Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578G10Rik |
T |
G |
4: 42,760,998 (GRCm39) |
W6G |
unknown |
Het |
Aatk |
A |
T |
11: 119,901,094 (GRCm39) |
C1101S |
probably benign |
Het |
Abcb4 |
A |
T |
5: 8,977,790 (GRCm39) |
D456V |
probably damaging |
Het |
Abcc8 |
T |
C |
7: 45,819,270 (GRCm39) |
E186G |
possibly damaging |
Het |
Adam18 |
T |
C |
8: 25,115,807 (GRCm39) |
N629S |
probably benign |
Het |
Angpt2 |
T |
G |
8: 18,764,143 (GRCm39) |
N133T |
probably benign |
Het |
Ankrd13c |
T |
A |
3: 157,697,396 (GRCm39) |
S334T |
probably benign |
Het |
Ankrd13d |
A |
T |
19: 4,320,289 (GRCm39) |
S151T |
unknown |
Het |
Ap3d1 |
G |
A |
10: 80,545,655 (GRCm39) |
P1025S |
probably benign |
Het |
Bhlhe41 |
G |
A |
6: 145,808,948 (GRCm39) |
A288V |
possibly damaging |
Het |
Cacna1b |
T |
C |
2: 24,540,058 (GRCm39) |
E1467G |
probably damaging |
Het |
Cacna1h |
T |
A |
17: 25,611,524 (GRCm39) |
T425S |
probably damaging |
Het |
Cdk13 |
A |
C |
13: 17,902,747 (GRCm39) |
C934W |
probably damaging |
Het |
Ces1b |
T |
A |
8: 93,799,890 (GRCm39) |
N162I |
probably damaging |
Het |
Clec9a |
T |
A |
6: 129,398,023 (GRCm39) |
I187K |
possibly damaging |
Het |
Cpsf3 |
A |
G |
12: 21,350,080 (GRCm39) |
I266M |
probably damaging |
Het |
Cr2 |
G |
T |
1: 194,840,416 (GRCm39) |
L509M |
probably damaging |
Het |
Creb3l2 |
C |
A |
6: 37,311,446 (GRCm39) |
G448W |
probably damaging |
Het |
Csmd1 |
T |
A |
8: 15,981,215 (GRCm39) |
|
probably null |
Het |
Cul9 |
G |
A |
17: 46,821,833 (GRCm39) |
R1881W |
probably damaging |
Het |
Cyth1 |
C |
T |
11: 118,076,206 (GRCm39) |
|
probably null |
Het |
Dnhd1 |
A |
T |
7: 105,352,889 (GRCm39) |
N2681Y |
possibly damaging |
Het |
Dnm1 |
T |
C |
2: 32,213,739 (GRCm39) |
M476V |
probably benign |
Het |
Dnmt3a |
A |
G |
12: 3,957,707 (GRCm39) |
H896R |
probably damaging |
Het |
Dock1 |
T |
G |
7: 134,592,279 (GRCm39) |
I938S |
probably benign |
Het |
Dock6 |
G |
A |
9: 21,724,821 (GRCm39) |
L1515F |
probably damaging |
Het |
Dusp16 |
T |
C |
6: 134,695,226 (GRCm39) |
H535R |
probably benign |
Het |
Fancd2os |
T |
A |
6: 113,574,994 (GRCm39) |
Y4F |
probably damaging |
Het |
Fat4 |
A |
T |
3: 39,037,886 (GRCm39) |
Q3846L |
probably benign |
Het |
Fbxw10 |
A |
C |
11: 62,743,814 (GRCm39) |
H240P |
probably benign |
Het |
Frmd4a |
A |
G |
2: 4,608,324 (GRCm39) |
T731A |
probably benign |
Het |
Gm44501 |
T |
A |
17: 40,889,820 (GRCm39) |
H111Q |
possibly damaging |
Het |
Gsdmc |
T |
C |
15: 63,650,551 (GRCm39) |
M277V |
probably benign |
Het |
Hira |
A |
G |
16: 18,772,789 (GRCm39) |
D867G |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,462,127 (GRCm39) |
S5184P |
probably benign |
Het |
Ighv1-26 |
A |
C |
12: 114,752,407 (GRCm39) |
F7V |
probably benign |
Het |
Igkv4-81 |
C |
T |
6: 68,967,796 (GRCm39) |
E102K |
possibly damaging |
Het |
Inmt |
G |
T |
6: 55,147,990 (GRCm39) |
S213Y |
possibly damaging |
Het |
Ints2 |
T |
A |
11: 86,135,335 (GRCm39) |
M360L |
probably benign |
Het |
Itih3 |
A |
G |
14: 30,631,416 (GRCm39) |
S827P |
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kcnk12 |
C |
A |
17: 88,054,122 (GRCm39) |
R180L |
probably benign |
Het |
Kndc1 |
G |
A |
7: 139,510,031 (GRCm39) |
S1291N |
probably benign |
Het |
Mettl21a |
T |
C |
1: 64,647,285 (GRCm39) |
T91A |
probably damaging |
Het |
Mmrn2 |
A |
G |
14: 34,120,407 (GRCm39) |
I426V |
possibly damaging |
Het |
Mrpl21 |
T |
G |
19: 3,337,704 (GRCm39) |
V137G |
probably damaging |
Het |
Nrbp2 |
T |
C |
15: 75,961,626 (GRCm39) |
N218S |
probably damaging |
Het |
Nrip1 |
T |
C |
16: 76,089,820 (GRCm39) |
N579S |
probably benign |
Het |
Nsf |
T |
C |
11: 103,763,988 (GRCm39) |
N365S |
probably damaging |
Het |
Or6c5 |
A |
G |
10: 129,074,656 (GRCm39) |
I213V |
probably damaging |
Het |
Or7g28 |
A |
T |
9: 19,272,383 (GRCm39) |
D89E |
probably benign |
Het |
Osbpl3 |
C |
T |
6: 50,313,194 (GRCm39) |
|
probably null |
Het |
Oscar |
T |
A |
7: 3,614,843 (GRCm39) |
H43L |
probably benign |
Het |
Pam |
C |
T |
1: 97,826,065 (GRCm39) |
|
probably null |
Het |
Parn |
A |
T |
16: 13,358,942 (GRCm39) |
M600K |
probably benign |
Het |
Pcdha11 |
C |
A |
18: 37,139,532 (GRCm39) |
T387N |
probably benign |
Het |
Plce1 |
G |
A |
19: 38,766,337 (GRCm39) |
E2121K |
possibly damaging |
Het |
Prune2 |
T |
A |
19: 17,096,706 (GRCm39) |
Y737N |
possibly damaging |
Het |
Ptch1 |
G |
A |
13: 63,681,448 (GRCm39) |
P613L |
probably benign |
Het |
Ptprt |
A |
C |
2: 161,397,381 (GRCm39) |
C1129G |
probably damaging |
Het |
Rara |
C |
T |
11: 98,860,983 (GRCm39) |
S157L |
probably benign |
Het |
Rest |
T |
A |
5: 77,416,098 (GRCm39) |
M104K |
probably damaging |
Het |
Rfc1 |
A |
G |
5: 65,437,142 (GRCm39) |
S513P |
probably damaging |
Het |
Rnf40 |
T |
A |
7: 127,201,808 (GRCm39) |
I1000N |
probably damaging |
Het |
Scube2 |
C |
T |
7: 109,430,969 (GRCm39) |
G410E |
probably damaging |
Het |
Sh3gl2 |
A |
G |
4: 85,304,089 (GRCm39) |
E264G |
probably benign |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Smc4 |
T |
G |
3: 68,914,662 (GRCm39) |
S92A |
probably damaging |
Het |
Spata31d1b |
A |
G |
13: 59,863,467 (GRCm39) |
D205G |
probably benign |
Het |
Spata31e4 |
A |
G |
13: 50,856,149 (GRCm39) |
T596A |
possibly damaging |
Het |
Spef2 |
T |
C |
15: 9,713,203 (GRCm39) |
R390G |
probably damaging |
Het |
Stk17b |
G |
T |
1: 53,796,898 (GRCm39) |
H290N |
probably damaging |
Het |
Stpg3 |
A |
T |
2: 25,103,516 (GRCm39) |
V191D |
probably benign |
Het |
Supt6 |
C |
T |
11: 78,120,290 (GRCm39) |
R350H |
probably damaging |
Het |
Tet3 |
T |
C |
6: 83,380,935 (GRCm39) |
E411G |
possibly damaging |
Het |
Tet3 |
T |
A |
6: 83,381,808 (GRCm39) |
|
probably null |
Het |
Tns3 |
A |
G |
11: 8,395,702 (GRCm39) |
I1234T |
probably damaging |
Het |
Trim34b |
A |
G |
7: 103,980,503 (GRCm39) |
E197G |
probably damaging |
Het |
Vcan |
G |
T |
13: 89,851,531 (GRCm39) |
T1143K |
possibly damaging |
Het |
Vmn2r61 |
T |
A |
7: 41,949,593 (GRCm39) |
V671E |
probably damaging |
Het |
Wdtc1 |
A |
G |
4: 133,049,529 (GRCm39) |
V29A |
probably damaging |
Het |
Zfp462 |
G |
A |
4: 55,080,735 (GRCm39) |
M2450I |
probably benign |
Het |
Zfp869 |
A |
T |
8: 70,159,849 (GRCm39) |
C241* |
probably null |
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 |
|
R1673:Speg
|
UTSW |
1 |
75,387,807 (GRCm39) |
missense |
possibly damaging |
0.60 |
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 |
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 |
|