Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf3 |
T |
C |
16: 20,367,796 (GRCm39) |
S52P |
possibly damaging |
Het |
Adamts19 |
G |
T |
18: 59,181,881 (GRCm39) |
G1107C |
probably damaging |
Het |
Afap1 |
A |
T |
5: 36,131,830 (GRCm39) |
T386S |
probably benign |
Het |
Alg12 |
T |
C |
15: 88,695,503 (GRCm39) |
Y331C |
probably null |
Het |
Aste1 |
T |
A |
9: 105,274,255 (GRCm39) |
I165N |
probably damaging |
Het |
Atp13a5 |
A |
G |
16: 29,167,805 (GRCm39) |
I118T |
probably damaging |
Het |
AW551984 |
A |
G |
9: 39,510,651 (GRCm39) |
V228A |
probably damaging |
Het |
Cachd1 |
A |
G |
4: 100,816,668 (GRCm39) |
Y357C |
possibly damaging |
Het |
Cacul1 |
T |
A |
19: 60,551,673 (GRCm39) |
H183L |
possibly damaging |
Het |
Casp16 |
T |
A |
17: 23,772,348 (GRCm39) |
I39F |
probably damaging |
Het |
Chd7 |
G |
T |
4: 8,839,529 (GRCm39) |
C1355F |
probably damaging |
Het |
Csnk1a1 |
A |
G |
18: 61,713,610 (GRCm39) |
|
probably null |
Het |
Ctif |
G |
A |
18: 75,698,115 (GRCm39) |
H182Y |
possibly damaging |
Het |
Cubn |
C |
T |
2: 13,329,971 (GRCm39) |
V2637I |
probably benign |
Het |
Dlx1 |
T |
A |
2: 71,360,652 (GRCm39) |
|
probably null |
Het |
Dsp |
A |
G |
13: 38,376,457 (GRCm39) |
N1414S |
possibly damaging |
Het |
Erich6 |
A |
T |
3: 58,544,449 (GRCm39) |
L46* |
probably null |
Het |
Fcho2 |
G |
A |
13: 98,862,282 (GRCm39) |
R804* |
probably null |
Het |
Gas7 |
T |
A |
11: 67,543,734 (GRCm39) |
I114N |
probably benign |
Het |
Gpr137b |
T |
C |
13: 13,533,929 (GRCm39) |
T376A |
probably benign |
Het |
H2-T24 |
T |
C |
17: 36,328,229 (GRCm39) |
M85V |
probably benign |
Het |
Klk1b16 |
T |
A |
7: 43,790,185 (GRCm39) |
C152S |
probably damaging |
Het |
Lrrc31 |
G |
A |
3: 30,753,932 (GRCm39) |
|
probably benign |
Het |
Magt1 |
C |
T |
X: 105,040,501 (GRCm39) |
A100T |
probably benign |
Het |
Nif3l1 |
A |
T |
1: 58,491,288 (GRCm39) |
T213S |
probably benign |
Het |
Oasl1 |
T |
A |
5: 115,075,465 (GRCm39) |
F508L |
probably benign |
Het |
Or10ak8 |
A |
T |
4: 118,773,723 (GRCm39) |
*314R |
probably null |
Het |
Or2a25 |
T |
C |
6: 42,888,976 (GRCm39) |
V173A |
possibly damaging |
Het |
Or4a80 |
C |
T |
2: 89,582,423 (GRCm39) |
V250I |
probably benign |
Het |
Or5b122 |
T |
C |
19: 13,562,764 (GRCm39) |
L32P |
probably damaging |
Het |
Psg23 |
T |
C |
7: 18,348,522 (GRCm39) |
D95G |
probably benign |
Het |
Ptprr |
T |
C |
10: 115,884,180 (GRCm39) |
I79T |
probably benign |
Het |
Resf1 |
C |
T |
6: 149,228,076 (GRCm39) |
T374I |
probably damaging |
Het |
Rhbg |
T |
A |
3: 88,152,525 (GRCm39) |
N340Y |
probably damaging |
Het |
Sash1 |
C |
A |
10: 8,605,745 (GRCm39) |
V882L |
probably benign |
Het |
Sharpin |
C |
T |
15: 76,232,197 (GRCm39) |
V220I |
probably damaging |
Het |
Slc22a22 |
T |
A |
15: 57,108,243 (GRCm39) |
D524V |
probably damaging |
Het |
Slc43a3 |
T |
C |
2: 84,780,860 (GRCm39) |
Y362H |
probably benign |
Het |
Slc4a3 |
T |
A |
1: 75,530,359 (GRCm39) |
D687E |
probably damaging |
Het |
Slco1a5 |
A |
G |
6: 142,208,411 (GRCm39) |
S127P |
probably benign |
Het |
Spg11 |
T |
C |
2: 121,910,739 (GRCm39) |
I1213V |
possibly damaging |
Het |
Synj2 |
T |
A |
17: 6,074,080 (GRCm39) |
Y813* |
probably null |
Het |
Tbc1d10a |
T |
C |
11: 4,155,837 (GRCm39) |
M131T |
probably damaging |
Het |
Tnfrsf19 |
C |
A |
14: 61,208,634 (GRCm39) |
V296F |
probably benign |
Het |
Trim45 |
T |
C |
3: 100,834,634 (GRCm39) |
V439A |
probably damaging |
Het |
Trim54 |
A |
G |
5: 31,294,338 (GRCm39) |
T325A |
probably benign |
Het |
Usp40 |
T |
C |
1: 87,908,770 (GRCm39) |
E577G |
possibly damaging |
Het |
Uts2r |
T |
A |
11: 121,051,345 (GRCm39) |
Y70N |
probably damaging |
Het |
Vmn1r72 |
T |
G |
7: 11,404,310 (GRCm39) |
D46A |
probably damaging |
Het |
Zfc3h1 |
T |
C |
10: 115,240,198 (GRCm39) |
V577A |
probably benign |
Het |
Zfp987 |
T |
G |
4: 146,061,343 (GRCm39) |
H258Q |
probably damaging |
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 |
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 |
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 |
|