm39) |
missense |
possibly damaging |
0.73 |
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 |
|