Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam29 |
A |
G |
8: 56,324,694 (GRCm39) |
C587R |
probably damaging |
Het |
Adgrg7 |
T |
C |
16: 56,562,769 (GRCm39) |
T523A |
probably damaging |
Het |
Arrdc3 |
A |
T |
13: 81,038,815 (GRCm39) |
K259M |
probably damaging |
Het |
Becn1 |
A |
T |
11: 101,186,150 (GRCm39) |
N151K |
probably benign |
Het |
Cars2 |
C |
T |
8: 11,579,649 (GRCm39) |
E270K |
probably damaging |
Het |
Ccp110 |
C |
A |
7: 118,331,628 (GRCm39) |
P943Q |
probably damaging |
Het |
Ccser2 |
A |
G |
14: 36,661,786 (GRCm39) |
I466T |
probably benign |
Het |
Cd164 |
A |
G |
10: 41,399,193 (GRCm39) |
E94G |
probably benign |
Het |
Cdon |
C |
T |
9: 35,415,446 (GRCm39) |
T1228I |
probably benign |
Het |
Cubn |
C |
A |
2: 13,311,091 (GRCm39) |
V3145L |
probably benign |
Het |
Cubn |
T |
A |
2: 13,311,092 (GRCm39) |
K3144N |
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,411,078 (GRCm39) |
V1649A |
probably benign |
Het |
Dgka |
A |
T |
10: 128,569,452 (GRCm39) |
D153E |
probably damaging |
Het |
Dip2b |
A |
G |
15: 100,055,853 (GRCm39) |
|
probably null |
Het |
Dnajc21 |
T |
C |
15: 10,449,717 (GRCm39) |
T435A |
probably benign |
Het |
F830016B08Rik |
A |
T |
18: 60,433,543 (GRCm39) |
I209F |
probably damaging |
Het |
Ghdc |
C |
A |
11: 100,660,540 (GRCm39) |
S111I |
possibly damaging |
Het |
Gm19965 |
T |
C |
1: 116,749,005 (GRCm39) |
C229R |
|
Het |
Gpm6a |
C |
T |
8: 55,490,486 (GRCm39) |
T54I |
probably damaging |
Het |
Gpr171 |
G |
T |
3: 59,005,577 (GRCm39) |
A66E |
probably damaging |
Het |
Grm7 |
A |
G |
6: 111,335,113 (GRCm39) |
D508G |
probably benign |
Het |
Has1 |
G |
A |
17: 18,064,068 (GRCm39) |
R524C |
probably damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Ighv3-8 |
A |
T |
12: 114,286,402 (GRCm39) |
L7Q |
probably damaging |
Het |
Ints10 |
A |
T |
8: 69,249,403 (GRCm39) |
R78* |
probably null |
Het |
Itpr1 |
A |
G |
6: 108,365,257 (GRCm39) |
I903V |
probably benign |
Het |
Lrp1 |
A |
G |
10: 127,386,052 (GRCm39) |
|
probably null |
Het |
Myh4 |
A |
G |
11: 67,143,999 (GRCm39) |
E1123G |
possibly damaging |
Het |
Neurog3 |
A |
G |
10: 61,969,359 (GRCm39) |
T40A |
probably benign |
Het |
Nipsnap3b |
T |
A |
4: 53,021,095 (GRCm39) |
|
probably null |
Het |
Nr4a3 |
G |
A |
4: 48,055,957 (GRCm39) |
V328I |
probably damaging |
Het |
Or11g27 |
T |
A |
14: 50,771,278 (GRCm39) |
Y136* |
probably null |
Het |
Or2d36 |
T |
C |
7: 106,747,236 (GRCm39) |
F238L |
probably damaging |
Het |
Or52u1 |
A |
T |
7: 104,237,430 (GRCm39) |
S140C |
probably damaging |
Het |
Or5af2 |
G |
A |
11: 58,707,990 (GRCm39) |
R52Q |
probably benign |
Het |
Or5b124 |
G |
T |
19: 13,611,244 (GRCm39) |
M256I |
possibly damaging |
Het |
Or5p63 |
A |
T |
7: 107,811,205 (GRCm39) |
V177D |
probably damaging |
Het |
Osbpl5 |
A |
G |
7: 143,263,577 (GRCm39) |
L102P |
probably benign |
Het |
Ppl |
C |
T |
16: 4,917,983 (GRCm39) |
R503Q |
probably damaging |
Het |
Ppp2r2d |
T |
C |
7: 138,478,326 (GRCm39) |
M321T |
possibly damaging |
Het |
Prex1 |
T |
C |
2: 166,475,302 (GRCm39) |
Y197C |
probably damaging |
Het |
Prss32 |
A |
G |
17: 24,072,895 (GRCm39) |
D42G |
possibly damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,768,361 (GRCm39) |
E1210G |
possibly damaging |
Het |
Sdr16c5 |
A |
G |
4: 4,006,591 (GRCm39) |
C234R |
probably damaging |
Het |
Slc23a4 |
A |
G |
6: 34,933,819 (GRCm39) |
S95P |
probably damaging |
Het |
Srp14 |
T |
C |
2: 118,309,871 (GRCm39) |
T29A |
probably damaging |
Het |
Tet2 |
T |
A |
3: 133,172,784 (GRCm39) |
H1826L |
possibly damaging |
Het |
Tfr2 |
A |
T |
5: 137,581,836 (GRCm39) |
Y641F |
probably damaging |
Het |
Tmco5b |
A |
G |
2: 113,117,766 (GRCm39) |
N27D |
probably damaging |
Het |
Tvp23a |
T |
C |
16: 10,246,599 (GRCm39) |
D62G |
probably benign |
Het |
Usp12 |
A |
G |
5: 146,674,562 (GRCm39) |
F347S |
possibly damaging |
Het |
Zfp407 |
A |
T |
18: 84,576,601 (GRCm39) |
L1504Q |
probably damaging |
Het |
Zfp524 |
A |
G |
7: 5,020,895 (GRCm39) |
D141G |
possibly damaging |
Het |
Zfp68 |
A |
G |
5: 138,605,201 (GRCm39) |
I374T |
possibly damaging |
Het |
Zfp758 |
C |
T |
17: 22,594,137 (GRCm39) |
H208Y |
probably benign |
Het |
Zfp804b |
T |
C |
5: 6,819,751 (GRCm39) |
H1104R |
probably benign |
Het |
Znrf2 |
T |
A |
6: 54,819,680 (GRCm39) |
*75K |
probably null |
Het |
Zzef1 |
T |
C |
11: 72,790,385 (GRCm39) |
V2113A |
probably benign |
Het |
|
Other mutations in Mki67 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00225:Mki67
|
APN |
7 |
135,291,849 (GRCm39) |
missense |
probably benign |
0.32 |
IGL00264:Mki67
|
APN |
7 |
135,309,549 (GRCm39) |
nonsense |
probably null |
|
IGL00328:Mki67
|
APN |
7 |
135,298,424 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00570:Mki67
|
APN |
7 |
135,309,830 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00584:Mki67
|
APN |
7 |
135,297,424 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00756:Mki67
|
APN |
7 |
135,300,460 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01063:Mki67
|
APN |
7 |
135,296,651 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01112:Mki67
|
APN |
7 |
135,315,745 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01360:Mki67
|
APN |
7 |
135,307,505 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Mki67
|
APN |
7 |
135,301,275 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01686:Mki67
|
APN |
7 |
135,309,542 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01731:Mki67
|
APN |
7 |
135,298,278 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01775:Mki67
|
APN |
7 |
135,300,005 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01806:Mki67
|
APN |
7 |
135,300,686 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01860:Mki67
|
APN |
7 |
135,300,686 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01938:Mki67
|
APN |
7 |
135,296,059 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02249:Mki67
|
APN |
7 |
135,302,251 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02260:Mki67
|
APN |
7 |
135,303,697 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02270:Mki67
|
APN |
7 |
135,300,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02406:Mki67
|
APN |
7 |
135,300,522 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02499:Mki67
|
APN |
7 |
135,296,056 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02655:Mki67
|
APN |
7 |
135,315,748 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02700:Mki67
|
APN |
7 |
135,309,931 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03370:Mki67
|
APN |
7 |
135,297,219 (GRCm39) |
missense |
probably benign |
0.00 |
Advisement
|
UTSW |
7 |
135,299,923 (GRCm39) |
missense |
probably damaging |
1.00 |
chocotoff
|
UTSW |
7 |
135,300,628 (GRCm39) |
missense |
possibly damaging |
0.92 |
Godiva
|
UTSW |
7 |
135,303,691 (GRCm39) |
missense |
probably benign |
0.10 |
sees
|
UTSW |
7 |
135,302,644 (GRCm39) |
missense |
possibly damaging |
0.68 |
Whitman
|
UTSW |
7 |
135,315,594 (GRCm39) |
missense |
probably damaging |
1.00 |
BB003:Mki67
|
UTSW |
7 |
135,298,869 (GRCm39) |
missense |
possibly damaging |
0.91 |
BB013:Mki67
|
UTSW |
7 |
135,298,869 (GRCm39) |
missense |
possibly damaging |
0.91 |
PIT4468001:Mki67
|
UTSW |
7 |
135,300,876 (GRCm39) |
missense |
probably benign |
0.00 |
R0001:Mki67
|
UTSW |
7 |
135,302,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R0001:Mki67
|
UTSW |
7 |
135,300,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R0043:Mki67
|
UTSW |
7 |
135,302,310 (GRCm39) |
missense |
probably benign |
0.16 |
R0043:Mki67
|
UTSW |
7 |
135,302,310 (GRCm39) |
missense |
probably benign |
0.16 |
R0102:Mki67
|
UTSW |
7 |
135,315,532 (GRCm39) |
missense |
probably benign |
0.16 |
R0130:Mki67
|
UTSW |
7 |
135,298,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R0149:Mki67
|
UTSW |
7 |
135,300,153 (GRCm39) |
missense |
probably benign |
0.00 |
R0356:Mki67
|
UTSW |
7 |
135,306,135 (GRCm39) |
missense |
probably benign |
0.34 |
R0482:Mki67
|
UTSW |
7 |
135,301,158 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0508:Mki67
|
UTSW |
7 |
135,302,075 (GRCm39) |
missense |
probably benign |
|
R0532:Mki67
|
UTSW |
7 |
135,299,893 (GRCm39) |
nonsense |
probably null |
|
R0548:Mki67
|
UTSW |
7 |
135,298,637 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0548:Mki67
|
UTSW |
7 |
135,296,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R0557:Mki67
|
UTSW |
7 |
135,300,990 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0627:Mki67
|
UTSW |
7 |
135,309,987 (GRCm39) |
missense |
probably benign |
0.31 |
R0631:Mki67
|
UTSW |
7 |
135,306,117 (GRCm39) |
missense |
probably damaging |
0.98 |
R0848:Mki67
|
UTSW |
7 |
135,302,772 (GRCm39) |
missense |
probably benign |
0.21 |
R1075:Mki67
|
UTSW |
7 |
135,299,040 (GRCm39) |
missense |
probably benign |
0.03 |
R1105:Mki67
|
UTSW |
7 |
135,302,779 (GRCm39) |
missense |
probably benign |
0.09 |
R1272:Mki67
|
UTSW |
7 |
135,302,143 (GRCm39) |
nonsense |
probably null |
|
R1331:Mki67
|
UTSW |
7 |
135,300,005 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1486:Mki67
|
UTSW |
7 |
135,301,449 (GRCm39) |
missense |
probably benign |
0.00 |
R1510:Mki67
|
UTSW |
7 |
135,297,900 (GRCm39) |
missense |
probably benign |
0.26 |
R1573:Mki67
|
UTSW |
7 |
135,296,845 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1586:Mki67
|
UTSW |
7 |
135,315,701 (GRCm39) |
nonsense |
probably null |
|
R1599:Mki67
|
UTSW |
7 |
135,301,663 (GRCm39) |
missense |
probably benign |
0.34 |
R1623:Mki67
|
UTSW |
7 |
135,310,547 (GRCm39) |
splice site |
probably null |
|
R1706:Mki67
|
UTSW |
7 |
135,302,295 (GRCm39) |
missense |
probably benign |
0.37 |
R1718:Mki67
|
UTSW |
7 |
135,297,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Mki67
|
UTSW |
7 |
135,305,970 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1816:Mki67
|
UTSW |
7 |
135,309,116 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1862:Mki67
|
UTSW |
7 |
135,301,090 (GRCm39) |
missense |
probably benign |
0.09 |
R1929:Mki67
|
UTSW |
7 |
135,299,794 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1957:Mki67
|
UTSW |
7 |
135,300,128 (GRCm39) |
missense |
probably benign |
0.01 |
R1971:Mki67
|
UTSW |
7 |
135,315,688 (GRCm39) |
critical splice donor site |
probably null |
|
R1998:Mki67
|
UTSW |
7 |
135,307,499 (GRCm39) |
missense |
probably benign |
0.00 |
R2004:Mki67
|
UTSW |
7 |
135,300,238 (GRCm39) |
nonsense |
probably null |
|
R2005:Mki67
|
UTSW |
7 |
135,300,238 (GRCm39) |
nonsense |
probably null |
|
R2006:Mki67
|
UTSW |
7 |
135,300,238 (GRCm39) |
nonsense |
probably null |
|
R2109:Mki67
|
UTSW |
7 |
135,299,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:Mki67
|
UTSW |
7 |
135,305,970 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2131:Mki67
|
UTSW |
7 |
135,305,970 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2133:Mki67
|
UTSW |
7 |
135,305,970 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2140:Mki67
|
UTSW |
7 |
135,297,321 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2141:Mki67
|
UTSW |
7 |
135,297,321 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2142:Mki67
|
UTSW |
7 |
135,297,321 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2284:Mki67
|
UTSW |
7 |
135,301,674 (GRCm39) |
missense |
probably damaging |
0.99 |
R2869:Mki67
|
UTSW |
7 |
135,309,878 (GRCm39) |
missense |
probably benign |
0.19 |
R2869:Mki67
|
UTSW |
7 |
135,309,878 (GRCm39) |
missense |
probably benign |
0.19 |
R2871:Mki67
|
UTSW |
7 |
135,309,878 (GRCm39) |
missense |
probably benign |
0.19 |
R2871:Mki67
|
UTSW |
7 |
135,309,878 (GRCm39) |
missense |
probably benign |
0.19 |
R2913:Mki67
|
UTSW |
7 |
135,302,415 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3404:Mki67
|
UTSW |
7 |
135,309,204 (GRCm39) |
missense |
probably benign |
0.01 |
R3405:Mki67
|
UTSW |
7 |
135,309,204 (GRCm39) |
missense |
probably benign |
0.01 |
R3406:Mki67
|
UTSW |
7 |
135,309,204 (GRCm39) |
missense |
probably benign |
0.01 |
R3777:Mki67
|
UTSW |
7 |
135,297,859 (GRCm39) |
missense |
probably benign |
0.10 |
R3778:Mki67
|
UTSW |
7 |
135,297,859 (GRCm39) |
missense |
probably benign |
0.10 |
R3787:Mki67
|
UTSW |
7 |
135,302,012 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3847:Mki67
|
UTSW |
7 |
135,297,859 (GRCm39) |
missense |
probably benign |
0.10 |
R3848:Mki67
|
UTSW |
7 |
135,297,859 (GRCm39) |
missense |
probably benign |
0.10 |
R3853:Mki67
|
UTSW |
7 |
135,297,859 (GRCm39) |
missense |
probably benign |
0.10 |
R3971:Mki67
|
UTSW |
7 |
135,297,859 (GRCm39) |
missense |
probably benign |
0.10 |
R3972:Mki67
|
UTSW |
7 |
135,297,859 (GRCm39) |
missense |
probably benign |
0.10 |
R4258:Mki67
|
UTSW |
7 |
135,297,017 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4343:Mki67
|
UTSW |
7 |
135,296,847 (GRCm39) |
missense |
probably benign |
0.10 |
R4488:Mki67
|
UTSW |
7 |
135,299,400 (GRCm39) |
missense |
probably benign |
0.01 |
R4528:Mki67
|
UTSW |
7 |
135,297,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R4713:Mki67
|
UTSW |
7 |
135,297,198 (GRCm39) |
missense |
probably benign |
0.35 |
R4867:Mki67
|
UTSW |
7 |
135,301,585 (GRCm39) |
missense |
probably damaging |
0.97 |
R4874:Mki67
|
UTSW |
7 |
135,310,500 (GRCm39) |
missense |
probably damaging |
0.97 |
R4897:Mki67
|
UTSW |
7 |
135,298,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Mki67
|
UTSW |
7 |
135,309,633 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5306:Mki67
|
UTSW |
7 |
135,315,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R5309:Mki67
|
UTSW |
7 |
135,302,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R5312:Mki67
|
UTSW |
7 |
135,302,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R5379:Mki67
|
UTSW |
7 |
135,299,190 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5506:Mki67
|
UTSW |
7 |
135,301,710 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5513:Mki67
|
UTSW |
7 |
135,309,479 (GRCm39) |
missense |
probably damaging |
0.98 |
R5742:Mki67
|
UTSW |
7 |
135,306,102 (GRCm39) |
missense |
probably benign |
0.20 |
R5806:Mki67
|
UTSW |
7 |
135,306,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R6008:Mki67
|
UTSW |
7 |
135,299,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R6037:Mki67
|
UTSW |
7 |
135,298,532 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6037:Mki67
|
UTSW |
7 |
135,298,532 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6221:Mki67
|
UTSW |
7 |
135,299,643 (GRCm39) |
missense |
probably benign |
0.18 |
R6294:Mki67
|
UTSW |
7 |
135,306,319 (GRCm39) |
missense |
probably benign |
0.09 |
R6377:Mki67
|
UTSW |
7 |
135,298,050 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6456:Mki67
|
UTSW |
7 |
135,301,204 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6608:Mki67
|
UTSW |
7 |
135,300,090 (GRCm39) |
missense |
probably benign |
0.01 |
R6609:Mki67
|
UTSW |
7 |
135,301,558 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6648:Mki67
|
UTSW |
7 |
135,299,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R6901:Mki67
|
UTSW |
7 |
135,310,489 (GRCm39) |
splice site |
probably null |
|
R6978:Mki67
|
UTSW |
7 |
135,303,691 (GRCm39) |
missense |
probably benign |
0.10 |
R6985:Mki67
|
UTSW |
7 |
135,315,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R7217:Mki67
|
UTSW |
7 |
135,305,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R7239:Mki67
|
UTSW |
7 |
135,301,905 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7250:Mki67
|
UTSW |
7 |
135,301,053 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7313:Mki67
|
UTSW |
7 |
135,296,400 (GRCm39) |
missense |
probably benign |
0.29 |
R7336:Mki67
|
UTSW |
7 |
135,315,568 (GRCm39) |
missense |
probably benign |
0.03 |
R7422:Mki67
|
UTSW |
7 |
135,300,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Mki67
|
UTSW |
7 |
135,301,080 (GRCm39) |
missense |
probably benign |
0.01 |
R7502:Mki67
|
UTSW |
7 |
135,302,512 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7513:Mki67
|
UTSW |
7 |
135,294,952 (GRCm39) |
missense |
probably benign |
|
R7578:Mki67
|
UTSW |
7 |
135,302,644 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7619:Mki67
|
UTSW |
7 |
135,301,106 (GRCm39) |
missense |
probably benign |
0.01 |
R7646:Mki67
|
UTSW |
7 |
135,298,498 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7659:Mki67
|
UTSW |
7 |
135,299,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R7691:Mki67
|
UTSW |
7 |
135,303,721 (GRCm39) |
missense |
not run |
|
R7780:Mki67
|
UTSW |
7 |
135,315,697 (GRCm39) |
missense |
probably benign |
0.02 |
R7796:Mki67
|
UTSW |
7 |
135,299,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R7904:Mki67
|
UTSW |
7 |
135,294,816 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7911:Mki67
|
UTSW |
7 |
135,306,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R7921:Mki67
|
UTSW |
7 |
135,296,933 (GRCm39) |
missense |
probably benign |
0.01 |
R7926:Mki67
|
UTSW |
7 |
135,298,869 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7950:Mki67
|
UTSW |
7 |
135,301,453 (GRCm39) |
nonsense |
probably null |
|
R8130:Mki67
|
UTSW |
7 |
135,299,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R8145:Mki67
|
UTSW |
7 |
135,296,065 (GRCm39) |
missense |
probably benign |
0.07 |
R8196:Mki67
|
UTSW |
7 |
135,297,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R8220:Mki67
|
UTSW |
7 |
135,299,850 (GRCm39) |
missense |
probably benign |
0.03 |
R8299:Mki67
|
UTSW |
7 |
135,306,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Mki67
|
UTSW |
7 |
135,298,245 (GRCm39) |
missense |
probably damaging |
0.98 |
R8350:Mki67
|
UTSW |
7 |
135,300,200 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8358:Mki67
|
UTSW |
7 |
135,301,855 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8529:Mki67
|
UTSW |
7 |
135,315,688 (GRCm39) |
critical splice donor site |
probably null |
|
R8698:Mki67
|
UTSW |
7 |
135,296,937 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8700:Mki67
|
UTSW |
7 |
135,307,436 (GRCm39) |
missense |
|
|
R8737:Mki67
|
UTSW |
7 |
135,315,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R8914:Mki67
|
UTSW |
7 |
135,299,595 (GRCm39) |
missense |
|
|
R8930:Mki67
|
UTSW |
7 |
135,300,628 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8932:Mki67
|
UTSW |
7 |
135,300,628 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8972:Mki67
|
UTSW |
7 |
135,297,364 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8973:Mki67
|
UTSW |
7 |
135,297,364 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8975:Mki67
|
UTSW |
7 |
135,300,129 (GRCm39) |
missense |
probably benign |
0.01 |
R8975:Mki67
|
UTSW |
7 |
135,297,364 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9071:Mki67
|
UTSW |
7 |
135,301,205 (GRCm39) |
missense |
probably benign |
0.00 |
R9241:Mki67
|
UTSW |
7 |
135,297,653 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9387:Mki67
|
UTSW |
7 |
135,302,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R9524:Mki67
|
UTSW |
7 |
135,305,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Mki67
|
UTSW |
7 |
135,309,233 (GRCm39) |
frame shift |
probably null |
|
R9782:Mki67
|
UTSW |
7 |
135,306,066 (GRCm39) |
critical splice donor site |
probably null |
|
X0020:Mki67
|
UTSW |
7 |
135,315,730 (GRCm39) |
missense |
probably damaging |
0.96 |
X0065:Mki67
|
UTSW |
7 |
135,315,573 (GRCm39) |
missense |
possibly damaging |
0.95 |
|