Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
C |
T |
5: 113,245,502 (GRCm39) |
V1584I |
probably benign |
Het |
Adamts12 |
A |
G |
15: 11,285,987 (GRCm39) |
D732G |
probably benign |
Het |
Agpat4 |
A |
G |
17: 12,370,637 (GRCm39) |
|
probably benign |
Het |
AI182371 |
T |
C |
2: 34,985,829 (GRCm39) |
D140G |
possibly damaging |
Het |
Apol11b |
T |
A |
15: 77,519,133 (GRCm39) |
T316S |
probably benign |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Bard1 |
T |
C |
1: 71,114,333 (GRCm39) |
E216G |
probably benign |
Het |
Bdp1 |
C |
A |
13: 100,186,376 (GRCm39) |
R1692L |
probably damaging |
Het |
Capn10 |
T |
C |
1: 92,871,141 (GRCm39) |
I101T |
probably damaging |
Het |
Ccdc175 |
C |
T |
12: 72,158,979 (GRCm39) |
M653I |
probably benign |
Het |
Ccdc9b |
C |
A |
2: 118,590,058 (GRCm39) |
R262L |
probably damaging |
Het |
Ccr8 |
G |
A |
9: 119,923,530 (GRCm39) |
C215Y |
probably damaging |
Het |
Cct3 |
T |
A |
3: 88,219,092 (GRCm39) |
L241* |
probably null |
Het |
Cd2ap |
A |
T |
17: 43,163,350 (GRCm39) |
I25N |
probably damaging |
Het |
Cdh19 |
T |
C |
1: 110,820,990 (GRCm39) |
K583E |
probably benign |
Het |
Cela3a |
A |
G |
4: 137,129,986 (GRCm39) |
S212P |
unknown |
Het |
Cfap44 |
T |
A |
16: 44,236,246 (GRCm39) |
|
probably null |
Het |
Clca3a1 |
A |
T |
3: 144,455,473 (GRCm39) |
L440Q |
probably damaging |
Het |
Crybg2 |
A |
G |
4: 133,816,663 (GRCm39) |
Y1676C |
probably damaging |
Het |
Dscam |
T |
C |
16: 96,445,188 (GRCm39) |
D1501G |
probably benign |
Het |
Eml6 |
C |
A |
11: 29,755,757 (GRCm39) |
L832F |
probably benign |
Het |
Enpp3 |
A |
G |
10: 24,649,825 (GRCm39) |
L867P |
probably damaging |
Het |
Erbb3 |
A |
G |
10: 128,422,107 (GRCm39) |
Y46H |
possibly damaging |
Het |
Fads3 |
T |
C |
19: 10,033,384 (GRCm39) |
I342T |
possibly damaging |
Het |
Flvcr1 |
A |
T |
1: 190,753,303 (GRCm39) |
S290T |
probably benign |
Het |
Fut9 |
A |
G |
4: 25,799,191 (GRCm39) |
|
probably benign |
Het |
Gad2 |
C |
T |
2: 22,512,679 (GRCm39) |
A2V |
probably damaging |
Het |
Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
Gm10715 |
T |
G |
9: 3,038,073 (GRCm39) |
|
probably benign |
Het |
Herc1 |
T |
G |
9: 66,349,211 (GRCm39) |
D2023E |
probably benign |
Het |
Hsd3b3 |
A |
G |
3: 98,649,801 (GRCm39) |
L174P |
probably damaging |
Het |
Impg2 |
TACCACCACCACCACCACCACCACCA |
TACCACCACCACCACCACCACCA |
16: 56,078,302 (GRCm39) |
|
probably benign |
Het |
Iqcf3 |
A |
G |
9: 106,438,148 (GRCm39) |
|
probably null |
Het |
Kcna4 |
G |
A |
2: 107,126,888 (GRCm39) |
V541M |
probably damaging |
Het |
Kcnj11 |
T |
C |
7: 45,749,240 (GRCm39) |
T28A |
probably benign |
Het |
Kcnmb2 |
T |
A |
3: 32,236,016 (GRCm39) |
N88K |
probably damaging |
Het |
Kdm2a |
TTCCTCCTCCTCCTCCTCTTCCTCCTCCTC |
TTCCTCCTCCTCCTCTTCCTCCTCCTC |
19: 4,374,535 (GRCm39) |
|
probably benign |
Het |
Krt1c |
T |
C |
15: 101,722,395 (GRCm39) |
E430G |
probably damaging |
Het |
Lins1 |
C |
T |
7: 66,360,389 (GRCm39) |
L384F |
possibly damaging |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Mfge8 |
T |
C |
7: 78,784,273 (GRCm39) |
N389D |
probably damaging |
Het |
Mug1 |
C |
T |
6: 121,861,213 (GRCm39) |
T1278I |
probably benign |
Het |
Myh9 |
T |
C |
15: 77,692,077 (GRCm39) |
M161V |
probably damaging |
Het |
Myl7 |
T |
A |
11: 5,848,171 (GRCm39) |
Y61F |
probably benign |
Het |
Nlrp4d |
A |
T |
7: 10,096,706 (GRCm39) |
|
unknown |
Het |
Nol3 |
A |
G |
8: 106,008,565 (GRCm39) |
|
probably null |
Het |
Nup85 |
T |
A |
11: 115,468,751 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
A |
11: 58,903,568 (GRCm39) |
T7619S |
probably damaging |
Het |
Or2t49 |
T |
A |
11: 58,392,494 (GRCm39) |
N296I |
probably damaging |
Het |
Or4k48 |
T |
C |
2: 111,476,226 (GRCm39) |
M39V |
probably benign |
Het |
Or52a24 |
C |
T |
7: 103,381,457 (GRCm39) |
T108I |
possibly damaging |
Het |
Or7g26 |
G |
A |
9: 19,230,141 (GRCm39) |
V104I |
probably benign |
Het |
Pax5 |
T |
A |
4: 44,679,494 (GRCm39) |
I184F |
probably damaging |
Het |
Pcdha7 |
T |
A |
18: 37,107,560 (GRCm39) |
V195D |
probably damaging |
Het |
Phf3 |
A |
T |
1: 30,853,020 (GRCm39) |
|
probably benign |
Het |
Pla2g15 |
G |
T |
8: 106,889,703 (GRCm39) |
G325V |
probably damaging |
Het |
Ppp1r21 |
T |
C |
17: 88,880,043 (GRCm39) |
F487L |
probably benign |
Het |
Ppp1r9a |
A |
G |
6: 5,157,016 (GRCm39) |
I965V |
probably benign |
Het |
Ptpru |
A |
G |
4: 131,548,275 (GRCm39) |
V74A |
probably damaging |
Het |
Rif1 |
T |
A |
2: 51,988,946 (GRCm39) |
Y780N |
probably damaging |
Het |
Rps25 |
T |
A |
9: 44,320,046 (GRCm39) |
Y23N |
possibly damaging |
Het |
Ryr1 |
T |
C |
7: 28,785,258 (GRCm39) |
D1811G |
probably damaging |
Het |
Scamp5 |
T |
G |
9: 57,359,319 (GRCm39) |
|
probably null |
Het |
Senp1 |
T |
C |
15: 97,943,777 (GRCm39) |
D602G |
probably damaging |
Het |
Sh2b2 |
T |
G |
5: 136,260,811 (GRCm39) |
D135A |
probably damaging |
Het |
Slc26a8 |
G |
A |
17: 28,857,635 (GRCm39) |
T836M |
probably benign |
Het |
Slfn4 |
T |
G |
11: 83,077,647 (GRCm39) |
I145S |
possibly damaging |
Het |
Spag6l |
G |
A |
16: 16,595,254 (GRCm39) |
T377I |
probably benign |
Het |
Spdye4b |
T |
C |
5: 143,182,089 (GRCm39) |
F129S |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,447,514 (GRCm39) |
G2360E |
probably benign |
Het |
Taar2 |
A |
T |
10: 23,816,669 (GRCm39) |
I70F |
probably damaging |
Het |
Taar7e |
A |
G |
10: 23,914,464 (GRCm39) |
N318S |
probably damaging |
Het |
Tor1a |
C |
A |
2: 30,857,742 (GRCm39) |
R42L |
probably benign |
Het |
Trdn |
A |
T |
10: 33,350,502 (GRCm39) |
Q690H |
probably benign |
Het |
Trim56 |
C |
A |
5: 137,141,579 (GRCm39) |
V646L |
probably benign |
Het |
Tspan15 |
T |
A |
10: 62,027,323 (GRCm39) |
K165I |
probably benign |
Het |
Usp45 |
A |
G |
4: 21,797,307 (GRCm39) |
T76A |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,785,506 (GRCm39) |
|
probably null |
Het |
Zfp512b |
T |
C |
2: 181,226,888 (GRCm39) |
|
probably benign |
Het |
Zyx |
C |
A |
6: 42,333,093 (GRCm39) |
|
probably null |
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 |
R0125:Usp24
|
UTSW |
4 |
106,254,496 (GRCm39) |
missense |
possibly damaging |
0.76 |
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 |
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 |
|