Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34 |
G |
T |
8: 44,105,192 (GRCm39) |
T151K |
probably benign |
Het |
Adnp2 |
C |
T |
18: 80,185,893 (GRCm39) |
G27S |
probably damaging |
Het |
Ank3 |
A |
G |
10: 69,660,292 (GRCm39) |
M265V |
probably benign |
Het |
Aoc1l1 |
G |
A |
6: 48,952,428 (GRCm39) |
E118K |
probably damaging |
Het |
Apoe |
T |
C |
7: 19,430,597 (GRCm39) |
D215G |
possibly damaging |
Het |
Atp5f1b |
A |
G |
10: 127,924,850 (GRCm39) |
I438V |
probably benign |
Het |
Bckdha |
A |
G |
7: 25,330,436 (GRCm39) |
S387P |
probably damaging |
Het |
Camkk1 |
T |
C |
11: 72,924,734 (GRCm39) |
F316L |
probably damaging |
Het |
Carmil1 |
A |
G |
13: 24,197,179 (GRCm39) |
Y158H |
|
Het |
Ccdc148 |
T |
C |
2: 58,894,054 (GRCm39) |
R29G |
probably benign |
Het |
Ccdc39 |
A |
G |
3: 33,884,274 (GRCm39) |
V356A |
probably benign |
Het |
Cdan1 |
G |
A |
2: 120,561,568 (GRCm39) |
Q66* |
probably null |
Het |
Ckap4 |
A |
T |
10: 84,364,290 (GRCm39) |
S258T |
probably benign |
Het |
Col5a2 |
T |
C |
1: 45,419,306 (GRCm39) |
D1258G |
probably benign |
Het |
Col6a1 |
G |
A |
10: 76,552,593 (GRCm39) |
P431L |
unknown |
Het |
Cplane1 |
A |
G |
15: 8,223,859 (GRCm39) |
Y874C |
probably damaging |
Het |
Csn1s2a |
A |
G |
5: 87,933,164 (GRCm39) |
I138V |
probably benign |
Het |
Dnah10 |
A |
G |
5: 124,878,015 (GRCm39) |
E2700G |
possibly damaging |
Het |
Eif3l |
T |
A |
15: 78,960,006 (GRCm39) |
Y23* |
probably null |
Het |
Fam72a |
A |
G |
1: 131,456,502 (GRCm39) |
K22E |
probably benign |
Het |
Golim4 |
A |
G |
3: 75,805,351 (GRCm39) |
V258A |
probably benign |
Het |
Gtf2ird2 |
C |
T |
5: 134,237,739 (GRCm39) |
A272V |
probably benign |
Het |
Hpse |
T |
C |
5: 100,846,872 (GRCm39) |
T186A |
possibly damaging |
Het |
Ift140 |
A |
T |
17: 25,305,862 (GRCm39) |
Q816H |
probably benign |
Het |
Iqca1 |
A |
T |
1: 90,067,750 (GRCm39) |
I167N |
probably damaging |
Het |
Iqgap1 |
A |
T |
7: 80,401,141 (GRCm39) |
F515L |
probably benign |
Het |
Itgb4 |
G |
A |
11: 115,879,295 (GRCm39) |
R558H |
probably benign |
Het |
Kcna10 |
G |
A |
3: 107,101,419 (GRCm39) |
D17N |
probably damaging |
Het |
Kcnj16 |
A |
G |
11: 110,915,829 (GRCm39) |
I164V |
probably damaging |
Het |
Lrrc55 |
G |
T |
2: 85,026,615 (GRCm39) |
N136K |
probably damaging |
Het |
Mdm4 |
A |
T |
1: 132,940,382 (GRCm39) |
M50K |
probably benign |
Het |
Mfge8 |
A |
G |
7: 78,786,530 (GRCm39) |
S290P |
probably damaging |
Het |
Mindy4 |
G |
A |
6: 55,201,115 (GRCm39) |
D267N |
probably benign |
Het |
Mllt10 |
T |
A |
2: 18,128,617 (GRCm39) |
S199R |
probably benign |
Het |
Mms22l |
T |
C |
4: 24,533,029 (GRCm39) |
S436P |
probably damaging |
Het |
Mpped2 |
A |
G |
2: 106,697,395 (GRCm39) |
N290S |
possibly damaging |
Het |
Mrgpra2a |
A |
G |
7: 47,076,445 (GRCm39) |
L271P |
probably benign |
Het |
Myrf |
T |
A |
19: 10,200,931 (GRCm39) |
E247D |
probably benign |
Het |
Ndrg3 |
A |
G |
2: 156,782,299 (GRCm39) |
I189T |
possibly damaging |
Het |
Nenf |
C |
T |
1: 191,050,148 (GRCm39) |
E48K |
probably benign |
Het |
Nlgn2 |
T |
A |
11: 69,718,994 (GRCm39) |
N232Y |
probably damaging |
Het |
Oog2 |
G |
T |
4: 143,920,685 (GRCm39) |
M39I |
probably benign |
Het |
Or9r7 |
A |
T |
10: 129,962,631 (GRCm39) |
N98K |
probably benign |
Het |
Osbpl3 |
A |
T |
6: 50,304,371 (GRCm39) |
N461K |
probably benign |
Het |
P4ha1 |
A |
G |
10: 59,175,130 (GRCm39) |
D30G |
possibly damaging |
Het |
Pappa2 |
A |
T |
1: 158,590,762 (GRCm39) |
C1631S |
probably damaging |
Het |
Pigk |
A |
G |
3: 152,445,871 (GRCm39) |
M161V |
possibly damaging |
Het |
Prdm1 |
G |
T |
10: 44,317,335 (GRCm39) |
S496Y |
probably damaging |
Het |
Prkg2 |
T |
C |
5: 99,095,299 (GRCm39) |
N624S |
possibly damaging |
Het |
Rgs6 |
A |
G |
12: 83,112,733 (GRCm39) |
D181G |
probably damaging |
Het |
Sbf2 |
A |
G |
7: 110,040,155 (GRCm39) |
|
probably null |
Het |
Sbno2 |
A |
C |
10: 79,898,042 (GRCm39) |
L728W |
probably damaging |
Het |
Selenbp2 |
A |
T |
3: 94,609,793 (GRCm39) |
I310F |
probably damaging |
Het |
Shank3 |
T |
A |
15: 89,432,986 (GRCm39) |
W1244R |
possibly damaging |
Het |
Slc34a1 |
A |
C |
13: 24,004,184 (GRCm39) |
I395L |
probably benign |
Het |
Slf1 |
A |
T |
13: 77,194,693 (GRCm39) |
D877E |
probably damaging |
Het |
Smtn |
T |
C |
11: 3,472,908 (GRCm39) |
S255G |
probably benign |
Het |
Tbx2 |
T |
A |
11: 85,725,533 (GRCm39) |
D161E |
probably damaging |
Het |
Tex14 |
C |
A |
11: 87,324,675 (GRCm39) |
L26M |
possibly damaging |
Het |
Traf7 |
A |
G |
17: 24,731,286 (GRCm39) |
F249S |
probably damaging |
Het |
Trpm6 |
A |
G |
19: 18,815,366 (GRCm39) |
K1151E |
possibly damaging |
Het |
Ttc7b |
A |
G |
12: 100,268,022 (GRCm39) |
V773A |
probably benign |
Het |
Ttn |
G |
A |
2: 76,747,912 (GRCm39) |
T4379I |
probably benign |
Het |
Ttn |
G |
A |
2: 76,602,854 (GRCm39) |
T18456I |
probably damaging |
Het |
Ttn |
G |
C |
2: 76,709,171 (GRCm39) |
L8703V |
unknown |
Het |
Ubb |
T |
A |
11: 62,442,979 (GRCm39) |
I3N |
probably damaging |
Het |
Vmn1r209 |
A |
T |
13: 22,990,343 (GRCm39) |
W116R |
probably damaging |
Het |
Vmn1r75 |
A |
G |
7: 11,614,838 (GRCm39) |
D190G |
probably damaging |
Het |
Wdr12 |
T |
A |
1: 60,130,202 (GRCm39) |
M70L |
probably benign |
Het |
Wdr48 |
C |
A |
9: 119,740,142 (GRCm39) |
T317K |
probably damaging |
Het |
Zbtb5 |
A |
G |
4: 44,993,962 (GRCm39) |
V474A |
probably benign |
Het |
Zfp128 |
C |
T |
7: 12,625,113 (GRCm39) |
R494C |
possibly damaging |
Het |
|
Other mutations in Cyp19a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01897:Cyp19a1
|
APN |
9 |
54,075,813 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02885:Cyp19a1
|
APN |
9 |
54,079,102 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02897:Cyp19a1
|
APN |
9 |
54,074,195 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0384:Cyp19a1
|
UTSW |
9 |
54,080,025 (GRCm39) |
missense |
probably benign |
0.01 |
R3104:Cyp19a1
|
UTSW |
9 |
54,094,083 (GRCm39) |
missense |
probably benign |
0.00 |
R4116:Cyp19a1
|
UTSW |
9 |
54,076,025 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4158:Cyp19a1
|
UTSW |
9 |
54,093,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R4160:Cyp19a1
|
UTSW |
9 |
54,093,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R4555:Cyp19a1
|
UTSW |
9 |
54,074,105 (GRCm39) |
missense |
probably damaging |
0.96 |
R4569:Cyp19a1
|
UTSW |
9 |
54,100,607 (GRCm39) |
missense |
probably benign |
0.06 |
R4570:Cyp19a1
|
UTSW |
9 |
54,100,607 (GRCm39) |
missense |
probably benign |
0.06 |
R4693:Cyp19a1
|
UTSW |
9 |
54,080,617 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4807:Cyp19a1
|
UTSW |
9 |
54,083,930 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4853:Cyp19a1
|
UTSW |
9 |
54,074,060 (GRCm39) |
missense |
probably benign |
|
R4938:Cyp19a1
|
UTSW |
9 |
54,080,647 (GRCm39) |
missense |
probably benign |
0.01 |
R5272:Cyp19a1
|
UTSW |
9 |
54,083,898 (GRCm39) |
missense |
probably benign |
0.19 |
R6148:Cyp19a1
|
UTSW |
9 |
54,087,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R7008:Cyp19a1
|
UTSW |
9 |
54,100,609 (GRCm39) |
missense |
probably benign |
0.35 |
R7472:Cyp19a1
|
UTSW |
9 |
54,074,277 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7807:Cyp19a1
|
UTSW |
9 |
54,074,126 (GRCm39) |
missense |
probably benign |
0.06 |
R7841:Cyp19a1
|
UTSW |
9 |
54,079,089 (GRCm39) |
missense |
probably benign |
0.03 |
R8367:Cyp19a1
|
UTSW |
9 |
54,087,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R9674:Cyp19a1
|
UTSW |
9 |
54,074,141 (GRCm39) |
missense |
possibly damaging |
0.88 |
X0025:Cyp19a1
|
UTSW |
9 |
54,075,852 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cyp19a1
|
UTSW |
9 |
54,083,883 (GRCm39) |
nonsense |
probably null |
|
|