Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
A |
G |
7: 78,743,951 (GRCm39) |
T661A |
probably damaging |
Het |
Actrt2 |
T |
C |
4: 154,751,383 (GRCm39) |
Y251C |
probably benign |
Het |
Adat3 |
T |
A |
10: 80,442,255 (GRCm39) |
V31D |
probably damaging |
Het |
Adgrf4 |
T |
C |
17: 42,980,548 (GRCm39) |
H179R |
possibly damaging |
Het |
Ahcyl1 |
A |
T |
3: 107,578,513 (GRCm39) |
Y241* |
probably null |
Het |
Anks1 |
C |
A |
17: 28,227,114 (GRCm39) |
T589K |
possibly damaging |
Het |
Arhgap15 |
A |
G |
2: 43,670,630 (GRCm39) |
T5A |
probably benign |
Het |
Cacna1e |
A |
T |
1: 154,344,734 (GRCm39) |
M1130K |
probably null |
Het |
Ccdc121rt1 |
G |
A |
1: 181,338,443 (GRCm39) |
Q170* |
probably null |
Het |
Ceacam18 |
A |
T |
7: 43,286,298 (GRCm39) |
D57V |
probably damaging |
Het |
Celf1 |
C |
T |
2: 90,835,100 (GRCm39) |
Q194* |
probably null |
Het |
Celsr2 |
T |
A |
3: 108,306,218 (GRCm39) |
T2029S |
probably benign |
Het |
Cep170 |
T |
C |
1: 176,583,595 (GRCm39) |
D163G |
probably damaging |
Het |
Cfap210 |
A |
T |
2: 69,606,488 (GRCm39) |
D309E |
probably benign |
Het |
Cftr |
T |
C |
6: 18,214,295 (GRCm39) |
F157S |
probably damaging |
Het |
Chchd3 |
T |
C |
6: 32,945,164 (GRCm39) |
E114G |
probably damaging |
Het |
Cntnap2 |
T |
A |
6: 46,460,963 (GRCm39) |
S666R |
possibly damaging |
Het |
Col6a5 |
C |
T |
9: 105,753,075 (GRCm39) |
V2266I |
probably benign |
Het |
Ctr9 |
A |
G |
7: 110,633,133 (GRCm39) |
D127G |
probably benign |
Het |
Ctsl |
A |
T |
13: 64,514,882 (GRCm39) |
F141I |
probably damaging |
Het |
Dcpp1 |
T |
A |
17: 24,101,615 (GRCm39) |
Y121* |
probably null |
Het |
Ddx42 |
T |
C |
11: 106,138,565 (GRCm39) |
V788A |
probably benign |
Het |
Ehd4 |
T |
C |
2: 119,921,874 (GRCm39) |
I461V |
probably benign |
Het |
Elp6 |
C |
A |
9: 110,134,376 (GRCm39) |
L5I |
possibly damaging |
Het |
Faap20 |
T |
C |
4: 155,334,793 (GRCm39) |
S2P |
|
Het |
Fam98b |
A |
C |
2: 117,094,344 (GRCm39) |
Y218S |
probably damaging |
Het |
Fbxl4 |
T |
A |
4: 22,376,655 (GRCm39) |
D30E |
probably benign |
Het |
Fcrlb |
T |
C |
1: 170,736,210 (GRCm39) |
T189A |
probably damaging |
Het |
Gfpt1 |
A |
G |
6: 87,043,671 (GRCm39) |
D302G |
probably benign |
Het |
Gzmg |
T |
G |
14: 56,394,284 (GRCm39) |
E203D |
not run |
Het |
Hsph1 |
A |
C |
5: 149,553,838 (GRCm39) |
V210G |
probably damaging |
Het |
Il20rb |
A |
T |
9: 100,350,479 (GRCm39) |
M138K |
probably damaging |
Het |
Itpr1 |
A |
T |
6: 108,360,639 (GRCm39) |
E688D |
probably benign |
Het |
Jmjd1c |
T |
G |
10: 67,067,794 (GRCm39) |
S1585A |
probably damaging |
Het |
Kcnk3 |
A |
T |
5: 30,780,062 (GRCm39) |
T371S |
possibly damaging |
Het |
Kif11 |
T |
A |
19: 37,398,255 (GRCm39) |
S694T |
possibly damaging |
Het |
Kpna7 |
T |
A |
5: 144,942,731 (GRCm39) |
H85L |
probably benign |
Het |
Lipf |
A |
T |
19: 33,954,006 (GRCm39) |
I366F |
probably damaging |
Het |
Lrrc27 |
A |
G |
7: 138,794,748 (GRCm39) |
H37R |
probably benign |
Het |
Mtss1 |
A |
G |
15: 58,820,210 (GRCm39) |
S120P |
probably damaging |
Het |
Nav1 |
A |
G |
1: 135,397,404 (GRCm39) |
W922R |
probably damaging |
Het |
Nwd1 |
A |
G |
8: 73,434,021 (GRCm39) |
E1206G |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,885,635 (GRCm39) |
S7933G |
unknown |
Het |
Or13j1 |
T |
C |
4: 43,706,316 (GRCm39) |
H84R |
probably damaging |
Het |
Or1p4-ps1 |
T |
C |
11: 74,208,010 (GRCm39) |
V53A |
probably benign |
Het |
Or2g25 |
T |
A |
17: 37,971,122 (GRCm39) |
Y34F |
probably damaging |
Het |
Or2k2 |
T |
C |
4: 58,785,648 (GRCm39) |
I25V |
probably benign |
Het |
Or4c52 |
T |
C |
2: 89,845,355 (GRCm39) |
L27S |
probably benign |
Het |
Otog |
A |
T |
7: 45,948,039 (GRCm39) |
I162F |
probably damaging |
Het |
Paf1 |
G |
A |
7: 28,095,293 (GRCm39) |
V153I |
possibly damaging |
Het |
Pcdhga11 |
T |
A |
18: 37,889,554 (GRCm39) |
D187E |
probably benign |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Pitrm1 |
G |
T |
13: 6,610,658 (GRCm39) |
R424L |
probably damaging |
Het |
Pla2g4e |
T |
A |
2: 120,004,819 (GRCm39) |
|
probably null |
Het |
Plaat1 |
T |
C |
16: 29,046,919 (GRCm39) |
V146A |
probably benign |
Het |
Prorp |
T |
C |
12: 55,351,206 (GRCm39) |
Y172H |
probably damaging |
Het |
Prrc2a |
T |
C |
17: 35,381,286 (GRCm39) |
N61S |
unknown |
Het |
Ror1 |
T |
A |
4: 100,190,827 (GRCm39) |
D61E |
probably benign |
Het |
Ryr3 |
G |
A |
2: 112,542,706 (GRCm39) |
P3168S |
probably benign |
Het |
Serinc4 |
T |
A |
2: 121,284,250 (GRCm39) |
I289F |
probably damaging |
Het |
Sez6l |
A |
T |
5: 112,623,347 (GRCm39) |
L68H |
possibly damaging |
Het |
Sez6l2 |
A |
G |
7: 126,560,915 (GRCm39) |
E460G |
probably benign |
Het |
Sh3tc1 |
C |
T |
5: 35,863,406 (GRCm39) |
G927D |
probably damaging |
Het |
Slc22a27 |
G |
C |
19: 7,903,747 (GRCm39) |
T130S |
probably damaging |
Het |
Slc38a8 |
C |
A |
8: 120,227,820 (GRCm39) |
A37S |
possibly damaging |
Het |
Slc40a1 |
T |
C |
1: 45,958,134 (GRCm39) |
N100D |
probably damaging |
Het |
Slc49a3 |
G |
A |
5: 108,591,646 (GRCm39) |
|
probably null |
Het |
Snx30 |
T |
C |
4: 59,894,567 (GRCm39) |
F382L |
possibly damaging |
Het |
Sox1 |
A |
G |
8: 12,446,913 (GRCm39) |
N185D |
possibly damaging |
Het |
Spsb1 |
C |
T |
4: 149,991,385 (GRCm39) |
R61H |
possibly damaging |
Het |
Sptbn2 |
T |
C |
19: 4,798,110 (GRCm39) |
V1945A |
probably benign |
Het |
St18 |
T |
A |
1: 6,898,194 (GRCm39) |
N665K |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,283,446 (GRCm39) |
S1540P |
probably damaging |
Het |
Syne2 |
G |
A |
12: 76,141,100 (GRCm39) |
V1331M |
probably damaging |
Het |
Tfap2c |
T |
C |
2: 172,393,639 (GRCm39) |
S185P |
probably benign |
Het |
Tnfsf8 |
T |
A |
4: 63,769,398 (GRCm39) |
D71V |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,937,929 (GRCm39) |
D1196G |
probably benign |
Het |
Ttll8 |
A |
G |
15: 88,817,639 (GRCm39) |
|
probably null |
Het |
Tubgcp3 |
A |
G |
8: 12,691,207 (GRCm39) |
F444L |
probably damaging |
Het |
Txndc11 |
G |
A |
16: 10,905,742 (GRCm39) |
P596L |
probably benign |
Het |
Ubr4 |
C |
T |
4: 139,139,983 (GRCm39) |
P1189S |
possibly damaging |
Het |
Usp32 |
T |
C |
11: 84,913,724 (GRCm39) |
D869G |
possibly damaging |
Het |
Vmn1r202 |
G |
T |
13: 22,686,188 (GRCm39) |
N76K |
probably damaging |
Het |
Wfdc6a |
C |
T |
2: 164,421,761 (GRCm39) |
M132I |
probably benign |
Het |
Wnk2 |
A |
T |
13: 49,300,720 (GRCm39) |
|
probably null |
Het |
Xbp1 |
A |
G |
11: 5,474,683 (GRCm39) |
|
probably null |
Het |
Zfp551 |
A |
T |
7: 12,149,725 (GRCm39) |
Y561* |
probably null |
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 |
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 |
|