Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apba1 |
A |
T |
19: 23,870,195 (GRCm39) |
E9V |
probably benign |
Het |
Armc8 |
T |
A |
9: 99,418,333 (GRCm39) |
T32S |
probably benign |
Het |
Atr |
T |
A |
9: 95,752,658 (GRCm39) |
|
probably null |
Het |
Blm |
A |
G |
7: 80,143,862 (GRCm39) |
L859P |
probably benign |
Het |
Cacna2d3 |
A |
T |
14: 28,691,171 (GRCm39) |
F51L |
probably damaging |
Het |
Cdcp2 |
A |
G |
4: 106,964,197 (GRCm39) |
N349S |
probably damaging |
Het |
Cfap57 |
G |
A |
4: 118,457,124 (GRCm39) |
H442Y |
possibly damaging |
Het |
Chrm3 |
A |
G |
13: 9,928,517 (GRCm39) |
L173P |
probably damaging |
Het |
Cpb1 |
C |
G |
3: 20,317,920 (GRCm39) |
M201I |
probably benign |
Het |
Dgcr8 |
A |
T |
16: 18,076,178 (GRCm39) |
N2K |
probably damaging |
Het |
Dnah3 |
A |
T |
7: 119,528,079 (GRCm39) |
|
probably null |
Het |
Dnah6 |
T |
A |
6: 73,077,071 (GRCm39) |
Q2398L |
probably benign |
Het |
Dpep2 |
A |
T |
8: 106,716,080 (GRCm39) |
|
probably null |
Het |
Eif2ak4 |
C |
A |
2: 118,303,142 (GRCm39) |
T1504K |
probably damaging |
Het |
Exoc6b |
A |
G |
6: 84,828,896 (GRCm39) |
V496A |
probably damaging |
Het |
Fam174a |
A |
C |
1: 95,241,620 (GRCm39) |
S27R |
probably benign |
Het |
Fat2 |
T |
A |
11: 55,182,840 (GRCm39) |
Q1339L |
probably benign |
Het |
Fkbpl |
T |
A |
17: 34,864,797 (GRCm39) |
D188E |
possibly damaging |
Het |
Focad |
A |
G |
4: 88,325,402 (GRCm39) |
D89G |
possibly damaging |
Het |
Fstl4 |
C |
A |
11: 53,077,225 (GRCm39) |
Q661K |
probably benign |
Het |
Gck |
T |
C |
11: 5,853,253 (GRCm39) |
Y289C |
probably benign |
Het |
Gm16181 |
T |
A |
17: 35,442,913 (GRCm39) |
|
probably benign |
Het |
Herc1 |
G |
A |
9: 66,358,073 (GRCm39) |
G2385S |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,902,606 (GRCm39) |
|
probably null |
Het |
Il12b |
T |
C |
11: 44,299,353 (GRCm39) |
W141R |
probably damaging |
Het |
Itga6 |
T |
A |
2: 71,664,414 (GRCm39) |
S517T |
probably benign |
Het |
Kank1 |
A |
G |
19: 25,388,813 (GRCm39) |
S801G |
probably benign |
Het |
Klrh1 |
A |
G |
6: 129,752,343 (GRCm39) |
|
probably null |
Het |
Lctl |
A |
G |
9: 64,039,003 (GRCm39) |
D205G |
probably damaging |
Het |
Lhx3 |
A |
C |
2: 26,093,986 (GRCm39) |
V79G |
probably damaging |
Het |
Lrrc9 |
T |
C |
12: 72,543,912 (GRCm39) |
I1127T |
probably damaging |
Het |
Ltbp3 |
A |
T |
19: 5,797,877 (GRCm39) |
E505D |
probably benign |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Map6 |
A |
G |
7: 98,965,083 (GRCm39) |
S291G |
probably damaging |
Het |
Mapk7 |
A |
G |
11: 61,380,239 (GRCm39) |
F671L |
probably benign |
Het |
Mau2 |
A |
G |
8: 70,484,142 (GRCm39) |
W149R |
probably damaging |
Het |
Mb21d2 |
C |
T |
16: 28,647,267 (GRCm39) |
V236I |
possibly damaging |
Het |
Mc5r |
C |
G |
18: 68,471,741 (GRCm39) |
|
probably null |
Het |
Mical1 |
C |
A |
10: 41,361,466 (GRCm39) |
P797Q |
probably benign |
Het |
Mnx1 |
G |
A |
5: 29,679,043 (GRCm39) |
R347C |
unknown |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Nlrp2 |
G |
T |
7: 5,330,715 (GRCm39) |
C560* |
probably null |
Het |
Npat |
T |
A |
9: 53,474,416 (GRCm39) |
L736H |
probably damaging |
Het |
Nup155 |
T |
A |
15: 8,145,010 (GRCm39) |
V147E |
probably damaging |
Het |
Nxpe2 |
A |
G |
9: 48,238,121 (GRCm39) |
F45L |
probably benign |
Het |
Obscn |
T |
C |
11: 58,951,741 (GRCm39) |
D4370G |
probably benign |
Het |
Or2d3b |
A |
G |
7: 106,514,273 (GRCm39) |
I289M |
probably damaging |
Het |
Or4a79 |
T |
C |
2: 89,551,550 (GRCm39) |
K302E |
probably benign |
Het |
Or4c35 |
T |
C |
2: 89,808,671 (GRCm39) |
L183S |
probably damaging |
Het |
Or4d10 |
A |
G |
19: 12,051,183 (GRCm39) |
V271A |
probably benign |
Het |
Or52n4 |
A |
G |
7: 104,294,004 (GRCm39) |
S190P |
probably benign |
Het |
Or5g23 |
T |
A |
2: 85,439,188 (GRCm39) |
H22L |
probably benign |
Het |
Or8k3 |
A |
C |
2: 86,059,072 (GRCm39) |
M81R |
probably damaging |
Het |
Pcx |
T |
C |
19: 4,671,249 (GRCm39) |
I1157T |
possibly damaging |
Het |
Pias2 |
T |
A |
18: 77,240,412 (GRCm39) |
S589R |
probably benign |
Het |
Plcb1 |
T |
C |
2: 135,186,093 (GRCm39) |
F687L |
probably benign |
Het |
Plk5 |
G |
T |
10: 80,196,403 (GRCm39) |
|
probably null |
Het |
Pnpla2 |
T |
A |
7: 141,035,329 (GRCm39) |
Y44N |
probably damaging |
Het |
Ppp1r12a |
T |
A |
10: 108,098,292 (GRCm39) |
D337E |
possibly damaging |
Het |
Prl2c5 |
G |
T |
13: 13,365,358 (GRCm39) |
|
probably null |
Het |
Prom2 |
T |
C |
2: 127,378,514 (GRCm39) |
D460G |
probably damaging |
Het |
Pros1 |
A |
G |
16: 62,748,498 (GRCm39) |
H657R |
possibly damaging |
Het |
Prune2 |
A |
G |
19: 17,100,856 (GRCm39) |
E2120G |
probably damaging |
Het |
Rap2a |
T |
A |
14: 120,716,347 (GRCm39) |
L70Q |
probably damaging |
Het |
Rbl2 |
A |
T |
8: 91,839,157 (GRCm39) |
E858D |
probably benign |
Het |
Rbm48 |
T |
C |
5: 3,645,997 (GRCm39) |
Y69C |
probably damaging |
Het |
Rgs12 |
T |
A |
5: 35,123,018 (GRCm39) |
I267N |
probably damaging |
Het |
Rpusd2 |
G |
T |
2: 118,865,728 (GRCm39) |
A142S |
probably benign |
Het |
Rspo2 |
A |
T |
15: 42,939,332 (GRCm39) |
W153R |
probably damaging |
Het |
Serinc5 |
T |
A |
13: 92,842,771 (GRCm39) |
M407K |
probably damaging |
Het |
Slain2 |
T |
C |
5: 73,114,665 (GRCm39) |
S299P |
probably damaging |
Het |
Slc17a4 |
A |
G |
13: 24,084,528 (GRCm39) |
Y419H |
possibly damaging |
Het |
Slc1a6 |
T |
A |
10: 78,627,183 (GRCm39) |
D173E |
probably damaging |
Het |
Slc22a19 |
A |
T |
19: 7,688,506 (GRCm39) |
I18N |
probably damaging |
Het |
Slc37a3 |
A |
T |
6: 39,336,902 (GRCm39) |
F91L |
probably damaging |
Het |
Spag5 |
C |
A |
11: 78,195,281 (GRCm39) |
T196K |
possibly damaging |
Het |
Susd2 |
G |
T |
10: 75,475,566 (GRCm39) |
A326D |
probably damaging |
Het |
Syna |
G |
T |
5: 134,588,769 (GRCm39) |
A60D |
probably damaging |
Het |
Tchh |
A |
T |
3: 93,355,067 (GRCm39) |
E1502D |
unknown |
Het |
Tecta |
T |
C |
9: 42,303,320 (GRCm39) |
H104R |
probably damaging |
Het |
Tmed1 |
T |
C |
9: 21,420,387 (GRCm39) |
D102G |
probably damaging |
Het |
Trip12 |
T |
C |
1: 84,722,781 (GRCm39) |
D128G |
probably damaging |
Het |
Uroc1 |
A |
G |
6: 90,338,506 (GRCm39) |
M656V |
probably benign |
Het |
Usp47 |
T |
A |
7: 111,701,077 (GRCm39) |
V1096D |
possibly damaging |
Het |
Utp20 |
T |
A |
10: 88,598,632 (GRCm39) |
K115* |
probably null |
Het |
Vmn2r19 |
G |
T |
6: 123,308,597 (GRCm39) |
|
probably null |
Het |
Vmn2r86 |
A |
T |
10: 130,282,255 (GRCm39) |
V787D |
probably damaging |
Het |
Vmn2r87 |
A |
T |
10: 130,308,441 (GRCm39) |
I599N |
possibly damaging |
Het |
Vwf |
A |
G |
6: 125,644,492 (GRCm39) |
D2449G |
possibly damaging |
Het |
Zbtb7c |
T |
A |
18: 76,269,977 (GRCm39) |
C22S |
probably benign |
Het |
Zc3h7a |
A |
G |
16: 10,965,168 (GRCm39) |
I655T |
possibly damaging |
Het |
Zfp764l1 |
A |
G |
7: 126,992,503 (GRCm39) |
W36R |
probably 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 |
|
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 |
R1964:Sdk2
|
UTSW |
11 |
113,671,843 (GRCm39) |
nonsense |
probably null |
|
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 |
|