Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010B08Rik |
A |
T |
2: 173,561,706 (GRCm39) |
H5L |
unknown |
Het |
Aatk |
A |
G |
11: 119,901,733 (GRCm39) |
S888P |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,985,786 (GRCm39) |
K2357* |
probably null |
Het |
Arl9 |
T |
A |
5: 77,155,139 (GRCm39) |
L90Q |
probably damaging |
Het |
Atosa |
A |
G |
9: 74,924,349 (GRCm39) |
D864G |
possibly damaging |
Het |
Atxn2 |
T |
C |
5: 121,949,055 (GRCm39) |
V1144A |
probably damaging |
Het |
Batf3 |
C |
T |
1: 190,830,623 (GRCm39) |
|
probably benign |
Het |
Bltp3b |
C |
A |
10: 89,626,593 (GRCm39) |
T429K |
probably benign |
Het |
Brpf3 |
G |
A |
17: 29,037,597 (GRCm39) |
E822K |
probably benign |
Het |
Cabin1 |
T |
A |
10: 75,575,239 (GRCm39) |
Q602L |
probably damaging |
Het |
Cadps |
T |
C |
14: 12,597,418 (GRCm38) |
E424G |
probably damaging |
Het |
Camta1 |
A |
G |
4: 151,216,004 (GRCm39) |
L972P |
possibly damaging |
Het |
Ccdc159 |
A |
G |
9: 21,840,672 (GRCm39) |
N80D |
possibly damaging |
Het |
Cdh1 |
A |
C |
8: 107,388,604 (GRCm39) |
E553D |
possibly damaging |
Het |
Cdk14 |
T |
A |
5: 5,423,477 (GRCm39) |
E35V |
probably benign |
Het |
Cfap70 |
A |
G |
14: 20,450,546 (GRCm39) |
L995P |
probably damaging |
Het |
Col18a1 |
T |
A |
10: 76,916,673 (GRCm39) |
E334V |
unknown |
Het |
Colec12 |
T |
A |
18: 9,877,000 (GRCm39) |
I741K |
unknown |
Het |
Crot |
A |
G |
5: 9,024,170 (GRCm39) |
V342A |
probably benign |
Het |
Ctnnal1 |
A |
G |
4: 56,865,036 (GRCm39) |
S27P |
possibly damaging |
Het |
Cyp2j9 |
A |
G |
4: 96,460,193 (GRCm39) |
S437P |
probably damaging |
Het |
Dennd4c |
A |
T |
4: 86,743,160 (GRCm39) |
T1001S |
probably benign |
Het |
Dffa |
G |
A |
4: 149,202,276 (GRCm39) |
V227I |
probably benign |
Het |
Dnaaf5 |
T |
A |
5: 139,159,909 (GRCm39) |
H602Q |
probably benign |
Het |
Efcab7 |
G |
T |
4: 99,761,902 (GRCm39) |
K397N |
probably damaging |
Het |
Egfl6 |
C |
T |
X: 165,319,235 (GRCm39) |
V379I |
probably benign |
Het |
Fadd |
G |
A |
7: 144,134,384 (GRCm39) |
T167I |
probably benign |
Het |
Fam184b |
T |
C |
5: 45,796,484 (GRCm39) |
D33G |
probably damaging |
Het |
Fam237b |
C |
T |
5: 5,625,549 (GRCm39) |
Q82* |
probably null |
Het |
Fam83h |
G |
A |
15: 75,877,976 (GRCm39) |
R141W |
probably damaging |
Het |
Fanci |
G |
A |
7: 79,076,954 (GRCm39) |
R564Q |
probably damaging |
Het |
Fat3 |
A |
T |
9: 15,908,054 (GRCm39) |
D2649E |
possibly damaging |
Het |
Fcrl1 |
A |
G |
3: 87,291,918 (GRCm39) |
T46A |
possibly damaging |
Het |
Fig4 |
C |
T |
10: 41,143,763 (GRCm39) |
G232D |
probably benign |
Het |
Frem3 |
A |
T |
8: 81,341,145 (GRCm39) |
H1146L |
probably damaging |
Het |
Fyttd1 |
T |
A |
16: 32,715,472 (GRCm39) |
F133L |
probably benign |
Het |
Gata2 |
A |
G |
6: 88,179,505 (GRCm39) |
N326D |
probably damaging |
Het |
Gm7298 |
A |
T |
6: 121,764,491 (GRCm39) |
T1457S |
probably damaging |
Het |
Hdac1-ps |
A |
T |
17: 78,799,075 (GRCm39) |
Y22F |
probably benign |
Het |
Heatr5b |
C |
T |
17: 79,141,524 (GRCm39) |
|
probably null |
Het |
Hfm1 |
T |
A |
5: 107,066,329 (GRCm39) |
D33V |
possibly damaging |
Het |
Hmcn2 |
G |
A |
2: 31,292,450 (GRCm39) |
A2447T |
possibly damaging |
Het |
Hs3st3b1 |
A |
G |
11: 63,812,331 (GRCm39) |
F128S |
probably benign |
Het |
Hs3st6 |
G |
T |
17: 24,972,226 (GRCm39) |
R56L |
possibly damaging |
Het |
Hsd17b3 |
C |
T |
13: 64,212,171 (GRCm39) |
M168I |
probably damaging |
Het |
Ighv1-34 |
G |
T |
12: 114,814,885 (GRCm39) |
D92E |
possibly damaging |
Het |
Itgb4 |
A |
T |
11: 115,885,171 (GRCm39) |
I1018F |
possibly damaging |
Het |
Itih3 |
T |
C |
14: 30,637,605 (GRCm39) |
D518G |
possibly damaging |
Het |
Kcnma1 |
C |
T |
14: 23,501,666 (GRCm39) |
|
probably null |
Het |
Klhl11 |
A |
T |
11: 100,363,506 (GRCm39) |
S17T |
probably benign |
Het |
Lilra6 |
T |
C |
7: 3,917,521 (GRCm39) |
E158G |
possibly damaging |
Het |
Loxl1 |
A |
G |
9: 58,220,037 (GRCm39) |
W45R |
probably damaging |
Het |
Lratd1 |
T |
C |
12: 14,200,190 (GRCm39) |
N179S |
probably benign |
Het |
Lrfn1 |
G |
T |
7: 28,166,255 (GRCm39) |
V550F |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,409,368 (GRCm39) |
K1584E |
probably benign |
Het |
Lrp4 |
C |
G |
2: 91,338,914 (GRCm39) |
P1782A |
possibly damaging |
Het |
Map3k1 |
A |
G |
13: 111,885,478 (GRCm39) |
S1480P |
probably damaging |
Het |
Mark4 |
G |
T |
7: 19,160,015 (GRCm39) |
N748K |
probably benign |
Het |
Mrpl38 |
G |
A |
11: 116,025,900 (GRCm39) |
T142M |
probably damaging |
Het |
Mrpl41 |
T |
C |
2: 24,864,481 (GRCm39) |
T64A |
probably benign |
Het |
Mrps2 |
G |
A |
2: 28,359,764 (GRCm39) |
R207K |
possibly damaging |
Het |
Myo5a |
A |
T |
9: 75,099,726 (GRCm39) |
E96D |
|
Het |
Nbas |
A |
T |
12: 13,633,417 (GRCm39) |
E2274V |
probably damaging |
Het |
Or4x13 |
T |
C |
2: 90,231,338 (GRCm39) |
F111S |
probably damaging |
Het |
Or51a8 |
T |
C |
7: 102,549,652 (GRCm39) |
I26T |
probably benign |
Het |
Or51ac3 |
T |
C |
7: 103,213,850 (GRCm39) |
D212G |
probably damaging |
Het |
Or5m10b |
T |
C |
2: 85,699,278 (GRCm39) |
L114P |
possibly damaging |
Het |
Or5m10b |
T |
A |
2: 85,699,819 (GRCm39) |
N294K |
probably damaging |
Het |
Or6c35 |
T |
A |
10: 129,169,368 (GRCm39) |
I206N |
possibly damaging |
Het |
Pcdhga12 |
T |
A |
18: 37,900,288 (GRCm39) |
D373E |
probably damaging |
Het |
Pgd |
A |
C |
4: 149,235,596 (GRCm39) |
F395V |
probably damaging |
Het |
Pi16 |
A |
G |
17: 29,538,363 (GRCm39) |
M59V |
possibly damaging |
Het |
Pik3r5 |
A |
T |
11: 68,381,720 (GRCm39) |
T255S |
probably benign |
Het |
Plch2 |
A |
T |
4: 155,068,516 (GRCm39) |
V1370E |
probably benign |
Het |
Plec |
A |
G |
15: 76,067,153 (GRCm39) |
I1309T |
unknown |
Het |
Ppp2r3d |
A |
T |
9: 124,440,831 (GRCm38) |
S22R |
|
Het |
Pramel26 |
A |
G |
4: 143,542,609 (GRCm39) |
C4R |
probably damaging |
Het |
Ptk2b |
C |
A |
14: 66,413,154 (GRCm39) |
E342* |
probably null |
Het |
Ptpn23 |
T |
C |
9: 110,215,226 (GRCm39) |
|
probably null |
Het |
Rfx8 |
A |
C |
1: 39,722,850 (GRCm39) |
S256A |
probably damaging |
Het |
Rnf115 |
C |
T |
3: 96,665,337 (GRCm39) |
T69I |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,370,457 (GRCm39) |
Y4753C |
|
Het |
S100a10 |
A |
C |
3: 93,471,590 (GRCm39) |
D58A |
possibly damaging |
Het |
Serpina12 |
T |
C |
12: 104,004,317 (GRCm39) |
K105R |
probably benign |
Het |
Slc20a2 |
G |
A |
8: 23,028,900 (GRCm39) |
G124S |
probably damaging |
Het |
Stard9 |
C |
A |
2: 120,526,635 (GRCm39) |
T964N |
probably benign |
Het |
Stxbp5 |
T |
A |
10: 9,774,938 (GRCm39) |
I72F |
probably damaging |
Het |
Sumf2 |
T |
A |
5: 129,891,482 (GRCm39) |
M282K |
possibly damaging |
Het |
Tle7 |
T |
C |
8: 110,837,580 (GRCm39) |
F375L |
probably damaging |
Het |
Tmem135 |
G |
C |
7: 88,797,186 (GRCm39) |
L357V |
probably benign |
Het |
Tmem185b |
G |
T |
1: 119,454,613 (GRCm39) |
V125L |
probably benign |
Het |
Tmtc1 |
A |
G |
6: 148,144,714 (GRCm39) |
M887T |
probably damaging |
Het |
Tnfaip8 |
C |
T |
18: 50,223,512 (GRCm39) |
Q83* |
probably null |
Het |
Tnks |
A |
G |
8: 35,306,089 (GRCm39) |
V1162A |
probably damaging |
Het |
Tomm70a |
T |
A |
16: 56,961,072 (GRCm39) |
Y342N |
possibly damaging |
Het |
Tpo |
T |
A |
12: 30,125,875 (GRCm39) |
D828V |
probably damaging |
Het |
Ugt8a |
A |
T |
3: 125,708,338 (GRCm39) |
N257K |
probably damaging |
Het |
Unc13d |
AATGCCTCCCATGCC |
AATGCCTCCCATGCCTCCCATGCC |
11: 115,958,998 (GRCm39) |
|
probably benign |
Het |
Vim |
T |
A |
2: 13,579,703 (GRCm39) |
M154K |
probably damaging |
Het |
Virma |
G |
T |
4: 11,486,045 (GRCm39) |
M1I |
probably null |
Het |
Zfp715 |
A |
T |
7: 42,950,653 (GRCm39) |
M100K |
probably benign |
Het |
Zfp748 |
A |
T |
13: 67,690,647 (GRCm39) |
C204* |
probably null |
Het |
Zmynd8 |
A |
T |
2: 165,680,772 (GRCm39) |
D236E |
probably 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 |
|
R0391:Stab2
|
UTSW |
10 |
86,783,008 (GRCm39) |
missense |
probably benign |
0.27 |
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 |
|
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 |
|