Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
C |
T |
17: 9,211,324 (GRCm39) |
H158Y |
probably damaging |
Het |
1810009J06Rik |
T |
A |
6: 40,945,141 (GRCm39) |
C207S |
probably damaging |
Het |
Aadac |
T |
A |
3: 59,944,759 (GRCm39) |
|
probably null |
Het |
Abca6 |
T |
A |
11: 110,075,502 (GRCm39) |
I1330F |
probably damaging |
Het |
Adar |
A |
T |
3: 89,653,202 (GRCm39) |
S263C |
probably benign |
Het |
Adra2b |
T |
C |
2: 127,205,734 (GRCm39) |
Y84H |
probably damaging |
Het |
Arnt2 |
A |
T |
7: 83,992,997 (GRCm39) |
V181E |
possibly damaging |
Het |
Atg7 |
T |
C |
6: 114,683,191 (GRCm39) |
L418P |
probably damaging |
Het |
Atp2c1 |
A |
G |
9: 105,323,322 (GRCm39) |
L181P |
probably damaging |
Het |
Awat2 |
G |
A |
X: 99,448,165 (GRCm39) |
P148S |
probably damaging |
Het |
Birc6 |
A |
G |
17: 74,941,880 (GRCm39) |
M2737V |
possibly damaging |
Het |
Ccdc81 |
A |
G |
7: 89,535,361 (GRCm39) |
C292R |
probably benign |
Het |
Cd14 |
T |
A |
18: 36,859,392 (GRCm39) |
E21V |
probably damaging |
Het |
Cdc14b |
A |
C |
13: 64,363,351 (GRCm39) |
C303W |
probably damaging |
Het |
Cdh23 |
T |
C |
10: 60,221,001 (GRCm39) |
I1248V |
probably benign |
Het |
Ceacam1 |
T |
C |
7: 25,174,133 (GRCm39) |
D174G |
probably benign |
Het |
Cgas |
T |
G |
9: 78,344,737 (GRCm39) |
Y228S |
probably damaging |
Het |
Chd7 |
A |
G |
4: 8,865,978 (GRCm39) |
M717V |
probably damaging |
Het |
Cib1 |
T |
C |
7: 79,882,120 (GRCm39) |
T20A |
possibly damaging |
Het |
Clec4d |
A |
G |
6: 123,239,319 (GRCm39) |
K9R |
probably benign |
Het |
Cntnap1 |
C |
A |
11: 101,068,850 (GRCm39) |
S131* |
probably null |
Het |
Crybg1 |
T |
C |
10: 43,834,326 (GRCm39) |
K1581R |
probably damaging |
Het |
Csf2 |
T |
G |
11: 54,139,284 (GRCm39) |
T100P |
probably benign |
Het |
Csrp2 |
T |
A |
10: 110,767,894 (GRCm39) |
D26E |
probably benign |
Het |
Cul1 |
T |
C |
6: 47,479,505 (GRCm39) |
V257A |
probably damaging |
Het |
Cul4a |
G |
A |
8: 13,186,406 (GRCm39) |
M505I |
possibly damaging |
Het |
Cul4a |
T |
C |
8: 13,186,854 (GRCm39) |
M530T |
probably benign |
Het |
Dcp2 |
T |
C |
18: 44,529,038 (GRCm39) |
M51T |
possibly damaging |
Het |
Ddx60 |
T |
A |
8: 62,401,903 (GRCm39) |
C260S |
probably benign |
Het |
Dennd2c |
G |
A |
3: 103,073,807 (GRCm39) |
R851H |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 118,106,027 (GRCm39) |
E625G |
possibly damaging |
Het |
Edem1 |
T |
C |
6: 108,821,908 (GRCm39) |
W322R |
probably benign |
Het |
Egflam |
T |
C |
15: 7,276,586 (GRCm39) |
T527A |
probably damaging |
Het |
Ephb1 |
T |
A |
9: 101,848,322 (GRCm39) |
M659L |
possibly damaging |
Het |
Fbxl2 |
A |
G |
9: 113,818,237 (GRCm39) |
I203T |
probably benign |
Het |
Gabbr1 |
G |
A |
17: 37,359,351 (GRCm39) |
G109R |
probably damaging |
Het |
Gabra2 |
T |
C |
5: 71,171,793 (GRCm39) |
I148V |
possibly damaging |
Het |
Golga1 |
A |
G |
2: 38,937,099 (GRCm39) |
V161A |
probably benign |
Het |
Gps2 |
T |
G |
11: 69,807,246 (GRCm39) |
S301A |
probably benign |
Het |
H2-D1 |
T |
C |
17: 35,482,595 (GRCm39) |
L105P |
probably benign |
Het |
Igdcc4 |
T |
C |
9: 65,030,051 (GRCm39) |
V367A |
probably benign |
Het |
Igkv4-69 |
T |
G |
6: 69,260,782 (GRCm39) |
Y115S |
probably benign |
Het |
Itga5 |
A |
G |
15: 103,262,741 (GRCm39) |
L309P |
probably damaging |
Het |
Itih1 |
A |
G |
14: 30,651,580 (GRCm39) |
Y871H |
probably damaging |
Het |
Itpr2 |
T |
A |
6: 146,013,191 (GRCm39) |
N2662I |
probably damaging |
Het |
Kctd19 |
T |
A |
8: 106,115,102 (GRCm39) |
E486D |
probably damaging |
Het |
Kif5b |
C |
T |
18: 6,209,059 (GRCm39) |
R901Q |
possibly damaging |
Het |
Kmt2a |
G |
A |
9: 44,731,941 (GRCm39) |
S2792F |
probably benign |
Het |
Magi3 |
A |
G |
3: 103,927,718 (GRCm39) |
V1023A |
probably damaging |
Het |
Mapk9 |
C |
A |
11: 49,745,160 (GRCm39) |
R25S |
probably null |
Het |
Memo1 |
T |
C |
17: 74,552,003 (GRCm39) |
T98A |
possibly damaging |
Het |
Mill2 |
A |
G |
7: 18,590,529 (GRCm39) |
K203R |
probably damaging |
Het |
Mios |
T |
A |
6: 8,215,798 (GRCm39) |
H331Q |
probably damaging |
Het |
Muc6 |
G |
T |
7: 141,226,329 (GRCm39) |
S1566* |
probably null |
Het |
Muc6 |
A |
G |
7: 141,226,330 (GRCm39) |
|
probably benign |
Het |
Napsa |
T |
C |
7: 44,231,109 (GRCm39) |
F113L |
probably benign |
Het |
Or5ac16 |
T |
A |
16: 59,022,271 (GRCm39) |
I173F |
possibly damaging |
Het |
Or9m1 |
A |
G |
2: 87,734,011 (GRCm39) |
V3A |
probably benign |
Het |
Oscp1 |
T |
G |
4: 125,977,415 (GRCm39) |
V226G |
possibly damaging |
Het |
Osgin2 |
G |
T |
4: 15,998,358 (GRCm39) |
S421R |
probably damaging |
Het |
Pclaf |
A |
G |
9: 65,800,677 (GRCm39) |
N50D |
probably damaging |
Het |
Pdgfc |
A |
T |
3: 81,082,292 (GRCm39) |
I162F |
probably benign |
Het |
Plag1 |
T |
C |
4: 3,903,956 (GRCm39) |
T412A |
probably benign |
Het |
Pogz |
A |
T |
3: 94,785,504 (GRCm39) |
T820S |
probably benign |
Het |
Ptpn9 |
T |
A |
9: 56,967,196 (GRCm39) |
V473D |
probably damaging |
Het |
Qdpr |
A |
T |
5: 45,596,660 (GRCm39) |
M66K |
possibly damaging |
Het |
Qrich1 |
A |
G |
9: 108,411,621 (GRCm39) |
N382S |
possibly damaging |
Het |
Rbbp8 |
T |
C |
18: 11,875,736 (GRCm39) |
V883A |
possibly damaging |
Het |
Rgl1 |
T |
A |
1: 152,424,855 (GRCm39) |
I375F |
probably damaging |
Het |
Rif1 |
C |
T |
2: 51,988,421 (GRCm39) |
T720I |
probably benign |
Het |
Rilp |
A |
T |
11: 75,401,328 (GRCm39) |
Q95L |
probably benign |
Het |
Rnf169 |
T |
A |
7: 99,574,732 (GRCm39) |
N621I |
probably damaging |
Het |
Rps27a |
T |
C |
11: 29,497,229 (GRCm39) |
K27R |
probably null |
Het |
Sar1a |
T |
C |
10: 61,520,947 (GRCm39) |
V54A |
probably benign |
Het |
Sash1 |
T |
A |
10: 8,605,477 (GRCm39) |
H971L |
probably benign |
Het |
Serpina1e |
T |
A |
12: 103,917,466 (GRCm39) |
I68F |
probably damaging |
Het |
Serpinb9e |
A |
C |
13: 33,437,474 (GRCm39) |
Q119P |
probably benign |
Het |
Sh3tc2 |
A |
T |
18: 62,124,226 (GRCm39) |
K965* |
probably null |
Het |
Slc16a1 |
A |
T |
3: 104,556,782 (GRCm39) |
S56C |
probably damaging |
Het |
Slc26a11 |
T |
A |
11: 119,271,020 (GRCm39) |
L563Q |
possibly damaging |
Het |
Smarca2 |
G |
T |
19: 26,650,124 (GRCm39) |
E24* |
probably null |
Het |
Smgc |
G |
A |
15: 91,744,468 (GRCm39) |
G239D |
probably damaging |
Het |
Sos2 |
A |
T |
12: 69,663,636 (GRCm39) |
M616K |
possibly damaging |
Het |
Tet1 |
T |
A |
10: 62,648,726 (GRCm39) |
D1902V |
possibly damaging |
Het |
Thap2 |
C |
T |
10: 115,220,152 (GRCm39) |
C10Y |
probably damaging |
Het |
Tln2 |
T |
C |
9: 67,249,417 (GRCm39) |
D890G |
probably benign |
Het |
Tor2a |
G |
A |
2: 32,648,716 (GRCm39) |
G62D |
probably damaging |
Het |
Ubqln5 |
A |
T |
7: 103,778,095 (GRCm39) |
V243E |
possibly damaging |
Het |
Utrn |
A |
T |
10: 12,560,181 (GRCm39) |
D1369E |
probably damaging |
Het |
Vcan |
A |
G |
13: 89,840,861 (GRCm39) |
V1561A |
probably benign |
Het |
Vmn1r70 |
T |
C |
7: 10,367,737 (GRCm39) |
F56S |
possibly damaging |
Het |
Vmn2r25 |
A |
G |
6: 123,800,254 (GRCm39) |
L696S |
possibly damaging |
Het |
Washc2 |
A |
G |
6: 116,185,948 (GRCm39) |
T53A |
probably damaging |
Het |
Wnk1 |
T |
A |
6: 119,911,343 (GRCm39) |
T2417S |
possibly damaging |
Het |
Zbtb49 |
A |
T |
5: 38,361,105 (GRCm39) |
C12* |
probably null |
Het |
Zfp472 |
C |
A |
17: 33,196,848 (GRCm39) |
P308T |
possibly damaging |
Het |
|
Other mutations in Sdk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00972:Sdk2
|
APN |
11 |
113,745,210 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01063:Sdk2
|
APN |
11 |
113,721,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01291:Sdk2
|
APN |
11 |
113,733,906 (GRCm39) |
missense |
probably benign |
|
IGL01316:Sdk2
|
APN |
11 |
113,758,791 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01614:Sdk2
|
APN |
11 |
113,684,684 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01998:Sdk2
|
APN |
11 |
113,729,358 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02014:Sdk2
|
APN |
11 |
113,729,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02095:Sdk2
|
APN |
11 |
113,725,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02115:Sdk2
|
APN |
11 |
113,725,639 (GRCm39) |
splice site |
probably benign |
|
IGL02543:Sdk2
|
APN |
11 |
113,759,747 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02976:Sdk2
|
APN |
11 |
113,742,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03001:Sdk2
|
APN |
11 |
113,712,452 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03122:Sdk2
|
APN |
11 |
113,732,894 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03183:Sdk2
|
APN |
11 |
113,741,810 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03222:Sdk2
|
APN |
11 |
113,729,257 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03310:Sdk2
|
APN |
11 |
113,684,151 (GRCm39) |
missense |
possibly damaging |
0.77 |
Curtailed
|
UTSW |
11 |
113,742,626 (GRCm39) |
missense |
probably damaging |
1.00 |
Trimmed
|
UTSW |
11 |
113,747,522 (GRCm39) |
nonsense |
probably null |
|
ANU05:Sdk2
|
UTSW |
11 |
113,733,906 (GRCm39) |
missense |
probably benign |
|
BB008:Sdk2
|
UTSW |
11 |
113,784,267 (GRCm39) |
missense |
possibly damaging |
0.79 |
BB018:Sdk2
|
UTSW |
11 |
113,784,267 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0008:Sdk2
|
UTSW |
11 |
113,747,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R0008:Sdk2
|
UTSW |
11 |
113,747,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R0088:Sdk2
|
UTSW |
11 |
113,717,912 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0096:Sdk2
|
UTSW |
11 |
113,793,970 (GRCm39) |
splice site |
probably benign |
|
R0386:Sdk2
|
UTSW |
11 |
113,784,290 (GRCm39) |
missense |
probably damaging |
0.96 |
R0396:Sdk2
|
UTSW |
11 |
113,720,793 (GRCm39) |
missense |
probably benign |
0.04 |
R0409:Sdk2
|
UTSW |
11 |
113,741,717 (GRCm39) |
splice site |
probably benign |
|
R0416:Sdk2
|
UTSW |
11 |
113,694,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R0456:Sdk2
|
UTSW |
11 |
113,682,292 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0544:Sdk2
|
UTSW |
11 |
113,671,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R0691:Sdk2
|
UTSW |
11 |
113,685,746 (GRCm39) |
splice site |
probably null |
|
R0711:Sdk2
|
UTSW |
11 |
113,793,970 (GRCm39) |
splice site |
probably benign |
|
R0717:Sdk2
|
UTSW |
11 |
113,723,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R0780:Sdk2
|
UTSW |
11 |
113,784,334 (GRCm39) |
missense |
probably benign |
0.07 |
R0831:Sdk2
|
UTSW |
11 |
113,723,084 (GRCm39) |
missense |
probably damaging |
0.96 |
R0853:Sdk2
|
UTSW |
11 |
113,712,241 (GRCm39) |
missense |
probably benign |
0.00 |
R0865:Sdk2
|
UTSW |
11 |
113,741,748 (GRCm39) |
missense |
probably benign |
0.12 |
R0930:Sdk2
|
UTSW |
11 |
113,729,271 (GRCm39) |
missense |
probably benign |
0.01 |
R0964:Sdk2
|
UTSW |
11 |
113,697,243 (GRCm39) |
splice site |
probably benign |
|
R1051:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1052:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1054:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1055:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1077:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1079:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1115:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1186:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1187:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1337:Sdk2
|
UTSW |
11 |
113,723,157 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1430:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1433:Sdk2
|
UTSW |
11 |
113,685,871 (GRCm39) |
missense |
probably damaging |
0.99 |
R1464:Sdk2
|
UTSW |
11 |
113,720,906 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1464:Sdk2
|
UTSW |
11 |
113,720,906 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1497:Sdk2
|
UTSW |
11 |
113,784,401 (GRCm39) |
splice site |
probably benign |
|
R1514:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1529:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1596:Sdk2
|
UTSW |
11 |
113,729,435 (GRCm39) |
splice site |
probably benign |
|
R1680:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1680:Sdk2
|
UTSW |
11 |
113,682,262 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1770:Sdk2
|
UTSW |
11 |
113,684,567 (GRCm39) |
missense |
probably benign |
0.05 |
R1858:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1866:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1874:Sdk2
|
UTSW |
11 |
113,725,782 (GRCm39) |
missense |
probably benign |
0.00 |
R1899:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1905:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1907:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1913:Sdk2
|
UTSW |
11 |
113,747,552 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2055:Sdk2
|
UTSW |
11 |
113,741,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R2059:Sdk2
|
UTSW |
11 |
113,745,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R2093:Sdk2
|
UTSW |
11 |
113,833,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Sdk2
|
UTSW |
11 |
113,721,620 (GRCm39) |
missense |
probably benign |
0.44 |
R3720:Sdk2
|
UTSW |
11 |
113,691,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R3795:Sdk2
|
UTSW |
11 |
113,747,522 (GRCm39) |
nonsense |
probably null |
|
R4037:Sdk2
|
UTSW |
11 |
113,685,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R4171:Sdk2
|
UTSW |
11 |
113,757,815 (GRCm39) |
splice site |
probably null |
|
R4717:Sdk2
|
UTSW |
11 |
113,745,195 (GRCm39) |
missense |
probably damaging |
0.96 |
R4758:Sdk2
|
UTSW |
11 |
113,717,880 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4857:Sdk2
|
UTSW |
11 |
113,712,208 (GRCm39) |
nonsense |
probably null |
|
R4924:Sdk2
|
UTSW |
11 |
113,748,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Sdk2
|
UTSW |
11 |
113,684,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R5171:Sdk2
|
UTSW |
11 |
113,741,808 (GRCm39) |
missense |
probably benign |
0.01 |
R5239:Sdk2
|
UTSW |
11 |
113,758,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R5243:Sdk2
|
UTSW |
11 |
113,715,912 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5279:Sdk2
|
UTSW |
11 |
113,757,857 (GRCm39) |
missense |
probably benign |
0.31 |
R5535:Sdk2
|
UTSW |
11 |
113,833,984 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5634:Sdk2
|
UTSW |
11 |
113,742,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R5637:Sdk2
|
UTSW |
11 |
113,724,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Sdk2
|
UTSW |
11 |
113,742,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R5793:Sdk2
|
UTSW |
11 |
113,759,778 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5798:Sdk2
|
UTSW |
11 |
113,717,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R5834:Sdk2
|
UTSW |
11 |
113,745,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5863:Sdk2
|
UTSW |
11 |
113,725,810 (GRCm39) |
missense |
probably damaging |
0.98 |
R5869:Sdk2
|
UTSW |
11 |
113,742,708 (GRCm39) |
missense |
probably damaging |
0.96 |
R5875:Sdk2
|
UTSW |
11 |
113,720,885 (GRCm39) |
missense |
probably benign |
0.00 |
R5953:Sdk2
|
UTSW |
11 |
113,684,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R5991:Sdk2
|
UTSW |
11 |
113,834,080 (GRCm39) |
missense |
probably damaging |
0.97 |
R6018:Sdk2
|
UTSW |
11 |
113,720,889 (GRCm39) |
missense |
probably benign |
0.00 |
R6116:Sdk2
|
UTSW |
11 |
113,745,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R6328:Sdk2
|
UTSW |
11 |
113,684,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R6348:Sdk2
|
UTSW |
11 |
113,784,334 (GRCm39) |
missense |
probably benign |
0.07 |
R6383:Sdk2
|
UTSW |
11 |
113,723,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6824:Sdk2
|
UTSW |
11 |
113,758,760 (GRCm39) |
missense |
probably benign |
0.43 |
R6835:Sdk2
|
UTSW |
11 |
113,720,874 (GRCm39) |
missense |
probably damaging |
0.98 |
R6853:Sdk2
|
UTSW |
11 |
113,671,755 (GRCm39) |
missense |
probably damaging |
0.99 |
R6912:Sdk2
|
UTSW |
11 |
113,793,946 (GRCm39) |
missense |
probably benign |
0.03 |
R7000:Sdk2
|
UTSW |
11 |
113,693,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R7099:Sdk2
|
UTSW |
11 |
113,725,731 (GRCm39) |
missense |
probably damaging |
0.98 |
R7102:Sdk2
|
UTSW |
11 |
113,733,516 (GRCm39) |
nonsense |
probably null |
|
R7177:Sdk2
|
UTSW |
11 |
113,720,795 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7381:Sdk2
|
UTSW |
11 |
113,729,315 (GRCm39) |
missense |
probably damaging |
0.98 |
R7412:Sdk2
|
UTSW |
11 |
113,758,909 (GRCm39) |
splice site |
probably null |
|
R7504:Sdk2
|
UTSW |
11 |
113,758,793 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7552:Sdk2
|
UTSW |
11 |
113,764,039 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7604:Sdk2
|
UTSW |
11 |
113,720,795 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7647:Sdk2
|
UTSW |
11 |
113,684,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R7897:Sdk2
|
UTSW |
11 |
113,764,027 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7931:Sdk2
|
UTSW |
11 |
113,784,267 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7998:Sdk2
|
UTSW |
11 |
113,750,764 (GRCm39) |
missense |
probably benign |
0.18 |
R8052:Sdk2
|
UTSW |
11 |
113,745,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Sdk2
|
UTSW |
11 |
113,745,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R8084:Sdk2
|
UTSW |
11 |
113,717,915 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8136:Sdk2
|
UTSW |
11 |
113,742,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R8151:Sdk2
|
UTSW |
11 |
113,763,683 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8394:Sdk2
|
UTSW |
11 |
113,729,542 (GRCm39) |
missense |
probably benign |
|
R8715:Sdk2
|
UTSW |
11 |
113,671,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Sdk2
|
UTSW |
11 |
113,730,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774-TAIL:Sdk2
|
UTSW |
11 |
113,730,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R8804:Sdk2
|
UTSW |
11 |
113,763,978 (GRCm39) |
nonsense |
probably null |
|
R9136:Sdk2
|
UTSW |
11 |
113,697,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Sdk2
|
UTSW |
11 |
113,714,226 (GRCm39) |
missense |
probably benign |
0.18 |
R9300:Sdk2
|
UTSW |
11 |
113,715,856 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9354:Sdk2
|
UTSW |
11 |
113,725,757 (GRCm39) |
missense |
probably benign |
0.00 |
R9450:Sdk2
|
UTSW |
11 |
113,697,105 (GRCm39) |
missense |
probably benign |
|
R9462:Sdk2
|
UTSW |
11 |
113,760,744 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9616:Sdk2
|
UTSW |
11 |
113,691,061 (GRCm39) |
missense |
probably benign |
0.05 |
R9678:Sdk2
|
UTSW |
11 |
113,685,789 (GRCm39) |
nonsense |
probably null |
|
RF002:Sdk2
|
UTSW |
11 |
113,776,078 (GRCm39) |
missense |
probably benign |
0.00 |
V1662:Sdk2
|
UTSW |
11 |
113,725,734 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Sdk2
|
UTSW |
11 |
113,742,662 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Sdk2
|
UTSW |
11 |
113,730,148 (GRCm39) |
missense |
probably benign |
0.41 |
Z1177:Sdk2
|
UTSW |
11 |
113,750,782 (GRCm39) |
missense |
probably benign |
|
Z1177:Sdk2
|
UTSW |
11 |
113,730,146 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sdk2
|
UTSW |
11 |
113,729,485 (GRCm39) |
missense |
probably damaging |
0.99 |
|