Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,103,165 (GRCm39) |
S809G |
probably benign |
Het |
Ap4b1 |
T |
A |
3: 103,725,161 (GRCm39) |
|
probably null |
Het |
Aqp12 |
A |
G |
1: 92,934,606 (GRCm39) |
Q161R |
possibly damaging |
Het |
Atp8a2 |
A |
G |
14: 60,028,689 (GRCm39) |
I926T |
probably benign |
Het |
Cacna2d1 |
A |
T |
5: 16,504,988 (GRCm39) |
N314I |
probably damaging |
Het |
Cd209d |
A |
G |
8: 3,927,113 (GRCm39) |
S81P |
probably damaging |
Het |
Cdcp1 |
T |
A |
9: 123,007,086 (GRCm39) |
K554* |
probably null |
Het |
Celsr1 |
A |
G |
15: 85,816,658 (GRCm39) |
Y1762H |
probably benign |
Het |
Cklf |
A |
G |
8: 104,983,983 (GRCm39) |
T49A |
possibly damaging |
Het |
Col12a1 |
T |
G |
9: 79,600,820 (GRCm39) |
I755L |
probably benign |
Het |
Cts3 |
G |
A |
13: 61,715,368 (GRCm39) |
Q140* |
probably null |
Het |
Ddx1 |
A |
T |
12: 13,294,967 (GRCm39) |
|
probably null |
Het |
Dnah3 |
C |
A |
7: 119,570,402 (GRCm39) |
E2262* |
probably null |
Het |
Dnah5 |
A |
G |
15: 28,290,294 (GRCm39) |
N1228S |
probably benign |
Het |
Dsg1a |
G |
A |
18: 20,464,561 (GRCm39) |
R352Q |
probably damaging |
Het |
Efcab5 |
A |
G |
11: 77,042,679 (GRCm39) |
F25L |
probably damaging |
Het |
Efhd1 |
T |
A |
1: 87,192,404 (GRCm39) |
V78D |
probably damaging |
Het |
Eif5a2 |
T |
C |
3: 28,847,967 (GRCm39) |
|
probably null |
Het |
Elp2 |
T |
A |
18: 24,744,983 (GRCm39) |
V101D |
possibly damaging |
Het |
Enpp2 |
A |
T |
15: 54,773,592 (GRCm39) |
|
probably null |
Het |
F5 |
A |
G |
1: 164,007,089 (GRCm39) |
T298A |
probably damaging |
Het |
Fbxo21 |
G |
T |
5: 118,146,129 (GRCm39) |
R584L |
probably benign |
Het |
Fbxw22 |
G |
T |
9: 109,211,196 (GRCm39) |
F368L |
possibly damaging |
Het |
Gcn1 |
T |
C |
5: 115,720,356 (GRCm39) |
I409T |
probably benign |
Het |
Gm12887 |
T |
C |
4: 121,473,655 (GRCm39) |
Y65C |
probably damaging |
Het |
Gria4 |
G |
A |
9: 4,537,637 (GRCm39) |
Q224* |
probably null |
Het |
Hdac5 |
C |
T |
11: 102,089,631 (GRCm39) |
V860M |
probably damaging |
Het |
Ino80 |
G |
A |
2: 119,212,417 (GRCm39) |
R1302C |
probably damaging |
Het |
Kcns2 |
A |
T |
15: 34,838,966 (GRCm39) |
I110F |
probably damaging |
Het |
Lrig3 |
A |
G |
10: 125,846,036 (GRCm39) |
T822A |
probably damaging |
Het |
Mapk6 |
T |
C |
9: 75,302,851 (GRCm39) |
D214G |
probably damaging |
Het |
Mcm2 |
A |
T |
6: 88,869,060 (GRCm39) |
L264Q |
probably benign |
Het |
Mpnd |
A |
T |
17: 56,317,455 (GRCm39) |
Y64F |
probably damaging |
Het |
Muc1 |
T |
A |
3: 89,139,079 (GRCm39) |
M520K |
possibly damaging |
Het |
Muc4 |
T |
A |
16: 32,577,276 (GRCm39) |
S189T |
probably benign |
Het |
Myh13 |
T |
C |
11: 67,242,945 (GRCm39) |
S953P |
possibly damaging |
Het |
Ncf2 |
A |
T |
1: 152,706,230 (GRCm39) |
M281L |
probably benign |
Het |
Nipal2 |
A |
G |
15: 34,648,841 (GRCm39) |
I116T |
probably damaging |
Het |
Nptn |
T |
C |
9: 58,531,015 (GRCm39) |
L46P |
probably benign |
Het |
Or2b6 |
A |
T |
13: 21,823,214 (GRCm39) |
S160T |
probably damaging |
Het |
Or4k77 |
A |
G |
2: 111,199,552 (GRCm39) |
T192A |
probably benign |
Het |
Or51ag1 |
C |
A |
7: 103,155,896 (GRCm39) |
V86F |
probably damaging |
Het |
Or5ae1 |
T |
A |
7: 84,565,325 (GRCm39) |
F113I |
probably damaging |
Het |
Pgr |
A |
T |
9: 8,902,069 (GRCm39) |
Y534F |
possibly damaging |
Het |
Pip4k2a |
A |
T |
2: 18,877,093 (GRCm39) |
|
probably null |
Het |
Pkd1l2 |
C |
G |
8: 117,767,514 (GRCm39) |
V1259L |
probably benign |
Het |
Ppp1r12a |
A |
G |
10: 108,085,426 (GRCm39) |
E457G |
probably damaging |
Het |
Rasa4 |
T |
A |
5: 136,133,491 (GRCm39) |
V650D |
probably benign |
Het |
Rem2 |
C |
T |
14: 54,713,766 (GRCm39) |
|
probably benign |
Het |
Rps18-ps6 |
A |
T |
13: 97,896,868 (GRCm39) |
Y77N |
possibly damaging |
Het |
Sdc1 |
G |
A |
12: 8,840,409 (GRCm39) |
R62Q |
possibly damaging |
Het |
Sdk1 |
A |
G |
5: 141,934,261 (GRCm39) |
E366G |
possibly damaging |
Het |
Setd2 |
T |
A |
9: 110,433,248 (GRCm39) |
H2406Q |
probably damaging |
Het |
Slc30a5 |
A |
G |
13: 100,949,891 (GRCm39) |
V397A |
probably benign |
Het |
Slc36a2 |
A |
T |
11: 55,075,739 (GRCm39) |
L16H |
possibly damaging |
Het |
Slc44a1 |
T |
C |
4: 53,542,468 (GRCm39) |
V334A |
probably benign |
Het |
Sox8 |
A |
T |
17: 25,786,456 (GRCm39) |
Y416N |
possibly damaging |
Het |
Stimate |
T |
C |
14: 30,586,391 (GRCm39) |
L72S |
possibly damaging |
Het |
Stk24 |
T |
A |
14: 121,574,983 (GRCm39) |
I42F |
probably damaging |
Het |
Tasor2 |
A |
G |
13: 3,634,498 (GRCm39) |
|
probably null |
Het |
Tcerg1 |
T |
A |
18: 42,685,646 (GRCm39) |
L661Q |
possibly damaging |
Het |
Tpp1 |
G |
A |
7: 105,396,880 (GRCm39) |
R417W |
probably damaging |
Het |
Trim12a |
T |
A |
7: 103,955,264 (GRCm39) |
D153V |
possibly damaging |
Het |
Trpm2 |
T |
C |
10: 77,778,778 (GRCm39) |
N396S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,637,427 (GRCm39) |
K5695R |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,640,631 (GRCm39) |
R11960C |
probably damaging |
Het |
Tulp3 |
A |
C |
6: 128,310,906 (GRCm39) |
|
probably null |
Het |
Uaca |
T |
A |
9: 60,779,438 (GRCm39) |
L1273H |
probably damaging |
Het |
Usp33 |
A |
G |
3: 152,073,919 (GRCm39) |
E255G |
probably damaging |
Het |
Vmn2r54 |
T |
G |
7: 12,350,138 (GRCm39) |
|
probably null |
Het |
Vwa8 |
C |
T |
14: 79,145,670 (GRCm39) |
R116C |
probably damaging |
Het |
Wnt5b |
A |
T |
6: 119,423,315 (GRCm39) |
F116L |
probably benign |
Het |
Zbtb12 |
CTTCAT |
CTTCATTCAT |
17: 35,115,284 (GRCm39) |
|
probably null |
Het |
Zbtb12 |
TCATC |
TCATCCATC |
17: 35,115,286 (GRCm39) |
|
probably null |
Het |
Zfp408 |
G |
A |
2: 91,476,353 (GRCm39) |
T367I |
probably damaging |
Het |
Zfp512b |
G |
A |
2: 181,230,286 (GRCm39) |
A480V |
possibly damaging |
Het |
Zfp560 |
T |
C |
9: 20,258,949 (GRCm39) |
T638A |
probably benign |
Het |
Zfp932 |
G |
T |
5: 110,156,854 (GRCm39) |
G151V |
probably damaging |
Het |
Zpbp |
T |
C |
11: 11,302,696 (GRCm39) |
K320E |
probably damaging |
Het |
Zranb2 |
C |
T |
3: 157,243,277 (GRCm39) |
P91L |
probably damaging |
Het |
|
Other mutations in Speg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00838:Speg
|
APN |
1 |
75,387,034 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00979:Speg
|
APN |
1 |
75,387,378 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01122:Speg
|
APN |
1 |
75,386,679 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01293:Speg
|
APN |
1 |
75,364,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01304:Speg
|
APN |
1 |
75,404,841 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01351:Speg
|
APN |
1 |
75,387,920 (GRCm39) |
splice site |
probably benign |
|
IGL01473:Speg
|
APN |
1 |
75,404,929 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01477:Speg
|
APN |
1 |
75,368,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01485:Speg
|
APN |
1 |
75,364,471 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01584:Speg
|
APN |
1 |
75,407,581 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01959:Speg
|
APN |
1 |
75,367,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02231:Speg
|
APN |
1 |
75,400,031 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02355:Speg
|
APN |
1 |
75,400,559 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02362:Speg
|
APN |
1 |
75,400,559 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03013:Speg
|
APN |
1 |
75,407,923 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03168:Speg
|
APN |
1 |
75,364,831 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Speg
|
UTSW |
1 |
75,392,241 (GRCm39) |
missense |
probably benign |
0.39 |
R0112:Speg
|
UTSW |
1 |
75,361,676 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0311:Speg
|
UTSW |
1 |
75,407,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R0315:Speg
|
UTSW |
1 |
75,391,780 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0393:Speg
|
UTSW |
1 |
75,400,568 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0403:Speg
|
UTSW |
1 |
75,407,428 (GRCm39) |
splice site |
probably benign |
|
R0483:Speg
|
UTSW |
1 |
75,361,676 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0648:Speg
|
UTSW |
1 |
75,404,622 (GRCm39) |
missense |
probably benign |
|
R0683:Speg
|
UTSW |
1 |
75,405,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0800:Speg
|
UTSW |
1 |
75,400,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R0815:Speg
|
UTSW |
1 |
75,392,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0835:Speg
|
UTSW |
1 |
75,352,318 (GRCm39) |
missense |
probably benign |
0.00 |
R0866:Speg
|
UTSW |
1 |
75,393,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R0880:Speg
|
UTSW |
1 |
75,381,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R1082:Speg
|
UTSW |
1 |
75,391,782 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1140:Speg
|
UTSW |
1 |
75,405,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R1252:Speg
|
UTSW |
1 |
75,403,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R1301:Speg
|
UTSW |
1 |
75,378,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1348:Speg
|
UTSW |
1 |
75,399,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R1388:Speg
|
UTSW |
1 |
75,407,104 (GRCm39) |
missense |
probably damaging |
0.99 |
R1465:Speg
|
UTSW |
1 |
75,405,128 (GRCm39) |
splice site |
probably benign |
|
R1505:Speg
|
UTSW |
1 |
75,352,186 (GRCm39) |
missense |
probably benign |
0.02 |
R1506:Speg
|
UTSW |
1 |
75,394,307 (GRCm39) |
missense |
probably benign |
0.03 |
R1531:Speg
|
UTSW |
1 |
75,377,866 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1543:Speg
|
UTSW |
1 |
75,398,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R1567:Speg
|
UTSW |
1 |
75,404,691 (GRCm39) |
missense |
probably benign |
|
R1630:Speg
|
UTSW |
1 |
75,399,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1667:Speg
|
UTSW |
1 |
75,387,193 (GRCm39) |
splice site |
probably benign |
|
R1718:Speg
|
UTSW |
1 |
75,398,388 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1718:Speg
|
UTSW |
1 |
75,394,507 (GRCm39) |
missense |
probably benign |
0.00 |
R1719:Speg
|
UTSW |
1 |
75,394,507 (GRCm39) |
missense |
probably benign |
0.00 |
R1759:Speg
|
UTSW |
1 |
75,377,806 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1861:Speg
|
UTSW |
1 |
75,365,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Speg
|
UTSW |
1 |
75,400,550 (GRCm39) |
missense |
probably benign |
|
R1936:Speg
|
UTSW |
1 |
75,408,052 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2192:Speg
|
UTSW |
1 |
75,394,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R2204:Speg
|
UTSW |
1 |
75,407,121 (GRCm39) |
missense |
probably benign |
0.30 |
R2287:Speg
|
UTSW |
1 |
75,407,109 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2696:Speg
|
UTSW |
1 |
75,383,570 (GRCm39) |
missense |
probably benign |
0.27 |
R2983:Speg
|
UTSW |
1 |
75,361,574 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3110:Speg
|
UTSW |
1 |
75,399,326 (GRCm39) |
nonsense |
probably null |
|
R3112:Speg
|
UTSW |
1 |
75,399,326 (GRCm39) |
nonsense |
probably null |
|
R3154:Speg
|
UTSW |
1 |
75,378,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R3720:Speg
|
UTSW |
1 |
75,403,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R3983:Speg
|
UTSW |
1 |
75,399,191 (GRCm39) |
missense |
probably benign |
0.27 |
R4133:Speg
|
UTSW |
1 |
75,404,548 (GRCm39) |
missense |
probably benign |
|
R4522:Speg
|
UTSW |
1 |
75,404,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R4564:Speg
|
UTSW |
1 |
75,368,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4577:Speg
|
UTSW |
1 |
75,392,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Speg
|
UTSW |
1 |
75,398,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Speg
|
UTSW |
1 |
75,400,508 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4965:Speg
|
UTSW |
1 |
75,404,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Speg
|
UTSW |
1 |
75,364,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5152:Speg
|
UTSW |
1 |
75,404,742 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5156:Speg
|
UTSW |
1 |
75,404,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R5371:Speg
|
UTSW |
1 |
75,408,037 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5550:Speg
|
UTSW |
1 |
75,405,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R5562:Speg
|
UTSW |
1 |
75,403,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R5687:Speg
|
UTSW |
1 |
75,395,773 (GRCm39) |
splice site |
probably null |
|
R5985:Speg
|
UTSW |
1 |
75,383,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6004:Speg
|
UTSW |
1 |
75,392,247 (GRCm39) |
nonsense |
probably null |
|
R6038:Speg
|
UTSW |
1 |
75,395,103 (GRCm39) |
critical splice donor site |
probably null |
|
R6038:Speg
|
UTSW |
1 |
75,395,103 (GRCm39) |
critical splice donor site |
probably null |
|
R6143:Speg
|
UTSW |
1 |
75,391,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Speg
|
UTSW |
1 |
75,383,323 (GRCm39) |
nonsense |
probably null |
|
R6347:Speg
|
UTSW |
1 |
75,403,519 (GRCm39) |
missense |
probably benign |
0.00 |
R6453:Speg
|
UTSW |
1 |
75,394,616 (GRCm39) |
missense |
probably benign |
0.06 |
R6505:Speg
|
UTSW |
1 |
75,406,167 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6505:Speg
|
UTSW |
1 |
75,383,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6531:Speg
|
UTSW |
1 |
75,399,401 (GRCm39) |
missense |
probably benign |
0.03 |
R6566:Speg
|
UTSW |
1 |
75,365,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Speg
|
UTSW |
1 |
75,387,039 (GRCm39) |
critical splice donor site |
probably null |
|
R6819:Speg
|
UTSW |
1 |
75,368,456 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6821:Speg
|
UTSW |
1 |
75,394,547 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6919:Speg
|
UTSW |
1 |
75,364,552 (GRCm39) |
nonsense |
probably null |
|
R6981:Speg
|
UTSW |
1 |
75,407,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R7002:Speg
|
UTSW |
1 |
75,399,912 (GRCm39) |
missense |
probably damaging |
0.98 |
R7082:Speg
|
UTSW |
1 |
75,388,091 (GRCm39) |
missense |
probably damaging |
0.96 |
R7140:Speg
|
UTSW |
1 |
75,383,414 (GRCm39) |
critical splice donor site |
probably null |
|
R7175:Speg
|
UTSW |
1 |
75,399,134 (GRCm39) |
missense |
probably benign |
0.01 |
R7178:Speg
|
UTSW |
1 |
75,399,027 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7345:Speg
|
UTSW |
1 |
75,361,479 (GRCm39) |
missense |
probably damaging |
0.97 |
R7420:Speg
|
UTSW |
1 |
75,407,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R7537:Speg
|
UTSW |
1 |
75,378,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R7562:Speg
|
UTSW |
1 |
75,407,923 (GRCm39) |
missense |
probably damaging |
0.97 |
R7615:Speg
|
UTSW |
1 |
75,405,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Speg
|
UTSW |
1 |
75,382,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R7692:Speg
|
UTSW |
1 |
75,377,834 (GRCm39) |
missense |
probably benign |
0.04 |
R7696:Speg
|
UTSW |
1 |
75,405,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R7719:Speg
|
UTSW |
1 |
75,352,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Speg
|
UTSW |
1 |
75,365,514 (GRCm39) |
missense |
probably benign |
0.00 |
R7824:Speg
|
UTSW |
1 |
75,360,661 (GRCm39) |
splice site |
probably null |
|
R7834:Speg
|
UTSW |
1 |
75,361,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R7892:Speg
|
UTSW |
1 |
75,403,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R8015:Speg
|
UTSW |
1 |
75,392,065 (GRCm39) |
splice site |
probably benign |
|
R8068:Speg
|
UTSW |
1 |
75,398,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Speg
|
UTSW |
1 |
75,391,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R8130:Speg
|
UTSW |
1 |
75,392,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R8132:Speg
|
UTSW |
1 |
75,399,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R8239:Speg
|
UTSW |
1 |
75,395,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R8287:Speg
|
UTSW |
1 |
75,398,880 (GRCm39) |
missense |
probably benign |
0.26 |
R8299:Speg
|
UTSW |
1 |
75,364,480 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8441:Speg
|
UTSW |
1 |
75,387,976 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8468:Speg
|
UTSW |
1 |
75,407,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8555:Speg
|
UTSW |
1 |
75,378,908 (GRCm39) |
splice site |
probably null |
|
R8781:Speg
|
UTSW |
1 |
75,383,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R8784:Speg
|
UTSW |
1 |
75,381,793 (GRCm39) |
critical splice donor site |
probably benign |
|
R8848:Speg
|
UTSW |
1 |
75,404,082 (GRCm39) |
critical splice donor site |
probably null |
|
R8881:Speg
|
UTSW |
1 |
75,377,795 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8898:Speg
|
UTSW |
1 |
75,365,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R8935:Speg
|
UTSW |
1 |
75,399,250 (GRCm39) |
missense |
probably benign |
0.30 |
R9019:Speg
|
UTSW |
1 |
75,405,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R9027:Speg
|
UTSW |
1 |
75,365,076 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9066:Speg
|
UTSW |
1 |
75,361,654 (GRCm39) |
missense |
probably damaging |
0.99 |
R9092:Speg
|
UTSW |
1 |
75,399,378 (GRCm39) |
missense |
probably benign |
0.01 |
R9117:Speg
|
UTSW |
1 |
75,364,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R9202:Speg
|
UTSW |
1 |
75,367,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Speg
|
UTSW |
1 |
75,361,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R9248:Speg
|
UTSW |
1 |
75,398,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R9451:Speg
|
UTSW |
1 |
75,394,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R9452:Speg
|
UTSW |
1 |
75,399,152 (GRCm39) |
missense |
probably benign |
|
R9475:Speg
|
UTSW |
1 |
75,364,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R9476:Speg
|
UTSW |
1 |
75,377,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R9510:Speg
|
UTSW |
1 |
75,377,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R9519:Speg
|
UTSW |
1 |
75,392,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R9528:Speg
|
UTSW |
1 |
75,364,447 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9542:Speg
|
UTSW |
1 |
75,399,426 (GRCm39) |
missense |
probably benign |
0.08 |
R9553:Speg
|
UTSW |
1 |
75,394,645 (GRCm39) |
missense |
probably benign |
0.00 |
R9767:Speg
|
UTSW |
1 |
75,403,825 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9768:Speg
|
UTSW |
1 |
75,395,617 (GRCm39) |
nonsense |
probably null |
|
R9800:Speg
|
UTSW |
1 |
75,399,358 (GRCm39) |
missense |
probably benign |
0.03 |
X0025:Speg
|
UTSW |
1 |
75,399,101 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Speg
|
UTSW |
1 |
75,400,119 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1176:Speg
|
UTSW |
1 |
75,383,238 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Speg
|
UTSW |
1 |
75,404,327 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Speg
|
UTSW |
1 |
75,407,099 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Speg
|
UTSW |
1 |
75,405,025 (GRCm39) |
missense |
probably damaging |
1.00 |
|