Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adar |
T |
C |
3: 89,642,950 (GRCm39) |
L277P |
probably damaging |
Het |
Adgrb3 |
C |
A |
1: 25,865,472 (GRCm39) |
D124Y |
probably damaging |
Het |
Afdn |
T |
C |
17: 14,108,641 (GRCm39) |
V1403A |
probably benign |
Het |
Afg3l1 |
T |
C |
8: 124,227,973 (GRCm39) |
V586A |
probably damaging |
Het |
Ajm1 |
A |
G |
2: 25,469,831 (GRCm39) |
S27P |
possibly damaging |
Het |
Aloxe3 |
A |
G |
11: 69,033,677 (GRCm39) |
D597G |
probably damaging |
Het |
Asb15 |
T |
C |
6: 24,570,666 (GRCm39) |
V548A |
probably benign |
Het |
Atp6v1a |
C |
T |
16: 43,921,991 (GRCm39) |
R388Q |
probably damaging |
Het |
Btbd8 |
A |
G |
5: 107,658,635 (GRCm39) |
D1735G |
probably benign |
Het |
C130074G19Rik |
G |
A |
1: 184,615,184 (GRCm39) |
T2M |
probably damaging |
Het |
Ccdc187 |
T |
C |
2: 26,165,505 (GRCm39) |
T884A |
probably benign |
Het |
Cdk5rap1 |
G |
A |
2: 154,195,148 (GRCm39) |
R356* |
probably null |
Het |
Cebpz |
A |
T |
17: 79,234,334 (GRCm39) |
H725Q |
probably damaging |
Het |
Celsr2 |
T |
C |
3: 108,314,176 (GRCm39) |
D1283G |
probably damaging |
Het |
Cldn11 |
G |
T |
3: 31,217,239 (GRCm39) |
V136F |
probably damaging |
Het |
Cpxm2 |
T |
C |
7: 131,681,783 (GRCm39) |
N249D |
probably benign |
Het |
Ctsz |
T |
C |
2: 174,280,072 (GRCm39) |
N67D |
probably benign |
Het |
Drd3 |
A |
C |
16: 43,643,075 (GRCm39) |
H405P |
probably damaging |
Het |
F2rl2 |
T |
C |
13: 95,837,339 (GRCm39) |
V128A |
probably benign |
Het |
Fh1 |
C |
T |
1: 175,448,126 (GRCm39) |
P43S |
probably benign |
Het |
Fndc7 |
C |
T |
3: 108,779,622 (GRCm39) |
W307* |
probably null |
Het |
Gmip |
G |
T |
8: 70,270,485 (GRCm39) |
V732L |
probably benign |
Het |
Heatr4 |
A |
G |
12: 84,027,038 (GRCm39) |
F73S |
probably damaging |
Het |
Iqcf4 |
T |
C |
9: 106,448,111 (GRCm39) |
|
probably benign |
Het |
Itln1 |
T |
A |
1: 171,359,279 (GRCm39) |
Q67L |
probably damaging |
Het |
Jak1 |
A |
G |
4: 101,013,704 (GRCm39) |
V1008A |
probably damaging |
Het |
Kcnh1 |
A |
T |
1: 191,921,031 (GRCm39) |
|
probably benign |
Het |
Kcnu1 |
T |
G |
8: 26,342,101 (GRCm39) |
|
probably benign |
Het |
Kif1b |
A |
G |
4: 149,305,024 (GRCm39) |
S967P |
probably damaging |
Het |
Klra17 |
A |
G |
6: 129,851,780 (GRCm39) |
S31P |
probably benign |
Het |
Kmt2d |
C |
T |
15: 98,742,615 (GRCm39) |
E4182K |
unknown |
Het |
Lama5 |
T |
C |
2: 179,822,677 (GRCm39) |
D2825G |
probably damaging |
Het |
Lmtk2 |
T |
C |
5: 144,108,566 (GRCm39) |
V336A |
probably damaging |
Het |
Mad1l1 |
A |
G |
5: 140,074,438 (GRCm39) |
I584T |
probably benign |
Het |
Magea1 |
T |
A |
X: 153,871,787 (GRCm39) |
N313I |
possibly damaging |
Het |
Mapt |
T |
C |
11: 104,189,440 (GRCm39) |
S153P |
probably benign |
Het |
Myo1e |
T |
C |
9: 70,291,172 (GRCm39) |
Y988H |
probably benign |
Het |
Ndufc2 |
A |
T |
7: 97,049,403 (GRCm39) |
N3I |
probably benign |
Het |
Nos2 |
T |
A |
11: 78,836,515 (GRCm39) |
V531D |
possibly damaging |
Het |
Npbwr1 |
T |
A |
1: 5,986,617 (GRCm39) |
Y299F |
probably damaging |
Het |
Or4a39 |
A |
G |
2: 89,237,378 (GRCm39) |
L15P |
probably damaging |
Het |
Or4a70 |
A |
G |
2: 89,324,171 (GRCm39) |
Y162H |
possibly damaging |
Het |
Or52n20 |
G |
T |
7: 104,320,296 (GRCm39) |
C129F |
probably damaging |
Het |
Or8h10 |
G |
A |
2: 86,808,591 (GRCm39) |
P183L |
probably damaging |
Het |
Pp2d1 |
T |
C |
17: 53,815,191 (GRCm39) |
Y511C |
probably benign |
Het |
Psmb4 |
T |
C |
3: 94,793,435 (GRCm39) |
N149D |
probably benign |
Het |
Setbp1 |
T |
C |
18: 78,901,516 (GRCm39) |
K717R |
probably damaging |
Het |
Slc25a11 |
T |
C |
11: 70,535,630 (GRCm39) |
M303V |
probably benign |
Het |
Spesp1 |
A |
T |
9: 62,180,242 (GRCm39) |
M222K |
probably benign |
Het |
Tmem132d |
A |
G |
5: 127,869,495 (GRCm39) |
M613T |
probably benign |
Het |
Ugt2a2 |
A |
G |
5: 87,612,029 (GRCm39) |
F294L |
probably damaging |
Het |
Zfp750 |
T |
A |
11: 121,404,456 (GRCm39) |
I140F |
possibly damaging |
Het |
Zscan4e |
A |
T |
7: 11,041,574 (GRCm39) |
H127Q |
possibly damaging |
Het |
|
Other mutations in Usp34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00477:Usp34
|
APN |
11 |
23,418,879 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01307:Usp34
|
APN |
11 |
23,367,676 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01313:Usp34
|
APN |
11 |
23,423,206 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01794:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01826:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01827:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01830:Usp34
|
APN |
11 |
23,386,020 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01867:Usp34
|
APN |
11 |
23,334,411 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01939:Usp34
|
APN |
11 |
23,295,141 (GRCm39) |
splice site |
probably benign |
|
IGL01977:Usp34
|
APN |
11 |
23,402,661 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01985:Usp34
|
APN |
11 |
23,402,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02011:Usp34
|
APN |
11 |
23,421,554 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02302:Usp34
|
APN |
11 |
23,417,243 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02423:Usp34
|
APN |
11 |
23,304,900 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02491:Usp34
|
APN |
11 |
23,382,630 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02532:Usp34
|
APN |
11 |
23,320,291 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02561:Usp34
|
APN |
11 |
23,301,652 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02706:Usp34
|
APN |
11 |
23,338,659 (GRCm39) |
splice site |
probably benign |
|
IGL02891:Usp34
|
APN |
11 |
23,437,166 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03079:Usp34
|
APN |
11 |
23,382,247 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03089:Usp34
|
APN |
11 |
23,396,958 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03175:Usp34
|
APN |
11 |
23,438,686 (GRCm39) |
missense |
probably benign |
|
IGL03256:Usp34
|
APN |
11 |
23,370,090 (GRCm39) |
nonsense |
probably null |
|
IGL03280:Usp34
|
APN |
11 |
23,304,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03289:Usp34
|
APN |
11 |
23,343,818 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03408:Usp34
|
APN |
11 |
23,396,957 (GRCm39) |
missense |
possibly damaging |
0.92 |
Chub
|
UTSW |
11 |
23,414,686 (GRCm39) |
missense |
probably damaging |
0.99 |
Cicione
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5571_Usp34_680
|
UTSW |
11 |
23,407,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R5713_Usp34_003
|
UTSW |
11 |
23,293,515 (GRCm39) |
missense |
possibly damaging |
0.94 |
Roebuck
|
UTSW |
11 |
23,436,810 (GRCm39) |
splice site |
probably benign |
|
stoat
|
UTSW |
11 |
23,437,203 (GRCm39) |
missense |
|
|
tunnelvision
|
UTSW |
11 |
23,396,968 (GRCm39) |
missense |
|
|
I2288:Usp34
|
UTSW |
11 |
23,382,473 (GRCm39) |
splice site |
probably benign |
|
R0047:Usp34
|
UTSW |
11 |
23,414,403 (GRCm39) |
missense |
probably benign |
0.34 |
R0047:Usp34
|
UTSW |
11 |
23,414,403 (GRCm39) |
missense |
probably benign |
0.34 |
R0099:Usp34
|
UTSW |
11 |
23,313,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Usp34
|
UTSW |
11 |
23,383,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R0240:Usp34
|
UTSW |
11 |
23,383,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R0403:Usp34
|
UTSW |
11 |
23,283,838 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0432:Usp34
|
UTSW |
11 |
23,351,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R0446:Usp34
|
UTSW |
11 |
23,417,207 (GRCm39) |
missense |
probably damaging |
0.97 |
R0455:Usp34
|
UTSW |
11 |
23,396,741 (GRCm39) |
splice site |
probably benign |
|
R0470:Usp34
|
UTSW |
11 |
23,386,001 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0472:Usp34
|
UTSW |
11 |
23,334,509 (GRCm39) |
splice site |
probably benign |
|
R0512:Usp34
|
UTSW |
11 |
23,401,997 (GRCm39) |
missense |
probably benign |
0.04 |
R0557:Usp34
|
UTSW |
11 |
23,353,848 (GRCm39) |
missense |
probably damaging |
0.98 |
R0562:Usp34
|
UTSW |
11 |
23,382,406 (GRCm39) |
splice site |
probably benign |
|
R0656:Usp34
|
UTSW |
11 |
23,422,967 (GRCm39) |
missense |
probably damaging |
0.99 |
R0693:Usp34
|
UTSW |
11 |
23,402,637 (GRCm39) |
missense |
probably damaging |
0.97 |
R0739:Usp34
|
UTSW |
11 |
23,417,243 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1061:Usp34
|
UTSW |
11 |
23,334,420 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1078:Usp34
|
UTSW |
11 |
23,383,175 (GRCm39) |
splice site |
probably benign |
|
R1223:Usp34
|
UTSW |
11 |
23,396,464 (GRCm39) |
splice site |
probably null |
|
R1295:Usp34
|
UTSW |
11 |
23,334,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R1430:Usp34
|
UTSW |
11 |
23,409,151 (GRCm39) |
missense |
probably damaging |
0.97 |
R1445:Usp34
|
UTSW |
11 |
23,301,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R1468:Usp34
|
UTSW |
11 |
23,391,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Usp34
|
UTSW |
11 |
23,391,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Usp34
|
UTSW |
11 |
23,438,862 (GRCm39) |
missense |
probably benign |
0.20 |
R1475:Usp34
|
UTSW |
11 |
23,423,253 (GRCm39) |
missense |
probably damaging |
0.99 |
R1628:Usp34
|
UTSW |
11 |
23,438,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R1631:Usp34
|
UTSW |
11 |
23,410,651 (GRCm39) |
missense |
probably damaging |
0.99 |
R1655:Usp34
|
UTSW |
11 |
23,325,051 (GRCm39) |
missense |
probably benign |
0.05 |
R1741:Usp34
|
UTSW |
11 |
23,314,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1854:Usp34
|
UTSW |
11 |
23,376,153 (GRCm39) |
missense |
probably benign |
0.24 |
R1867:Usp34
|
UTSW |
11 |
23,311,593 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1869:Usp34
|
UTSW |
11 |
23,314,479 (GRCm39) |
missense |
probably benign |
0.37 |
R1870:Usp34
|
UTSW |
11 |
23,314,479 (GRCm39) |
missense |
probably benign |
0.37 |
R1871:Usp34
|
UTSW |
11 |
23,314,479 (GRCm39) |
missense |
probably benign |
0.37 |
R1967:Usp34
|
UTSW |
11 |
23,314,503 (GRCm39) |
missense |
probably benign |
0.01 |
R2051:Usp34
|
UTSW |
11 |
23,414,468 (GRCm39) |
missense |
probably damaging |
0.97 |
R2132:Usp34
|
UTSW |
11 |
23,414,556 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2156:Usp34
|
UTSW |
11 |
23,332,602 (GRCm39) |
missense |
probably damaging |
0.98 |
R2205:Usp34
|
UTSW |
11 |
23,335,147 (GRCm39) |
missense |
probably damaging |
0.97 |
R2342:Usp34
|
UTSW |
11 |
23,353,599 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3431:Usp34
|
UTSW |
11 |
23,320,466 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3812:Usp34
|
UTSW |
11 |
23,414,517 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3872:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3873:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3874:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3875:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3925:Usp34
|
UTSW |
11 |
23,293,640 (GRCm39) |
missense |
probably benign |
0.28 |
R3972:Usp34
|
UTSW |
11 |
23,407,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R4018:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4042:Usp34
|
UTSW |
11 |
23,439,033 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4155:Usp34
|
UTSW |
11 |
23,367,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R4197:Usp34
|
UTSW |
11 |
23,394,189 (GRCm39) |
missense |
probably damaging |
0.98 |
R4352:Usp34
|
UTSW |
11 |
23,270,727 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4379:Usp34
|
UTSW |
11 |
23,334,499 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4444:Usp34
|
UTSW |
11 |
23,385,998 (GRCm39) |
missense |
probably damaging |
0.98 |
R4475:Usp34
|
UTSW |
11 |
23,407,975 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4501:Usp34
|
UTSW |
11 |
23,351,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R4527:Usp34
|
UTSW |
11 |
23,371,257 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4603:Usp34
|
UTSW |
11 |
23,414,633 (GRCm39) |
missense |
probably damaging |
0.97 |
R4612:Usp34
|
UTSW |
11 |
23,382,268 (GRCm39) |
missense |
probably damaging |
0.99 |
R4673:Usp34
|
UTSW |
11 |
23,314,480 (GRCm39) |
small deletion |
probably benign |
|
R4707:Usp34
|
UTSW |
11 |
23,437,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Usp34
|
UTSW |
11 |
23,343,749 (GRCm39) |
splice site |
probably null |
|
R4867:Usp34
|
UTSW |
11 |
23,401,999 (GRCm39) |
missense |
probably benign |
0.28 |
R4879:Usp34
|
UTSW |
11 |
23,323,410 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4977:Usp34
|
UTSW |
11 |
23,438,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Usp34
|
UTSW |
11 |
23,414,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Usp34
|
UTSW |
11 |
23,408,086 (GRCm39) |
intron |
probably benign |
|
R5068:Usp34
|
UTSW |
11 |
23,410,665 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5304:Usp34
|
UTSW |
11 |
23,293,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Usp34
|
UTSW |
11 |
23,283,739 (GRCm39) |
missense |
probably benign |
|
R5327:Usp34
|
UTSW |
11 |
23,418,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Usp34
|
UTSW |
11 |
23,438,659 (GRCm39) |
missense |
probably benign |
0.04 |
R5328:Usp34
|
UTSW |
11 |
23,414,616 (GRCm39) |
missense |
probably benign |
0.01 |
R5390:Usp34
|
UTSW |
11 |
23,394,202 (GRCm39) |
critical splice donor site |
probably null |
|
R5434:Usp34
|
UTSW |
11 |
23,362,271 (GRCm39) |
missense |
probably damaging |
0.99 |
R5523:Usp34
|
UTSW |
11 |
23,299,198 (GRCm39) |
missense |
probably benign |
0.39 |
R5567:Usp34
|
UTSW |
11 |
23,438,336 (GRCm39) |
missense |
probably damaging |
0.97 |
R5571:Usp34
|
UTSW |
11 |
23,407,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R5645:Usp34
|
UTSW |
11 |
23,325,024 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5713:Usp34
|
UTSW |
11 |
23,293,515 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5719:Usp34
|
UTSW |
11 |
23,304,846 (GRCm39) |
missense |
probably benign |
0.00 |
R5813:Usp34
|
UTSW |
11 |
23,371,340 (GRCm39) |
missense |
probably benign |
0.38 |
R5921:Usp34
|
UTSW |
11 |
23,414,686 (GRCm39) |
missense |
probably damaging |
0.99 |
R5928:Usp34
|
UTSW |
11 |
23,386,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R5944:Usp34
|
UTSW |
11 |
23,313,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R6198:Usp34
|
UTSW |
11 |
23,434,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R6229:Usp34
|
UTSW |
11 |
23,396,778 (GRCm39) |
missense |
probably damaging |
0.99 |
R6306:Usp34
|
UTSW |
11 |
23,362,260 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6320:Usp34
|
UTSW |
11 |
23,402,520 (GRCm39) |
missense |
probably damaging |
0.98 |
R6341:Usp34
|
UTSW |
11 |
23,331,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R6374:Usp34
|
UTSW |
11 |
23,388,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R6398:Usp34
|
UTSW |
11 |
23,438,666 (GRCm39) |
missense |
probably benign |
|
R6438:Usp34
|
UTSW |
11 |
23,314,266 (GRCm39) |
missense |
probably benign |
0.02 |
R6668:Usp34
|
UTSW |
11 |
23,410,659 (GRCm39) |
missense |
probably damaging |
0.97 |
R6700:Usp34
|
UTSW |
11 |
23,389,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R6783:Usp34
|
UTSW |
11 |
23,362,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R6821:Usp34
|
UTSW |
11 |
23,317,491 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6855:Usp34
|
UTSW |
11 |
23,402,569 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6916:Usp34
|
UTSW |
11 |
23,408,023 (GRCm39) |
missense |
probably damaging |
0.98 |
R7020:Usp34
|
UTSW |
11 |
23,343,954 (GRCm39) |
missense |
probably benign |
0.05 |
R7026:Usp34
|
UTSW |
11 |
23,311,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R7085:Usp34
|
UTSW |
11 |
23,313,097 (GRCm39) |
missense |
|
|
R7101:Usp34
|
UTSW |
11 |
23,376,183 (GRCm39) |
missense |
|
|
R7168:Usp34
|
UTSW |
11 |
23,414,585 (GRCm39) |
missense |
|
|
R7192:Usp34
|
UTSW |
11 |
23,410,571 (GRCm39) |
missense |
|
|
R7264:Usp34
|
UTSW |
11 |
23,283,566 (GRCm39) |
missense |
probably benign |
0.00 |
R7325:Usp34
|
UTSW |
11 |
23,369,052 (GRCm39) |
missense |
|
|
R7343:Usp34
|
UTSW |
11 |
23,438,868 (GRCm39) |
missense |
|
|
R7358:Usp34
|
UTSW |
11 |
23,311,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R7369:Usp34
|
UTSW |
11 |
23,382,361 (GRCm39) |
missense |
|
|
R7389:Usp34
|
UTSW |
11 |
23,295,200 (GRCm39) |
missense |
|
|
R7459:Usp34
|
UTSW |
11 |
23,314,458 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7517:Usp34
|
UTSW |
11 |
23,396,968 (GRCm39) |
missense |
|
|
R7729:Usp34
|
UTSW |
11 |
23,399,268 (GRCm39) |
missense |
|
|
R7777:Usp34
|
UTSW |
11 |
23,332,638 (GRCm39) |
missense |
|
|
R7810:Usp34
|
UTSW |
11 |
23,362,314 (GRCm39) |
missense |
|
|
R7836:Usp34
|
UTSW |
11 |
23,396,614 (GRCm39) |
missense |
|
|
R7862:Usp34
|
UTSW |
11 |
23,414,718 (GRCm39) |
missense |
|
|
R7993:Usp34
|
UTSW |
11 |
23,327,622 (GRCm39) |
missense |
|
|
R8050:Usp34
|
UTSW |
11 |
23,396,787 (GRCm39) |
missense |
|
|
R8054:Usp34
|
UTSW |
11 |
23,311,295 (GRCm39) |
missense |
|
|
R8239:Usp34
|
UTSW |
11 |
23,396,750 (GRCm39) |
missense |
|
|
R8266:Usp34
|
UTSW |
11 |
23,436,810 (GRCm39) |
splice site |
probably benign |
|
R8347:Usp34
|
UTSW |
11 |
23,362,345 (GRCm39) |
missense |
|
|
R8409:Usp34
|
UTSW |
11 |
23,407,811 (GRCm39) |
missense |
|
|
R8692:Usp34
|
UTSW |
11 |
23,379,325 (GRCm39) |
missense |
|
|
R8734:Usp34
|
UTSW |
11 |
23,394,184 (GRCm39) |
missense |
|
|
R8806:Usp34
|
UTSW |
11 |
23,434,143 (GRCm39) |
missense |
|
|
R8914:Usp34
|
UTSW |
11 |
23,293,604 (GRCm39) |
missense |
|
|
R8987:Usp34
|
UTSW |
11 |
23,414,267 (GRCm39) |
missense |
|
|
R9013:Usp34
|
UTSW |
11 |
23,320,302 (GRCm39) |
missense |
|
|
R9108:Usp34
|
UTSW |
11 |
23,320,528 (GRCm39) |
missense |
|
|
R9264:Usp34
|
UTSW |
11 |
23,439,064 (GRCm39) |
missense |
|
|
R9301:Usp34
|
UTSW |
11 |
23,422,951 (GRCm39) |
missense |
|
|
R9375:Usp34
|
UTSW |
11 |
23,437,203 (GRCm39) |
missense |
|
|
R9385:Usp34
|
UTSW |
11 |
23,399,223 (GRCm39) |
missense |
|
|
R9500:Usp34
|
UTSW |
11 |
23,331,337 (GRCm39) |
missense |
probably damaging |
0.99 |
R9566:Usp34
|
UTSW |
11 |
23,317,529 (GRCm39) |
missense |
|
|
R9629:Usp34
|
UTSW |
11 |
23,314,364 (GRCm39) |
missense |
|
|
R9679:Usp34
|
UTSW |
11 |
23,394,369 (GRCm39) |
missense |
|
|
R9680:Usp34
|
UTSW |
11 |
23,317,385 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9686:Usp34
|
UTSW |
11 |
23,424,351 (GRCm39) |
missense |
|
|
R9752:Usp34
|
UTSW |
11 |
23,409,182 (GRCm39) |
missense |
probably benign |
0.11 |
X0023:Usp34
|
UTSW |
11 |
23,325,028 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0057:Usp34
|
UTSW |
11 |
23,407,824 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Usp34
|
UTSW |
11 |
23,423,221 (GRCm39) |
missense |
probably damaging |
1.00 |
|