Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam4 |
A |
T |
12: 81,466,596 (GRCm39) |
V675D |
possibly damaging |
Het |
Adamts16 |
T |
C |
13: 70,901,345 (GRCm39) |
T911A |
probably benign |
Het |
Adgra1 |
T |
C |
7: 139,427,619 (GRCm39) |
F62S |
possibly damaging |
Het |
Adgra3 |
A |
G |
5: 50,159,272 (GRCm39) |
V326A |
probably damaging |
Het |
Aff1 |
T |
A |
5: 103,902,572 (GRCm39) |
M1K |
probably null |
Het |
AI429214 |
C |
T |
8: 37,461,071 (GRCm39) |
S73L |
probably benign |
Het |
Apcs |
T |
C |
1: 172,722,130 (GRCm39) |
Y72C |
probably damaging |
Het |
Arid4a |
T |
C |
12: 71,108,299 (GRCm39) |
|
probably benign |
Het |
Armcx4 |
C |
A |
X: 133,591,774 (GRCm39) |
Q561K |
probably benign |
Het |
Atp5po |
C |
T |
16: 91,725,794 (GRCm39) |
R64H |
probably damaging |
Het |
Bank1 |
G |
A |
3: 135,953,534 (GRCm39) |
|
probably benign |
Het |
Ccdc150 |
A |
G |
1: 54,395,932 (GRCm39) |
D805G |
probably benign |
Het |
Ccdc88a |
T |
A |
11: 29,436,006 (GRCm39) |
C10S |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 30,991,774 (GRCm39) |
M3076K |
possibly damaging |
Het |
Dnpep |
A |
G |
1: 75,293,270 (GRCm39) |
V33A |
probably damaging |
Het |
Egfem1 |
C |
T |
3: 29,637,170 (GRCm39) |
T202I |
probably damaging |
Het |
Fam120b |
T |
A |
17: 15,651,897 (GRCm39) |
|
probably benign |
Het |
Frem1 |
T |
C |
4: 82,881,416 (GRCm39) |
T1263A |
possibly damaging |
Het |
Gm6802 |
C |
A |
12: 19,540,621 (GRCm39) |
|
noncoding transcript |
Het |
Golga2 |
C |
A |
2: 32,192,954 (GRCm39) |
A424E |
probably damaging |
Het |
Gpat2 |
G |
A |
2: 127,270,211 (GRCm39) |
V75M |
probably damaging |
Het |
Grik5 |
T |
C |
7: 24,762,397 (GRCm39) |
D198G |
probably benign |
Het |
Hcrtr2 |
A |
G |
9: 76,140,290 (GRCm39) |
F333L |
probably benign |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Htr1b |
A |
C |
9: 81,514,094 (GRCm39) |
V171G |
probably benign |
Het |
Kalrn |
G |
T |
16: 34,032,642 (GRCm39) |
D1117E |
probably benign |
Het |
Kcp |
T |
C |
6: 29,482,845 (GRCm39) |
N1408S |
possibly damaging |
Het |
Klhl7 |
G |
T |
5: 24,343,319 (GRCm39) |
V212L |
probably damaging |
Het |
Klra17 |
T |
A |
6: 129,851,809 (GRCm39) |
N21I |
probably damaging |
Het |
Lrrc8d |
A |
T |
5: 105,974,572 (GRCm39) |
|
noncoding transcript |
Het |
Mast2 |
C |
G |
4: 116,168,107 (GRCm39) |
E881Q |
possibly damaging |
Het |
Mcm6 |
T |
C |
1: 128,279,322 (GRCm39) |
T155A |
probably benign |
Het |
Mslnl |
T |
C |
17: 25,963,491 (GRCm39) |
F326L |
probably benign |
Het |
Nlrp4c |
A |
G |
7: 6,095,569 (GRCm39) |
K816E |
possibly damaging |
Het |
Or10g1 |
T |
A |
14: 52,647,818 (GRCm39) |
R170S |
possibly damaging |
Het |
Or5b101 |
G |
C |
19: 13,005,411 (GRCm39) |
A94G |
probably benign |
Het |
Or5p69 |
A |
T |
7: 107,967,551 (GRCm39) |
I285F |
possibly damaging |
Het |
Or8k3 |
T |
C |
2: 86,058,986 (GRCm39) |
S110G |
probably benign |
Het |
Otoa |
A |
G |
7: 120,721,266 (GRCm39) |
Q427R |
probably damaging |
Het |
Pcdhb6 |
A |
G |
18: 37,468,945 (GRCm39) |
E622G |
probably damaging |
Het |
Pdzd8 |
A |
G |
19: 59,333,845 (GRCm39) |
Y59H |
probably damaging |
Het |
Psmc3 |
A |
C |
2: 90,886,263 (GRCm39) |
D159A |
probably damaging |
Het |
Ripk4 |
T |
C |
16: 97,545,157 (GRCm39) |
T497A |
probably benign |
Het |
Rpn2 |
C |
A |
2: 157,132,572 (GRCm39) |
A108E |
possibly damaging |
Het |
Serpina3n |
A |
G |
12: 104,377,536 (GRCm39) |
E263G |
possibly damaging |
Het |
Six4 |
A |
G |
12: 73,159,657 (GRCm39) |
F101S |
probably damaging |
Het |
Slc16a4 |
G |
A |
3: 107,208,188 (GRCm39) |
E233K |
probably benign |
Het |
Smu1 |
T |
C |
4: 40,752,008 (GRCm39) |
T183A |
probably benign |
Het |
Sptb |
T |
G |
12: 76,657,589 (GRCm39) |
K1311Q |
possibly damaging |
Het |
Styxl1 |
T |
C |
5: 135,794,618 (GRCm39) |
Y83C |
probably damaging |
Het |
Sypl2 |
C |
T |
3: 108,124,045 (GRCm39) |
V166I |
possibly damaging |
Het |
Tal2 |
A |
G |
4: 53,785,843 (GRCm39) |
N8S |
probably damaging |
Het |
Tenm4 |
T |
C |
7: 96,501,737 (GRCm39) |
Y1314H |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,772,749 (GRCm39) |
N2415K |
possibly damaging |
Het |
Usp53 |
T |
C |
3: 122,743,507 (GRCm39) |
|
probably null |
Het |
Vmn2r65 |
T |
C |
7: 84,595,896 (GRCm39) |
I263V |
probably benign |
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 |
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 |
|