Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
T |
C |
13: 77,471,843 (GRCm39) |
W1083R |
possibly damaging |
Het |
Adamts10 |
T |
A |
17: 33,747,726 (GRCm39) |
L54Q |
probably damaging |
Het |
Ankrd24 |
A |
C |
10: 81,479,149 (GRCm39) |
|
probably benign |
Het |
Atg2b |
A |
G |
12: 105,618,888 (GRCm39) |
S813P |
probably benign |
Het |
Atp13a3 |
T |
A |
16: 30,160,058 (GRCm39) |
I716F |
probably damaging |
Het |
Atp6v1c1 |
T |
A |
15: 38,689,420 (GRCm39) |
W294R |
probably damaging |
Het |
Atrnl1 |
G |
T |
19: 58,030,793 (GRCm39) |
A1312S |
probably benign |
Het |
Bcl2 |
A |
T |
1: 106,640,338 (GRCm39) |
H91Q |
possibly damaging |
Het |
Cacna1c |
G |
A |
6: 118,607,263 (GRCm39) |
Q1214* |
probably null |
Het |
Cacna1g |
C |
A |
11: 94,324,673 (GRCm39) |
G1183W |
probably damaging |
Het |
Capsl |
A |
T |
15: 9,461,828 (GRCm39) |
M75L |
probably benign |
Het |
Ccdc122 |
T |
G |
14: 77,349,047 (GRCm39) |
|
probably benign |
Het |
Ccdc57 |
T |
G |
11: 120,772,683 (GRCm39) |
R645S |
possibly damaging |
Het |
Cdh8 |
T |
A |
8: 99,751,558 (GRCm39) |
R720* |
probably null |
Het |
Cenpx |
T |
G |
11: 120,602,610 (GRCm39) |
|
probably benign |
Het |
Clic3 |
T |
C |
2: 25,348,194 (GRCm39) |
S114P |
probably damaging |
Het |
Cracdl |
A |
T |
1: 37,664,046 (GRCm39) |
D617E |
probably benign |
Het |
Crtac1 |
A |
T |
19: 42,312,240 (GRCm39) |
W158R |
possibly damaging |
Het |
Dennd2b |
C |
T |
7: 109,156,240 (GRCm39) |
G170D |
probably damaging |
Het |
Dhrs11 |
T |
A |
11: 84,719,626 (GRCm39) |
Q33L |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dpp9 |
G |
T |
17: 56,498,016 (GRCm39) |
Q647K |
probably damaging |
Het |
Egf |
C |
T |
3: 129,510,327 (GRCm39) |
G64D |
probably damaging |
Het |
Eif2b4 |
C |
T |
5: 31,346,864 (GRCm39) |
|
probably benign |
Het |
Epas1 |
A |
G |
17: 87,113,267 (GRCm39) |
N151S |
probably benign |
Het |
Fastkd1 |
A |
T |
2: 69,521,651 (GRCm39) |
I707K |
probably benign |
Het |
Fbln2 |
A |
G |
6: 91,246,168 (GRCm39) |
T1005A |
probably benign |
Het |
Fgfrl1 |
T |
A |
5: 108,851,363 (GRCm39) |
Y93* |
probably null |
Het |
Fktn |
A |
G |
4: 53,744,637 (GRCm39) |
T306A |
probably benign |
Het |
Gabbr2 |
T |
G |
4: 46,991,139 (GRCm39) |
Y96S |
possibly damaging |
Het |
Gm16332 |
A |
T |
1: 139,819,396 (GRCm39) |
|
noncoding transcript |
Het |
Gm5145 |
G |
T |
17: 20,790,810 (GRCm39) |
V63F |
probably damaging |
Het |
Gm9970 |
G |
T |
5: 31,398,429 (GRCm39) |
|
probably benign |
Het |
Gpr158 |
A |
G |
2: 21,787,993 (GRCm39) |
T545A |
probably damaging |
Het |
Heatr1 |
G |
A |
13: 12,426,929 (GRCm39) |
E685K |
probably benign |
Het |
Herc6 |
A |
T |
6: 57,581,151 (GRCm39) |
I284F |
probably damaging |
Het |
Hook1 |
C |
G |
4: 95,890,794 (GRCm39) |
A301G |
possibly damaging |
Het |
Hpcal4 |
T |
A |
4: 123,084,491 (GRCm39) |
M140K |
possibly damaging |
Het |
Il11ra1 |
T |
C |
4: 41,766,096 (GRCm39) |
|
probably benign |
Het |
Ildr1 |
A |
T |
16: 36,542,917 (GRCm39) |
H439L |
possibly damaging |
Het |
Itga11 |
A |
G |
9: 62,684,009 (GRCm39) |
|
probably null |
Het |
Jag2 |
A |
T |
12: 112,880,252 (GRCm39) |
D337E |
probably benign |
Het |
Krt82 |
C |
T |
15: 101,458,923 (GRCm39) |
R39Q |
probably benign |
Het |
L3mbtl4 |
T |
A |
17: 68,666,475 (GRCm39) |
M1K |
probably null |
Het |
Lrrc32 |
T |
G |
7: 98,148,224 (GRCm39) |
F335V |
probably damaging |
Het |
Lurap1l |
T |
A |
4: 80,829,650 (GRCm39) |
V20E |
probably damaging |
Het |
Lyar |
T |
A |
5: 38,385,230 (GRCm39) |
V90D |
possibly damaging |
Het |
Man2c1 |
C |
T |
9: 57,048,469 (GRCm39) |
R778* |
probably null |
Het |
Mapk6 |
A |
G |
9: 75,295,714 (GRCm39) |
F595L |
probably benign |
Het |
Mccc1 |
A |
G |
3: 36,039,150 (GRCm39) |
I281T |
probably damaging |
Het |
Mep1b |
T |
C |
18: 21,226,311 (GRCm39) |
V391A |
probably damaging |
Het |
Mier1 |
G |
A |
4: 102,988,195 (GRCm39) |
D40N |
probably damaging |
Het |
Mkx |
T |
C |
18: 7,002,432 (GRCm39) |
H38R |
probably benign |
Het |
Mroh4 |
A |
G |
15: 74,498,028 (GRCm39) |
L184P |
probably damaging |
Het |
Muc2 |
C |
A |
7: 141,307,877 (GRCm39) |
N834K |
probably benign |
Het |
Mycl |
A |
G |
4: 122,894,049 (GRCm39) |
D283G |
probably damaging |
Het |
Myh6 |
T |
C |
14: 55,190,750 (GRCm39) |
N975S |
probably damaging |
Het |
Myl12a |
A |
G |
17: 71,303,297 (GRCm39) |
|
probably benign |
Het |
Mysm1 |
T |
C |
4: 94,853,910 (GRCm39) |
T230A |
probably benign |
Het |
Naca |
A |
G |
10: 127,883,672 (GRCm39) |
K2099R |
probably null |
Het |
Nedd1 |
A |
G |
10: 92,534,772 (GRCm39) |
V246A |
probably benign |
Het |
Nid2 |
A |
G |
14: 19,839,829 (GRCm39) |
D806G |
probably benign |
Het |
Ninl |
G |
A |
2: 150,801,801 (GRCm39) |
R156* |
probably null |
Het |
Obscn |
T |
A |
11: 58,960,685 (GRCm39) |
I3418F |
probably damaging |
Het |
Or8g37 |
T |
A |
9: 39,731,193 (GRCm39) |
V86E |
probably benign |
Het |
Pappa2 |
T |
C |
1: 158,684,949 (GRCm39) |
N730S |
probably damaging |
Het |
Pcm1 |
G |
A |
8: 41,746,715 (GRCm39) |
D1305N |
probably damaging |
Het |
Pcsk4 |
A |
T |
10: 80,158,938 (GRCm39) |
I485N |
probably damaging |
Het |
Phldb2 |
T |
C |
16: 45,646,237 (GRCm39) |
R111G |
probably damaging |
Het |
Prdm10 |
T |
C |
9: 31,252,569 (GRCm39) |
F385S |
probably damaging |
Het |
Prkcsh |
C |
T |
9: 21,923,034 (GRCm39) |
P351L |
probably damaging |
Het |
Prrc2a |
G |
A |
17: 35,369,018 (GRCm39) |
P2006L |
probably damaging |
Het |
Rad51c |
T |
C |
11: 87,286,204 (GRCm39) |
D251G |
probably damaging |
Het |
Radil |
A |
G |
5: 142,470,918 (GRCm39) |
F1088L |
probably benign |
Het |
Rere |
C |
A |
4: 150,699,624 (GRCm39) |
|
probably benign |
Het |
Rnf167 |
T |
A |
11: 70,540,961 (GRCm39) |
C196S |
probably benign |
Het |
Robo2 |
T |
A |
16: 74,149,633 (GRCm39) |
Y65F |
probably damaging |
Het |
Scarf2 |
G |
A |
16: 17,621,371 (GRCm39) |
C319Y |
probably damaging |
Het |
Sec24c |
A |
G |
14: 20,743,780 (GRCm39) |
D995G |
probably damaging |
Het |
Selenbp1 |
T |
C |
3: 94,851,211 (GRCm39) |
L369S |
probably benign |
Het |
Sgpl1 |
A |
T |
10: 60,959,123 (GRCm39) |
I53K |
possibly damaging |
Het |
Sh3bp5 |
C |
A |
14: 31,099,452 (GRCm39) |
R265L |
probably benign |
Het |
Slc1a6 |
A |
T |
10: 78,635,952 (GRCm39) |
Y339F |
probably damaging |
Het |
Smchd1 |
G |
T |
17: 71,667,048 (GRCm39) |
Y1781* |
probably null |
Het |
Smg1 |
T |
C |
7: 117,779,697 (GRCm39) |
S1233G |
probably benign |
Het |
Snap91 |
A |
T |
9: 86,665,507 (GRCm39) |
|
probably benign |
Het |
Snx29 |
T |
A |
16: 11,238,600 (GRCm39) |
L112Q |
probably damaging |
Het |
Sptbn5 |
T |
C |
2: 119,889,622 (GRCm39) |
|
probably benign |
Het |
Srl |
A |
T |
16: 4,310,222 (GRCm39) |
H502Q |
possibly damaging |
Het |
St8sia3 |
A |
G |
18: 64,404,820 (GRCm39) |
M366V |
probably benign |
Het |
Stk19 |
A |
T |
17: 35,041,485 (GRCm39) |
|
probably benign |
Het |
Syngap1 |
G |
A |
17: 27,180,423 (GRCm39) |
A611T |
probably benign |
Het |
Tas2r113 |
A |
G |
6: 132,870,670 (GRCm39) |
T233A |
possibly damaging |
Het |
Tbcc |
G |
A |
17: 47,202,145 (GRCm39) |
W177* |
probably null |
Het |
Tcstv3 |
T |
A |
13: 120,779,618 (GRCm39) |
|
probably null |
Het |
Trav13-5 |
T |
A |
14: 54,033,408 (GRCm39) |
C106S |
probably damaging |
Het |
Trmt61a |
G |
A |
12: 111,645,147 (GRCm39) |
V28M |
possibly damaging |
Het |
Ubap2l |
G |
A |
3: 89,928,210 (GRCm39) |
T553M |
probably damaging |
Het |
Urb1 |
T |
C |
16: 90,554,715 (GRCm39) |
N1839S |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,475,742 (GRCm39) |
L2893P |
probably damaging |
Het |
Usp24 |
G |
A |
4: 106,217,359 (GRCm39) |
V421M |
possibly damaging |
Het |
Vmn1r43 |
T |
C |
6: 89,846,892 (GRCm39) |
E198G |
probably benign |
Het |
Vps13d |
A |
C |
4: 144,904,626 (GRCm39) |
S130A |
probably damaging |
Het |
Zfp426 |
T |
A |
9: 20,382,310 (GRCm39) |
I211F |
probably benign |
Het |
Znfx1 |
T |
C |
2: 166,880,489 (GRCm39) |
|
probably null |
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 |
|
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 |
R6143:Nbeal1
|
UTSW |
1 |
60,290,466 (GRCm39) |
missense |
possibly damaging |
0.81 |
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 |
|
|