Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
A |
G |
1: 179,596,599 (GRCm39) |
V126A |
probably damaging |
Het |
Ank2 |
C |
A |
3: 126,749,519 (GRCm39) |
E503D |
probably damaging |
Het |
Arhgap45 |
C |
A |
10: 79,853,768 (GRCm39) |
T94N |
probably benign |
Het |
Arid1b |
T |
C |
17: 5,392,166 (GRCm39) |
S1899P |
possibly damaging |
Het |
Atad5 |
T |
A |
11: 79,980,601 (GRCm39) |
V2E |
probably damaging |
Het |
Calr |
A |
T |
8: 85,571,528 (GRCm39) |
V155E |
probably benign |
Het |
Cckbr |
C |
T |
7: 105,083,238 (GRCm39) |
A147V |
probably damaging |
Het |
Ces1d |
C |
A |
8: 93,896,346 (GRCm39) |
|
probably null |
Het |
Cetn1 |
T |
C |
18: 9,619,422 (GRCm39) |
|
probably benign |
Het |
Chl1 |
A |
T |
6: 103,618,949 (GRCm39) |
L6F |
probably damaging |
Het |
Chrnb1 |
C |
T |
11: 69,675,935 (GRCm39) |
V436I |
possibly damaging |
Het |
Col4a4 |
T |
C |
1: 82,506,204 (GRCm39) |
E292G |
unknown |
Het |
Ddx56 |
A |
G |
11: 6,217,667 (GRCm39) |
L18P |
probably damaging |
Het |
Dhx36 |
A |
C |
3: 62,384,797 (GRCm39) |
|
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,453,358 (GRCm39) |
R4376S |
possibly damaging |
Het |
Dnah6 |
T |
A |
6: 73,185,582 (GRCm39) |
D113V |
probably benign |
Het |
Dnah7a |
A |
G |
1: 53,512,118 (GRCm39) |
|
probably benign |
Het |
Dock7 |
T |
A |
4: 98,833,442 (GRCm39) |
K1920* |
probably null |
Het |
Dysf |
A |
G |
6: 84,076,471 (GRCm39) |
D628G |
probably benign |
Het |
Exoc3l2 |
A |
G |
7: 19,229,109 (GRCm39) |
I176V |
probably benign |
Het |
Fcrl1 |
A |
G |
3: 87,292,012 (GRCm39) |
Y57C |
probably damaging |
Het |
Fzd4 |
C |
T |
7: 89,057,162 (GRCm39) |
T403M |
probably damaging |
Het |
Gpr171 |
A |
T |
3: 59,005,288 (GRCm39) |
N162K |
probably benign |
Het |
Impdh1 |
T |
A |
6: 29,206,924 (GRCm39) |
K132* |
probably null |
Het |
Itgb2l |
A |
T |
16: 96,223,850 (GRCm39) |
W730R |
possibly damaging |
Het |
Jmjd8 |
T |
C |
17: 26,049,134 (GRCm39) |
F230S |
probably damaging |
Het |
Krt72 |
G |
A |
15: 101,690,556 (GRCm39) |
T232M |
probably damaging |
Het |
Lpin3 |
T |
C |
2: 160,740,540 (GRCm39) |
|
probably benign |
Het |
Nup214 |
A |
C |
2: 31,900,384 (GRCm39) |
|
probably benign |
Het |
Or11g7 |
A |
T |
14: 50,690,507 (GRCm39) |
|
probably benign |
Het |
Or7d10 |
A |
G |
9: 19,831,747 (GRCm39) |
M81V |
probably damaging |
Het |
Or8c20 |
A |
G |
9: 38,260,469 (GRCm39) |
Q24R |
probably benign |
Het |
Or8g26 |
A |
G |
9: 39,095,822 (GRCm39) |
Y113C |
probably damaging |
Het |
Pdgfra |
T |
A |
5: 75,355,635 (GRCm39) |
S1048R |
probably damaging |
Het |
Sall3 |
G |
T |
18: 81,012,728 (GRCm39) |
A1236E |
probably damaging |
Het |
Sipa1 |
T |
C |
19: 5,705,736 (GRCm39) |
T411A |
probably damaging |
Het |
Thsd7a |
T |
G |
6: 12,500,994 (GRCm39) |
D471A |
probably benign |
Het |
Tm2d1 |
T |
A |
4: 98,263,192 (GRCm39) |
E100D |
probably damaging |
Het |
Tmcc1 |
A |
G |
6: 116,110,849 (GRCm39) |
V148A |
probably damaging |
Het |
Tubgcp6 |
A |
T |
15: 88,986,518 (GRCm39) |
Y19* |
probably null |
Het |
Ubr3 |
A |
G |
2: 69,783,203 (GRCm39) |
Y713C |
probably damaging |
Het |
Uevld |
A |
G |
7: 46,605,377 (GRCm39) |
V39A |
probably benign |
Het |
Vmn2r28 |
A |
T |
7: 5,484,003 (GRCm39) |
H732Q |
probably damaging |
Het |
Zfp629 |
A |
T |
7: 127,209,484 (GRCm39) |
F775Y |
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 |
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 |
|
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 |
|