Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
T |
C |
6: 86,936,024 (GRCm39) |
|
probably benign |
Het |
Aldh18a1 |
A |
G |
19: 40,558,944 (GRCm39) |
S299P |
probably damaging |
Het |
Ankrd6 |
A |
C |
4: 32,806,206 (GRCm39) |
S618R |
probably benign |
Het |
Apobec3 |
G |
T |
15: 79,783,301 (GRCm39) |
R126M |
possibly damaging |
Het |
Arl8b |
T |
A |
6: 108,790,658 (GRCm39) |
V65D |
probably damaging |
Het |
AW554918 |
C |
T |
18: 25,533,104 (GRCm39) |
R253C |
probably benign |
Het |
Cd177 |
A |
G |
7: 24,453,817 (GRCm39) |
V358A |
probably benign |
Het |
Cdca7l |
G |
A |
12: 117,835,948 (GRCm39) |
V95I |
probably damaging |
Het |
Ces1e |
A |
G |
8: 93,928,467 (GRCm39) |
|
probably null |
Het |
Cfap90 |
A |
G |
13: 68,759,344 (GRCm39) |
H106R |
probably damaging |
Het |
Coq5 |
T |
G |
5: 115,433,957 (GRCm39) |
F306V |
probably damaging |
Het |
Cpsf1 |
A |
G |
15: 76,485,349 (GRCm39) |
V501A |
probably benign |
Het |
Csmd1 |
C |
T |
8: 16,052,522 (GRCm39) |
A2201T |
probably damaging |
Het |
Cul5 |
T |
A |
9: 53,534,243 (GRCm39) |
I630L |
probably benign |
Het |
Cyp4a12b |
A |
T |
4: 115,289,667 (GRCm39) |
D178V |
probably damaging |
Het |
Dedd |
A |
G |
1: 171,166,469 (GRCm39) |
E135G |
probably benign |
Het |
Ecel1 |
A |
G |
1: 87,080,622 (GRCm39) |
F368S |
probably damaging |
Het |
Ext1 |
A |
C |
15: 53,208,485 (GRCm39) |
I92S |
probably benign |
Het |
Fbxw5 |
A |
T |
2: 25,393,576 (GRCm39) |
D268V |
possibly damaging |
Het |
Flacc1 |
T |
G |
1: 58,698,164 (GRCm39) |
N379T |
probably damaging |
Het |
Gen1 |
A |
T |
12: 11,302,034 (GRCm39) |
V192E |
possibly damaging |
Het |
Gm11077 |
T |
G |
6: 140,675,041 (GRCm39) |
V11G |
unknown |
Het |
Ift88 |
A |
T |
14: 57,678,438 (GRCm39) |
E150V |
possibly damaging |
Het |
Kcna1 |
T |
C |
6: 126,620,009 (GRCm39) |
R104G |
probably damaging |
Het |
Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
Krt82 |
A |
G |
15: 101,459,035 (GRCm39) |
S2P |
probably damaging |
Het |
Luc7l2 |
T |
C |
6: 38,547,526 (GRCm39) |
S69P |
possibly damaging |
Het |
Ly9 |
G |
T |
1: 171,416,653 (GRCm39) |
T537N |
possibly damaging |
Het |
Mamstr |
G |
T |
7: 45,293,956 (GRCm39) |
R20L |
probably damaging |
Het |
Nav1 |
C |
A |
1: 135,398,862 (GRCm39) |
K573N |
possibly damaging |
Het |
Or5b104 |
T |
C |
19: 13,072,277 (GRCm39) |
H245R |
probably damaging |
Het |
Or8b12c |
C |
T |
9: 37,715,465 (GRCm39) |
S86L |
probably benign |
Het |
Or8b40 |
A |
T |
9: 38,027,922 (GRCm39) |
T277S |
possibly damaging |
Het |
Or8b55 |
A |
G |
9: 38,727,722 (GRCm39) |
K308E |
possibly damaging |
Het |
Palld |
T |
A |
8: 62,002,871 (GRCm39) |
|
probably benign |
Het |
Pcdha2 |
A |
G |
18: 37,074,748 (GRCm39) |
Y793C |
probably benign |
Het |
Pcdhb4 |
A |
T |
18: 37,441,065 (GRCm39) |
D125V |
probably damaging |
Het |
Pomgnt1 |
T |
A |
4: 116,011,139 (GRCm39) |
|
probably null |
Het |
Ppp1r9b |
A |
T |
11: 94,883,359 (GRCm39) |
E329V |
probably damaging |
Het |
Rarres1 |
T |
A |
3: 67,422,654 (GRCm39) |
D32V |
probably benign |
Het |
Rhobtb1 |
A |
G |
10: 69,121,523 (GRCm39) |
H53R |
possibly damaging |
Het |
Ryr1 |
A |
T |
7: 28,772,327 (GRCm39) |
S2494T |
probably damaging |
Het |
Sapcd2 |
G |
A |
2: 25,263,518 (GRCm39) |
|
probably benign |
Het |
Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
Senp1 |
A |
C |
15: 97,954,713 (GRCm39) |
D490E |
probably damaging |
Het |
Sfrp5 |
C |
T |
19: 42,187,230 (GRCm39) |
R280H |
probably benign |
Het |
Skint5 |
A |
G |
4: 113,486,319 (GRCm39) |
|
probably benign |
Het |
Skint5 |
G |
A |
4: 113,703,496 (GRCm39) |
T499I |
possibly damaging |
Het |
Smad1 |
G |
A |
8: 80,070,359 (GRCm39) |
A393V |
probably benign |
Het |
Sorl1 |
A |
G |
9: 41,975,345 (GRCm39) |
L487P |
possibly damaging |
Het |
Spire1 |
G |
T |
18: 67,639,733 (GRCm39) |
T273K |
probably benign |
Het |
Tep1 |
T |
C |
14: 51,105,772 (GRCm39) |
T83A |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,552,077 (GRCm39) |
R29441* |
probably null |
Het |
Wdr37 |
A |
G |
13: 8,903,632 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Top2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00430:Top2b
|
APN |
14 |
16,422,692 (GRCm38) |
missense |
probably benign |
0.00 |
IGL00730:Top2b
|
APN |
14 |
16,389,831 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00917:Top2b
|
APN |
14 |
16,407,354 (GRCm38) |
missense |
probably benign |
0.05 |
IGL01959:Top2b
|
APN |
14 |
16,422,695 (GRCm38) |
missense |
probably benign |
0.19 |
IGL02019:Top2b
|
APN |
14 |
16,409,965 (GRCm38) |
missense |
probably benign |
0.44 |
IGL02119:Top2b
|
APN |
14 |
16,406,733 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02136:Top2b
|
APN |
14 |
16,407,103 (GRCm38) |
unclassified |
probably benign |
|
IGL02148:Top2b
|
APN |
14 |
16,400,488 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02496:Top2b
|
APN |
14 |
16,387,335 (GRCm38) |
missense |
probably benign |
|
IGL02503:Top2b
|
APN |
14 |
16,407,163 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL02672:Top2b
|
APN |
14 |
16,409,166 (GRCm38) |
unclassified |
probably benign |
|
IGL02721:Top2b
|
APN |
14 |
16,409,236 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02886:Top2b
|
APN |
14 |
16,365,688 (GRCm38) |
missense |
possibly damaging |
0.73 |
IGL03252:Top2b
|
APN |
14 |
16,393,163 (GRCm38) |
missense |
possibly damaging |
0.60 |
PIT4434001:Top2b
|
UTSW |
14 |
16,423,780 (GRCm38) |
critical splice donor site |
probably null |
|
R0092:Top2b
|
UTSW |
14 |
16,409,263 (GRCm38) |
missense |
probably damaging |
1.00 |
R0201:Top2b
|
UTSW |
14 |
16,383,174 (GRCm38) |
missense |
probably damaging |
1.00 |
R0390:Top2b
|
UTSW |
14 |
16,418,442 (GRCm38) |
missense |
probably benign |
0.00 |
R0394:Top2b
|
UTSW |
14 |
16,413,556 (GRCm38) |
splice site |
probably null |
|
R1159:Top2b
|
UTSW |
14 |
16,430,329 (GRCm38) |
missense |
possibly damaging |
0.81 |
R1424:Top2b
|
UTSW |
14 |
16,383,177 (GRCm38) |
missense |
probably damaging |
1.00 |
R1519:Top2b
|
UTSW |
14 |
16,408,953 (GRCm38) |
splice site |
probably null |
|
R1561:Top2b
|
UTSW |
14 |
16,398,993 (GRCm38) |
missense |
possibly damaging |
0.80 |
R1713:Top2b
|
UTSW |
14 |
16,409,823 (GRCm38) |
missense |
probably benign |
0.05 |
R1987:Top2b
|
UTSW |
14 |
16,398,916 (GRCm38) |
missense |
probably damaging |
0.99 |
R2219:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R2287:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R2422:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R2679:Top2b
|
UTSW |
14 |
16,413,947 (GRCm38) |
missense |
probably damaging |
1.00 |
R3687:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R3707:Top2b
|
UTSW |
14 |
16,388,447 (GRCm38) |
missense |
probably damaging |
1.00 |
R3810:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R3812:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R3816:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R3818:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4023:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4025:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4026:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4133:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4157:Top2b
|
UTSW |
14 |
16,384,491 (GRCm38) |
missense |
probably benign |
0.42 |
R4179:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4180:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4300:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4376:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4377:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4492:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4549:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4550:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4581:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4582:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4628:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4630:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4667:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4668:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4669:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R4698:Top2b
|
UTSW |
14 |
16,387,331 (GRCm38) |
nonsense |
probably null |
|
R4769:Top2b
|
UTSW |
14 |
16,398,991 (GRCm38) |
missense |
probably damaging |
1.00 |
R4809:Top2b
|
UTSW |
14 |
16,383,125 (GRCm38) |
missense |
probably benign |
0.06 |
R4899:Top2b
|
UTSW |
14 |
16,387,313 (GRCm38) |
missense |
probably damaging |
1.00 |
R5035:Top2b
|
UTSW |
14 |
16,409,966 (GRCm38) |
missense |
probably benign |
0.01 |
R5621:Top2b
|
UTSW |
14 |
16,387,280 (GRCm38) |
missense |
probably damaging |
1.00 |
R5631:Top2b
|
UTSW |
14 |
16,409,882 (GRCm38) |
missense |
probably damaging |
1.00 |
R5685:Top2b
|
UTSW |
14 |
16,413,666 (GRCm38) |
missense |
probably damaging |
1.00 |
R5732:Top2b
|
UTSW |
14 |
16,400,106 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5939:Top2b
|
UTSW |
14 |
16,422,786 (GRCm38) |
missense |
probably damaging |
0.96 |
R6007:Top2b
|
UTSW |
14 |
16,423,779 (GRCm38) |
critical splice donor site |
probably null |
|
R6087:Top2b
|
UTSW |
14 |
16,409,864 (GRCm38) |
missense |
probably benign |
0.14 |
R6144:Top2b
|
UTSW |
14 |
16,423,740 (GRCm38) |
missense |
possibly damaging |
0.48 |
R6196:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R6218:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R6229:Top2b
|
UTSW |
14 |
16,409,838 (GRCm38) |
missense |
probably damaging |
1.00 |
R6249:Top2b
|
UTSW |
14 |
16,399,006 (GRCm38) |
missense |
probably damaging |
1.00 |
R6337:Top2b
|
UTSW |
14 |
16,399,026 (GRCm38) |
missense |
possibly damaging |
0.77 |
R6353:Top2b
|
UTSW |
14 |
16,416,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R6512:Top2b
|
UTSW |
14 |
16,409,854 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6573:Top2b
|
UTSW |
14 |
16,398,991 (GRCm38) |
missense |
probably damaging |
1.00 |
R6614:Top2b
|
UTSW |
14 |
16,407,142 (GRCm38) |
nonsense |
probably null |
|
R6844:Top2b
|
UTSW |
14 |
16,429,383 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6848:Top2b
|
UTSW |
14 |
16,409,958 (GRCm38) |
missense |
possibly damaging |
0.89 |
R6871:Top2b
|
UTSW |
14 |
16,409,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R6895:Top2b
|
UTSW |
14 |
16,413,604 (GRCm38) |
missense |
probably benign |
0.06 |
R7162:Top2b
|
UTSW |
14 |
16,416,653 (GRCm38) |
missense |
probably benign |
0.00 |
R7247:Top2b
|
UTSW |
14 |
16,416,962 (GRCm38) |
missense |
probably benign |
0.08 |
R7250:Top2b
|
UTSW |
14 |
16,420,411 (GRCm38) |
missense |
probably benign |
|
R7359:Top2b
|
UTSW |
14 |
16,407,376 (GRCm38) |
missense |
probably null |
1.00 |
R7365:Top2b
|
UTSW |
14 |
16,416,649 (GRCm38) |
missense |
probably benign |
0.04 |
R7493:Top2b
|
UTSW |
14 |
16,416,605 (GRCm38) |
missense |
probably benign |
0.00 |
R7528:Top2b
|
UTSW |
14 |
16,395,427 (GRCm38) |
nonsense |
probably null |
|
R7562:Top2b
|
UTSW |
14 |
16,412,946 (GRCm38) |
missense |
probably benign |
0.04 |
R7594:Top2b
|
UTSW |
14 |
16,428,587 (GRCm38) |
missense |
probably benign |
|
R7670:Top2b
|
UTSW |
14 |
16,416,620 (GRCm38) |
missense |
possibly damaging |
0.61 |
R7894:Top2b
|
UTSW |
14 |
16,413,081 (GRCm38) |
missense |
possibly damaging |
0.68 |
R8031:Top2b
|
UTSW |
14 |
16,412,986 (GRCm38) |
missense |
probably damaging |
0.98 |
R8150:Top2b
|
UTSW |
14 |
16,393,291 (GRCm38) |
missense |
probably damaging |
0.99 |
R8214:Top2b
|
UTSW |
14 |
16,383,177 (GRCm38) |
missense |
probably damaging |
1.00 |
R8299:Top2b
|
UTSW |
14 |
16,386,123 (GRCm38) |
missense |
possibly damaging |
0.68 |
R8977:Top2b
|
UTSW |
14 |
16,393,239 (GRCm38) |
missense |
probably benign |
0.36 |
R9562:Top2b
|
UTSW |
14 |
16,365,718 (GRCm38) |
missense |
probably benign |
0.09 |
R9565:Top2b
|
UTSW |
14 |
16,365,718 (GRCm38) |
missense |
probably benign |
0.09 |
R9798:Top2b
|
UTSW |
14 |
16,389,845 (GRCm38) |
missense |
probably damaging |
1.00 |
X0028:Top2b
|
UTSW |
14 |
16,384,499 (GRCm38) |
nonsense |
probably null |
|
Z1176:Top2b
|
UTSW |
14 |
16,395,434 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Top2b
|
UTSW |
14 |
16,416,953 (GRCm38) |
missense |
probably benign |
|
|