Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
G |
5: 8,871,322 (GRCm39) |
I292S |
possibly damaging |
Het |
Abcc4 |
T |
C |
14: 118,763,694 (GRCm39) |
N1047S |
probably benign |
Het |
Abcc8 |
G |
T |
7: 45,766,847 (GRCm39) |
|
probably null |
Het |
Alox5 |
T |
A |
6: 116,392,424 (GRCm39) |
I366F |
probably damaging |
Het |
Amn |
A |
G |
12: 111,242,526 (GRCm39) |
N447S |
probably damaging |
Het |
Ankrd22 |
A |
T |
19: 34,143,174 (GRCm39) |
M1K |
probably null |
Het |
Asic1 |
G |
T |
15: 99,569,765 (GRCm39) |
G29C |
probably damaging |
Het |
Atxn7l1 |
A |
G |
12: 33,395,976 (GRCm39) |
N235S |
probably benign |
Het |
AY358078 |
T |
A |
14: 52,063,519 (GRCm39) |
D388E |
probably damaging |
Het |
Bod1l |
A |
G |
5: 41,974,679 (GRCm39) |
S2212P |
probably damaging |
Het |
Cacna1e |
T |
A |
1: 154,353,563 (GRCm39) |
Q423L |
probably damaging |
Het |
Calu |
T |
C |
6: 29,366,974 (GRCm39) |
I62T |
possibly damaging |
Het |
Cars2 |
A |
G |
8: 11,564,515 (GRCm39) |
V75A |
probably benign |
Het |
Catsperb |
T |
A |
12: 101,569,026 (GRCm39) |
N899K |
possibly damaging |
Het |
Ccdc50 |
T |
A |
16: 27,228,089 (GRCm39) |
C86* |
probably null |
Het |
Cdh5 |
G |
T |
8: 104,864,447 (GRCm39) |
L469F |
probably damaging |
Het |
Clrn3 |
A |
T |
7: 135,115,848 (GRCm39) |
D167E |
probably benign |
Het |
Csmd1 |
A |
T |
8: 16,396,698 (GRCm39) |
C411S |
probably damaging |
Het |
Dchs1 |
A |
T |
7: 105,411,755 (GRCm39) |
S1454T |
probably benign |
Het |
Ddx20 |
G |
A |
3: 105,586,660 (GRCm39) |
Q562* |
probably null |
Het |
Dgkg |
T |
G |
16: 22,419,344 (GRCm39) |
Y52S |
probably damaging |
Het |
Dhx58 |
T |
C |
11: 100,594,316 (GRCm39) |
|
probably null |
Het |
Dpp6 |
A |
T |
5: 27,604,004 (GRCm39) |
I145L |
probably benign |
Het |
Efna2 |
A |
T |
10: 80,022,711 (GRCm39) |
Y85F |
possibly damaging |
Het |
Eif3a |
C |
T |
19: 60,769,954 (GRCm39) |
V127I |
probably benign |
Het |
Exph5 |
A |
T |
9: 53,284,935 (GRCm39) |
H672L |
possibly damaging |
Het |
Fam131b |
T |
C |
6: 42,297,818 (GRCm39) |
T112A |
possibly damaging |
Het |
Fcgr1 |
A |
T |
3: 96,193,184 (GRCm39) |
V271E |
probably damaging |
Het |
Fgfr4 |
A |
G |
13: 55,313,715 (GRCm39) |
D508G |
probably damaging |
Het |
Fndc3b |
A |
G |
3: 27,473,549 (GRCm39) |
M1172T |
probably benign |
Het |
Fryl |
G |
T |
5: 73,265,836 (GRCm39) |
T495K |
probably damaging |
Het |
Garin5b |
A |
T |
7: 4,761,017 (GRCm39) |
V565E |
probably damaging |
Het |
Gm5134 |
A |
T |
10: 75,802,227 (GRCm39) |
I93F |
probably damaging |
Het |
Gpbar1 |
G |
A |
1: 74,318,603 (GRCm39) |
G282D |
possibly damaging |
Het |
Gria2 |
G |
A |
3: 80,709,664 (GRCm39) |
L10F |
probably benign |
Het |
Grm7 |
T |
C |
6: 111,184,769 (GRCm39) |
Y367H |
probably benign |
Het |
H1f9 |
T |
A |
11: 94,858,858 (GRCm39) |
V51E |
probably damaging |
Het |
Hivep1 |
G |
A |
13: 42,310,969 (GRCm39) |
A1070T |
probably benign |
Het |
Il33 |
A |
G |
19: 29,934,304 (GRCm39) |
D155G |
possibly damaging |
Het |
Kdm6b |
T |
C |
11: 69,297,129 (GRCm39) |
S408G |
probably null |
Het |
Kntc1 |
A |
G |
5: 123,948,874 (GRCm39) |
|
probably null |
Het |
Kntc1 |
G |
A |
5: 123,897,162 (GRCm39) |
|
probably null |
Het |
Ltbp2 |
T |
G |
12: 84,855,220 (GRCm39) |
|
probably null |
Het |
Mapk8ip3 |
G |
T |
17: 25,133,562 (GRCm39) |
L83I |
probably damaging |
Het |
Meltf |
C |
A |
16: 31,711,440 (GRCm39) |
Y554* |
probably null |
Het |
Mov10 |
A |
C |
3: 104,706,735 (GRCm39) |
F725C |
probably damaging |
Het |
Ms4a6d |
A |
C |
19: 11,567,523 (GRCm39) |
L18R |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,298,515 (GRCm39) |
N507S |
probably benign |
Het |
Nodal |
A |
G |
10: 61,254,113 (GRCm39) |
Q12R |
probably benign |
Het |
Npy6r |
T |
C |
18: 44,409,575 (GRCm39) |
L332P |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,227,181 (GRCm39) |
K272R |
possibly damaging |
Het |
Obox2 |
G |
T |
7: 15,131,174 (GRCm39) |
K93N |
probably benign |
Het |
Or10j27 |
C |
T |
1: 172,958,418 (GRCm39) |
R122H |
possibly damaging |
Het |
Or51a6 |
G |
T |
7: 102,603,953 (GRCm39) |
P285Q |
probably damaging |
Het |
Or5b112 |
A |
G |
19: 13,319,178 (GRCm39) |
T19A |
possibly damaging |
Het |
Or5w13 |
C |
T |
2: 87,523,777 (GRCm39) |
V150M |
probably benign |
Het |
Pcdh12 |
T |
A |
18: 38,415,196 (GRCm39) |
D643V |
possibly damaging |
Het |
Pcsk2 |
A |
G |
2: 143,529,539 (GRCm39) |
D112G |
probably benign |
Het |
Pms1 |
A |
G |
1: 53,234,174 (GRCm39) |
S781P |
probably benign |
Het |
Prtg |
A |
G |
9: 72,752,178 (GRCm39) |
D188G |
probably benign |
Het |
Psg21 |
A |
T |
7: 18,388,695 (GRCm39) |
N132K |
probably benign |
Het |
Psip1 |
A |
G |
4: 83,400,769 (GRCm39) |
V25A |
probably damaging |
Het |
Psmd13 |
T |
A |
7: 140,478,107 (GRCm39) |
I319N |
probably damaging |
Het |
Ptges2 |
A |
G |
2: 32,290,104 (GRCm39) |
T173A |
probably benign |
Het |
Ptprm |
G |
A |
17: 67,054,155 (GRCm39) |
R975W |
probably damaging |
Het |
Rdh1 |
A |
G |
10: 127,601,214 (GRCm39) |
D254G |
probably benign |
Het |
Rnf138 |
T |
G |
18: 21,157,540 (GRCm39) |
N212K |
probably damaging |
Het |
Serpine2 |
A |
G |
1: 79,799,159 (GRCm39) |
S32P |
probably damaging |
Het |
Serpini1 |
G |
T |
3: 75,521,971 (GRCm39) |
W154L |
probably damaging |
Het |
Sf3a1 |
C |
A |
11: 4,129,177 (GRCm39) |
Q713K |
possibly damaging |
Het |
Sgo2b |
A |
T |
8: 64,379,867 (GRCm39) |
H988Q |
probably benign |
Het |
Sin3a |
T |
C |
9: 57,008,483 (GRCm39) |
F468L |
probably damaging |
Het |
Slamf6 |
A |
T |
1: 171,761,776 (GRCm39) |
I66F |
possibly damaging |
Het |
Slc22a28 |
A |
T |
19: 8,094,488 (GRCm39) |
C178S |
possibly damaging |
Het |
Slc35a1 |
A |
C |
4: 34,675,181 (GRCm39) |
V119G |
probably damaging |
Het |
Slc39a12 |
A |
T |
2: 14,439,030 (GRCm39) |
H428L |
probably damaging |
Het |
Speer2 |
A |
G |
16: 69,654,965 (GRCm39) |
S167P |
probably benign |
Het |
Sphkap |
G |
A |
1: 83,255,236 (GRCm39) |
R838* |
probably null |
Het |
Spsb2 |
T |
C |
6: 124,786,329 (GRCm39) |
|
probably null |
Het |
Stam2 |
A |
T |
2: 52,593,168 (GRCm39) |
Y341* |
probably null |
Het |
Sv2b |
G |
A |
7: 74,856,089 (GRCm39) |
A67V |
probably benign |
Het |
Svep1 |
A |
G |
4: 58,064,170 (GRCm39) |
|
probably null |
Het |
Syt15 |
A |
T |
14: 33,944,969 (GRCm39) |
Q172L |
probably benign |
Het |
T |
G |
A |
17: 8,660,634 (GRCm39) |
S415N |
probably benign |
Het |
Tep1 |
A |
G |
14: 51,061,641 (GRCm39) |
F2625S |
possibly damaging |
Het |
Tex14 |
T |
C |
11: 87,427,581 (GRCm39) |
V11A |
possibly damaging |
Het |
Tiam2 |
A |
T |
17: 3,465,401 (GRCm39) |
R377* |
probably null |
Het |
Tirap |
A |
G |
9: 35,102,312 (GRCm39) |
|
probably null |
Het |
Tm4sf20 |
T |
C |
1: 82,737,938 (GRCm39) |
T118A |
probably benign |
Het |
Trank1 |
A |
T |
9: 111,207,900 (GRCm39) |
Q1715L |
probably benign |
Het |
Trpm2 |
C |
T |
10: 77,783,823 (GRCm39) |
V217M |
probably damaging |
Het |
Ubap1l |
G |
A |
9: 65,279,078 (GRCm39) |
E126K |
possibly damaging |
Het |
Urgcp |
G |
T |
11: 5,666,526 (GRCm39) |
P604Q |
probably damaging |
Het |
Vmn1r63 |
A |
G |
7: 5,806,254 (GRCm39) |
V126A |
probably benign |
Het |
Vmn2r90 |
T |
C |
17: 17,933,525 (GRCm39) |
C362R |
probably damaging |
Het |
Vmn2r96 |
A |
G |
17: 18,804,138 (GRCm39) |
I271V |
probably damaging |
Het |
Vps13a |
A |
T |
19: 16,699,822 (GRCm39) |
I740K |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,883,138 (GRCm39) |
T3562A |
probably damaging |
Het |
Wdr91 |
T |
A |
6: 34,869,297 (GRCm39) |
H409L |
probably damaging |
Het |
Wnt7a |
T |
A |
6: 91,342,938 (GRCm39) |
T315S |
possibly damaging |
Het |
Zfp616 |
A |
G |
11: 73,975,795 (GRCm39) |
H688R |
probably benign |
Het |
Zfp763 |
A |
T |
17: 33,237,413 (GRCm39) |
H577Q |
probably damaging |
Het |
Zfp808 |
G |
A |
13: 62,320,721 (GRCm39) |
S650N |
probably benign |
Het |
Zfp977 |
A |
T |
7: 42,229,409 (GRCm39) |
M372K |
probably benign |
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 |
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 |
|