Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr3 |
A |
T |
1: 125,322,874 (GRCm39) |
D364E |
probably benign |
Het |
Adra2c |
C |
T |
5: 35,437,423 (GRCm39) |
T65I |
probably damaging |
Het |
Agap2 |
T |
A |
10: 126,925,229 (GRCm39) |
|
probably null |
Het |
Ager |
T |
C |
17: 34,817,728 (GRCm39) |
V126A |
possibly damaging |
Het |
Arhgap39 |
T |
C |
15: 76,621,736 (GRCm39) |
I288M |
probably benign |
Het |
Arhgap45 |
A |
T |
10: 79,862,068 (GRCm39) |
S541C |
probably benign |
Het |
Asb4 |
A |
G |
6: 5,431,043 (GRCm39) |
Y426C |
probably damaging |
Het |
Azi2 |
C |
T |
9: 117,878,406 (GRCm39) |
T82I |
probably damaging |
Het |
Baz2b |
T |
A |
2: 59,778,567 (GRCm39) |
R764S |
probably damaging |
Het |
Ccdc146 |
A |
C |
5: 21,506,338 (GRCm39) |
I701S |
probably damaging |
Het |
Ccnq |
T |
C |
11: 78,642,056 (GRCm39) |
K145E |
probably damaging |
Het |
Cd55b |
T |
A |
1: 130,345,903 (GRCm39) |
I172F |
probably damaging |
Het |
Cdk11b |
A |
G |
4: 155,718,647 (GRCm39) |
E199G |
probably benign |
Het |
Cntnap4 |
A |
T |
8: 113,478,921 (GRCm39) |
T216S |
possibly damaging |
Het |
D5Ertd579e |
A |
T |
5: 36,761,858 (GRCm39) |
N1336K |
possibly damaging |
Het |
Dmxl1 |
A |
G |
18: 49,979,653 (GRCm39) |
E96G |
probably benign |
Het |
Dscaml1 |
C |
T |
9: 45,579,458 (GRCm39) |
T335I |
possibly damaging |
Het |
Epb41l2 |
G |
T |
10: 25,378,022 (GRCm39) |
G695C |
probably damaging |
Het |
Erbb4 |
C |
T |
1: 68,599,735 (GRCm39) |
R114H |
probably damaging |
Het |
F2rl1 |
G |
T |
13: 95,650,446 (GRCm39) |
Y145* |
probably null |
Het |
Fsip2 |
A |
T |
2: 82,810,785 (GRCm39) |
Y2368F |
possibly damaging |
Het |
Galnt7 |
C |
T |
8: 57,989,612 (GRCm39) |
|
probably null |
Het |
Garre1 |
A |
T |
7: 33,941,802 (GRCm39) |
Y627* |
probably null |
Het |
Gm6811 |
T |
A |
17: 21,314,245 (GRCm39) |
|
noncoding transcript |
Het |
Gm6811 |
T |
G |
17: 21,314,952 (GRCm39) |
|
noncoding transcript |
Het |
H2-M1 |
G |
A |
17: 36,982,602 (GRCm39) |
T86M |
possibly damaging |
Het |
Hk2 |
T |
C |
6: 82,720,347 (GRCm39) |
D170G |
probably benign |
Het |
Hmcn1 |
C |
T |
1: 150,614,432 (GRCm39) |
A1325T |
possibly damaging |
Het |
Insrr |
T |
A |
3: 87,707,826 (GRCm39) |
Y89* |
probably null |
Het |
Itga1 |
T |
C |
13: 115,117,388 (GRCm39) |
E871G |
probably benign |
Het |
Kat6a |
T |
C |
8: 23,429,421 (GRCm39) |
L1592P |
possibly damaging |
Het |
Kndc1 |
C |
A |
7: 139,500,979 (GRCm39) |
A756E |
probably benign |
Het |
Krt12 |
A |
T |
11: 99,312,728 (GRCm39) |
C105* |
probably null |
Het |
Lama1 |
G |
A |
17: 68,091,083 (GRCm39) |
|
probably null |
Het |
Lama3 |
A |
G |
18: 12,640,006 (GRCm39) |
N67S |
probably benign |
Het |
Lrrk1 |
A |
G |
7: 65,956,587 (GRCm39) |
|
probably null |
Het |
Lypd9 |
T |
A |
11: 58,337,192 (GRCm39) |
I94L |
possibly damaging |
Het |
Map2 |
T |
C |
1: 66,438,578 (GRCm39) |
V34A |
probably damaging |
Het |
Mroh6 |
A |
G |
15: 75,757,549 (GRCm39) |
L487P |
probably damaging |
Het |
Myo18b |
A |
T |
5: 112,959,508 (GRCm39) |
S1430T |
probably benign |
Het |
Notch3 |
G |
A |
17: 32,373,723 (GRCm39) |
T495I |
probably benign |
Het |
Or1e31 |
A |
T |
11: 73,690,229 (GRCm39) |
M118K |
probably damaging |
Het |
Palld |
C |
T |
8: 61,966,457 (GRCm39) |
A980T |
probably damaging |
Het |
Paxip1 |
A |
T |
5: 27,966,666 (GRCm39) |
I620N |
probably damaging |
Het |
Pcdha6 |
A |
G |
18: 37,102,820 (GRCm39) |
|
probably null |
Het |
Pcdhb11 |
G |
A |
18: 37,554,813 (GRCm39) |
V48M |
probably benign |
Het |
Pcdhga6 |
A |
G |
18: 37,840,697 (GRCm39) |
E139G |
probably benign |
Het |
Pck1 |
T |
C |
2: 172,999,112 (GRCm39) |
V426A |
probably damaging |
Het |
Pck2 |
T |
A |
14: 55,780,081 (GRCm39) |
I110N |
probably damaging |
Het |
Peg10 |
GAT |
GATCAT |
6: 4,756,449 (GRCm39) |
|
probably benign |
Het |
Phactr3 |
G |
A |
2: 177,920,812 (GRCm39) |
E222K |
probably damaging |
Het |
Ppip5k1 |
A |
T |
2: 121,153,684 (GRCm39) |
|
probably benign |
Het |
Prodh2 |
A |
G |
7: 30,206,076 (GRCm39) |
H278R |
probably benign |
Het |
Rspry1 |
T |
A |
8: 95,349,886 (GRCm39) |
H91Q |
probably damaging |
Het |
Slc13a2 |
CGTTATCTGT |
CGT |
11: 78,294,306 (GRCm39) |
|
probably benign |
Het |
Smn1 |
A |
G |
13: 100,264,503 (GRCm39) |
N78S |
possibly damaging |
Het |
Spta1 |
T |
A |
1: 174,046,078 (GRCm39) |
I1614N |
probably damaging |
Het |
Syt17 |
T |
C |
7: 118,033,513 (GRCm39) |
D165G |
probably damaging |
Het |
Tbck |
A |
G |
3: 132,448,766 (GRCm39) |
Y593C |
probably damaging |
Het |
Tcaf2 |
G |
C |
6: 42,606,687 (GRCm39) |
F422L |
probably benign |
Het |
Tex15 |
T |
A |
8: 34,067,217 (GRCm39) |
F2216I |
possibly damaging |
Het |
Trpc4 |
A |
G |
3: 54,225,441 (GRCm39) |
E846G |
probably benign |
Het |
Ttc41 |
T |
C |
10: 86,580,313 (GRCm39) |
I753T |
probably benign |
Het |
Vdac1 |
C |
T |
11: 52,267,309 (GRCm39) |
T70M |
possibly damaging |
Het |
Vmn1r124 |
A |
C |
7: 20,994,104 (GRCm39) |
F147V |
probably benign |
Het |
Vmn1r220 |
T |
C |
13: 23,368,465 (GRCm39) |
D77G |
probably damaging |
Het |
Vmn2r28 |
T |
C |
7: 5,493,730 (GRCm39) |
H72R |
probably benign |
Het |
Vmn2r78 |
A |
T |
7: 86,570,318 (GRCm39) |
I279L |
probably benign |
Het |
Vmn2r95 |
G |
T |
17: 18,671,732 (GRCm39) |
A490S |
possibly damaging |
Het |
Wdfy4 |
C |
T |
14: 32,831,482 (GRCm39) |
A915T |
possibly damaging |
Het |
Zmiz2 |
G |
T |
11: 6,345,604 (GRCm39) |
|
probably null |
Het |
Zscan2 |
A |
G |
7: 80,525,557 (GRCm39) |
N426S |
probably benign |
Het |
|
Other mutations in Dlg5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00160:Dlg5
|
APN |
14 |
24,241,229 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00164:Dlg5
|
APN |
14 |
24,208,532 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL00767:Dlg5
|
APN |
14 |
24,215,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01284:Dlg5
|
APN |
14 |
24,196,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01328:Dlg5
|
APN |
14 |
24,252,419 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01532:Dlg5
|
APN |
14 |
24,208,660 (GRCm39) |
missense |
probably benign |
|
IGL01621:Dlg5
|
APN |
14 |
24,198,289 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01649:Dlg5
|
APN |
14 |
24,188,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01733:Dlg5
|
APN |
14 |
24,220,517 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02048:Dlg5
|
APN |
14 |
24,222,271 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02103:Dlg5
|
APN |
14 |
24,194,414 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02138:Dlg5
|
APN |
14 |
24,208,419 (GRCm39) |
missense |
probably benign |
|
IGL02146:Dlg5
|
APN |
14 |
24,252,429 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02392:Dlg5
|
APN |
14 |
24,200,277 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02427:Dlg5
|
APN |
14 |
24,216,275 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02643:Dlg5
|
APN |
14 |
24,241,250 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02649:Dlg5
|
APN |
14 |
24,196,319 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02933:Dlg5
|
APN |
14 |
24,208,567 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02965:Dlg5
|
APN |
14 |
24,222,091 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02988:Dlg5
|
APN |
14 |
24,216,323 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03351:Dlg5
|
APN |
14 |
24,220,522 (GRCm39) |
missense |
probably benign |
0.03 |
legerdemain
|
UTSW |
14 |
24,214,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R0123:Dlg5
|
UTSW |
14 |
24,197,274 (GRCm39) |
missense |
probably benign |
|
R0131:Dlg5
|
UTSW |
14 |
24,188,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R0709:Dlg5
|
UTSW |
14 |
24,196,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R0920:Dlg5
|
UTSW |
14 |
24,226,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R0924:Dlg5
|
UTSW |
14 |
24,185,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R0930:Dlg5
|
UTSW |
14 |
24,185,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R0981:Dlg5
|
UTSW |
14 |
24,204,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R1402:Dlg5
|
UTSW |
14 |
24,226,676 (GRCm39) |
missense |
probably benign |
0.06 |
R1402:Dlg5
|
UTSW |
14 |
24,226,676 (GRCm39) |
missense |
probably benign |
0.06 |
R1438:Dlg5
|
UTSW |
14 |
24,204,673 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1449:Dlg5
|
UTSW |
14 |
24,185,711 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1465:Dlg5
|
UTSW |
14 |
24,204,764 (GRCm39) |
splice site |
probably null |
|
R1465:Dlg5
|
UTSW |
14 |
24,204,764 (GRCm39) |
splice site |
probably null |
|
R1543:Dlg5
|
UTSW |
14 |
24,194,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Dlg5
|
UTSW |
14 |
24,199,512 (GRCm39) |
missense |
probably benign |
0.28 |
R1899:Dlg5
|
UTSW |
14 |
24,198,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1920:Dlg5
|
UTSW |
14 |
24,226,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1921:Dlg5
|
UTSW |
14 |
24,226,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Dlg5
|
UTSW |
14 |
24,206,537 (GRCm39) |
splice site |
probably benign |
|
R1968:Dlg5
|
UTSW |
14 |
24,214,187 (GRCm39) |
nonsense |
probably null |
|
R2049:Dlg5
|
UTSW |
14 |
24,204,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Dlg5
|
UTSW |
14 |
24,186,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Dlg5
|
UTSW |
14 |
24,227,826 (GRCm39) |
nonsense |
probably null |
|
R2139:Dlg5
|
UTSW |
14 |
24,220,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Dlg5
|
UTSW |
14 |
24,187,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R2283:Dlg5
|
UTSW |
14 |
24,208,731 (GRCm39) |
missense |
probably benign |
0.00 |
R2293:Dlg5
|
UTSW |
14 |
24,208,180 (GRCm39) |
missense |
probably benign |
|
R2356:Dlg5
|
UTSW |
14 |
24,220,496 (GRCm39) |
critical splice donor site |
probably null |
|
R2362:Dlg5
|
UTSW |
14 |
24,208,755 (GRCm39) |
missense |
probably benign |
0.04 |
R2513:Dlg5
|
UTSW |
14 |
24,214,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R3084:Dlg5
|
UTSW |
14 |
24,216,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R3086:Dlg5
|
UTSW |
14 |
24,216,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R3750:Dlg5
|
UTSW |
14 |
24,215,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R3780:Dlg5
|
UTSW |
14 |
24,240,378 (GRCm39) |
unclassified |
probably benign |
|
R3782:Dlg5
|
UTSW |
14 |
24,240,378 (GRCm39) |
unclassified |
probably benign |
|
R3828:Dlg5
|
UTSW |
14 |
24,196,226 (GRCm39) |
missense |
probably damaging |
0.99 |
R4079:Dlg5
|
UTSW |
14 |
24,198,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4393:Dlg5
|
UTSW |
14 |
24,228,057 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4615:Dlg5
|
UTSW |
14 |
24,208,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Dlg5
|
UTSW |
14 |
24,187,249 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4712:Dlg5
|
UTSW |
14 |
24,228,051 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4796:Dlg5
|
UTSW |
14 |
24,194,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Dlg5
|
UTSW |
14 |
24,204,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Dlg5
|
UTSW |
14 |
24,204,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R4946:Dlg5
|
UTSW |
14 |
24,204,429 (GRCm39) |
missense |
probably damaging |
0.99 |
R5022:Dlg5
|
UTSW |
14 |
24,186,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5023:Dlg5
|
UTSW |
14 |
24,186,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Dlg5
|
UTSW |
14 |
24,186,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5234:Dlg5
|
UTSW |
14 |
24,242,930 (GRCm39) |
missense |
probably damaging |
0.98 |
R5561:Dlg5
|
UTSW |
14 |
24,227,860 (GRCm39) |
missense |
probably benign |
0.03 |
R5567:Dlg5
|
UTSW |
14 |
24,242,981 (GRCm39) |
nonsense |
probably null |
|
R5570:Dlg5
|
UTSW |
14 |
24,242,981 (GRCm39) |
nonsense |
probably null |
|
R5640:Dlg5
|
UTSW |
14 |
24,220,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R5646:Dlg5
|
UTSW |
14 |
24,208,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R5711:Dlg5
|
UTSW |
14 |
24,200,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R5810:Dlg5
|
UTSW |
14 |
24,196,322 (GRCm39) |
missense |
probably damaging |
0.99 |
R5900:Dlg5
|
UTSW |
14 |
24,199,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R5964:Dlg5
|
UTSW |
14 |
24,214,157 (GRCm39) |
missense |
probably benign |
|
R6190:Dlg5
|
UTSW |
14 |
24,240,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R6240:Dlg5
|
UTSW |
14 |
24,199,596 (GRCm39) |
splice site |
probably null |
|
R6339:Dlg5
|
UTSW |
14 |
24,208,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R6508:Dlg5
|
UTSW |
14 |
24,188,774 (GRCm39) |
missense |
probably benign |
0.45 |
R6527:Dlg5
|
UTSW |
14 |
24,240,516 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6593:Dlg5
|
UTSW |
14 |
24,200,720 (GRCm39) |
missense |
probably benign |
0.01 |
R6687:Dlg5
|
UTSW |
14 |
24,240,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R6965:Dlg5
|
UTSW |
14 |
24,199,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Dlg5
|
UTSW |
14 |
24,196,263 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7075:Dlg5
|
UTSW |
14 |
24,227,865 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7149:Dlg5
|
UTSW |
14 |
24,240,492 (GRCm39) |
missense |
probably benign |
0.00 |
R7182:Dlg5
|
UTSW |
14 |
24,294,924 (GRCm39) |
missense |
|
|
R7203:Dlg5
|
UTSW |
14 |
24,188,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R7216:Dlg5
|
UTSW |
14 |
24,186,706 (GRCm39) |
nonsense |
probably null |
|
R7359:Dlg5
|
UTSW |
14 |
24,214,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Dlg5
|
UTSW |
14 |
24,295,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Dlg5
|
UTSW |
14 |
24,227,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R7485:Dlg5
|
UTSW |
14 |
24,198,390 (GRCm39) |
missense |
probably benign |
|
R7629:Dlg5
|
UTSW |
14 |
24,295,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7666:Dlg5
|
UTSW |
14 |
24,207,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R7804:Dlg5
|
UTSW |
14 |
24,215,388 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7861:Dlg5
|
UTSW |
14 |
24,295,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7862:Dlg5
|
UTSW |
14 |
24,295,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7864:Dlg5
|
UTSW |
14 |
24,295,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7874:Dlg5
|
UTSW |
14 |
24,185,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R7913:Dlg5
|
UTSW |
14 |
24,187,192 (GRCm39) |
splice site |
probably null |
|
R7981:Dlg5
|
UTSW |
14 |
24,208,213 (GRCm39) |
missense |
probably benign |
|
R8147:Dlg5
|
UTSW |
14 |
24,208,395 (GRCm39) |
missense |
probably benign |
0.07 |
R8204:Dlg5
|
UTSW |
14 |
24,210,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R8206:Dlg5
|
UTSW |
14 |
24,210,336 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8287:Dlg5
|
UTSW |
14 |
24,214,453 (GRCm39) |
missense |
probably benign |
0.40 |
R8296:Dlg5
|
UTSW |
14 |
24,198,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8317:Dlg5
|
UTSW |
14 |
24,241,298 (GRCm39) |
missense |
probably damaging |
0.98 |
R8327:Dlg5
|
UTSW |
14 |
24,196,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R8352:Dlg5
|
UTSW |
14 |
24,241,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Dlg5
|
UTSW |
14 |
24,208,213 (GRCm39) |
missense |
probably benign |
|
R8409:Dlg5
|
UTSW |
14 |
24,226,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R8452:Dlg5
|
UTSW |
14 |
24,241,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8453:Dlg5
|
UTSW |
14 |
24,208,213 (GRCm39) |
missense |
probably benign |
|
R8540:Dlg5
|
UTSW |
14 |
24,208,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R8701:Dlg5
|
UTSW |
14 |
24,226,768 (GRCm39) |
missense |
probably benign |
0.04 |
R8925:Dlg5
|
UTSW |
14 |
24,206,547 (GRCm39) |
missense |
|
|
R8927:Dlg5
|
UTSW |
14 |
24,206,547 (GRCm39) |
missense |
|
|
R9025:Dlg5
|
UTSW |
14 |
24,199,546 (GRCm39) |
missense |
probably benign |
0.00 |
R9102:Dlg5
|
UTSW |
14 |
24,199,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R9138:Dlg5
|
UTSW |
14 |
24,295,376 (GRCm39) |
missense |
probably damaging |
0.98 |
R9165:Dlg5
|
UTSW |
14 |
24,196,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R9250:Dlg5
|
UTSW |
14 |
24,240,543 (GRCm39) |
missense |
probably benign |
0.07 |
R9267:Dlg5
|
UTSW |
14 |
24,204,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R9269:Dlg5
|
UTSW |
14 |
24,242,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R9291:Dlg5
|
UTSW |
14 |
24,241,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R9387:Dlg5
|
UTSW |
14 |
24,197,168 (GRCm39) |
missense |
probably damaging |
0.99 |
R9729:Dlg5
|
UTSW |
14 |
24,204,681 (GRCm39) |
missense |
probably benign |
0.00 |
RF005:Dlg5
|
UTSW |
14 |
24,208,561 (GRCm39) |
nonsense |
probably null |
|
YA93:Dlg5
|
UTSW |
14 |
24,205,201 (GRCm39) |
unclassified |
probably benign |
|
Z1088:Dlg5
|
UTSW |
14 |
24,208,162 (GRCm39) |
missense |
probably damaging |
1.00 |
|