Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810064F22Rik |
A |
G |
9: 22,119,177 (GRCm39) |
|
noncoding transcript |
Het |
5530400C23Rik |
A |
T |
6: 133,269,287 (GRCm39) |
|
probably benign |
Het |
Aco2 |
T |
C |
15: 81,787,666 (GRCm39) |
|
probably benign |
Het |
Arap3 |
A |
T |
18: 38,129,760 (GRCm39) |
S134T |
probably benign |
Het |
Arsa |
T |
A |
15: 89,358,539 (GRCm39) |
M288L |
possibly damaging |
Het |
Atg2b |
A |
T |
12: 105,614,708 (GRCm39) |
D1074E |
probably benign |
Het |
Baiap2l1 |
A |
T |
5: 144,221,372 (GRCm39) |
I174N |
probably damaging |
Het |
Bpifb9a |
A |
T |
2: 154,108,761 (GRCm39) |
N421Y |
possibly damaging |
Het |
Btn2a2 |
T |
A |
13: 23,662,655 (GRCm39) |
I432L |
probably benign |
Het |
Ccdc150 |
A |
G |
1: 54,395,850 (GRCm39) |
I778V |
probably benign |
Het |
Cd200r2 |
G |
A |
16: 44,730,037 (GRCm39) |
V194I |
possibly damaging |
Het |
Cep350 |
A |
C |
1: 155,786,964 (GRCm39) |
L1421R |
probably damaging |
Het |
Col24a1 |
G |
A |
3: 145,250,899 (GRCm39) |
A1633T |
probably damaging |
Het |
Col6a6 |
A |
T |
9: 105,579,412 (GRCm39) |
C1938S |
probably damaging |
Het |
Cspg4 |
A |
T |
9: 56,795,418 (GRCm39) |
D1051V |
probably damaging |
Het |
Cstf1 |
T |
A |
2: 172,214,976 (GRCm39) |
N32K |
probably benign |
Het |
Ctrb1 |
G |
A |
8: 112,413,269 (GRCm39) |
R248* |
probably null |
Het |
Cyp2d11 |
T |
A |
15: 82,275,958 (GRCm39) |
M208L |
probably benign |
Het |
Dbt |
A |
G |
3: 116,337,478 (GRCm39) |
Q334R |
probably benign |
Het |
Dcaf12 |
A |
G |
4: 41,298,338 (GRCm39) |
V270A |
probably damaging |
Het |
Dis3l |
T |
A |
9: 64,226,447 (GRCm39) |
N361I |
probably benign |
Het |
Dnah10 |
A |
T |
5: 124,840,140 (GRCm39) |
D1315V |
probably benign |
Het |
Dnah11 |
A |
G |
12: 118,090,621 (GRCm39) |
F1080S |
probably benign |
Het |
Dnm3 |
A |
G |
1: 162,234,930 (GRCm39) |
V70A |
probably damaging |
Het |
Dpy19l1 |
A |
C |
9: 24,325,705 (GRCm39) |
M700R |
possibly damaging |
Het |
Dpy19l2 |
G |
A |
9: 24,557,679 (GRCm39) |
|
probably benign |
Het |
Dst |
C |
A |
1: 34,228,634 (GRCm39) |
H2254N |
possibly damaging |
Het |
Epm2aip1 |
A |
G |
9: 111,101,531 (GRCm39) |
N168S |
probably benign |
Het |
Fchsd2 |
A |
G |
7: 100,927,631 (GRCm39) |
Y691C |
possibly damaging |
Het |
Fndc8 |
A |
T |
11: 82,788,398 (GRCm39) |
D76V |
probably benign |
Het |
Frmd4a |
T |
C |
2: 4,477,963 (GRCm39) |
L48P |
probably damaging |
Het |
Gimap6 |
T |
A |
6: 48,679,404 (GRCm39) |
I211F |
probably damaging |
Het |
Gm15130 |
A |
G |
2: 110,969,284 (GRCm39) |
|
probably benign |
Het |
Gm43302 |
T |
A |
5: 105,438,766 (GRCm39) |
I41F |
probably damaging |
Het |
Gm5698 |
C |
T |
1: 31,016,614 (GRCm39) |
V146I |
probably benign |
Het |
Gpatch1 |
G |
A |
7: 34,986,652 (GRCm39) |
S768L |
probably damaging |
Het |
Grb14 |
T |
G |
2: 64,768,836 (GRCm39) |
|
probably null |
Het |
Hnrnpd |
T |
C |
5: 100,112,560 (GRCm39) |
E222G |
probably damaging |
Het |
Il4ra |
C |
T |
7: 125,175,403 (GRCm39) |
P537L |
possibly damaging |
Het |
Kalrn |
T |
C |
16: 34,024,327 (GRCm39) |
D610G |
probably damaging |
Het |
Kcnh4 |
T |
C |
11: 100,648,626 (GRCm39) |
H26R |
probably benign |
Het |
Kctd2 |
T |
G |
11: 115,320,343 (GRCm39) |
|
probably benign |
Het |
Khdrbs3 |
T |
A |
15: 68,866,886 (GRCm39) |
|
probably benign |
Het |
Macf1 |
G |
A |
4: 123,325,943 (GRCm39) |
Q3066* |
probably null |
Het |
Mfn2 |
G |
A |
4: 147,969,902 (GRCm39) |
|
probably benign |
Het |
Mmab |
T |
C |
5: 114,574,526 (GRCm39) |
|
probably benign |
Het |
Mrc1 |
T |
C |
2: 14,266,011 (GRCm39) |
S310P |
probably benign |
Het |
Mrps21 |
T |
C |
3: 95,770,197 (GRCm39) |
Y44C |
probably null |
Het |
Myh10 |
T |
A |
11: 68,590,317 (GRCm39) |
F121Y |
probably damaging |
Het |
Myo1f |
A |
G |
17: 33,820,677 (GRCm39) |
D840G |
probably damaging |
Het |
Neb |
T |
A |
2: 52,196,542 (GRCm39) |
D553V |
probably damaging |
Het |
Nol6 |
G |
T |
4: 41,119,572 (GRCm39) |
|
probably benign |
Het |
Npr2 |
G |
T |
4: 43,632,329 (GRCm39) |
V49L |
probably benign |
Het |
Ntsr2 |
T |
C |
12: 16,704,120 (GRCm39) |
I207T |
probably benign |
Het |
Nwd1 |
T |
A |
8: 73,438,484 (GRCm39) |
S1552T |
probably benign |
Het |
Oas3 |
T |
A |
5: 120,896,940 (GRCm39) |
I894F |
probably damaging |
Het |
Oprd1 |
A |
G |
4: 131,841,299 (GRCm39) |
F220L |
probably benign |
Het |
Or11j4 |
T |
A |
14: 50,630,659 (GRCm39) |
F149I |
probably benign |
Het |
Or2aj4 |
T |
A |
16: 19,384,799 (GRCm39) |
Y278F |
probably damaging |
Het |
Or2r2 |
A |
T |
6: 42,463,869 (GRCm39) |
M86K |
probably benign |
Het |
Or8b57 |
T |
C |
9: 40,003,983 (GRCm39) |
N93S |
possibly damaging |
Het |
Pkd1l3 |
G |
T |
8: 110,347,103 (GRCm39) |
G159C |
unknown |
Het |
Plcb4 |
T |
C |
2: 135,803,689 (GRCm39) |
S521P |
probably benign |
Het |
Plcl1 |
A |
T |
1: 55,752,634 (GRCm39) |
I993F |
probably damaging |
Het |
Plcxd1 |
T |
A |
5: 110,249,368 (GRCm39) |
V65E |
probably damaging |
Het |
Plekha7 |
T |
C |
7: 115,756,743 (GRCm39) |
S640G |
probably damaging |
Het |
Ptprn2 |
A |
C |
12: 117,240,222 (GRCm39) |
N993T |
probably benign |
Het |
Rabepk |
T |
C |
2: 34,685,318 (GRCm39) |
D26G |
possibly damaging |
Het |
Reck |
A |
G |
4: 43,930,936 (GRCm39) |
N646D |
probably damaging |
Het |
Rfx2 |
A |
T |
17: 57,093,736 (GRCm39) |
|
probably benign |
Het |
Ripk2 |
G |
A |
4: 16,123,868 (GRCm39) |
Q436* |
probably null |
Het |
Ryr1 |
C |
T |
7: 28,704,992 (GRCm39) |
|
probably benign |
Het |
Sema6b |
A |
G |
17: 56,435,271 (GRCm39) |
V324A |
possibly damaging |
Het |
Sik2 |
C |
A |
9: 50,909,833 (GRCm39) |
M73I |
probably benign |
Het |
Slc39a6 |
T |
C |
18: 24,732,326 (GRCm39) |
K321E |
probably damaging |
Het |
Slc7a4 |
C |
A |
16: 17,391,875 (GRCm39) |
V520F |
probably benign |
Het |
Slitrk6 |
A |
T |
14: 110,987,364 (GRCm39) |
L781H |
probably damaging |
Het |
Spink14 |
T |
C |
18: 44,161,830 (GRCm39) |
V2A |
probably benign |
Het |
Sptan1 |
C |
A |
2: 29,893,679 (GRCm39) |
|
probably benign |
Het |
Tbc1d17 |
C |
T |
7: 44,493,495 (GRCm39) |
|
probably benign |
Het |
Tbcd |
T |
A |
11: 121,394,590 (GRCm39) |
L49* |
probably null |
Het |
Tmco6 |
A |
G |
18: 36,875,160 (GRCm39) |
T477A |
probably benign |
Het |
Tmem208 |
C |
T |
8: 106,054,857 (GRCm39) |
A53V |
probably benign |
Het |
Tpp2 |
A |
G |
1: 44,020,908 (GRCm39) |
T837A |
possibly damaging |
Het |
Tulp4 |
A |
T |
17: 6,252,008 (GRCm39) |
N60I |
probably damaging |
Het |
Ubqlnl |
A |
T |
7: 103,798,145 (GRCm39) |
W451R |
probably damaging |
Het |
Usp53 |
G |
T |
3: 122,746,956 (GRCm39) |
C363* |
probably null |
Het |
Usp7 |
A |
T |
16: 8,509,282 (GRCm39) |
H1017Q |
probably benign |
Het |
Utp4 |
A |
G |
8: 107,649,530 (GRCm39) |
T660A |
possibly damaging |
Het |
Vmn1r194 |
A |
T |
13: 22,428,641 (GRCm39) |
Y86F |
probably benign |
Het |
Vmn1r195 |
A |
T |
13: 22,463,409 (GRCm39) |
H293L |
possibly damaging |
Het |
Vmn1r231 |
T |
C |
17: 21,109,998 (GRCm39) |
R306G |
probably benign |
Het |
Vmn2r63 |
T |
C |
7: 42,576,514 (GRCm39) |
|
probably benign |
Het |
Vmn2r77 |
T |
C |
7: 86,449,964 (GRCm39) |
V70A |
probably benign |
Het |
Vmn2r85 |
T |
C |
10: 130,261,770 (GRCm39) |
D189G |
probably damaging |
Het |
Vps8 |
A |
G |
16: 21,296,273 (GRCm39) |
E515G |
possibly damaging |
Het |
Wdr18 |
C |
A |
10: 79,796,937 (GRCm39) |
Y104* |
probably null |
Het |
Wnk4 |
A |
T |
11: 101,156,261 (GRCm39) |
D43V |
probably damaging |
Het |
Xab2 |
A |
T |
8: 3,663,880 (GRCm39) |
N346K |
probably damaging |
Het |
Xirp2 |
T |
C |
2: 67,342,484 (GRCm39) |
V1575A |
possibly damaging |
Het |
Zdhhc12 |
C |
T |
2: 29,982,547 (GRCm39) |
R50H |
probably damaging |
Het |
Zdhhc8 |
A |
G |
16: 18,043,064 (GRCm39) |
S379P |
probably benign |
Het |
Zfp458 |
G |
A |
13: 67,407,673 (GRCm39) |
Q58* |
probably null |
Het |
Zfp747 |
A |
T |
7: 126,973,772 (GRCm39) |
S133T |
probably benign |
Het |
|
Other mutations in Stab1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Stab1
|
APN |
14 |
30,883,314 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00323:Stab1
|
APN |
14 |
30,861,263 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00515:Stab1
|
APN |
14 |
30,881,686 (GRCm39) |
missense |
probably benign |
0.20 |
IGL00844:Stab1
|
APN |
14 |
30,869,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01374:Stab1
|
APN |
14 |
30,869,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01384:Stab1
|
APN |
14 |
30,872,365 (GRCm39) |
missense |
probably benign |
|
IGL01431:Stab1
|
APN |
14 |
30,870,952 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01787:Stab1
|
APN |
14 |
30,861,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02128:Stab1
|
APN |
14 |
30,872,398 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02138:Stab1
|
APN |
14 |
30,865,470 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02256:Stab1
|
APN |
14 |
30,863,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02340:Stab1
|
APN |
14 |
30,862,367 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02507:Stab1
|
APN |
14 |
30,861,167 (GRCm39) |
unclassified |
probably benign |
|
IGL02695:Stab1
|
APN |
14 |
30,881,228 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02755:Stab1
|
APN |
14 |
30,861,595 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02870:Stab1
|
APN |
14 |
30,861,354 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02884:Stab1
|
APN |
14 |
30,872,100 (GRCm39) |
splice site |
probably null |
|
IGL03035:Stab1
|
APN |
14 |
30,869,726 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03267:Stab1
|
APN |
14 |
30,864,686 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03286:Stab1
|
APN |
14 |
30,881,283 (GRCm39) |
splice site |
probably benign |
|
IGL03366:Stab1
|
APN |
14 |
30,872,220 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL03412:Stab1
|
APN |
14 |
30,876,364 (GRCm39) |
missense |
probably benign |
0.42 |
R0906_Stab1_335
|
UTSW |
14 |
30,867,206 (GRCm39) |
missense |
probably benign |
0.19 |
R5086_Stab1_467
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Stab1
|
UTSW |
14 |
30,867,981 (GRCm39) |
critical splice donor site |
probably null |
|
K7371:Stab1
|
UTSW |
14 |
30,872,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Stab1
|
UTSW |
14 |
30,862,644 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0053:Stab1
|
UTSW |
14 |
30,862,644 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0066:Stab1
|
UTSW |
14 |
30,879,027 (GRCm39) |
splice site |
probably benign |
|
R0363:Stab1
|
UTSW |
14 |
30,880,965 (GRCm39) |
splice site |
probably benign |
|
R0387:Stab1
|
UTSW |
14 |
30,870,058 (GRCm39) |
missense |
probably benign |
0.00 |
R0391:Stab1
|
UTSW |
14 |
30,865,375 (GRCm39) |
missense |
probably benign |
0.21 |
R0513:Stab1
|
UTSW |
14 |
30,870,902 (GRCm39) |
missense |
probably benign |
0.08 |
R0546:Stab1
|
UTSW |
14 |
30,861,507 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0825:Stab1
|
UTSW |
14 |
30,874,557 (GRCm39) |
missense |
probably benign |
0.16 |
R0906:Stab1
|
UTSW |
14 |
30,867,206 (GRCm39) |
missense |
probably benign |
0.19 |
R0963:Stab1
|
UTSW |
14 |
30,869,231 (GRCm39) |
missense |
probably damaging |
0.97 |
R1219:Stab1
|
UTSW |
14 |
30,862,578 (GRCm39) |
splice site |
probably null |
|
R1234:Stab1
|
UTSW |
14 |
30,872,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R1260:Stab1
|
UTSW |
14 |
30,873,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R1400:Stab1
|
UTSW |
14 |
30,861,787 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1405:Stab1
|
UTSW |
14 |
30,870,958 (GRCm39) |
missense |
probably benign |
0.19 |
R1405:Stab1
|
UTSW |
14 |
30,870,958 (GRCm39) |
missense |
probably benign |
0.19 |
R1440:Stab1
|
UTSW |
14 |
30,873,647 (GRCm39) |
nonsense |
probably null |
|
R1472:Stab1
|
UTSW |
14 |
30,863,543 (GRCm39) |
missense |
probably benign |
0.01 |
R1474:Stab1
|
UTSW |
14 |
30,871,818 (GRCm39) |
missense |
probably benign |
0.45 |
R1475:Stab1
|
UTSW |
14 |
30,885,785 (GRCm39) |
missense |
probably benign |
|
R1509:Stab1
|
UTSW |
14 |
30,873,541 (GRCm39) |
splice site |
probably benign |
|
R1551:Stab1
|
UTSW |
14 |
30,882,456 (GRCm39) |
missense |
probably benign |
0.00 |
R1572:Stab1
|
UTSW |
14 |
30,872,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Stab1
|
UTSW |
14 |
30,872,337 (GRCm39) |
splice site |
probably null |
|
R1719:Stab1
|
UTSW |
14 |
30,867,985 (GRCm39) |
nonsense |
probably null |
|
R1733:Stab1
|
UTSW |
14 |
30,867,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:Stab1
|
UTSW |
14 |
30,890,373 (GRCm39) |
missense |
probably benign |
0.04 |
R1808:Stab1
|
UTSW |
14 |
30,863,101 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1816:Stab1
|
UTSW |
14 |
30,879,422 (GRCm39) |
missense |
probably benign |
0.03 |
R1853:Stab1
|
UTSW |
14 |
30,862,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Stab1
|
UTSW |
14 |
30,863,287 (GRCm39) |
missense |
probably benign |
0.07 |
R1984:Stab1
|
UTSW |
14 |
30,872,605 (GRCm39) |
missense |
probably benign |
0.20 |
R1998:Stab1
|
UTSW |
14 |
30,884,110 (GRCm39) |
nonsense |
probably null |
|
R2165:Stab1
|
UTSW |
14 |
30,890,392 (GRCm39) |
missense |
probably benign |
0.20 |
R2191:Stab1
|
UTSW |
14 |
30,881,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Stab1
|
UTSW |
14 |
30,864,757 (GRCm39) |
missense |
probably benign |
0.03 |
R2233:Stab1
|
UTSW |
14 |
30,883,837 (GRCm39) |
missense |
probably benign |
0.08 |
R2303:Stab1
|
UTSW |
14 |
30,868,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R2496:Stab1
|
UTSW |
14 |
30,883,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Stab1
|
UTSW |
14 |
30,884,997 (GRCm39) |
critical splice donor site |
probably null |
|
R2519:Stab1
|
UTSW |
14 |
30,876,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R2926:Stab1
|
UTSW |
14 |
30,883,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R4025:Stab1
|
UTSW |
14 |
30,876,909 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4113:Stab1
|
UTSW |
14 |
30,890,436 (GRCm39) |
missense |
probably damaging |
0.98 |
R4258:Stab1
|
UTSW |
14 |
30,876,629 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4588:Stab1
|
UTSW |
14 |
30,879,402 (GRCm39) |
missense |
probably benign |
0.01 |
R4644:Stab1
|
UTSW |
14 |
30,862,444 (GRCm39) |
unclassified |
probably benign |
|
R4660:Stab1
|
UTSW |
14 |
30,876,872 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4801:Stab1
|
UTSW |
14 |
30,863,328 (GRCm39) |
nonsense |
probably null |
|
R4802:Stab1
|
UTSW |
14 |
30,863,328 (GRCm39) |
nonsense |
probably null |
|
R4870:Stab1
|
UTSW |
14 |
30,864,000 (GRCm39) |
missense |
probably benign |
0.13 |
R4872:Stab1
|
UTSW |
14 |
30,862,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R4881:Stab1
|
UTSW |
14 |
30,865,629 (GRCm39) |
missense |
probably benign |
0.32 |
R4941:Stab1
|
UTSW |
14 |
30,873,528 (GRCm39) |
missense |
probably benign |
0.00 |
R5061:Stab1
|
UTSW |
14 |
30,885,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Stab1
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Stab1
|
UTSW |
14 |
30,865,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5087:Stab1
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Stab1
|
UTSW |
14 |
30,867,812 (GRCm39) |
missense |
probably benign |
0.01 |
R5102:Stab1
|
UTSW |
14 |
30,869,974 (GRCm39) |
critical splice donor site |
probably null |
|
R5107:Stab1
|
UTSW |
14 |
30,885,752 (GRCm39) |
splice site |
probably null |
|
R5195:Stab1
|
UTSW |
14 |
30,862,478 (GRCm39) |
unclassified |
probably benign |
|
R5217:Stab1
|
UTSW |
14 |
30,881,476 (GRCm39) |
missense |
probably benign |
0.25 |
R5285:Stab1
|
UTSW |
14 |
30,865,433 (GRCm39) |
unclassified |
probably benign |
|
R5327:Stab1
|
UTSW |
14 |
30,883,793 (GRCm39) |
nonsense |
probably null |
|
R5647:Stab1
|
UTSW |
14 |
30,879,397 (GRCm39) |
nonsense |
probably null |
|
R5696:Stab1
|
UTSW |
14 |
30,882,178 (GRCm39) |
missense |
probably benign |
|
R5996:Stab1
|
UTSW |
14 |
30,861,508 (GRCm39) |
missense |
probably benign |
0.39 |
R6016:Stab1
|
UTSW |
14 |
30,880,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R6017:Stab1
|
UTSW |
14 |
30,863,501 (GRCm39) |
missense |
probably benign |
0.00 |
R6174:Stab1
|
UTSW |
14 |
30,884,476 (GRCm39) |
nonsense |
probably null |
|
R6366:Stab1
|
UTSW |
14 |
30,863,395 (GRCm39) |
missense |
probably benign |
0.10 |
R6754:Stab1
|
UTSW |
14 |
30,863,038 (GRCm39) |
missense |
probably benign |
|
R6788:Stab1
|
UTSW |
14 |
30,861,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R6898:Stab1
|
UTSW |
14 |
30,880,920 (GRCm39) |
missense |
probably benign |
0.00 |
R7124:Stab1
|
UTSW |
14 |
30,882,824 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7145:Stab1
|
UTSW |
14 |
30,867,030 (GRCm39) |
critical splice donor site |
probably null |
|
R7153:Stab1
|
UTSW |
14 |
30,882,541 (GRCm39) |
missense |
probably benign |
0.16 |
R7213:Stab1
|
UTSW |
14 |
30,865,630 (GRCm39) |
missense |
probably benign |
|
R7215:Stab1
|
UTSW |
14 |
30,882,754 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7319:Stab1
|
UTSW |
14 |
30,862,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7389:Stab1
|
UTSW |
14 |
30,869,196 (GRCm39) |
missense |
probably benign |
0.00 |
R7400:Stab1
|
UTSW |
14 |
30,879,341 (GRCm39) |
missense |
probably null |
1.00 |
R7427:Stab1
|
UTSW |
14 |
30,881,216 (GRCm39) |
missense |
probably benign |
0.00 |
R7428:Stab1
|
UTSW |
14 |
30,881,216 (GRCm39) |
missense |
probably benign |
0.00 |
R7484:Stab1
|
UTSW |
14 |
30,882,274 (GRCm39) |
missense |
probably benign |
0.00 |
R7568:Stab1
|
UTSW |
14 |
30,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Stab1
|
UTSW |
14 |
30,876,622 (GRCm39) |
missense |
probably benign |
|
R7619:Stab1
|
UTSW |
14 |
30,867,194 (GRCm39) |
missense |
probably benign |
|
R7623:Stab1
|
UTSW |
14 |
30,862,578 (GRCm39) |
missense |
probably benign |
0.03 |
R7721:Stab1
|
UTSW |
14 |
30,863,413 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7869:Stab1
|
UTSW |
14 |
30,876,429 (GRCm39) |
missense |
probably benign |
0.01 |
R7936:Stab1
|
UTSW |
14 |
30,879,372 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7956:Stab1
|
UTSW |
14 |
30,881,981 (GRCm39) |
missense |
probably benign |
0.02 |
R7973:Stab1
|
UTSW |
14 |
30,881,590 (GRCm39) |
critical splice donor site |
probably null |
|
R8059:Stab1
|
UTSW |
14 |
30,882,198 (GRCm39) |
missense |
probably benign |
0.02 |
R8116:Stab1
|
UTSW |
14 |
30,880,910 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8304:Stab1
|
UTSW |
14 |
30,870,911 (GRCm39) |
missense |
probably benign |
0.14 |
R8368:Stab1
|
UTSW |
14 |
30,870,368 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8495:Stab1
|
UTSW |
14 |
30,877,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8513:Stab1
|
UTSW |
14 |
30,871,747 (GRCm39) |
critical splice donor site |
probably null |
|
R8544:Stab1
|
UTSW |
14 |
30,885,008 (GRCm39) |
nonsense |
probably null |
|
R8671:Stab1
|
UTSW |
14 |
30,879,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Stab1
|
UTSW |
14 |
30,883,771 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8974:Stab1
|
UTSW |
14 |
30,882,779 (GRCm39) |
missense |
probably benign |
|
R9022:Stab1
|
UTSW |
14 |
30,882,226 (GRCm39) |
missense |
probably benign |
0.01 |
R9059:Stab1
|
UTSW |
14 |
30,876,805 (GRCm39) |
missense |
probably benign |
0.01 |
R9226:Stab1
|
UTSW |
14 |
30,867,812 (GRCm39) |
missense |
probably benign |
0.00 |
R9272:Stab1
|
UTSW |
14 |
30,867,298 (GRCm39) |
missense |
probably benign |
0.05 |
R9388:Stab1
|
UTSW |
14 |
30,876,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R9401:Stab1
|
UTSW |
14 |
30,883,069 (GRCm39) |
missense |
probably benign |
|
R9433:Stab1
|
UTSW |
14 |
30,865,531 (GRCm39) |
missense |
probably benign |
0.00 |
R9450:Stab1
|
UTSW |
14 |
30,884,896 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9505:Stab1
|
UTSW |
14 |
30,877,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Stab1
|
UTSW |
14 |
30,864,638 (GRCm39) |
missense |
probably benign |
0.01 |
R9624:Stab1
|
UTSW |
14 |
30,863,345 (GRCm39) |
missense |
|
|
R9694:Stab1
|
UTSW |
14 |
30,876,901 (GRCm39) |
missense |
probably benign |
0.06 |
R9723:Stab1
|
UTSW |
14 |
30,885,848 (GRCm39) |
missense |
probably benign |
0.10 |
X0026:Stab1
|
UTSW |
14 |
30,884,148 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1176:Stab1
|
UTSW |
14 |
30,872,617 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Stab1
|
UTSW |
14 |
30,863,995 (GRCm39) |
missense |
probably benign |
0.00 |
|