Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,285,215 (GRCm39) |
H3283L |
probably damaging |
Het |
Abcb1a |
T |
G |
5: 8,744,072 (GRCm39) |
S233A |
probably benign |
Het |
Actr10 |
T |
C |
12: 70,999,805 (GRCm39) |
|
probably null |
Het |
Acvr2b |
C |
T |
9: 119,261,619 (GRCm39) |
A380V |
probably damaging |
Het |
Adcy5 |
A |
G |
16: 35,119,995 (GRCm39) |
E1168G |
probably damaging |
Het |
Akap12 |
C |
T |
10: 4,303,226 (GRCm39) |
T117I |
probably damaging |
Het |
Alox5 |
T |
A |
6: 116,390,429 (GRCm39) |
Y516F |
probably benign |
Het |
Amigo2 |
T |
C |
15: 97,143,741 (GRCm39) |
N227S |
probably damaging |
Het |
Anpep |
C |
A |
7: 79,486,061 (GRCm39) |
V554L |
probably benign |
Het |
Ap5b1 |
T |
A |
19: 5,620,215 (GRCm39) |
V545E |
possibly damaging |
Het |
Bbs9 |
C |
T |
9: 22,490,849 (GRCm39) |
L326F |
probably damaging |
Het |
Bltp1 |
T |
G |
3: 36,994,947 (GRCm39) |
Y990D |
probably damaging |
Het |
Cadps |
C |
T |
14: 12,603,738 (GRCm38) |
G361R |
probably damaging |
Het |
Ccdc57 |
C |
A |
11: 120,812,557 (GRCm39) |
E66* |
probably null |
Het |
Ccr6 |
G |
A |
17: 8,475,019 (GRCm39) |
V75I |
probably benign |
Het |
Cdk6 |
T |
C |
5: 3,570,709 (GRCm39) |
F300S |
probably damaging |
Het |
Cenpb |
A |
C |
2: 131,020,799 (GRCm39) |
V333G |
probably damaging |
Het |
Clca4a |
T |
C |
3: 144,667,670 (GRCm39) |
I434V |
probably benign |
Het |
Coro2b |
T |
A |
9: 62,328,667 (GRCm39) |
D447V |
possibly damaging |
Het |
Cpeb3 |
T |
C |
19: 37,152,119 (GRCm39) |
S86G |
probably benign |
Het |
Cry2 |
C |
A |
2: 92,243,438 (GRCm39) |
A468S |
probably damaging |
Het |
Csf2rb2 |
T |
C |
15: 78,181,272 (GRCm39) |
Y40C |
probably damaging |
Het |
Ddx49 |
T |
A |
8: 70,753,726 (GRCm39) |
T48S |
probably damaging |
Het |
Dennd10 |
T |
A |
19: 60,821,034 (GRCm39) |
M272K |
probably damaging |
Het |
Dip2c |
A |
G |
13: 9,654,572 (GRCm39) |
T727A |
probably benign |
Het |
Dnai3 |
A |
T |
3: 145,761,459 (GRCm39) |
S632R |
possibly damaging |
Het |
Ebf4 |
A |
T |
2: 130,151,651 (GRCm39) |
I183F |
probably benign |
Het |
Elavl3 |
G |
T |
9: 21,930,025 (GRCm39) |
P293Q |
possibly damaging |
Het |
Esyt1 |
A |
T |
10: 128,352,105 (GRCm39) |
L768Q |
probably damaging |
Het |
Fat2 |
G |
A |
11: 55,174,260 (GRCm39) |
P2151L |
probably damaging |
Het |
Fgfbp3 |
G |
T |
19: 36,896,606 (GRCm39) |
A4E |
possibly damaging |
Het |
Flg |
T |
A |
3: 93,200,335 (GRCm39) |
V277D |
unknown |
Het |
Fndc3b |
T |
C |
3: 27,524,383 (GRCm39) |
D459G |
possibly damaging |
Het |
Fras1 |
A |
G |
5: 96,718,900 (GRCm39) |
Q438R |
probably benign |
Het |
Glipr1l2 |
A |
T |
10: 111,928,330 (GRCm39) |
|
probably null |
Het |
Gm7347 |
T |
A |
5: 26,262,382 (GRCm39) |
|
probably null |
Het |
Grm6 |
G |
A |
11: 50,753,804 (GRCm39) |
V703I |
possibly damaging |
Het |
Gtf2h1 |
T |
A |
7: 46,468,550 (GRCm39) |
V496E |
probably benign |
Het |
Ifna12 |
A |
G |
4: 88,521,388 (GRCm39) |
L53P |
probably damaging |
Het |
Invs |
T |
A |
4: 48,407,674 (GRCm39) |
S550T |
probably benign |
Het |
Irak2 |
G |
T |
6: 113,663,810 (GRCm39) |
C453F |
probably damaging |
Het |
Itih2 |
G |
T |
2: 10,110,574 (GRCm39) |
Q506K |
probably benign |
Het |
Kidins220 |
T |
C |
12: 25,107,662 (GRCm39) |
I1614T |
probably benign |
Het |
Krtap5-3 |
T |
A |
7: 141,755,992 (GRCm39) |
C276* |
probably null |
Het |
Lama3 |
T |
A |
18: 12,685,870 (GRCm39) |
M1128K |
possibly damaging |
Het |
Lhfpl4 |
C |
T |
6: 113,171,106 (GRCm39) |
A27T |
possibly damaging |
Het |
Lyplal1 |
A |
G |
1: 185,832,524 (GRCm39) |
V77A |
probably damaging |
Het |
Malrd1 |
A |
T |
2: 16,147,114 (GRCm39) |
E1985D |
unknown |
Het |
Mlx |
A |
C |
11: 100,979,802 (GRCm39) |
Q161P |
probably benign |
Het |
Myh7b |
A |
G |
2: 155,464,119 (GRCm39) |
E540G |
probably damaging |
Het |
Neb |
T |
A |
2: 52,194,067 (GRCm39) |
D653V |
probably damaging |
Het |
Nek10 |
T |
A |
14: 14,828,517 (GRCm38) |
L113Q |
probably damaging |
Het |
Nlrp4c |
T |
A |
7: 6,068,708 (GRCm39) |
L203* |
probably null |
Het |
Nscme3l |
T |
A |
19: 5,553,623 (GRCm39) |
T53S |
probably benign |
Het |
Ntpcr |
T |
A |
8: 126,456,794 (GRCm39) |
C5S |
unknown |
Het |
Nwd1 |
A |
G |
8: 73,421,957 (GRCm39) |
D1001G |
probably damaging |
Het |
Or12j5 |
T |
A |
7: 140,084,229 (GRCm39) |
T48S |
probably benign |
Het |
Or14a256 |
C |
T |
7: 86,265,475 (GRCm39) |
C126Y |
probably benign |
Het |
Or4p22 |
T |
A |
2: 88,317,492 (GRCm39) |
C139S |
probably damaging |
Het |
Or6c208 |
A |
C |
10: 129,224,036 (GRCm39) |
D178A |
probably damaging |
Het |
Osbpl3 |
T |
A |
6: 50,297,115 (GRCm39) |
S564C |
probably damaging |
Het |
Pax6 |
C |
A |
2: 105,522,604 (GRCm39) |
P264T |
probably damaging |
Het |
Plppr4 |
T |
C |
3: 117,116,832 (GRCm39) |
R342G |
probably damaging |
Het |
Prg4 |
C |
T |
1: 150,328,005 (GRCm39) |
C220Y |
probably damaging |
Het |
Prune2 |
T |
A |
19: 17,098,577 (GRCm39) |
D1360E |
probably benign |
Het |
Ranbp2 |
T |
A |
10: 58,299,772 (GRCm39) |
S469T |
probably damaging |
Het |
Rbfox1 |
A |
T |
16: 7,187,698 (GRCm39) |
K43N |
probably benign |
Het |
Rgs22 |
T |
C |
15: 36,122,459 (GRCm39) |
D25G |
probably damaging |
Het |
Rnf113a2 |
G |
A |
12: 84,464,545 (GRCm39) |
G146S |
probably damaging |
Het |
Sbpl |
T |
A |
17: 24,173,608 (GRCm39) |
K55* |
probably null |
Het |
Scel |
G |
A |
14: 103,781,268 (GRCm39) |
W138* |
probably null |
Het |
Scgb2b19 |
T |
C |
7: 32,979,711 (GRCm39) |
I12V |
probably null |
Het |
Scn9a |
T |
A |
2: 66,379,359 (GRCm39) |
M358L |
probably damaging |
Het |
Sdk2 |
C |
A |
11: 113,733,516 (GRCm39) |
E924* |
probably null |
Het |
Sipa1l3 |
T |
C |
7: 29,048,012 (GRCm39) |
Q1292R |
possibly damaging |
Het |
Skint4 |
G |
A |
4: 111,975,298 (GRCm39) |
G86D |
probably damaging |
Het |
Slc28a3 |
C |
T |
13: 58,736,028 (GRCm39) |
V57I |
probably benign |
Het |
Slc9a4 |
T |
C |
1: 40,662,559 (GRCm39) |
S609P |
probably damaging |
Het |
Slc9a4 |
C |
T |
1: 40,619,799 (GRCm39) |
P42S |
probably benign |
Het |
Slitrk1 |
T |
A |
14: 109,150,061 (GRCm39) |
T217S |
probably benign |
Het |
Spindoc |
C |
T |
19: 7,335,807 (GRCm39) |
R327H |
probably benign |
Het |
Stk36 |
T |
C |
1: 74,661,382 (GRCm39) |
S470P |
probably benign |
Het |
Sypl1 |
C |
T |
12: 33,024,254 (GRCm39) |
P196L |
probably benign |
Het |
Tekt4 |
T |
A |
17: 25,693,718 (GRCm39) |
I285N |
probably damaging |
Het |
Tgm5 |
T |
A |
2: 120,876,979 (GRCm39) |
I686F |
possibly damaging |
Het |
Thsd4 |
C |
A |
9: 59,883,587 (GRCm39) |
R933L |
probably damaging |
Het |
Treml1 |
T |
A |
17: 48,673,700 (GRCm39) |
I237N |
probably damaging |
Het |
Txndc16 |
T |
C |
14: 45,442,839 (GRCm39) |
I119V |
probably benign |
Het |
Ubr3 |
C |
A |
2: 69,728,166 (GRCm39) |
N176K |
probably damaging |
Het |
Vit |
A |
G |
17: 78,932,426 (GRCm39) |
Y511C |
probably damaging |
Het |
Vwa5b2 |
G |
A |
16: 20,422,984 (GRCm39) |
G994D |
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,925,268 (GRCm39) |
T1648A |
unknown |
Het |
Ythdf1 |
G |
A |
2: 180,553,315 (GRCm39) |
T300I |
probably damaging |
Het |
Zan |
A |
G |
5: 137,452,462 (GRCm39) |
|
probably null |
Het |
Zbbx |
A |
G |
3: 75,019,401 (GRCm39) |
L103P |
probably benign |
Het |
Zfp105 |
A |
G |
9: 122,758,869 (GRCm39) |
D180G |
probably damaging |
Het |
Zfp114 |
T |
A |
7: 23,880,083 (GRCm39) |
L144Q |
possibly damaging |
Het |
Zfp128 |
T |
C |
7: 12,624,399 (GRCm39) |
C256R |
probably damaging |
Het |
|
Other mutations in Mroh2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Mroh2b
|
APN |
15 |
4,928,679 (GRCm39) |
missense |
probably benign |
|
IGL00507:Mroh2b
|
APN |
15 |
4,991,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00548:Mroh2b
|
APN |
15 |
4,960,798 (GRCm39) |
missense |
probably benign |
0.35 |
IGL00902:Mroh2b
|
APN |
15 |
4,944,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00944:Mroh2b
|
APN |
15 |
4,980,609 (GRCm39) |
splice site |
probably benign |
|
IGL00954:Mroh2b
|
APN |
15 |
4,932,536 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01015:Mroh2b
|
APN |
15 |
4,971,024 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01134:Mroh2b
|
APN |
15 |
4,944,634 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01337:Mroh2b
|
APN |
15 |
4,934,506 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01780:Mroh2b
|
APN |
15 |
4,941,482 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01919:Mroh2b
|
APN |
15 |
4,953,170 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02069:Mroh2b
|
APN |
15 |
4,933,806 (GRCm39) |
splice site |
probably benign |
|
IGL02146:Mroh2b
|
APN |
15 |
4,980,776 (GRCm39) |
splice site |
probably null |
|
IGL02221:Mroh2b
|
APN |
15 |
4,953,123 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02281:Mroh2b
|
APN |
15 |
4,981,745 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02350:Mroh2b
|
APN |
15 |
4,941,482 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02357:Mroh2b
|
APN |
15 |
4,941,482 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02401:Mroh2b
|
APN |
15 |
4,929,983 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02427:Mroh2b
|
APN |
15 |
4,981,042 (GRCm39) |
splice site |
probably benign |
|
IGL02432:Mroh2b
|
APN |
15 |
4,943,668 (GRCm39) |
missense |
probably benign |
|
IGL02582:Mroh2b
|
APN |
15 |
4,937,997 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02632:Mroh2b
|
APN |
15 |
4,960,583 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02741:Mroh2b
|
APN |
15 |
4,935,114 (GRCm39) |
missense |
probably benign |
|
IGL02811:Mroh2b
|
APN |
15 |
4,944,718 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02826:Mroh2b
|
APN |
15 |
4,991,630 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03412:Mroh2b
|
APN |
15 |
4,973,854 (GRCm39) |
missense |
probably benign |
0.14 |
PIT4468001:Mroh2b
|
UTSW |
15 |
4,942,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R0024:Mroh2b
|
UTSW |
15 |
4,955,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R0333:Mroh2b
|
UTSW |
15 |
4,960,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Mroh2b
|
UTSW |
15 |
4,971,116 (GRCm39) |
missense |
probably benign |
0.01 |
R0530:Mroh2b
|
UTSW |
15 |
4,963,877 (GRCm39) |
missense |
probably damaging |
0.97 |
R1411:Mroh2b
|
UTSW |
15 |
4,947,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R1457:Mroh2b
|
UTSW |
15 |
4,955,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Mroh2b
|
UTSW |
15 |
4,955,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Mroh2b
|
UTSW |
15 |
4,955,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Mroh2b
|
UTSW |
15 |
4,978,137 (GRCm39) |
missense |
probably benign |
0.00 |
R1525:Mroh2b
|
UTSW |
15 |
4,980,612 (GRCm39) |
splice site |
probably null |
|
R1584:Mroh2b
|
UTSW |
15 |
4,955,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Mroh2b
|
UTSW |
15 |
4,974,572 (GRCm39) |
missense |
probably benign |
0.08 |
R1657:Mroh2b
|
UTSW |
15 |
4,960,525 (GRCm39) |
nonsense |
probably null |
|
R1671:Mroh2b
|
UTSW |
15 |
4,980,776 (GRCm39) |
splice site |
probably null |
|
R1698:Mroh2b
|
UTSW |
15 |
4,943,622 (GRCm39) |
missense |
probably benign |
0.02 |
R2002:Mroh2b
|
UTSW |
15 |
4,955,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Mroh2b
|
UTSW |
15 |
4,946,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R2077:Mroh2b
|
UTSW |
15 |
4,974,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R2179:Mroh2b
|
UTSW |
15 |
4,950,928 (GRCm39) |
critical splice donor site |
probably null |
|
R2183:Mroh2b
|
UTSW |
15 |
4,947,707 (GRCm39) |
splice site |
probably null |
|
R3713:Mroh2b
|
UTSW |
15 |
4,973,131 (GRCm39) |
missense |
probably benign |
0.01 |
R3714:Mroh2b
|
UTSW |
15 |
4,973,131 (GRCm39) |
missense |
probably benign |
0.01 |
R3747:Mroh2b
|
UTSW |
15 |
4,981,728 (GRCm39) |
nonsense |
probably null |
|
R3748:Mroh2b
|
UTSW |
15 |
4,981,728 (GRCm39) |
nonsense |
probably null |
|
R3749:Mroh2b
|
UTSW |
15 |
4,981,728 (GRCm39) |
nonsense |
probably null |
|
R3750:Mroh2b
|
UTSW |
15 |
4,981,728 (GRCm39) |
nonsense |
probably null |
|
R3792:Mroh2b
|
UTSW |
15 |
4,953,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R3872:Mroh2b
|
UTSW |
15 |
4,954,543 (GRCm39) |
nonsense |
probably null |
|
R4021:Mroh2b
|
UTSW |
15 |
4,954,582 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4329:Mroh2b
|
UTSW |
15 |
4,960,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R4456:Mroh2b
|
UTSW |
15 |
4,977,407 (GRCm39) |
missense |
probably benign |
0.21 |
R4592:Mroh2b
|
UTSW |
15 |
4,947,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R4836:Mroh2b
|
UTSW |
15 |
4,933,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R5050:Mroh2b
|
UTSW |
15 |
4,929,932 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5230:Mroh2b
|
UTSW |
15 |
4,971,004 (GRCm39) |
missense |
probably benign |
0.07 |
R5342:Mroh2b
|
UTSW |
15 |
4,943,615 (GRCm39) |
nonsense |
probably null |
|
R5353:Mroh2b
|
UTSW |
15 |
4,946,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R5368:Mroh2b
|
UTSW |
15 |
4,935,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R5424:Mroh2b
|
UTSW |
15 |
4,971,094 (GRCm39) |
missense |
probably damaging |
0.98 |
R5484:Mroh2b
|
UTSW |
15 |
4,938,463 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5999:Mroh2b
|
UTSW |
15 |
4,942,366 (GRCm39) |
splice site |
probably null |
|
R6046:Mroh2b
|
UTSW |
15 |
4,980,763 (GRCm39) |
missense |
probably benign |
0.01 |
R6081:Mroh2b
|
UTSW |
15 |
4,973,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6162:Mroh2b
|
UTSW |
15 |
4,944,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R6165:Mroh2b
|
UTSW |
15 |
4,947,832 (GRCm39) |
missense |
probably benign |
0.23 |
R6240:Mroh2b
|
UTSW |
15 |
4,964,126 (GRCm39) |
missense |
probably benign |
0.38 |
R6487:Mroh2b
|
UTSW |
15 |
4,976,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R6539:Mroh2b
|
UTSW |
15 |
4,935,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R6616:Mroh2b
|
UTSW |
15 |
4,982,764 (GRCm39) |
missense |
probably benign |
0.36 |
R6663:Mroh2b
|
UTSW |
15 |
4,977,417 (GRCm39) |
missense |
probably benign |
0.21 |
R6820:Mroh2b
|
UTSW |
15 |
4,982,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R6900:Mroh2b
|
UTSW |
15 |
4,938,469 (GRCm39) |
missense |
probably benign |
0.00 |
R6990:Mroh2b
|
UTSW |
15 |
4,942,284 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7067:Mroh2b
|
UTSW |
15 |
4,929,986 (GRCm39) |
missense |
probably benign |
0.35 |
R7092:Mroh2b
|
UTSW |
15 |
4,964,160 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7264:Mroh2b
|
UTSW |
15 |
4,950,844 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7436:Mroh2b
|
UTSW |
15 |
4,971,036 (GRCm39) |
missense |
probably benign |
0.21 |
R7462:Mroh2b
|
UTSW |
15 |
4,938,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7529:Mroh2b
|
UTSW |
15 |
4,978,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7575:Mroh2b
|
UTSW |
15 |
4,964,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R7579:Mroh2b
|
UTSW |
15 |
4,960,543 (GRCm39) |
missense |
probably benign |
0.09 |
R7605:Mroh2b
|
UTSW |
15 |
4,974,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R7624:Mroh2b
|
UTSW |
15 |
4,946,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R7797:Mroh2b
|
UTSW |
15 |
4,978,587 (GRCm39) |
missense |
probably benign |
0.36 |
R7848:Mroh2b
|
UTSW |
15 |
4,967,861 (GRCm39) |
nonsense |
probably null |
|
R7952:Mroh2b
|
UTSW |
15 |
4,980,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R7995:Mroh2b
|
UTSW |
15 |
4,950,839 (GRCm39) |
nonsense |
probably null |
|
R8088:Mroh2b
|
UTSW |
15 |
4,929,985 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8207:Mroh2b
|
UTSW |
15 |
4,967,892 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8242:Mroh2b
|
UTSW |
15 |
4,938,522 (GRCm39) |
missense |
probably benign |
0.04 |
R8248:Mroh2b
|
UTSW |
15 |
4,960,586 (GRCm39) |
missense |
probably benign |
0.40 |
R8258:Mroh2b
|
UTSW |
15 |
4,941,391 (GRCm39) |
missense |
probably benign |
0.01 |
R8259:Mroh2b
|
UTSW |
15 |
4,941,391 (GRCm39) |
missense |
probably benign |
0.01 |
R8304:Mroh2b
|
UTSW |
15 |
4,955,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R8316:Mroh2b
|
UTSW |
15 |
4,980,746 (GRCm39) |
nonsense |
probably null |
|
R8345:Mroh2b
|
UTSW |
15 |
4,973,808 (GRCm39) |
missense |
probably benign |
0.09 |
R8507:Mroh2b
|
UTSW |
15 |
4,978,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R8728:Mroh2b
|
UTSW |
15 |
4,935,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8747:Mroh2b
|
UTSW |
15 |
4,964,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:Mroh2b
|
UTSW |
15 |
4,978,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R8814:Mroh2b
|
UTSW |
15 |
4,971,107 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8856:Mroh2b
|
UTSW |
15 |
4,960,510 (GRCm39) |
nonsense |
probably null |
|
R8910:Mroh2b
|
UTSW |
15 |
4,960,855 (GRCm39) |
missense |
probably benign |
0.01 |
R8913:Mroh2b
|
UTSW |
15 |
4,947,010 (GRCm39) |
intron |
probably benign |
|
R8941:Mroh2b
|
UTSW |
15 |
4,991,606 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9014:Mroh2b
|
UTSW |
15 |
4,928,670 (GRCm39) |
start codon destroyed |
probably null |
0.95 |
R9086:Mroh2b
|
UTSW |
15 |
4,982,754 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9101:Mroh2b
|
UTSW |
15 |
4,929,935 (GRCm39) |
missense |
probably benign |
0.20 |
R9118:Mroh2b
|
UTSW |
15 |
4,991,573 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9393:Mroh2b
|
UTSW |
15 |
4,980,666 (GRCm39) |
missense |
probably benign |
|
R9429:Mroh2b
|
UTSW |
15 |
4,963,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R9431:Mroh2b
|
UTSW |
15 |
4,963,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R9443:Mroh2b
|
UTSW |
15 |
4,973,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R9447:Mroh2b
|
UTSW |
15 |
4,960,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R9497:Mroh2b
|
UTSW |
15 |
4,950,845 (GRCm39) |
missense |
probably damaging |
0.98 |
R9588:Mroh2b
|
UTSW |
15 |
4,978,130 (GRCm39) |
missense |
probably benign |
0.00 |
R9631:Mroh2b
|
UTSW |
15 |
4,946,556 (GRCm39) |
missense |
probably damaging |
0.97 |
R9686:Mroh2b
|
UTSW |
15 |
4,974,605 (GRCm39) |
missense |
probably benign |
0.34 |
R9774:Mroh2b
|
UTSW |
15 |
4,943,613 (GRCm39) |
missense |
probably benign |
0.08 |
X0067:Mroh2b
|
UTSW |
15 |
4,981,073 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1177:Mroh2b
|
UTSW |
15 |
4,934,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|