Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
A |
G |
1: 130,670,428 (GRCm39) |
S217G |
probably benign |
Het |
Adrb3 |
C |
A |
8: 27,717,591 (GRCm39) |
R286L |
probably damaging |
Het |
Akap11 |
T |
A |
14: 78,749,306 (GRCm39) |
D1027V |
probably benign |
Het |
Ank3 |
A |
T |
10: 69,733,913 (GRCm39) |
I726F |
probably damaging |
Het |
Ankmy2 |
T |
A |
12: 36,215,930 (GRCm39) |
D43E |
possibly damaging |
Het |
Ankrd34b |
A |
G |
13: 92,576,064 (GRCm39) |
D432G |
probably damaging |
Het |
Ano3 |
A |
C |
2: 110,715,217 (GRCm39) |
S74A |
probably benign |
Het |
B4galnt4 |
T |
A |
7: 140,650,439 (GRCm39) |
S769T |
probably damaging |
Het |
Bicral |
T |
A |
17: 47,136,104 (GRCm39) |
T369S |
probably benign |
Het |
Blm |
A |
G |
7: 80,147,166 (GRCm39) |
L738P |
probably damaging |
Het |
Bpifb3 |
A |
G |
2: 153,767,760 (GRCm39) |
T278A |
probably benign |
Het |
Bpifb5 |
A |
G |
2: 154,069,122 (GRCm39) |
|
probably benign |
Het |
Brd8 |
G |
C |
18: 34,743,527 (GRCm39) |
P266R |
probably damaging |
Het |
Btaf1 |
A |
T |
19: 36,957,983 (GRCm39) |
M587L |
probably benign |
Het |
Casz1 |
C |
G |
4: 149,027,668 (GRCm39) |
T1015S |
probably damaging |
Het |
Cdh23 |
A |
G |
10: 60,272,597 (GRCm39) |
I524T |
possibly damaging |
Het |
Celsr3 |
T |
C |
9: 108,713,037 (GRCm39) |
V1825A |
probably benign |
Het |
Cenpf |
A |
G |
1: 189,416,013 (GRCm39) |
L104P |
probably damaging |
Het |
Clasp1 |
G |
T |
1: 118,528,315 (GRCm39) |
|
probably null |
Het |
Coprs |
A |
G |
8: 13,935,112 (GRCm39) |
W148R |
probably damaging |
Het |
Cpne1 |
A |
G |
2: 155,920,302 (GRCm39) |
S168P |
probably damaging |
Het |
Cpxm2 |
T |
C |
7: 131,661,563 (GRCm39) |
Y408C |
probably damaging |
Het |
Ctnna3 |
A |
G |
10: 63,339,886 (GRCm39) |
E24G |
possibly damaging |
Het |
Cubn |
T |
A |
2: 13,327,813 (GRCm39) |
S2671C |
probably damaging |
Het |
Cyp4f39 |
T |
A |
17: 32,702,298 (GRCm39) |
F265Y |
probably damaging |
Het |
Dgkq |
C |
A |
5: 108,808,461 (GRCm39) |
R34L |
probably benign |
Het |
Dnajc7 |
C |
T |
11: 100,490,139 (GRCm39) |
|
probably benign |
Het |
Eml6 |
T |
G |
11: 29,781,136 (GRCm39) |
D632A |
probably damaging |
Het |
Fbxl18 |
G |
A |
5: 142,871,978 (GRCm39) |
A419V |
probably damaging |
Het |
Fbxw22 |
A |
T |
9: 109,214,179 (GRCm39) |
C212* |
probably null |
Het |
Ffar2 |
A |
G |
7: 30,518,839 (GRCm39) |
|
probably null |
Het |
Fga |
A |
T |
3: 82,940,028 (GRCm39) |
T561S |
probably damaging |
Het |
Fry |
A |
G |
5: 150,269,386 (GRCm39) |
Y159C |
probably damaging |
Het |
Gal3st1 |
A |
G |
11: 3,948,231 (GRCm39) |
Y146C |
probably damaging |
Het |
Gapvd1 |
A |
T |
2: 34,596,033 (GRCm39) |
H788Q |
probably damaging |
Het |
Gimap7 |
G |
A |
6: 48,700,449 (GRCm39) |
V12I |
possibly damaging |
Het |
Gli2 |
C |
A |
1: 118,929,779 (GRCm39) |
A43S |
possibly damaging |
Het |
Gm15446 |
T |
C |
5: 110,090,419 (GRCm39) |
F224L |
probably damaging |
Het |
Gm21738 |
C |
T |
14: 19,418,824 (GRCm38) |
V35I |
possibly damaging |
Het |
Grhl1 |
T |
C |
12: 24,636,155 (GRCm39) |
|
probably benign |
Het |
Grk6 |
T |
C |
13: 55,598,086 (GRCm39) |
Y53H |
probably damaging |
Het |
Hcar1 |
C |
T |
5: 124,017,328 (GRCm39) |
R121K |
probably damaging |
Het |
Hmcn1 |
A |
C |
1: 150,596,446 (GRCm39) |
S1797A |
probably damaging |
Het |
Hsd17b7 |
A |
T |
1: 169,783,562 (GRCm39) |
L282Q |
possibly damaging |
Het |
Irs1 |
TTCTCTGAGTGGCCACAGCGTCT |
TTCT |
1: 82,267,574 (GRCm39) |
|
probably null |
Het |
Kif1b |
C |
T |
4: 149,272,089 (GRCm39) |
V1571I |
probably benign |
Het |
Lpl |
T |
A |
8: 69,349,271 (GRCm39) |
C266S |
probably damaging |
Het |
Mag |
G |
A |
7: 30,608,476 (GRCm39) |
H213Y |
probably benign |
Het |
Mansc4 |
T |
G |
6: 146,976,688 (GRCm39) |
R309S |
probably benign |
Het |
Mlh3 |
A |
G |
12: 85,284,287 (GRCm39) |
|
probably null |
Het |
Mndal |
G |
A |
1: 173,687,933 (GRCm39) |
|
probably benign |
Het |
Mrgpra2b |
T |
A |
7: 47,113,742 (GRCm39) |
E330V |
probably damaging |
Het |
Myh3 |
A |
G |
11: 66,984,005 (GRCm39) |
I990V |
probably benign |
Het |
Myoz2 |
A |
T |
3: 122,819,765 (GRCm39) |
S65T |
probably damaging |
Het |
Naa16 |
T |
C |
14: 79,593,183 (GRCm39) |
E463G |
possibly damaging |
Het |
Nadsyn1 |
A |
G |
7: 143,351,581 (GRCm39) |
F684S |
probably damaging |
Het |
Notch1 |
T |
C |
2: 26,371,591 (GRCm39) |
E286G |
possibly damaging |
Het |
Nynrin |
A |
T |
14: 56,100,950 (GRCm39) |
I247L |
probably benign |
Het |
Oprm1 |
A |
G |
10: 6,739,035 (GRCm39) |
H54R |
probably benign |
Het |
Or10g6 |
T |
A |
9: 39,934,151 (GRCm39) |
I154N |
possibly damaging |
Het |
Or2n1d |
C |
T |
17: 38,646,860 (GRCm39) |
P271S |
probably damaging |
Het |
Or51a43 |
T |
C |
7: 103,717,336 (GRCm39) |
I301V |
probably null |
Het |
P4hb |
C |
T |
11: 120,452,992 (GRCm39) |
D483N |
probably benign |
Het |
Pak1 |
T |
C |
7: 97,520,787 (GRCm39) |
S149P |
probably benign |
Het |
Pars2 |
T |
C |
4: 106,510,913 (GRCm39) |
F232L |
possibly damaging |
Het |
Pih1d2 |
A |
G |
9: 50,532,245 (GRCm39) |
M88V |
possibly damaging |
Het |
Pms1 |
A |
T |
1: 53,246,392 (GRCm39) |
N382K |
probably benign |
Het |
Pnliprp2 |
G |
T |
19: 58,751,821 (GRCm39) |
V189L |
probably benign |
Het |
Pole |
G |
A |
5: 110,471,530 (GRCm39) |
V1425M |
possibly damaging |
Het |
Pot1b |
T |
A |
17: 55,961,805 (GRCm39) |
Q591L |
probably benign |
Het |
Ppp1r9a |
C |
T |
6: 4,906,348 (GRCm39) |
T301M |
possibly damaging |
Het |
Psg21 |
T |
C |
7: 18,384,741 (GRCm39) |
E335G |
probably benign |
Het |
Ptpru |
T |
A |
4: 131,497,066 (GRCm39) |
M1416L |
probably benign |
Het |
Pxn |
T |
C |
5: 115,683,049 (GRCm39) |
V117A |
probably damaging |
Het |
Qsox1 |
C |
T |
1: 155,688,385 (GRCm39) |
R54H |
possibly damaging |
Het |
Rad1 |
A |
G |
15: 10,488,092 (GRCm39) |
E42G |
probably damaging |
Het |
Rpp14 |
A |
G |
14: 8,090,145 (GRCm38) |
Y23C |
probably benign |
Het |
Serpina3j |
G |
T |
12: 104,285,958 (GRCm39) |
R371L |
probably benign |
Het |
Serpinb9d |
T |
A |
13: 33,381,946 (GRCm39) |
|
probably null |
Het |
Sirt5 |
C |
T |
13: 43,524,267 (GRCm39) |
S13F |
possibly damaging |
Het |
Slc6a7 |
T |
A |
18: 61,134,470 (GRCm39) |
|
probably benign |
Het |
Slx4 |
A |
G |
16: 3,804,712 (GRCm39) |
S701P |
probably benign |
Het |
Snx29 |
A |
G |
16: 11,185,545 (GRCm39) |
T43A |
probably benign |
Het |
Speg |
T |
C |
1: 75,400,550 (GRCm39) |
V2570A |
probably benign |
Het |
Srrm4 |
T |
A |
5: 116,591,565 (GRCm39) |
|
probably benign |
Het |
Stk32a |
A |
G |
18: 43,394,381 (GRCm39) |
Y110C |
probably damaging |
Het |
Tbc1d31 |
G |
A |
15: 57,779,506 (GRCm39) |
G73E |
probably benign |
Het |
Thsd7a |
A |
T |
6: 12,555,434 (GRCm39) |
I150N |
possibly damaging |
Het |
Tjp1 |
A |
T |
7: 64,969,001 (GRCm39) |
D699E |
probably damaging |
Het |
Tmem143 |
A |
G |
7: 45,565,988 (GRCm39) |
D437G |
possibly damaging |
Het |
Tmem45a2 |
A |
G |
16: 56,867,447 (GRCm39) |
Y85H |
possibly damaging |
Het |
Tmem45b |
T |
A |
9: 31,340,383 (GRCm39) |
T7S |
probably damaging |
Het |
Tut4 |
T |
A |
4: 108,407,922 (GRCm39) |
V1397D |
probably damaging |
Het |
Ube4b |
A |
G |
4: 149,432,428 (GRCm39) |
L832P |
probably damaging |
Het |
Ugp2 |
G |
T |
11: 21,279,048 (GRCm39) |
F379L |
probably damaging |
Het |
Ugt3a1 |
A |
T |
15: 9,365,437 (GRCm39) |
D350V |
probably damaging |
Het |
Vmn2r8 |
T |
A |
5: 108,950,284 (GRCm39) |
T188S |
possibly damaging |
Het |
Vwa7 |
C |
G |
17: 35,236,088 (GRCm39) |
P14R |
probably benign |
Het |
Vwc2 |
C |
A |
11: 11,211,495 (GRCm39) |
T317K |
probably damaging |
Het |
Vwf |
A |
T |
6: 125,605,335 (GRCm39) |
Q906L |
probably benign |
Het |
Wdr49 |
A |
G |
3: 75,336,654 (GRCm39) |
V351A |
probably damaging |
Het |
Wdr7 |
A |
G |
18: 63,861,575 (GRCm39) |
S196G |
probably benign |
Het |
Xkr6 |
C |
A |
14: 64,035,745 (GRCm39) |
A26E |
unknown |
Het |
Zfp955b |
T |
C |
17: 33,524,427 (GRCm39) |
I47V |
probably benign |
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 |
|
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 |
|