Other mutations in this stock |
Total: 109 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd4 |
G |
A |
12: 84,662,156 (GRCm39) |
S30F |
probably benign |
Het |
Abtb1 |
T |
C |
6: 88,813,601 (GRCm39) |
D379G |
possibly damaging |
Het |
Adgre1 |
A |
G |
17: 57,748,350 (GRCm39) |
I517V |
probably benign |
Het |
Ajm1 |
C |
T |
2: 25,468,000 (GRCm39) |
G637D |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Angpt4 |
G |
A |
2: 151,780,909 (GRCm39) |
V386M |
probably damaging |
Het |
Asic1 |
A |
G |
15: 99,594,535 (GRCm39) |
H360R |
probably null |
Het |
Asxl1 |
G |
A |
2: 153,243,526 (GRCm39) |
A1359T |
probably benign |
Het |
Atp8a2 |
C |
T |
14: 60,258,207 (GRCm39) |
|
probably null |
Het |
Bltp3a |
T |
C |
17: 28,109,045 (GRCm39) |
F1088S |
possibly damaging |
Het |
C1qtnf2 |
T |
A |
11: 43,382,114 (GRCm39) |
F279I |
probably damaging |
Het |
Car8 |
A |
T |
4: 8,221,671 (GRCm39) |
L100* |
probably null |
Het |
Cd52 |
T |
C |
4: 133,822,295 (GRCm39) |
M1V |
probably null |
Het |
Celf5 |
T |
C |
10: 81,303,053 (GRCm39) |
I163V |
possibly damaging |
Het |
Cep250 |
A |
T |
2: 155,834,107 (GRCm39) |
T2010S |
possibly damaging |
Het |
Cfap65 |
C |
T |
1: 74,958,107 (GRCm39) |
V934M |
probably damaging |
Het |
Colec11 |
A |
T |
12: 28,644,858 (GRCm39) |
I212N |
probably damaging |
Het |
Cpa3 |
C |
T |
3: 20,277,391 (GRCm39) |
|
probably null |
Het |
Ctnnd1 |
G |
T |
2: 84,445,553 (GRCm39) |
H495N |
probably damaging |
Het |
Cyb5a |
T |
C |
18: 84,869,686 (GRCm39) |
V28A |
probably benign |
Het |
Ddo |
A |
T |
10: 40,523,625 (GRCm39) |
Q205L |
probably benign |
Het |
Dnah1 |
T |
A |
14: 30,983,050 (GRCm39) |
N4195I |
probably benign |
Het |
E2f1 |
A |
T |
2: 154,402,849 (GRCm39) |
V306E |
probably benign |
Het |
Ece1 |
C |
T |
4: 137,685,312 (GRCm39) |
R601W |
probably damaging |
Het |
Eef1d |
A |
C |
15: 75,773,024 (GRCm39) |
F25C |
probably damaging |
Het |
Ehd3 |
A |
T |
17: 74,137,354 (GRCm39) |
I508F |
probably damaging |
Het |
Eml6 |
T |
A |
11: 29,831,975 (GRCm39) |
I232F |
probably benign |
Het |
Enc1 |
T |
A |
13: 97,382,991 (GRCm39) |
D500E |
probably benign |
Het |
Enc1 |
C |
A |
13: 97,382,993 (GRCm39) |
T501K |
possibly damaging |
Het |
Fam83f |
C |
T |
15: 80,574,283 (GRCm39) |
R213W |
possibly damaging |
Het |
Fbxo31 |
A |
T |
8: 122,287,177 (GRCm39) |
L158* |
probably null |
Het |
Fcgbpl1 |
C |
T |
7: 27,854,797 (GRCm39) |
P1808S |
probably damaging |
Het |
Foxi3 |
C |
A |
6: 70,937,794 (GRCm39) |
T342N |
possibly damaging |
Het |
Gpr179 |
T |
A |
11: 97,227,382 (GRCm39) |
D1591V |
possibly damaging |
Het |
Gpsm2 |
A |
G |
3: 108,609,166 (GRCm39) |
V151A |
probably damaging |
Het |
Grk2 |
T |
G |
19: 4,337,968 (GRCm39) |
I513L |
probably benign |
Het |
H2-Ab1 |
A |
G |
17: 34,486,346 (GRCm39) |
E135G |
probably damaging |
Het |
Herc1 |
A |
T |
9: 66,296,138 (GRCm39) |
K578* |
probably null |
Het |
Hycc1 |
T |
G |
5: 24,191,149 (GRCm39) |
T173P |
probably damaging |
Het |
Itpr2 |
T |
C |
6: 146,198,171 (GRCm39) |
N1533S |
probably benign |
Het |
Kif3c |
A |
G |
12: 3,417,299 (GRCm39) |
N440S |
probably benign |
Het |
Klhdc2 |
T |
C |
12: 69,347,071 (GRCm39) |
|
probably null |
Het |
Kmo |
G |
T |
1: 175,465,461 (GRCm39) |
V72L |
probably benign |
Het |
Krt71 |
A |
G |
15: 101,651,315 (GRCm39) |
I56T |
possibly damaging |
Het |
Krt72 |
T |
C |
15: 101,689,987 (GRCm39) |
|
probably null |
Het |
Krt78 |
T |
A |
15: 101,859,300 (GRCm39) |
Q299L |
probably damaging |
Het |
Loxhd1 |
C |
T |
18: 77,493,603 (GRCm39) |
R1521C |
probably damaging |
Het |
Loxhd1 |
G |
A |
18: 77,513,335 (GRCm39) |
E1774K |
possibly damaging |
Het |
Ly6g6f |
T |
C |
17: 35,302,478 (GRCm39) |
S20G |
probably benign |
Het |
Mecr |
T |
A |
4: 131,592,382 (GRCm39) |
M282K |
probably damaging |
Het |
Mfsd14a |
G |
T |
3: 116,428,596 (GRCm39) |
A353D |
probably damaging |
Het |
Mroh9 |
A |
T |
1: 162,873,279 (GRCm39) |
N564K |
probably damaging |
Het |
Mrs2 |
T |
A |
13: 25,181,111 (GRCm39) |
T237S |
possibly damaging |
Het |
Mycbpap |
A |
G |
11: 94,398,377 (GRCm39) |
L534S |
probably damaging |
Het |
Myh1 |
T |
C |
11: 67,115,183 (GRCm39) |
I1906T |
probably benign |
Het |
Myh4 |
T |
A |
11: 67,151,150 (GRCm39) |
V1935D |
probably benign |
Het |
Myo18a |
T |
C |
11: 77,720,170 (GRCm39) |
I684T |
possibly damaging |
Het |
Myo7b |
C |
T |
18: 32,119,728 (GRCm39) |
R788H |
possibly damaging |
Het |
Nbea |
A |
T |
3: 55,551,129 (GRCm39) |
D2678E |
possibly damaging |
Het |
Ndufs3 |
A |
C |
2: 90,729,050 (GRCm39) |
Y145* |
probably null |
Het |
Nrros |
A |
G |
16: 31,962,329 (GRCm39) |
F563L |
probably damaging |
Het |
Ntn4 |
T |
C |
10: 93,581,633 (GRCm39) |
V602A |
probably damaging |
Het |
Obscn |
C |
A |
11: 58,920,163 (GRCm39) |
R6736L |
possibly damaging |
Het |
Odr4 |
T |
C |
1: 150,251,305 (GRCm39) |
N283S |
probably benign |
Het |
Or13c7d |
T |
A |
4: 43,770,495 (GRCm39) |
D172V |
possibly damaging |
Het |
Or2ag16 |
T |
C |
7: 106,351,756 (GRCm39) |
I280V |
probably benign |
Het |
Or7g22 |
C |
A |
9: 19,049,213 (GRCm39) |
T308K |
probably benign |
Het |
Or8d1 |
T |
A |
9: 38,766,820 (GRCm39) |
V154D |
probably benign |
Het |
Or8g54 |
C |
T |
9: 39,707,301 (GRCm39) |
P210L |
possibly damaging |
Het |
Or8g55 |
A |
G |
9: 39,785,267 (GRCm39) |
E232G |
probably benign |
Het |
Pik3cd |
A |
G |
4: 149,738,576 (GRCm39) |
F751L |
possibly damaging |
Het |
Plekhh2 |
A |
G |
17: 84,906,561 (GRCm39) |
|
probably null |
Het |
Postn |
A |
G |
3: 54,281,177 (GRCm39) |
H434R |
probably damaging |
Het |
Prss39 |
A |
G |
1: 34,539,114 (GRCm39) |
D118G |
possibly damaging |
Het |
Ralyl |
G |
T |
3: 14,208,493 (GRCm39) |
G211V |
possibly damaging |
Het |
Rbak |
T |
A |
5: 143,159,202 (GRCm39) |
E617V |
probably damaging |
Het |
Rbms3 |
A |
T |
9: 116,548,401 (GRCm39) |
W80R |
probably damaging |
Het |
Retnlg |
A |
T |
16: 48,694,610 (GRCm39) |
Y86F |
probably benign |
Het |
Rtel1 |
T |
A |
2: 180,993,896 (GRCm39) |
S643T |
probably benign |
Het |
Semp2l2a |
A |
T |
8: 13,886,816 (GRCm39) |
L425* |
probably null |
Het |
Serpina11 |
A |
T |
12: 103,950,954 (GRCm39) |
F256I |
probably damaging |
Het |
Setd2 |
A |
T |
9: 110,379,413 (GRCm39) |
Y1076F |
probably benign |
Het |
Setd2 |
A |
T |
9: 110,446,884 (GRCm39) |
|
probably null |
Het |
Sgsm1 |
T |
C |
5: 113,421,483 (GRCm39) |
T248A |
possibly damaging |
Het |
Slc6a21 |
T |
C |
7: 44,930,179 (GRCm39) |
Y193H |
probably damaging |
Het |
Slfn9 |
T |
C |
11: 82,872,781 (GRCm39) |
K652E |
probably benign |
Het |
Stt3b |
A |
T |
9: 115,077,675 (GRCm39) |
Y692* |
probably null |
Het |
Sval3 |
A |
G |
6: 41,945,096 (GRCm39) |
Q8R |
probably benign |
Het |
Synm |
T |
A |
7: 67,383,748 (GRCm39) |
I1305F |
possibly damaging |
Het |
Tdrd1 |
T |
C |
19: 56,826,215 (GRCm39) |
F169L |
probably damaging |
Het |
Tecta |
T |
A |
9: 42,295,493 (GRCm39) |
D334V |
probably damaging |
Het |
Tle2 |
G |
A |
10: 81,425,331 (GRCm39) |
|
probably null |
Het |
Tmem243 |
A |
G |
5: 9,166,489 (GRCm39) |
I30V |
probably benign |
Het |
Treml2 |
T |
C |
17: 48,616,530 (GRCm39) |
*330R |
probably null |
Het |
Trpm6 |
A |
G |
19: 18,804,931 (GRCm39) |
D961G |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,155,907 (GRCm39) |
V2244A |
probably benign |
Het |
Ush2a |
A |
C |
1: 188,643,024 (GRCm39) |
T4129P |
probably benign |
Het |
Vgll2 |
G |
A |
10: 51,901,324 (GRCm39) |
V85I |
probably damaging |
Het |
Vmn1r16 |
T |
C |
6: 57,300,256 (GRCm39) |
Y122C |
probably benign |
Het |
Vmn1r22 |
A |
T |
6: 57,877,134 (GRCm39) |
I91N |
probably damaging |
Het |
Vmn2r70 |
A |
T |
7: 85,213,011 (GRCm39) |
Y465* |
probably null |
Het |
Wdr64 |
A |
T |
1: 175,544,897 (GRCm39) |
E110V |
probably damaging |
Het |
Wfdc6a |
A |
T |
2: 164,422,231 (GRCm39) |
C123S |
probably damaging |
Het |
Xrcc1 |
A |
G |
7: 24,247,252 (GRCm39) |
Y30C |
probably damaging |
Het |
Zdhhc7 |
T |
C |
8: 120,812,157 (GRCm39) |
K155R |
probably benign |
Het |
Zfp560 |
A |
G |
9: 20,263,226 (GRCm39) |
F50S |
possibly damaging |
Het |
Zfp616 |
C |
T |
11: 73,976,671 (GRCm39) |
T980I |
probably damaging |
Het |
Zfp808 |
C |
T |
13: 62,319,670 (GRCm39) |
P300S |
probably damaging |
Het |
Zfp979 |
G |
A |
4: 147,697,740 (GRCm39) |
T323I |
probably damaging |
Het |
|
Other mutations in Unc79 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00718:Unc79
|
APN |
12 |
103,135,906 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL00835:Unc79
|
APN |
12 |
103,108,149 (GRCm39) |
splice site |
probably benign |
|
IGL00917:Unc79
|
APN |
12 |
103,054,766 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01012:Unc79
|
APN |
12 |
103,078,714 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01121:Unc79
|
APN |
12 |
103,131,890 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01303:Unc79
|
APN |
12 |
103,128,126 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01305:Unc79
|
APN |
12 |
102,968,130 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01315:Unc79
|
APN |
12 |
103,054,780 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01388:Unc79
|
APN |
12 |
103,136,018 (GRCm39) |
splice site |
probably benign |
|
IGL01415:Unc79
|
APN |
12 |
103,074,944 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01447:Unc79
|
APN |
12 |
103,045,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01655:Unc79
|
APN |
12 |
103,134,546 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01662:Unc79
|
APN |
12 |
103,115,279 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01728:Unc79
|
APN |
12 |
103,131,943 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01767:Unc79
|
APN |
12 |
103,108,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02080:Unc79
|
APN |
12 |
102,968,234 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02115:Unc79
|
APN |
12 |
102,964,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02176:Unc79
|
APN |
12 |
102,965,006 (GRCm39) |
splice site |
probably null |
|
IGL02186:Unc79
|
APN |
12 |
102,977,542 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02205:Unc79
|
APN |
12 |
103,045,260 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02337:Unc79
|
APN |
12 |
103,122,705 (GRCm39) |
splice site |
probably benign |
|
IGL02498:Unc79
|
APN |
12 |
103,137,837 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02508:Unc79
|
APN |
12 |
103,078,535 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02508:Unc79
|
APN |
12 |
103,078,277 (GRCm39) |
splice site |
probably benign |
|
IGL02557:Unc79
|
APN |
12 |
103,148,418 (GRCm39) |
splice site |
probably benign |
|
IGL02589:Unc79
|
APN |
12 |
103,139,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02611:Unc79
|
APN |
12 |
103,131,967 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02728:Unc79
|
APN |
12 |
103,088,688 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02827:Unc79
|
APN |
12 |
103,041,105 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03028:Unc79
|
APN |
12 |
103,139,785 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03144:Unc79
|
APN |
12 |
103,008,401 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03229:Unc79
|
APN |
12 |
103,100,798 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03269:Unc79
|
APN |
12 |
103,054,936 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03325:Unc79
|
APN |
12 |
103,135,869 (GRCm39) |
missense |
probably damaging |
0.98 |
pencil-thin
|
UTSW |
12 |
103,075,040 (GRCm39) |
splice site |
probably null |
|
sweetpea
|
UTSW |
12 |
103,025,777 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Unc79
|
UTSW |
12 |
103,039,009 (GRCm39) |
nonsense |
probably null |
|
ANU22:Unc79
|
UTSW |
12 |
102,968,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R0046:Unc79
|
UTSW |
12 |
103,091,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R0046:Unc79
|
UTSW |
12 |
103,091,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R0067:Unc79
|
UTSW |
12 |
103,025,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R0067:Unc79
|
UTSW |
12 |
103,025,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Unc79
|
UTSW |
12 |
103,100,784 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0110:Unc79
|
UTSW |
12 |
103,045,329 (GRCm39) |
critical splice donor site |
probably null |
|
R0128:Unc79
|
UTSW |
12 |
103,054,693 (GRCm39) |
splice site |
probably benign |
|
R0166:Unc79
|
UTSW |
12 |
103,122,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Unc79
|
UTSW |
12 |
103,058,286 (GRCm39) |
missense |
probably benign |
0.00 |
R0211:Unc79
|
UTSW |
12 |
103,039,051 (GRCm39) |
missense |
probably benign |
0.01 |
R0211:Unc79
|
UTSW |
12 |
103,039,051 (GRCm39) |
missense |
probably benign |
0.01 |
R0218:Unc79
|
UTSW |
12 |
103,075,040 (GRCm39) |
splice site |
probably null |
|
R0244:Unc79
|
UTSW |
12 |
103,079,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R0305:Unc79
|
UTSW |
12 |
103,079,459 (GRCm39) |
missense |
probably benign |
0.18 |
R0310:Unc79
|
UTSW |
12 |
103,027,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Unc79
|
UTSW |
12 |
103,137,903 (GRCm39) |
missense |
probably damaging |
0.98 |
R0369:Unc79
|
UTSW |
12 |
103,055,031 (GRCm39) |
critical splice donor site |
probably null |
|
R0450:Unc79
|
UTSW |
12 |
103,045,329 (GRCm39) |
critical splice donor site |
probably null |
|
R0503:Unc79
|
UTSW |
12 |
103,045,127 (GRCm39) |
missense |
probably benign |
0.01 |
R0542:Unc79
|
UTSW |
12 |
103,060,437 (GRCm39) |
splice site |
probably benign |
|
R0845:Unc79
|
UTSW |
12 |
103,139,703 (GRCm39) |
splice site |
probably benign |
|
R0893:Unc79
|
UTSW |
12 |
102,957,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Unc79
|
UTSW |
12 |
103,041,112 (GRCm39) |
missense |
probably benign |
0.03 |
R1148:Unc79
|
UTSW |
12 |
103,078,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Unc79
|
UTSW |
12 |
103,078,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1159:Unc79
|
UTSW |
12 |
103,013,311 (GRCm39) |
splice site |
probably benign |
|
R1191:Unc79
|
UTSW |
12 |
103,013,271 (GRCm39) |
nonsense |
probably null |
|
R1307:Unc79
|
UTSW |
12 |
103,036,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R1368:Unc79
|
UTSW |
12 |
103,122,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R1476:Unc79
|
UTSW |
12 |
103,149,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Unc79
|
UTSW |
12 |
103,079,052 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1777:Unc79
|
UTSW |
12 |
103,078,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Unc79
|
UTSW |
12 |
103,025,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R1830:Unc79
|
UTSW |
12 |
103,100,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R1927:Unc79
|
UTSW |
12 |
103,135,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Unc79
|
UTSW |
12 |
103,041,178 (GRCm39) |
missense |
probably benign |
0.19 |
R1958:Unc79
|
UTSW |
12 |
102,957,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1980:Unc79
|
UTSW |
12 |
102,977,538 (GRCm39) |
nonsense |
probably null |
|
R2019:Unc79
|
UTSW |
12 |
103,137,830 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2290:Unc79
|
UTSW |
12 |
103,112,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2939:Unc79
|
UTSW |
12 |
102,957,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R2962:Unc79
|
UTSW |
12 |
103,061,378 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3176:Unc79
|
UTSW |
12 |
103,079,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R3276:Unc79
|
UTSW |
12 |
103,079,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Unc79
|
UTSW |
12 |
103,041,062 (GRCm39) |
missense |
probably benign |
0.00 |
R3684:Unc79
|
UTSW |
12 |
103,041,062 (GRCm39) |
missense |
probably benign |
0.00 |
R3686:Unc79
|
UTSW |
12 |
103,054,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R3760:Unc79
|
UTSW |
12 |
103,058,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R4031:Unc79
|
UTSW |
12 |
103,039,018 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4039:Unc79
|
UTSW |
12 |
103,041,208 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4110:Unc79
|
UTSW |
12 |
103,025,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4113:Unc79
|
UTSW |
12 |
103,025,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4159:Unc79
|
UTSW |
12 |
103,036,512 (GRCm39) |
intron |
probably benign |
|
R4273:Unc79
|
UTSW |
12 |
103,088,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R4292:Unc79
|
UTSW |
12 |
103,149,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R4334:Unc79
|
UTSW |
12 |
103,045,233 (GRCm39) |
missense |
probably benign |
|
R4513:Unc79
|
UTSW |
12 |
102,988,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R4562:Unc79
|
UTSW |
12 |
102,957,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Unc79
|
UTSW |
12 |
102,968,062 (GRCm39) |
splice site |
probably benign |
|
R4645:Unc79
|
UTSW |
12 |
103,079,081 (GRCm39) |
missense |
probably benign |
|
R4758:Unc79
|
UTSW |
12 |
103,128,080 (GRCm39) |
nonsense |
probably null |
|
R4787:Unc79
|
UTSW |
12 |
103,013,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R4852:Unc79
|
UTSW |
12 |
103,139,725 (GRCm39) |
missense |
probably damaging |
0.98 |
R4883:Unc79
|
UTSW |
12 |
103,060,592 (GRCm39) |
missense |
probably damaging |
0.99 |
R4898:Unc79
|
UTSW |
12 |
103,128,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R4979:Unc79
|
UTSW |
12 |
103,078,691 (GRCm39) |
missense |
probably benign |
|
R5044:Unc79
|
UTSW |
12 |
103,078,962 (GRCm39) |
missense |
probably benign |
0.32 |
R5053:Unc79
|
UTSW |
12 |
103,071,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5061:Unc79
|
UTSW |
12 |
103,134,700 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5075:Unc79
|
UTSW |
12 |
103,041,213 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5101:Unc79
|
UTSW |
12 |
103,078,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R5236:Unc79
|
UTSW |
12 |
103,060,654 (GRCm39) |
critical splice donor site |
probably null |
|
R5240:Unc79
|
UTSW |
12 |
103,037,010 (GRCm39) |
missense |
probably damaging |
0.99 |
R5383:Unc79
|
UTSW |
12 |
103,070,886 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5461:Unc79
|
UTSW |
12 |
103,078,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R5535:Unc79
|
UTSW |
12 |
103,135,962 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5609:Unc79
|
UTSW |
12 |
103,094,527 (GRCm39) |
missense |
probably benign |
|
R5639:Unc79
|
UTSW |
12 |
103,137,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R5704:Unc79
|
UTSW |
12 |
102,968,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R5923:Unc79
|
UTSW |
12 |
103,078,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R5925:Unc79
|
UTSW |
12 |
103,091,989 (GRCm39) |
splice site |
probably null |
|
R5975:Unc79
|
UTSW |
12 |
103,091,885 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6047:Unc79
|
UTSW |
12 |
103,027,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R6156:Unc79
|
UTSW |
12 |
103,027,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Unc79
|
UTSW |
12 |
103,149,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R6292:Unc79
|
UTSW |
12 |
103,108,991 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6313:Unc79
|
UTSW |
12 |
103,078,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R6391:Unc79
|
UTSW |
12 |
102,987,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R6405:Unc79
|
UTSW |
12 |
103,134,595 (GRCm39) |
missense |
probably damaging |
0.97 |
R6416:Unc79
|
UTSW |
12 |
103,097,905 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6467:Unc79
|
UTSW |
12 |
103,139,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Unc79
|
UTSW |
12 |
103,027,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R6614:Unc79
|
UTSW |
12 |
102,957,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Unc79
|
UTSW |
12 |
103,045,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Unc79
|
UTSW |
12 |
103,045,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R6700:Unc79
|
UTSW |
12 |
103,091,962 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6724:Unc79
|
UTSW |
12 |
103,071,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R6819:Unc79
|
UTSW |
12 |
103,108,267 (GRCm39) |
missense |
probably benign |
0.12 |
R6869:Unc79
|
UTSW |
12 |
103,079,331 (GRCm39) |
missense |
probably benign |
0.33 |
R6879:Unc79
|
UTSW |
12 |
103,115,046 (GRCm39) |
splice site |
probably null |
|
R6942:Unc79
|
UTSW |
12 |
103,088,704 (GRCm39) |
critical splice donor site |
probably null |
|
R6961:Unc79
|
UTSW |
12 |
103,079,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R6973:Unc79
|
UTSW |
12 |
102,964,699 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6980:Unc79
|
UTSW |
12 |
103,025,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R7124:Unc79
|
UTSW |
12 |
103,027,652 (GRCm39) |
missense |
probably damaging |
0.99 |
R7144:Unc79
|
UTSW |
12 |
103,108,885 (GRCm39) |
missense |
probably benign |
0.06 |
R7197:Unc79
|
UTSW |
12 |
103,078,765 (GRCm39) |
missense |
probably benign |
|
R7209:Unc79
|
UTSW |
12 |
103,091,883 (GRCm39) |
missense |
probably benign |
|
R7232:Unc79
|
UTSW |
12 |
103,100,734 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7304:Unc79
|
UTSW |
12 |
103,029,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R7354:Unc79
|
UTSW |
12 |
103,108,961 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7384:Unc79
|
UTSW |
12 |
103,137,837 (GRCm39) |
missense |
probably benign |
0.11 |
R7400:Unc79
|
UTSW |
12 |
103,070,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R7417:Unc79
|
UTSW |
12 |
103,055,017 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7470:Unc79
|
UTSW |
12 |
103,061,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Unc79
|
UTSW |
12 |
103,058,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R8037:Unc79
|
UTSW |
12 |
103,016,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R8041:Unc79
|
UTSW |
12 |
103,054,726 (GRCm39) |
missense |
probably benign |
0.06 |
R8146:Unc79
|
UTSW |
12 |
103,036,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R8276:Unc79
|
UTSW |
12 |
102,968,122 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8427:Unc79
|
UTSW |
12 |
103,045,297 (GRCm39) |
missense |
probably benign |
0.24 |
R8501:Unc79
|
UTSW |
12 |
103,058,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R8510:Unc79
|
UTSW |
12 |
103,070,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Unc79
|
UTSW |
12 |
103,013,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Unc79
|
UTSW |
12 |
103,049,855 (GRCm39) |
missense |
probably benign |
0.13 |
R8795:Unc79
|
UTSW |
12 |
103,074,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R9017:Unc79
|
UTSW |
12 |
103,074,874 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9121:Unc79
|
UTSW |
12 |
102,968,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R9196:Unc79
|
UTSW |
12 |
103,078,613 (GRCm39) |
missense |
probably benign |
|
R9443:Unc79
|
UTSW |
12 |
103,037,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R9548:Unc79
|
UTSW |
12 |
102,977,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R9600:Unc79
|
UTSW |
12 |
103,135,972 (GRCm39) |
missense |
probably benign |
0.07 |
R9767:Unc79
|
UTSW |
12 |
103,079,234 (GRCm39) |
missense |
probably benign |
|
R9787:Unc79
|
UTSW |
12 |
103,112,620 (GRCm39) |
missense |
probably benign |
0.00 |
RF010:Unc79
|
UTSW |
12 |
103,079,046 (GRCm39) |
missense |
probably benign |
0.17 |
X0017:Unc79
|
UTSW |
12 |
103,074,520 (GRCm39) |
missense |
probably damaging |
0.99 |
X0028:Unc79
|
UTSW |
12 |
102,957,662 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Unc79
|
UTSW |
12 |
102,987,271 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Unc79
|
UTSW |
12 |
103,108,312 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Unc79
|
UTSW |
12 |
103,054,937 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Unc79
|
UTSW |
12 |
103,131,948 (GRCm39) |
missense |
probably benign |
|
|