Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
G |
A |
5: 109,737,393 |
R200C |
probably benign |
Het |
Ak7 |
G |
A |
12: 105,713,575 |
V123M |
probably benign |
Het |
Apc |
T |
C |
18: 34,318,565 |
L2804P |
probably damaging |
Het |
Apob |
C |
A |
12: 8,011,331 |
A3271E |
probably damaging |
Het |
Asl |
G |
T |
5: 130,018,316 |
A147E |
probably damaging |
Het |
Atp1a1 |
A |
G |
3: 101,586,943 |
V447A |
probably benign |
Het |
AY358078 |
T |
A |
14: 51,826,075 |
C393S |
possibly damaging |
Het |
Bcl11b |
T |
C |
12: 107,916,530 |
K509E |
probably damaging |
Het |
Btnl1 |
T |
C |
17: 34,379,725 |
I105T |
probably damaging |
Het |
Btnl10 |
A |
G |
11: 58,920,357 |
T169A |
probably damaging |
Het |
C8b |
T |
C |
4: 104,790,644 |
I278T |
probably damaging |
Het |
Ccdc66 |
T |
C |
14: 27,500,420 |
N122S |
probably damaging |
Het |
Cd8b1 |
T |
C |
6: 71,332,475 |
V181A |
probably benign |
Het |
Cdan1 |
A |
T |
2: 120,730,720 |
V189D |
probably damaging |
Het |
Celf2 |
G |
T |
2: 6,586,020 |
N279K |
possibly damaging |
Het |
Cfap52 |
T |
C |
11: 67,926,421 |
N549D |
probably damaging |
Het |
Cmklr1 |
C |
T |
5: 113,614,869 |
V24M |
probably benign |
Het |
Cntnap4 |
G |
T |
8: 112,773,739 |
|
probably null |
Het |
Col27a1 |
G |
A |
4: 63,293,506 |
G91R |
probably damaging |
Het |
Col5a3 |
A |
G |
9: 20,814,896 |
|
probably benign |
Het |
Dcc |
C |
T |
18: 71,548,998 |
|
probably null |
Het |
Deaf1 |
T |
A |
7: 141,310,971 |
T433S |
possibly damaging |
Het |
Dnajc7 |
A |
T |
11: 100,590,977 |
Y228* |
probably null |
Het |
Doxl2 |
A |
T |
6: 48,975,156 |
Q5L |
probably benign |
Het |
Eno1b |
T |
C |
18: 48,047,703 |
V316A |
probably damaging |
Het |
Exoc4 |
T |
C |
6: 33,438,405 |
M404T |
possibly damaging |
Het |
Fignl1 |
A |
T |
11: 11,801,268 |
C596S |
probably benign |
Het |
Fn1 |
A |
C |
1: 71,624,178 |
Y1050* |
probably null |
Het |
Frem2 |
A |
G |
3: 53,547,807 |
L2116S |
possibly damaging |
Het |
Gba2 |
T |
A |
4: 43,568,092 |
S732C |
probably damaging |
Het |
Gcnt4 |
C |
A |
13: 96,946,482 |
S95R |
probably benign |
Het |
Gpr37 |
A |
G |
6: 25,669,624 |
V407A |
probably benign |
Het |
Gria2 |
A |
T |
3: 80,692,492 |
M695K |
probably damaging |
Het |
Hoxa9 |
T |
C |
6: 52,225,710 |
K132R |
probably damaging |
Het |
Ifi213 |
T |
A |
1: 173,589,914 |
T311S |
possibly damaging |
Het |
Itgb2 |
T |
A |
10: 77,550,050 |
N282K |
probably damaging |
Het |
Kcnh8 |
A |
T |
17: 52,602,836 |
Q11L |
probably benign |
Het |
Klk14 |
T |
C |
7: 43,694,357 |
C163R |
probably damaging |
Het |
Klk1b3 |
T |
A |
7: 44,201,265 |
W74R |
possibly damaging |
Het |
Krtap13-1 |
G |
T |
16: 88,729,254 |
C122F |
possibly damaging |
Het |
Luzp2 |
T |
C |
7: 55,063,356 |
|
probably null |
Het |
Mbtps1 |
A |
T |
8: 119,535,347 |
D354E |
probably damaging |
Het |
Mcpt9 |
C |
T |
14: 56,028,592 |
V60M |
probably damaging |
Het |
Mical3 |
C |
A |
6: 120,934,838 |
E1083* |
probably null |
Het |
Mrc2 |
G |
A |
11: 105,348,431 |
|
probably null |
Het |
Mtor |
T |
A |
4: 148,486,119 |
V1211E |
probably benign |
Het |
Myb |
T |
A |
10: 21,145,324 |
D402V |
probably damaging |
Het |
Ncor2 |
G |
A |
5: 125,030,859 |
T1593I |
probably damaging |
Het |
Ndst3 |
A |
G |
3: 123,671,549 |
I258T |
probably benign |
Het |
Npy6r |
C |
A |
18: 44,276,401 |
H296Q |
probably damaging |
Het |
Olfml2b |
T |
A |
1: 170,644,947 |
L9H |
probably damaging |
Het |
Olfr1364 |
A |
T |
13: 21,573,574 |
V294D |
probably damaging |
Het |
Olfr1442 |
T |
A |
19: 12,674,954 |
Y250N |
probably damaging |
Het |
Olfr145 |
T |
A |
9: 37,898,326 |
S307R |
probably benign |
Het |
Olfr1475 |
C |
T |
19: 13,480,012 |
C62Y |
probably damaging |
Het |
Olfr43 |
A |
T |
11: 74,206,535 |
V227D |
possibly damaging |
Het |
Olfr519 |
A |
G |
7: 108,894,117 |
C97R |
probably damaging |
Het |
Olfr727 |
C |
A |
14: 50,127,073 |
N165K |
probably benign |
Het |
Olfr777 |
G |
A |
10: 129,268,405 |
A306V |
probably benign |
Het |
Ovgp1 |
T |
C |
3: 105,986,567 |
|
probably benign |
Het |
Parg |
G |
A |
14: 32,274,864 |
R304Q |
probably damaging |
Het |
Pdf |
T |
G |
8: 107,048,535 |
S22R |
probably benign |
Het |
Phlpp2 |
A |
T |
8: 109,876,883 |
R60S |
possibly damaging |
Het |
Piwil2 |
C |
T |
14: 70,402,197 |
E401K |
probably benign |
Het |
Pla2g4e |
T |
G |
2: 120,186,382 |
H226P |
possibly damaging |
Het |
Polr3a |
T |
C |
14: 24,452,508 |
|
probably null |
Het |
Ppp3cb |
T |
C |
14: 20,520,646 |
N339S |
possibly damaging |
Het |
Ptch2 |
G |
A |
4: 117,110,378 |
D748N |
probably benign |
Het |
Rai14 |
A |
C |
15: 10,592,138 |
Y224D |
probably damaging |
Het |
Rft1 |
A |
G |
14: 30,689,790 |
I432V |
probably damaging |
Het |
Rictor |
C |
T |
15: 6,787,144 |
A1299V |
possibly damaging |
Het |
Sall2 |
A |
G |
14: 52,313,753 |
C662R |
probably damaging |
Het |
Scn4b |
A |
G |
9: 45,150,439 |
N208D |
probably damaging |
Het |
Sdhb |
G |
A |
4: 140,972,915 |
G109R |
probably damaging |
Het |
Sec16a |
A |
G |
2: 26,441,805 |
V66A |
probably benign |
Het |
Sema4g |
A |
G |
19: 45,001,612 |
Y710C |
probably damaging |
Het |
Serpinb12 |
T |
A |
1: 106,949,153 |
D66E |
probably benign |
Het |
Shc4 |
T |
A |
2: 125,655,682 |
D369V |
probably benign |
Het |
Siglech |
T |
C |
7: 55,771,693 |
L285P |
probably damaging |
Het |
Skint6 |
A |
G |
4: 113,074,076 |
M506T |
probably benign |
Het |
Slco1a6 |
C |
A |
6: 142,101,652 |
C404F |
probably benign |
Het |
Slfn14 |
T |
A |
11: 83,283,314 |
K284* |
probably null |
Het |
Sox14 |
A |
G |
9: 99,875,662 |
I8T |
probably damaging |
Het |
Srpk3 |
A |
G |
X: 73,774,941 |
H79R |
possibly damaging |
Het |
Tdpoz3 |
A |
T |
3: 93,827,023 |
H335L |
probably damaging |
Het |
Tdrd5 |
T |
A |
1: 156,284,374 |
T479S |
probably benign |
Het |
Tnik |
T |
C |
3: 28,542,100 |
|
probably null |
Het |
Tnpo2 |
T |
C |
8: 85,053,803 |
S720P |
probably benign |
Het |
Tpst1 |
A |
G |
5: 130,101,706 |
K6E |
probably damaging |
Het |
Trank1 |
T |
A |
9: 111,362,261 |
I446N |
probably damaging |
Het |
Trmt44 |
A |
T |
5: 35,575,007 |
D13E |
probably benign |
Het |
Ubr4 |
T |
A |
4: 139,399,579 |
V471E |
possibly damaging |
Het |
Ubtd1 |
A |
G |
19: 42,033,591 |
T101A |
probably benign |
Het |
Ugt3a1 |
A |
T |
15: 9,306,400 |
K212* |
probably null |
Het |
Zbtb7c |
C |
T |
18: 76,136,847 |
A2V |
possibly damaging |
Het |
Zfp423 |
C |
T |
8: 87,688,081 |
G1182D |
possibly damaging |
Het |
Zfp618 |
G |
A |
4: 63,132,979 |
V666M |
probably damaging |
Het |
Zmat1 |
A |
T |
X: 134,972,945 |
S566T |
probably damaging |
Homo |
Zscan20 |
T |
C |
4: 128,588,106 |
T588A |
probably benign |
Het |
Zscan25 |
G |
A |
5: 145,291,116 |
R530H |
probably damaging |
Het |
|