Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaa1b |
T |
C |
9: 118,983,038 (GRCm39) |
N120S |
probably damaging |
Het |
Acsbg3 |
A |
T |
17: 57,190,631 (GRCm39) |
I400F |
probably benign |
Het |
Acvr1c |
T |
C |
2: 58,174,850 (GRCm39) |
T313A |
probably damaging |
Het |
Adamtsl3 |
A |
T |
7: 82,171,198 (GRCm39) |
D417V |
probably damaging |
Het |
Adgrf4 |
A |
T |
17: 42,978,204 (GRCm39) |
C380S |
probably damaging |
Het |
AI597479 |
T |
G |
1: 43,150,277 (GRCm39) |
L129R |
probably benign |
Het |
AI661453 |
G |
A |
17: 47,757,571 (GRCm39) |
R76Q |
probably damaging |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Anxa7 |
A |
C |
14: 20,519,566 (GRCm39) |
|
probably null |
Het |
Arhgap12 |
T |
A |
18: 6,039,382 (GRCm39) |
D455V |
probably damaging |
Het |
Arhgap22 |
A |
G |
14: 33,091,374 (GRCm39) |
R650G |
possibly damaging |
Het |
Arhgef12 |
A |
C |
9: 42,931,982 (GRCm39) |
H168Q |
probably damaging |
Het |
Arhgef2 |
A |
G |
3: 88,549,808 (GRCm39) |
H592R |
probably damaging |
Het |
BC049715 |
A |
G |
6: 136,817,035 (GRCm39) |
T92A |
possibly damaging |
Het |
Bcr |
C |
T |
10: 75,017,466 (GRCm39) |
T1209I |
possibly damaging |
Het |
Bmpr1a |
C |
T |
14: 34,151,734 (GRCm39) |
S185N |
probably benign |
Het |
Calcoco1 |
A |
T |
15: 102,624,198 (GRCm39) |
M246K |
probably benign |
Het |
Capn8 |
T |
A |
1: 182,457,703 (GRCm39) |
I689N |
probably benign |
Het |
Ccno |
T |
A |
13: 113,126,530 (GRCm39) |
L333Q |
probably damaging |
Het |
Cep57 |
G |
A |
9: 13,728,281 (GRCm39) |
R148W |
probably damaging |
Het |
Cftr |
T |
A |
6: 18,226,096 (GRCm39) |
M318K |
probably null |
Het |
Chd3 |
T |
G |
11: 69,247,159 (GRCm39) |
D1003A |
probably damaging |
Het |
Ckmt2 |
T |
A |
13: 92,011,322 (GRCm39) |
D96V |
possibly damaging |
Het |
Cldn13 |
A |
G |
5: 134,944,176 (GRCm39) |
V3A |
probably benign |
Het |
Col17a1 |
T |
C |
19: 47,658,871 (GRCm39) |
T413A |
probably benign |
Het |
Cpne5 |
A |
T |
17: 29,430,634 (GRCm39) |
L92H |
probably damaging |
Het |
Dnaaf2 |
C |
A |
12: 69,244,518 (GRCm39) |
R181L |
probably damaging |
Het |
Erbin |
C |
A |
13: 104,005,373 (GRCm39) |
C114F |
probably damaging |
Het |
Fads2b |
T |
A |
2: 85,348,895 (GRCm39) |
R72S |
probably benign |
Het |
Fanca |
A |
T |
8: 124,000,911 (GRCm39) |
C1156* |
probably null |
Het |
Flot2 |
T |
A |
11: 77,949,784 (GRCm39) |
I322N |
possibly damaging |
Het |
Fstl5 |
T |
C |
3: 76,615,060 (GRCm39) |
V707A |
possibly damaging |
Het |
Gli3 |
T |
G |
13: 15,898,143 (GRCm39) |
L741R |
probably damaging |
Het |
Gmip |
G |
T |
8: 70,263,468 (GRCm39) |
S70I |
probably benign |
Het |
Gnptab |
T |
C |
10: 88,276,171 (GRCm39) |
S1153P |
probably damaging |
Het |
Gramd1a |
T |
C |
7: 30,837,679 (GRCm39) |
D360G |
possibly damaging |
Het |
Gtf2i |
T |
C |
5: 134,280,740 (GRCm39) |
E518G |
probably damaging |
Het |
Hsp90b1 |
T |
C |
10: 86,530,019 (GRCm39) |
E226G |
probably damaging |
Het |
Impg2 |
A |
G |
16: 56,072,627 (GRCm39) |
Y353C |
probably damaging |
Het |
Kank1 |
A |
G |
19: 25,401,677 (GRCm39) |
K1095E |
probably benign |
Het |
Kcnh4 |
C |
T |
11: 100,648,569 (GRCm39) |
C45Y |
probably damaging |
Het |
Kif13b |
A |
G |
14: 65,040,669 (GRCm39) |
T1590A |
probably benign |
Het |
Lpin3 |
T |
C |
2: 160,747,225 (GRCm39) |
V827A |
probably benign |
Het |
Lrp1b |
A |
T |
2: 40,591,773 (GRCm39) |
C73* |
probably null |
Het |
Mcm8 |
A |
G |
2: 132,661,914 (GRCm39) |
K83E |
possibly damaging |
Het |
Med12l |
A |
G |
3: 59,135,123 (GRCm39) |
E757G |
probably damaging |
Het |
Mep1a |
A |
G |
17: 43,808,789 (GRCm39) |
|
probably null |
Het |
Mybpc2 |
C |
T |
7: 44,158,453 (GRCm39) |
A710T |
possibly damaging |
Het |
Myof |
A |
C |
19: 37,924,326 (GRCm39) |
I1297S |
probably damaging |
Het |
Nacad |
A |
G |
11: 6,550,903 (GRCm39) |
S763P |
probably benign |
Het |
Nbea |
A |
G |
3: 55,550,238 (GRCm39) |
V2730A |
probably benign |
Het |
Nbeal1 |
A |
G |
1: 60,307,222 (GRCm39) |
Y1684C |
probably damaging |
Het |
Optn |
A |
T |
2: 5,039,066 (GRCm39) |
N352K |
possibly damaging |
Het |
Or10k2 |
A |
G |
8: 84,268,142 (GRCm39) |
Y123C |
probably damaging |
Het |
Or2g1 |
A |
T |
17: 38,106,880 (GRCm39) |
M182L |
probably benign |
Het |
Or7g16 |
A |
G |
9: 18,726,937 (GRCm39) |
Y218H |
probably damaging |
Het |
Or9g4b |
T |
A |
2: 85,616,147 (GRCm39) |
C97* |
probably null |
Het |
Pcif1 |
G |
T |
2: 164,731,364 (GRCm39) |
R466L |
probably damaging |
Het |
Phxr2 |
T |
C |
10: 98,961,979 (GRCm39) |
|
probably benign |
Het |
Plaat5 |
T |
A |
19: 7,614,663 (GRCm39) |
|
probably null |
Het |
Plb1 |
T |
A |
5: 32,512,701 (GRCm39) |
F1353Y |
probably damaging |
Het |
Plec |
A |
G |
15: 76,075,618 (GRCm39) |
|
probably null |
Het |
Polr1a |
T |
A |
6: 71,943,400 (GRCm39) |
C1212S |
possibly damaging |
Het |
Primpol |
A |
T |
8: 47,063,496 (GRCm39) |
N53K |
probably damaging |
Het |
Pygo2 |
T |
A |
3: 89,340,461 (GRCm39) |
N286K |
possibly damaging |
Het |
Rttn |
G |
A |
18: 89,004,204 (GRCm39) |
|
probably null |
Het |
Serpinb3b |
G |
T |
1: 107,087,433 (GRCm39) |
N25K |
probably damaging |
Het |
Sidt2 |
A |
G |
9: 45,866,200 (GRCm39) |
I2T |
probably benign |
Het |
Slc12a3 |
A |
T |
8: 95,072,974 (GRCm39) |
N699I |
possibly damaging |
Het |
Slc25a30 |
G |
A |
14: 76,000,112 (GRCm39) |
Q285* |
probably null |
Het |
Slc4a9 |
A |
T |
18: 36,668,592 (GRCm39) |
H724L |
probably damaging |
Het |
Ssbp2 |
T |
A |
13: 91,828,698 (GRCm39) |
|
probably null |
Het |
Stac3 |
C |
A |
10: 127,343,616 (GRCm39) |
|
probably null |
Het |
Stk32a |
A |
G |
18: 43,446,566 (GRCm39) |
K339E |
probably benign |
Het |
Stoml2 |
A |
G |
4: 43,030,238 (GRCm39) |
|
probably null |
Het |
Syne2 |
G |
T |
12: 76,013,727 (GRCm39) |
G2974C |
probably benign |
Het |
Tbc1d16 |
A |
G |
11: 119,049,555 (GRCm39) |
|
probably null |
Het |
Tfdp2 |
T |
G |
9: 96,188,946 (GRCm39) |
F200V |
probably damaging |
Het |
Tie1 |
C |
A |
4: 118,341,924 (GRCm39) |
R175L |
probably benign |
Het |
Trappc12 |
A |
G |
12: 28,797,259 (GRCm39) |
V91A |
probably benign |
Het |
Trim46 |
G |
T |
3: 89,143,820 (GRCm39) |
P536Q |
probably damaging |
Het |
Tshz3 |
T |
A |
7: 36,469,458 (GRCm39) |
D482E |
probably benign |
Het |
Tspan33 |
T |
C |
6: 29,711,091 (GRCm39) |
|
probably null |
Het |
Unc80 |
T |
C |
1: 66,713,246 (GRCm39) |
L2788P |
possibly damaging |
Het |
Utp20 |
T |
A |
10: 88,653,841 (GRCm39) |
T260S |
probably benign |
Het |
Vmn2r118 |
G |
T |
17: 55,917,717 (GRCm39) |
T265K |
probably damaging |
Het |
Vmn2r98 |
A |
C |
17: 19,286,609 (GRCm39) |
H369P |
probably benign |
Het |
Vps39 |
A |
T |
2: 120,169,268 (GRCm39) |
Y245N |
possibly damaging |
Het |
Vps4a |
A |
C |
8: 107,769,698 (GRCm39) |
I336L |
probably benign |
Het |
Xylb |
T |
C |
9: 119,210,653 (GRCm39) |
S379P |
probably damaging |
Het |
Zbtb37 |
T |
C |
1: 160,860,066 (GRCm39) |
T80A |
probably benign |
Het |
Zfhx3 |
A |
G |
8: 109,675,589 (GRCm39) |
D2213G |
probably damaging |
Het |
Zfp729a |
G |
T |
13: 67,768,473 (GRCm39) |
H585Q |
probably damaging |
Het |
Zfp804b |
A |
T |
5: 6,821,029 (GRCm39) |
I642N |
possibly damaging |
Het |
Zfp804b |
A |
T |
5: 6,821,994 (GRCm39) |
N356K |
possibly damaging |
Het |
|
Other mutations in Mtor |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01123:Mtor
|
APN |
4 |
148,537,494 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01447:Mtor
|
APN |
4 |
148,615,214 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01551:Mtor
|
APN |
4 |
148,556,494 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01661:Mtor
|
APN |
4 |
148,599,308 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01675:Mtor
|
APN |
4 |
148,569,111 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01743:Mtor
|
APN |
4 |
148,615,070 (GRCm39) |
splice site |
probably benign |
|
IGL02015:Mtor
|
APN |
4 |
148,624,570 (GRCm39) |
nonsense |
probably null |
|
IGL02084:Mtor
|
APN |
4 |
148,555,137 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02095:Mtor
|
APN |
4 |
148,628,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02129:Mtor
|
APN |
4 |
148,634,302 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02260:Mtor
|
APN |
4 |
148,622,758 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02329:Mtor
|
APN |
4 |
148,619,396 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02440:Mtor
|
APN |
4 |
148,576,104 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02440:Mtor
|
APN |
4 |
148,630,886 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02449:Mtor
|
APN |
4 |
148,618,378 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02479:Mtor
|
APN |
4 |
148,555,041 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02904:Mtor
|
APN |
4 |
148,576,069 (GRCm39) |
splice site |
probably benign |
|
IGL02904:Mtor
|
APN |
4 |
148,536,851 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02931:Mtor
|
APN |
4 |
148,549,421 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03048:Mtor
|
APN |
4 |
148,630,847 (GRCm39) |
splice site |
probably benign |
|
IGL03133:Mtor
|
APN |
4 |
148,568,776 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03142:Mtor
|
APN |
4 |
148,538,356 (GRCm39) |
missense |
probably benign |
0.00 |
Brushes
|
UTSW |
4 |
148,548,205 (GRCm39) |
missense |
probably benign |
0.00 |
Dynamo
|
UTSW |
4 |
148,547,367 (GRCm39) |
missense |
probably benign |
0.00 |
engine
|
UTSW |
4 |
148,641,312 (GRCm39) |
splice site |
probably null |
|
Erg
|
UTSW |
4 |
148,630,053 (GRCm39) |
missense |
probably damaging |
1.00 |
Lindor
|
UTSW |
4 |
148,539,103 (GRCm39) |
missense |
probably damaging |
1.00 |
motor
|
UTSW |
4 |
148,575,817 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4858_Mtor_211
|
UTSW |
4 |
148,539,273 (GRCm39) |
makesense |
probably null |
|
Vigor
|
UTSW |
4 |
148,623,356 (GRCm39) |
missense |
probably damaging |
1.00 |
Vim
|
UTSW |
4 |
148,610,260 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4519001:Mtor
|
UTSW |
4 |
148,608,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R0045:Mtor
|
UTSW |
4 |
148,549,406 (GRCm39) |
missense |
probably benign |
0.42 |
R0048:Mtor
|
UTSW |
4 |
148,623,338 (GRCm39) |
nonsense |
probably null |
|
R0048:Mtor
|
UTSW |
4 |
148,623,338 (GRCm39) |
nonsense |
probably null |
|
R0103:Mtor
|
UTSW |
4 |
148,618,359 (GRCm39) |
missense |
probably benign |
0.05 |
R0112:Mtor
|
UTSW |
4 |
148,565,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0137:Mtor
|
UTSW |
4 |
148,555,081 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0184:Mtor
|
UTSW |
4 |
148,549,428 (GRCm39) |
missense |
probably benign |
0.05 |
R0208:Mtor
|
UTSW |
4 |
148,549,432 (GRCm39) |
missense |
probably benign |
0.43 |
R0329:Mtor
|
UTSW |
4 |
148,568,837 (GRCm39) |
missense |
probably benign |
|
R0365:Mtor
|
UTSW |
4 |
148,570,507 (GRCm39) |
missense |
probably benign |
0.01 |
R0537:Mtor
|
UTSW |
4 |
148,622,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R0542:Mtor
|
UTSW |
4 |
148,624,907 (GRCm39) |
missense |
probably benign |
0.02 |
R0556:Mtor
|
UTSW |
4 |
148,553,837 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0613:Mtor
|
UTSW |
4 |
148,610,503 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0646:Mtor
|
UTSW |
4 |
148,568,811 (GRCm39) |
nonsense |
probably null |
|
R0710:Mtor
|
UTSW |
4 |
148,548,848 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0791:Mtor
|
UTSW |
4 |
148,547,367 (GRCm39) |
missense |
probably benign |
0.00 |
R0792:Mtor
|
UTSW |
4 |
148,547,367 (GRCm39) |
missense |
probably benign |
0.00 |
R0866:Mtor
|
UTSW |
4 |
148,570,513 (GRCm39) |
missense |
probably benign |
0.04 |
R0973:Mtor
|
UTSW |
4 |
148,634,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R1027:Mtor
|
UTSW |
4 |
148,624,456 (GRCm39) |
missense |
probably benign |
0.03 |
R1028:Mtor
|
UTSW |
4 |
148,623,287 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1289:Mtor
|
UTSW |
4 |
148,554,764 (GRCm39) |
missense |
probably benign |
0.10 |
R1416:Mtor
|
UTSW |
4 |
148,575,871 (GRCm39) |
nonsense |
probably null |
|
R1465:Mtor
|
UTSW |
4 |
148,610,450 (GRCm39) |
splice site |
probably benign |
|
R1506:Mtor
|
UTSW |
4 |
148,620,962 (GRCm39) |
splice site |
probably benign |
|
R1624:Mtor
|
UTSW |
4 |
148,632,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Mtor
|
UTSW |
4 |
148,623,364 (GRCm39) |
missense |
probably benign |
0.08 |
R1771:Mtor
|
UTSW |
4 |
148,555,081 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1800:Mtor
|
UTSW |
4 |
148,547,349 (GRCm39) |
missense |
probably benign |
0.00 |
R1855:Mtor
|
UTSW |
4 |
148,637,546 (GRCm39) |
missense |
probably benign |
0.02 |
R1857:Mtor
|
UTSW |
4 |
148,565,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R1867:Mtor
|
UTSW |
4 |
148,539,089 (GRCm39) |
missense |
probably damaging |
0.97 |
R1954:Mtor
|
UTSW |
4 |
148,552,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R2054:Mtor
|
UTSW |
4 |
148,550,482 (GRCm39) |
missense |
probably benign |
0.00 |
R2054:Mtor
|
UTSW |
4 |
148,547,309 (GRCm39) |
missense |
probably benign |
0.05 |
R2099:Mtor
|
UTSW |
4 |
148,634,649 (GRCm39) |
nonsense |
probably null |
|
R2148:Mtor
|
UTSW |
4 |
148,540,469 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2214:Mtor
|
UTSW |
4 |
148,623,327 (GRCm39) |
missense |
probably benign |
0.39 |
R2281:Mtor
|
UTSW |
4 |
148,574,012 (GRCm39) |
missense |
probably benign |
0.02 |
R2512:Mtor
|
UTSW |
4 |
148,614,948 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2870:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2870:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2871:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2871:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2872:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2872:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R2873:Mtor
|
UTSW |
4 |
148,624,487 (GRCm39) |
missense |
probably benign |
0.00 |
R4032:Mtor
|
UTSW |
4 |
148,621,209 (GRCm39) |
missense |
probably benign |
0.03 |
R4073:Mtor
|
UTSW |
4 |
148,633,832 (GRCm39) |
missense |
probably damaging |
0.99 |
R4273:Mtor
|
UTSW |
4 |
148,634,609 (GRCm39) |
missense |
probably benign |
0.21 |
R4611:Mtor
|
UTSW |
4 |
148,570,576 (GRCm39) |
missense |
probably benign |
0.03 |
R4858:Mtor
|
UTSW |
4 |
148,539,273 (GRCm39) |
makesense |
probably null |
|
R4942:Mtor
|
UTSW |
4 |
148,556,599 (GRCm39) |
missense |
probably benign |
0.03 |
R4967:Mtor
|
UTSW |
4 |
148,575,817 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4995:Mtor
|
UTSW |
4 |
148,610,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R5054:Mtor
|
UTSW |
4 |
148,641,312 (GRCm39) |
splice site |
probably null |
|
R5215:Mtor
|
UTSW |
4 |
148,538,440 (GRCm39) |
missense |
probably benign |
|
R5249:Mtor
|
UTSW |
4 |
148,548,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R5289:Mtor
|
UTSW |
4 |
148,550,549 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5365:Mtor
|
UTSW |
4 |
148,634,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R5498:Mtor
|
UTSW |
4 |
148,624,821 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5514:Mtor
|
UTSW |
4 |
148,630,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R5540:Mtor
|
UTSW |
4 |
148,539,165 (GRCm39) |
missense |
probably benign |
0.01 |
R5600:Mtor
|
UTSW |
4 |
148,575,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R5615:Mtor
|
UTSW |
4 |
148,622,733 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5632:Mtor
|
UTSW |
4 |
148,553,463 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5641:Mtor
|
UTSW |
4 |
148,630,882 (GRCm39) |
missense |
probably damaging |
0.98 |
R5834:Mtor
|
UTSW |
4 |
148,620,993 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5984:Mtor
|
UTSW |
4 |
148,623,284 (GRCm39) |
missense |
probably benign |
0.02 |
R6056:Mtor
|
UTSW |
4 |
148,621,892 (GRCm39) |
missense |
probably benign |
0.00 |
R6225:Mtor
|
UTSW |
4 |
148,605,794 (GRCm39) |
missense |
probably benign |
0.04 |
R6262:Mtor
|
UTSW |
4 |
148,610,552 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6335:Mtor
|
UTSW |
4 |
148,550,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R6479:Mtor
|
UTSW |
4 |
148,635,457 (GRCm39) |
missense |
probably benign |
0.16 |
R6543:Mtor
|
UTSW |
4 |
148,630,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R6711:Mtor
|
UTSW |
4 |
148,536,824 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6715:Mtor
|
UTSW |
4 |
148,623,004 (GRCm39) |
missense |
probably benign |
0.00 |
R6744:Mtor
|
UTSW |
4 |
148,543,112 (GRCm39) |
missense |
probably benign |
0.01 |
R6748:Mtor
|
UTSW |
4 |
148,634,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R6762:Mtor
|
UTSW |
4 |
148,622,938 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6836:Mtor
|
UTSW |
4 |
148,573,955 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6948:Mtor
|
UTSW |
4 |
148,621,209 (GRCm39) |
missense |
probably benign |
0.12 |
R6979:Mtor
|
UTSW |
4 |
148,608,930 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6992:Mtor
|
UTSW |
4 |
148,548,932 (GRCm39) |
missense |
probably benign |
|
R7271:Mtor
|
UTSW |
4 |
148,630,942 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7423:Mtor
|
UTSW |
4 |
148,640,801 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7434:Mtor
|
UTSW |
4 |
148,549,416 (GRCm39) |
missense |
probably benign |
0.39 |
R7619:Mtor
|
UTSW |
4 |
148,547,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R7634:Mtor
|
UTSW |
4 |
148,536,807 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7697:Mtor
|
UTSW |
4 |
148,624,765 (GRCm39) |
nonsense |
probably null |
|
R7737:Mtor
|
UTSW |
4 |
148,623,195 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7791:Mtor
|
UTSW |
4 |
148,547,397 (GRCm39) |
missense |
probably benign |
0.00 |
R7858:Mtor
|
UTSW |
4 |
148,539,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R8035:Mtor
|
UTSW |
4 |
148,630,856 (GRCm39) |
missense |
probably benign |
0.29 |
R8076:Mtor
|
UTSW |
4 |
148,610,260 (GRCm39) |
critical splice donor site |
probably null |
|
R8078:Mtor
|
UTSW |
4 |
148,552,744 (GRCm39) |
missense |
probably benign |
|
R8928:Mtor
|
UTSW |
4 |
148,623,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R9040:Mtor
|
UTSW |
4 |
148,548,205 (GRCm39) |
missense |
probably benign |
0.00 |
R9116:Mtor
|
UTSW |
4 |
148,637,198 (GRCm39) |
missense |
probably benign |
|
R9284:Mtor
|
UTSW |
4 |
148,543,537 (GRCm39) |
missense |
probably benign |
0.03 |
R9310:Mtor
|
UTSW |
4 |
148,553,834 (GRCm39) |
missense |
probably benign |
0.03 |
R9374:Mtor
|
UTSW |
4 |
148,599,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9417:Mtor
|
UTSW |
4 |
148,622,776 (GRCm39) |
nonsense |
probably null |
|
R9465:Mtor
|
UTSW |
4 |
148,624,839 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9492:Mtor
|
UTSW |
4 |
148,568,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R9499:Mtor
|
UTSW |
4 |
148,599,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9516:Mtor
|
UTSW |
4 |
148,569,103 (GRCm39) |
missense |
probably benign |
0.23 |
R9600:Mtor
|
UTSW |
4 |
148,632,092 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9622:Mtor
|
UTSW |
4 |
148,568,169 (GRCm39) |
missense |
probably damaging |
0.99 |
X0025:Mtor
|
UTSW |
4 |
148,615,171 (GRCm39) |
missense |
probably benign |
0.09 |
Z1176:Mtor
|
UTSW |
4 |
148,634,587 (GRCm39) |
missense |
possibly damaging |
0.69 |
Z1176:Mtor
|
UTSW |
4 |
148,634,582 (GRCm39) |
missense |
probably benign |
0.08 |
|