Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933411K16Rik |
T |
G |
19: 42,041,515 (GRCm39) |
S215R |
possibly damaging |
Het |
Abcc9 |
T |
C |
6: 142,627,867 (GRCm39) |
M388V |
probably benign |
Het |
Acbd6 |
A |
C |
1: 155,477,275 (GRCm39) |
T154P |
probably benign |
Het |
Ago1 |
T |
C |
4: 126,347,447 (GRCm39) |
D434G |
probably damaging |
Het |
Ankib1 |
A |
T |
5: 3,819,652 (GRCm39) |
M89K |
probably benign |
Het |
Arap2 |
A |
T |
5: 62,833,868 (GRCm39) |
H866Q |
probably damaging |
Het |
Armh3 |
T |
C |
19: 45,939,146 (GRCm39) |
T335A |
probably benign |
Het |
Capn12 |
A |
T |
7: 28,589,795 (GRCm39) |
H622L |
probably benign |
Het |
Capns2 |
T |
G |
8: 93,628,530 (GRCm39) |
F140V |
probably damaging |
Het |
Catsper1 |
T |
G |
19: 5,385,991 (GRCm39) |
F75V |
probably benign |
Het |
Ccdc24 |
T |
C |
4: 117,729,297 (GRCm39) |
N16S |
probably benign |
Het |
Cdkn2aip |
A |
T |
8: 48,165,964 (GRCm39) |
L114Q |
probably damaging |
Het |
Cenpe |
T |
A |
3: 134,940,689 (GRCm39) |
S649R |
probably damaging |
Het |
Chgb |
A |
T |
2: 132,635,602 (GRCm39) |
R515W |
probably damaging |
Het |
Chrnb1 |
A |
G |
11: 69,684,804 (GRCm39) |
F123S |
probably damaging |
Het |
Copz2 |
A |
T |
11: 96,748,377 (GRCm39) |
|
probably null |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Daw1 |
C |
A |
1: 83,165,719 (GRCm39) |
A178E |
probably benign |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Epb41l5 |
T |
C |
1: 119,482,801 (GRCm39) |
D629G |
probably benign |
Het |
Erap1 |
A |
G |
13: 74,838,829 (GRCm39) |
E925G |
probably benign |
Het |
Exoc7 |
A |
C |
11: 116,180,095 (GRCm39) |
F657V |
probably damaging |
Het |
Fam210b |
G |
C |
2: 172,187,585 (GRCm39) |
A2P |
probably damaging |
Homo |
Fry |
A |
G |
5: 150,321,719 (GRCm39) |
E1018G |
probably damaging |
Het |
Galc |
A |
T |
12: 98,209,027 (GRCm39) |
L15* |
probably null |
Het |
Gm11232 |
T |
A |
4: 71,675,138 (GRCm39) |
K121N |
possibly damaging |
Het |
Hectd1 |
A |
T |
12: 51,831,045 (GRCm39) |
D931E |
probably benign |
Het |
Hecw2 |
T |
C |
1: 53,871,830 (GRCm39) |
H1372R |
probably benign |
Het |
Ighv3-2 |
T |
A |
12: 113,997,606 (GRCm39) |
|
noncoding transcript |
Het |
Kcns2 |
T |
G |
15: 34,839,751 (GRCm39) |
S371R |
probably damaging |
Het |
Kif23 |
T |
C |
9: 61,843,985 (GRCm39) |
K175E |
probably benign |
Het |
Kmt2c |
G |
A |
5: 25,500,509 (GRCm39) |
R436W |
possibly damaging |
Het |
Lama5 |
A |
G |
2: 179,835,242 (GRCm39) |
S1317P |
probably benign |
Het |
Lce1e |
T |
C |
3: 92,615,135 (GRCm39) |
S71G |
unknown |
Het |
Lrrc37a |
T |
A |
11: 103,388,444 (GRCm39) |
E2327V |
unknown |
Het |
Map3k20 |
A |
G |
2: 72,232,411 (GRCm39) |
M356V |
probably benign |
Het |
Metap2 |
G |
T |
10: 93,725,462 (GRCm39) |
T30K |
possibly damaging |
Het |
Mysm1 |
T |
A |
4: 94,861,207 (GRCm39) |
T53S |
probably benign |
Het |
Nasp |
A |
T |
4: 116,459,382 (GRCm39) |
D717E |
probably damaging |
Het |
Ndnf |
G |
A |
6: 65,680,555 (GRCm39) |
R278H |
possibly damaging |
Het |
Neb |
A |
T |
2: 52,106,273 (GRCm39) |
N4205K |
probably damaging |
Het |
Nebl |
A |
T |
2: 17,380,082 (GRCm39) |
I764N |
possibly damaging |
Het |
Nucb1 |
A |
G |
7: 45,148,313 (GRCm39) |
Y131H |
probably damaging |
Het |
Or14c39 |
A |
C |
7: 86,343,687 (GRCm39) |
T8P |
probably benign |
Het |
Or1e22 |
A |
G |
11: 73,377,623 (GRCm39) |
I9T |
probably benign |
Het |
Or5l14 |
G |
T |
2: 87,793,042 (GRCm39) |
H65N |
probably benign |
Het |
Oscp1 |
T |
A |
4: 125,970,555 (GRCm39) |
C115S |
probably benign |
Het |
Paip2 |
C |
T |
18: 35,746,412 (GRCm39) |
R59C |
possibly damaging |
Het |
Pate10 |
T |
G |
9: 35,653,465 (GRCm39) |
F90V |
probably benign |
Het |
Pcdhga4 |
G |
A |
18: 37,819,572 (GRCm39) |
D374N |
probably damaging |
Het |
Pcolce |
G |
T |
5: 137,603,936 (GRCm39) |
|
probably benign |
Het |
Pcyox1l |
T |
C |
18: 61,832,468 (GRCm39) |
E193G |
probably damaging |
Het |
Pde6b |
A |
T |
5: 108,573,196 (GRCm39) |
Q522L |
probably benign |
Het |
Peg10 |
T |
TCCG |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Phf11a |
A |
G |
14: 59,521,887 (GRCm39) |
F95L |
probably benign |
Het |
Pja2 |
A |
C |
17: 64,616,053 (GRCm39) |
S281A |
probably benign |
Het |
Plekhm2 |
A |
G |
4: 141,361,687 (GRCm39) |
F272S |
probably damaging |
Het |
Pom121l2 |
T |
C |
13: 22,167,984 (GRCm39) |
S752P |
probably benign |
Het |
Ppl |
T |
C |
16: 4,906,582 (GRCm39) |
T1238A |
possibly damaging |
Het |
Prmt7 |
A |
G |
8: 106,976,995 (GRCm39) |
Y569C |
probably damaging |
Het |
Prss37 |
G |
A |
6: 40,493,070 (GRCm39) |
T132I |
probably benign |
Het |
Psmf1 |
A |
T |
2: 151,571,377 (GRCm39) |
|
probably benign |
Het |
Ptprj |
A |
C |
2: 90,290,876 (GRCm39) |
I528S |
probably damaging |
Het |
Reg1 |
A |
G |
6: 78,405,196 (GRCm39) |
T140A |
possibly damaging |
Het |
Rtn4 |
A |
G |
11: 29,657,217 (GRCm39) |
N457S |
probably benign |
Het |
Rusf1 |
C |
T |
7: 127,875,645 (GRCm39) |
|
probably benign |
Het |
Scn9a |
T |
C |
2: 66,396,614 (GRCm39) |
K93R |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,329,531 (GRCm39) |
V828A |
probably benign |
Het |
Sec23b |
T |
A |
2: 144,423,873 (GRCm39) |
D507E |
probably benign |
Het |
Sirt4 |
A |
T |
5: 115,620,850 (GRCm39) |
F107L |
probably benign |
Het |
Slc14a2 |
A |
T |
18: 78,193,616 (GRCm39) |
L862Q |
probably damaging |
Het |
Slc16a4 |
T |
C |
3: 107,208,176 (GRCm39) |
S229P |
probably benign |
Het |
Slc37a3 |
A |
T |
6: 39,329,651 (GRCm39) |
C185* |
probably null |
Het |
Slc5a2 |
A |
T |
7: 127,870,982 (GRCm39) |
*154C |
probably null |
Het |
Snx17 |
A |
G |
5: 31,353,138 (GRCm39) |
S42G |
possibly damaging |
Het |
Tgm6 |
T |
C |
2: 129,983,113 (GRCm39) |
V234A |
probably damaging |
Het |
Thbs4 |
A |
G |
13: 92,927,207 (GRCm39) |
M94T |
probably benign |
Het |
Thtpa |
A |
G |
14: 55,309,605 (GRCm39) |
|
probably benign |
Het |
Tie1 |
T |
C |
4: 118,340,952 (GRCm39) |
E343G |
probably damaging |
Het |
Tmem145 |
A |
G |
7: 25,008,027 (GRCm39) |
I238V |
probably benign |
Het |
Tmprss11f |
T |
C |
5: 86,685,858 (GRCm39) |
S170G |
probably benign |
Het |
Tnk2 |
T |
A |
16: 32,499,283 (GRCm39) |
D865E |
probably damaging |
Het |
Ttll8 |
T |
C |
15: 88,809,785 (GRCm39) |
E337G |
probably benign |
Het |
Ttn |
G |
A |
2: 76,697,790 (GRCm39) |
|
probably benign |
Het |
Tubgcp6 |
T |
C |
15: 88,990,494 (GRCm39) |
E710G |
probably damaging |
Het |
Txndc2 |
T |
A |
17: 65,945,055 (GRCm39) |
H374L |
probably benign |
Het |
Unc80 |
G |
T |
1: 66,713,891 (GRCm39) |
|
probably null |
Het |
Vmn2r23 |
G |
A |
6: 123,710,308 (GRCm39) |
C537Y |
probably damaging |
Het |
Vmn2r45 |
A |
G |
7: 8,486,116 (GRCm39) |
F391L |
probably damaging |
Het |
Vstm4 |
A |
T |
14: 32,641,202 (GRCm39) |
T262S |
probably benign |
Het |
Zfp180 |
C |
T |
7: 23,805,503 (GRCm39) |
R641C |
probably damaging |
Het |
Zfp979 |
A |
T |
4: 147,698,371 (GRCm39) |
S113T |
possibly damaging |
Het |
Zswim4 |
C |
T |
8: 84,953,296 (GRCm39) |
|
probably null |
Het |
Zswim5 |
T |
A |
4: 116,842,883 (GRCm39) |
M876K |
possibly damaging |
Het |
|
Other mutations in Med12l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Med12l
|
APN |
3 |
58,949,757 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00561:Med12l
|
APN |
3 |
59,135,245 (GRCm39) |
missense |
probably benign |
|
IGL00974:Med12l
|
APN |
3 |
58,990,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01024:Med12l
|
APN |
3 |
58,980,762 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01094:Med12l
|
APN |
3 |
59,001,076 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01134:Med12l
|
APN |
3 |
58,949,696 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01535:Med12l
|
APN |
3 |
59,169,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01653:Med12l
|
APN |
3 |
59,169,314 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01735:Med12l
|
APN |
3 |
59,170,675 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01972:Med12l
|
APN |
3 |
59,169,314 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02005:Med12l
|
APN |
3 |
59,152,368 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02098:Med12l
|
APN |
3 |
59,183,276 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02115:Med12l
|
APN |
3 |
58,975,740 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02231:Med12l
|
APN |
3 |
59,153,303 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02259:Med12l
|
APN |
3 |
59,153,264 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02369:Med12l
|
APN |
3 |
59,164,794 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02424:Med12l
|
APN |
3 |
59,000,143 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02501:Med12l
|
APN |
3 |
59,169,397 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02525:Med12l
|
APN |
3 |
58,975,789 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02530:Med12l
|
APN |
3 |
58,984,510 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02735:Med12l
|
APN |
3 |
59,001,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02865:Med12l
|
APN |
3 |
59,201,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03183:Med12l
|
APN |
3 |
58,944,976 (GRCm39) |
splice site |
probably null |
|
IGL03264:Med12l
|
APN |
3 |
59,208,788 (GRCm39) |
nonsense |
probably null |
|
FR4304:Med12l
|
UTSW |
3 |
59,183,403 (GRCm39) |
small insertion |
probably benign |
|
FR4340:Med12l
|
UTSW |
3 |
59,183,406 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Med12l
|
UTSW |
3 |
59,183,415 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Med12l
|
UTSW |
3 |
59,183,409 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Med12l
|
UTSW |
3 |
59,183,384 (GRCm39) |
nonsense |
probably null |
|
FR4548:Med12l
|
UTSW |
3 |
59,183,403 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Med12l
|
UTSW |
3 |
59,183,377 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Med12l
|
UTSW |
3 |
59,183,398 (GRCm39) |
small insertion |
probably benign |
|
P0007:Med12l
|
UTSW |
3 |
58,998,816 (GRCm39) |
splice site |
probably benign |
|
P0045:Med12l
|
UTSW |
3 |
58,998,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R0030:Med12l
|
UTSW |
3 |
59,156,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R0030:Med12l
|
UTSW |
3 |
59,156,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R0148:Med12l
|
UTSW |
3 |
58,945,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Med12l
|
UTSW |
3 |
58,984,480 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0330:Med12l
|
UTSW |
3 |
59,135,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R0388:Med12l
|
UTSW |
3 |
59,000,925 (GRCm39) |
splice site |
probably benign |
|
R0542:Med12l
|
UTSW |
3 |
58,949,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Med12l
|
UTSW |
3 |
58,945,123 (GRCm39) |
nonsense |
probably null |
|
R0625:Med12l
|
UTSW |
3 |
59,154,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Med12l
|
UTSW |
3 |
59,172,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R0706:Med12l
|
UTSW |
3 |
59,169,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R0785:Med12l
|
UTSW |
3 |
59,168,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R1054:Med12l
|
UTSW |
3 |
59,156,072 (GRCm39) |
missense |
probably damaging |
0.99 |
R1102:Med12l
|
UTSW |
3 |
59,152,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R1391:Med12l
|
UTSW |
3 |
58,945,159 (GRCm39) |
missense |
probably benign |
0.00 |
R1501:Med12l
|
UTSW |
3 |
59,168,256 (GRCm39) |
critical splice donor site |
probably null |
|
R1544:Med12l
|
UTSW |
3 |
59,172,661 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1662:Med12l
|
UTSW |
3 |
59,001,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R1670:Med12l
|
UTSW |
3 |
59,183,379 (GRCm39) |
small insertion |
probably benign |
|
R1839:Med12l
|
UTSW |
3 |
58,975,740 (GRCm39) |
missense |
probably benign |
|
R1854:Med12l
|
UTSW |
3 |
59,168,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Med12l
|
UTSW |
3 |
59,169,731 (GRCm39) |
nonsense |
probably null |
|
R2070:Med12l
|
UTSW |
3 |
59,152,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Med12l
|
UTSW |
3 |
59,172,703 (GRCm39) |
splice site |
probably null |
|
R2290:Med12l
|
UTSW |
3 |
59,152,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R2325:Med12l
|
UTSW |
3 |
59,139,875 (GRCm39) |
missense |
probably damaging |
0.99 |
R2352:Med12l
|
UTSW |
3 |
59,148,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R2484:Med12l
|
UTSW |
3 |
59,205,259 (GRCm39) |
missense |
probably benign |
0.18 |
R2906:Med12l
|
UTSW |
3 |
59,164,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R3735:Med12l
|
UTSW |
3 |
58,998,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R3736:Med12l
|
UTSW |
3 |
58,998,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R3774:Med12l
|
UTSW |
3 |
59,155,363 (GRCm39) |
missense |
probably damaging |
0.97 |
R3957:Med12l
|
UTSW |
3 |
58,980,589 (GRCm39) |
missense |
probably damaging |
0.99 |
R4020:Med12l
|
UTSW |
3 |
59,155,363 (GRCm39) |
missense |
probably damaging |
0.97 |
R4087:Med12l
|
UTSW |
3 |
59,205,342 (GRCm39) |
missense |
probably benign |
0.00 |
R4231:Med12l
|
UTSW |
3 |
59,164,644 (GRCm39) |
splice site |
probably null |
|
R4233:Med12l
|
UTSW |
3 |
59,164,644 (GRCm39) |
splice site |
probably null |
|
R4235:Med12l
|
UTSW |
3 |
59,164,644 (GRCm39) |
splice site |
probably null |
|
R4236:Med12l
|
UTSW |
3 |
59,164,644 (GRCm39) |
splice site |
probably null |
|
R4327:Med12l
|
UTSW |
3 |
59,172,688 (GRCm39) |
missense |
probably benign |
0.01 |
R4328:Med12l
|
UTSW |
3 |
59,172,688 (GRCm39) |
missense |
probably benign |
0.01 |
R4346:Med12l
|
UTSW |
3 |
58,938,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R4543:Med12l
|
UTSW |
3 |
58,998,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R4559:Med12l
|
UTSW |
3 |
58,914,523 (GRCm39) |
critical splice donor site |
probably null |
|
R4776:Med12l
|
UTSW |
3 |
59,140,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R4877:Med12l
|
UTSW |
3 |
59,152,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R5114:Med12l
|
UTSW |
3 |
59,167,109 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5125:Med12l
|
UTSW |
3 |
59,174,635 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5230:Med12l
|
UTSW |
3 |
59,153,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R5407:Med12l
|
UTSW |
3 |
59,165,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R5426:Med12l
|
UTSW |
3 |
59,156,143 (GRCm39) |
missense |
probably damaging |
0.98 |
R5439:Med12l
|
UTSW |
3 |
59,170,634 (GRCm39) |
missense |
probably null |
1.00 |
R5449:Med12l
|
UTSW |
3 |
59,167,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R5596:Med12l
|
UTSW |
3 |
59,159,771 (GRCm39) |
missense |
probably benign |
0.45 |
R5716:Med12l
|
UTSW |
3 |
59,208,798 (GRCm39) |
critical splice donor site |
probably null |
|
R5833:Med12l
|
UTSW |
3 |
59,172,647 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5883:Med12l
|
UTSW |
3 |
58,998,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R6264:Med12l
|
UTSW |
3 |
59,163,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R6269:Med12l
|
UTSW |
3 |
59,135,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R6394:Med12l
|
UTSW |
3 |
59,142,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6400:Med12l
|
UTSW |
3 |
59,155,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R6475:Med12l
|
UTSW |
3 |
59,164,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R6489:Med12l
|
UTSW |
3 |
59,164,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R6654:Med12l
|
UTSW |
3 |
59,169,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R6881:Med12l
|
UTSW |
3 |
59,174,586 (GRCm39) |
missense |
probably benign |
0.00 |
R7110:Med12l
|
UTSW |
3 |
59,169,645 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7134:Med12l
|
UTSW |
3 |
59,001,180 (GRCm39) |
nonsense |
probably null |
|
R7137:Med12l
|
UTSW |
3 |
59,165,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R7159:Med12l
|
UTSW |
3 |
59,183,438 (GRCm39) |
missense |
probably benign |
|
R7341:Med12l
|
UTSW |
3 |
58,949,824 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7349:Med12l
|
UTSW |
3 |
59,165,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7413:Med12l
|
UTSW |
3 |
58,998,971 (GRCm39) |
missense |
probably benign |
0.00 |
R7495:Med12l
|
UTSW |
3 |
59,152,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Med12l
|
UTSW |
3 |
58,984,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R7697:Med12l
|
UTSW |
3 |
59,148,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R7714:Med12l
|
UTSW |
3 |
59,001,007 (GRCm39) |
missense |
probably benign |
0.17 |
R7725:Med12l
|
UTSW |
3 |
59,163,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Med12l
|
UTSW |
3 |
59,172,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R7852:Med12l
|
UTSW |
3 |
59,155,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R8080:Med12l
|
UTSW |
3 |
59,172,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R8181:Med12l
|
UTSW |
3 |
59,169,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R8223:Med12l
|
UTSW |
3 |
58,993,784 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8560:Med12l
|
UTSW |
3 |
58,945,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Med12l
|
UTSW |
3 |
59,159,751 (GRCm39) |
missense |
probably benign |
0.00 |
R8865:Med12l
|
UTSW |
3 |
58,979,303 (GRCm39) |
missense |
probably benign |
|
R8947:Med12l
|
UTSW |
3 |
58,984,443 (GRCm39) |
splice site |
probably benign |
|
R8976:Med12l
|
UTSW |
3 |
59,183,329 (GRCm39) |
missense |
probably damaging |
0.99 |
R9016:Med12l
|
UTSW |
3 |
59,163,294 (GRCm39) |
missense |
probably damaging |
0.96 |
R9183:Med12l
|
UTSW |
3 |
58,984,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R9487:Med12l
|
UTSW |
3 |
59,155,353 (GRCm39) |
missense |
probably benign |
|
R9526:Med12l
|
UTSW |
3 |
58,984,207 (GRCm39) |
missense |
probably damaging |
0.96 |
R9802:Med12l
|
UTSW |
3 |
59,169,346 (GRCm39) |
missense |
probably damaging |
1.00 |
RF004:Med12l
|
UTSW |
3 |
59,183,390 (GRCm39) |
small insertion |
probably benign |
|
RF011:Med12l
|
UTSW |
3 |
59,183,401 (GRCm39) |
small insertion |
probably benign |
|
RF013:Med12l
|
UTSW |
3 |
59,183,387 (GRCm39) |
small insertion |
probably benign |
|
RF020:Med12l
|
UTSW |
3 |
59,183,379 (GRCm39) |
small insertion |
probably benign |
|
RF021:Med12l
|
UTSW |
3 |
58,980,711 (GRCm39) |
missense |
probably benign |
0.19 |
RF027:Med12l
|
UTSW |
3 |
59,183,402 (GRCm39) |
small insertion |
probably benign |
|
RF027:Med12l
|
UTSW |
3 |
59,183,388 (GRCm39) |
small insertion |
probably benign |
|
RF030:Med12l
|
UTSW |
3 |
59,183,410 (GRCm39) |
small insertion |
probably benign |
|
RF032:Med12l
|
UTSW |
3 |
59,183,410 (GRCm39) |
small insertion |
probably benign |
|
RF032:Med12l
|
UTSW |
3 |
59,183,406 (GRCm39) |
small insertion |
probably benign |
|
RF032:Med12l
|
UTSW |
3 |
59,183,402 (GRCm39) |
small insertion |
probably benign |
|
RF033:Med12l
|
UTSW |
3 |
59,183,416 (GRCm39) |
small insertion |
probably benign |
|
RF033:Med12l
|
UTSW |
3 |
59,183,408 (GRCm39) |
small insertion |
probably benign |
|
RF033:Med12l
|
UTSW |
3 |
59,183,402 (GRCm39) |
small insertion |
probably benign |
|
RF037:Med12l
|
UTSW |
3 |
59,183,377 (GRCm39) |
small insertion |
probably benign |
|
RF040:Med12l
|
UTSW |
3 |
59,183,410 (GRCm39) |
small insertion |
probably benign |
|
RF040:Med12l
|
UTSW |
3 |
59,183,388 (GRCm39) |
small insertion |
probably benign |
|
RF041:Med12l
|
UTSW |
3 |
59,183,416 (GRCm39) |
small insertion |
probably benign |
|
RF041:Med12l
|
UTSW |
3 |
59,183,406 (GRCm39) |
small insertion |
probably benign |
|
RF042:Med12l
|
UTSW |
3 |
59,183,402 (GRCm39) |
small insertion |
probably benign |
|
RF042:Med12l
|
UTSW |
3 |
59,183,388 (GRCm39) |
small insertion |
probably benign |
|
RF042:Med12l
|
UTSW |
3 |
59,183,377 (GRCm39) |
small insertion |
probably benign |
|
RF042:Med12l
|
UTSW |
3 |
59,183,416 (GRCm39) |
small insertion |
probably benign |
|
RF049:Med12l
|
UTSW |
3 |
59,183,390 (GRCm39) |
small insertion |
probably benign |
|
RF050:Med12l
|
UTSW |
3 |
59,183,394 (GRCm39) |
small insertion |
probably benign |
|
RF053:Med12l
|
UTSW |
3 |
59,183,414 (GRCm39) |
small insertion |
probably benign |
|
RF055:Med12l
|
UTSW |
3 |
59,183,404 (GRCm39) |
small insertion |
probably benign |
|
RF056:Med12l
|
UTSW |
3 |
59,183,414 (GRCm39) |
small insertion |
probably benign |
|
RF057:Med12l
|
UTSW |
3 |
59,183,401 (GRCm39) |
small insertion |
probably benign |
|
RF063:Med12l
|
UTSW |
3 |
59,183,394 (GRCm39) |
small insertion |
probably benign |
|
RF063:Med12l
|
UTSW |
3 |
59,183,379 (GRCm39) |
small insertion |
probably benign |
|
X0062:Med12l
|
UTSW |
3 |
59,140,600 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Med12l
|
UTSW |
3 |
59,203,538 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Med12l
|
UTSW |
3 |
59,152,364 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Med12l
|
UTSW |
3 |
58,998,838 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Med12l
|
UTSW |
3 |
59,155,296 (GRCm39) |
missense |
probably damaging |
1.00 |
|