Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930453N24Rik |
C |
T |
16: 64,591,151 (GRCm39) |
A26T |
probably benign |
Het |
Acly |
T |
C |
11: 100,383,117 (GRCm39) |
|
probably null |
Het |
Adam29 |
A |
C |
8: 56,324,439 (GRCm39) |
L672V |
probably benign |
Het |
Adgrf1 |
T |
C |
17: 43,621,493 (GRCm39) |
S577P |
probably benign |
Het |
Ankar |
T |
C |
1: 72,682,452 (GRCm39) |
K1371R |
probably damaging |
Het |
Arid5b |
T |
C |
10: 67,934,009 (GRCm39) |
D631G |
probably damaging |
Het |
Brpf3 |
T |
C |
17: 29,025,611 (GRCm39) |
V228A |
probably benign |
Het |
Calr4 |
A |
T |
4: 109,099,426 (GRCm39) |
N143I |
probably benign |
Het |
Catsperd |
T |
G |
17: 56,935,811 (GRCm39) |
|
probably null |
Het |
Cobl |
T |
A |
11: 12,246,540 (GRCm39) |
H154L |
|
Het |
Cryzl2 |
G |
A |
1: 157,316,154 (GRCm39) |
|
probably benign |
Het |
Dennd1c |
A |
G |
17: 57,374,915 (GRCm39) |
|
probably null |
Het |
Dnah8 |
A |
T |
17: 30,923,698 (GRCm39) |
D1222V |
possibly damaging |
Het |
Errfi1 |
T |
C |
4: 150,951,225 (GRCm39) |
S218P |
probably benign |
Het |
Fbxw27 |
G |
T |
9: 109,599,223 (GRCm39) |
T398N |
probably damaging |
Het |
Fhod3 |
A |
G |
18: 25,223,219 (GRCm39) |
D855G |
probably benign |
Het |
Flii |
A |
G |
11: 60,611,481 (GRCm39) |
V410A |
probably benign |
Het |
Fsip2 |
C |
A |
2: 82,817,968 (GRCm39) |
P4567Q |
probably benign |
Het |
Fxyd1 |
T |
G |
7: 30,752,458 (GRCm39) |
Q66H |
probably damaging |
Het |
Gdi1 |
G |
A |
X: 73,350,461 (GRCm39) |
R55H |
probably benign |
Het |
Gramd2b |
C |
T |
18: 56,625,017 (GRCm39) |
T370I |
probably benign |
Het |
Kdr |
A |
G |
5: 76,104,993 (GRCm39) |
V1079A |
probably damaging |
Het |
Lmx1a |
G |
A |
1: 167,658,115 (GRCm39) |
G166D |
probably damaging |
Het |
Lrrfip2 |
A |
G |
9: 111,002,176 (GRCm39) |
R92G |
probably benign |
Het |
Map1a |
T |
A |
2: 121,130,998 (GRCm39) |
S605T |
probably benign |
Het |
Megf8 |
A |
T |
7: 25,045,945 (GRCm39) |
D1496V |
probably damaging |
Het |
Mgam |
T |
C |
6: 40,638,650 (GRCm39) |
V461A |
probably benign |
Het |
Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,214,363 (GRCm39) |
|
probably null |
Het |
Nav3 |
T |
C |
10: 109,539,195 (GRCm39) |
T2069A |
probably benign |
Het |
Nbeal2 |
A |
T |
9: 110,474,506 (GRCm39) |
|
probably null |
Het |
Ndst1 |
A |
G |
18: 60,828,572 (GRCm39) |
F661L |
possibly damaging |
Het |
Neu3 |
G |
A |
7: 99,463,027 (GRCm39) |
T232M |
possibly damaging |
Het |
Nf1 |
T |
C |
11: 79,461,156 (GRCm39) |
S741P |
probably benign |
Het |
Nr5a1 |
G |
T |
2: 38,584,148 (GRCm39) |
L424M |
probably damaging |
Het |
Nuf2 |
G |
A |
1: 169,333,641 (GRCm39) |
T345M |
probably benign |
Het |
Or4d10c |
A |
G |
19: 12,065,530 (GRCm39) |
F209L |
possibly damaging |
Het |
Or4k51 |
A |
T |
2: 111,585,421 (GRCm39) |
T276S |
probably benign |
Het |
Or6d12 |
T |
A |
6: 116,493,721 (GRCm39) |
*328R |
probably null |
Het |
Or8g33 |
G |
A |
9: 39,337,599 (GRCm39) |
T256I |
probably benign |
Het |
Otud7a |
A |
G |
7: 63,407,203 (GRCm39) |
E502G |
possibly damaging |
Het |
Otulin |
A |
G |
15: 27,608,832 (GRCm39) |
L237S |
probably damaging |
Het |
Pias1 |
A |
G |
9: 62,788,427 (GRCm39) |
M79T |
|
Het |
Prom2 |
T |
C |
2: 127,381,698 (GRCm39) |
E206G |
probably benign |
Het |
Scarb1 |
A |
T |
5: 125,381,414 (GRCm39) |
N43K |
probably damaging |
Het |
Sdad1 |
A |
G |
5: 92,441,832 (GRCm39) |
V365A |
possibly damaging |
Het |
Sdk2 |
T |
C |
11: 113,725,731 (GRCm39) |
T1173A |
probably damaging |
Het |
Sidt1 |
A |
G |
16: 44,063,860 (GRCm39) |
S803P |
probably damaging |
Het |
Slc45a1 |
A |
T |
4: 150,714,030 (GRCm39) |
D738E |
probably benign |
Het |
Slc4a7 |
T |
A |
14: 14,733,750 (GRCm38) |
H53Q |
probably damaging |
Het |
Spata22 |
T |
C |
11: 73,231,225 (GRCm39) |
F160L |
probably benign |
Het |
Stag1 |
G |
A |
9: 100,826,879 (GRCm39) |
V949I |
probably benign |
Het |
Syne1 |
T |
C |
10: 5,073,744 (GRCm39) |
S1200G |
probably benign |
Het |
Tbc1d9 |
A |
G |
8: 83,981,520 (GRCm39) |
E729G |
probably damaging |
Het |
Tcaf2 |
C |
T |
6: 42,607,275 (GRCm39) |
M226I |
probably benign |
Het |
Tep1 |
T |
C |
14: 51,081,944 (GRCm39) |
|
probably null |
Het |
Tigd2 |
C |
A |
6: 59,187,166 (GRCm39) |
T11K |
probably damaging |
Het |
Trappc9 |
A |
G |
15: 72,565,468 (GRCm39) |
V941A |
probably benign |
Het |
Ugt2b37 |
A |
G |
5: 87,388,848 (GRCm39) |
M455T |
probably benign |
Het |
Usp42 |
A |
T |
5: 143,712,400 (GRCm39) |
S95T |
probably damaging |
Het |
Usp44 |
T |
C |
10: 93,686,049 (GRCm39) |
I488T |
possibly damaging |
Het |
Vmn1r73 |
T |
C |
7: 11,490,320 (GRCm39) |
I46T |
probably damaging |
Het |
Vmn2r34 |
A |
T |
7: 7,675,540 (GRCm39) |
I616N |
probably damaging |
Het |
Zfp352 |
A |
G |
4: 90,113,117 (GRCm39) |
K419R |
probably benign |
Het |
Zfp595 |
T |
A |
13: 67,465,711 (GRCm39) |
H187L |
probably damaging |
Het |
Zfp804b |
A |
T |
5: 6,822,161 (GRCm39) |
S301T |
probably benign |
Het |
Zzef1 |
T |
C |
11: 72,763,475 (GRCm39) |
V1374A |
possibly damaging |
Het |
|
Other mutations in C3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:C3
|
APN |
17 |
57,533,004 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00741:C3
|
APN |
17 |
57,527,206 (GRCm39) |
intron |
probably benign |
|
IGL01093:C3
|
APN |
17 |
57,530,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01309:C3
|
APN |
17 |
57,516,652 (GRCm39) |
intron |
probably benign |
|
IGL01312:C3
|
APN |
17 |
57,532,993 (GRCm39) |
unclassified |
probably benign |
|
IGL01344:C3
|
APN |
17 |
57,531,880 (GRCm39) |
missense |
probably benign |
|
IGL01514:C3
|
APN |
17 |
57,522,866 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01913:C3
|
APN |
17 |
57,520,767 (GRCm39) |
missense |
probably null |
0.01 |
IGL02165:C3
|
APN |
17 |
57,532,092 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02176:C3
|
APN |
17 |
57,533,337 (GRCm39) |
unclassified |
probably benign |
|
IGL02189:C3
|
APN |
17 |
57,527,113 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02378:C3
|
APN |
17 |
57,519,698 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02422:C3
|
APN |
17 |
57,533,823 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02715:C3
|
APN |
17 |
57,511,158 (GRCm39) |
intron |
probably benign |
|
IGL02737:C3
|
APN |
17 |
57,511,281 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03201:C3
|
APN |
17 |
57,529,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03210:C3
|
APN |
17 |
57,522,846 (GRCm39) |
nonsense |
probably null |
|
IGL03345:C3
|
APN |
17 |
57,526,585 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4431001:C3
|
UTSW |
17 |
57,513,242 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4494001:C3
|
UTSW |
17 |
57,516,263 (GRCm39) |
missense |
probably benign |
0.01 |
R0158:C3
|
UTSW |
17 |
57,531,851 (GRCm39) |
critical splice donor site |
probably null |
|
R0318:C3
|
UTSW |
17 |
57,531,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R1132:C3
|
UTSW |
17 |
57,514,531 (GRCm39) |
critical splice donor site |
probably null |
|
R1765:C3
|
UTSW |
17 |
57,531,401 (GRCm39) |
splice site |
probably null |
|
R1793:C3
|
UTSW |
17 |
57,526,592 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1852:C3
|
UTSW |
17 |
57,529,823 (GRCm39) |
missense |
probably damaging |
0.98 |
R1908:C3
|
UTSW |
17 |
57,516,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:C3
|
UTSW |
17 |
57,527,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:C3
|
UTSW |
17 |
57,525,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R2026:C3
|
UTSW |
17 |
57,525,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:C3
|
UTSW |
17 |
57,530,974 (GRCm39) |
splice site |
probably null |
|
R2197:C3
|
UTSW |
17 |
57,526,623 (GRCm39) |
missense |
probably benign |
0.32 |
R2394:C3
|
UTSW |
17 |
57,529,303 (GRCm39) |
nonsense |
probably null |
|
R2998:C3
|
UTSW |
17 |
57,517,284 (GRCm39) |
missense |
probably benign |
0.00 |
R3727:C3
|
UTSW |
17 |
57,514,379 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3767:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3768:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3769:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3770:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3784:C3
|
UTSW |
17 |
57,533,067 (GRCm39) |
missense |
probably damaging |
0.99 |
R3883:C3
|
UTSW |
17 |
57,524,173 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3884:C3
|
UTSW |
17 |
57,524,173 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3950:C3
|
UTSW |
17 |
57,532,286 (GRCm39) |
missense |
probably benign |
0.02 |
R3966:C3
|
UTSW |
17 |
57,525,664 (GRCm39) |
missense |
probably damaging |
0.99 |
R4077:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4078:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4079:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4168:C3
|
UTSW |
17 |
57,525,608 (GRCm39) |
missense |
probably benign |
0.00 |
R4208:C3
|
UTSW |
17 |
57,512,303 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4695:C3
|
UTSW |
17 |
57,528,057 (GRCm39) |
missense |
probably benign |
|
R4909:C3
|
UTSW |
17 |
57,533,830 (GRCm39) |
critical splice donor site |
probably null |
|
R5011:C3
|
UTSW |
17 |
57,530,236 (GRCm39) |
missense |
probably benign |
0.06 |
R5094:C3
|
UTSW |
17 |
57,532,033 (GRCm39) |
critical splice donor site |
probably null |
|
R5141:C3
|
UTSW |
17 |
57,526,570 (GRCm39) |
missense |
probably damaging |
0.98 |
R5170:C3
|
UTSW |
17 |
57,530,938 (GRCm39) |
missense |
probably damaging |
0.96 |
R5339:C3
|
UTSW |
17 |
57,531,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R5369:C3
|
UTSW |
17 |
57,528,159 (GRCm39) |
missense |
probably benign |
0.45 |
R5412:C3
|
UTSW |
17 |
57,527,187 (GRCm39) |
missense |
probably benign |
0.01 |
R5439:C3
|
UTSW |
17 |
57,511,502 (GRCm39) |
missense |
probably benign |
0.28 |
R5463:C3
|
UTSW |
17 |
57,518,720 (GRCm39) |
missense |
probably benign |
0.08 |
R5546:C3
|
UTSW |
17 |
57,529,976 (GRCm39) |
missense |
probably damaging |
0.99 |
R5572:C3
|
UTSW |
17 |
57,531,673 (GRCm39) |
missense |
probably damaging |
0.99 |
R5851:C3
|
UTSW |
17 |
57,518,612 (GRCm39) |
missense |
probably null |
0.14 |
R5863:C3
|
UTSW |
17 |
57,530,141 (GRCm39) |
missense |
probably benign |
0.06 |
R5888:C3
|
UTSW |
17 |
57,521,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R5940:C3
|
UTSW |
17 |
57,517,244 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6073:C3
|
UTSW |
17 |
57,513,223 (GRCm39) |
missense |
probably null |
|
R6091:C3
|
UTSW |
17 |
57,528,967 (GRCm39) |
nonsense |
probably null |
|
R6286:C3
|
UTSW |
17 |
57,531,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:C3
|
UTSW |
17 |
57,524,264 (GRCm39) |
critical splice donor site |
probably null |
|
R6868:C3
|
UTSW |
17 |
57,511,029 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6896:C3
|
UTSW |
17 |
57,527,864 (GRCm39) |
splice site |
probably null |
|
R7007:C3
|
UTSW |
17 |
57,525,809 (GRCm39) |
missense |
probably benign |
0.00 |
R7022:C3
|
UTSW |
17 |
57,524,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:C3
|
UTSW |
17 |
57,519,655 (GRCm39) |
missense |
probably benign |
0.01 |
R7347:C3
|
UTSW |
17 |
57,530,215 (GRCm39) |
missense |
probably benign |
0.09 |
R7366:C3
|
UTSW |
17 |
57,528,162 (GRCm39) |
missense |
probably benign |
0.00 |
R7423:C3
|
UTSW |
17 |
57,521,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R7425:C3
|
UTSW |
17 |
57,511,039 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7481:C3
|
UTSW |
17 |
57,527,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R7540:C3
|
UTSW |
17 |
57,513,220 (GRCm39) |
missense |
probably benign |
0.01 |
R7746:C3
|
UTSW |
17 |
57,525,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7771:C3
|
UTSW |
17 |
57,522,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:C3
|
UTSW |
17 |
57,533,264 (GRCm39) |
missense |
probably benign |
0.05 |
R8144:C3
|
UTSW |
17 |
57,533,276 (GRCm39) |
missense |
probably damaging |
0.98 |
R8279:C3
|
UTSW |
17 |
57,522,809 (GRCm39) |
missense |
probably benign |
0.28 |
R8284:C3
|
UTSW |
17 |
57,530,938 (GRCm39) |
missense |
probably benign |
0.39 |
R8328:C3
|
UTSW |
17 |
57,527,973 (GRCm39) |
missense |
probably benign |
0.00 |
R8353:C3
|
UTSW |
17 |
57,519,643 (GRCm39) |
missense |
probably benign |
0.00 |
R8396:C3
|
UTSW |
17 |
57,528,029 (GRCm39) |
missense |
probably benign |
|
R8429:C3
|
UTSW |
17 |
57,529,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R8453:C3
|
UTSW |
17 |
57,519,643 (GRCm39) |
missense |
probably benign |
0.00 |
R8557:C3
|
UTSW |
17 |
57,531,383 (GRCm39) |
missense |
probably benign |
0.00 |
R8738:C3
|
UTSW |
17 |
57,511,015 (GRCm39) |
makesense |
probably null |
|
R8794:C3
|
UTSW |
17 |
57,528,011 (GRCm39) |
missense |
probably benign |
|
R9130:C3
|
UTSW |
17 |
57,518,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R9296:C3
|
UTSW |
17 |
57,511,291 (GRCm39) |
missense |
probably benign |
|
R9432:C3
|
UTSW |
17 |
57,530,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R9451:C3
|
UTSW |
17 |
57,531,169 (GRCm39) |
missense |
probably benign |
0.03 |
R9542:C3
|
UTSW |
17 |
57,532,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R9615:C3
|
UTSW |
17 |
57,518,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R9624:C3
|
UTSW |
17 |
57,527,189 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:C3
|
UTSW |
17 |
57,533,171 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:C3
|
UTSW |
17 |
57,524,144 (GRCm39) |
missense |
probably benign |
0.07 |
|