Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actmap |
T |
A |
7: 26,900,468 (GRCm39) |
M149K |
probably damaging |
Het |
Adamts12 |
A |
T |
15: 11,270,748 (GRCm39) |
S668C |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,626,711 (GRCm39) |
V709A |
possibly damaging |
Het |
Aim2 |
T |
A |
1: 173,291,442 (GRCm39) |
D282E |
possibly damaging |
Het |
Aloxe3 |
A |
T |
11: 69,019,480 (GRCm39) |
D131V |
probably null |
Het |
Ankrd28 |
A |
C |
14: 31,477,698 (GRCm39) |
C115G |
probably benign |
Het |
Anxa2 |
A |
T |
9: 69,393,812 (GRCm39) |
M217L |
probably benign |
Het |
Asah2 |
T |
C |
19: 31,972,758 (GRCm39) |
N659S |
probably benign |
Het |
Btaf1 |
A |
G |
19: 36,958,478 (GRCm39) |
D665G |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,361,221 (GRCm39) |
V282E |
probably damaging |
Het |
Cdh15 |
G |
A |
8: 123,588,763 (GRCm39) |
R279Q |
probably damaging |
Het |
Cdipt |
T |
A |
7: 126,577,530 (GRCm39) |
L92H |
probably damaging |
Het |
Cep104 |
T |
A |
4: 154,072,883 (GRCm39) |
D380E |
probably damaging |
Het |
Cfap74 |
T |
A |
4: 155,548,059 (GRCm39) |
|
probably benign |
Het |
Chd1 |
A |
T |
17: 17,598,079 (GRCm39) |
E55D |
probably benign |
Het |
Cldnd2 |
T |
A |
7: 43,091,613 (GRCm39) |
C65S |
possibly damaging |
Het |
Clec9a |
G |
T |
6: 129,393,299 (GRCm39) |
A108S |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,563,467 (GRCm39) |
D215G |
probably benign |
Het |
Col9a3 |
G |
A |
2: 180,252,474 (GRCm39) |
E373K |
probably damaging |
Het |
Deptor |
C |
A |
15: 55,044,406 (GRCm39) |
H191N |
probably benign |
Het |
Dgkz |
A |
T |
2: 91,768,684 (GRCm39) |
I699N |
probably damaging |
Het |
Dnah7c |
T |
A |
1: 46,809,333 (GRCm39) |
N3550K |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,994,035 (GRCm39) |
K3384R |
probably null |
Het |
Dnajc13 |
CT |
C |
9: 104,064,004 (GRCm39) |
|
probably benign |
Het |
Dnhd1 |
C |
A |
7: 105,323,056 (GRCm39) |
N521K |
probably benign |
Het |
Efhb |
G |
A |
17: 53,733,272 (GRCm39) |
T533I |
probably damaging |
Het |
Ercc4 |
A |
T |
16: 12,965,471 (GRCm39) |
H701L |
probably damaging |
Het |
Ern1 |
A |
T |
11: 106,325,676 (GRCm39) |
|
probably benign |
Het |
Etfb |
T |
C |
7: 43,093,624 (GRCm39) |
V17A |
probably damaging |
Het |
Evc |
T |
A |
5: 37,481,141 (GRCm39) |
M235L |
probably benign |
Het |
Fbxw22 |
T |
C |
9: 109,207,937 (GRCm39) |
I445V |
probably benign |
Het |
Fmnl2 |
A |
G |
2: 53,007,081 (GRCm39) |
T764A |
possibly damaging |
Het |
Fto |
T |
A |
8: 92,136,342 (GRCm39) |
D205E |
probably damaging |
Het |
Galntl6 |
G |
A |
8: 58,880,847 (GRCm39) |
P147L |
probably damaging |
Het |
Gm6871 |
T |
C |
7: 41,196,173 (GRCm39) |
I39V |
probably benign |
Het |
Gpr83 |
A |
G |
9: 14,777,470 (GRCm39) |
|
probably benign |
Het |
Gucy1a2 |
A |
T |
9: 3,759,424 (GRCm39) |
H410L |
probably benign |
Het |
Helb |
T |
C |
10: 119,930,193 (GRCm39) |
|
probably null |
Het |
Ifi214 |
T |
C |
1: 173,354,157 (GRCm39) |
Q171R |
probably benign |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,721 (GRCm39) |
I245M |
probably benign |
Het |
Igdcc3 |
A |
G |
9: 65,089,279 (GRCm39) |
T492A |
probably damaging |
Het |
Ighv13-1 |
T |
C |
12: 114,231,252 (GRCm39) |
|
probably benign |
Het |
Igkv4-50 |
T |
C |
6: 69,677,984 (GRCm39) |
K40R |
probably benign |
Het |
Igkv8-18 |
T |
A |
6: 70,333,280 (GRCm39) |
I74N |
probably damaging |
Het |
Iho1 |
A |
G |
9: 108,282,584 (GRCm39) |
V368A |
probably benign |
Het |
Kbtbd7 |
T |
C |
14: 79,666,240 (GRCm39) |
*691Q |
probably null |
Het |
Khnyn |
T |
A |
14: 56,123,946 (GRCm39) |
|
probably null |
Het |
Kif26a |
G |
A |
12: 112,142,007 (GRCm39) |
A754T |
probably benign |
Het |
Llgl1 |
T |
A |
11: 60,597,051 (GRCm39) |
L194* |
probably null |
Het |
Map3k12 |
G |
T |
15: 102,409,717 (GRCm39) |
T686N |
probably benign |
Het |
Myo18a |
C |
A |
11: 77,720,585 (GRCm39) |
P741Q |
probably benign |
Het |
Ncaph2 |
G |
A |
15: 89,240,030 (GRCm39) |
|
probably benign |
Het |
Nfkb2 |
A |
G |
19: 46,297,403 (GRCm39) |
Q406R |
possibly damaging |
Het |
Or10g9b |
A |
T |
9: 39,917,564 (GRCm39) |
I227N |
probably damaging |
Het |
Or11g2 |
T |
A |
14: 50,856,026 (GRCm39) |
C116S |
probably benign |
Het |
Or1ad6 |
G |
A |
11: 50,860,093 (GRCm39) |
V83M |
possibly damaging |
Het |
Or2i1 |
T |
C |
17: 37,507,915 (GRCm39) |
T315A |
probably damaging |
Het |
Or2n1e |
T |
A |
17: 38,586,438 (GRCm39) |
Y259N |
probably damaging |
Het |
Or8b12 |
A |
T |
9: 37,657,831 (GRCm39) |
T134S |
probably benign |
Het |
Ostm1 |
C |
T |
10: 42,554,975 (GRCm39) |
|
probably benign |
Het |
Pabpc1 |
A |
T |
15: 36,599,528 (GRCm39) |
V389E |
probably benign |
Het |
Pank4 |
A |
T |
4: 155,055,847 (GRCm39) |
M291L |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,033,214 (GRCm39) |
D579G |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,035,633 (GRCm39) |
|
probably null |
Het |
Phc2 |
C |
T |
4: 128,601,764 (GRCm39) |
T73M |
probably damaging |
Het |
Pkp4 |
G |
A |
2: 59,165,276 (GRCm39) |
|
probably null |
Het |
Plekhg1 |
T |
A |
10: 3,907,506 (GRCm39) |
S808T |
probably benign |
Het |
Plk5 |
A |
T |
10: 80,194,631 (GRCm39) |
H118L |
probably damaging |
Het |
Pnlip |
T |
C |
19: 58,664,919 (GRCm39) |
I249T |
probably benign |
Het |
Ptov1 |
T |
C |
7: 44,516,533 (GRCm39) |
D134G |
probably benign |
Het |
Ptprb |
T |
C |
10: 116,155,238 (GRCm39) |
V664A |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,002,609 (GRCm39) |
S1566R |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,445,504 (GRCm39) |
S158P |
probably benign |
Het |
Rae1 |
G |
T |
2: 172,857,185 (GRCm39) |
|
probably benign |
Het |
Ros1 |
A |
C |
10: 52,018,325 (GRCm39) |
W778G |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,592,795 (GRCm39) |
M4653K |
possibly damaging |
Het |
Sacm1l |
G |
A |
9: 123,419,895 (GRCm39) |
V553I |
probably benign |
Het |
Samd4b |
G |
A |
7: 28,106,088 (GRCm39) |
R377W |
probably benign |
Het |
Selenoo |
A |
G |
15: 88,983,531 (GRCm39) |
Q524R |
probably benign |
Het |
Slc30a3 |
T |
C |
5: 31,250,638 (GRCm39) |
S22G |
probably benign |
Het |
Slc35g2 |
A |
C |
9: 100,434,555 (GRCm39) |
V372G |
probably benign |
Het |
Slc5a8 |
T |
C |
10: 88,761,649 (GRCm39) |
|
probably null |
Het |
Slc7a7 |
T |
C |
14: 54,646,190 (GRCm39) |
Y91C |
probably damaging |
Het |
Slc7a9 |
T |
A |
7: 35,152,988 (GRCm39) |
Y135* |
probably null |
Het |
Slfn1 |
A |
T |
11: 83,012,661 (GRCm39) |
E259V |
probably damaging |
Het |
Slmap |
T |
C |
14: 26,189,690 (GRCm39) |
N156S |
probably damaging |
Het |
Smim29 |
A |
G |
17: 27,784,244 (GRCm39) |
|
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,303,133 (GRCm39) |
R485S |
probably benign |
Het |
Sptbn2 |
T |
A |
19: 4,792,508 (GRCm39) |
F1388I |
probably damaging |
Het |
Stac2 |
C |
T |
11: 97,930,521 (GRCm39) |
G349E |
probably damaging |
Het |
Tigd2 |
T |
A |
6: 59,188,400 (GRCm39) |
H422Q |
probably benign |
Het |
Tle1 |
T |
C |
4: 72,043,256 (GRCm39) |
N538D |
possibly damaging |
Het |
Tmtc1 |
A |
C |
6: 148,186,478 (GRCm39) |
|
probably null |
Het |
Tns3 |
C |
T |
11: 8,400,986 (GRCm39) |
R1104H |
probably benign |
Het |
Tom1l2 |
C |
G |
11: 60,161,259 (GRCm39) |
R84P |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,219,478 (GRCm39) |
F2072L |
probably damaging |
Het |
Trim6 |
T |
C |
7: 103,881,855 (GRCm39) |
Y369H |
probably damaging |
Het |
Trpc7 |
A |
G |
13: 56,952,366 (GRCm39) |
S541P |
probably damaging |
Het |
Trpv4 |
T |
C |
5: 114,760,814 (GRCm39) |
D732G |
possibly damaging |
Het |
Tsc2 |
C |
A |
17: 24,822,249 (GRCm39) |
V1141F |
possibly damaging |
Het |
Tspoap1 |
T |
A |
11: 87,656,473 (GRCm39) |
V257E |
probably benign |
Het |
Ttn |
A |
T |
2: 76,773,355 (GRCm39) |
M2395K |
unknown |
Het |
Ubd |
A |
C |
17: 37,506,593 (GRCm39) |
T160P |
probably benign |
Het |
Ubr7 |
A |
G |
12: 102,735,485 (GRCm39) |
T315A |
probably benign |
Het |
Ugt2b36 |
G |
T |
5: 87,229,397 (GRCm39) |
Y156* |
probably null |
Het |
Ulk4 |
G |
A |
9: 121,092,704 (GRCm39) |
R178* |
probably null |
Het |
Urod |
G |
A |
4: 116,848,870 (GRCm39) |
A92V |
possibly damaging |
Het |
Utp20 |
T |
C |
10: 88,590,382 (GRCm39) |
D2364G |
possibly damaging |
Het |
Vmn1r87 |
A |
T |
7: 12,866,254 (GRCm39) |
M11K |
possibly damaging |
Het |
Vstm4 |
A |
G |
14: 32,639,859 (GRCm39) |
K96E |
possibly damaging |
Het |
Wwp1 |
T |
C |
4: 19,661,990 (GRCm39) |
D172G |
probably benign |
Het |
Zfhx3 |
A |
G |
8: 109,682,716 (GRCm39) |
Q3385R |
unknown |
Het |
Zfp229 |
C |
T |
17: 21,964,267 (GRCm39) |
H166Y |
possibly damaging |
Het |
Zfp738 |
A |
T |
13: 67,818,033 (GRCm39) |
C653S |
probably damaging |
Het |
Zp2 |
C |
A |
7: 119,737,343 (GRCm39) |
V282L |
probably 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 |
R1872:Akap9
|
UTSW |
5 |
4,051,406 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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 |
|