Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
C |
7: 119,854,626 (GRCm39) |
V930A |
probably benign |
Het |
Ankrd13b |
T |
C |
11: 77,362,494 (GRCm39) |
R677G |
probably benign |
Het |
Apold1 |
A |
G |
6: 134,961,032 (GRCm39) |
Y162C |
probably damaging |
Het |
Atp6v0a4 |
T |
C |
6: 38,055,737 (GRCm39) |
I325V |
probably benign |
Het |
Cab39 |
A |
G |
1: 85,776,050 (GRCm39) |
Y249C |
probably damaging |
Het |
Cd22 |
T |
A |
7: 30,575,325 (GRCm39) |
H239L |
probably damaging |
Het |
Chrna7 |
A |
G |
7: 62,753,538 (GRCm39) |
M327T |
probably damaging |
Het |
Cimip2b |
T |
C |
4: 43,427,574 (GRCm39) |
H250R |
possibly damaging |
Het |
Clock |
T |
C |
5: 76,383,657 (GRCm39) |
M499V |
probably benign |
Het |
Clspn |
A |
G |
4: 126,475,253 (GRCm39) |
E1002G |
probably benign |
Het |
Clta |
C |
T |
4: 44,012,819 (GRCm39) |
P10S |
probably damaging |
Het |
Col5a3 |
A |
G |
9: 20,685,855 (GRCm39) |
|
probably null |
Het |
Coq6 |
T |
C |
12: 84,408,913 (GRCm39) |
V30A |
probably benign |
Het |
Csmd2 |
G |
T |
4: 127,881,921 (GRCm39) |
R20L |
probably benign |
Het |
D430041D05Rik |
A |
T |
2: 104,038,528 (GRCm39) |
V1547D |
probably damaging |
Het |
Dapk1 |
C |
T |
13: 60,865,861 (GRCm39) |
P153S |
probably benign |
Het |
Dock2 |
T |
A |
11: 34,189,536 (GRCm39) |
Y1545F |
probably damaging |
Het |
Dpp6 |
G |
T |
5: 27,839,546 (GRCm39) |
G354C |
probably damaging |
Het |
Dyrk1b |
T |
C |
7: 27,881,856 (GRCm39) |
L105P |
probably damaging |
Het |
Epor |
A |
G |
9: 21,873,155 (GRCm39) |
S86P |
probably benign |
Het |
Gale |
C |
A |
4: 135,695,148 (GRCm39) |
S341* |
probably null |
Het |
Galnt4 |
T |
A |
10: 98,945,355 (GRCm39) |
V360E |
probably damaging |
Het |
Gart |
A |
T |
16: 91,419,833 (GRCm39) |
C24* |
probably null |
Het |
Gcnt2 |
G |
T |
13: 41,040,966 (GRCm39) |
V42L |
probably benign |
Het |
Herc6 |
A |
G |
6: 57,636,698 (GRCm39) |
I805V |
probably benign |
Het |
Ints12 |
T |
A |
3: 132,804,214 (GRCm39) |
I67N |
probably benign |
Het |
Irx1 |
C |
A |
13: 72,108,232 (GRCm39) |
R150L |
probably damaging |
Het |
Kif26b |
A |
G |
1: 178,358,024 (GRCm39) |
Y45C |
unknown |
Het |
Krt35 |
T |
C |
11: 99,984,834 (GRCm39) |
T275A |
probably damaging |
Het |
Laptm5 |
G |
T |
4: 130,643,316 (GRCm39) |
|
probably benign |
Het |
Lin7a |
T |
C |
10: 107,248,027 (GRCm39) |
S111P |
unknown |
Het |
Med27 |
A |
G |
2: 29,414,470 (GRCm39) |
D159G |
probably damaging |
Het |
Msh2 |
A |
G |
17: 88,016,006 (GRCm39) |
K546R |
probably damaging |
Het |
Myo1a |
A |
T |
10: 127,556,020 (GRCm39) |
|
probably null |
Het |
Myo1c |
T |
C |
11: 75,559,019 (GRCm39) |
F604L |
probably damaging |
Het |
Myrip |
A |
G |
9: 120,293,850 (GRCm39) |
K782E |
probably damaging |
Het |
Ndc80 |
T |
C |
17: 71,828,063 (GRCm39) |
D88G |
probably damaging |
Het |
Nrxn2 |
A |
G |
19: 6,505,282 (GRCm39) |
D375G |
probably damaging |
Het |
Or2y10 |
T |
C |
11: 49,455,545 (GRCm39) |
S266P |
probably damaging |
Het |
Or52e7 |
A |
G |
7: 104,685,280 (GRCm39) |
I292V |
probably benign |
Het |
Padi3 |
T |
C |
4: 140,525,422 (GRCm39) |
H187R |
probably damaging |
Het |
Pcdhgb1 |
A |
T |
18: 37,814,610 (GRCm39) |
N367I |
probably damaging |
Het |
Pdrg1 |
T |
C |
2: 152,854,310 (GRCm39) |
I77V |
probably benign |
Het |
Pfas |
T |
C |
11: 68,881,895 (GRCm39) |
E930G |
probably benign |
Het |
Pik3cb |
C |
T |
9: 98,943,817 (GRCm39) |
R662Q |
probably benign |
Het |
Pla2g4e |
T |
G |
2: 120,016,863 (GRCm39) |
H226P |
possibly damaging |
Het |
Plxnd1 |
A |
T |
6: 115,971,237 (GRCm39) |
V177E |
probably damaging |
Het |
Prmt7 |
A |
G |
8: 106,976,961 (GRCm39) |
S558G |
possibly damaging |
Het |
Pspc1 |
A |
C |
14: 57,015,246 (GRCm39) |
|
probably null |
Het |
Rilp |
T |
C |
11: 75,403,586 (GRCm39) |
S343P |
probably benign |
Het |
Ror1 |
A |
G |
4: 100,265,107 (GRCm39) |
M194V |
probably damaging |
Het |
Rsu1 |
T |
C |
2: 13,174,815 (GRCm39) |
Y225C |
probably damaging |
Het |
Rundc1 |
A |
G |
11: 101,324,752 (GRCm39) |
N486S |
probably damaging |
Het |
Sema6d |
T |
A |
2: 124,496,151 (GRCm39) |
I65N |
probably damaging |
Het |
Slc5a11 |
A |
G |
7: 122,857,601 (GRCm39) |
E230G |
probably benign |
Het |
Spint1 |
T |
C |
2: 119,076,941 (GRCm39) |
S342P |
probably damaging |
Het |
Stard3nl |
A |
G |
13: 19,551,923 (GRCm39) |
S214P |
probably damaging |
Het |
Tcp10a |
A |
C |
17: 7,604,323 (GRCm39) |
T271P |
probably damaging |
Het |
Tie1 |
A |
G |
4: 118,329,831 (GRCm39) |
Y1091H |
probably benign |
Het |
Tlr12 |
T |
C |
4: 128,511,125 (GRCm39) |
Y375C |
probably benign |
Het |
Tmem107 |
T |
A |
11: 68,962,274 (GRCm39) |
M77K |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Tns3 |
T |
C |
11: 8,481,747 (GRCm39) |
K202E |
probably damaging |
Het |
Tspoap1 |
C |
T |
11: 87,670,347 (GRCm39) |
P1634L |
probably damaging |
Het |
Ttc7b |
G |
A |
12: 100,466,376 (GRCm39) |
R79C |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,643,844 (GRCm39) |
N4402S |
probably benign |
Het |
Vmn2r13 |
A |
T |
5: 109,304,322 (GRCm39) |
I703N |
probably damaging |
Het |
Xrcc4 |
A |
G |
13: 90,210,126 (GRCm39) |
|
probably null |
Het |
Zp3 |
A |
T |
5: 136,013,089 (GRCm39) |
K168* |
probably null |
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 |
|
R2013:Apc
|
UTSW |
18 |
34,448,644 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
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 |
|