Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
A |
G |
5: 8,773,187 (GRCm39) |
N805S |
probably damaging |
Het |
Acat2 |
A |
G |
17: 13,178,893 (GRCm39) |
V60A |
probably benign |
Het |
Adam6b |
A |
G |
12: 113,454,754 (GRCm39) |
I524V |
probably benign |
Het |
Adamts16 |
C |
T |
13: 70,921,074 (GRCm39) |
W590* |
probably null |
Het |
Adamts9 |
C |
T |
6: 92,835,102 (GRCm39) |
G1257D |
probably damaging |
Het |
Adgrf5 |
C |
T |
17: 43,755,974 (GRCm39) |
T644I |
probably benign |
Het |
Adgrf5 |
T |
G |
17: 43,763,368 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,668,634 (GRCm39) |
T2641A |
possibly damaging |
Het |
Agap3 |
T |
C |
5: 24,657,382 (GRCm39) |
F60L |
probably benign |
Het |
Akap9 |
C |
A |
5: 4,054,933 (GRCm39) |
T1626K |
probably damaging |
Het |
Ampd3 |
C |
A |
7: 110,405,261 (GRCm39) |
D603E |
probably damaging |
Het |
Angpt4 |
T |
A |
2: 151,767,326 (GRCm39) |
V119E |
probably benign |
Het |
Atp6v1a |
T |
C |
16: 43,934,980 (GRCm39) |
T70A |
probably benign |
Het |
B4galt3 |
T |
A |
1: 171,100,319 (GRCm39) |
I163N |
probably damaging |
Het |
Borcs5 |
C |
T |
6: 134,687,143 (GRCm39) |
T167M |
probably damaging |
Het |
Btbd19 |
T |
A |
4: 116,978,616 (GRCm39) |
S156C |
probably damaging |
Het |
Camkk2 |
C |
T |
5: 122,875,574 (GRCm39) |
R492Q |
possibly damaging |
Het |
Casr |
T |
C |
16: 36,330,033 (GRCm39) |
I434V |
probably damaging |
Het |
Cd4 |
G |
T |
6: 124,844,066 (GRCm39) |
T394K |
probably benign |
Het |
Cps1 |
T |
C |
1: 67,237,517 (GRCm39) |
L1006P |
probably damaging |
Het |
Crx |
G |
A |
7: 15,601,857 (GRCm39) |
P274S |
probably damaging |
Het |
Crybg1 |
T |
A |
10: 43,865,107 (GRCm39) |
I1457F |
probably damaging |
Het |
Cul4a |
C |
A |
8: 13,171,676 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
T |
A |
2: 104,085,910 (GRCm39) |
T196S |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,580,567 (GRCm39) |
E1995G |
probably benign |
Het |
Dnm1 |
T |
A |
2: 32,226,021 (GRCm39) |
T353S |
probably damaging |
Het |
Ect2l |
T |
A |
10: 18,044,149 (GRCm39) |
T329S |
probably damaging |
Het |
Elp2 |
T |
A |
18: 24,742,716 (GRCm39) |
S83T |
probably benign |
Het |
Exosc7 |
A |
G |
9: 122,948,013 (GRCm39) |
T39A |
probably benign |
Het |
Fam135a |
C |
A |
1: 24,096,473 (GRCm39) |
V91F |
probably damaging |
Het |
Gab2 |
G |
T |
7: 96,731,005 (GRCm39) |
|
probably benign |
Het |
Gbf1 |
A |
T |
19: 46,268,793 (GRCm39) |
I1408F |
possibly damaging |
Het |
Glis3 |
C |
T |
19: 28,508,419 (GRCm39) |
E522K |
probably damaging |
Het |
Gm10375 |
A |
T |
14: 43,842,314 (GRCm39) |
C139S |
possibly damaging |
Het |
Gm26558 |
T |
C |
2: 70,492,211 (GRCm39) |
E81G |
unknown |
Het |
Gm35315 |
C |
T |
5: 110,227,091 (GRCm39) |
C116Y |
probably benign |
Het |
Gm3676 |
T |
A |
14: 41,366,064 (GRCm39) |
I84F |
probably damaging |
Het |
Gm7145 |
T |
A |
1: 117,913,932 (GRCm39) |
H271Q |
probably damaging |
Het |
Gpat2 |
T |
A |
2: 127,270,215 (GRCm39) |
I76N |
probably damaging |
Het |
Hipk1 |
A |
T |
3: 103,685,574 (GRCm39) |
S14T |
unknown |
Het |
Hlcs |
C |
A |
16: 94,068,362 (GRCm39) |
S286I |
probably damaging |
Het |
Ighg1 |
A |
T |
12: 113,293,078 (GRCm39) |
F204Y |
|
Het |
Igsf10 |
T |
C |
3: 59,236,837 (GRCm39) |
I1115V |
probably benign |
Het |
Klk7 |
A |
T |
7: 43,462,299 (GRCm39) |
H97L |
probably damaging |
Het |
Kmt2d |
A |
T |
15: 98,754,504 (GRCm39) |
D1605E |
unknown |
Het |
Leng8 |
T |
A |
7: 4,142,525 (GRCm39) |
I49N |
possibly damaging |
Het |
Lingo4 |
A |
T |
3: 94,310,451 (GRCm39) |
D463V |
possibly damaging |
Het |
Lrp1 |
T |
A |
10: 127,389,337 (GRCm39) |
N3193I |
probably damaging |
Het |
Lrrc7 |
T |
A |
3: 157,866,111 (GRCm39) |
Y1210F |
probably damaging |
Het |
Mki67 |
G |
C |
7: 135,296,400 (GRCm39) |
A2878G |
probably benign |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Mtcl3 |
T |
A |
10: 29,072,875 (GRCm39) |
Y722* |
probably null |
Het |
Mucl2 |
C |
T |
15: 103,929,445 (GRCm39) |
|
probably null |
Het |
Myh6 |
A |
T |
14: 55,197,727 (GRCm39) |
D470E |
probably benign |
Het |
Myo1e |
T |
C |
9: 70,266,667 (GRCm39) |
|
probably null |
Het |
Myo7a |
G |
A |
7: 97,713,402 (GRCm39) |
R1647W |
probably damaging |
Het |
Nmral1 |
C |
T |
16: 4,531,660 (GRCm39) |
M198I |
probably benign |
Het |
Nrap |
C |
A |
19: 56,330,700 (GRCm39) |
L1120F |
probably damaging |
Het |
Nup155 |
T |
A |
15: 8,184,406 (GRCm39) |
I1267N |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,898,414 (GRCm39) |
P6616S |
unknown |
Het |
Ocstamp |
T |
G |
2: 165,239,229 (GRCm39) |
D319A |
probably damaging |
Het |
Ooep |
T |
C |
9: 78,285,433 (GRCm39) |
D61G |
probably damaging |
Het |
Or10p1 |
A |
G |
10: 129,443,949 (GRCm39) |
S134P |
probably benign |
Het |
Or1e25 |
A |
T |
11: 73,493,810 (GRCm39) |
I135F |
probably damaging |
Het |
Or52ad1 |
A |
G |
7: 102,995,538 (GRCm39) |
V199A |
probably benign |
Het |
Or6c5c |
T |
C |
10: 129,298,856 (GRCm39) |
S104P |
probably damaging |
Het |
Or7g35 |
A |
G |
9: 19,495,938 (GRCm39) |
Y35C |
probably damaging |
Het |
Otoa |
A |
G |
7: 120,701,765 (GRCm39) |
E148G |
probably benign |
Het |
Ovgp1 |
A |
T |
3: 105,894,387 (GRCm39) |
D720V |
unknown |
Het |
Padi2 |
T |
A |
4: 140,660,079 (GRCm39) |
F294I |
probably damaging |
Het |
Pcdha7 |
T |
A |
18: 37,107,471 (GRCm39) |
N165K |
probably damaging |
Het |
Pcdhb6 |
C |
A |
18: 37,468,261 (GRCm39) |
P394H |
probably damaging |
Het |
Pcdhga6 |
T |
C |
18: 37,841,072 (GRCm39) |
V264A |
possibly damaging |
Het |
Pik3ap1 |
G |
T |
19: 41,284,815 (GRCm39) |
D623E |
possibly damaging |
Het |
Prdm10 |
A |
T |
9: 31,268,456 (GRCm39) |
K802* |
probably null |
Het |
Ptgfrn |
G |
A |
3: 100,980,363 (GRCm39) |
L326F |
possibly damaging |
Het |
Rgsl1 |
T |
G |
1: 153,683,622 (GRCm39) |
|
probably null |
Het |
Rock1 |
T |
G |
18: 10,129,317 (GRCm39) |
T347P |
possibly damaging |
Het |
Rprd2 |
G |
A |
3: 95,684,022 (GRCm39) |
P338S |
probably damaging |
Het |
Sdk1 |
A |
T |
5: 141,923,377 (GRCm39) |
N333Y |
probably damaging |
Het |
Setd4 |
T |
A |
16: 93,388,132 (GRCm39) |
H118L |
probably benign |
Het |
Sirt3 |
G |
A |
7: 140,458,039 (GRCm39) |
P37S |
|
Het |
Slc16a9 |
G |
T |
10: 70,119,000 (GRCm39) |
G440W |
probably damaging |
Het |
Slc22a23 |
T |
A |
13: 34,367,161 (GRCm39) |
I616F |
probably damaging |
Het |
Slc30a8 |
A |
C |
15: 52,180,707 (GRCm39) |
D102A |
probably damaging |
Het |
Slc6a4 |
T |
A |
11: 76,901,527 (GRCm39) |
D87E |
possibly damaging |
Het |
Slc9a4 |
A |
C |
1: 40,668,663 (GRCm39) |
T769P |
probably benign |
Het |
Sspo |
A |
T |
6: 48,431,762 (GRCm39) |
Y685F |
probably damaging |
Het |
Sspo |
C |
A |
6: 48,450,390 (GRCm39) |
Q2560K |
probably benign |
Het |
Stpg1 |
T |
A |
4: 135,256,827 (GRCm39) |
L206Q |
probably damaging |
Het |
Stt3b |
A |
T |
9: 115,095,183 (GRCm39) |
Y283N |
probably damaging |
Het |
Sult4a1 |
T |
C |
15: 83,970,814 (GRCm39) |
E197G |
probably damaging |
Het |
Syne1 |
T |
G |
10: 4,997,635 (GRCm39) |
D444A |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,064,845 (GRCm39) |
V1425E |
possibly damaging |
Het |
Tgm4 |
A |
G |
9: 122,891,556 (GRCm39) |
D557G |
probably benign |
Het |
Tmcc3 |
A |
G |
10: 94,266,434 (GRCm39) |
|
probably benign |
Het |
Tnfrsf8 |
T |
A |
4: 145,000,952 (GRCm39) |
N385Y |
probably benign |
Het |
Ttc4 |
T |
C |
4: 106,536,017 (GRCm39) |
D15G |
possibly damaging |
Het |
Tut1 |
A |
G |
19: 8,941,413 (GRCm39) |
N400S |
probably benign |
Het |
Usp39 |
T |
C |
6: 72,313,413 (GRCm39) |
K259R |
probably benign |
Het |
Vmn1r215 |
C |
T |
13: 23,260,484 (GRCm39) |
H175Y |
probably benign |
Het |
Vmn1r36 |
A |
T |
6: 66,693,107 (GRCm39) |
M256K |
probably benign |
Het |
Zfp128 |
T |
A |
7: 12,624,461 (GRCm39) |
H276Q |
possibly damaging |
Het |
Zfp276 |
T |
C |
8: 123,994,562 (GRCm39) |
M543T |
probably damaging |
Het |
Zfp354c |
A |
T |
11: 50,705,483 (GRCm39) |
Y531N |
probably damaging |
Het |
Zfp532 |
T |
A |
18: 65,756,076 (GRCm39) |
M3K |
probably damaging |
Het |
Zfp64 |
T |
G |
2: 168,741,810 (GRCm39) |
K373Q |
probably damaging |
Het |
Zfp764l1 |
C |
T |
7: 126,990,856 (GRCm39) |
S377N |
probably benign |
Het |
Zfp983 |
T |
G |
17: 21,880,413 (GRCm39) |
S114A |
probably damaging |
Het |
Zranb1 |
G |
A |
7: 132,584,481 (GRCm39) |
R583K |
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 |
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 |
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 |
|
|