Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003H04Rik |
C |
T |
3: 124,350,493 (GRCm39) |
C133Y |
unknown |
Het |
Abce1 |
A |
G |
8: 80,416,880 (GRCm39) |
M377T |
possibly damaging |
Het |
Adam25 |
A |
T |
8: 41,208,263 (GRCm39) |
R510* |
probably null |
Het |
Adamts12 |
G |
T |
15: 11,217,966 (GRCm39) |
E308* |
probably null |
Het |
Adgrg3 |
C |
A |
8: 95,760,070 (GRCm39) |
N96K |
possibly damaging |
Het |
Afdn |
T |
C |
17: 14,101,578 (GRCm39) |
V1022A |
probably damaging |
Het |
Akip1 |
A |
G |
7: 109,310,982 (GRCm39) |
Y174C |
probably damaging |
Het |
Aoc1l1 |
A |
G |
6: 48,952,554 (GRCm39) |
I160V |
probably benign |
Het |
Ap3b2 |
T |
C |
7: 81,113,898 (GRCm39) |
T830A |
unknown |
Het |
Aph1a |
A |
G |
3: 95,802,876 (GRCm39) |
T159A |
probably damaging |
Het |
Ccdc146 |
T |
C |
5: 21,506,288 (GRCm39) |
T718A |
probably benign |
Het |
Cdk5r2 |
T |
C |
1: 74,894,981 (GRCm39) |
L242P |
probably damaging |
Het |
Cep97 |
T |
A |
16: 55,748,229 (GRCm39) |
N67I |
probably damaging |
Het |
Cgas |
T |
C |
9: 78,340,484 (GRCm39) |
D416G |
probably benign |
Het |
Chic2 |
A |
T |
5: 75,172,140 (GRCm39) |
W121R |
possibly damaging |
Het |
Clock |
A |
G |
5: 76,396,309 (GRCm39) |
S147P |
possibly damaging |
Het |
Cntnap5a |
T |
G |
1: 116,016,940 (GRCm39) |
S178A |
probably benign |
Het |
Col11a2 |
C |
A |
17: 34,281,529 (GRCm39) |
|
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,757,936 (GRCm39) |
H6L |
probably damaging |
Het |
Cpne5 |
T |
C |
17: 29,423,667 (GRCm39) |
N154D |
probably benign |
Het |
Ctsz |
T |
G |
2: 174,269,769 (GRCm39) |
K273Q |
probably benign |
Het |
Cybrd1 |
G |
A |
2: 70,960,104 (GRCm39) |
V101M |
probably benign |
Het |
Cyp2c23 |
T |
A |
19: 43,993,990 (GRCm39) |
K459* |
probably null |
Het |
Cyp4a31 |
A |
T |
4: 115,431,933 (GRCm39) |
H419L |
probably damaging |
Het |
D930020B18Rik |
G |
A |
10: 121,477,879 (GRCm39) |
V35M |
probably damaging |
Het |
Depp1 |
G |
A |
6: 116,628,683 (GRCm39) |
V9M |
possibly damaging |
Het |
Dnah9 |
C |
T |
11: 65,928,316 (GRCm39) |
V2118M |
probably benign |
Het |
Dtna |
T |
C |
18: 23,730,617 (GRCm39) |
|
probably null |
Het |
Ednra |
C |
T |
8: 78,447,025 (GRCm39) |
V18I |
possibly damaging |
Het |
Elac1 |
T |
C |
18: 73,875,717 (GRCm39) |
R105G |
probably benign |
Het |
Exoc2 |
A |
G |
13: 31,006,644 (GRCm39) |
S844P |
probably benign |
Het |
Fam185a |
A |
T |
5: 21,685,328 (GRCm39) |
|
probably null |
Het |
Fam204a |
A |
G |
19: 60,187,881 (GRCm39) |
M233T |
possibly damaging |
Het |
Fat1 |
C |
A |
8: 45,406,341 (GRCm39) |
H1031N |
probably benign |
Het |
Fat1 |
T |
A |
8: 45,491,386 (GRCm39) |
Y3816N |
probably damaging |
Het |
Fbxo38 |
C |
T |
18: 62,650,094 (GRCm39) |
R621Q |
probably benign |
Het |
Fhod3 |
C |
A |
18: 25,263,667 (GRCm39) |
R1524S |
probably damaging |
Het |
Fnip1 |
A |
T |
11: 54,378,561 (GRCm39) |
R192W |
probably damaging |
Het |
Frem3 |
T |
A |
8: 81,339,205 (GRCm39) |
H499Q |
probably damaging |
Het |
Gab2 |
C |
T |
7: 96,948,250 (GRCm39) |
T280I |
probably damaging |
Het |
Gdpgp1 |
A |
G |
7: 79,888,172 (GRCm39) |
R68G |
probably benign |
Het |
Gm10382 |
C |
T |
5: 125,466,624 (GRCm39) |
|
probably benign |
Het |
Gmps |
A |
G |
3: 63,908,938 (GRCm39) |
H480R |
probably benign |
Het |
Hecw1 |
G |
A |
13: 14,455,034 (GRCm39) |
R674* |
probably null |
Het |
Herc2 |
T |
A |
7: 55,807,257 (GRCm39) |
F2478L |
probably benign |
Het |
Homer2 |
C |
T |
7: 81,286,150 (GRCm39) |
V21M |
probably damaging |
Het |
Ifna9 |
A |
G |
4: 88,510,492 (GRCm39) |
M44T |
probably damaging |
Het |
Igfl3 |
A |
G |
7: 17,913,821 (GRCm39) |
D57G |
possibly damaging |
Het |
Jcad |
T |
C |
18: 4,673,048 (GRCm39) |
M270T |
probably benign |
Het |
Kdm5b |
T |
C |
1: 134,552,732 (GRCm39) |
L1236P |
probably damaging |
Het |
Kif14 |
T |
A |
1: 136,414,096 (GRCm39) |
L724Q |
probably damaging |
Het |
Lhb |
T |
C |
7: 45,070,757 (GRCm39) |
V45A |
probably damaging |
Het |
Lhpp |
A |
G |
7: 132,235,816 (GRCm39) |
N134D |
probably benign |
Het |
Mas1 |
T |
C |
17: 13,061,078 (GRCm39) |
Y115C |
probably damaging |
Het |
Mgam |
A |
T |
6: 40,638,234 (GRCm39) |
K395* |
probably null |
Het |
Mms22l |
A |
G |
4: 24,598,807 (GRCm39) |
N1134S |
probably damaging |
Het |
Mrc1 |
A |
G |
2: 14,330,192 (GRCm39) |
|
probably null |
Het |
Mrgprg |
G |
A |
7: 143,318,281 (GRCm39) |
S277L |
probably damaging |
Het |
Mrpl49 |
G |
T |
19: 6,107,010 (GRCm39) |
P60T |
possibly damaging |
Het |
Mrps10 |
G |
A |
17: 47,683,377 (GRCm39) |
G104D |
possibly damaging |
Het |
Msantd3 |
A |
G |
4: 48,552,771 (GRCm39) |
Y120C |
probably damaging |
Het |
Mtcl2 |
A |
G |
2: 156,882,181 (GRCm39) |
C624R |
possibly damaging |
Het |
N4bp2 |
C |
T |
5: 65,951,861 (GRCm39) |
|
probably benign |
Het |
Nbea |
A |
G |
3: 55,550,310 (GRCm39) |
V2706A |
probably benign |
Het |
Nfic |
T |
A |
10: 81,256,518 (GRCm39) |
M71L |
possibly damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Or12e1 |
A |
G |
2: 87,022,222 (GRCm39) |
T64A |
possibly damaging |
Het |
Or14j4 |
G |
T |
17: 37,920,803 (GRCm39) |
P280T |
probably damaging |
Het |
Or4a15 |
A |
G |
2: 89,192,933 (GRCm39) |
L280P |
probably damaging |
Het |
Or4c105 |
T |
A |
2: 88,648,280 (GRCm39) |
V255E |
probably benign |
Het |
Pak5 |
T |
C |
2: 135,927,508 (GRCm39) |
I655V |
possibly damaging |
Het |
Pip5k1c |
A |
G |
10: 81,142,153 (GRCm39) |
N121S |
probably damaging |
Het |
Plce1 |
A |
T |
19: 38,748,521 (GRCm39) |
I1737F |
probably damaging |
Het |
Prrt1 |
T |
C |
17: 34,849,925 (GRCm39) |
L113P |
probably damaging |
Het |
Ptprq |
T |
A |
10: 107,479,860 (GRCm39) |
T1137S |
probably benign |
Het |
Recql5 |
T |
C |
11: 115,814,135 (GRCm39) |
I223V |
probably benign |
Het |
Reg3g |
A |
T |
6: 78,444,836 (GRCm39) |
Y47* |
probably null |
Het |
Rgs12 |
T |
G |
5: 35,123,165 (GRCm39) |
M316R |
probably damaging |
Het |
Ric1 |
T |
C |
19: 29,580,068 (GRCm39) |
S1290P |
probably benign |
Het |
Rpl36al |
A |
G |
12: 69,229,697 (GRCm39) |
C72R |
probably damaging |
Het |
Rplp0 |
T |
A |
5: 115,701,374 (GRCm39) |
F275L |
possibly damaging |
Het |
Rpp30 |
G |
A |
19: 36,064,793 (GRCm39) |
V89I |
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,539,482 (GRCm39) |
F3253L |
possibly damaging |
Het |
Serpina3n |
A |
T |
12: 104,375,203 (GRCm39) |
N92Y |
probably benign |
Het |
Setd7 |
G |
T |
3: 51,450,252 (GRCm39) |
T58N |
probably benign |
Het |
Sh3tc2 |
T |
A |
18: 62,144,954 (GRCm39) |
L1136Q |
probably damaging |
Het |
Slc35b4 |
G |
A |
6: 34,135,440 (GRCm39) |
Q291* |
probably null |
Het |
Sort1 |
A |
G |
3: 108,248,011 (GRCm39) |
N452S |
probably benign |
Het |
Sympk |
A |
G |
7: 18,763,070 (GRCm39) |
I46V |
probably benign |
Het |
Syngr2 |
T |
C |
11: 117,703,364 (GRCm39) |
V60A |
probably damaging |
Het |
Syt17 |
A |
T |
7: 118,007,341 (GRCm39) |
F318I |
probably benign |
Het |
Tdpoz8 |
T |
A |
3: 92,981,729 (GRCm39) |
L249H |
probably damaging |
Het |
Tgfb1 |
T |
A |
7: 25,391,891 (GRCm39) |
L149M |
probably damaging |
Het |
Ticam1 |
A |
T |
17: 56,578,897 (GRCm39) |
M66K |
probably benign |
Het |
Tmem131 |
G |
T |
1: 36,847,008 (GRCm39) |
D1363E |
probably benign |
Het |
Tns4 |
A |
C |
11: 98,970,926 (GRCm39) |
D261E |
probably damaging |
Het |
Trim30a |
T |
C |
7: 104,078,417 (GRCm39) |
N220D |
probably benign |
Het |
Trmt10a |
T |
C |
3: 137,862,481 (GRCm39) |
L257P |
probably damaging |
Het |
Troap |
G |
T |
15: 98,973,233 (GRCm39) |
|
probably benign |
Het |
Ttc6 |
T |
C |
12: 57,751,338 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Vav1 |
A |
C |
17: 57,631,750 (GRCm39) |
K775T |
probably damaging |
Het |
Vmn1r236 |
A |
G |
17: 21,507,673 (GRCm39) |
K264E |
possibly damaging |
Het |
Vmn1r84 |
A |
G |
7: 12,096,555 (GRCm39) |
V46A |
probably benign |
Het |
Wdr59 |
A |
T |
8: 112,185,649 (GRCm39) |
W835R |
probably damaging |
Het |
Zfp513 |
T |
G |
5: 31,357,767 (GRCm39) |
K202T |
probably damaging |
Het |
Zfp7 |
T |
G |
15: 76,775,977 (GRCm39) |
I673S |
probably benign |
Het |
Zmynd11 |
A |
G |
13: 9,748,737 (GRCm39) |
I108T |
possibly damaging |
Het |
|
Other mutations in Akap9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00478:Akap9
|
APN |
5 |
4,096,639 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00642:Akap9
|
APN |
5 |
4,010,842 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00786:Akap9
|
APN |
5 |
4,120,522 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00788:Akap9
|
APN |
5 |
4,110,480 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00969:Akap9
|
APN |
5 |
4,051,550 (GRCm39) |
missense |
probably benign |
|
IGL01014:Akap9
|
APN |
5 |
4,018,683 (GRCm39) |
missense |
probably benign |
0.41 |
IGL01302:Akap9
|
APN |
5 |
4,020,711 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01610:Akap9
|
APN |
5 |
4,082,839 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01620:Akap9
|
APN |
5 |
4,010,218 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01862:Akap9
|
APN |
5 |
4,115,856 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01862:Akap9
|
APN |
5 |
4,001,705 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02151:Akap9
|
APN |
5 |
4,082,728 (GRCm39) |
nonsense |
probably null |
|
IGL02635:Akap9
|
APN |
5 |
4,120,500 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02858:Akap9
|
APN |
5 |
4,119,130 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02967:Akap9
|
APN |
5 |
4,026,164 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03064:Akap9
|
APN |
5 |
4,018,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03289:Akap9
|
APN |
5 |
4,127,261 (GRCm39) |
missense |
probably damaging |
1.00 |
Andy
|
UTSW |
5 |
4,011,764 (GRCm39) |
nonsense |
probably null |
|
blimey
|
UTSW |
5 |
4,120,397 (GRCm39) |
nonsense |
probably null |
|
hoarder
|
UTSW |
5 |
4,119,089 (GRCm39) |
missense |
probably benign |
0.00 |
marinarum
|
UTSW |
5 |
4,063,875 (GRCm39) |
nonsense |
probably null |
|
miser
|
UTSW |
5 |
4,096,064 (GRCm39) |
missense |
probably benign |
0.13 |
naviculus
|
UTSW |
5 |
4,010,865 (GRCm39) |
missense |
probably damaging |
0.98 |
thrifty
|
UTSW |
5 |
4,026,209 (GRCm39) |
missense |
probably damaging |
0.99 |
wee_one
|
UTSW |
5 |
4,093,925 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Akap9
|
UTSW |
5 |
4,031,214 (GRCm39) |
unclassified |
probably benign |
|
PIT1430001:Akap9
|
UTSW |
5 |
4,079,849 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4366001:Akap9
|
UTSW |
5 |
4,096,221 (GRCm39) |
missense |
probably benign |
0.24 |
R0088:Akap9
|
UTSW |
5 |
4,011,946 (GRCm39) |
missense |
probably benign |
0.22 |
R0309:Akap9
|
UTSW |
5 |
4,119,038 (GRCm39) |
missense |
probably benign |
0.01 |
R0387:Akap9
|
UTSW |
5 |
4,001,678 (GRCm39) |
splice site |
probably benign |
|
R0440:Akap9
|
UTSW |
5 |
4,114,569 (GRCm39) |
missense |
probably damaging |
0.99 |
R0441:Akap9
|
UTSW |
5 |
4,011,714 (GRCm39) |
missense |
probably benign |
0.15 |
R0491:Akap9
|
UTSW |
5 |
4,022,851 (GRCm39) |
unclassified |
probably benign |
|
R0501:Akap9
|
UTSW |
5 |
4,020,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R0507:Akap9
|
UTSW |
5 |
4,119,043 (GRCm39) |
missense |
probably benign |
0.41 |
R0544:Akap9
|
UTSW |
5 |
4,119,185 (GRCm39) |
missense |
probably benign |
0.22 |
R0581:Akap9
|
UTSW |
5 |
4,100,620 (GRCm39) |
missense |
probably benign |
0.03 |
R0611:Akap9
|
UTSW |
5 |
4,004,870 (GRCm39) |
missense |
probably benign |
0.00 |
R0620:Akap9
|
UTSW |
5 |
4,114,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R0639:Akap9
|
UTSW |
5 |
4,110,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R0932:Akap9
|
UTSW |
5 |
4,096,492 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0944:Akap9
|
UTSW |
5 |
4,114,742 (GRCm39) |
splice site |
probably null |
|
R1101:Akap9
|
UTSW |
5 |
4,096,205 (GRCm39) |
missense |
probably benign |
0.00 |
R1159:Akap9
|
UTSW |
5 |
4,010,865 (GRCm39) |
missense |
probably damaging |
0.98 |
R1170:Akap9
|
UTSW |
5 |
4,105,671 (GRCm39) |
missense |
probably benign |
|
R1185:Akap9
|
UTSW |
5 |
3,998,783 (GRCm39) |
missense |
probably benign |
0.13 |
R1185:Akap9
|
UTSW |
5 |
3,998,783 (GRCm39) |
missense |
probably benign |
0.13 |
R1185:Akap9
|
UTSW |
5 |
3,998,783 (GRCm39) |
missense |
probably benign |
0.13 |
R1453:Akap9
|
UTSW |
5 |
4,025,614 (GRCm39) |
splice site |
probably null |
|
R1551:Akap9
|
UTSW |
5 |
4,119,174 (GRCm39) |
missense |
probably benign |
0.02 |
R1608:Akap9
|
UTSW |
5 |
4,011,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R1652:Akap9
|
UTSW |
5 |
4,127,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R1659:Akap9
|
UTSW |
5 |
4,114,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Akap9
|
UTSW |
5 |
4,089,345 (GRCm39) |
critical splice donor site |
probably null |
|
R1719:Akap9
|
UTSW |
5 |
4,007,645 (GRCm39) |
nonsense |
probably null |
|
R1720:Akap9
|
UTSW |
5 |
4,022,791 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1757:Akap9
|
UTSW |
5 |
4,051,667 (GRCm39) |
missense |
probably benign |
0.41 |
R1876:Akap9
|
UTSW |
5 |
4,011,809 (GRCm39) |
missense |
probably benign |
0.28 |
R1881:Akap9
|
UTSW |
5 |
4,100,173 (GRCm39) |
missense |
probably benign |
|
R1950:Akap9
|
UTSW |
5 |
4,010,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R1980:Akap9
|
UTSW |
5 |
4,022,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R1993:Akap9
|
UTSW |
5 |
4,088,520 (GRCm39) |
splice site |
probably null |
|
R2008:Akap9
|
UTSW |
5 |
4,010,131 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2020:Akap9
|
UTSW |
5 |
4,011,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R2051:Akap9
|
UTSW |
5 |
4,025,685 (GRCm39) |
nonsense |
probably null |
|
R2061:Akap9
|
UTSW |
5 |
4,011,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Akap9
|
UTSW |
5 |
4,094,847 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2135:Akap9
|
UTSW |
5 |
4,114,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R2225:Akap9
|
UTSW |
5 |
4,127,271 (GRCm39) |
missense |
probably damaging |
0.96 |
R2232:Akap9
|
UTSW |
5 |
4,096,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R2424:Akap9
|
UTSW |
5 |
4,115,279 (GRCm39) |
missense |
probably damaging |
0.97 |
R2483:Akap9
|
UTSW |
5 |
4,026,235 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2879:Akap9
|
UTSW |
5 |
4,026,353 (GRCm39) |
intron |
probably benign |
|
R3622:Akap9
|
UTSW |
5 |
4,026,235 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3623:Akap9
|
UTSW |
5 |
4,026,235 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3624:Akap9
|
UTSW |
5 |
4,026,235 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3722:Akap9
|
UTSW |
5 |
4,120,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Akap9
|
UTSW |
5 |
4,004,410 (GRCm39) |
missense |
probably benign |
0.00 |
R3919:Akap9
|
UTSW |
5 |
4,011,764 (GRCm39) |
nonsense |
probably null |
|
R4023:Akap9
|
UTSW |
5 |
4,042,077 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4093:Akap9
|
UTSW |
5 |
4,093,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R4434:Akap9
|
UTSW |
5 |
4,082,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R4529:Akap9
|
UTSW |
5 |
4,093,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4530:Akap9
|
UTSW |
5 |
4,093,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4532:Akap9
|
UTSW |
5 |
4,093,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4533:Akap9
|
UTSW |
5 |
4,093,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R4585:Akap9
|
UTSW |
5 |
4,026,151 (GRCm39) |
missense |
probably benign |
0.00 |
R4586:Akap9
|
UTSW |
5 |
4,026,151 (GRCm39) |
missense |
probably benign |
0.00 |
R4655:Akap9
|
UTSW |
5 |
4,096,403 (GRCm39) |
missense |
probably benign |
0.14 |
R4676:Akap9
|
UTSW |
5 |
4,114,515 (GRCm39) |
nonsense |
probably null |
|
R4676:Akap9
|
UTSW |
5 |
4,082,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Akap9
|
UTSW |
5 |
4,105,339 (GRCm39) |
missense |
probably benign |
|
R4731:Akap9
|
UTSW |
5 |
4,012,266 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4732:Akap9
|
UTSW |
5 |
4,063,901 (GRCm39) |
missense |
probably damaging |
0.98 |
R4733:Akap9
|
UTSW |
5 |
4,063,901 (GRCm39) |
missense |
probably damaging |
0.98 |
R4743:Akap9
|
UTSW |
5 |
4,011,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Akap9
|
UTSW |
5 |
4,018,737 (GRCm39) |
missense |
probably benign |
0.41 |
R4756:Akap9
|
UTSW |
5 |
4,051,418 (GRCm39) |
missense |
probably damaging |
0.99 |
R4757:Akap9
|
UTSW |
5 |
4,058,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R4860:Akap9
|
UTSW |
5 |
4,084,916 (GRCm39) |
intron |
probably benign |
|
R4937:Akap9
|
UTSW |
5 |
4,100,145 (GRCm39) |
splice site |
probably null |
|
R4960:Akap9
|
UTSW |
5 |
4,007,664 (GRCm39) |
missense |
probably benign |
0.15 |
R4974:Akap9
|
UTSW |
5 |
4,011,466 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5101:Akap9
|
UTSW |
5 |
4,051,748 (GRCm39) |
missense |
probably damaging |
0.96 |
R5160:Akap9
|
UTSW |
5 |
4,080,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5200:Akap9
|
UTSW |
5 |
4,010,734 (GRCm39) |
missense |
probably benign |
0.00 |
R5245:Akap9
|
UTSW |
5 |
4,026,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R5293:Akap9
|
UTSW |
5 |
3,998,687 (GRCm39) |
missense |
probably damaging |
0.99 |
R5408:Akap9
|
UTSW |
5 |
4,108,458 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5507:Akap9
|
UTSW |
5 |
4,018,683 (GRCm39) |
missense |
probably benign |
0.41 |
R5517:Akap9
|
UTSW |
5 |
4,051,665 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5579:Akap9
|
UTSW |
5 |
4,114,714 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5619:Akap9
|
UTSW |
5 |
4,004,760 (GRCm39) |
intron |
probably benign |
|
R5645:Akap9
|
UTSW |
5 |
4,100,590 (GRCm39) |
missense |
probably benign |
0.09 |
R5669:Akap9
|
UTSW |
5 |
4,100,540 (GRCm39) |
nonsense |
probably null |
|
R5686:Akap9
|
UTSW |
5 |
4,021,926 (GRCm39) |
missense |
probably benign |
0.00 |
R5697:Akap9
|
UTSW |
5 |
4,010,170 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5821:Akap9
|
UTSW |
5 |
4,096,064 (GRCm39) |
missense |
probably benign |
0.13 |
R5875:Akap9
|
UTSW |
5 |
4,127,285 (GRCm39) |
missense |
probably benign |
0.01 |
R5897:Akap9
|
UTSW |
5 |
4,127,904 (GRCm39) |
missense |
probably benign |
0.23 |
R5999:Akap9
|
UTSW |
5 |
4,093,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R6025:Akap9
|
UTSW |
5 |
4,082,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R6078:Akap9
|
UTSW |
5 |
4,117,924 (GRCm39) |
critical splice donor site |
probably null |
|
R6138:Akap9
|
UTSW |
5 |
4,117,924 (GRCm39) |
critical splice donor site |
probably null |
|
R6225:Akap9
|
UTSW |
5 |
4,012,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R6243:Akap9
|
UTSW |
5 |
4,115,000 (GRCm39) |
splice site |
probably null |
|
R6326:Akap9
|
UTSW |
5 |
4,012,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R6564:Akap9
|
UTSW |
5 |
4,078,491 (GRCm39) |
missense |
probably damaging |
0.98 |
R6617:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R6625:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R6632:Akap9
|
UTSW |
5 |
4,063,842 (GRCm39) |
splice site |
probably null |
|
R6677:Akap9
|
UTSW |
5 |
4,079,869 (GRCm39) |
missense |
probably benign |
0.21 |
R6717:Akap9
|
UTSW |
5 |
4,114,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R6893:Akap9
|
UTSW |
5 |
4,011,709 (GRCm39) |
missense |
probably benign |
0.32 |
R6915:Akap9
|
UTSW |
5 |
4,010,551 (GRCm39) |
missense |
probably benign |
0.03 |
R6938:Akap9
|
UTSW |
5 |
4,096,628 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6972:Akap9
|
UTSW |
5 |
4,096,699 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6973:Akap9
|
UTSW |
5 |
4,096,699 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6993:Akap9
|
UTSW |
5 |
4,115,866 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7032:Akap9
|
UTSW |
5 |
4,004,896 (GRCm39) |
missense |
probably benign |
|
R7164:Akap9
|
UTSW |
5 |
4,110,364 (GRCm39) |
missense |
probably damaging |
0.96 |
R7170:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7192:Akap9
|
UTSW |
5 |
4,055,723 (GRCm39) |
splice site |
probably null |
|
R7284:Akap9
|
UTSW |
5 |
4,006,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Akap9
|
UTSW |
5 |
4,082,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Akap9
|
UTSW |
5 |
4,054,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Akap9
|
UTSW |
5 |
4,095,930 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7343:Akap9
|
UTSW |
5 |
4,096,364 (GRCm39) |
missense |
probably damaging |
0.99 |
R7455:Akap9
|
UTSW |
5 |
4,022,792 (GRCm39) |
missense |
probably benign |
0.03 |
R7482:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7489:Akap9
|
UTSW |
5 |
4,054,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7525:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7528:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7576:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7577:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7578:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7610:Akap9
|
UTSW |
5 |
4,007,677 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7658:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R7754:Akap9
|
UTSW |
5 |
4,096,736 (GRCm39) |
missense |
probably benign |
0.03 |
R7818:Akap9
|
UTSW |
5 |
4,063,875 (GRCm39) |
nonsense |
probably null |
|
R7979:Akap9
|
UTSW |
5 |
4,100,381 (GRCm39) |
missense |
probably benign |
|
R7991:Akap9
|
UTSW |
5 |
4,114,949 (GRCm39) |
splice site |
probably null |
|
R8036:Akap9
|
UTSW |
5 |
4,120,397 (GRCm39) |
nonsense |
probably null |
|
R8054:Akap9
|
UTSW |
5 |
4,088,707 (GRCm39) |
critical splice donor site |
probably null |
|
R8116:Akap9
|
UTSW |
5 |
4,111,183 (GRCm39) |
missense |
probably benign |
0.04 |
R8150:Akap9
|
UTSW |
5 |
4,011,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R8234:Akap9
|
UTSW |
5 |
4,094,845 (GRCm39) |
missense |
probably benign |
0.18 |
R8348:Akap9
|
UTSW |
5 |
3,998,897 (GRCm39) |
critical splice donor site |
probably null |
|
R8365:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R8366:Akap9
|
UTSW |
5 |
4,018,745 (GRCm39) |
missense |
probably benign |
0.04 |
R8448:Akap9
|
UTSW |
5 |
3,998,897 (GRCm39) |
critical splice donor site |
probably null |
|
R8466:Akap9
|
UTSW |
5 |
4,088,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R8772:Akap9
|
UTSW |
5 |
4,096,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R8881:Akap9
|
UTSW |
5 |
4,011,279 (GRCm39) |
missense |
|
|
R8937:Akap9
|
UTSW |
5 |
4,094,048 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8956:Akap9
|
UTSW |
5 |
3,998,805 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9000:Akap9
|
UTSW |
5 |
4,105,650 (GRCm39) |
missense |
probably benign |
|
R9049:Akap9
|
UTSW |
5 |
4,114,597 (GRCm39) |
missense |
|
|
R9074:Akap9
|
UTSW |
5 |
4,127,959 (GRCm39) |
missense |
probably benign |
0.40 |
R9124:Akap9
|
UTSW |
5 |
4,111,284 (GRCm39) |
missense |
probably damaging |
0.99 |
R9129:Akap9
|
UTSW |
5 |
4,119,089 (GRCm39) |
missense |
probably benign |
0.00 |
R9371:Akap9
|
UTSW |
5 |
4,011,852 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9424:Akap9
|
UTSW |
5 |
4,012,224 (GRCm39) |
nonsense |
probably null |
|
R9424:Akap9
|
UTSW |
5 |
4,012,223 (GRCm39) |
nonsense |
probably null |
|
R9509:Akap9
|
UTSW |
5 |
4,096,349 (GRCm39) |
missense |
probably benign |
|
R9515:Akap9
|
UTSW |
5 |
4,105,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R9567:Akap9
|
UTSW |
5 |
4,127,311 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9587:Akap9
|
UTSW |
5 |
4,119,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R9619:Akap9
|
UTSW |
5 |
4,094,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9635:Akap9
|
UTSW |
5 |
4,100,545 (GRCm39) |
missense |
probably benign |
0.20 |
R9680:Akap9
|
UTSW |
5 |
4,011,587 (GRCm39) |
missense |
probably benign |
0.03 |
R9691:Akap9
|
UTSW |
5 |
4,010,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R9726:Akap9
|
UTSW |
5 |
4,053,757 (GRCm39) |
missense |
probably benign |
0.39 |
U15987:Akap9
|
UTSW |
5 |
4,117,924 (GRCm39) |
critical splice donor site |
probably null |
|
X0026:Akap9
|
UTSW |
5 |
4,064,039 (GRCm39) |
missense |
probably damaging |
1.00 |
X0057:Akap9
|
UTSW |
5 |
4,025,598 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Akap9
|
UTSW |
5 |
4,012,251 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Akap9
|
UTSW |
5 |
4,096,189 (GRCm39) |
missense |
probably damaging |
1.00 |
|