Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
T |
C |
1: 156,468,979 (GRCm39) |
S748P |
possibly damaging |
Het |
Alppl2 |
T |
C |
1: 87,016,833 (GRCm39) |
D104G |
probably damaging |
Het |
Als2 |
C |
A |
1: 59,206,673 (GRCm39) |
W1590L |
possibly damaging |
Het |
Aopep |
G |
T |
13: 63,338,339 (GRCm39) |
V571F |
possibly damaging |
Het |
Aplf |
C |
T |
6: 87,630,805 (GRCm39) |
W210* |
probably null |
Het |
Ash1l |
A |
T |
3: 88,889,978 (GRCm39) |
H619L |
probably benign |
Het |
Baiap3 |
G |
A |
17: 25,462,814 (GRCm39) |
R1075C |
probably benign |
Het |
Bpifb1 |
G |
T |
2: 154,044,589 (GRCm39) |
V19F |
probably damaging |
Het |
Capn1 |
A |
T |
19: 6,064,349 (GRCm39) |
L50Q |
probably benign |
Het |
Carmil1 |
A |
G |
13: 24,323,318 (GRCm39) |
S245P |
probably damaging |
Het |
Cavin4 |
A |
G |
4: 48,672,479 (GRCm39) |
H308R |
probably benign |
Het |
Cd4 |
C |
T |
6: 124,847,217 (GRCm39) |
V316M |
probably damaging |
Het |
Cdcp1 |
T |
C |
9: 123,002,662 (GRCm39) |
Y803C |
probably damaging |
Het |
Cep295nl |
A |
G |
11: 118,223,815 (GRCm39) |
I343T |
probably benign |
Het |
Cgn |
T |
G |
3: 94,670,392 (GRCm39) |
T1021P |
possibly damaging |
Het |
Cilk1 |
C |
T |
9: 78,016,484 (GRCm39) |
|
probably benign |
Het |
Col6a5 |
A |
G |
9: 105,822,937 (GRCm39) |
V140A |
unknown |
Het |
Cops8 |
T |
C |
1: 90,531,320 (GRCm39) |
|
probably benign |
Het |
Crhbp |
A |
G |
13: 95,580,699 (GRCm39) |
Y54H |
probably damaging |
Het |
Cyp2c29 |
G |
A |
19: 39,275,571 (GRCm39) |
V4I |
probably benign |
Het |
Cyp2j6 |
T |
A |
4: 96,423,708 (GRCm39) |
Y220F |
probably benign |
Het |
D130043K22Rik |
A |
G |
13: 25,077,391 (GRCm39) |
D1008G |
probably damaging |
Het |
Ddx47 |
T |
A |
6: 135,000,336 (GRCm39) |
V444E |
possibly damaging |
Het |
Dnttip2 |
T |
A |
3: 122,070,181 (GRCm39) |
C465* |
probably null |
Het |
Dst |
C |
A |
1: 34,221,879 (GRCm39) |
S2561* |
probably null |
Het |
Dstyk |
T |
C |
1: 132,381,847 (GRCm39) |
S534P |
probably benign |
Het |
Eif4e |
A |
G |
3: 138,232,943 (GRCm39) |
|
probably benign |
Het |
Eipr1 |
C |
T |
12: 28,801,817 (GRCm39) |
|
probably benign |
Het |
Fastkd2 |
T |
A |
1: 63,771,032 (GRCm39) |
D129E |
possibly damaging |
Het |
Fndc3b |
C |
T |
3: 27,555,618 (GRCm39) |
G312D |
probably benign |
Het |
Gab2 |
T |
A |
7: 96,952,290 (GRCm39) |
I562N |
probably damaging |
Het |
Gata5 |
C |
A |
2: 179,975,685 (GRCm39) |
D160Y |
possibly damaging |
Het |
Gcn1 |
G |
A |
5: 115,749,203 (GRCm39) |
V1912I |
probably damaging |
Het |
Gdf5 |
C |
A |
2: 155,786,655 (GRCm39) |
Q107H |
probably damaging |
Het |
Gdpd1 |
A |
G |
11: 86,926,118 (GRCm39) |
Y276H |
probably damaging |
Het |
Gins1 |
A |
G |
2: 150,759,791 (GRCm39) |
Y81C |
probably damaging |
Het |
Gm28360 |
T |
C |
1: 117,781,329 (GRCm39) |
C107R |
probably damaging |
Het |
Hadha |
T |
C |
5: 30,324,998 (GRCm39) |
|
probably null |
Het |
Hcn4 |
A |
T |
9: 58,730,867 (GRCm39) |
I25F |
unknown |
Het |
Hectd4 |
A |
G |
5: 121,437,660 (GRCm39) |
Y1095C |
possibly damaging |
Het |
Hsp90b1 |
A |
T |
10: 86,531,730 (GRCm39) |
L73Q |
probably damaging |
Het |
Hspa12a |
A |
G |
19: 58,793,132 (GRCm39) |
V351A |
probably damaging |
Het |
Htr1b |
T |
A |
9: 81,514,296 (GRCm39) |
M104L |
probably benign |
Het |
Igf2r |
T |
C |
17: 12,917,212 (GRCm39) |
T1563A |
probably benign |
Het |
Kif13a |
C |
T |
13: 46,905,931 (GRCm39) |
V671M |
possibly damaging |
Het |
Liph |
A |
T |
16: 21,795,009 (GRCm39) |
V201E |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,221,759 (GRCm39) |
D196G |
probably damaging |
Het |
Med15 |
C |
T |
16: 17,470,591 (GRCm39) |
D589N |
possibly damaging |
Het |
Mknk1 |
A |
G |
4: 115,714,307 (GRCm39) |
D26G |
probably damaging |
Het |
Mpi |
T |
C |
9: 57,452,500 (GRCm39) |
D344G |
probably damaging |
Het |
Mrc2 |
A |
G |
11: 105,223,062 (GRCm39) |
E435G |
possibly damaging |
Het |
Mrps5 |
A |
G |
2: 127,442,786 (GRCm39) |
E285G |
probably damaging |
Het |
Ms4a20 |
A |
T |
19: 11,087,675 (GRCm39) |
F85L |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,531,764 (GRCm39) |
M6197L |
probably damaging |
Het |
Myo3b |
A |
T |
2: 69,925,552 (GRCm39) |
E34D |
probably benign |
Het |
Nsd3 |
T |
C |
8: 26,131,279 (GRCm39) |
S215P |
probably damaging |
Het |
Nsmce2 |
T |
A |
15: 59,368,679 (GRCm39) |
|
probably benign |
Het |
Ntan1 |
T |
C |
16: 13,644,774 (GRCm39) |
S37P |
probably benign |
Het |
Nup210l |
T |
A |
3: 90,067,254 (GRCm39) |
Y765N |
probably damaging |
Het |
Or10q12 |
A |
T |
19: 13,745,715 (GRCm39) |
D3V |
probably benign |
Het |
Or2aa1 |
T |
C |
11: 59,480,408 (GRCm39) |
Y169C |
possibly damaging |
Het |
Or4s2b |
A |
T |
2: 88,509,085 (GRCm39) |
R288S |
probably damaging |
Het |
Or7g30 |
A |
C |
9: 19,352,888 (GRCm39) |
L226F |
possibly damaging |
Het |
Pald1 |
T |
C |
10: 61,175,078 (GRCm39) |
H724R |
probably benign |
Het |
Pcdhb7 |
A |
T |
18: 37,475,257 (GRCm39) |
D131V |
possibly damaging |
Het |
Pds5b |
G |
T |
5: 150,724,225 (GRCm39) |
R1269S |
probably benign |
Het |
Pikfyve |
T |
C |
1: 65,273,520 (GRCm39) |
V645A |
probably damaging |
Het |
Plag1 |
G |
T |
4: 3,904,676 (GRCm39) |
H172N |
probably damaging |
Het |
Plch2 |
G |
C |
4: 155,074,489 (GRCm39) |
|
probably null |
Het |
Plxnb1 |
T |
A |
9: 108,929,453 (GRCm39) |
V103E |
probably damaging |
Het |
Prpf8 |
T |
A |
11: 75,386,984 (GRCm39) |
M1143K |
probably benign |
Het |
Ptpn18 |
T |
A |
1: 34,498,906 (GRCm39) |
M1K |
probably null |
Het |
Rasgrf2 |
G |
A |
13: 92,130,952 (GRCm39) |
T703I |
possibly damaging |
Het |
Rassf6 |
A |
T |
5: 90,757,584 (GRCm39) |
H125Q |
probably benign |
Het |
Sdad1 |
A |
G |
5: 92,446,049 (GRCm39) |
|
probably null |
Het |
Sf3a3 |
T |
A |
4: 124,622,219 (GRCm39) |
F426L |
probably benign |
Het |
Sgsm3 |
T |
C |
15: 80,892,576 (GRCm39) |
F6L |
possibly damaging |
Het |
Slc14a2 |
A |
T |
18: 78,202,252 (GRCm39) |
I626N |
probably damaging |
Het |
Slc17a8 |
T |
C |
10: 89,436,083 (GRCm39) |
N165S |
probably benign |
Het |
Slc41a1 |
C |
A |
1: 131,769,795 (GRCm39) |
A305D |
possibly damaging |
Het |
Smyd4 |
C |
A |
11: 75,281,340 (GRCm39) |
P271Q |
probably damaging |
Het |
Spata2 |
A |
T |
2: 167,327,283 (GRCm39) |
V38E |
possibly damaging |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
Syt14 |
T |
A |
1: 192,665,966 (GRCm39) |
|
probably benign |
Het |
Tbx21 |
A |
G |
11: 96,990,597 (GRCm39) |
S329P |
probably damaging |
Het |
Tex2 |
A |
T |
11: 106,402,726 (GRCm39) |
|
probably null |
Het |
Tmem62 |
A |
G |
2: 120,824,058 (GRCm39) |
I244M |
possibly damaging |
Het |
Tnks |
A |
T |
8: 35,318,790 (GRCm39) |
N830K |
probably damaging |
Het |
Tox2 |
A |
G |
2: 163,156,264 (GRCm39) |
E145G |
probably damaging |
Het |
Tpcn1 |
T |
C |
5: 120,723,342 (GRCm39) |
D7G |
probably damaging |
Het |
Ttc28 |
T |
A |
5: 111,414,445 (GRCm39) |
M1320K |
probably benign |
Het |
Tubgcp5 |
T |
G |
7: 55,455,114 (GRCm39) |
V270G |
probably damaging |
Het |
Unc5a |
A |
G |
13: 55,152,297 (GRCm39) |
R62G |
probably damaging |
Het |
Unc5d |
A |
G |
8: 29,205,749 (GRCm39) |
|
probably null |
Het |
Utrn |
T |
C |
10: 12,558,082 (GRCm39) |
H1459R |
probably damaging |
Het |
Vmn2r100 |
T |
A |
17: 19,725,263 (GRCm39) |
L64Q |
possibly damaging |
Het |
Wdr55 |
T |
G |
18: 36,893,473 (GRCm39) |
L45R |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,816,357 (GRCm39) |
Y306H |
probably damaging |
Het |
Zfp398 |
G |
T |
6: 47,843,243 (GRCm39) |
D300Y |
probably damaging |
Het |
Zfp407 |
A |
G |
18: 84,579,982 (GRCm39) |
V377A |
probably damaging |
Het |
Zfp457 |
G |
A |
13: 67,441,997 (GRCm39) |
H97Y |
probably benign |
Het |
Zfp467 |
T |
C |
6: 48,415,072 (GRCm39) |
T527A |
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 |
|
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 |
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 |
|