Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530002B09Rik |
T |
A |
4: 122,594,970 (GRCm39) |
|
probably benign |
Het |
Abcc2 |
G |
A |
19: 43,810,044 (GRCm39) |
|
probably benign |
Het |
Abcc8 |
C |
G |
7: 45,771,597 (GRCm39) |
G838A |
probably damaging |
Het |
Akr1c21 |
G |
A |
13: 4,631,199 (GRCm39) |
A245T |
probably damaging |
Het |
Anapc15-ps |
T |
C |
10: 95,509,139 (GRCm39) |
E47G |
probably damaging |
Het |
Apoa1 |
A |
G |
9: 46,141,140 (GRCm39) |
T79A |
probably benign |
Het |
Atp6v1b1 |
A |
G |
6: 83,733,903 (GRCm39) |
H378R |
possibly damaging |
Het |
C4b |
A |
G |
17: 34,954,588 (GRCm39) |
|
probably benign |
Het |
Catsperd |
A |
T |
17: 56,969,821 (GRCm39) |
E638D |
probably benign |
Het |
Cckar |
C |
T |
5: 53,863,595 (GRCm39) |
|
probably null |
Het |
Cfap100 |
C |
T |
6: 90,382,321 (GRCm39) |
|
probably benign |
Het |
Chd1 |
G |
T |
17: 15,970,156 (GRCm39) |
G970C |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,309,655 (GRCm39) |
|
probably benign |
Het |
Col17a1 |
C |
T |
19: 47,652,263 (GRCm39) |
V698M |
probably damaging |
Het |
Cpeb1 |
T |
C |
7: 81,011,473 (GRCm39) |
D156G |
possibly damaging |
Het |
Cryl1 |
A |
G |
14: 57,541,232 (GRCm39) |
Y151H |
possibly damaging |
Het |
Csmd3 |
C |
A |
15: 47,520,969 (GRCm39) |
V1881L |
probably damaging |
Het |
Ctnnal1 |
C |
T |
4: 56,847,921 (GRCm39) |
A73T |
probably damaging |
Het |
Cyp2c37 |
T |
C |
19: 39,982,950 (GRCm39) |
S180P |
probably damaging |
Het |
Cyp2c54 |
T |
C |
19: 40,060,613 (GRCm39) |
T123A |
possibly damaging |
Het |
Dennd6b |
T |
C |
15: 89,071,417 (GRCm39) |
D304G |
probably damaging |
Het |
Dnmt3l |
T |
C |
10: 77,887,750 (GRCm39) |
|
probably benign |
Het |
Eci1 |
G |
A |
17: 24,652,234 (GRCm39) |
|
probably null |
Het |
Efhc1 |
A |
G |
1: 21,030,412 (GRCm39) |
Y115C |
probably damaging |
Het |
Ern1 |
T |
A |
11: 106,298,004 (GRCm39) |
K706* |
probably null |
Het |
Ghrl |
T |
C |
6: 113,696,299 (GRCm39) |
E31G |
probably damaging |
Het |
Gpr108 |
A |
C |
17: 57,550,101 (GRCm39) |
V179G |
probably benign |
Het |
Henmt1 |
A |
G |
3: 108,865,851 (GRCm39) |
|
probably benign |
Het |
Ift172 |
A |
G |
5: 31,444,011 (GRCm39) |
V69A |
probably damaging |
Het |
Il17ra |
T |
C |
6: 120,453,940 (GRCm39) |
|
probably benign |
Het |
Il17rb |
T |
C |
14: 29,726,304 (GRCm39) |
N95D |
probably benign |
Het |
Il17rb |
G |
T |
14: 29,728,112 (GRCm39) |
|
probably null |
Het |
Iqub |
G |
A |
6: 24,446,154 (GRCm39) |
L757F |
probably benign |
Het |
Itpr1 |
T |
C |
6: 108,355,128 (GRCm39) |
V473A |
probably benign |
Het |
Itpr2 |
T |
G |
6: 146,131,271 (GRCm39) |
N1978H |
probably damaging |
Het |
Klk1b26 |
T |
A |
7: 43,662,151 (GRCm39) |
F3Y |
probably damaging |
Het |
Lars1 |
A |
G |
18: 42,384,428 (GRCm39) |
V50A |
probably benign |
Het |
Lax1 |
G |
T |
1: 133,607,804 (GRCm39) |
H312Q |
probably benign |
Het |
Lctl |
T |
C |
9: 64,029,596 (GRCm39) |
|
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,287,202 (GRCm39) |
D3745V |
probably damaging |
Het |
Lrp2 |
G |
A |
2: 69,290,681 (GRCm39) |
|
probably benign |
Het |
Lvrn |
A |
T |
18: 46,983,533 (GRCm39) |
H92L |
probably benign |
Het |
Marchf1 |
A |
G |
8: 66,871,625 (GRCm39) |
T385A |
probably damaging |
Het |
Marf1 |
C |
T |
16: 13,960,398 (GRCm39) |
A549T |
probably damaging |
Het |
Mbd5 |
T |
C |
2: 49,162,428 (GRCm39) |
V970A |
possibly damaging |
Het |
Mccc1 |
A |
G |
3: 36,017,719 (GRCm39) |
|
probably benign |
Het |
Mpp4 |
A |
T |
1: 59,182,988 (GRCm39) |
|
probably benign |
Het |
Mrnip |
G |
A |
11: 50,090,747 (GRCm39) |
A304T |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,418,819 (GRCm39) |
S3922P |
possibly damaging |
Het |
Myh3 |
T |
A |
11: 66,987,333 (GRCm39) |
|
probably benign |
Het |
Nbea |
A |
T |
3: 55,944,698 (GRCm39) |
H555Q |
probably damaging |
Het |
Niban3 |
T |
A |
8: 72,055,143 (GRCm39) |
|
probably benign |
Het |
Nlrp9c |
A |
T |
7: 26,070,901 (GRCm39) |
|
probably benign |
Het |
Nmur1 |
A |
T |
1: 86,315,400 (GRCm39) |
V178E |
probably damaging |
Het |
Nod2 |
T |
G |
8: 89,390,406 (GRCm39) |
S238A |
probably benign |
Het |
Ogfod1 |
A |
T |
8: 94,789,651 (GRCm39) |
T451S |
probably damaging |
Het |
Or1e17 |
T |
C |
11: 73,831,935 (GRCm39) |
F288L |
probably damaging |
Het |
Or2d36 |
T |
A |
7: 106,747,394 (GRCm39) |
Y290* |
probably null |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or8b8 |
G |
A |
9: 37,809,138 (GRCm39) |
G146D |
probably benign |
Het |
Pcdh20 |
T |
C |
14: 88,706,104 (GRCm39) |
I399V |
probably benign |
Het |
Pdlim1 |
G |
T |
19: 40,232,017 (GRCm39) |
H120Q |
probably damaging |
Het |
Plg |
T |
C |
17: 12,637,968 (GRCm39) |
V798A |
probably damaging |
Het |
Polr2c |
A |
G |
8: 95,584,403 (GRCm39) |
I39V |
possibly damaging |
Het |
Ppfia2 |
C |
A |
10: 106,666,575 (GRCm39) |
|
probably benign |
Het |
Ppp1r3a |
A |
T |
6: 14,719,696 (GRCm39) |
I406N |
probably benign |
Het |
Psg28 |
A |
T |
7: 18,160,098 (GRCm39) |
M366K |
probably benign |
Het |
Rad54b |
T |
C |
4: 11,601,702 (GRCm39) |
I419T |
probably damaging |
Het |
Rnf43 |
A |
G |
11: 87,622,108 (GRCm39) |
Q403R |
possibly damaging |
Het |
Sema6a |
G |
A |
18: 47,423,112 (GRCm39) |
|
probably null |
Het |
Slc28a3 |
A |
G |
13: 58,717,229 (GRCm39) |
|
probably benign |
Het |
Smad2 |
A |
T |
18: 76,422,108 (GRCm39) |
|
probably null |
Het |
Smad4 |
G |
A |
18: 73,791,720 (GRCm39) |
P274S |
probably benign |
Het |
Smchd1 |
A |
T |
17: 71,710,149 (GRCm39) |
V906D |
probably damaging |
Het |
Soat2 |
C |
A |
15: 102,067,188 (GRCm39) |
R320S |
possibly damaging |
Het |
Spata33 |
C |
T |
8: 123,948,626 (GRCm39) |
A57V |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,865,375 (GRCm39) |
L1814P |
probably benign |
Het |
Stil |
A |
G |
4: 114,898,369 (GRCm39) |
|
probably null |
Het |
Sympk |
T |
A |
7: 18,780,774 (GRCm39) |
L759H |
probably benign |
Het |
Tet1 |
A |
T |
10: 62,650,325 (GRCm39) |
|
probably null |
Het |
Tfpi2 |
A |
T |
6: 3,965,460 (GRCm39) |
N117K |
probably benign |
Het |
Tle3 |
A |
G |
9: 61,323,943 (GRCm39) |
Y766C |
probably damaging |
Het |
Trpt1 |
C |
A |
19: 6,975,298 (GRCm39) |
|
probably null |
Het |
Tshz1 |
A |
G |
18: 84,034,174 (GRCm39) |
F78S |
possibly damaging |
Het |
Ttc1 |
T |
C |
11: 43,629,635 (GRCm39) |
D177G |
probably damaging |
Het |
Ttc13 |
T |
A |
8: 125,401,140 (GRCm39) |
Y741F |
probably damaging |
Het |
Ulk3 |
C |
T |
9: 57,502,115 (GRCm39) |
S462L |
probably benign |
Het |
Utrn |
C |
T |
10: 12,401,077 (GRCm39) |
|
probably benign |
Het |
V1rd19 |
A |
C |
7: 23,703,010 (GRCm39) |
T159P |
probably damaging |
Het |
Vars1 |
T |
C |
17: 35,230,462 (GRCm39) |
V515A |
possibly damaging |
Het |
Vmn1r85 |
A |
G |
7: 12,818,515 (GRCm39) |
Y210H |
probably benign |
Het |
Vmn2r89 |
A |
G |
14: 51,693,435 (GRCm39) |
T262A |
probably damaging |
Het |
Vps53 |
G |
A |
11: 76,012,405 (GRCm39) |
T209I |
probably benign |
Het |
Wdfy2 |
T |
C |
14: 63,162,582 (GRCm39) |
F95L |
possibly damaging |
Het |
Wwp1 |
G |
T |
4: 19,627,911 (GRCm39) |
S694Y |
probably damaging |
Het |
Zbtb8b |
T |
A |
4: 129,326,463 (GRCm39) |
D201V |
probably damaging |
Het |
Zmym5 |
A |
C |
14: 57,041,908 (GRCm39) |
N123K |
possibly damaging |
Het |
|
Other mutations in Stab2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Stab2
|
APN |
10 |
86,705,070 (GRCm39) |
splice site |
probably null |
|
IGL00809:Stab2
|
APN |
10 |
86,684,038 (GRCm39) |
splice site |
probably benign |
|
IGL00911:Stab2
|
APN |
10 |
86,805,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01347:Stab2
|
APN |
10 |
86,737,567 (GRCm39) |
splice site |
probably null |
|
IGL01411:Stab2
|
APN |
10 |
86,815,872 (GRCm39) |
splice site |
probably benign |
|
IGL01503:Stab2
|
APN |
10 |
86,776,477 (GRCm39) |
splice site |
probably benign |
|
IGL01599:Stab2
|
APN |
10 |
86,758,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01635:Stab2
|
APN |
10 |
86,816,992 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01640:Stab2
|
APN |
10 |
86,790,035 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01671:Stab2
|
APN |
10 |
86,805,141 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02023:Stab2
|
APN |
10 |
86,707,695 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02075:Stab2
|
APN |
10 |
86,803,514 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02174:Stab2
|
APN |
10 |
86,695,606 (GRCm39) |
splice site |
probably null |
|
IGL02600:Stab2
|
APN |
10 |
86,790,123 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Stab2
|
APN |
10 |
86,686,766 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02668:Stab2
|
APN |
10 |
86,682,027 (GRCm39) |
splice site |
probably benign |
|
IGL02709:Stab2
|
APN |
10 |
86,682,029 (GRCm39) |
splice site |
probably benign |
|
IGL02728:Stab2
|
APN |
10 |
86,692,420 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02803:Stab2
|
APN |
10 |
86,786,133 (GRCm39) |
splice site |
probably benign |
|
IGL02938:Stab2
|
APN |
10 |
86,707,785 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03033:Stab2
|
APN |
10 |
86,832,667 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03238:Stab2
|
APN |
10 |
86,690,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03402:Stab2
|
APN |
10 |
86,805,165 (GRCm39) |
missense |
probably benign |
0.03 |
prospector
|
UTSW |
10 |
86,737,431 (GRCm39) |
splice site |
probably null |
|
songbird
|
UTSW |
10 |
86,694,016 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Stab2
|
UTSW |
10 |
86,705,041 (GRCm39) |
missense |
probably damaging |
0.96 |
F6893:Stab2
|
UTSW |
10 |
86,691,035 (GRCm39) |
missense |
probably damaging |
1.00 |
K7371:Stab2
|
UTSW |
10 |
86,779,153 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4142001:Stab2
|
UTSW |
10 |
86,703,039 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4362001:Stab2
|
UTSW |
10 |
86,697,299 (GRCm39) |
nonsense |
probably null |
|
R0015:Stab2
|
UTSW |
10 |
86,679,481 (GRCm39) |
missense |
probably benign |
|
R0254:Stab2
|
UTSW |
10 |
86,733,824 (GRCm39) |
missense |
probably benign |
|
R0310:Stab2
|
UTSW |
10 |
86,803,477 (GRCm39) |
splice site |
probably benign |
|
R0333:Stab2
|
UTSW |
10 |
86,677,491 (GRCm39) |
missense |
probably benign |
|
R0400:Stab2
|
UTSW |
10 |
86,708,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Stab2
|
UTSW |
10 |
86,679,355 (GRCm39) |
splice site |
probably benign |
|
R0440:Stab2
|
UTSW |
10 |
86,785,792 (GRCm39) |
missense |
probably benign |
0.23 |
R0743:Stab2
|
UTSW |
10 |
86,723,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R0847:Stab2
|
UTSW |
10 |
86,805,735 (GRCm39) |
missense |
probably benign |
0.00 |
R0883:Stab2
|
UTSW |
10 |
86,760,314 (GRCm39) |
splice site |
probably benign |
|
R1078:Stab2
|
UTSW |
10 |
86,742,997 (GRCm39) |
splice site |
probably null |
|
R1118:Stab2
|
UTSW |
10 |
86,721,582 (GRCm39) |
splice site |
probably null |
|
R1119:Stab2
|
UTSW |
10 |
86,695,619 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1179:Stab2
|
UTSW |
10 |
86,786,165 (GRCm39) |
missense |
probably damaging |
0.98 |
R1440:Stab2
|
UTSW |
10 |
86,697,231 (GRCm39) |
splice site |
probably null |
|
R1550:Stab2
|
UTSW |
10 |
86,714,790 (GRCm39) |
missense |
probably benign |
0.01 |
R1616:Stab2
|
UTSW |
10 |
86,721,582 (GRCm39) |
splice site |
probably null |
|
R1728:Stab2
|
UTSW |
10 |
86,773,903 (GRCm39) |
missense |
probably benign |
0.41 |
R1768:Stab2
|
UTSW |
10 |
86,838,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R1772:Stab2
|
UTSW |
10 |
86,790,098 (GRCm39) |
missense |
probably benign |
0.06 |
R1776:Stab2
|
UTSW |
10 |
86,793,680 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1784:Stab2
|
UTSW |
10 |
86,773,903 (GRCm39) |
missense |
probably benign |
0.41 |
R1892:Stab2
|
UTSW |
10 |
86,773,913 (GRCm39) |
missense |
probably damaging |
0.99 |
R1957:Stab2
|
UTSW |
10 |
86,697,334 (GRCm39) |
missense |
probably benign |
0.13 |
R1972:Stab2
|
UTSW |
10 |
86,796,180 (GRCm39) |
missense |
probably damaging |
0.99 |
R1975:Stab2
|
UTSW |
10 |
86,732,360 (GRCm39) |
critical splice donor site |
probably null |
|
R1976:Stab2
|
UTSW |
10 |
86,732,360 (GRCm39) |
critical splice donor site |
probably null |
|
R1996:Stab2
|
UTSW |
10 |
86,838,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R2085:Stab2
|
UTSW |
10 |
86,790,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Stab2
|
UTSW |
10 |
86,700,904 (GRCm39) |
nonsense |
probably null |
|
R2169:Stab2
|
UTSW |
10 |
86,723,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Stab2
|
UTSW |
10 |
86,776,503 (GRCm39) |
missense |
probably benign |
0.22 |
R2296:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2297:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2298:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2326:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2434:Stab2
|
UTSW |
10 |
86,805,183 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2519:Stab2
|
UTSW |
10 |
86,770,704 (GRCm39) |
splice site |
probably benign |
|
R2696:Stab2
|
UTSW |
10 |
86,697,363 (GRCm39) |
missense |
probably benign |
0.45 |
R2883:Stab2
|
UTSW |
10 |
86,803,550 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2923:Stab2
|
UTSW |
10 |
86,697,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R3711:Stab2
|
UTSW |
10 |
86,702,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Stab2
|
UTSW |
10 |
86,805,141 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3834:Stab2
|
UTSW |
10 |
86,785,776 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3970:Stab2
|
UTSW |
10 |
86,714,750 (GRCm39) |
missense |
probably damaging |
0.97 |
R3979:Stab2
|
UTSW |
10 |
86,699,320 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4003:Stab2
|
UTSW |
10 |
86,693,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Stab2
|
UTSW |
10 |
86,758,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R4151:Stab2
|
UTSW |
10 |
86,838,847 (GRCm39) |
missense |
probably benign |
0.12 |
R4190:Stab2
|
UTSW |
10 |
86,714,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R4556:Stab2
|
UTSW |
10 |
86,803,543 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4773:Stab2
|
UTSW |
10 |
86,743,235 (GRCm39) |
nonsense |
probably null |
|
R4825:Stab2
|
UTSW |
10 |
86,783,011 (GRCm39) |
missense |
probably benign |
0.08 |
R4865:Stab2
|
UTSW |
10 |
86,679,364 (GRCm39) |
splice site |
probably null |
|
R4871:Stab2
|
UTSW |
10 |
86,778,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R4943:Stab2
|
UTSW |
10 |
86,790,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R4981:Stab2
|
UTSW |
10 |
86,796,087 (GRCm39) |
missense |
probably benign |
|
R4994:Stab2
|
UTSW |
10 |
86,785,771 (GRCm39) |
missense |
probably benign |
|
R4999:Stab2
|
UTSW |
10 |
86,773,773 (GRCm39) |
missense |
probably damaging |
0.97 |
R5061:Stab2
|
UTSW |
10 |
86,743,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Stab2
|
UTSW |
10 |
86,699,422 (GRCm39) |
missense |
probably benign |
0.23 |
R5073:Stab2
|
UTSW |
10 |
86,699,422 (GRCm39) |
missense |
probably benign |
0.23 |
R5074:Stab2
|
UTSW |
10 |
86,699,422 (GRCm39) |
missense |
probably benign |
0.23 |
R5134:Stab2
|
UTSW |
10 |
86,707,674 (GRCm39) |
splice site |
probably null |
|
R5213:Stab2
|
UTSW |
10 |
86,743,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R5508:Stab2
|
UTSW |
10 |
86,796,143 (GRCm39) |
missense |
probably benign |
0.01 |
R5530:Stab2
|
UTSW |
10 |
86,783,026 (GRCm39) |
missense |
probably benign |
0.04 |
R5540:Stab2
|
UTSW |
10 |
86,683,989 (GRCm39) |
missense |
probably benign |
0.30 |
R5839:Stab2
|
UTSW |
10 |
86,708,555 (GRCm39) |
missense |
probably damaging |
0.97 |
R5949:Stab2
|
UTSW |
10 |
86,805,713 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6015:Stab2
|
UTSW |
10 |
86,773,906 (GRCm39) |
missense |
probably damaging |
0.99 |
R6019:Stab2
|
UTSW |
10 |
86,838,886 (GRCm39) |
missense |
probably benign |
0.00 |
R6116:Stab2
|
UTSW |
10 |
86,743,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6131:Stab2
|
UTSW |
10 |
86,719,642 (GRCm39) |
splice site |
probably null |
|
R6209:Stab2
|
UTSW |
10 |
86,758,867 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6243:Stab2
|
UTSW |
10 |
86,743,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R6433:Stab2
|
UTSW |
10 |
86,737,431 (GRCm39) |
splice site |
probably null |
|
R6787:Stab2
|
UTSW |
10 |
86,754,948 (GRCm39) |
missense |
probably benign |
0.07 |
R6841:Stab2
|
UTSW |
10 |
86,778,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6873:Stab2
|
UTSW |
10 |
86,697,230 (GRCm39) |
critical splice donor site |
probably null |
|
R7025:Stab2
|
UTSW |
10 |
86,686,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R7043:Stab2
|
UTSW |
10 |
86,706,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R7047:Stab2
|
UTSW |
10 |
86,694,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R7107:Stab2
|
UTSW |
10 |
86,741,456 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7214:Stab2
|
UTSW |
10 |
86,735,705 (GRCm39) |
missense |
probably damaging |
0.99 |
R7271:Stab2
|
UTSW |
10 |
86,838,972 (GRCm39) |
splice site |
probably null |
|
R7291:Stab2
|
UTSW |
10 |
86,782,084 (GRCm39) |
missense |
probably damaging |
0.96 |
R7336:Stab2
|
UTSW |
10 |
86,805,049 (GRCm39) |
nonsense |
probably null |
|
R7432:Stab2
|
UTSW |
10 |
86,721,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R7580:Stab2
|
UTSW |
10 |
86,705,028 (GRCm39) |
missense |
probably benign |
0.00 |
R7622:Stab2
|
UTSW |
10 |
86,709,766 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7629:Stab2
|
UTSW |
10 |
86,719,646 (GRCm39) |
critical splice donor site |
probably null |
|
R7658:Stab2
|
UTSW |
10 |
86,816,999 (GRCm39) |
missense |
probably benign |
0.12 |
R7798:Stab2
|
UTSW |
10 |
86,793,776 (GRCm39) |
missense |
probably damaging |
0.98 |
R7835:Stab2
|
UTSW |
10 |
86,708,483 (GRCm39) |
missense |
probably benign |
0.06 |
R7845:Stab2
|
UTSW |
10 |
86,832,758 (GRCm39) |
missense |
probably benign |
0.09 |
R7863:Stab2
|
UTSW |
10 |
86,808,745 (GRCm39) |
missense |
probably benign |
0.30 |
R7885:Stab2
|
UTSW |
10 |
86,714,776 (GRCm39) |
missense |
probably benign |
0.03 |
R7904:Stab2
|
UTSW |
10 |
86,790,056 (GRCm39) |
nonsense |
probably null |
|
R7947:Stab2
|
UTSW |
10 |
86,681,897 (GRCm39) |
missense |
probably benign |
0.31 |
R7963:Stab2
|
UTSW |
10 |
86,683,887 (GRCm39) |
critical splice donor site |
probably null |
|
R8014:Stab2
|
UTSW |
10 |
86,686,767 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8021:Stab2
|
UTSW |
10 |
86,741,403 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8024:Stab2
|
UTSW |
10 |
86,681,916 (GRCm39) |
missense |
probably benign |
0.34 |
R8097:Stab2
|
UTSW |
10 |
86,704,959 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8281:Stab2
|
UTSW |
10 |
86,709,728 (GRCm39) |
missense |
probably damaging |
0.98 |
R8462:Stab2
|
UTSW |
10 |
86,803,598 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8670:Stab2
|
UTSW |
10 |
86,776,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R8692:Stab2
|
UTSW |
10 |
86,808,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R8744:Stab2
|
UTSW |
10 |
86,805,213 (GRCm39) |
missense |
probably benign |
0.32 |
R8745:Stab2
|
UTSW |
10 |
86,805,213 (GRCm39) |
missense |
probably benign |
0.32 |
R8782:Stab2
|
UTSW |
10 |
86,735,685 (GRCm39) |
missense |
probably benign |
0.00 |
R8875:Stab2
|
UTSW |
10 |
86,832,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R8978:Stab2
|
UTSW |
10 |
86,785,782 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9141:Stab2
|
UTSW |
10 |
86,704,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R9248:Stab2
|
UTSW |
10 |
86,727,481 (GRCm39) |
missense |
probably damaging |
0.98 |
R9326:Stab2
|
UTSW |
10 |
86,791,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R9426:Stab2
|
UTSW |
10 |
86,704,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R9568:Stab2
|
UTSW |
10 |
86,699,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R9627:Stab2
|
UTSW |
10 |
86,793,704 (GRCm39) |
missense |
probably damaging |
0.98 |
R9635:Stab2
|
UTSW |
10 |
86,686,651 (GRCm39) |
nonsense |
probably null |
|
R9648:Stab2
|
UTSW |
10 |
86,692,561 (GRCm39) |
frame shift |
probably null |
|
R9649:Stab2
|
UTSW |
10 |
86,692,561 (GRCm39) |
frame shift |
probably null |
|
R9650:Stab2
|
UTSW |
10 |
86,692,561 (GRCm39) |
frame shift |
probably null |
|
R9726:Stab2
|
UTSW |
10 |
86,790,095 (GRCm39) |
missense |
probably benign |
0.00 |
R9756:Stab2
|
UTSW |
10 |
86,803,553 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9786:Stab2
|
UTSW |
10 |
86,757,997 (GRCm39) |
missense |
probably benign |
0.03 |
RF061:Stab2
|
UTSW |
10 |
86,702,622 (GRCm39) |
critical splice acceptor site |
probably benign |
|
X0023:Stab2
|
UTSW |
10 |
86,758,062 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0025:Stab2
|
UTSW |
10 |
86,723,680 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Stab2
|
UTSW |
10 |
86,785,778 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Stab2
|
UTSW |
10 |
86,732,460 (GRCm39) |
missense |
probably damaging |
1.00 |
|