Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447F04Rik |
T |
C |
X: 65,347,274 (GRCm39) |
E91G |
unknown |
Het |
Acot1 |
A |
G |
12: 84,064,113 (GRCm39) |
Q407R |
probably benign |
Het |
Adcy10 |
T |
A |
1: 165,398,297 (GRCm39) |
Y1465N |
probably damaging |
Het |
Ahsa2 |
T |
A |
11: 23,440,702 (GRCm39) |
I249F |
probably damaging |
Het |
Arhgap10 |
T |
C |
8: 77,977,594 (GRCm39) |
N721S |
probably damaging |
Het |
Arrdc4 |
T |
G |
7: 68,391,619 (GRCm39) |
E216A |
probably damaging |
Het |
Axin1 |
T |
C |
17: 26,392,637 (GRCm39) |
V306A |
probably benign |
Het |
Cct3 |
T |
C |
3: 88,210,173 (GRCm39) |
|
probably null |
Het |
Cfap58 |
G |
A |
19: 47,963,119 (GRCm39) |
|
probably null |
Het |
Chd9 |
T |
C |
8: 91,699,859 (GRCm39) |
S49P |
possibly damaging |
Het |
Clcn2 |
C |
A |
16: 20,529,178 (GRCm39) |
|
probably null |
Het |
Col26a1 |
T |
C |
5: 136,783,047 (GRCm39) |
N286D |
probably benign |
Het |
Cpt1b |
T |
A |
15: 89,308,596 (GRCm39) |
I111F |
possibly damaging |
Het |
Cyp4f16 |
T |
A |
17: 32,756,061 (GRCm39) |
I30N |
probably damaging |
Het |
Ddc |
T |
G |
11: 11,830,587 (GRCm39) |
D19A |
possibly damaging |
Het |
Depdc1a |
T |
A |
3: 159,222,537 (GRCm39) |
|
probably null |
Het |
Evc2 |
T |
A |
5: 37,574,828 (GRCm39) |
C1028S |
possibly damaging |
Het |
Fam228a |
T |
C |
12: 4,781,457 (GRCm39) |
E134G |
probably damaging |
Het |
Fasl |
T |
C |
1: 161,615,523 (GRCm39) |
E111G |
probably benign |
Het |
Fbxw10 |
A |
G |
11: 62,767,564 (GRCm39) |
N800S |
possibly damaging |
Het |
Fras1 |
T |
C |
5: 96,910,524 (GRCm39) |
S3318P |
probably damaging |
Het |
G3bp1 |
T |
C |
11: 55,389,452 (GRCm39) |
F383L |
probably damaging |
Het |
Gad1 |
T |
A |
2: 70,409,545 (GRCm39) |
M212K |
probably damaging |
Het |
Gm17455 |
T |
G |
10: 60,238,752 (GRCm39) |
S6A |
probably benign |
Het |
Grm5 |
T |
C |
7: 87,779,997 (GRCm39) |
S1146P |
probably damaging |
Het |
Gsn |
T |
C |
2: 35,194,651 (GRCm39) |
L649P |
probably damaging |
Het |
H2-DMb1 |
A |
G |
17: 34,374,685 (GRCm39) |
T112A |
probably benign |
Het |
Hcn3 |
T |
A |
3: 89,060,201 (GRCm39) |
I148F |
probably damaging |
Het |
Hdac10 |
T |
C |
15: 89,009,961 (GRCm39) |
|
probably null |
Het |
Hk3 |
C |
A |
13: 55,156,518 (GRCm39) |
D619Y |
probably damaging |
Het |
Ifi44 |
T |
A |
3: 151,451,134 (GRCm39) |
R272S |
possibly damaging |
Het |
Il1rap |
A |
C |
16: 26,517,625 (GRCm39) |
D275A |
probably damaging |
Het |
Irag2 |
A |
G |
6: 145,113,710 (GRCm39) |
R293G |
possibly damaging |
Het |
Itgam |
A |
T |
7: 127,707,152 (GRCm39) |
N660I |
probably benign |
Het |
Itpr3 |
T |
C |
17: 27,332,793 (GRCm39) |
M1853T |
probably benign |
Het |
Lrrc8c |
A |
C |
5: 105,754,965 (GRCm39) |
K247Q |
probably damaging |
Het |
Map3k21 |
T |
C |
8: 126,668,858 (GRCm39) |
S815P |
probably benign |
Het |
Myh8 |
C |
T |
11: 67,194,591 (GRCm39) |
Q1601* |
probably null |
Het |
Nhlrc2 |
A |
G |
19: 56,558,959 (GRCm39) |
D148G |
probably damaging |
Het |
Nos1 |
T |
A |
5: 118,081,385 (GRCm39) |
S1196T |
probably benign |
Het |
Nsmaf |
C |
T |
4: 6,424,874 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
C |
11: 58,890,449 (GRCm39) |
D7361G |
unknown |
Het |
Or2t35 |
T |
C |
14: 14,407,777 (GRCm38) |
V183A |
probably damaging |
Het |
Or52ad1 |
C |
A |
7: 102,996,085 (GRCm39) |
A17S |
probably benign |
Het |
Or5bw2 |
C |
T |
7: 6,573,359 (GRCm39) |
A123V |
probably damaging |
Het |
Pank3 |
T |
G |
11: 35,668,536 (GRCm39) |
M175R |
probably benign |
Het |
Papolg |
A |
G |
11: 23,829,868 (GRCm39) |
|
probably null |
Het |
Pcdhb21 |
G |
A |
18: 37,647,566 (GRCm39) |
D232N |
probably damaging |
Het |
Pcdhb22 |
T |
C |
18: 37,651,925 (GRCm39) |
F131S |
probably damaging |
Het |
Pik3r6 |
G |
A |
11: 68,419,608 (GRCm39) |
A140T |
possibly damaging |
Het |
Pinlyp |
T |
C |
7: 24,241,947 (GRCm39) |
T87A |
possibly damaging |
Het |
Pld1 |
T |
C |
3: 28,178,724 (GRCm39) |
S873P |
probably damaging |
Het |
Pld5 |
T |
A |
1: 176,102,295 (GRCm39) |
Y49F |
probably benign |
Het |
Polq |
T |
C |
16: 36,855,252 (GRCm39) |
V449A |
probably damaging |
Het |
Prkca |
A |
G |
11: 107,869,106 (GRCm39) |
V69A |
probably benign |
Het |
Ptk6 |
A |
G |
2: 180,844,075 (GRCm39) |
S75P |
possibly damaging |
Het |
Ptprq |
G |
A |
10: 107,418,391 (GRCm39) |
Q1662* |
probably null |
Het |
Ptprt |
C |
A |
2: 161,395,742 (GRCm39) |
A1144S |
probably damaging |
Het |
Rrm1 |
T |
A |
7: 102,116,133 (GRCm39) |
W684R |
probably damaging |
Het |
Ryr1 |
T |
A |
7: 28,735,500 (GRCm39) |
M4093L |
probably damaging |
Het |
Scnn1a |
C |
T |
6: 125,299,189 (GRCm39) |
L90F |
probably damaging |
Het |
Slc25a19 |
G |
T |
11: 115,508,423 (GRCm39) |
Y188* |
probably null |
Het |
Slc31a1 |
C |
T |
4: 62,303,866 (GRCm39) |
|
probably benign |
Het |
Slc5a11 |
C |
G |
7: 122,864,458 (GRCm39) |
S351R |
possibly damaging |
Het |
Slc6a17 |
A |
G |
3: 107,384,183 (GRCm39) |
L387P |
probably benign |
Het |
Slitrk6 |
A |
T |
14: 110,987,364 (GRCm39) |
L781H |
probably damaging |
Het |
Spam1 |
T |
A |
6: 24,797,837 (GRCm39) |
L331Q |
probably damaging |
Het |
Spata32 |
A |
G |
11: 103,100,125 (GRCm39) |
W127R |
probably damaging |
Het |
Spring1 |
A |
G |
5: 118,393,886 (GRCm39) |
E88G |
possibly damaging |
Het |
Spta1 |
T |
G |
1: 174,041,508 (GRCm39) |
I1324S |
probably damaging |
Het |
St6galnac4 |
A |
G |
2: 32,484,330 (GRCm39) |
Y176C |
probably damaging |
Het |
Stk10 |
A |
G |
11: 32,546,724 (GRCm39) |
E327G |
probably damaging |
Het |
Stxbp5l |
T |
A |
16: 36,954,646 (GRCm39) |
Y912F |
possibly damaging |
Het |
Tchp |
G |
A |
5: 114,858,243 (GRCm39) |
E459K |
probably benign |
Het |
Terf2 |
C |
T |
8: 107,822,842 (GRCm39) |
W100* |
probably null |
Het |
Thoc2l |
T |
G |
5: 104,666,077 (GRCm39) |
S200A |
probably benign |
Het |
Thrsp |
T |
C |
7: 97,066,634 (GRCm39) |
N26S |
probably damaging |
Het |
Tln1 |
C |
A |
4: 43,553,504 (GRCm39) |
R297L |
probably benign |
Het |
Tmeff2 |
C |
A |
1: 50,967,234 (GRCm39) |
T43N |
possibly damaging |
Het |
Tmx1 |
C |
T |
12: 70,499,947 (GRCm39) |
A2V |
possibly damaging |
Het |
Tnks1bp1 |
T |
A |
2: 84,902,481 (GRCm39) |
L1053Q |
probably damaging |
Het |
Trmt10b |
A |
T |
4: 45,304,286 (GRCm39) |
K107N |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,955,972 (GRCm39) |
|
probably null |
Het |
Trrap |
A |
G |
5: 144,783,287 (GRCm39) |
K3371R |
probably damaging |
Het |
Tuba3b |
G |
A |
6: 145,563,995 (GRCm39) |
V14I |
probably benign |
Het |
Usp19 |
T |
C |
9: 108,371,439 (GRCm39) |
|
probably null |
Het |
Usp28 |
C |
A |
9: 48,950,401 (GRCm39) |
D615E |
possibly damaging |
Het |
Utp20 |
T |
C |
10: 88,657,931 (GRCm39) |
D43G |
probably benign |
Het |
Vmn1r58 |
T |
G |
7: 5,413,997 (GRCm39) |
K78Q |
possibly damaging |
Het |
Vmn2r10 |
T |
C |
5: 109,151,327 (GRCm39) |
M96V |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,079,023 (GRCm39) |
E273G |
probably damaging |
Het |
Xpc |
C |
T |
6: 91,468,208 (GRCm39) |
A860T |
probably benign |
Het |
Zscan21 |
T |
C |
5: 138,131,865 (GRCm39) |
I463T |
possibly 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 |
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 |
R2062:Mast4
|
UTSW |
13 |
102,895,601 (GRCm39) |
missense |
probably benign |
0.18 |
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 |
|