Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700019A02Rik |
C |
T |
1: 53,221,665 (GRCm39) |
D55N |
possibly damaging |
Het |
Abcc2 |
G |
A |
19: 43,806,471 (GRCm39) |
G762S |
probably damaging |
Het |
Acta2 |
C |
A |
19: 34,225,865 (GRCm39) |
A110S |
probably damaging |
Het |
Adam26a |
T |
C |
8: 44,022,456 (GRCm39) |
T345A |
possibly damaging |
Het |
Anapc11 |
T |
C |
11: 120,496,250 (GRCm39) |
*85R |
probably null |
Het |
Ang2 |
A |
C |
14: 51,433,071 (GRCm39) |
C104G |
probably damaging |
Het |
Ankzf1 |
G |
A |
1: 75,174,596 (GRCm39) |
V529I |
probably benign |
Het |
Aox4 |
G |
T |
1: 58,288,097 (GRCm39) |
V737F |
probably benign |
Het |
Aqr |
T |
C |
2: 113,934,528 (GRCm39) |
N1371S |
probably benign |
Het |
Bach1 |
T |
A |
16: 87,526,733 (GRCm39) |
S732T |
probably benign |
Het |
Bcr |
T |
A |
10: 74,967,431 (GRCm39) |
I555N |
probably damaging |
Het |
Bicra |
T |
C |
7: 15,705,717 (GRCm39) |
T1575A |
probably damaging |
Het |
Bop1 |
A |
G |
15: 76,338,076 (GRCm39) |
L598P |
probably damaging |
Het |
Cacna1d |
A |
T |
14: 29,845,419 (GRCm39) |
F605L |
possibly damaging |
Het |
Capn15 |
C |
T |
17: 26,184,353 (GRCm39) |
V109I |
possibly damaging |
Het |
Cdkn1b |
T |
C |
6: 134,897,815 (GRCm39) |
|
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,406,617 (GRCm39) |
T542A |
possibly damaging |
Het |
Dsc2 |
A |
T |
18: 20,180,276 (GRCm39) |
I159N |
probably damaging |
Het |
Ecel1 |
A |
T |
1: 87,075,716 (GRCm39) |
V774E |
probably damaging |
Het |
Eif5b |
T |
G |
1: 38,084,560 (GRCm39) |
C849W |
probably damaging |
Het |
Eif5b |
T |
A |
1: 38,058,451 (GRCm39) |
L251* |
probably null |
Het |
Ext2 |
T |
C |
2: 93,592,956 (GRCm39) |
D416G |
probably damaging |
Het |
Fancm |
G |
A |
12: 65,153,388 (GRCm39) |
W1281* |
probably null |
Het |
Flvcr1 |
A |
T |
1: 190,743,829 (GRCm39) |
I409K |
possibly damaging |
Het |
Foxk1 |
T |
C |
5: 142,437,389 (GRCm39) |
|
probably null |
Het |
Frem2 |
T |
A |
3: 53,560,905 (GRCm39) |
I1201F |
possibly damaging |
Het |
Gabra5 |
A |
G |
7: 57,157,873 (GRCm39) |
|
probably benign |
Het |
Gmpr2 |
G |
A |
14: 55,915,778 (GRCm39) |
V319I |
probably damaging |
Het |
Gna12 |
A |
T |
5: 140,746,338 (GRCm39) |
L369Q |
probably damaging |
Het |
Gpr160 |
A |
G |
3: 30,950,914 (GRCm39) |
R329G |
probably benign |
Het |
H2-M10.3 |
T |
C |
17: 36,677,423 (GRCm39) |
H285R |
probably benign |
Het |
H2-M2 |
A |
T |
17: 37,793,424 (GRCm39) |
V194E |
probably benign |
Het |
Hephl1 |
G |
A |
9: 14,995,830 (GRCm39) |
R431W |
possibly damaging |
Het |
Hr |
A |
G |
14: 70,793,877 (GRCm39) |
T46A |
probably benign |
Het |
Hr |
A |
G |
14: 70,794,205 (GRCm39) |
H126R |
possibly damaging |
Het |
Hsf1 |
T |
G |
15: 76,382,398 (GRCm39) |
D256E |
probably benign |
Het |
Ifi208 |
C |
T |
1: 173,510,961 (GRCm39) |
T372I |
probably damaging |
Het |
Ifi47 |
T |
G |
11: 48,986,620 (GRCm39) |
F129C |
probably damaging |
Het |
Il1rl2 |
CTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTTATT |
CTTTATTTTATTTTATTTTATTTTATTTTATTTTATT |
1: 40,366,470 (GRCm39) |
|
probably benign |
Het |
Irag2 |
A |
G |
6: 145,120,257 (GRCm39) |
I491V |
probably benign |
Het |
Itga11 |
A |
T |
9: 62,670,171 (GRCm39) |
N765I |
probably benign |
Het |
Klhl22 |
T |
A |
16: 17,589,663 (GRCm39) |
I108K |
probably benign |
Het |
Lancl1 |
T |
G |
1: 67,073,381 (GRCm39) |
H34P |
probably benign |
Het |
Lcor |
C |
A |
19: 41,573,685 (GRCm39) |
N813K |
probably damaging |
Het |
Mbd3l1 |
G |
A |
9: 18,396,274 (GRCm39) |
G133D |
probably benign |
Het |
Mrm1 |
A |
T |
11: 84,705,531 (GRCm39) |
N289K |
probably damaging |
Het |
Myf6 |
A |
G |
10: 107,330,073 (GRCm39) |
Y165H |
probably benign |
Het |
Myo1g |
C |
A |
11: 6,456,913 (GRCm39) |
C971F |
probably benign |
Het |
Myo3a |
T |
C |
2: 22,245,862 (GRCm39) |
M3T |
probably benign |
Het |
Nsrp1 |
G |
A |
11: 76,937,114 (GRCm39) |
R361* |
probably null |
Het |
Or10d4 |
A |
C |
9: 39,580,611 (GRCm39) |
Q86P |
possibly damaging |
Het |
Or10h1b |
C |
A |
17: 33,395,548 (GRCm39) |
H57Q |
possibly damaging |
Het |
Or4a69 |
T |
C |
2: 89,312,756 (GRCm39) |
H241R |
probably damaging |
Het |
Or4a77 |
T |
C |
2: 89,487,731 (GRCm39) |
D18G |
probably damaging |
Het |
Or5p6 |
A |
T |
7: 107,631,163 (GRCm39) |
I129N |
possibly damaging |
Het |
Or8b41 |
G |
A |
9: 38,054,866 (GRCm39) |
C140Y |
probably benign |
Het |
Or8k53 |
T |
A |
2: 86,177,846 (GRCm39) |
D88V |
probably benign |
Het |
Oscar |
T |
G |
7: 3,614,663 (GRCm39) |
Y103S |
probably damaging |
Het |
Pdpr |
A |
G |
8: 111,852,925 (GRCm39) |
N610S |
probably benign |
Het |
Ppp4r3b |
T |
C |
11: 29,124,697 (GRCm39) |
I56T |
probably damaging |
Het |
Pxdn |
T |
A |
12: 30,044,552 (GRCm39) |
V510D |
possibly damaging |
Het |
Rab11fip5 |
T |
C |
6: 85,324,913 (GRCm39) |
S465G |
possibly damaging |
Het |
Rasgrf2 |
T |
C |
13: 92,267,759 (GRCm39) |
T82A |
probably benign |
Het |
Scmh1 |
G |
A |
4: 120,320,284 (GRCm39) |
W30* |
probably null |
Het |
Sema4g |
T |
C |
19: 44,981,071 (GRCm39) |
Y40H |
probably benign |
Het |
Serpinf2 |
A |
T |
11: 75,323,494 (GRCm39) |
M404K |
probably damaging |
Het |
Sgk3 |
T |
C |
1: 9,950,616 (GRCm39) |
|
probably null |
Het |
Slc16a5 |
A |
T |
11: 115,360,738 (GRCm39) |
Y307F |
possibly damaging |
Het |
Slc39a5 |
G |
A |
10: 128,233,628 (GRCm39) |
L290F |
probably damaging |
Het |
Snx32 |
A |
C |
19: 5,547,736 (GRCm39) |
D191E |
probably damaging |
Het |
Sp4 |
T |
C |
12: 118,262,859 (GRCm39) |
I396V |
probably benign |
Het |
Srrd |
A |
G |
5: 112,490,765 (GRCm39) |
V42A |
unknown |
Het |
Stim1 |
A |
G |
7: 102,080,257 (GRCm39) |
H547R |
unknown |
Het |
Svep1 |
G |
A |
4: 58,070,517 (GRCm39) |
A2423V |
probably benign |
Het |
Tep1 |
A |
G |
14: 51,066,687 (GRCm39) |
S2304P |
possibly damaging |
Het |
Tkt |
C |
G |
14: 30,281,795 (GRCm39) |
S104R |
probably benign |
Het |
Tkt |
T |
C |
14: 30,281,796 (GRCm39) |
S105P |
probably damaging |
Het |
Tln1 |
A |
T |
4: 43,542,893 (GRCm39) |
N1365K |
probably damaging |
Het |
Topaz1 |
G |
T |
9: 122,604,707 (GRCm39) |
A1104S |
probably benign |
Het |
Trmt2a |
A |
G |
16: 18,068,814 (GRCm39) |
H270R |
probably damaging |
Het |
Ttll10 |
G |
T |
4: 156,127,616 (GRCm39) |
T389K |
probably benign |
Het |
Tubal3 |
A |
G |
13: 3,980,674 (GRCm39) |
I129V |
probably benign |
Het |
Ucp3 |
A |
G |
7: 100,131,123 (GRCm39) |
E192G |
probably damaging |
Het |
Usp47 |
A |
G |
7: 111,677,063 (GRCm39) |
D448G |
probably damaging |
Het |
Vmn2r98 |
T |
A |
17: 19,301,496 (GRCm39) |
L833M |
possibly damaging |
Het |
Vps13d |
A |
G |
4: 144,807,869 (GRCm39) |
|
probably null |
Het |
Wdr7 |
A |
G |
18: 63,910,939 (GRCm39) |
D777G |
possibly damaging |
Het |
Zcchc8 |
A |
G |
5: 123,847,300 (GRCm39) |
I213T |
probably damaging |
Het |
Zfp281 |
T |
C |
1: 136,555,143 (GRCm39) |
I707T |
probably damaging |
Het |
Zfp335 |
T |
C |
2: 164,735,395 (GRCm39) |
H1158R |
probably damaging |
Het |
Zfp692 |
C |
T |
11: 58,199,765 (GRCm39) |
T118M |
probably damaging |
Het |
Zfr2 |
T |
A |
10: 81,075,969 (GRCm39) |
L192Q |
probably benign |
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 |
R4983:Med12l
|
UTSW |
3 |
59,169,350 (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 |
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 |
|