Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730061H03Rik |
A |
G |
14: 55,797,736 (GRCm39) |
|
probably benign |
Het |
Abcd2 |
A |
T |
15: 91,075,150 (GRCm39) |
V221E |
possibly damaging |
Het |
Arhgap39 |
T |
A |
15: 76,614,606 (GRCm39) |
K853* |
probably null |
Het |
Art2a |
T |
C |
7: 101,204,430 (GRCm39) |
D36G |
possibly damaging |
Het |
Atp13a1 |
C |
T |
8: 70,258,010 (GRCm39) |
P922S |
probably benign |
Het |
Brwd1 |
C |
T |
16: 95,804,156 (GRCm39) |
G2005R |
probably benign |
Het |
Bzw2 |
A |
T |
12: 36,170,725 (GRCm39) |
M133K |
probably benign |
Het |
Cacna1s |
T |
G |
1: 136,004,496 (GRCm39) |
S346A |
probably damaging |
Het |
Cebpb |
C |
A |
2: 167,531,220 (GRCm39) |
D93E |
probably benign |
Het |
Cep162 |
C |
A |
9: 87,094,904 (GRCm39) |
|
probably null |
Het |
Col9a2 |
A |
T |
4: 120,911,060 (GRCm39) |
Y565F |
probably damaging |
Het |
Csgalnact1 |
T |
A |
8: 68,826,202 (GRCm39) |
N372I |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,138,315 (GRCm39) |
D1579G |
probably damaging |
Het |
Cyfip2 |
A |
C |
11: 46,144,792 (GRCm39) |
Y687* |
probably null |
Het |
Cyp2d34 |
G |
A |
15: 82,504,977 (GRCm39) |
R28W |
probably benign |
Het |
Dbndd2 |
C |
A |
2: 164,330,206 (GRCm39) |
Q13K |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,233,377 (GRCm39) |
S245R |
probably benign |
Het |
Dnajb5 |
A |
T |
4: 42,956,990 (GRCm39) |
T226S |
probably damaging |
Het |
Dnmt1 |
T |
C |
9: 20,838,430 (GRCm39) |
E211G |
probably benign |
Het |
Dnpep |
G |
A |
1: 75,291,872 (GRCm39) |
H214Y |
probably damaging |
Het |
Drc3 |
G |
A |
11: 60,261,406 (GRCm39) |
V186M |
possibly damaging |
Het |
Dvl3 |
A |
G |
16: 20,345,789 (GRCm39) |
D413G |
possibly damaging |
Het |
Dyrk4 |
C |
T |
6: 126,863,614 (GRCm39) |
|
probably null |
Het |
Edc4 |
T |
A |
8: 106,612,506 (GRCm39) |
D181E |
probably damaging |
Het |
Enthd1 |
T |
C |
15: 80,393,487 (GRCm39) |
Y247C |
possibly damaging |
Het |
Gm5622 |
A |
T |
14: 51,892,372 (GRCm39) |
R50S |
possibly damaging |
Het |
Gpbp1 |
G |
A |
13: 111,603,389 (GRCm39) |
T20I |
probably damaging |
Het |
Hnrnpdl |
A |
T |
5: 100,184,410 (GRCm39) |
Y276* |
probably null |
Het |
Hsd3b7 |
A |
C |
7: 127,400,404 (GRCm39) |
E51A |
probably damaging |
Het |
Ighv5-16 |
G |
T |
12: 113,802,238 (GRCm39) |
F87L |
probably damaging |
Het |
Iqsec1 |
C |
T |
6: 90,786,666 (GRCm39) |
|
probably null |
Het |
Irgm2 |
A |
T |
11: 58,111,435 (GRCm39) |
E387D |
possibly damaging |
Het |
Klhl23 |
C |
A |
2: 69,664,040 (GRCm39) |
P463Q |
possibly damaging |
Het |
Mast4 |
A |
T |
13: 102,990,391 (GRCm39) |
N43K |
probably damaging |
Het |
Mme |
T |
G |
3: 63,207,532 (GRCm39) |
|
probably null |
Het |
Mrps31 |
T |
G |
8: 22,901,539 (GRCm39) |
S20A |
probably benign |
Het |
Myo5c |
A |
G |
9: 75,157,091 (GRCm39) |
R176G |
probably damaging |
Het |
Naf1 |
T |
C |
8: 67,330,347 (GRCm39) |
V291A |
possibly damaging |
Het |
Ncaph2 |
T |
C |
15: 89,248,206 (GRCm39) |
|
probably null |
Het |
Neurod4 |
T |
G |
10: 130,106,869 (GRCm39) |
Y135S |
probably damaging |
Het |
Nrp2 |
A |
T |
1: 62,799,974 (GRCm39) |
N396I |
probably damaging |
Het |
Nvl |
T |
G |
1: 180,962,560 (GRCm39) |
T137P |
probably benign |
Het |
Or5p59 |
A |
G |
7: 107,703,335 (GRCm39) |
D273G |
probably damaging |
Het |
Papola |
T |
C |
12: 105,793,219 (GRCm39) |
V513A |
probably benign |
Het |
Pcdhgc4 |
T |
A |
18: 37,950,653 (GRCm39) |
S690T |
possibly damaging |
Het |
Pck1 |
A |
T |
2: 172,995,805 (GRCm39) |
D101V |
probably damaging |
Het |
Pdilt |
T |
A |
7: 119,094,265 (GRCm39) |
N329Y |
probably damaging |
Het |
Pfkl |
T |
A |
10: 77,825,447 (GRCm39) |
R648W |
probably damaging |
Het |
Prtn3 |
T |
A |
10: 79,716,382 (GRCm39) |
I63N |
probably damaging |
Het |
Psg22 |
C |
T |
7: 18,456,723 (GRCm39) |
A163V |
probably benign |
Het |
Pten |
A |
G |
19: 32,777,485 (GRCm39) |
T160A |
possibly damaging |
Het |
Retreg2 |
A |
G |
1: 75,123,530 (GRCm39) |
D449G |
probably damaging |
Het |
Scn9a |
T |
C |
2: 66,317,868 (GRCm39) |
Y1531C |
probably benign |
Het |
Sgk2 |
T |
A |
2: 162,841,174 (GRCm39) |
C195S |
probably damaging |
Het |
Slc19a3 |
C |
T |
1: 83,004,060 (GRCm39) |
V14I |
probably benign |
Het |
Snai2 |
A |
T |
16: 14,526,107 (GRCm39) |
R253* |
probably null |
Het |
Speg |
G |
A |
1: 75,391,031 (GRCm39) |
V1512I |
probably damaging |
Het |
Srsf1 |
G |
A |
11: 87,940,425 (GRCm39) |
|
probably benign |
Het |
Tctn3 |
G |
T |
19: 40,597,671 (GRCm39) |
T190N |
probably benign |
Het |
Tmprss11f |
T |
A |
5: 86,687,558 (GRCm39) |
I117L |
probably benign |
Het |
Ttn |
G |
A |
2: 76,682,413 (GRCm39) |
R959* |
probably null |
Het |
Vmn2r118 |
G |
T |
17: 55,899,871 (GRCm39) |
L678I |
possibly damaging |
Het |
Vps13b |
T |
C |
15: 35,668,884 (GRCm39) |
S1594P |
probably damaging |
Het |
Vps13d |
G |
T |
4: 144,875,135 (GRCm39) |
H1791N |
possibly damaging |
Het |
|
Other mutations in Nbeal1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Nbeal1
|
APN |
1 |
60,274,350 (GRCm39) |
nonsense |
probably null |
0.00 |
IGL00334:Nbeal1
|
APN |
1 |
60,321,042 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00334:Nbeal1
|
APN |
1 |
60,367,262 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00514:Nbeal1
|
APN |
1 |
60,256,384 (GRCm39) |
missense |
probably benign |
0.31 |
IGL00596:Nbeal1
|
APN |
1 |
60,220,900 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00654:Nbeal1
|
APN |
1 |
60,234,170 (GRCm39) |
critical splice acceptor site |
probably benign |
0.00 |
IGL00757:Nbeal1
|
APN |
1 |
60,234,302 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL00771:Nbeal1
|
APN |
1 |
60,274,512 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01315:Nbeal1
|
APN |
1 |
60,320,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01445:Nbeal1
|
APN |
1 |
60,281,784 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01456:Nbeal1
|
APN |
1 |
60,269,787 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01458:Nbeal1
|
APN |
1 |
60,281,784 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01535:Nbeal1
|
APN |
1 |
60,256,414 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01608:Nbeal1
|
APN |
1 |
60,281,694 (GRCm39) |
critical splice acceptor site |
probably benign |
0.00 |
IGL02006:Nbeal1
|
APN |
1 |
60,311,418 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02105:Nbeal1
|
APN |
1 |
60,292,660 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02409:Nbeal1
|
APN |
1 |
60,368,494 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02713:Nbeal1
|
APN |
1 |
60,274,396 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02720:Nbeal1
|
APN |
1 |
60,323,146 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02887:Nbeal1
|
APN |
1 |
60,326,603 (GRCm39) |
splice site |
probably benign |
|
IGL02945:Nbeal1
|
APN |
1 |
60,245,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03023:Nbeal1
|
APN |
1 |
60,292,572 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03114:Nbeal1
|
APN |
1 |
60,317,886 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03231:Nbeal1
|
APN |
1 |
60,275,618 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03241:Nbeal1
|
APN |
1 |
60,274,027 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL03241:Nbeal1
|
APN |
1 |
60,274,028 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03382:Nbeal1
|
APN |
1 |
60,300,745 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03412:Nbeal1
|
APN |
1 |
60,281,726 (GRCm39) |
nonsense |
probably null |
|
coach
|
UTSW |
1 |
60,292,640 (GRCm39) |
nonsense |
probably null |
|
Committee
|
UTSW |
1 |
60,332,062 (GRCm39) |
missense |
probably damaging |
1.00 |
Disgrace
|
UTSW |
1 |
60,320,469 (GRCm39) |
nonsense |
probably null |
|
Dravrah
|
UTSW |
1 |
60,323,251 (GRCm39) |
missense |
probably damaging |
1.00 |
Harvard
|
UTSW |
1 |
60,274,722 (GRCm39) |
splice site |
probably null |
|
horrified
|
UTSW |
1 |
60,283,983 (GRCm39) |
missense |
probably damaging |
1.00 |
Lampoon
|
UTSW |
1 |
60,300,745 (GRCm39) |
critical splice donor site |
probably null |
|
lawyer
|
UTSW |
1 |
60,349,383 (GRCm39) |
nonsense |
probably null |
|
magistrate
|
UTSW |
1 |
60,233,756 (GRCm39) |
critical splice donor site |
probably null |
|
Maratimus
|
UTSW |
1 |
60,331,047 (GRCm39) |
missense |
probably damaging |
1.00 |
National
|
UTSW |
1 |
60,261,422 (GRCm39) |
missense |
possibly damaging |
0.95 |
phainopepla
|
UTSW |
1 |
60,358,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R3875_Nbeal1_770
|
UTSW |
1 |
60,233,758 (GRCm39) |
splice site |
probably benign |
|
satirical
|
UTSW |
1 |
60,274,721 (GRCm39) |
critical splice donor site |
probably null |
|
silky
|
UTSW |
1 |
60,370,037 (GRCm39) |
splice site |
probably benign |
|
stiggs
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
3-1:Nbeal1
|
UTSW |
1 |
60,303,431 (GRCm39) |
splice site |
probably benign |
|
P0007:Nbeal1
|
UTSW |
1 |
60,358,847 (GRCm39) |
missense |
probably damaging |
0.98 |
P0028:Nbeal1
|
UTSW |
1 |
60,331,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Nbeal1
|
UTSW |
1 |
60,321,030 (GRCm39) |
missense |
probably benign |
0.05 |
R0051:Nbeal1
|
UTSW |
1 |
60,349,422 (GRCm39) |
missense |
probably benign |
0.19 |
R0052:Nbeal1
|
UTSW |
1 |
60,267,771 (GRCm39) |
splice site |
probably benign |
|
R0054:Nbeal1
|
UTSW |
1 |
60,326,560 (GRCm39) |
utr 3 prime |
probably benign |
|
R0062:Nbeal1
|
UTSW |
1 |
60,286,876 (GRCm39) |
missense |
probably benign |
0.01 |
R0062:Nbeal1
|
UTSW |
1 |
60,286,876 (GRCm39) |
missense |
probably benign |
0.01 |
R0094:Nbeal1
|
UTSW |
1 |
60,344,468 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0310:Nbeal1
|
UTSW |
1 |
60,344,529 (GRCm39) |
splice site |
probably benign |
|
R0324:Nbeal1
|
UTSW |
1 |
60,332,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R0329:Nbeal1
|
UTSW |
1 |
60,307,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R0330:Nbeal1
|
UTSW |
1 |
60,307,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R0417:Nbeal1
|
UTSW |
1 |
60,286,893 (GRCm39) |
missense |
probably benign |
0.00 |
R0421:Nbeal1
|
UTSW |
1 |
60,307,598 (GRCm39) |
missense |
probably benign |
0.08 |
R0617:Nbeal1
|
UTSW |
1 |
60,320,991 (GRCm39) |
nonsense |
probably null |
|
R1034:Nbeal1
|
UTSW |
1 |
60,329,165 (GRCm39) |
nonsense |
probably null |
|
R1082:Nbeal1
|
UTSW |
1 |
60,351,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R1123:Nbeal1
|
UTSW |
1 |
60,299,428 (GRCm39) |
missense |
probably benign |
|
R1187:Nbeal1
|
UTSW |
1 |
60,233,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Nbeal1
|
UTSW |
1 |
60,240,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1594:Nbeal1
|
UTSW |
1 |
60,344,450 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1651:Nbeal1
|
UTSW |
1 |
60,239,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R1678:Nbeal1
|
UTSW |
1 |
60,299,493 (GRCm39) |
missense |
probably benign |
0.00 |
R1806:Nbeal1
|
UTSW |
1 |
60,323,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Nbeal1
|
UTSW |
1 |
60,307,100 (GRCm39) |
nonsense |
probably null |
|
R1952:Nbeal1
|
UTSW |
1 |
60,273,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R1953:Nbeal1
|
UTSW |
1 |
60,273,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R2038:Nbeal1
|
UTSW |
1 |
60,245,503 (GRCm39) |
missense |
probably benign |
0.00 |
R2044:Nbeal1
|
UTSW |
1 |
60,358,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Nbeal1
|
UTSW |
1 |
60,332,123 (GRCm39) |
splice site |
probably null |
|
R2055:Nbeal1
|
UTSW |
1 |
60,350,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Nbeal1
|
UTSW |
1 |
60,309,515 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2100:Nbeal1
|
UTSW |
1 |
60,344,430 (GRCm39) |
splice site |
probably null |
|
R2181:Nbeal1
|
UTSW |
1 |
60,317,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R2192:Nbeal1
|
UTSW |
1 |
60,321,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R2203:Nbeal1
|
UTSW |
1 |
60,323,165 (GRCm39) |
missense |
probably benign |
0.21 |
R2267:Nbeal1
|
UTSW |
1 |
60,370,037 (GRCm39) |
splice site |
probably benign |
|
R2268:Nbeal1
|
UTSW |
1 |
60,370,037 (GRCm39) |
splice site |
probably benign |
|
R2351:Nbeal1
|
UTSW |
1 |
60,276,257 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2366:Nbeal1
|
UTSW |
1 |
60,290,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R2393:Nbeal1
|
UTSW |
1 |
60,290,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R3545:Nbeal1
|
UTSW |
1 |
60,317,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R3546:Nbeal1
|
UTSW |
1 |
60,317,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R3547:Nbeal1
|
UTSW |
1 |
60,317,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R3701:Nbeal1
|
UTSW |
1 |
60,290,572 (GRCm39) |
splice site |
probably benign |
|
R3747:Nbeal1
|
UTSW |
1 |
60,234,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R3875:Nbeal1
|
UTSW |
1 |
60,233,758 (GRCm39) |
splice site |
probably benign |
|
R4119:Nbeal1
|
UTSW |
1 |
60,331,029 (GRCm39) |
missense |
probably damaging |
0.99 |
R4256:Nbeal1
|
UTSW |
1 |
60,370,107 (GRCm39) |
missense |
probably benign |
0.19 |
R4371:Nbeal1
|
UTSW |
1 |
60,329,105 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4450:Nbeal1
|
UTSW |
1 |
60,306,933 (GRCm39) |
missense |
probably damaging |
0.97 |
R4558:Nbeal1
|
UTSW |
1 |
60,320,469 (GRCm39) |
nonsense |
probably null |
|
R4618:Nbeal1
|
UTSW |
1 |
60,267,890 (GRCm39) |
intron |
probably benign |
|
R4673:Nbeal1
|
UTSW |
1 |
60,368,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Nbeal1
|
UTSW |
1 |
60,274,722 (GRCm39) |
splice site |
probably null |
|
R4798:Nbeal1
|
UTSW |
1 |
60,261,352 (GRCm39) |
splice site |
probably null |
|
R4826:Nbeal1
|
UTSW |
1 |
60,290,501 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4841:Nbeal1
|
UTSW |
1 |
60,292,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R4842:Nbeal1
|
UTSW |
1 |
60,292,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R4895:Nbeal1
|
UTSW |
1 |
60,332,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R4929:Nbeal1
|
UTSW |
1 |
60,277,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R5026:Nbeal1
|
UTSW |
1 |
60,276,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R5243:Nbeal1
|
UTSW |
1 |
60,309,487 (GRCm39) |
missense |
probably damaging |
0.99 |
R5300:Nbeal1
|
UTSW |
1 |
60,274,718 (GRCm39) |
nonsense |
probably null |
|
R5345:Nbeal1
|
UTSW |
1 |
60,367,369 (GRCm39) |
critical splice donor site |
probably null |
|
R5502:Nbeal1
|
UTSW |
1 |
60,350,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R5542:Nbeal1
|
UTSW |
1 |
60,316,353 (GRCm39) |
missense |
probably benign |
0.00 |
R5555:Nbeal1
|
UTSW |
1 |
60,276,311 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5580:Nbeal1
|
UTSW |
1 |
60,281,761 (GRCm39) |
missense |
probably benign |
0.45 |
R5765:Nbeal1
|
UTSW |
1 |
60,331,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R5802:Nbeal1
|
UTSW |
1 |
60,311,380 (GRCm39) |
missense |
probably benign |
0.01 |
R5907:Nbeal1
|
UTSW |
1 |
60,267,950 (GRCm39) |
intron |
probably benign |
|
R5918:Nbeal1
|
UTSW |
1 |
60,307,051 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5923:Nbeal1
|
UTSW |
1 |
60,287,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R6066:Nbeal1
|
UTSW |
1 |
60,287,564 (GRCm39) |
missense |
probably benign |
0.29 |
R6091:Nbeal1
|
UTSW |
1 |
60,220,715 (GRCm39) |
start gained |
probably benign |
|
R6113:Nbeal1
|
UTSW |
1 |
60,261,422 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6194:Nbeal1
|
UTSW |
1 |
60,296,643 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6197:Nbeal1
|
UTSW |
1 |
60,261,287 (GRCm39) |
missense |
probably damaging |
0.99 |
R6228:Nbeal1
|
UTSW |
1 |
60,335,083 (GRCm39) |
missense |
probably benign |
0.00 |
R6229:Nbeal1
|
UTSW |
1 |
60,287,524 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6309:Nbeal1
|
UTSW |
1 |
60,277,878 (GRCm39) |
missense |
probably benign |
|
R6457:Nbeal1
|
UTSW |
1 |
60,292,633 (GRCm39) |
missense |
probably benign |
0.31 |
R6489:Nbeal1
|
UTSW |
1 |
60,370,101 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6845:Nbeal1
|
UTSW |
1 |
60,320,469 (GRCm39) |
nonsense |
probably null |
|
R7021:Nbeal1
|
UTSW |
1 |
60,300,745 (GRCm39) |
critical splice donor site |
probably null |
|
R7033:Nbeal1
|
UTSW |
1 |
60,350,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7145:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7146:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7157:Nbeal1
|
UTSW |
1 |
60,299,793 (GRCm39) |
nonsense |
probably null |
|
R7157:Nbeal1
|
UTSW |
1 |
60,276,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R7209:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7210:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7211:Nbeal1
|
UTSW |
1 |
60,240,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R7212:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7213:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7214:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7283:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7285:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7287:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7296:Nbeal1
|
UTSW |
1 |
60,349,383 (GRCm39) |
nonsense |
probably null |
|
R7312:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7313:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7329:Nbeal1
|
UTSW |
1 |
60,256,355 (GRCm39) |
missense |
probably benign |
0.39 |
R7380:Nbeal1
|
UTSW |
1 |
60,283,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7414:Nbeal1
|
UTSW |
1 |
60,233,756 (GRCm39) |
critical splice donor site |
probably null |
|
R7477:Nbeal1
|
UTSW |
1 |
60,300,743 (GRCm39) |
missense |
probably benign |
|
R7507:Nbeal1
|
UTSW |
1 |
60,274,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R7642:Nbeal1
|
UTSW |
1 |
60,316,386 (GRCm39) |
missense |
probably benign |
0.31 |
R7678:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7689:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7728:Nbeal1
|
UTSW |
1 |
60,283,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7757:Nbeal1
|
UTSW |
1 |
60,296,609 (GRCm39) |
missense |
probably damaging |
0.97 |
R7761:Nbeal1
|
UTSW |
1 |
60,358,500 (GRCm39) |
missense |
probably benign |
0.00 |
R7813:Nbeal1
|
UTSW |
1 |
60,331,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R7829:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R7891:Nbeal1
|
UTSW |
1 |
60,299,591 (GRCm39) |
missense |
probably benign |
|
R7902:Nbeal1
|
UTSW |
1 |
60,331,029 (GRCm39) |
missense |
probably damaging |
0.99 |
R8022:Nbeal1
|
UTSW |
1 |
60,299,431 (GRCm39) |
nonsense |
probably null |
|
R8053:Nbeal1
|
UTSW |
1 |
60,318,954 (GRCm39) |
missense |
probably damaging |
0.98 |
R8169:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R8170:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R8178:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R8182:Nbeal1
|
UTSW |
1 |
60,239,292 (GRCm39) |
missense |
probably benign |
0.00 |
R8186:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R8187:Nbeal1
|
UTSW |
1 |
60,276,310 (GRCm39) |
missense |
probably benign |
0.11 |
R8193:Nbeal1
|
UTSW |
1 |
60,292,640 (GRCm39) |
nonsense |
probably null |
|
R8209:Nbeal1
|
UTSW |
1 |
60,316,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R8226:Nbeal1
|
UTSW |
1 |
60,316,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R8549:Nbeal1
|
UTSW |
1 |
60,274,721 (GRCm39) |
critical splice donor site |
probably null |
|
R8560:Nbeal1
|
UTSW |
1 |
60,274,316 (GRCm39) |
missense |
probably benign |
0.38 |
R8753:Nbeal1
|
UTSW |
1 |
60,307,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R8769:Nbeal1
|
UTSW |
1 |
60,274,370 (GRCm39) |
missense |
probably damaging |
0.99 |
R8771:Nbeal1
|
UTSW |
1 |
60,300,743 (GRCm39) |
missense |
probably benign |
|
R8952:Nbeal1
|
UTSW |
1 |
60,299,459 (GRCm39) |
missense |
probably benign |
0.01 |
R9014:Nbeal1
|
UTSW |
1 |
60,329,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R9056:Nbeal1
|
UTSW |
1 |
60,317,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R9091:Nbeal1
|
UTSW |
1 |
60,307,548 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9138:Nbeal1
|
UTSW |
1 |
60,286,904 (GRCm39) |
nonsense |
probably null |
|
R9168:Nbeal1
|
UTSW |
1 |
60,331,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R9200:Nbeal1
|
UTSW |
1 |
60,320,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R9205:Nbeal1
|
UTSW |
1 |
60,317,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R9270:Nbeal1
|
UTSW |
1 |
60,307,548 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9322:Nbeal1
|
UTSW |
1 |
60,297,818 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9405:Nbeal1
|
UTSW |
1 |
60,349,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R9554:Nbeal1
|
UTSW |
1 |
60,290,287 (GRCm39) |
nonsense |
probably null |
|
R9557:Nbeal1
|
UTSW |
1 |
60,274,509 (GRCm39) |
missense |
probably benign |
|
R9560:Nbeal1
|
UTSW |
1 |
60,368,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Nbeal1
|
UTSW |
1 |
60,350,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R9784:Nbeal1
|
UTSW |
1 |
60,299,741 (GRCm39) |
nonsense |
probably null |
|
X0022:Nbeal1
|
UTSW |
1 |
60,316,391 (GRCm39) |
missense |
probably benign |
|
|