Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
T |
G |
17: 48,347,723 (GRCm39) |
T194P |
possibly damaging |
Het |
4921504E06Rik |
T |
A |
2: 19,545,124 (GRCm39) |
M110L |
probably benign |
Het |
Acad9 |
T |
G |
3: 36,127,737 (GRCm39) |
I113R |
probably damaging |
Het |
Adam34l |
T |
C |
8: 44,079,442 (GRCm39) |
S261G |
possibly damaging |
Het |
Adamts6 |
A |
T |
13: 104,450,812 (GRCm39) |
I332F |
probably damaging |
Het |
Adcy8 |
C |
T |
15: 64,639,727 (GRCm39) |
G678S |
probably benign |
Het |
Afg3l2 |
C |
T |
18: 67,564,842 (GRCm39) |
V211I |
probably damaging |
Het |
Ahnak |
T |
C |
19: 8,991,937 (GRCm39) |
I4407T |
probably damaging |
Het |
Alpl |
G |
T |
4: 137,482,458 (GRCm39) |
H79N |
probably benign |
Het |
Ascc3 |
T |
C |
10: 50,525,908 (GRCm39) |
M540T |
probably damaging |
Het |
Blm |
T |
C |
7: 80,152,147 (GRCm39) |
E600G |
probably damaging |
Het |
Btbd8 |
T |
C |
5: 107,658,655 (GRCm39) |
W1742R |
probably damaging |
Het |
Cadps |
T |
A |
14: 12,522,337 (GRCm38) |
D609V |
probably damaging |
Het |
Ccdc69 |
C |
T |
11: 54,941,983 (GRCm39) |
M174I |
probably benign |
Het |
Cdk13 |
A |
T |
13: 17,913,748 (GRCm39) |
L877* |
probably null |
Het |
Cdk14 |
T |
C |
5: 5,143,047 (GRCm39) |
Y228C |
probably damaging |
Het |
Dip2c |
C |
T |
13: 9,617,882 (GRCm39) |
Q426* |
probably null |
Het |
Dsp |
A |
G |
13: 38,375,434 (GRCm39) |
N1073S |
probably damaging |
Het |
Epyc |
T |
C |
10: 97,511,655 (GRCm39) |
I216T |
probably damaging |
Het |
Erbin |
A |
G |
13: 103,994,041 (GRCm39) |
S300P |
probably damaging |
Het |
Ercc3 |
A |
G |
18: 32,381,482 (GRCm39) |
T433A |
probably benign |
Het |
Exoc4 |
A |
G |
6: 33,243,026 (GRCm39) |
T80A |
probably damaging |
Het |
Foxm1 |
T |
A |
6: 128,352,465 (GRCm39) |
|
probably null |
Het |
Gaa |
A |
G |
11: 119,175,409 (GRCm39) |
|
probably null |
Het |
H2-Q4 |
A |
G |
17: 35,599,526 (GRCm39) |
E203G |
probably damaging |
Het |
Helt |
T |
C |
8: 46,745,355 (GRCm39) |
D214G |
probably damaging |
Het |
Hlcs |
A |
G |
16: 94,063,599 (GRCm39) |
V487A |
probably benign |
Het |
Hmmr |
A |
T |
11: 40,619,259 (GRCm39) |
S74T |
possibly damaging |
Het |
Hspa9 |
A |
T |
18: 35,079,701 (GRCm39) |
Y243N |
probably damaging |
Het |
Htt |
T |
G |
5: 35,010,215 (GRCm39) |
L1556R |
probably damaging |
Het |
Ift80 |
T |
C |
3: 68,898,117 (GRCm39) |
K73E |
possibly damaging |
Het |
Il6st |
G |
A |
13: 112,635,423 (GRCm39) |
A551T |
probably null |
Het |
Kdm5a |
T |
C |
6: 120,408,951 (GRCm39) |
S1545P |
probably benign |
Het |
Lef1 |
T |
A |
3: 130,905,236 (GRCm39) |
I39N |
probably damaging |
Het |
Lmo2 |
T |
C |
2: 103,811,407 (GRCm39) |
Y147H |
probably damaging |
Het |
Lrp6 |
A |
G |
6: 134,457,337 (GRCm39) |
|
probably null |
Het |
Macf1 |
T |
C |
4: 123,577,807 (GRCm39) |
D59G |
probably damaging |
Het |
Maged1 |
T |
C |
X: 93,580,523 (GRCm39) |
Y636C |
possibly damaging |
Het |
Mamdc4 |
T |
A |
2: 25,453,584 (GRCm39) |
D1195V |
probably damaging |
Het |
Mob3b |
A |
G |
4: 35,083,922 (GRCm39) |
V89A |
probably benign |
Het |
Mogs |
C |
T |
6: 83,094,631 (GRCm39) |
R483* |
probably null |
Het |
Mybphl |
A |
C |
3: 108,282,718 (GRCm39) |
T203P |
probably benign |
Het |
Myo15a |
A |
G |
11: 60,385,057 (GRCm39) |
T1720A |
probably damaging |
Het |
Myo16 |
T |
A |
8: 10,552,796 (GRCm39) |
F945I |
probably damaging |
Het |
Nbeal2 |
G |
A |
9: 110,463,139 (GRCm39) |
L1309F |
probably benign |
Het |
Nes |
A |
G |
3: 87,883,985 (GRCm39) |
Q748R |
possibly damaging |
Het |
Nhsl1 |
A |
T |
10: 18,387,340 (GRCm39) |
R205W |
probably damaging |
Het |
Nlrc3 |
A |
C |
16: 3,782,974 (GRCm39) |
L161R |
probably damaging |
Het |
Npy2r |
T |
A |
3: 82,448,487 (GRCm39) |
D96V |
probably damaging |
Het |
Or4d11 |
T |
A |
19: 12,013,518 (GRCm39) |
E196V |
probably damaging |
Het |
Or5w18 |
T |
G |
2: 87,632,847 (GRCm39) |
V38G |
probably damaging |
Het |
Pappa2 |
C |
T |
1: 158,662,498 (GRCm39) |
C1159Y |
probably damaging |
Het |
Phf21a |
T |
C |
2: 92,058,828 (GRCm39) |
|
probably null |
Het |
Pik3c2a |
T |
A |
7: 115,950,166 (GRCm39) |
|
probably null |
Het |
Psg22 |
A |
T |
7: 18,453,560 (GRCm39) |
Y85F |
possibly damaging |
Het |
Pttg1ip2 |
T |
A |
5: 5,505,964 (GRCm39) |
I106L |
probably benign |
Het |
Qtrt2 |
A |
G |
16: 43,689,455 (GRCm39) |
I181T |
probably damaging |
Het |
Sash1 |
A |
T |
10: 8,605,177 (GRCm39) |
V1071D |
probably benign |
Het |
Scn10a |
A |
T |
9: 119,442,802 (GRCm39) |
I1481N |
probably damaging |
Het |
Slc15a1 |
G |
A |
14: 121,713,399 (GRCm39) |
A376V |
possibly damaging |
Het |
Slc25a46 |
A |
T |
18: 31,742,778 (GRCm39) |
H29Q |
probably benign |
Het |
Slit2 |
T |
C |
5: 48,459,832 (GRCm39) |
C1354R |
probably damaging |
Het |
Ssu2 |
C |
T |
6: 112,360,902 (GRCm39) |
E52K |
possibly damaging |
Het |
Taar7e |
A |
T |
10: 23,913,732 (GRCm39) |
H74L |
possibly damaging |
Het |
Tcte1 |
A |
T |
17: 45,852,237 (GRCm39) |
N490I |
probably benign |
Het |
Tent4b |
T |
A |
8: 88,972,223 (GRCm39) |
|
probably null |
Het |
Tpst2 |
G |
T |
5: 112,455,880 (GRCm39) |
G140C |
probably damaging |
Het |
Trip11 |
A |
T |
12: 101,803,981 (GRCm39) |
F1634I |
probably damaging |
Het |
Trpm2 |
A |
G |
10: 77,761,600 (GRCm39) |
F1017L |
probably damaging |
Het |
Utp18 |
A |
G |
11: 93,766,948 (GRCm39) |
V253A |
possibly damaging |
Het |
Vmn2r102 |
A |
G |
17: 19,897,006 (GRCm39) |
T118A |
probably benign |
Het |
Vmn2r14 |
T |
C |
5: 109,369,109 (GRCm39) |
T155A |
probably benign |
Het |
Vmn2r19 |
T |
A |
6: 123,292,954 (GRCm39) |
M332K |
probably benign |
Het |
Vmn2r71 |
T |
A |
7: 85,269,845 (GRCm39) |
M452K |
probably benign |
Het |
Vmn2r79 |
T |
G |
7: 86,653,289 (GRCm39) |
L518R |
possibly damaging |
Het |
Vps13b |
T |
C |
15: 35,607,288 (GRCm39) |
S1074P |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,835,078 (GRCm39) |
S2757P |
probably damaging |
Het |
Wdr33 |
C |
A |
18: 32,022,029 (GRCm39) |
Q860K |
unknown |
Het |
Zfp423 |
T |
A |
8: 88,509,025 (GRCm39) |
I440F |
probably benign |
Het |
Zup1 |
A |
G |
10: 33,805,820 (GRCm39) |
V437A |
possibly damaging |
Het |
|
Other mutations in Apc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00507:Apc
|
APN |
18 |
34,449,979 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00898:Apc
|
APN |
18 |
34,450,147 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01111:Apc
|
APN |
18 |
34,448,189 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01347:Apc
|
APN |
18 |
34,450,723 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01375:Apc
|
APN |
18 |
34,446,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01805:Apc
|
APN |
18 |
34,451,271 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01997:Apc
|
APN |
18 |
34,448,476 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02033:Apc
|
APN |
18 |
34,443,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02323:Apc
|
APN |
18 |
34,448,863 (GRCm39) |
nonsense |
probably null |
|
IGL02373:Apc
|
APN |
18 |
34,449,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02379:Apc
|
APN |
18 |
34,431,798 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02456:Apc
|
APN |
18 |
34,446,935 (GRCm39) |
nonsense |
probably null |
|
IGL02552:Apc
|
APN |
18 |
34,446,035 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02676:Apc
|
APN |
18 |
34,448,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02756:Apc
|
APN |
18 |
34,447,588 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02938:Apc
|
APN |
18 |
34,448,281 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02974:Apc
|
APN |
18 |
34,401,436 (GRCm39) |
splice site |
probably benign |
|
IGL03124:Apc
|
APN |
18 |
34,433,038 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03201:Apc
|
APN |
18 |
34,445,429 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03339:Apc
|
APN |
18 |
34,431,527 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Apc
|
UTSW |
18 |
34,415,050 (GRCm39) |
intron |
probably benign |
|
FR4342:Apc
|
UTSW |
18 |
34,415,052 (GRCm39) |
intron |
probably benign |
|
FR4449:Apc
|
UTSW |
18 |
34,415,058 (GRCm39) |
intron |
probably benign |
|
FR4449:Apc
|
UTSW |
18 |
34,415,053 (GRCm39) |
intron |
probably benign |
|
FR4548:Apc
|
UTSW |
18 |
34,415,051 (GRCm39) |
intron |
probably benign |
|
FR4737:Apc
|
UTSW |
18 |
34,415,052 (GRCm39) |
intron |
probably benign |
|
FR4976:Apc
|
UTSW |
18 |
34,415,057 (GRCm39) |
nonsense |
probably null |
|
FR4976:Apc
|
UTSW |
18 |
34,415,053 (GRCm39) |
intron |
probably benign |
|
FR4976:Apc
|
UTSW |
18 |
34,415,051 (GRCm39) |
intron |
probably benign |
|
R0385:Apc
|
UTSW |
18 |
34,448,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R0535:Apc
|
UTSW |
18 |
34,394,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R0561:Apc
|
UTSW |
18 |
34,446,356 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0590:Apc
|
UTSW |
18 |
34,449,283 (GRCm39) |
nonsense |
probably null |
|
R0626:Apc
|
UTSW |
18 |
34,451,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R0991:Apc
|
UTSW |
18 |
34,449,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R1564:Apc
|
UTSW |
18 |
34,448,202 (GRCm39) |
missense |
probably benign |
0.00 |
R1663:Apc
|
UTSW |
18 |
34,401,378 (GRCm39) |
missense |
probably damaging |
0.98 |
R1737:Apc
|
UTSW |
18 |
34,450,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Apc
|
UTSW |
18 |
34,445,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Apc
|
UTSW |
18 |
34,450,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1887:Apc
|
UTSW |
18 |
34,405,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Apc
|
UTSW |
18 |
34,450,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R1974:Apc
|
UTSW |
18 |
34,433,057 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2005:Apc
|
UTSW |
18 |
34,443,962 (GRCm39) |
critical splice donor site |
probably null |
|
R2014:Apc
|
UTSW |
18 |
34,448,644 (GRCm39) |
missense |
probably damaging |
0.98 |
R2015:Apc
|
UTSW |
18 |
34,448,644 (GRCm39) |
missense |
probably damaging |
0.98 |
R2017:Apc
|
UTSW |
18 |
34,446,655 (GRCm39) |
missense |
probably benign |
0.00 |
R2056:Apc
|
UTSW |
18 |
34,449,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Apc
|
UTSW |
18 |
34,402,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Apc
|
UTSW |
18 |
34,409,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Apc
|
UTSW |
18 |
34,445,098 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2133:Apc
|
UTSW |
18 |
34,445,098 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2291:Apc
|
UTSW |
18 |
34,445,544 (GRCm39) |
missense |
probably benign |
0.45 |
R2332:Apc
|
UTSW |
18 |
34,450,112 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2360:Apc
|
UTSW |
18 |
34,394,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R2407:Apc
|
UTSW |
18 |
34,447,315 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2507:Apc
|
UTSW |
18 |
34,449,590 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2940:Apc
|
UTSW |
18 |
34,409,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R3404:Apc
|
UTSW |
18 |
34,446,655 (GRCm39) |
missense |
probably benign |
0.00 |
R3411:Apc
|
UTSW |
18 |
34,402,312 (GRCm39) |
splice site |
probably benign |
|
R3778:Apc
|
UTSW |
18 |
34,446,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Apc
|
UTSW |
18 |
34,412,388 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4599:Apc
|
UTSW |
18 |
34,451,040 (GRCm39) |
nonsense |
probably null |
|
R4611:Apc
|
UTSW |
18 |
34,451,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Apc
|
UTSW |
18 |
34,431,647 (GRCm39) |
missense |
probably damaging |
0.98 |
R4969:Apc
|
UTSW |
18 |
34,445,971 (GRCm39) |
nonsense |
probably null |
|
R5007:Apc
|
UTSW |
18 |
34,446,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R5066:Apc
|
UTSW |
18 |
34,449,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Apc
|
UTSW |
18 |
34,449,162 (GRCm39) |
nonsense |
probably null |
|
R5259:Apc
|
UTSW |
18 |
34,447,343 (GRCm39) |
missense |
probably benign |
0.29 |
R5440:Apc
|
UTSW |
18 |
34,354,213 (GRCm39) |
unclassified |
probably benign |
|
R5508:Apc
|
UTSW |
18 |
34,431,633 (GRCm39) |
missense |
probably damaging |
0.97 |
R5512:Apc
|
UTSW |
18 |
34,443,962 (GRCm39) |
critical splice donor site |
probably benign |
|
R5850:Apc
|
UTSW |
18 |
34,451,116 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5951:Apc
|
UTSW |
18 |
34,450,199 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5966:Apc
|
UTSW |
18 |
34,354,140 (GRCm39) |
utr 5 prime |
probably benign |
|
R6081:Apc
|
UTSW |
18 |
34,423,164 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6116:Apc
|
UTSW |
18 |
34,449,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6351:Apc
|
UTSW |
18 |
34,445,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R6354:Apc
|
UTSW |
18 |
34,445,581 (GRCm39) |
missense |
probably benign |
0.02 |
R6467:Apc
|
UTSW |
18 |
34,402,252 (GRCm39) |
missense |
probably benign |
0.22 |
R6974:Apc
|
UTSW |
18 |
34,431,480 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7027:Apc
|
UTSW |
18 |
34,445,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R7096:Apc
|
UTSW |
18 |
34,449,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R7289:Apc
|
UTSW |
18 |
34,448,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R7439:Apc
|
UTSW |
18 |
34,445,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R7441:Apc
|
UTSW |
18 |
34,445,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R7534:Apc
|
UTSW |
18 |
34,450,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R7685:Apc
|
UTSW |
18 |
34,447,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R7814:Apc
|
UTSW |
18 |
34,405,592 (GRCm39) |
missense |
probably damaging |
0.98 |
R7954:Apc
|
UTSW |
18 |
34,447,321 (GRCm39) |
missense |
probably damaging |
0.99 |
R8352:Apc
|
UTSW |
18 |
34,445,804 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8452:Apc
|
UTSW |
18 |
34,445,804 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8497:Apc
|
UTSW |
18 |
34,446,083 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8545:Apc
|
UTSW |
18 |
34,450,084 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8554:Apc
|
UTSW |
18 |
34,445,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Apc
|
UTSW |
18 |
34,401,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R9014:Apc
|
UTSW |
18 |
34,354,074 (GRCm39) |
start gained |
probably benign |
|
R9061:Apc
|
UTSW |
18 |
34,446,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Apc
|
UTSW |
18 |
34,450,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Apc
|
UTSW |
18 |
34,447,040 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9521:Apc
|
UTSW |
18 |
34,445,738 (GRCm39) |
missense |
probably benign |
0.24 |
R9546:Apc
|
UTSW |
18 |
34,445,311 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9547:Apc
|
UTSW |
18 |
34,445,311 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9557:Apc
|
UTSW |
18 |
34,451,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R9592:Apc
|
UTSW |
18 |
34,443,823 (GRCm39) |
nonsense |
probably null |
|
R9675:Apc
|
UTSW |
18 |
34,449,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R9736:Apc
|
UTSW |
18 |
34,450,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R9792:Apc
|
UTSW |
18 |
34,447,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9793:Apc
|
UTSW |
18 |
34,447,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9795:Apc
|
UTSW |
18 |
34,447,628 (GRCm39) |
missense |
probably damaging |
1.00 |
RF046:Apc
|
UTSW |
18 |
34,415,062 (GRCm39) |
critical splice donor site |
probably benign |
|
RF063:Apc
|
UTSW |
18 |
34,415,062 (GRCm39) |
critical splice donor site |
probably benign |
|
X0021:Apc
|
UTSW |
18 |
34,445,161 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Apc
|
UTSW |
18 |
34,445,429 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Apc
|
UTSW |
18 |
34,446,220 (GRCm39) |
nonsense |
probably null |
|
Z1177:Apc
|
UTSW |
18 |
34,447,516 (GRCm39) |
missense |
probably benign |
0.06 |
|