Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
T |
7: 120,140,463 (GRCm39) |
I1588F |
probably benign |
Het |
Abcc2 |
A |
T |
19: 43,795,683 (GRCm39) |
T480S |
probably benign |
Het |
Acnat1 |
A |
G |
4: 49,447,498 (GRCm39) |
I361T |
probably damaging |
Het |
Adamts10 |
A |
T |
17: 33,768,529 (GRCm39) |
H869L |
probably benign |
Het |
Agpat5 |
T |
C |
8: 18,929,629 (GRCm39) |
C253R |
probably benign |
Het |
Agtrap |
T |
A |
4: 148,168,434 (GRCm39) |
H15L |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,985,286 (GRCm39) |
V2190E |
probably damaging |
Het |
Alx4 |
A |
G |
2: 93,505,732 (GRCm39) |
E278G |
probably damaging |
Het |
Amz2 |
T |
C |
11: 109,319,697 (GRCm39) |
S28P |
probably damaging |
Het |
Atr |
T |
A |
9: 95,748,786 (GRCm39) |
Y444N |
probably benign |
Het |
Brdt |
T |
C |
5: 107,496,479 (GRCm39) |
I197T |
probably benign |
Het |
Ccser1 |
G |
T |
6: 62,356,878 (GRCm39) |
S772I |
probably damaging |
Het |
Cdh16 |
T |
C |
8: 105,343,100 (GRCm39) |
H657R |
probably benign |
Het |
Ceacam5 |
A |
T |
7: 17,493,502 (GRCm39) |
K842* |
probably null |
Het |
Cep120 |
G |
A |
18: 53,856,358 (GRCm39) |
T353I |
probably benign |
Het |
Chrnb1 |
T |
C |
11: 69,684,410 (GRCm39) |
N164S |
possibly damaging |
Het |
Cse1l |
T |
C |
2: 166,764,111 (GRCm39) |
F123L |
probably damaging |
Het |
Cul7 |
T |
A |
17: 46,974,116 (GRCm39) |
L1467H |
probably damaging |
Het |
Dcx |
G |
C |
X: 142,706,099 (GRCm39) |
L231V |
probably damaging |
Het |
Dnah12 |
T |
C |
14: 26,514,221 (GRCm39) |
|
probably null |
Het |
Dnah2 |
A |
T |
11: 69,355,756 (GRCm39) |
M2227K |
probably damaging |
Het |
Dnajc30 |
G |
A |
5: 135,093,186 (GRCm39) |
A28T |
probably benign |
Het |
Dnm1l |
T |
C |
16: 16,147,830 (GRCm39) |
T306A |
probably benign |
Het |
Elapor2 |
T |
G |
5: 9,316,275 (GRCm39) |
L2R |
probably damaging |
Het |
Enpp3 |
C |
A |
10: 24,652,669 (GRCm39) |
E763* |
probably null |
Het |
Esyt3 |
T |
C |
9: 99,202,364 (GRCm39) |
S516G |
probably benign |
Het |
Exoc3 |
T |
C |
13: 74,330,435 (GRCm39) |
Q498R |
probably damaging |
Het |
Fbn2 |
T |
A |
18: 58,194,814 (GRCm39) |
N1449I |
probably damaging |
Het |
Fgb |
T |
C |
3: 82,952,287 (GRCm39) |
D194G |
probably benign |
Het |
Fgd3 |
T |
C |
13: 49,417,324 (GRCm39) |
D713G |
possibly damaging |
Het |
Foxb1 |
T |
A |
9: 69,667,383 (GRCm39) |
Y49F |
possibly damaging |
Het |
Fpr3 |
A |
G |
17: 18,191,670 (GRCm39) |
I314V |
probably damaging |
Het |
Gfod1 |
A |
T |
13: 43,456,921 (GRCm39) |
I18N |
probably damaging |
Het |
Gm5407 |
T |
C |
16: 49,117,283 (GRCm39) |
|
noncoding transcript |
Het |
Gpr89 |
A |
G |
3: 96,782,949 (GRCm39) |
F334L |
possibly damaging |
Het |
Gucy2d |
G |
T |
7: 98,093,054 (GRCm39) |
V144F |
probably benign |
Het |
H2-M10.5 |
C |
A |
17: 37,085,660 (GRCm39) |
P273H |
probably damaging |
Het |
H2-T13 |
T |
A |
17: 36,391,908 (GRCm39) |
K237M |
probably damaging |
Het |
Hcn2 |
A |
G |
10: 79,566,777 (GRCm39) |
M485V |
probably benign |
Het |
Helz2 |
G |
T |
2: 180,875,543 (GRCm39) |
S1650R |
probably damaging |
Het |
Ifnar2 |
T |
C |
16: 91,201,058 (GRCm39) |
V433A |
probably benign |
Het |
Igsf21 |
T |
A |
4: 139,834,623 (GRCm39) |
Y83F |
probably benign |
Het |
Kcnk18 |
A |
G |
19: 59,223,490 (GRCm39) |
I212V |
possibly damaging |
Het |
Kcns2 |
T |
C |
15: 34,839,855 (GRCm39) |
I406T |
probably damaging |
Het |
Krt42 |
C |
T |
11: 100,158,075 (GRCm39) |
V166M |
possibly damaging |
Het |
Lama3 |
T |
C |
18: 12,628,336 (GRCm39) |
M1476T |
probably benign |
Het |
Lcor |
A |
G |
19: 41,546,913 (GRCm39) |
R166G |
probably benign |
Het |
Mapt |
C |
T |
11: 104,218,901 (GRCm39) |
P354L |
probably damaging |
Het |
Mep1b |
A |
T |
18: 21,226,286 (GRCm39) |
I383F |
probably benign |
Het |
Mpzl1 |
C |
A |
1: 165,429,374 (GRCm39) |
C222F |
probably benign |
Het |
Mug2 |
T |
C |
6: 122,047,829 (GRCm39) |
L780P |
probably damaging |
Het |
Naip2 |
C |
T |
13: 100,288,665 (GRCm39) |
|
probably null |
Het |
Ndufab1 |
T |
C |
7: 121,695,914 (GRCm39) |
D41G |
probably benign |
Het |
Ntn1 |
A |
G |
11: 68,104,011 (GRCm39) |
C546R |
probably damaging |
Het |
Or2a5 |
T |
A |
6: 42,873,687 (GRCm39) |
F101I |
probably damaging |
Het |
Pakap |
A |
G |
4: 57,892,963 (GRCm39) |
E880G |
probably damaging |
Het |
Pde6b |
A |
G |
5: 108,575,056 (GRCm39) |
E639G |
probably benign |
Het |
Phf10 |
T |
C |
17: 15,177,071 (GRCm39) |
T83A |
probably benign |
Het |
Phkb |
T |
A |
8: 86,628,549 (GRCm39) |
I186N |
possibly damaging |
Het |
Pkhd1 |
A |
G |
1: 20,636,980 (GRCm39) |
|
probably null |
Het |
Plxnd1 |
C |
A |
6: 115,954,978 (GRCm39) |
A595S |
possibly damaging |
Het |
Ppara |
T |
A |
15: 85,685,300 (GRCm39) |
H416Q |
probably damaging |
Het |
Prodh |
T |
A |
16: 17,898,891 (GRCm39) |
D188V |
probably damaging |
Het |
Psmd14 |
A |
T |
2: 61,615,800 (GRCm39) |
K223M |
possibly damaging |
Het |
Ptpn5 |
A |
G |
7: 46,728,616 (GRCm39) |
M528T |
possibly damaging |
Het |
Rassf9 |
G |
A |
10: 102,380,800 (GRCm39) |
E59K |
probably benign |
Het |
Rnf2 |
A |
T |
1: 151,351,936 (GRCm39) |
L140H |
probably damaging |
Het |
Scai |
A |
G |
2: 38,970,093 (GRCm39) |
F557S |
probably damaging |
Het |
Sec24c |
A |
G |
14: 20,739,179 (GRCm39) |
D534G |
probably benign |
Het |
Semp2l2a |
T |
A |
8: 13,887,143 (GRCm39) |
Q316L |
probably benign |
Het |
Septin4 |
T |
C |
11: 87,457,838 (GRCm39) |
S71P |
probably benign |
Het |
Serinc1 |
A |
G |
10: 57,395,561 (GRCm39) |
V375A |
probably benign |
Het |
Serpinb9f |
C |
T |
13: 33,509,829 (GRCm39) |
A7V |
probably damaging |
Het |
Smco1 |
T |
C |
16: 32,092,700 (GRCm39) |
S124P |
probably damaging |
Het |
Smim23 |
C |
A |
11: 32,774,441 (GRCm39) |
C26F |
possibly damaging |
Het |
Sppl2c |
T |
A |
11: 104,078,715 (GRCm39) |
M505K |
probably benign |
Het |
Sprr1b |
C |
A |
3: 92,344,775 (GRCm39) |
V34F |
possibly damaging |
Het |
Sun1 |
G |
A |
5: 139,221,487 (GRCm39) |
|
probably null |
Het |
Supt16 |
A |
G |
14: 52,415,592 (GRCm39) |
L381P |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 75,946,020 (GRCm39) |
D364G |
possibly damaging |
Het |
Tax1bp1 |
G |
T |
6: 52,742,937 (GRCm39) |
V775F |
probably damaging |
Het |
Tial1 |
T |
A |
7: 128,046,383 (GRCm39) |
I231F |
probably damaging |
Het |
Tiam1 |
C |
A |
16: 89,595,582 (GRCm39) |
V1300L |
probably damaging |
Het |
Tmem132e |
A |
G |
11: 82,334,243 (GRCm39) |
T585A |
probably damaging |
Het |
Tnni3k |
C |
T |
3: 154,684,836 (GRCm39) |
A165T |
probably benign |
Het |
Tomm40 |
A |
T |
7: 19,444,886 (GRCm39) |
I165N |
probably damaging |
Het |
Tomt |
T |
C |
7: 101,550,454 (GRCm39) |
E104G |
probably damaging |
Het |
Topaz1 |
T |
C |
9: 122,596,078 (GRCm39) |
S950P |
possibly damaging |
Het |
Traf3ip2 |
C |
G |
10: 39,501,936 (GRCm39) |
P28R |
probably benign |
Het |
Trim24 |
C |
T |
6: 37,934,750 (GRCm39) |
P822S |
probably damaging |
Het |
Upf3a |
T |
G |
8: 13,842,108 (GRCm39) |
Y175D |
probably damaging |
Het |
Vars2 |
G |
A |
17: 35,977,814 (GRCm39) |
P69S |
probably benign |
Het |
Veph1 |
T |
C |
3: 66,151,976 (GRCm39) |
Y151C |
probably damaging |
Het |
Vmn2r11 |
T |
A |
5: 109,202,654 (GRCm39) |
D141V |
probably benign |
Het |
Vwa5b1 |
G |
A |
4: 138,319,331 (GRCm39) |
Q442* |
probably null |
Het |
Wdr17 |
T |
A |
8: 55,140,761 (GRCm39) |
D197V |
probably damaging |
Het |
Wdr70 |
G |
T |
15: 7,913,891 (GRCm39) |
T586N |
possibly damaging |
Het |
Wfdc18 |
G |
A |
11: 83,600,754 (GRCm39) |
G52R |
probably benign |
Het |
Zc3h6 |
T |
C |
2: 128,858,540 (GRCm39) |
I857T |
probably damaging |
Het |
Zfp318 |
TGAAGAAGAAGAAGAAGAAGAAGAAGAAG |
TGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAG |
17: 46,723,440 (GRCm39) |
|
probably benign |
Het |
Zfp318 |
GAAGAA |
GAAGAACAAGAA |
17: 46,723,450 (GRCm39) |
|
probably benign |
Het |
Zfp647 |
C |
T |
15: 76,796,151 (GRCm39) |
V170I |
probably benign |
Het |
Zfp871 |
T |
C |
17: 32,994,891 (GRCm39) |
N76D |
possibly damaging |
Het |
Zpld2 |
A |
G |
4: 133,919,986 (GRCm39) |
|
probably null |
Het |
Zwilch |
A |
G |
9: 64,068,234 (GRCm39) |
Y194H |
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 |
|
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 |
|
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 |
|