Other mutations in this stock |
Total: 142 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
C |
6: 128,523,210 (GRCm39) |
|
probably null |
Het |
Aars1 |
A |
G |
8: 111,768,974 (GRCm39) |
Y258C |
probably damaging |
Het |
Acaa2 |
A |
T |
18: 74,938,943 (GRCm39) |
Y376F |
probably benign |
Het |
Adcy1 |
C |
T |
11: 7,119,543 (GRCm39) |
S1062F |
possibly damaging |
Het |
Adgrb3 |
A |
T |
1: 25,571,000 (GRCm39) |
C492* |
probably null |
Het |
Adgrg6 |
A |
G |
10: 14,411,636 (GRCm39) |
F22S |
probably benign |
Het |
Adh1 |
A |
G |
3: 137,994,648 (GRCm39) |
|
probably null |
Het |
Afm |
T |
A |
5: 90,699,259 (GRCm39) |
C568S |
probably benign |
Het |
Ago4 |
C |
T |
4: 126,405,257 (GRCm39) |
E439K |
probably benign |
Het |
Aifm2 |
T |
G |
10: 61,563,496 (GRCm39) |
V122G |
possibly damaging |
Het |
Akap6 |
A |
G |
12: 53,189,357 (GRCm39) |
N2257S |
probably benign |
Het |
Ap3m2 |
A |
G |
8: 23,294,026 (GRCm39) |
I8T |
probably benign |
Het |
Apc2 |
C |
A |
10: 80,147,228 (GRCm39) |
L761I |
probably damaging |
Het |
Asap2 |
A |
G |
12: 21,162,052 (GRCm39) |
D3G |
probably benign |
Het |
Asxl1 |
T |
C |
2: 153,243,913 (GRCm39) |
C1489R |
probably damaging |
Het |
Atm |
T |
G |
9: 53,364,737 (GRCm39) |
|
probably null |
Het |
Bmal1 |
C |
A |
7: 112,898,415 (GRCm39) |
T281K |
probably benign |
Het |
Bpifa6 |
C |
A |
2: 153,828,353 (GRCm39) |
A153E |
probably damaging |
Het |
Cav2 |
A |
G |
6: 17,282,059 (GRCm39) |
T106A |
probably benign |
Het |
Cavin4 |
A |
G |
4: 48,663,631 (GRCm39) |
N4D |
probably benign |
Het |
Cenpc1 |
T |
C |
5: 86,194,358 (GRCm39) |
N136S |
probably benign |
Het |
Cfap45 |
T |
A |
1: 172,365,910 (GRCm39) |
|
probably null |
Het |
Col3a1 |
G |
A |
1: 45,366,807 (GRCm39) |
|
probably null |
Het |
Crocc2 |
C |
T |
1: 93,121,809 (GRCm39) |
L653F |
probably damaging |
Het |
Cry2 |
A |
G |
2: 92,244,009 (GRCm39) |
L388P |
probably damaging |
Het |
Cstb |
T |
C |
10: 78,262,822 (GRCm39) |
F43S |
probably damaging |
Het |
Ctcfl |
A |
G |
2: 172,954,051 (GRCm39) |
Y349H |
probably damaging |
Het |
Ctu2 |
T |
A |
8: 123,208,238 (GRCm39) |
V485D |
probably damaging |
Het |
Cwc25 |
A |
C |
11: 97,638,823 (GRCm39) |
L367R |
possibly damaging |
Het |
Dock4 |
T |
A |
12: 40,838,243 (GRCm39) |
H1061Q |
possibly damaging |
Het |
Dpy19l3 |
C |
A |
7: 35,452,067 (GRCm39) |
V26L |
probably benign |
Het |
Efcab3 |
T |
C |
11: 104,605,528 (GRCm39) |
I298T |
probably benign |
Het |
Elmo1 |
A |
T |
13: 20,465,105 (GRCm39) |
I225F |
probably benign |
Het |
Ep300 |
T |
C |
15: 81,534,746 (GRCm39) |
S2268P |
probably damaging |
Het |
F2r |
C |
T |
13: 95,754,836 (GRCm39) |
C16Y |
probably damaging |
Het |
Fbxo33 |
C |
A |
12: 59,251,157 (GRCm39) |
E453* |
probably null |
Het |
Flot1 |
A |
T |
17: 36,136,405 (GRCm39) |
D186V |
probably damaging |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,436,769 (GRCm39) |
|
probably benign |
Het |
Fras1 |
T |
C |
5: 96,744,644 (GRCm39) |
C560R |
probably damaging |
Het |
Get3 |
A |
T |
8: 85,746,492 (GRCm39) |
F119I |
probably benign |
Het |
Gfi1 |
A |
T |
5: 107,871,095 (GRCm39) |
S165T |
possibly damaging |
Het |
Gli2 |
T |
C |
1: 118,776,222 (GRCm39) |
D400G |
probably damaging |
Het |
Gm37240 |
T |
A |
3: 84,879,944 (GRCm39) |
|
probably null |
Het |
Gml |
C |
T |
15: 74,688,970 (GRCm39) |
V27I |
possibly damaging |
Het |
Htt |
A |
T |
5: 34,961,143 (GRCm39) |
I257F |
probably benign |
Het |
Hycc2 |
T |
C |
1: 58,569,193 (GRCm39) |
K462R |
probably benign |
Het |
Ier5 |
C |
T |
1: 154,974,438 (GRCm39) |
V247M |
probably damaging |
Het |
Ift46 |
C |
T |
9: 44,689,892 (GRCm39) |
|
probably benign |
Het |
Il12b |
A |
G |
11: 44,298,721 (GRCm39) |
T59A |
probably benign |
Het |
Insr |
A |
G |
8: 3,248,231 (GRCm39) |
L438P |
probably damaging |
Het |
Iqgap2 |
C |
T |
13: 95,869,398 (GRCm39) |
|
probably null |
Het |
Irx4 |
A |
T |
13: 73,415,672 (GRCm39) |
T154S |
possibly damaging |
Het |
Itgbl1 |
A |
G |
14: 124,094,901 (GRCm39) |
K309E |
probably benign |
Het |
Kcns2 |
T |
A |
15: 34,839,849 (GRCm39) |
L404* |
probably null |
Het |
Kif2c |
T |
C |
4: 117,019,226 (GRCm39) |
E644G |
possibly damaging |
Het |
Klhl22 |
T |
C |
16: 17,594,669 (GRCm39) |
L266P |
probably damaging |
Het |
Krt71 |
T |
A |
15: 101,646,764 (GRCm39) |
K315* |
probably null |
Het |
Lca5 |
T |
C |
9: 83,277,583 (GRCm39) |
N587S |
probably benign |
Het |
Lrp1b |
T |
A |
2: 41,185,681 (GRCm39) |
M1459L |
|
Het |
Lrrtm2 |
T |
C |
18: 35,346,645 (GRCm39) |
K219R |
probably damaging |
Het |
Mcmbp |
T |
C |
7: 128,306,241 (GRCm39) |
D459G |
probably damaging |
Het |
Megf8 |
A |
G |
7: 25,048,367 (GRCm39) |
H1680R |
probably damaging |
Het |
Mia3 |
A |
G |
1: 183,115,629 (GRCm39) |
S301P |
probably benign |
Het |
Mtrr |
A |
G |
13: 68,712,521 (GRCm39) |
Y622H |
probably damaging |
Het |
Myo7b |
T |
A |
18: 32,099,292 (GRCm39) |
Q1710L |
probably damaging |
Het |
Nab1 |
T |
C |
1: 52,520,154 (GRCm39) |
N276D |
probably damaging |
Het |
Nalcn |
C |
T |
14: 123,540,302 (GRCm39) |
R1127H |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,324,220 (GRCm39) |
I110N |
probably damaging |
Het |
Nfe2l3 |
C |
T |
6: 51,434,276 (GRCm39) |
Q279* |
probably null |
Het |
Nlrp9c |
C |
T |
7: 26,064,440 (GRCm39) |
E963K |
probably benign |
Het |
Nsmaf |
A |
G |
4: 6,416,586 (GRCm39) |
V569A |
probably benign |
Het |
Or10ak14 |
T |
C |
4: 118,611,372 (GRCm39) |
Y123C |
possibly damaging |
Het |
Or13c3 |
C |
T |
4: 52,856,421 (GRCm39) |
V31I |
probably benign |
Het |
Or52a5b |
T |
A |
7: 103,417,137 (GRCm39) |
I156F |
probably benign |
Het |
Or52n5 |
A |
T |
7: 104,588,638 (GRCm39) |
I302F |
probably benign |
Het |
Or5ac17 |
T |
A |
16: 59,036,283 (GRCm39) |
D231V |
probably benign |
Het |
Or5p4 |
T |
C |
7: 107,680,399 (GRCm39) |
S133P |
not run |
Het |
Or7e166 |
A |
T |
9: 19,624,183 (GRCm39) |
D20V |
probably damaging |
Het |
Or7g32 |
T |
A |
9: 19,408,398 (GRCm39) |
M118K |
probably damaging |
Het |
Or8d1b |
T |
A |
9: 38,887,017 (GRCm39) |
V15E |
probably benign |
Het |
Or8k28 |
T |
C |
2: 86,286,412 (GRCm39) |
T68A |
probably benign |
Het |
Paf1 |
A |
G |
7: 28,096,353 (GRCm39) |
Y322C |
probably damaging |
Het |
Pcdha2 |
C |
A |
18: 37,072,438 (GRCm39) |
A23D |
possibly damaging |
Het |
Pcdhb6 |
G |
A |
18: 37,468,225 (GRCm39) |
C382Y |
probably damaging |
Het |
Pdzd7 |
C |
T |
19: 45,034,045 (GRCm39) |
G13D |
probably damaging |
Het |
Pik3r2 |
T |
C |
8: 71,222,025 (GRCm39) |
N586S |
probably benign |
Het |
Pik3r3 |
T |
A |
4: 116,128,027 (GRCm39) |
D119E |
probably benign |
Het |
Pkd2l1 |
T |
A |
19: 44,142,154 (GRCm39) |
I535F |
probably benign |
Het |
Ppfia3 |
T |
C |
7: 45,010,870 (GRCm39) |
|
probably null |
Het |
Ppl |
T |
A |
16: 4,930,860 (GRCm39) |
Q53L |
possibly damaging |
Het |
Rimbp3 |
T |
G |
16: 17,029,068 (GRCm39) |
S831A |
probably benign |
Het |
Rnps1 |
A |
G |
17: 24,637,504 (GRCm39) |
T49A |
unknown |
Het |
Rpl7a |
T |
A |
2: 26,802,019 (GRCm39) |
|
probably null |
Het |
Rrm2b |
T |
A |
15: 37,931,891 (GRCm39) |
E248D |
probably benign |
Het |
Sdhaf4 |
A |
G |
1: 24,035,439 (GRCm39) |
F70L |
probably damaging |
Het |
Sel1l3 |
A |
T |
5: 53,273,751 (GRCm39) |
S1038R |
probably benign |
Het |
Selenoo |
T |
A |
15: 88,973,681 (GRCm39) |
F124I |
probably benign |
Het |
Setbp1 |
A |
T |
18: 78,900,701 (GRCm39) |
Y989N |
probably damaging |
Het |
Slc1a7 |
A |
G |
4: 107,859,400 (GRCm39) |
E163G |
possibly damaging |
Het |
Slc22a2 |
T |
C |
17: 12,831,278 (GRCm39) |
F356S |
probably damaging |
Het |
Slc24a4 |
C |
T |
12: 102,205,435 (GRCm39) |
P378L |
probably benign |
Het |
Slc4a1ap |
A |
G |
5: 31,684,871 (GRCm39) |
D169G |
probably benign |
Het |
Slc4a7 |
T |
A |
14: 14,757,421 (GRCm38) |
V422D |
probably damaging |
Het |
Slitrk6 |
T |
C |
14: 110,987,295 (GRCm39) |
Y804C |
probably damaging |
Het |
Smarcad1 |
T |
A |
6: 65,087,360 (GRCm39) |
H906Q |
probably benign |
Het |
Smn1 |
A |
G |
13: 100,264,373 (GRCm39) |
T109A |
probably damaging |
Het |
Sntb2 |
A |
G |
8: 107,707,944 (GRCm39) |
N236S |
probably damaging |
Het |
Spg11 |
C |
A |
2: 121,888,910 (GRCm39) |
G2154W |
probably damaging |
Het |
Srsf6 |
T |
C |
2: 162,776,489 (GRCm39) |
S278P |
unknown |
Het |
Stag3 |
G |
A |
5: 138,280,222 (GRCm39) |
R29H |
probably benign |
Het |
Stambp |
C |
T |
6: 83,540,888 (GRCm39) |
V98I |
not run |
Het |
Styxl2 |
G |
T |
1: 165,939,632 (GRCm39) |
S58* |
probably null |
Het |
Suco |
T |
C |
1: 161,689,780 (GRCm39) |
D89G |
possibly damaging |
Het |
Suox |
C |
T |
10: 128,506,910 (GRCm39) |
V373I |
probably benign |
Het |
Sv2b |
T |
A |
7: 74,797,476 (GRCm39) |
|
probably null |
Het |
Tatdn2 |
T |
C |
6: 113,681,662 (GRCm39) |
L565P |
probably damaging |
Het |
Tbpl2 |
T |
A |
2: 23,984,712 (GRCm39) |
E145V |
probably benign |
Het |
Tlr1 |
T |
C |
5: 65,082,571 (GRCm39) |
I669V |
not run |
Het |
Tmc1 |
A |
T |
19: 20,845,753 (GRCm39) |
F157I |
probably damaging |
Het |
Tmem26 |
T |
G |
10: 68,559,922 (GRCm39) |
|
probably null |
Het |
Tmem33 |
A |
T |
5: 67,443,476 (GRCm39) |
I218F |
probably benign |
Het |
Tmem94 |
T |
A |
11: 115,685,000 (GRCm39) |
D862E |
probably damaging |
Het |
Tnr |
T |
C |
1: 159,712,432 (GRCm39) |
|
probably null |
Het |
Tnrc6c |
T |
C |
11: 117,632,606 (GRCm39) |
S1103P |
probably benign |
Het |
Tomm70a |
T |
A |
16: 56,966,407 (GRCm39) |
Y453* |
probably null |
Het |
Trabd |
C |
A |
15: 88,969,493 (GRCm39) |
R229S |
possibly damaging |
Het |
Trappc10 |
T |
C |
10: 78,029,252 (GRCm39) |
D1095G |
probably damaging |
Het |
Trim27 |
A |
G |
13: 21,376,631 (GRCm39) |
T460A |
possibly damaging |
Het |
Tsen54 |
T |
G |
11: 115,712,531 (GRCm39) |
D433E |
probably benign |
Het |
Ubap2 |
A |
G |
4: 41,235,515 (GRCm39) |
|
probably null |
Het |
Vat1l |
A |
T |
8: 115,016,132 (GRCm39) |
N341Y |
possibly damaging |
Het |
Vmn2r82 |
C |
G |
10: 79,232,276 (GRCm39) |
Y758* |
probably null |
Het |
Vps16 |
T |
G |
2: 130,280,099 (GRCm39) |
V108G |
probably damaging |
Het |
Vps53 |
T |
A |
11: 75,967,900 (GRCm39) |
I585F |
possibly damaging |
Het |
Wrnip1 |
G |
A |
13: 33,000,264 (GRCm39) |
V424M |
probably benign |
Het |
Yif1a |
G |
A |
19: 5,139,818 (GRCm39) |
V88M |
possibly damaging |
Het |
Zfat |
T |
C |
15: 68,052,969 (GRCm39) |
Y275C |
probably damaging |
Het |
Zfhx3 |
A |
G |
8: 109,519,880 (GRCm39) |
E334G |
probably damaging |
Het |
Zfp277 |
T |
C |
12: 40,365,852 (GRCm39) |
D539G |
possibly damaging |
Het |
Zfp292 |
A |
T |
4: 34,808,384 (GRCm39) |
N1558K |
probably benign |
Het |
Zfp3 |
A |
G |
11: 70,662,899 (GRCm39) |
K286R |
probably benign |
Het |
Zfp366 |
T |
C |
13: 99,366,023 (GRCm39) |
C395R |
probably damaging |
Het |
|
Other mutations in Spag9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00422:Spag9
|
APN |
11 |
93,988,692 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01776:Spag9
|
APN |
11 |
94,007,553 (GRCm39) |
splice site |
probably benign |
|
IGL02095:Spag9
|
APN |
11 |
93,999,408 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02307:Spag9
|
APN |
11 |
93,992,986 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02417:Spag9
|
APN |
11 |
94,007,567 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02480:Spag9
|
APN |
11 |
93,999,413 (GRCm39) |
nonsense |
probably null |
|
IGL02864:Spag9
|
APN |
11 |
93,997,487 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02976:Spag9
|
APN |
11 |
93,974,779 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02979:Spag9
|
APN |
11 |
93,988,190 (GRCm39) |
missense |
probably benign |
|
IGL03349:Spag9
|
APN |
11 |
93,984,335 (GRCm39) |
missense |
possibly damaging |
0.51 |
dazzle
|
UTSW |
11 |
93,984,450 (GRCm39) |
nonsense |
probably null |
|
R0128:Spag9
|
UTSW |
11 |
93,984,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R0418:Spag9
|
UTSW |
11 |
93,982,579 (GRCm39) |
splice site |
probably benign |
|
R1463:Spag9
|
UTSW |
11 |
94,007,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R1593:Spag9
|
UTSW |
11 |
93,988,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Spag9
|
UTSW |
11 |
93,939,365 (GRCm39) |
missense |
probably damaging |
0.99 |
R1649:Spag9
|
UTSW |
11 |
93,999,278 (GRCm39) |
splice site |
probably null |
|
R1697:Spag9
|
UTSW |
11 |
93,887,391 (GRCm39) |
missense |
probably benign |
0.00 |
R1952:Spag9
|
UTSW |
11 |
93,988,184 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2011:Spag9
|
UTSW |
11 |
93,983,201 (GRCm39) |
nonsense |
probably null |
|
R2012:Spag9
|
UTSW |
11 |
93,983,201 (GRCm39) |
nonsense |
probably null |
|
R2351:Spag9
|
UTSW |
11 |
93,983,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Spag9
|
UTSW |
11 |
94,007,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R3027:Spag9
|
UTSW |
11 |
93,977,203 (GRCm39) |
missense |
probably null |
1.00 |
R3766:Spag9
|
UTSW |
11 |
93,951,109 (GRCm39) |
intron |
probably benign |
|
R3777:Spag9
|
UTSW |
11 |
93,989,852 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3937:Spag9
|
UTSW |
11 |
93,935,305 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3937:Spag9
|
UTSW |
11 |
93,935,243 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4417:Spag9
|
UTSW |
11 |
93,951,172 (GRCm39) |
intron |
probably benign |
|
R4445:Spag9
|
UTSW |
11 |
93,988,079 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4711:Spag9
|
UTSW |
11 |
94,005,177 (GRCm39) |
critical splice donor site |
probably null |
|
R4799:Spag9
|
UTSW |
11 |
93,939,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R4799:Spag9
|
UTSW |
11 |
93,939,342 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4816:Spag9
|
UTSW |
11 |
93,939,425 (GRCm39) |
intron |
probably benign |
|
R4843:Spag9
|
UTSW |
11 |
93,988,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R5020:Spag9
|
UTSW |
11 |
93,988,612 (GRCm39) |
missense |
probably benign |
0.08 |
R5119:Spag9
|
UTSW |
11 |
94,013,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5298:Spag9
|
UTSW |
11 |
93,990,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R5304:Spag9
|
UTSW |
11 |
93,959,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5305:Spag9
|
UTSW |
11 |
93,959,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5395:Spag9
|
UTSW |
11 |
93,982,577 (GRCm39) |
splice site |
probably null |
|
R5636:Spag9
|
UTSW |
11 |
93,959,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5638:Spag9
|
UTSW |
11 |
93,959,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5654:Spag9
|
UTSW |
11 |
93,981,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R5779:Spag9
|
UTSW |
11 |
94,005,079 (GRCm39) |
missense |
probably benign |
0.20 |
R5814:Spag9
|
UTSW |
11 |
93,973,654 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5912:Spag9
|
UTSW |
11 |
93,935,251 (GRCm39) |
missense |
probably damaging |
0.98 |
R6038:Spag9
|
UTSW |
11 |
94,002,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R6038:Spag9
|
UTSW |
11 |
94,002,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R6269:Spag9
|
UTSW |
11 |
93,935,333 (GRCm39) |
missense |
probably benign |
0.05 |
R6294:Spag9
|
UTSW |
11 |
93,984,311 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6389:Spag9
|
UTSW |
11 |
93,977,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R6420:Spag9
|
UTSW |
11 |
93,977,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R6460:Spag9
|
UTSW |
11 |
93,959,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R6482:Spag9
|
UTSW |
11 |
93,984,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6860:Spag9
|
UTSW |
11 |
93,972,196 (GRCm39) |
missense |
probably benign |
0.25 |
R7086:Spag9
|
UTSW |
11 |
93,988,690 (GRCm39) |
missense |
probably benign |
|
R7179:Spag9
|
UTSW |
11 |
93,980,258 (GRCm39) |
splice site |
probably null |
|
R7225:Spag9
|
UTSW |
11 |
93,988,184 (GRCm39) |
missense |
probably damaging |
0.98 |
R7351:Spag9
|
UTSW |
11 |
93,983,802 (GRCm39) |
missense |
probably benign |
0.00 |
R7366:Spag9
|
UTSW |
11 |
93,999,347 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7401:Spag9
|
UTSW |
11 |
93,988,515 (GRCm39) |
missense |
probably benign |
|
R7506:Spag9
|
UTSW |
11 |
93,999,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R7507:Spag9
|
UTSW |
11 |
93,958,906 (GRCm39) |
missense |
probably benign |
0.00 |
R7513:Spag9
|
UTSW |
11 |
94,002,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R7655:Spag9
|
UTSW |
11 |
93,887,389 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7656:Spag9
|
UTSW |
11 |
93,887,389 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7664:Spag9
|
UTSW |
11 |
93,992,986 (GRCm39) |
critical splice donor site |
probably null |
|
R7665:Spag9
|
UTSW |
11 |
93,904,480 (GRCm39) |
missense |
probably damaging |
0.98 |
R7862:Spag9
|
UTSW |
11 |
94,002,892 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8074:Spag9
|
UTSW |
11 |
94,002,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Spag9
|
UTSW |
11 |
93,989,870 (GRCm39) |
missense |
probably benign |
|
R8469:Spag9
|
UTSW |
11 |
93,982,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R8547:Spag9
|
UTSW |
11 |
94,013,647 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8709:Spag9
|
UTSW |
11 |
93,958,916 (GRCm39) |
missense |
probably benign |
0.02 |
R8732:Spag9
|
UTSW |
11 |
93,962,514 (GRCm39) |
critical splice donor site |
probably null |
|
R8899:Spag9
|
UTSW |
11 |
93,983,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R8983:Spag9
|
UTSW |
11 |
93,958,815 (GRCm39) |
missense |
probably benign |
|
R9043:Spag9
|
UTSW |
11 |
93,951,085 (GRCm39) |
missense |
|
|
R9050:Spag9
|
UTSW |
11 |
93,935,294 (GRCm39) |
missense |
probably damaging |
0.97 |
R9502:Spag9
|
UTSW |
11 |
93,959,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R9575:Spag9
|
UTSW |
11 |
93,962,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R9667:Spag9
|
UTSW |
11 |
93,887,119 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9683:Spag9
|
UTSW |
11 |
93,988,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R9774:Spag9
|
UTSW |
11 |
94,005,062 (GRCm39) |
missense |
probably damaging |
0.96 |
|