Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
A2ml1 |
A |
T |
6: 128,529,271 (GRCm39) |
M957K |
probably benign |
Het |
Adam7 |
C |
A |
14: 68,742,610 (GRCm39) |
V668F |
probably benign |
Het |
Adcy7 |
T |
G |
8: 89,038,902 (GRCm39) |
L306R |
probably damaging |
Het |
Akt3 |
A |
G |
1: 176,930,551 (GRCm39) |
S136P |
possibly damaging |
Het |
Alox12e |
G |
A |
11: 70,206,828 (GRCm39) |
R620W |
probably damaging |
Het |
Amy2a1 |
T |
C |
3: 113,324,217 (GRCm39) |
I108V |
probably benign |
Het |
Ano7 |
T |
C |
1: 93,318,035 (GRCm39) |
V249A |
probably benign |
Het |
Aox1 |
T |
C |
1: 58,098,351 (GRCm39) |
|
probably null |
Het |
Asah2 |
A |
T |
19: 32,002,274 (GRCm39) |
V290E |
probably damaging |
Het |
Ascc2 |
A |
T |
11: 4,631,496 (GRCm39) |
M646L |
probably benign |
Het |
Atxn2l |
T |
A |
7: 126,095,038 (GRCm39) |
K421N |
probably damaging |
Het |
Cars2 |
T |
C |
8: 11,597,747 (GRCm39) |
I110V |
probably damaging |
Het |
Ccdc74a |
A |
G |
16: 17,467,890 (GRCm39) |
N249S |
probably benign |
Het |
Cenpe |
T |
C |
3: 134,928,082 (GRCm39) |
|
probably benign |
Het |
Clptm1l |
C |
T |
13: 73,755,842 (GRCm39) |
Q153* |
probably null |
Het |
Cnep1r1 |
G |
T |
8: 88,845,445 (GRCm39) |
|
probably benign |
Het |
Cyp2d37-ps |
C |
T |
15: 82,574,289 (GRCm39) |
|
noncoding transcript |
Het |
Cyp3a25 |
A |
G |
5: 145,923,779 (GRCm39) |
|
probably benign |
Het |
Dis3l |
G |
T |
9: 64,246,855 (GRCm39) |
Q67K |
probably benign |
Het |
Dnah1 |
A |
G |
14: 30,993,086 (GRCm39) |
V2936A |
probably damaging |
Het |
Dnah5 |
C |
T |
15: 28,366,416 (GRCm39) |
R2710C |
probably damaging |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
Dvl3 |
G |
A |
16: 20,345,101 (GRCm39) |
S361N |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Eif2ak3 |
T |
C |
6: 70,881,181 (GRCm39) |
V1085A |
probably benign |
Het |
Eif3b |
T |
C |
5: 140,412,208 (GRCm39) |
Y226H |
probably damaging |
Het |
Endov |
T |
C |
11: 119,390,408 (GRCm39) |
F12S |
probably damaging |
Het |
Ercc1 |
A |
G |
7: 19,088,295 (GRCm39) |
*37W |
probably null |
Het |
Evi2a |
G |
A |
11: 79,418,593 (GRCm39) |
Q6* |
probably null |
Het |
Faah |
C |
T |
4: 115,855,770 (GRCm39) |
V552M |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,477,369 (GRCm39) |
N2138K |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,479,741 (GRCm39) |
V2929E |
probably damaging |
Het |
Gm2959 |
A |
G |
14: 42,235,658 (GRCm39) |
|
noncoding transcript |
Het |
Gm6327 |
A |
T |
16: 12,578,979 (GRCm39) |
|
noncoding transcript |
Het |
Gm9912 |
T |
C |
3: 148,890,795 (GRCm39) |
T113A |
unknown |
Het |
Gtf2f2 |
A |
G |
14: 76,155,136 (GRCm39) |
S142P |
possibly damaging |
Het |
Hspg2 |
A |
T |
4: 137,286,678 (GRCm39) |
T3666S |
possibly damaging |
Het |
Htt |
C |
T |
5: 34,983,326 (GRCm39) |
T975I |
probably benign |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Iqgap1 |
G |
A |
7: 80,373,727 (GRCm39) |
Q1421* |
probably null |
Het |
Itga3 |
T |
A |
11: 94,944,902 (GRCm39) |
Q802L |
possibly damaging |
Het |
Lonp2 |
A |
G |
8: 87,392,403 (GRCm39) |
T490A |
probably damaging |
Het |
Lztr1 |
T |
C |
16: 17,327,534 (GRCm39) |
V79A |
probably damaging |
Het |
Mpp4 |
G |
A |
1: 59,182,941 (GRCm39) |
P322L |
possibly damaging |
Het |
Mrto4 |
T |
C |
4: 139,076,334 (GRCm39) |
K86E |
probably benign |
Het |
Myof |
A |
G |
19: 37,904,194 (GRCm39) |
V2A |
possibly damaging |
Het |
Naf1 |
A |
G |
8: 67,340,432 (GRCm39) |
D414G |
probably damaging |
Het |
Nav3 |
G |
A |
10: 109,555,882 (GRCm39) |
T1683M |
probably damaging |
Het |
Nbea |
A |
G |
3: 55,993,578 (GRCm39) |
|
probably benign |
Het |
Nebl |
A |
T |
2: 17,401,932 (GRCm39) |
M427K |
probably benign |
Het |
Ngdn |
T |
C |
14: 55,259,564 (GRCm39) |
V205A |
possibly damaging |
Het |
Nup133 |
C |
A |
8: 124,641,314 (GRCm39) |
D869Y |
probably damaging |
Het |
Oas1g |
T |
C |
5: 121,023,946 (GRCm39) |
E121G |
probably damaging |
Het |
Or10j3b |
T |
C |
1: 173,043,277 (GRCm39) |
F20L |
probably benign |
Het |
Or2ab1 |
A |
G |
11: 58,488,396 (GRCm39) |
N58S |
probably damaging |
Het |
Or2w3 |
G |
T |
11: 58,556,808 (GRCm39) |
C141F |
probably damaging |
Het |
Or5m9 |
A |
G |
2: 85,877,299 (GRCm39) |
T158A |
probably damaging |
Het |
Or6c205 |
T |
A |
10: 129,087,001 (GRCm39) |
Y199* |
probably null |
Het |
Park7 |
T |
C |
4: 150,989,732 (GRCm39) |
N76S |
probably benign |
Het |
Pcdh8 |
A |
T |
14: 80,005,651 (GRCm39) |
S912R |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,271,559 (GRCm39) |
I2998T |
probably damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Ppard |
A |
G |
17: 28,518,663 (GRCm39) |
H388R |
probably damaging |
Het |
Psma1 |
A |
G |
7: 113,869,001 (GRCm39) |
S142P |
possibly damaging |
Het |
Pth2r |
T |
C |
1: 65,382,721 (GRCm39) |
I158T |
probably damaging |
Het |
Rbl2 |
C |
A |
8: 91,833,367 (GRCm39) |
P714Q |
probably damaging |
Het |
Rexo2 |
A |
T |
9: 48,385,813 (GRCm39) |
S104T |
possibly damaging |
Het |
Sema5a |
T |
C |
15: 32,609,363 (GRCm39) |
|
probably benign |
Het |
Spmip10 |
C |
T |
18: 56,721,535 (GRCm39) |
Q25* |
probably null |
Het |
Sun2 |
A |
G |
15: 79,622,852 (GRCm39) |
L109P |
probably damaging |
Het |
Tdg |
A |
G |
10: 82,477,368 (GRCm39) |
T116A |
probably benign |
Het |
Terb1 |
A |
T |
8: 105,195,380 (GRCm39) |
M587K |
possibly damaging |
Het |
Tmcc1 |
C |
T |
6: 116,020,019 (GRCm39) |
V118M |
probably benign |
Het |
Tnfsf11 |
T |
A |
14: 78,516,362 (GRCm39) |
N202I |
probably damaging |
Het |
Togaram2 |
T |
C |
17: 72,023,360 (GRCm39) |
S759P |
probably benign |
Het |
Ttc7b |
G |
A |
12: 100,291,948 (GRCm39) |
A208V |
probably damaging |
Het |
Tti2 |
T |
C |
8: 31,644,338 (GRCm39) |
|
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,905,118 (GRCm39) |
|
probably null |
Het |
Zfyve26 |
T |
C |
12: 79,330,806 (GRCm39) |
|
probably null |
Het |
Zfyve28 |
T |
C |
5: 34,391,681 (GRCm39) |
M157V |
probably null |
Het |
Zgrf1 |
T |
C |
3: 127,406,999 (GRCm39) |
C1589R |
probably damaging |
Het |
|
Other mutations in Mast4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00703:Mast4
|
APN |
13 |
102,907,275 (GRCm39) |
nonsense |
probably null |
|
IGL00933:Mast4
|
APN |
13 |
102,871,874 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01113:Mast4
|
APN |
13 |
102,910,744 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01461:Mast4
|
APN |
13 |
102,890,576 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01569:Mast4
|
APN |
13 |
102,897,523 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01697:Mast4
|
APN |
13 |
102,904,401 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01725:Mast4
|
APN |
13 |
102,887,020 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01734:Mast4
|
APN |
13 |
102,874,123 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01738:Mast4
|
APN |
13 |
102,873,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01739:Mast4
|
APN |
13 |
102,910,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02299:Mast4
|
APN |
13 |
102,874,482 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02479:Mast4
|
APN |
13 |
102,878,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02485:Mast4
|
APN |
13 |
102,872,004 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02528:Mast4
|
APN |
13 |
102,990,331 (GRCm39) |
makesense |
probably null |
|
IGL02850:Mast4
|
APN |
13 |
102,890,740 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02900:Mast4
|
APN |
13 |
102,872,184 (GRCm39) |
missense |
probably benign |
|
IGL03064:Mast4
|
APN |
13 |
102,897,472 (GRCm39) |
nonsense |
probably null |
|
IGL03124:Mast4
|
APN |
13 |
102,874,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03146:Mast4
|
APN |
13 |
102,874,163 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03221:Mast4
|
APN |
13 |
102,890,764 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03284:Mast4
|
APN |
13 |
102,887,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03406:Mast4
|
APN |
13 |
102,873,615 (GRCm39) |
missense |
possibly damaging |
0.46 |
buck
|
UTSW |
13 |
102,897,801 (GRCm39) |
critical splice donor site |
probably null |
|
doe
|
UTSW |
13 |
103,042,185 (GRCm39) |
missense |
possibly damaging |
0.85 |
skinnybones
|
UTSW |
13 |
102,941,149 (GRCm39) |
critical splice donor site |
probably null |
|
BB010:Mast4
|
UTSW |
13 |
102,909,071 (GRCm39) |
missense |
probably damaging |
0.99 |
BB020:Mast4
|
UTSW |
13 |
102,909,071 (GRCm39) |
missense |
probably damaging |
0.99 |
FR4304:Mast4
|
UTSW |
13 |
102,871,370 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4340:Mast4
|
UTSW |
13 |
102,872,825 (GRCm39) |
small insertion |
probably benign |
|
FR4340:Mast4
|
UTSW |
13 |
102,871,365 (GRCm39) |
frame shift |
probably null |
|
FR4548:Mast4
|
UTSW |
13 |
102,872,826 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Mast4
|
UTSW |
13 |
102,875,755 (GRCm39) |
frame shift |
probably null |
|
FR4976:Mast4
|
UTSW |
13 |
102,872,820 (GRCm39) |
small insertion |
probably benign |
|
NA:Mast4
|
UTSW |
13 |
102,878,565 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4466001:Mast4
|
UTSW |
13 |
102,941,226 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4469001:Mast4
|
UTSW |
13 |
102,941,226 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4472001:Mast4
|
UTSW |
13 |
102,941,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R0009:Mast4
|
UTSW |
13 |
102,878,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Mast4
|
UTSW |
13 |
103,470,723 (GRCm39) |
start gained |
probably benign |
|
R0242:Mast4
|
UTSW |
13 |
102,990,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R0310:Mast4
|
UTSW |
13 |
102,890,669 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0395:Mast4
|
UTSW |
13 |
102,871,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Mast4
|
UTSW |
13 |
102,888,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Mast4
|
UTSW |
13 |
102,895,252 (GRCm39) |
splice site |
probably benign |
|
R0744:Mast4
|
UTSW |
13 |
102,873,895 (GRCm39) |
missense |
probably damaging |
0.98 |
R0883:Mast4
|
UTSW |
13 |
102,990,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R0905:Mast4
|
UTSW |
13 |
102,907,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R1023:Mast4
|
UTSW |
13 |
102,872,004 (GRCm39) |
missense |
probably benign |
0.02 |
R1281:Mast4
|
UTSW |
13 |
102,887,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R1376:Mast4
|
UTSW |
13 |
102,872,916 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1376:Mast4
|
UTSW |
13 |
102,872,916 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1473:Mast4
|
UTSW |
13 |
102,909,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Mast4
|
UTSW |
13 |
102,873,431 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1575:Mast4
|
UTSW |
13 |
102,875,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Mast4
|
UTSW |
13 |
102,930,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Mast4
|
UTSW |
13 |
102,887,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Mast4
|
UTSW |
13 |
102,875,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R2106:Mast4
|
UTSW |
13 |
102,887,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R2118:Mast4
|
UTSW |
13 |
102,890,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R2143:Mast4
|
UTSW |
13 |
102,871,983 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2256:Mast4
|
UTSW |
13 |
102,872,259 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2261:Mast4
|
UTSW |
13 |
102,934,715 (GRCm39) |
splice site |
probably benign |
|
R2370:Mast4
|
UTSW |
13 |
102,910,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Mast4
|
UTSW |
13 |
102,875,147 (GRCm39) |
missense |
probably damaging |
0.96 |
R2509:Mast4
|
UTSW |
13 |
102,990,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R2842:Mast4
|
UTSW |
13 |
102,872,939 (GRCm39) |
missense |
probably benign |
0.01 |
R3087:Mast4
|
UTSW |
13 |
102,990,434 (GRCm39) |
splice site |
probably benign |
|
R3434:Mast4
|
UTSW |
13 |
102,923,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R3435:Mast4
|
UTSW |
13 |
102,923,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R3763:Mast4
|
UTSW |
13 |
102,923,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Mast4
|
UTSW |
13 |
102,875,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R3829:Mast4
|
UTSW |
13 |
102,875,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R3830:Mast4
|
UTSW |
13 |
102,875,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R3913:Mast4
|
UTSW |
13 |
102,895,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R3914:Mast4
|
UTSW |
13 |
102,875,829 (GRCm39) |
nonsense |
probably null |
|
R4021:Mast4
|
UTSW |
13 |
102,875,829 (GRCm39) |
nonsense |
probably null |
|
R4022:Mast4
|
UTSW |
13 |
102,990,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R4022:Mast4
|
UTSW |
13 |
102,875,829 (GRCm39) |
nonsense |
probably null |
|
R4210:Mast4
|
UTSW |
13 |
102,875,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R4342:Mast4
|
UTSW |
13 |
102,910,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R4580:Mast4
|
UTSW |
13 |
102,873,766 (GRCm39) |
nonsense |
probably null |
|
R4627:Mast4
|
UTSW |
13 |
103,470,529 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4711:Mast4
|
UTSW |
13 |
103,470,627 (GRCm39) |
missense |
probably benign |
0.01 |
R4732:Mast4
|
UTSW |
13 |
102,909,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R4733:Mast4
|
UTSW |
13 |
102,909,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R4833:Mast4
|
UTSW |
13 |
102,910,692 (GRCm39) |
critical splice donor site |
probably null |
|
R4995:Mast4
|
UTSW |
13 |
103,042,262 (GRCm39) |
intron |
probably benign |
|
R5059:Mast4
|
UTSW |
13 |
102,887,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R5073:Mast4
|
UTSW |
13 |
102,875,391 (GRCm39) |
nonsense |
probably null |
|
R5101:Mast4
|
UTSW |
13 |
102,872,864 (GRCm39) |
missense |
probably benign |
0.01 |
R5526:Mast4
|
UTSW |
13 |
102,890,723 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5599:Mast4
|
UTSW |
13 |
102,873,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R5673:Mast4
|
UTSW |
13 |
102,930,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R5694:Mast4
|
UTSW |
13 |
102,910,701 (GRCm39) |
nonsense |
probably null |
|
R5906:Mast4
|
UTSW |
13 |
102,872,252 (GRCm39) |
missense |
probably benign |
0.31 |
R5908:Mast4
|
UTSW |
13 |
102,874,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R5947:Mast4
|
UTSW |
13 |
102,872,148 (GRCm39) |
missense |
probably benign |
|
R5987:Mast4
|
UTSW |
13 |
102,895,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R6143:Mast4
|
UTSW |
13 |
102,990,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R6154:Mast4
|
UTSW |
13 |
102,923,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Mast4
|
UTSW |
13 |
102,923,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R6239:Mast4
|
UTSW |
13 |
102,872,717 (GRCm39) |
missense |
probably benign |
0.01 |
R6327:Mast4
|
UTSW |
13 |
102,897,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R6356:Mast4
|
UTSW |
13 |
102,872,493 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6432:Mast4
|
UTSW |
13 |
103,042,185 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6522:Mast4
|
UTSW |
13 |
102,897,801 (GRCm39) |
critical splice donor site |
probably null |
|
R6667:Mast4
|
UTSW |
13 |
102,874,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R6941:Mast4
|
UTSW |
13 |
102,941,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Mast4
|
UTSW |
13 |
102,934,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R6970:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6980:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6991:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6992:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6993:Mast4
|
UTSW |
13 |
102,872,482 (GRCm39) |
missense |
probably benign |
0.28 |
R6993:Mast4
|
UTSW |
13 |
102,941,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R7083:Mast4
|
UTSW |
13 |
102,874,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R7241:Mast4
|
UTSW |
13 |
103,470,508 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7242:Mast4
|
UTSW |
13 |
102,874,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R7246:Mast4
|
UTSW |
13 |
102,930,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R7332:Mast4
|
UTSW |
13 |
102,887,932 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7453:Mast4
|
UTSW |
13 |
102,941,149 (GRCm39) |
critical splice donor site |
probably null |
|
R7514:Mast4
|
UTSW |
13 |
102,923,934 (GRCm39) |
nonsense |
probably null |
|
R7697:Mast4
|
UTSW |
13 |
102,875,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R7820:Mast4
|
UTSW |
13 |
102,890,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R7874:Mast4
|
UTSW |
13 |
102,875,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7933:Mast4
|
UTSW |
13 |
102,909,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R8042:Mast4
|
UTSW |
13 |
102,917,753 (GRCm39) |
missense |
probably damaging |
0.96 |
R8060:Mast4
|
UTSW |
13 |
102,874,184 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8172:Mast4
|
UTSW |
13 |
103,089,633 (GRCm39) |
critical splice donor site |
probably null |
|
R8206:Mast4
|
UTSW |
13 |
102,872,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R8248:Mast4
|
UTSW |
13 |
102,875,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R8283:Mast4
|
UTSW |
13 |
102,895,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R8346:Mast4
|
UTSW |
13 |
102,887,986 (GRCm39) |
missense |
probably damaging |
0.99 |
R8434:Mast4
|
UTSW |
13 |
102,897,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R8796:Mast4
|
UTSW |
13 |
102,919,899 (GRCm39) |
missense |
probably benign |
0.07 |
R8850:Mast4
|
UTSW |
13 |
102,895,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R9012:Mast4
|
UTSW |
13 |
102,934,606 (GRCm39) |
missense |
probably benign |
0.05 |
R9375:Mast4
|
UTSW |
13 |
102,917,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R9389:Mast4
|
UTSW |
13 |
103,470,438 (GRCm39) |
missense |
probably benign |
0.00 |
R9404:Mast4
|
UTSW |
13 |
102,887,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R9520:Mast4
|
UTSW |
13 |
102,925,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R9525:Mast4
|
UTSW |
13 |
102,872,944 (GRCm39) |
missense |
probably benign |
0.00 |
R9526:Mast4
|
UTSW |
13 |
102,873,593 (GRCm39) |
missense |
probably benign |
0.00 |
R9709:Mast4
|
UTSW |
13 |
102,910,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R9790:Mast4
|
UTSW |
13 |
102,890,705 (GRCm39) |
missense |
probably benign |
0.01 |
R9791:Mast4
|
UTSW |
13 |
102,890,705 (GRCm39) |
missense |
probably benign |
0.01 |
RF005:Mast4
|
UTSW |
13 |
102,872,815 (GRCm39) |
small insertion |
probably benign |
|
RF015:Mast4
|
UTSW |
13 |
102,875,755 (GRCm39) |
frame shift |
probably null |
|
RF019:Mast4
|
UTSW |
13 |
102,872,815 (GRCm39) |
small insertion |
probably benign |
|
RF037:Mast4
|
UTSW |
13 |
102,875,749 (GRCm39) |
small deletion |
probably benign |
|
RF039:Mast4
|
UTSW |
13 |
102,875,749 (GRCm39) |
small deletion |
probably benign |
|
RF040:Mast4
|
UTSW |
13 |
102,875,749 (GRCm39) |
small deletion |
probably benign |
|
Z1088:Mast4
|
UTSW |
13 |
102,875,027 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mast4
|
UTSW |
13 |
102,874,968 (GRCm39) |
missense |
probably damaging |
1.00 |
|