Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1600012H06Rik |
A |
T |
17: 15,164,001 (GRCm39) |
I43L |
possibly damaging |
Het |
4930449A18Rik |
T |
A |
3: 59,749,153 (GRCm39) |
|
noncoding transcript |
Het |
Abcc8 |
T |
C |
7: 45,800,252 (GRCm39) |
K510R |
probably damaging |
Het |
Adamtsl3 |
C |
T |
7: 82,178,069 (GRCm39) |
R511C |
probably damaging |
Het |
Arhgap11a |
T |
C |
2: 113,670,107 (GRCm39) |
S339G |
probably damaging |
Het |
C2cd3 |
A |
G |
7: 100,065,397 (GRCm39) |
T728A |
probably benign |
Het |
Cand1 |
C |
A |
10: 119,049,451 (GRCm39) |
|
probably null |
Het |
Catspere1 |
A |
T |
1: 177,699,624 (GRCm39) |
|
noncoding transcript |
Het |
Ccdc121rt2 |
A |
T |
5: 112,598,106 (GRCm39) |
K218* |
probably null |
Het |
Cd209c |
G |
T |
8: 3,995,905 (GRCm39) |
R2S |
probably benign |
Het |
Cdc16 |
A |
G |
8: 13,831,644 (GRCm39) |
|
probably benign |
Het |
Ces1g |
C |
T |
8: 94,060,323 (GRCm39) |
E99K |
probably benign |
Het |
Chrna7 |
A |
C |
7: 62,862,196 (GRCm39) |
L10R |
probably benign |
Het |
Clnk |
C |
T |
5: 38,870,412 (GRCm39) |
|
probably null |
Het |
Cntrob |
C |
G |
11: 69,206,220 (GRCm39) |
L315F |
possibly damaging |
Het |
Ctdp1 |
A |
G |
18: 80,451,941 (GRCm39) |
S145P |
unknown |
Het |
Dennd2a |
T |
C |
6: 39,474,044 (GRCm39) |
D430G |
probably damaging |
Het |
Dnajc16 |
A |
G |
4: 141,501,936 (GRCm39) |
F298S |
probably damaging |
Het |
Dock5 |
T |
C |
14: 68,055,012 (GRCm39) |
D618G |
probably damaging |
Het |
Drc3 |
G |
A |
11: 60,261,361 (GRCm39) |
A171T |
probably benign |
Het |
Ecel1 |
A |
T |
1: 87,081,023 (GRCm39) |
N322K |
probably damaging |
Het |
Eftud2 |
A |
G |
11: 102,745,640 (GRCm39) |
F362L |
probably damaging |
Het |
Egfr |
C |
T |
11: 16,861,607 (GRCm39) |
H1129Y |
probably benign |
Het |
Eif2b1 |
A |
G |
5: 124,714,971 (GRCm39) |
S102P |
probably damaging |
Het |
Erich3 |
T |
A |
3: 154,410,480 (GRCm39) |
F112I |
possibly damaging |
Het |
Fam107b |
T |
C |
2: 3,779,580 (GRCm39) |
L261S |
probably damaging |
Het |
Fat3 |
A |
C |
9: 15,908,883 (GRCm39) |
V2373G |
probably damaging |
Het |
Fcgbpl1 |
T |
A |
7: 27,850,147 (GRCm39) |
C1198S |
probably damaging |
Het |
Gadd45a |
A |
T |
6: 67,013,873 (GRCm39) |
L58Q |
probably damaging |
Het |
Gask1b |
G |
A |
3: 79,843,912 (GRCm39) |
R377H |
probably damaging |
Het |
Gipr |
C |
T |
7: 18,896,601 (GRCm39) |
R165H |
probably damaging |
Het |
Gje1 |
C |
T |
10: 14,593,082 (GRCm39) |
G45R |
probably null |
Het |
Gldc |
T |
A |
19: 30,111,132 (GRCm39) |
N548I |
possibly damaging |
Het |
Gm13035 |
A |
G |
4: 146,009,993 (GRCm39) |
|
noncoding transcript |
Het |
Gm27013 |
T |
A |
6: 130,497,700 (GRCm39) |
|
noncoding transcript |
Het |
Gm5436 |
A |
T |
12: 84,305,584 (GRCm39) |
|
noncoding transcript |
Het |
Grik3 |
C |
A |
4: 125,584,969 (GRCm39) |
N612K |
probably damaging |
Het |
H2bc13 |
C |
T |
13: 21,900,234 (GRCm39) |
|
probably benign |
Het |
Hfm1 |
C |
A |
5: 107,040,617 (GRCm39) |
W716L |
probably damaging |
Het |
Il5ra |
T |
C |
6: 106,715,336 (GRCm39) |
Y166C |
probably damaging |
Het |
Iqcb1 |
A |
G |
16: 36,655,952 (GRCm39) |
E113G |
probably benign |
Het |
Kcnk10 |
A |
T |
12: 98,401,175 (GRCm39) |
M486K |
probably benign |
Het |
Kcnv2 |
A |
G |
19: 27,301,190 (GRCm39) |
D347G |
probably damaging |
Het |
Kif21b |
C |
A |
1: 136,072,958 (GRCm39) |
H119N |
probably damaging |
Het |
Lamb1 |
C |
T |
12: 31,337,432 (GRCm39) |
H388Y |
probably damaging |
Het |
Leng9 |
T |
C |
7: 4,152,385 (GRCm39) |
D97G |
probably damaging |
Het |
Lmbr1 |
G |
A |
5: 29,492,424 (GRCm39) |
T55I |
probably damaging |
Het |
Lrp1 |
G |
T |
10: 127,419,805 (GRCm39) |
R935S |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,299,755 (GRCm39) |
V3099E |
probably benign |
Het |
Lrrcc1 |
C |
A |
3: 14,627,571 (GRCm39) |
D503E |
probably benign |
Het |
Map1a |
T |
A |
2: 121,132,567 (GRCm39) |
S890T |
probably damaging |
Het |
Msh2 |
C |
A |
17: 88,030,841 (GRCm39) |
A906E |
probably benign |
Het |
Mybph |
A |
T |
1: 134,126,233 (GRCm39) |
E349V |
probably damaging |
Het |
Myh7b |
C |
A |
2: 155,475,909 (GRCm39) |
L1935M |
probably benign |
Het |
Myh9 |
T |
C |
15: 77,653,453 (GRCm39) |
E1348G |
probably damaging |
Het |
Myzap |
A |
G |
9: 71,456,037 (GRCm39) |
S328P |
probably damaging |
Het |
Nepro |
G |
A |
16: 44,555,160 (GRCm39) |
S412N |
probably null |
Het |
Nr1h3 |
A |
G |
2: 91,020,563 (GRCm39) |
F257L |
probably benign |
Het |
Nudt5 |
T |
C |
2: 5,869,239 (GRCm39) |
V155A |
probably benign |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Or13a25 |
A |
T |
7: 140,247,502 (GRCm39) |
I94F |
probably damaging |
Het |
Or52d3 |
A |
T |
7: 104,229,422 (GRCm39) |
I190L |
probably benign |
Het |
Or6ae1 |
A |
G |
7: 139,742,602 (GRCm39) |
L87P |
possibly damaging |
Het |
Pde1a |
T |
A |
2: 79,959,181 (GRCm39) |
|
probably benign |
Het |
Pde4dip |
T |
A |
3: 97,700,844 (GRCm39) |
H220L |
probably damaging |
Het |
Pde9a |
T |
A |
17: 31,662,135 (GRCm39) |
|
probably null |
Het |
Pnkp |
C |
A |
7: 44,511,070 (GRCm39) |
|
probably null |
Het |
Pnpla7 |
A |
G |
2: 24,870,064 (GRCm39) |
T15A |
probably benign |
Het |
Polq |
G |
T |
16: 36,869,145 (GRCm39) |
|
probably null |
Het |
Ppfia2 |
C |
T |
10: 106,690,818 (GRCm39) |
T553I |
probably benign |
Het |
Ptk6 |
T |
G |
2: 180,838,784 (GRCm39) |
N323T |
possibly damaging |
Het |
Rhox3c |
G |
A |
X: 36,652,077 (GRCm39) |
A60T |
probably damaging |
Het |
Rnf4 |
T |
A |
5: 34,506,053 (GRCm39) |
V61E |
probably damaging |
Het |
Rnf5 |
A |
G |
17: 34,820,977 (GRCm39) |
|
probably benign |
Het |
Sardh |
A |
G |
2: 27,081,967 (GRCm39) |
V853A |
probably benign |
Het |
Scfd1 |
T |
C |
12: 51,436,109 (GRCm39) |
V86A |
probably damaging |
Het |
Scube3 |
G |
A |
17: 28,383,097 (GRCm39) |
C425Y |
probably damaging |
Het |
Sema5a |
C |
T |
15: 32,609,563 (GRCm39) |
H490Y |
probably benign |
Het |
Sfta2 |
T |
C |
17: 35,960,773 (GRCm39) |
|
probably benign |
Het |
Sh3d19 |
T |
C |
3: 86,031,049 (GRCm39) |
Y738H |
probably damaging |
Het |
Shc2 |
T |
C |
10: 79,458,295 (GRCm39) |
R463G |
probably damaging |
Het |
Socs7 |
T |
A |
11: 97,267,829 (GRCm39) |
I320N |
possibly damaging |
Het |
Speer2 |
A |
T |
16: 69,654,988 (GRCm39) |
M159K |
probably benign |
Het |
Sppl2c |
A |
C |
11: 104,078,478 (GRCm39) |
H426P |
probably benign |
Het |
Stag3 |
T |
G |
5: 138,307,627 (GRCm39) |
|
probably null |
Het |
Stxbp5 |
C |
A |
10: 9,638,635 (GRCm39) |
V1055L |
probably benign |
Het |
Synpo |
A |
T |
18: 60,736,684 (GRCm39) |
S421T |
probably damaging |
Het |
Taf6l |
A |
G |
19: 8,759,770 (GRCm39) |
V135A |
possibly damaging |
Het |
Tas2r116 |
G |
A |
6: 132,832,660 (GRCm39) |
S87N |
probably benign |
Het |
Tomm6 |
T |
C |
17: 47,998,994 (GRCm39) |
|
probably benign |
Het |
Trabd |
T |
C |
15: 88,966,915 (GRCm39) |
M113T |
probably benign |
Het |
Trim58 |
G |
A |
11: 58,542,150 (GRCm39) |
G370E |
probably damaging |
Het |
Ttc41 |
C |
T |
10: 86,566,989 (GRCm39) |
R552C |
probably benign |
Het |
Vit |
T |
C |
17: 78,909,308 (GRCm39) |
S252P |
probably benign |
Het |
Vma21-ps |
T |
A |
4: 52,496,943 (GRCm39) |
D101V |
probably damaging |
Het |
Vmn1r173 |
A |
T |
7: 23,402,361 (GRCm39) |
I199F |
probably damaging |
Het |
Vmn2r114 |
T |
A |
17: 23,529,336 (GRCm39) |
R255S |
probably benign |
Het |
Vmn2r17 |
A |
G |
5: 109,582,246 (GRCm39) |
N545S |
probably damaging |
Het |
Zfp865 |
A |
G |
7: 5,034,640 (GRCm39) |
Y875C |
probably 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 |
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 |
|
|