Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
A |
G |
14: 118,727,978 (GRCm39) |
L1268P |
possibly damaging |
Het |
Acot3 |
T |
A |
12: 84,103,860 (GRCm39) |
V223E |
probably damaging |
Het |
Afap1 |
T |
G |
5: 36,154,895 (GRCm39) |
S680A |
probably damaging |
Het |
Aox1 |
C |
T |
1: 58,116,672 (GRCm39) |
A801V |
probably damaging |
Het |
Atp8b1 |
G |
T |
18: 64,710,687 (GRCm39) |
T155K |
probably damaging |
Het |
Bard1 |
C |
A |
1: 71,069,909 (GRCm39) |
V690F |
possibly damaging |
Het |
Btnl9 |
C |
A |
11: 49,073,792 (GRCm39) |
|
probably null |
Het |
C1rl |
A |
G |
6: 124,470,147 (GRCm39) |
N13S |
probably benign |
Het |
Cad |
C |
A |
5: 31,226,456 (GRCm39) |
T1166K |
probably damaging |
Het |
Ckap5 |
T |
A |
2: 91,393,334 (GRCm39) |
M405K |
probably damaging |
Het |
Csn1s1 |
T |
C |
5: 87,825,944 (GRCm39) |
|
probably null |
Het |
Ctnna2 |
A |
G |
6: 76,892,811 (GRCm39) |
L792P |
probably damaging |
Het |
Dennd3 |
T |
A |
15: 73,438,929 (GRCm39) |
V1099D |
possibly damaging |
Het |
Dnai2 |
A |
G |
11: 114,643,816 (GRCm39) |
N482S |
probably benign |
Het |
Dock10 |
T |
C |
1: 80,583,890 (GRCm39) |
T184A |
probably damaging |
Het |
Ear2 |
T |
A |
14: 44,340,546 (GRCm39) |
L68H |
probably damaging |
Het |
Edn3 |
A |
G |
2: 174,621,525 (GRCm39) |
T149A |
probably benign |
Het |
Erf |
C |
T |
7: 24,945,041 (GRCm39) |
V131M |
probably benign |
Het |
Esp34 |
A |
G |
17: 38,865,118 (GRCm39) |
|
probably benign |
Het |
Gm7247 |
C |
T |
14: 51,601,805 (GRCm39) |
S26F |
probably benign |
Het |
Golga1 |
A |
G |
2: 38,937,099 (GRCm39) |
V161A |
probably benign |
Het |
Gpr17 |
T |
A |
18: 32,080,530 (GRCm39) |
T178S |
probably benign |
Het |
Gsg1l2 |
T |
A |
11: 67,665,537 (GRCm39) |
I35N |
possibly damaging |
Het |
Hmgn3 |
T |
A |
9: 82,994,284 (GRCm39) |
T46S |
probably damaging |
Het |
Hydin |
A |
C |
8: 111,325,717 (GRCm39) |
I4709L |
probably benign |
Het |
Ifna9 |
A |
T |
4: 88,510,600 (GRCm39) |
L8Q |
probably null |
Het |
Iftap |
A |
T |
2: 101,413,898 (GRCm39) |
M133K |
possibly damaging |
Het |
Kpna4 |
T |
C |
3: 69,034,066 (GRCm39) |
E125G |
probably null |
Het |
Lrriq1 |
A |
G |
10: 103,006,325 (GRCm39) |
S1267P |
probably damaging |
Het |
Mab21l1 |
G |
T |
3: 55,690,518 (GRCm39) |
C35F |
possibly damaging |
Het |
Map3k2 |
A |
G |
18: 32,336,104 (GRCm39) |
D97G |
probably damaging |
Het |
Matcap2 |
G |
A |
9: 22,335,422 (GRCm39) |
W13* |
probably null |
Het |
Mdn1 |
T |
A |
4: 32,741,073 (GRCm39) |
I3799N |
probably damaging |
Het |
Mroh1 |
A |
T |
15: 76,335,557 (GRCm39) |
H1400L |
possibly damaging |
Het |
Mroh4 |
T |
A |
15: 74,497,321 (GRCm39) |
K167* |
probably null |
Het |
Mroh8 |
A |
G |
2: 157,094,984 (GRCm39) |
I334T |
probably benign |
Het |
Or51a25 |
T |
A |
7: 102,373,574 (GRCm39) |
Y41F |
probably damaging |
Het |
Phf11d |
T |
A |
14: 59,602,898 (GRCm39) |
|
probably benign |
Het |
Phf21a |
C |
T |
2: 92,182,097 (GRCm39) |
T342I |
possibly damaging |
Het |
Pira12 |
G |
T |
7: 3,897,599 (GRCm39) |
H499N |
probably damaging |
Het |
Plekhh3 |
T |
C |
11: 101,055,591 (GRCm39) |
E483G |
possibly damaging |
Het |
Ppp1r3b |
G |
A |
8: 35,851,355 (GRCm39) |
A65T |
probably damaging |
Het |
Pramel30 |
C |
T |
4: 144,057,777 (GRCm39) |
T128I |
probably benign |
Het |
Prkcq |
A |
G |
2: 11,261,097 (GRCm39) |
H383R |
probably damaging |
Het |
Pum1 |
T |
C |
4: 130,496,158 (GRCm39) |
V961A |
probably damaging |
Het |
Scgb2b27 |
T |
C |
7: 33,711,561 (GRCm39) |
E96G |
probably benign |
Het |
Sel1l2 |
T |
A |
2: 140,086,025 (GRCm39) |
E522V |
probably damaging |
Het |
Socs4 |
T |
G |
14: 47,527,618 (GRCm39) |
C184W |
probably damaging |
Het |
Spdye4c |
A |
T |
2: 128,438,553 (GRCm39) |
I304F |
probably benign |
Het |
Sptbn2 |
A |
G |
19: 4,789,306 (GRCm39) |
I1249V |
possibly damaging |
Het |
Sys1 |
T |
C |
2: 164,306,507 (GRCm39) |
S154P |
probably benign |
Het |
Taf6l |
T |
C |
19: 8,755,530 (GRCm39) |
Q275R |
possibly damaging |
Het |
Tas2r107 |
A |
G |
6: 131,636,875 (GRCm39) |
V58A |
possibly damaging |
Het |
Thada |
T |
A |
17: 84,744,062 (GRCm39) |
I749F |
probably damaging |
Het |
Tubb1 |
T |
A |
2: 174,299,567 (GRCm39) |
H416Q |
probably benign |
Het |
Vmn2r109 |
G |
A |
17: 20,760,981 (GRCm39) |
T792I |
probably damaging |
Het |
Zfp988 |
A |
G |
4: 147,416,259 (GRCm39) |
Q231R |
probably benign |
Het |
Zmynd8 |
T |
C |
2: 165,684,707 (GRCm39) |
I182V |
possibly damaging |
Het |
Zzz3 |
T |
C |
3: 152,133,788 (GRCm39) |
V282A |
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 |
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 |
R7076:Mki67
|
UTSW |
7 |
135,307,358 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
|