Other mutations in this stock |
Total: 130 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930555F03Rik |
A |
T |
8: 49,953,527 (GRCm39) |
|
noncoding transcript |
Het |
A630073D07Rik |
T |
C |
6: 132,603,700 (GRCm39) |
|
probably benign |
Het |
Abca16 |
G |
A |
7: 120,032,834 (GRCm39) |
|
probably benign |
Het |
Abca5 |
A |
T |
11: 110,170,515 (GRCm39) |
D1265E |
probably damaging |
Het |
Abcf1 |
C |
T |
17: 36,272,079 (GRCm39) |
V312I |
probably benign |
Het |
Abhd12 |
T |
A |
2: 150,688,285 (GRCm39) |
|
probably null |
Het |
Adam23 |
A |
G |
1: 63,582,306 (GRCm39) |
H318R |
probably benign |
Het |
Adcy2 |
T |
A |
13: 68,826,725 (GRCm39) |
K660* |
probably null |
Het |
Adgrf3 |
T |
C |
5: 30,400,078 (GRCm39) |
T972A |
probably benign |
Het |
Adipoq |
T |
A |
16: 22,974,160 (GRCm39) |
D62E |
probably damaging |
Het |
Alk |
G |
T |
17: 72,910,578 (GRCm39) |
P43T |
probably damaging |
Het |
Arap2 |
AT |
ATT |
5: 62,807,250 (GRCm39) |
|
probably benign |
Het |
Arhgef28 |
G |
T |
13: 98,106,863 (GRCm39) |
T687K |
probably benign |
Het |
Arrb1 |
T |
C |
7: 99,243,884 (GRCm39) |
L278P |
probably damaging |
Het |
Atad2b |
C |
A |
12: 4,987,401 (GRCm39) |
D76E |
probably benign |
Het |
Atm |
A |
T |
9: 53,370,241 (GRCm39) |
Y2290* |
probably null |
Het |
Atrn |
T |
A |
2: 130,837,005 (GRCm39) |
|
probably null |
Het |
Bpifb1 |
A |
G |
2: 154,054,867 (GRCm39) |
D253G |
possibly damaging |
Het |
Bpifb9b |
C |
T |
2: 154,161,545 (GRCm39) |
T559M |
probably benign |
Het |
Bsn |
T |
C |
9: 107,984,439 (GRCm39) |
E3205G |
unknown |
Het |
Cacna1c |
T |
C |
6: 118,579,174 (GRCm39) |
Y1599C |
probably damaging |
Het |
Ccdc40 |
A |
G |
11: 119,133,630 (GRCm39) |
D590G |
probably damaging |
Het |
Ccdc68 |
A |
G |
18: 70,079,623 (GRCm39) |
|
probably null |
Het |
Ccdc97 |
G |
A |
7: 25,413,845 (GRCm39) |
R279C |
probably damaging |
Het |
Ccm2l |
A |
G |
2: 152,912,820 (GRCm39) |
T120A |
probably damaging |
Het |
Cfap54 |
T |
C |
10: 92,665,512 (GRCm39) |
|
probably benign |
Het |
Cfh |
A |
G |
1: 140,028,621 (GRCm39) |
S1043P |
probably benign |
Het |
Chil3 |
T |
C |
3: 106,063,072 (GRCm39) |
K173E |
probably benign |
Het |
Cib2 |
T |
C |
9: 54,461,780 (GRCm39) |
D26G |
possibly damaging |
Het |
Col24a1 |
T |
C |
3: 145,019,881 (GRCm39) |
V84A |
probably damaging |
Het |
Csn3 |
T |
C |
5: 88,077,730 (GRCm39) |
Y79H |
probably benign |
Het |
Ddx47 |
T |
A |
6: 134,994,085 (GRCm39) |
V149E |
probably damaging |
Het |
Dennd5b |
A |
T |
6: 148,934,760 (GRCm39) |
|
probably benign |
Het |
Desi1 |
T |
C |
15: 81,882,399 (GRCm39) |
N109D |
probably damaging |
Het |
Fam13c |
T |
C |
10: 70,372,182 (GRCm39) |
|
probably benign |
Het |
Fam234a |
A |
T |
17: 26,435,591 (GRCm39) |
D264E |
probably benign |
Het |
Fanca |
A |
G |
8: 124,014,809 (GRCm39) |
F831S |
probably damaging |
Het |
Fancm |
C |
T |
12: 65,144,091 (GRCm39) |
R518* |
probably null |
Het |
Fat2 |
A |
G |
11: 55,202,669 (GRCm39) |
V135A |
possibly damaging |
Het |
Fbxl17 |
A |
C |
17: 63,691,987 (GRCm39) |
F42V |
probably damaging |
Het |
Fgd3 |
A |
T |
13: 49,418,173 (GRCm39) |
V631E |
possibly damaging |
Het |
Fhod3 |
G |
A |
18: 25,245,736 (GRCm39) |
|
probably benign |
Het |
Focad |
T |
C |
4: 88,039,525 (GRCm39) |
|
probably benign |
Het |
Foxn4 |
C |
A |
5: 114,399,129 (GRCm39) |
|
probably benign |
Het |
Gm2381 |
A |
T |
7: 42,469,402 (GRCm39) |
C241S |
probably damaging |
Het |
Gm6483 |
T |
G |
8: 19,743,725 (GRCm39) |
F117V |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,481,295 (GRCm39) |
|
probably benign |
Het |
Hecw1 |
T |
A |
13: 14,455,027 (GRCm39) |
Q676L |
probably benign |
Het |
Hipk2 |
G |
A |
6: 38,724,420 (GRCm39) |
R437C |
possibly damaging |
Het |
Ifnar1 |
T |
C |
16: 91,298,570 (GRCm39) |
Y396H |
probably damaging |
Het |
Ints5 |
A |
T |
19: 8,873,383 (GRCm39) |
K447N |
probably damaging |
Het |
Iqsec1 |
T |
C |
6: 90,666,952 (GRCm39) |
Y495C |
probably damaging |
Het |
Itga5 |
C |
T |
15: 103,264,742 (GRCm39) |
|
probably null |
Het |
Kcnk4 |
T |
A |
19: 6,905,528 (GRCm39) |
|
probably benign |
Het |
Kmo |
A |
G |
1: 175,474,756 (GRCm39) |
T174A |
possibly damaging |
Het |
Krt36 |
T |
C |
11: 99,993,101 (GRCm39) |
D458G |
probably damaging |
Het |
Krtap16-1 |
G |
T |
11: 99,877,321 (GRCm39) |
P28T |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,552,315 (GRCm39) |
|
probably null |
Het |
Lrrc9 |
T |
C |
12: 72,529,788 (GRCm39) |
S920P |
probably damaging |
Het |
Lrrk2 |
A |
T |
15: 91,636,481 (GRCm39) |
Y1485F |
probably benign |
Het |
Mical1 |
C |
T |
10: 41,357,311 (GRCm39) |
A372V |
probably damaging |
Het |
Ms4a20 |
C |
A |
19: 11,089,764 (GRCm39) |
L40F |
probably damaging |
Het |
Mtr |
C |
T |
13: 12,236,318 (GRCm39) |
R636Q |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,570,925 (GRCm39) |
T662S |
possibly damaging |
Het |
Myo10 |
G |
A |
15: 25,738,091 (GRCm39) |
V546M |
probably damaging |
Het |
Nhlrc3 |
T |
C |
3: 53,366,044 (GRCm39) |
T150A |
probably damaging |
Het |
Nicol1 |
T |
C |
5: 34,140,896 (GRCm39) |
|
probably benign |
Het |
Nkx2-1 |
T |
C |
12: 56,581,640 (GRCm39) |
H69R |
possibly damaging |
Het |
Nlrp4g |
A |
T |
9: 124,349,540 (GRCm38) |
|
noncoding transcript |
Het |
Nod2 |
A |
G |
8: 89,379,859 (GRCm39) |
N120S |
probably benign |
Het |
Nol8 |
T |
C |
13: 49,807,921 (GRCm39) |
F46L |
possibly damaging |
Het |
Ntrk1 |
T |
C |
3: 87,691,240 (GRCm39) |
D308G |
possibly damaging |
Het |
Oog3 |
A |
T |
4: 143,886,784 (GRCm39) |
V112D |
probably benign |
Het |
Or10ag58 |
A |
G |
2: 87,265,005 (GRCm39) |
D58G |
probably damaging |
Het |
Or4a66 |
A |
G |
2: 88,531,040 (GRCm39) |
V211A |
probably damaging |
Het |
Or51i1 |
A |
T |
7: 103,671,196 (GRCm39) |
S110T |
probably damaging |
Het |
Or5af2 |
T |
C |
11: 58,707,975 (GRCm39) |
V47A |
probably damaging |
Het |
Or5b106 |
T |
C |
19: 13,123,727 (GRCm39) |
M99V |
probably benign |
Het |
Or5b120 |
C |
A |
19: 13,479,900 (GRCm39) |
N64K |
probably damaging |
Het |
Or5m9b |
A |
G |
2: 85,905,485 (GRCm39) |
M134V |
probably benign |
Het |
Or9s18 |
A |
T |
13: 65,300,692 (GRCm39) |
Y218F |
possibly damaging |
Het |
Pakap |
T |
C |
4: 57,829,434 (GRCm39) |
|
probably benign |
Het |
Pcdhb8 |
C |
T |
18: 37,490,100 (GRCm39) |
R593C |
probably benign |
Het |
Pgm3 |
A |
G |
9: 86,438,243 (GRCm39) |
|
probably null |
Het |
Pirt |
T |
A |
11: 66,816,998 (GRCm39) |
V103E |
probably damaging |
Het |
Plxnc1 |
T |
A |
10: 94,635,230 (GRCm39) |
D1332V |
probably damaging |
Het |
Ppfia4 |
A |
T |
1: 134,256,518 (GRCm39) |
V122E |
probably damaging |
Het |
Pramel14 |
A |
G |
4: 143,720,088 (GRCm39) |
|
probably benign |
Het |
Prmt2 |
C |
T |
10: 76,044,517 (GRCm39) |
|
probably benign |
Het |
Prrc2a |
G |
T |
17: 35,372,536 (GRCm39) |
P1702T |
probably damaging |
Het |
Prss39 |
A |
T |
1: 34,539,279 (GRCm39) |
H173L |
probably damaging |
Het |
Rabl6 |
A |
G |
2: 25,476,878 (GRCm39) |
|
probably null |
Het |
Rb1cc1 |
T |
A |
1: 6,319,014 (GRCm39) |
I794K |
possibly damaging |
Het |
Reln |
T |
C |
5: 22,125,535 (GRCm39) |
D2716G |
probably damaging |
Het |
Sbf2 |
ACC |
AC |
7: 109,929,890 (GRCm39) |
|
probably null |
Het |
Sema6d |
T |
A |
2: 124,502,665 (GRCm39) |
F583L |
possibly damaging |
Het |
Setx |
T |
A |
2: 29,036,819 (GRCm39) |
H1101Q |
possibly damaging |
Het |
Sis |
A |
G |
3: 72,872,938 (GRCm39) |
C67R |
probably damaging |
Het |
Skint1 |
T |
A |
4: 111,886,596 (GRCm39) |
|
probably benign |
Het |
Smg6 |
C |
A |
11: 75,053,757 (GRCm39) |
T1413K |
probably benign |
Het |
Spata31d1a |
A |
T |
13: 59,850,073 (GRCm39) |
I685N |
possibly damaging |
Het |
Spef2 |
T |
A |
15: 9,592,844 (GRCm39) |
N1499I |
probably damaging |
Het |
Stk11ip |
T |
A |
1: 75,508,932 (GRCm39) |
|
probably null |
Het |
Stxbp1 |
A |
C |
2: 32,692,795 (GRCm39) |
I407S |
probably damaging |
Het |
Svil |
T |
C |
18: 5,117,002 (GRCm39) |
S2059P |
probably damaging |
Het |
Syne1 |
C |
T |
10: 5,300,933 (GRCm39) |
V932M |
probably damaging |
Het |
Tacc1 |
A |
C |
8: 25,668,020 (GRCm39) |
|
probably benign |
Het |
Tbc1d13 |
C |
A |
2: 30,025,576 (GRCm39) |
|
probably benign |
Het |
Tbc1d15 |
A |
C |
10: 115,075,204 (GRCm39) |
D59E |
probably damaging |
Het |
Tcaf2 |
A |
G |
6: 42,619,445 (GRCm39) |
F194S |
probably damaging |
Het |
Terf2ip |
T |
A |
8: 112,738,127 (GRCm39) |
M5K |
probably benign |
Het |
Tgfbr2 |
A |
T |
9: 115,987,388 (GRCm39) |
D40E |
probably benign |
Het |
Tm4sf5 |
T |
A |
11: 70,401,495 (GRCm39) |
S165T |
probably damaging |
Het |
Tmprss3 |
A |
T |
17: 31,412,886 (GRCm39) |
C129S |
probably damaging |
Het |
Tmx2 |
T |
C |
2: 84,502,740 (GRCm39) |
D256G |
probably benign |
Het |
Tnr |
A |
G |
1: 159,695,673 (GRCm39) |
D532G |
probably damaging |
Het |
Tnrc18 |
T |
A |
5: 142,762,494 (GRCm39) |
H465L |
unknown |
Het |
Togaram2 |
A |
T |
17: 72,007,504 (GRCm39) |
Q350L |
possibly damaging |
Het |
Topaz1 |
G |
A |
9: 122,578,971 (GRCm39) |
C627Y |
possibly damaging |
Het |
Tpx2 |
A |
T |
2: 152,715,058 (GRCm39) |
Q93L |
probably benign |
Het |
Trim54 |
T |
C |
5: 31,293,526 (GRCm39) |
|
probably null |
Het |
Troap |
T |
A |
15: 98,980,541 (GRCm39) |
C574S |
probably damaging |
Het |
Tut7 |
A |
T |
13: 59,964,669 (GRCm39) |
|
probably null |
Het |
Ubr4 |
T |
C |
4: 139,206,373 (GRCm39) |
|
probably null |
Het |
Vmn2r51 |
A |
G |
7: 9,834,396 (GRCm39) |
V214A |
possibly damaging |
Het |
Vmn2r66 |
A |
T |
7: 84,644,484 (GRCm39) |
M642K |
probably benign |
Het |
Vwa5a |
T |
A |
9: 38,635,191 (GRCm39) |
I232N |
probably damaging |
Het |
Zfp820 |
A |
T |
17: 22,038,685 (GRCm39) |
S214R |
probably damaging |
Het |
Zfp955b |
A |
T |
17: 33,524,437 (GRCm39) |
S43R |
probably damaging |
Het |
Zgrf1 |
C |
T |
3: 127,381,687 (GRCm39) |
T1162M |
probably benign |
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 |
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 |
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 |
|
|