Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930012K11Rik |
T |
C |
14: 70,394,096 (GRCm39) |
|
probably benign |
Het |
Adam23 |
T |
C |
1: 63,573,515 (GRCm39) |
L261P |
probably benign |
Het |
Adgra3 |
G |
A |
5: 50,159,194 (GRCm39) |
|
probably benign |
Het |
Agtr1b |
A |
G |
3: 20,369,704 (GRCm39) |
F301L |
probably benign |
Het |
Ahnak2 |
G |
A |
12: 112,748,776 (GRCm39) |
T357I |
probably benign |
Het |
Aldh1a7 |
T |
C |
19: 20,704,430 (GRCm39) |
|
probably benign |
Het |
Apoh |
A |
T |
11: 108,302,899 (GRCm39) |
N288I |
probably damaging |
Het |
Arfgap3 |
A |
G |
15: 83,227,340 (GRCm39) |
V24A |
probably benign |
Het |
Atp6v0a1 |
A |
G |
11: 100,929,677 (GRCm39) |
|
probably null |
Het |
Axl |
A |
T |
7: 25,486,368 (GRCm39) |
M112K |
probably benign |
Het |
Bnc2 |
A |
C |
4: 84,211,169 (GRCm39) |
I425S |
probably damaging |
Het |
Ccn4 |
T |
C |
15: 66,789,194 (GRCm39) |
S227P |
possibly damaging |
Het |
Cdc42bpa |
C |
T |
1: 179,788,763 (GRCm39) |
T30M |
probably damaging |
Het |
Cebpz |
C |
A |
17: 79,227,317 (GRCm39) |
R1051M |
possibly damaging |
Het |
Ces1d |
A |
C |
8: 93,901,810 (GRCm39) |
|
probably benign |
Het |
Chd1l |
T |
C |
3: 97,494,465 (GRCm39) |
N405S |
probably benign |
Het |
Chodl |
G |
T |
16: 78,738,311 (GRCm39) |
G93V |
probably damaging |
Het |
Cpeb2 |
C |
T |
5: 43,395,743 (GRCm39) |
|
probably benign |
Het |
Crebbp |
A |
G |
16: 3,935,105 (GRCm39) |
|
probably benign |
Het |
Crybb3 |
T |
C |
5: 113,227,675 (GRCm39) |
T49A |
possibly damaging |
Het |
Ctps1 |
A |
G |
4: 120,418,722 (GRCm39) |
|
probably benign |
Het |
Cyp26b1 |
A |
G |
6: 84,551,497 (GRCm39) |
Y240H |
probably damaging |
Het |
Cyp2d11 |
A |
C |
15: 82,273,422 (GRCm39) |
V483G |
probably benign |
Het |
Dennd2b |
T |
C |
7: 109,155,545 (GRCm39) |
K402E |
probably benign |
Het |
Dnah14 |
A |
T |
1: 181,579,628 (GRCm39) |
N3054Y |
probably damaging |
Het |
Dspp |
A |
C |
5: 104,325,905 (GRCm39) |
D756A |
unknown |
Het |
Dst |
T |
C |
1: 34,309,984 (GRCm39) |
S1553P |
probably damaging |
Het |
Elp4 |
A |
G |
2: 105,622,559 (GRCm39) |
|
probably null |
Het |
Eml6 |
G |
T |
11: 29,832,088 (GRCm39) |
T194K |
probably benign |
Het |
Evi5 |
A |
G |
5: 107,943,638 (GRCm39) |
I569T |
probably benign |
Het |
Fancm |
C |
T |
12: 65,168,730 (GRCm39) |
P1698S |
possibly damaging |
Het |
Fhdc1 |
T |
C |
3: 84,352,852 (GRCm39) |
D791G |
probably benign |
Het |
Frem1 |
A |
G |
4: 82,930,188 (GRCm39) |
Y253H |
probably damaging |
Het |
Gpn3 |
A |
G |
5: 122,519,481 (GRCm39) |
Y196C |
probably benign |
Het |
Hcls1 |
A |
G |
16: 36,782,525 (GRCm39) |
D398G |
probably benign |
Het |
Hydin |
T |
C |
8: 111,189,163 (GRCm39) |
V1189A |
probably benign |
Het |
Itgb3 |
G |
A |
11: 104,534,789 (GRCm39) |
D549N |
probably damaging |
Het |
Itpr2 |
A |
G |
6: 146,141,951 (GRCm39) |
F1697S |
probably benign |
Het |
Klk1b11 |
A |
G |
7: 43,648,475 (GRCm39) |
T161A |
probably benign |
Het |
Kntc1 |
G |
A |
5: 123,903,120 (GRCm39) |
|
probably benign |
Het |
Map3k19 |
A |
T |
1: 127,750,837 (GRCm39) |
F838Y |
probably benign |
Het |
Map6 |
T |
A |
7: 98,985,187 (GRCm39) |
|
probably null |
Het |
Mcrs1 |
A |
G |
15: 99,142,608 (GRCm39) |
|
probably benign |
Het |
Mdn1 |
A |
T |
4: 32,729,956 (GRCm39) |
Y2766F |
probably damaging |
Het |
Med23 |
C |
T |
10: 24,776,686 (GRCm39) |
H739Y |
probably damaging |
Het |
Mmp17 |
T |
A |
5: 129,671,646 (GRCm39) |
D65E |
possibly damaging |
Het |
Mmp9 |
T |
A |
2: 164,793,177 (GRCm39) |
L442Q |
probably damaging |
Het |
Myo19 |
T |
C |
11: 84,779,001 (GRCm39) |
|
probably benign |
Het |
Nedd1 |
A |
C |
10: 92,527,791 (GRCm39) |
S468A |
possibly damaging |
Het |
Niban2 |
T |
A |
2: 32,813,833 (GRCm39) |
V682D |
probably benign |
Het |
Nlrp4d |
A |
C |
7: 10,116,316 (GRCm39) |
V152G |
probably damaging |
Het |
Nxf1 |
T |
A |
19: 8,740,170 (GRCm39) |
D112E |
probably benign |
Het |
Oas1h |
A |
T |
5: 121,000,626 (GRCm39) |
K79* |
probably null |
Het |
Omg |
T |
A |
11: 79,393,679 (GRCm39) |
I60F |
possibly damaging |
Het |
Or5p69 |
A |
G |
7: 107,967,576 (GRCm39) |
Y293C |
probably damaging |
Het |
Or8b101 |
A |
G |
9: 38,020,815 (GRCm39) |
T278A |
probably benign |
Het |
Or8b1b |
T |
A |
9: 38,375,757 (GRCm39) |
L140* |
probably null |
Het |
Pck1 |
G |
A |
2: 172,997,874 (GRCm39) |
W314* |
probably null |
Het |
Pla2g15 |
T |
C |
8: 106,889,756 (GRCm39) |
Y343H |
probably benign |
Het |
Plcb3 |
T |
C |
19: 6,936,276 (GRCm39) |
E749G |
probably damaging |
Het |
Plgrkt |
A |
G |
19: 29,328,442 (GRCm39) |
|
probably null |
Het |
Pprc1 |
A |
G |
19: 46,057,951 (GRCm39) |
|
probably benign |
Het |
Prkdc |
A |
T |
16: 15,516,871 (GRCm39) |
I1082F |
probably damaging |
Het |
Rapgef6 |
T |
A |
11: 54,516,701 (GRCm39) |
Y172* |
probably null |
Het |
Ros1 |
G |
T |
10: 52,001,885 (GRCm39) |
A1079D |
probably benign |
Het |
Sap30 |
T |
C |
8: 57,938,545 (GRCm39) |
E147G |
probably null |
Het |
Sell |
T |
C |
1: 163,899,674 (GRCm39) |
|
probably benign |
Het |
Senp1 |
A |
T |
15: 97,946,112 (GRCm39) |
D544E |
probably damaging |
Het |
Shpk |
G |
A |
11: 73,105,048 (GRCm39) |
|
probably benign |
Het |
Slc35b1 |
A |
T |
11: 95,277,353 (GRCm39) |
T74S |
probably benign |
Het |
Slc6a3 |
T |
A |
13: 73,718,098 (GRCm39) |
|
probably benign |
Het |
Slf1 |
T |
C |
13: 77,191,864 (GRCm39) |
N990S |
probably benign |
Het |
Smgc |
A |
G |
15: 91,738,746 (GRCm39) |
|
probably benign |
Het |
Snx19 |
T |
A |
9: 30,351,515 (GRCm39) |
V861D |
probably damaging |
Het |
Sprr2e |
C |
T |
3: 92,260,285 (GRCm39) |
P39S |
unknown |
Het |
Sstr2 |
T |
A |
11: 113,515,303 (GRCm39) |
M74K |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,099,937 (GRCm39) |
|
probably benign |
Het |
Tas2r143 |
A |
G |
6: 42,377,889 (GRCm39) |
I240V |
probably benign |
Het |
Tbrg1 |
T |
C |
9: 37,563,937 (GRCm39) |
I233V |
probably benign |
Het |
Tecpr1 |
G |
T |
5: 144,134,717 (GRCm39) |
D1055E |
probably damaging |
Het |
Thap2 |
A |
T |
10: 115,212,277 (GRCm39) |
|
probably null |
Het |
Tinagl1 |
A |
G |
4: 130,060,101 (GRCm39) |
Y388H |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,585,896 (GRCm39) |
Y21945F |
probably damaging |
Het |
Ugt2b1 |
A |
T |
5: 87,073,961 (GRCm39) |
W133R |
probably benign |
Het |
Utp15 |
A |
G |
13: 98,387,390 (GRCm39) |
S395P |
possibly damaging |
Het |
Vav1 |
T |
A |
17: 57,606,847 (GRCm39) |
L254Q |
probably damaging |
Het |
Vmn2r104 |
T |
C |
17: 20,250,069 (GRCm39) |
Y734C |
probably damaging |
Het |
Vps8 |
T |
A |
16: 21,288,904 (GRCm39) |
V421E |
probably benign |
Het |
Xkr7 |
G |
T |
2: 152,874,346 (GRCm39) |
A138S |
probably benign |
Het |
|
Other mutations in Usp24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00329:Usp24
|
APN |
4 |
106,216,288 (GRCm39) |
missense |
probably benign |
|
IGL00340:Usp24
|
APN |
4 |
106,258,336 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00480:Usp24
|
APN |
4 |
106,225,303 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00548:Usp24
|
APN |
4 |
106,198,495 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00655:Usp24
|
APN |
4 |
106,247,515 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00674:Usp24
|
APN |
4 |
106,229,876 (GRCm39) |
splice site |
probably benign |
|
IGL00718:Usp24
|
APN |
4 |
106,266,901 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00803:Usp24
|
APN |
4 |
106,242,723 (GRCm39) |
splice site |
probably benign |
|
IGL01161:Usp24
|
APN |
4 |
106,294,041 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01344:Usp24
|
APN |
4 |
106,236,582 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01374:Usp24
|
APN |
4 |
106,237,296 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01485:Usp24
|
APN |
4 |
106,219,429 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01736:Usp24
|
APN |
4 |
106,280,658 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01737:Usp24
|
APN |
4 |
106,244,931 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01862:Usp24
|
APN |
4 |
106,266,095 (GRCm39) |
splice site |
probably benign |
|
IGL01981:Usp24
|
APN |
4 |
106,232,965 (GRCm39) |
splice site |
probably benign |
|
IGL02090:Usp24
|
APN |
4 |
106,268,623 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02275:Usp24
|
APN |
4 |
106,244,690 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02352:Usp24
|
APN |
4 |
106,261,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02359:Usp24
|
APN |
4 |
106,261,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02391:Usp24
|
APN |
4 |
106,264,326 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02418:Usp24
|
APN |
4 |
106,293,557 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02537:Usp24
|
APN |
4 |
106,249,564 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02638:Usp24
|
APN |
4 |
106,295,969 (GRCm39) |
splice site |
probably benign |
|
IGL02638:Usp24
|
APN |
4 |
106,295,967 (GRCm39) |
splice site |
probably benign |
|
IGL02830:Usp24
|
APN |
4 |
106,204,584 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03125:Usp24
|
APN |
4 |
106,249,599 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03280:Usp24
|
APN |
4 |
106,237,627 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03350:Usp24
|
APN |
4 |
106,228,276 (GRCm39) |
nonsense |
probably null |
|
BB010:Usp24
|
UTSW |
4 |
106,285,686 (GRCm39) |
missense |
probably benign |
|
BB020:Usp24
|
UTSW |
4 |
106,285,686 (GRCm39) |
missense |
probably benign |
|
IGL03098:Usp24
|
UTSW |
4 |
106,228,230 (GRCm39) |
missense |
probably benign |
0.11 |
R0035:Usp24
|
UTSW |
4 |
106,225,224 (GRCm39) |
missense |
probably benign |
0.18 |
R0044:Usp24
|
UTSW |
4 |
106,269,281 (GRCm39) |
splice site |
probably benign |
|
R0086:Usp24
|
UTSW |
4 |
106,249,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R0197:Usp24
|
UTSW |
4 |
106,264,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Usp24
|
UTSW |
4 |
106,271,601 (GRCm39) |
nonsense |
probably null |
|
R0240:Usp24
|
UTSW |
4 |
106,271,601 (GRCm39) |
nonsense |
probably null |
|
R0491:Usp24
|
UTSW |
4 |
106,259,302 (GRCm39) |
missense |
probably benign |
0.41 |
R0687:Usp24
|
UTSW |
4 |
106,277,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Usp24
|
UTSW |
4 |
106,270,875 (GRCm39) |
splice site |
probably null |
|
R0973:Usp24
|
UTSW |
4 |
106,228,276 (GRCm39) |
nonsense |
probably null |
|
R0973:Usp24
|
UTSW |
4 |
106,228,276 (GRCm39) |
nonsense |
probably null |
|
R0974:Usp24
|
UTSW |
4 |
106,270,875 (GRCm39) |
splice site |
probably null |
|
R0974:Usp24
|
UTSW |
4 |
106,228,276 (GRCm39) |
nonsense |
probably null |
|
R1163:Usp24
|
UTSW |
4 |
106,278,157 (GRCm39) |
missense |
probably benign |
|
R1293:Usp24
|
UTSW |
4 |
106,280,750 (GRCm39) |
missense |
probably benign |
0.19 |
R1333:Usp24
|
UTSW |
4 |
106,199,550 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1476:Usp24
|
UTSW |
4 |
106,219,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1699:Usp24
|
UTSW |
4 |
106,296,024 (GRCm39) |
missense |
probably damaging |
0.99 |
R1728:Usp24
|
UTSW |
4 |
106,217,618 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1729:Usp24
|
UTSW |
4 |
106,217,618 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1753:Usp24
|
UTSW |
4 |
106,234,756 (GRCm39) |
missense |
probably benign |
0.04 |
R1917:Usp24
|
UTSW |
4 |
106,267,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Usp24
|
UTSW |
4 |
106,258,177 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2424:Usp24
|
UTSW |
4 |
106,256,310 (GRCm39) |
critical splice donor site |
probably null |
|
R2436:Usp24
|
UTSW |
4 |
106,266,842 (GRCm39) |
nonsense |
probably null |
|
R2513:Usp24
|
UTSW |
4 |
106,236,602 (GRCm39) |
splice site |
probably null |
|
R3824:Usp24
|
UTSW |
4 |
106,236,263 (GRCm39) |
missense |
probably benign |
|
R3831:Usp24
|
UTSW |
4 |
106,219,209 (GRCm39) |
critical splice donor site |
probably null |
|
R3833:Usp24
|
UTSW |
4 |
106,219,209 (GRCm39) |
critical splice donor site |
probably null |
|
R3982:Usp24
|
UTSW |
4 |
106,245,080 (GRCm39) |
missense |
probably benign |
0.38 |
R4022:Usp24
|
UTSW |
4 |
106,236,421 (GRCm39) |
splice site |
probably benign |
|
R4067:Usp24
|
UTSW |
4 |
106,216,286 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4175:Usp24
|
UTSW |
4 |
106,173,970 (GRCm39) |
missense |
probably benign |
0.00 |
R4766:Usp24
|
UTSW |
4 |
106,273,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Usp24
|
UTSW |
4 |
106,219,377 (GRCm39) |
splice site |
probably null |
|
R4798:Usp24
|
UTSW |
4 |
106,217,359 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4809:Usp24
|
UTSW |
4 |
106,270,873 (GRCm39) |
critical splice donor site |
probably null |
|
R4822:Usp24
|
UTSW |
4 |
106,273,244 (GRCm39) |
missense |
probably damaging |
0.98 |
R4906:Usp24
|
UTSW |
4 |
106,245,834 (GRCm39) |
missense |
probably benign |
0.20 |
R4934:Usp24
|
UTSW |
4 |
106,283,743 (GRCm39) |
missense |
probably benign |
0.29 |
R5074:Usp24
|
UTSW |
4 |
106,277,644 (GRCm39) |
missense |
probably benign |
0.12 |
R5151:Usp24
|
UTSW |
4 |
106,256,309 (GRCm39) |
critical splice donor site |
probably null |
|
R5220:Usp24
|
UTSW |
4 |
106,239,500 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5279:Usp24
|
UTSW |
4 |
106,242,621 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5280:Usp24
|
UTSW |
4 |
106,198,411 (GRCm39) |
missense |
probably benign |
0.18 |
R5285:Usp24
|
UTSW |
4 |
106,264,230 (GRCm39) |
missense |
probably benign |
0.00 |
R5292:Usp24
|
UTSW |
4 |
106,275,460 (GRCm39) |
missense |
probably benign |
0.06 |
R5294:Usp24
|
UTSW |
4 |
106,219,554 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5394:Usp24
|
UTSW |
4 |
106,265,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Usp24
|
UTSW |
4 |
106,232,871 (GRCm39) |
missense |
probably benign |
0.02 |
R5522:Usp24
|
UTSW |
4 |
106,229,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R5546:Usp24
|
UTSW |
4 |
106,273,244 (GRCm39) |
missense |
probably damaging |
0.98 |
R5756:Usp24
|
UTSW |
4 |
106,219,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R5910:Usp24
|
UTSW |
4 |
106,237,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R5972:Usp24
|
UTSW |
4 |
106,225,264 (GRCm39) |
missense |
probably damaging |
0.98 |
R6285:Usp24
|
UTSW |
4 |
106,231,297 (GRCm39) |
splice site |
probably null |
|
R6370:Usp24
|
UTSW |
4 |
106,237,718 (GRCm39) |
missense |
probably null |
0.20 |
R6630:Usp24
|
UTSW |
4 |
106,245,032 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6754:Usp24
|
UTSW |
4 |
106,217,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7027:Usp24
|
UTSW |
4 |
106,219,441 (GRCm39) |
missense |
probably benign |
0.21 |
R7088:Usp24
|
UTSW |
4 |
106,244,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R7129:Usp24
|
UTSW |
4 |
106,219,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R7131:Usp24
|
UTSW |
4 |
106,239,500 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7156:Usp24
|
UTSW |
4 |
106,245,116 (GRCm39) |
critical splice donor site |
probably null |
|
R7174:Usp24
|
UTSW |
4 |
106,219,878 (GRCm39) |
splice site |
probably null |
|
R7236:Usp24
|
UTSW |
4 |
106,263,502 (GRCm39) |
splice site |
probably null |
|
R7403:Usp24
|
UTSW |
4 |
106,264,232 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7424:Usp24
|
UTSW |
4 |
106,236,304 (GRCm39) |
missense |
probably benign |
0.00 |
R7475:Usp24
|
UTSW |
4 |
106,199,550 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7505:Usp24
|
UTSW |
4 |
106,236,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R7782:Usp24
|
UTSW |
4 |
106,173,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R7900:Usp24
|
UTSW |
4 |
106,266,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R7933:Usp24
|
UTSW |
4 |
106,285,686 (GRCm39) |
missense |
probably benign |
|
R7940:Usp24
|
UTSW |
4 |
106,287,741 (GRCm39) |
missense |
probably damaging |
0.98 |
R8271:Usp24
|
UTSW |
4 |
106,285,711 (GRCm39) |
missense |
probably damaging |
0.98 |
R8348:Usp24
|
UTSW |
4 |
106,225,933 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8448:Usp24
|
UTSW |
4 |
106,225,933 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8483:Usp24
|
UTSW |
4 |
106,230,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8546:Usp24
|
UTSW |
4 |
106,259,326 (GRCm39) |
missense |
probably benign |
0.01 |
R8798:Usp24
|
UTSW |
4 |
106,236,436 (GRCm39) |
missense |
probably benign |
0.00 |
R8822:Usp24
|
UTSW |
4 |
106,269,410 (GRCm39) |
missense |
probably benign |
0.17 |
R8992:Usp24
|
UTSW |
4 |
106,234,762 (GRCm39) |
missense |
probably benign |
0.36 |
R9002:Usp24
|
UTSW |
4 |
106,275,412 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9037:Usp24
|
UTSW |
4 |
106,236,251 (GRCm39) |
missense |
probably damaging |
0.99 |
R9068:Usp24
|
UTSW |
4 |
106,232,875 (GRCm39) |
missense |
probably benign |
0.09 |
R9096:Usp24
|
UTSW |
4 |
106,254,508 (GRCm39) |
missense |
probably benign |
0.00 |
R9180:Usp24
|
UTSW |
4 |
106,216,247 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9199:Usp24
|
UTSW |
4 |
106,244,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R9201:Usp24
|
UTSW |
4 |
106,277,727 (GRCm39) |
missense |
probably benign |
0.36 |
R9251:Usp24
|
UTSW |
4 |
106,217,715 (GRCm39) |
missense |
probably benign |
0.19 |
R9423:Usp24
|
UTSW |
4 |
106,288,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R9459:Usp24
|
UTSW |
4 |
106,199,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R9472:Usp24
|
UTSW |
4 |
106,261,128 (GRCm39) |
missense |
probably benign |
0.00 |
R9483:Usp24
|
UTSW |
4 |
106,219,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R9534:Usp24
|
UTSW |
4 |
106,264,312 (GRCm39) |
missense |
probably damaging |
0.97 |
R9653:Usp24
|
UTSW |
4 |
106,204,564 (GRCm39) |
missense |
probably benign |
0.03 |
R9712:Usp24
|
UTSW |
4 |
106,204,564 (GRCm39) |
missense |
probably benign |
0.03 |
X0024:Usp24
|
UTSW |
4 |
106,217,643 (GRCm39) |
missense |
probably benign |
0.09 |
X0028:Usp24
|
UTSW |
4 |
106,225,252 (GRCm39) |
missense |
probably benign |
0.01 |
X0066:Usp24
|
UTSW |
4 |
106,212,928 (GRCm39) |
missense |
possibly damaging |
0.82 |
|