Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
C |
14: 32,383,809 (GRCm39) |
T719A |
possibly damaging |
Het |
Abcc1 |
A |
G |
16: 14,290,873 (GRCm39) |
|
probably null |
Het |
Aftph |
C |
T |
11: 20,658,676 (GRCm39) |
|
probably null |
Het |
Als2 |
C |
A |
1: 59,254,276 (GRCm39) |
K360N |
probably benign |
Het |
Atg2a |
T |
A |
19: 6,308,076 (GRCm39) |
|
probably null |
Het |
Axl |
T |
C |
7: 25,486,941 (GRCm39) |
D22G |
probably benign |
Het |
Baiap2 |
G |
A |
11: 119,890,052 (GRCm39) |
A438T |
probably benign |
Het |
Bean1 |
G |
C |
8: 104,908,643 (GRCm39) |
A7P |
probably benign |
Het |
Birc6 |
C |
G |
17: 74,954,724 (GRCm39) |
P3431R |
probably damaging |
Het |
Camk1d |
A |
G |
2: 5,719,047 (GRCm39) |
M1T |
probably null |
Het |
Carmil3 |
T |
C |
14: 55,741,295 (GRCm39) |
Y1027H |
probably damaging |
Het |
Ccdc6 |
G |
A |
10: 70,023,658 (GRCm39) |
|
probably benign |
Het |
Cemip |
C |
A |
7: 83,591,233 (GRCm39) |
V1280L |
probably benign |
Het |
Cfap58 |
C |
A |
19: 47,950,981 (GRCm39) |
N447K |
probably benign |
Het |
Chd3 |
A |
G |
11: 69,251,471 (GRCm39) |
L520P |
probably damaging |
Het |
Col1a2 |
T |
A |
6: 4,531,223 (GRCm39) |
|
probably null |
Het |
Cpne7 |
A |
C |
8: 123,844,406 (GRCm39) |
|
probably null |
Het |
Ctla4 |
T |
C |
1: 60,951,723 (GRCm39) |
V84A |
probably damaging |
Het |
Dap3 |
A |
G |
3: 88,835,565 (GRCm39) |
V263A |
probably benign |
Het |
Dhx57 |
T |
A |
17: 80,549,378 (GRCm39) |
|
probably null |
Het |
Dsg3 |
C |
A |
18: 20,656,719 (GRCm39) |
F196L |
possibly damaging |
Het |
Eif2ak4 |
C |
A |
2: 118,257,064 (GRCm39) |
D402E |
probably damaging |
Het |
Fance |
T |
C |
17: 28,537,068 (GRCm39) |
V24A |
probably benign |
Het |
Fasn |
A |
T |
11: 120,705,574 (GRCm39) |
L1149Q |
probably damaging |
Het |
Fcgbpl1 |
C |
G |
7: 27,831,060 (GRCm39) |
S91C |
probably damaging |
Het |
Flg |
T |
A |
3: 93,187,093 (GRCm39) |
S182T |
possibly damaging |
Het |
Gm128 |
T |
A |
3: 95,147,293 (GRCm39) |
S334C |
possibly damaging |
Het |
Gm3727 |
A |
C |
14: 7,264,561 (GRCm38) |
H31Q |
probably damaging |
Het |
Gm4841 |
T |
G |
18: 60,403,977 (GRCm39) |
T39P |
probably damaging |
Het |
Golgb1 |
G |
T |
16: 36,735,513 (GRCm39) |
V1587L |
possibly damaging |
Het |
Golm1 |
G |
A |
13: 59,790,072 (GRCm39) |
P243S |
probably benign |
Het |
Gstcd |
C |
A |
3: 132,788,081 (GRCm39) |
A206S |
possibly damaging |
Het |
Gstcd |
C |
A |
3: 132,788,082 (GRCm39) |
K205N |
possibly damaging |
Het |
Gtf3c1 |
A |
G |
7: 125,280,345 (GRCm39) |
V355A |
probably benign |
Het |
Hhatl |
T |
C |
9: 121,618,236 (GRCm39) |
D173G |
probably benign |
Het |
Kcnu1 |
T |
A |
8: 26,395,994 (GRCm39) |
C660S |
probably benign |
Het |
Kctd8 |
T |
C |
5: 69,267,988 (GRCm39) |
D374G |
probably benign |
Het |
Kif21a |
T |
C |
15: 90,878,594 (GRCm39) |
I229V |
possibly damaging |
Het |
L3mbtl1 |
A |
T |
2: 162,809,505 (GRCm39) |
I702F |
probably benign |
Het |
Lce1d |
T |
C |
3: 92,593,066 (GRCm39) |
|
probably benign |
Het |
Lrig1 |
C |
T |
6: 94,594,347 (GRCm39) |
|
probably null |
Het |
Lrp12 |
A |
T |
15: 39,739,507 (GRCm39) |
D563E |
probably damaging |
Het |
Lrp2 |
C |
T |
2: 69,336,718 (GRCm39) |
|
probably null |
Het |
Map3k5 |
G |
A |
10: 19,970,201 (GRCm39) |
V703I |
possibly damaging |
Het |
Mecr |
A |
G |
4: 131,581,076 (GRCm39) |
R110G |
probably benign |
Het |
Mtrr |
T |
A |
13: 68,715,092 (GRCm39) |
K445* |
probably null |
Het |
Nanos1 |
T |
A |
19: 60,744,990 (GRCm39) |
L96Q |
probably benign |
Het |
Or13a24 |
T |
G |
7: 140,154,069 (GRCm39) |
M1R |
probably null |
Het |
Or51t4 |
T |
A |
7: 102,598,700 (GRCm39) |
F333I |
probably benign |
Het |
Or6c214 |
T |
A |
10: 129,591,021 (GRCm39) |
L99F |
probably damaging |
Het |
Otog |
T |
C |
7: 45,955,014 (GRCm39) |
|
probably null |
Het |
Pcdhb3 |
G |
T |
18: 37,434,294 (GRCm39) |
V87F |
probably benign |
Het |
Pcdhb3 |
T |
A |
18: 37,434,292 (GRCm39) |
L86* |
probably null |
Het |
Pcdhb3 |
A |
T |
18: 37,434,293 (GRCm39) |
L86F |
probably damaging |
Het |
Pdgfd |
A |
G |
9: 6,359,894 (GRCm39) |
K322E |
probably damaging |
Het |
Picalm |
T |
C |
7: 89,846,217 (GRCm39) |
S648P |
probably damaging |
Het |
Pigr |
T |
C |
1: 130,774,357 (GRCm39) |
S446P |
possibly damaging |
Het |
Pik3cb |
A |
C |
9: 98,943,895 (GRCm39) |
L636W |
probably damaging |
Het |
Pla2g2f |
A |
T |
4: 138,481,473 (GRCm39) |
L92Q |
probably damaging |
Het |
Plod3 |
G |
C |
5: 137,017,000 (GRCm39) |
A50P |
probably benign |
Het |
Prkar2b |
C |
T |
12: 32,025,928 (GRCm39) |
V191I |
possibly damaging |
Het |
Prune1 |
C |
A |
3: 95,165,430 (GRCm39) |
A281S |
probably benign |
Het |
Ptges3l |
A |
T |
11: 101,314,868 (GRCm39) |
C42S |
possibly damaging |
Het |
Reg3b |
A |
T |
6: 78,348,802 (GRCm39) |
I33L |
probably benign |
Het |
Rel |
A |
G |
11: 23,695,823 (GRCm39) |
I188T |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Ripor1 |
G |
T |
8: 106,344,254 (GRCm39) |
V463L |
probably benign |
Het |
Rrm1 |
T |
A |
7: 102,109,896 (GRCm39) |
D510E |
probably damaging |
Het |
Setd7 |
A |
G |
3: 51,440,436 (GRCm39) |
S202P |
probably damaging |
Het |
Shank3 |
T |
A |
15: 89,432,889 (GRCm39) |
D1211E |
probably benign |
Het |
Slc30a1 |
A |
T |
1: 191,639,674 (GRCm39) |
T186S |
possibly damaging |
Het |
Slc4a4 |
G |
A |
5: 89,304,257 (GRCm39) |
V523I |
probably benign |
Het |
Slc9a2 |
T |
A |
1: 40,781,768 (GRCm39) |
|
probably null |
Het |
Smg6 |
A |
G |
11: 74,820,502 (GRCm39) |
T258A |
probably damaging |
Het |
Sptlc1 |
C |
T |
13: 53,491,676 (GRCm39) |
D408N |
possibly damaging |
Het |
Tasor2 |
G |
T |
13: 3,632,150 (GRCm39) |
L784I |
possibly damaging |
Het |
Tbl3 |
T |
C |
17: 24,923,524 (GRCm39) |
|
probably null |
Het |
Tdo2 |
T |
C |
3: 81,876,812 (GRCm39) |
D139G |
possibly damaging |
Het |
Ticam1 |
T |
A |
17: 56,578,612 (GRCm39) |
H161L |
possibly damaging |
Het |
Tnfaip3 |
T |
A |
10: 18,881,407 (GRCm39) |
D293V |
probably benign |
Het |
Trim72 |
G |
A |
7: 127,603,878 (GRCm39) |
V75M |
possibly damaging |
Het |
Trip11 |
T |
A |
12: 101,803,986 (GRCm39) |
N1632I |
possibly damaging |
Het |
Tspan18 |
A |
T |
2: 93,050,440 (GRCm39) |
M61K |
possibly damaging |
Het |
Tuba8 |
A |
T |
6: 121,202,932 (GRCm39) |
E415V |
probably damaging |
Het |
Ung |
A |
G |
5: 114,275,253 (GRCm39) |
H214R |
probably benign |
Het |
Uqcrc1 |
T |
C |
9: 108,765,836 (GRCm39) |
L17P |
probably damaging |
Het |
Usp24 |
A |
G |
4: 106,236,602 (GRCm39) |
|
probably null |
Het |
Vps39 |
A |
C |
2: 120,169,268 (GRCm39) |
Y245D |
probably damaging |
Het |
Whrn |
T |
A |
4: 63,353,649 (GRCm39) |
T373S |
probably benign |
Het |
Zc2hc1a |
C |
T |
3: 7,581,596 (GRCm39) |
|
probably null |
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 |
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 |
|
R6276:Dlg5
|
UTSW |
14 |
24,214,636 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|