Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap31 |
T |
C |
16: 38,422,593 (GRCm39) |
T1158A |
probably damaging |
Het |
Arhgap32 |
A |
G |
9: 32,171,810 (GRCm39) |
E1530G |
possibly damaging |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Csmd1 |
T |
C |
8: 16,011,418 (GRCm39) |
N2545S |
probably damaging |
Het |
Ctsh |
A |
G |
9: 89,943,476 (GRCm39) |
D49G |
probably benign |
Het |
Cyp7a1 |
T |
A |
4: 6,272,697 (GRCm39) |
Y172F |
probably benign |
Het |
Ddx52 |
A |
G |
11: 83,842,911 (GRCm39) |
|
probably null |
Het |
Dmxl1 |
A |
G |
18: 50,026,474 (GRCm39) |
T1861A |
possibly damaging |
Het |
Dnah7c |
C |
T |
1: 46,830,929 (GRCm39) |
L3813F |
probably benign |
Het |
Efl1 |
A |
G |
7: 82,307,307 (GRCm39) |
I68V |
probably damaging |
Het |
Etnk2 |
T |
C |
1: 133,293,438 (GRCm39) |
V127A |
possibly damaging |
Het |
Fank1 |
G |
C |
7: 133,478,554 (GRCm39) |
R206P |
probably damaging |
Het |
Fbxl9 |
A |
G |
8: 106,042,165 (GRCm39) |
I221T |
probably benign |
Het |
Fbxw27 |
G |
A |
9: 109,618,468 (GRCm39) |
R73* |
probably null |
Het |
Fndc1 |
A |
T |
17: 7,992,029 (GRCm39) |
S556T |
unknown |
Het |
Gnb3 |
T |
C |
6: 124,814,055 (GRCm39) |
T178A |
probably benign |
Het |
H2bc12 |
T |
C |
13: 22,220,225 (GRCm39) |
S57P |
probably damaging |
Het |
H2-M10.3 |
A |
T |
17: 36,677,174 (GRCm39) |
L326Q |
probably benign |
Het |
Idh2 |
GGTCCCAG |
GG |
7: 79,748,077 (GRCm39) |
|
probably benign |
Het |
Itfg2 |
T |
C |
6: 128,393,344 (GRCm39) |
|
probably benign |
Het |
Kcnma1 |
G |
A |
14: 23,387,057 (GRCm39) |
P995L |
probably benign |
Het |
Lama1 |
G |
A |
17: 68,076,430 (GRCm39) |
G1068D |
|
Het |
Lats1 |
A |
T |
10: 7,573,290 (GRCm39) |
K125* |
probably null |
Het |
Lipg |
C |
T |
18: 75,081,078 (GRCm39) |
M334I |
probably damaging |
Het |
Loxhd1 |
A |
T |
18: 77,518,909 (GRCm39) |
E1905V |
probably damaging |
Het |
Lpin1 |
C |
T |
12: 16,612,370 (GRCm39) |
G544D |
|
Het |
Lyst |
A |
T |
13: 13,882,268 (GRCm39) |
N2853I |
probably benign |
Het |
Mars1 |
A |
G |
10: 127,136,114 (GRCm39) |
I525T |
probably damaging |
Het |
Miga2 |
T |
A |
2: 30,261,216 (GRCm39) |
D170E |
probably benign |
Het |
Mrpl34 |
T |
C |
8: 71,917,911 (GRCm39) |
V28A |
probably benign |
Het |
Muc16 |
A |
T |
9: 18,553,990 (GRCm39) |
V4101E |
unknown |
Het |
Muc5ac |
G |
C |
7: 141,363,040 (GRCm39) |
G2117A |
unknown |
Het |
Myo1f |
A |
G |
17: 33,817,270 (GRCm39) |
Y771C |
probably damaging |
Het |
Nr2f1 |
G |
A |
13: 78,337,988 (GRCm39) |
T376I |
probably benign |
Het |
Nsd1 |
A |
G |
13: 55,461,068 (GRCm39) |
T2535A |
probably damaging |
Het |
Nup98 |
T |
A |
7: 101,825,556 (GRCm39) |
T428S |
probably benign |
Het |
Omd |
A |
G |
13: 49,743,630 (GRCm39) |
M227V |
probably damaging |
Het |
Osbpl7 |
A |
C |
11: 96,951,283 (GRCm39) |
I657L |
possibly damaging |
Het |
Pdgfrb |
T |
C |
18: 61,205,730 (GRCm39) |
V572A |
probably damaging |
Het |
Pik3c3 |
T |
C |
18: 30,445,624 (GRCm39) |
V537A |
probably benign |
Het |
Pou2f2 |
T |
C |
7: 24,815,489 (GRCm39) |
M93V |
probably benign |
Het |
Ppip5k2 |
T |
C |
1: 97,668,207 (GRCm39) |
T640A |
probably benign |
Het |
Ptar1 |
C |
T |
19: 23,686,158 (GRCm39) |
P157S |
probably benign |
Het |
Rapgef2 |
T |
A |
3: 78,973,933 (GRCm39) |
D1471V |
possibly damaging |
Het |
Rgs7 |
A |
T |
1: 174,977,216 (GRCm39) |
|
probably null |
Het |
Rhag |
A |
G |
17: 41,142,536 (GRCm39) |
Y247C |
probably benign |
Het |
Sardh |
A |
G |
2: 27,129,383 (GRCm39) |
I305T |
probably damaging |
Het |
Scn11a |
A |
G |
9: 119,633,617 (GRCm39) |
I372T |
probably benign |
Het |
Scn3a |
G |
T |
2: 65,366,859 (GRCm39) |
D54E |
probably damaging |
Het |
Senp2 |
A |
G |
16: 21,832,981 (GRCm39) |
T90A |
probably benign |
Het |
Serpinh1 |
C |
T |
7: 98,998,495 (GRCm39) |
R45H |
probably benign |
Het |
Siglecg |
T |
C |
7: 43,058,703 (GRCm39) |
V152A |
probably benign |
Het |
Sipa1l2 |
T |
A |
8: 126,174,337 (GRCm39) |
M1314L |
probably benign |
Het |
Slc23a1 |
A |
G |
18: 35,759,002 (GRCm39) |
F63S |
possibly damaging |
Het |
Slc25a40 |
T |
A |
5: 8,492,509 (GRCm39) |
L133Q |
probably damaging |
Het |
Slc6a16 |
A |
G |
7: 44,908,771 (GRCm39) |
E117G |
probably damaging |
Het |
Thoc2l |
T |
C |
5: 104,669,212 (GRCm39) |
S1245P |
possibly damaging |
Het |
Tmem235 |
G |
A |
11: 117,755,033 (GRCm39) |
V162M |
probably benign |
Het |
Trank1 |
A |
G |
9: 111,221,584 (GRCm39) |
T2774A |
probably benign |
Het |
Trav10n |
A |
T |
14: 53,359,587 (GRCm39) |
H6L |
probably benign |
Het |
Trav13d-3 |
G |
A |
14: 53,270,704 (GRCm39) |
W55* |
probably null |
Het |
Zfp654 |
G |
T |
16: 64,672,011 (GRCm39) |
A2E |
probably damaging |
Het |
Zkscan5 |
A |
C |
5: 145,157,676 (GRCm39) |
H726P |
probably 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 |
R7099:C3
|
UTSW |
17 |
57,513,276 (GRCm39) |
missense |
probably benign |
0.28 |
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 |
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 |
|