Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
C |
5: 8,957,267 (GRCm39) |
V132A |
possibly damaging |
Het |
Acp3 |
A |
T |
9: 104,184,174 (GRCm39) |
V292E |
probably damaging |
Het |
Adamts10 |
T |
C |
17: 33,747,870 (GRCm39) |
V102A |
possibly damaging |
Het |
Add2 |
A |
G |
6: 86,073,728 (GRCm39) |
T206A |
probably benign |
Het |
Alg12 |
A |
T |
15: 88,700,391 (GRCm39) |
L15Q |
probably damaging |
Het |
Ankrd27 |
T |
A |
7: 35,307,800 (GRCm39) |
D346E |
probably damaging |
Het |
Armc2 |
A |
T |
10: 41,799,790 (GRCm39) |
N689K |
probably damaging |
Het |
Best3 |
T |
A |
10: 116,860,460 (GRCm39) |
D573E |
probably benign |
Het |
Bltp1 |
T |
G |
3: 37,020,086 (GRCm39) |
N2108K |
probably damaging |
Het |
Ccdc80 |
A |
T |
16: 44,916,261 (GRCm39) |
Q339L |
probably benign |
Het |
Cdh9 |
T |
C |
15: 16,778,242 (GRCm39) |
V19A |
probably benign |
Het |
Cimap1a |
G |
A |
7: 140,428,398 (GRCm39) |
|
probably benign |
Het |
Cnksr1 |
A |
T |
4: 133,956,986 (GRCm39) |
|
probably null |
Het |
Col7a1 |
T |
A |
9: 108,786,345 (GRCm39) |
V525E |
unknown |
Het |
Cplane1 |
T |
C |
15: 8,251,421 (GRCm39) |
S1898P |
probably benign |
Het |
Crebrf |
T |
C |
17: 26,961,394 (GRCm39) |
S172P |
possibly damaging |
Het |
Csmd1 |
T |
C |
8: 16,059,439 (GRCm39) |
I2099V |
probably benign |
Het |
Dcaf4 |
T |
A |
12: 83,586,233 (GRCm39) |
M400K |
possibly damaging |
Het |
Dnah11 |
A |
T |
12: 117,958,935 (GRCm39) |
F2983I |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,735,733 (GRCm39) |
V1005A |
possibly damaging |
Het |
Dyrk2 |
C |
A |
10: 118,704,153 (GRCm39) |
G34C |
probably damaging |
Het |
Eif4a1 |
A |
T |
11: 69,559,423 (GRCm39) |
|
probably benign |
Het |
Eno4 |
G |
T |
19: 58,952,975 (GRCm39) |
D330Y |
probably damaging |
Het |
Faf1 |
G |
A |
4: 109,699,496 (GRCm39) |
C347Y |
probably benign |
Het |
Fam169a |
A |
G |
13: 97,234,100 (GRCm39) |
Y124C |
probably damaging |
Het |
Fam227a |
G |
T |
15: 79,521,255 (GRCm39) |
F269L |
probably benign |
Het |
Fancm |
C |
A |
12: 65,122,605 (GRCm39) |
D42E |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,404,317 (GRCm39) |
I356N |
possibly damaging |
Het |
Fer1l6 |
A |
T |
15: 58,509,869 (GRCm39) |
T1444S |
probably damaging |
Het |
Galr1 |
A |
G |
18: 82,412,065 (GRCm39) |
L267P |
probably damaging |
Het |
Gbx1 |
T |
C |
5: 24,709,837 (GRCm39) |
H336R |
probably damaging |
Het |
Gimap8 |
A |
T |
6: 48,636,281 (GRCm39) |
Q682L |
possibly damaging |
Het |
Gm2396 |
T |
G |
9: 88,813,281 (GRCm39) |
|
noncoding transcript |
Het |
Gm5798 |
T |
C |
14: 41,070,614 (GRCm39) |
L8S |
probably damaging |
Het |
Hmgcll1 |
C |
T |
9: 75,963,460 (GRCm39) |
S39F |
possibly damaging |
Het |
Hspg2 |
C |
T |
4: 137,246,251 (GRCm39) |
R1010C |
probably damaging |
Het |
Il3ra |
A |
T |
14: 14,355,381 (GRCm38) |
E289D |
probably benign |
Het |
Isoc1 |
T |
A |
18: 58,806,350 (GRCm39) |
L220Q |
probably damaging |
Het |
Itga2 |
T |
A |
13: 114,990,302 (GRCm39) |
K918* |
probably null |
Het |
Kat6a |
C |
T |
8: 23,428,329 (GRCm39) |
T1228I |
probably benign |
Het |
Klhl30 |
T |
A |
1: 91,287,046 (GRCm39) |
|
probably null |
Het |
Krtap6-2 |
A |
T |
16: 89,216,806 (GRCm39) |
C54S |
unknown |
Het |
Lmf2 |
G |
A |
15: 89,236,003 (GRCm39) |
P634S |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,490,906 (GRCm39) |
V175A |
possibly damaging |
Het |
Mcm3 |
A |
C |
1: 20,890,480 (GRCm39) |
|
probably benign |
Het |
Mon1b |
T |
C |
8: 114,365,859 (GRCm39) |
S396P |
probably damaging |
Het |
Ncor2 |
A |
G |
5: 125,126,404 (GRCm39) |
|
probably null |
Het |
Nlrc5 |
T |
G |
8: 95,247,844 (GRCm39) |
|
probably benign |
Het |
Nlrp14 |
GT |
GTT |
7: 106,796,386 (GRCm39) |
|
probably null |
Het |
Nwd2 |
T |
G |
5: 63,962,151 (GRCm39) |
S578R |
probably damaging |
Het |
Or12k7 |
A |
G |
2: 36,958,422 (GRCm39) |
Y35C |
probably damaging |
Het |
Or4f4b |
G |
A |
2: 111,314,005 (GRCm39) |
V105I |
possibly damaging |
Het |
Otoa |
C |
A |
7: 120,701,902 (GRCm39) |
P194T |
probably damaging |
Het |
Pde1b |
A |
C |
15: 103,429,801 (GRCm39) |
D98A |
probably damaging |
Het |
Pi4ka |
A |
T |
16: 17,195,033 (GRCm39) |
C122S |
probably damaging |
Het |
Pole2 |
C |
T |
12: 69,269,924 (GRCm39) |
V67M |
probably damaging |
Het |
Prickle2 |
A |
T |
6: 92,393,736 (GRCm39) |
D312E |
probably benign |
Het |
Prkd1 |
T |
C |
12: 50,436,745 (GRCm39) |
D453G |
probably damaging |
Het |
Prrc1 |
T |
A |
18: 57,507,626 (GRCm39) |
V260E |
probably damaging |
Het |
Reg3g |
A |
T |
6: 78,444,793 (GRCm39) |
Y62N |
probably benign |
Het |
Reln |
C |
T |
5: 22,160,236 (GRCm39) |
G2111E |
probably damaging |
Het |
Rsph6a |
A |
T |
7: 18,791,665 (GRCm39) |
E278V |
possibly damaging |
Het |
Scpep1 |
T |
A |
11: 88,832,122 (GRCm39) |
I203F |
probably damaging |
Het |
Sec24d |
T |
C |
3: 123,148,596 (GRCm39) |
C747R |
probably damaging |
Het |
Sec31a |
A |
T |
5: 100,516,192 (GRCm39) |
N967K |
probably damaging |
Het |
Sell |
T |
C |
1: 163,890,631 (GRCm39) |
W5R |
probably benign |
Het |
Siglec1 |
C |
T |
2: 130,911,789 (GRCm39) |
V1697M |
probably benign |
Het |
Sinhcaf |
A |
G |
6: 148,834,498 (GRCm39) |
|
probably null |
Het |
Slc22a26 |
T |
A |
19: 7,768,419 (GRCm39) |
I213L |
probably benign |
Het |
Slc2a13 |
G |
A |
15: 91,296,415 (GRCm39) |
P300S |
probably benign |
Het |
Slco1a4 |
A |
G |
6: 141,761,231 (GRCm39) |
Y461H |
possibly damaging |
Het |
Slco3a1 |
G |
C |
7: 73,970,304 (GRCm39) |
C434W |
probably null |
Het |
Sp3 |
A |
T |
2: 72,768,633 (GRCm39) |
V666D |
probably benign |
Het |
Spidr |
A |
T |
16: 15,936,806 (GRCm39) |
W100R |
possibly damaging |
Het |
Stk33 |
T |
A |
7: 108,926,802 (GRCm39) |
M286L |
probably damaging |
Het |
Sult1c2 |
T |
A |
17: 54,139,163 (GRCm39) |
I183F |
probably benign |
Het |
Svep1 |
G |
T |
4: 58,087,751 (GRCm39) |
T1776K |
probably benign |
Het |
Tesk2 |
A |
G |
4: 116,660,190 (GRCm39) |
H436R |
probably benign |
Het |
Tex2 |
T |
C |
11: 106,459,230 (GRCm39) |
T67A |
probably damaging |
Het |
Timm10 |
T |
C |
2: 84,660,192 (GRCm39) |
S44P |
possibly damaging |
Het |
Tmed11 |
C |
A |
5: 108,943,048 (GRCm39) |
|
probably null |
Het |
Trim12c |
G |
A |
7: 103,990,155 (GRCm39) |
R441C |
probably damaging |
Het |
Trmt2a |
A |
G |
16: 18,070,793 (GRCm39) |
K509E |
probably damaging |
Het |
Upk3a |
A |
G |
15: 84,903,624 (GRCm39) |
T108A |
probably benign |
Het |
Usp29 |
A |
G |
7: 6,965,158 (GRCm39) |
M334V |
probably benign |
Het |
Vash1 |
A |
G |
12: 86,726,916 (GRCm39) |
D52G |
probably benign |
Het |
Vmn2r14 |
T |
G |
5: 109,368,246 (GRCm39) |
T249P |
probably benign |
Het |
Vmn2r43 |
A |
T |
7: 8,247,848 (GRCm39) |
F772I |
probably damaging |
Het |
Vmn2r75 |
G |
T |
7: 85,820,787 (GRCm39) |
S49Y |
probably benign |
Het |
Xdh |
T |
C |
17: 74,217,238 (GRCm39) |
T677A |
probably damaging |
Het |
Zan |
A |
G |
5: 137,384,718 (GRCm39) |
L5102P |
unknown |
Het |
Zfp160 |
T |
A |
17: 21,240,343 (GRCm39) |
S9T |
probably benign |
Het |
Zfp273 |
A |
T |
13: 67,973,673 (GRCm39) |
H267L |
probably damaging |
Het |
Zfp97 |
T |
A |
17: 17,365,038 (GRCm39) |
I179K |
probably benign |
Het |
Zfp975 |
T |
C |
7: 42,311,716 (GRCm39) |
Y299C |
probably damaging |
Het |
|
Other mutations in Mroh2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Mroh2a
|
APN |
1 |
88,172,692 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00990:Mroh2a
|
APN |
1 |
88,161,842 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL00990:Mroh2a
|
APN |
1 |
88,158,468 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03097:Mroh2a
|
UTSW |
1 |
88,163,098 (GRCm39) |
missense |
probably benign |
0.30 |
R0032:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
R0068:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
R0139:Mroh2a
|
UTSW |
1 |
88,185,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R0197:Mroh2a
|
UTSW |
1 |
88,173,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0322:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R0374:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0387:Mroh2a
|
UTSW |
1 |
88,173,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R0412:Mroh2a
|
UTSW |
1 |
88,162,938 (GRCm39) |
missense |
probably benign |
0.01 |
R0536:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R0548:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0580:Mroh2a
|
UTSW |
1 |
88,171,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0581:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
R0583:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
R0613:Mroh2a
|
UTSW |
1 |
88,171,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R0657:Mroh2a
|
UTSW |
1 |
88,183,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R0659:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0659:Mroh2a
|
UTSW |
1 |
88,178,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0675:Mroh2a
|
UTSW |
1 |
88,156,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R0675:Mroh2a
|
UTSW |
1 |
88,178,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R0689:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R0689:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R0735:Mroh2a
|
UTSW |
1 |
88,171,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Mroh2a
|
UTSW |
1 |
88,171,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R0845:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R0853:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R0959:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R0960:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1004:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1013:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R1028:Mroh2a
|
UTSW |
1 |
88,163,098 (GRCm39) |
missense |
probably benign |
0.30 |
R1268:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R1281:Mroh2a
|
UTSW |
1 |
88,183,889 (GRCm39) |
frame shift |
probably null |
|
R1414:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R1439:Mroh2a
|
UTSW |
1 |
88,185,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R1441:Mroh2a
|
UTSW |
1 |
88,169,353 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1442:Mroh2a
|
UTSW |
1 |
88,160,075 (GRCm39) |
splice site |
probably benign |
|
R1442:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1465:Mroh2a
|
UTSW |
1 |
88,185,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Mroh2a
|
UTSW |
1 |
88,169,340 (GRCm39) |
missense |
probably benign |
0.07 |
R1686:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R1686:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R1780:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R1846:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R1899:Mroh2a
|
UTSW |
1 |
88,163,098 (GRCm39) |
missense |
probably benign |
0.30 |
R1958:Mroh2a
|
UTSW |
1 |
88,165,213 (GRCm39) |
nonsense |
probably null |
|
R2122:Mroh2a
|
UTSW |
1 |
88,184,476 (GRCm39) |
missense |
probably benign |
0.37 |
R2248:Mroh2a
|
UTSW |
1 |
88,184,476 (GRCm39) |
missense |
probably benign |
0.37 |
R2306:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R2869:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R2870:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R2871:Mroh2a
|
UTSW |
1 |
88,183,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R3408:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R3608:Mroh2a
|
UTSW |
1 |
88,172,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R3730:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R3937:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4022:Mroh2a
|
UTSW |
1 |
88,173,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R4049:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4133:Mroh2a
|
UTSW |
1 |
88,182,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4361:Mroh2a
|
UTSW |
1 |
88,182,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4392:Mroh2a
|
UTSW |
1 |
88,187,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R4401:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4402:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4575:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4625:Mroh2a
|
UTSW |
1 |
88,182,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4631:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4665:Mroh2a
|
UTSW |
1 |
88,169,340 (GRCm39) |
missense |
probably benign |
0.07 |
R4701:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R4701:Mroh2a
|
UTSW |
1 |
88,169,340 (GRCm39) |
missense |
probably benign |
0.07 |
R4771:Mroh2a
|
UTSW |
1 |
88,179,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4839:Mroh2a
|
UTSW |
1 |
88,165,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R4873:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4875:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5007:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R5031:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R5062:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R5301:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5367:Mroh2a
|
UTSW |
1 |
88,182,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5371:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5446:Mroh2a
|
UTSW |
1 |
88,182,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5484:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5506:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5561:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R5615:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R5825:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R5891:Mroh2a
|
UTSW |
1 |
88,169,337 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5906:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5928:Mroh2a
|
UTSW |
1 |
88,169,340 (GRCm39) |
missense |
probably benign |
0.07 |
R6004:Mroh2a
|
UTSW |
1 |
88,176,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R6035:Mroh2a
|
UTSW |
1 |
88,158,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R6064:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R6074:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R6091:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R6127:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R6234:Mroh2a
|
UTSW |
1 |
88,184,476 (GRCm39) |
missense |
probably benign |
0.37 |
R6234:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R6244:Mroh2a
|
UTSW |
1 |
88,184,476 (GRCm39) |
missense |
probably benign |
0.37 |
R6464:Mroh2a
|
UTSW |
1 |
88,185,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R6465:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R6575:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R6809:Mroh2a
|
UTSW |
1 |
88,162,938 (GRCm39) |
missense |
probably benign |
0.01 |
R6819:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6854:Mroh2a
|
UTSW |
1 |
88,171,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R6860:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7126:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7818:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R8350:Mroh2a
|
UTSW |
1 |
88,171,805 (GRCm39) |
splice site |
probably null |
|
R9414:Mroh2a
|
UTSW |
1 |
88,179,096 (GRCm39) |
missense |
probably benign |
0.26 |
RF024:Mroh2a
|
UTSW |
1 |
88,170,207 (GRCm39) |
missense |
probably damaging |
1.00 |
V5622:Mroh2a
|
UTSW |
1 |
88,154,813 (GRCm39) |
start gained |
probably benign |
|
V8831:Mroh2a
|
UTSW |
1 |
88,183,889 (GRCm39) |
frame shift |
probably null |
|
X0027:Mroh2a
|
UTSW |
1 |
88,176,335 (GRCm39) |
missense |
possibly damaging |
0.86 |
X0028:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
X0028:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
X0033:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
X0034:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
X0034:Mroh2a
|
UTSW |
1 |
88,160,014 (GRCm39) |
missense |
probably damaging |
1.00 |
X0034:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
X0039:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
X0057:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
X0057:Mroh2a
|
UTSW |
1 |
88,183,377 (GRCm39) |
missense |
probably benign |
0.25 |
X0057:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
X0063:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
Z1188:Mroh2a
|
UTSW |
1 |
88,162,938 (GRCm39) |
missense |
probably benign |
0.01 |
Z1190:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
Z1192:Mroh2a
|
UTSW |
1 |
88,162,938 (GRCm39) |
missense |
probably benign |
0.01 |
|