Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
T |
A |
4: 144,349,782 (GRCm39) |
N346K |
possibly damaging |
Het |
Abca15 |
A |
G |
7: 119,987,439 (GRCm39) |
M1242V |
probably benign |
Het |
Abca6 |
T |
A |
11: 110,139,374 (GRCm39) |
E33D |
probably damaging |
Het |
Abca8a |
T |
C |
11: 109,961,177 (GRCm39) |
K582E |
possibly damaging |
Het |
Abcb6 |
A |
G |
1: 75,154,646 (GRCm39) |
L263P |
probably damaging |
Het |
Adamts2 |
A |
C |
11: 50,678,106 (GRCm39) |
E795A |
probably damaging |
Het |
Avil |
T |
A |
10: 126,844,864 (GRCm39) |
I292N |
probably damaging |
Het |
Cd300ld2 |
T |
C |
11: 114,904,576 (GRCm39) |
D97G |
probably benign |
Het |
Cfh |
A |
C |
1: 140,030,137 (GRCm39) |
I912R |
probably damaging |
Het |
Cyp26c1 |
A |
T |
19: 37,675,604 (GRCm39) |
Q156L |
probably benign |
Het |
Dhx57 |
T |
C |
17: 80,574,978 (GRCm39) |
I614V |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,660,826 (GRCm39) |
S896T |
probably damaging |
Het |
Dmtn |
G |
T |
14: 70,853,518 (GRCm39) |
P97Q |
probably damaging |
Het |
Dock6 |
A |
T |
9: 21,713,160 (GRCm39) |
V1931E |
probably damaging |
Het |
Dpep2 |
C |
A |
8: 106,717,227 (GRCm39) |
|
probably null |
Het |
Dsg1c |
T |
A |
18: 20,400,986 (GRCm39) |
L163Q |
probably benign |
Het |
Esyt3 |
A |
G |
9: 99,202,960 (GRCm39) |
|
probably benign |
Het |
Fcgbp |
T |
A |
7: 27,816,783 (GRCm39) |
I2415N |
possibly damaging |
Het |
Fpr-rs6 |
T |
C |
17: 20,403,307 (GRCm39) |
D18G |
probably benign |
Het |
Fras1 |
T |
C |
5: 96,682,725 (GRCm39) |
V74A |
possibly damaging |
Het |
Fut8 |
T |
A |
12: 77,496,987 (GRCm39) |
V399E |
probably benign |
Het |
Galntl5 |
G |
T |
5: 25,391,237 (GRCm39) |
K45N |
probably benign |
Het |
Gbe1 |
A |
G |
16: 70,357,983 (GRCm39) |
Y669C |
possibly damaging |
Het |
Gcnt1 |
T |
C |
19: 17,307,493 (GRCm39) |
I77M |
probably benign |
Het |
Itprid1 |
T |
A |
6: 55,875,075 (GRCm39) |
W342R |
probably damaging |
Het |
Mark2 |
A |
G |
19: 7,255,405 (GRCm39) |
|
probably null |
Het |
Muc2 |
A |
T |
7: 141,300,450 (GRCm39) |
|
probably benign |
Het |
Nacc2 |
C |
T |
2: 25,980,329 (GRCm39) |
V36I |
probably damaging |
Het |
Nphp1 |
T |
C |
2: 127,611,543 (GRCm39) |
I268V |
probably benign |
Het |
Oosp3 |
A |
G |
19: 11,678,332 (GRCm39) |
I5V |
probably benign |
Het |
Or9m1 |
T |
G |
2: 87,733,724 (GRCm39) |
T99P |
possibly damaging |
Het |
Pex7 |
A |
G |
10: 19,769,990 (GRCm39) |
|
probably benign |
Het |
Prr14l |
T |
C |
5: 32,988,440 (GRCm39) |
K352E |
probably benign |
Het |
Rheb |
T |
A |
5: 25,008,709 (GRCm39) |
I170F |
probably benign |
Het |
Rpgrip1 |
A |
G |
14: 52,382,714 (GRCm39) |
|
probably null |
Het |
Rps2 |
T |
A |
17: 24,939,650 (GRCm39) |
L107Q |
probably damaging |
Het |
Rrp1 |
A |
T |
10: 78,240,874 (GRCm39) |
|
probably benign |
Het |
Rtcb |
A |
T |
10: 85,779,806 (GRCm39) |
V288D |
possibly damaging |
Het |
Sec14l3 |
T |
C |
11: 4,020,084 (GRCm39) |
F174L |
probably benign |
Het |
Slc28a1 |
G |
A |
7: 80,775,909 (GRCm39) |
V202M |
probably damaging |
Het |
Slc44a3 |
A |
T |
3: 121,325,366 (GRCm39) |
C32S |
probably damaging |
Het |
Syne1 |
G |
A |
10: 5,359,875 (GRCm39) |
|
probably benign |
Het |
Synrg |
C |
A |
11: 83,892,804 (GRCm39) |
|
probably benign |
Het |
Tmem219 |
A |
T |
7: 126,488,121 (GRCm39) |
F265I |
probably benign |
Het |
Tmem94 |
T |
C |
11: 115,683,765 (GRCm39) |
I726T |
probably damaging |
Het |
Trim37 |
T |
C |
11: 87,087,785 (GRCm39) |
M632T |
probably benign |
Het |
Trpm6 |
A |
T |
19: 18,790,846 (GRCm39) |
Q627L |
probably damaging |
Het |
Uvrag |
A |
G |
7: 98,628,984 (GRCm39) |
V361A |
possibly damaging |
Het |
Yipf3 |
C |
A |
17: 46,562,520 (GRCm39) |
N308K |
possibly damaging |
Het |
Zfp438 |
A |
G |
18: 5,245,427 (GRCm39) |
|
probably benign |
Het |
Zmiz1 |
T |
A |
14: 25,657,166 (GRCm39) |
|
probably benign |
Het |
Zranb3 |
A |
G |
1: 127,888,562 (GRCm39) |
V841A |
probably benign |
Het |
|
Other mutations in Frem3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Frem3
|
APN |
8 |
81,395,439 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01019:Frem3
|
APN |
8 |
81,341,763 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01470:Frem3
|
APN |
8 |
81,340,944 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01609:Frem3
|
APN |
8 |
81,339,333 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01622:Frem3
|
APN |
8 |
81,340,544 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01623:Frem3
|
APN |
8 |
81,340,544 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01751:Frem3
|
APN |
8 |
81,342,372 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02037:Frem3
|
APN |
8 |
81,338,118 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02039:Frem3
|
APN |
8 |
81,339,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02084:Frem3
|
APN |
8 |
81,339,072 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02124:Frem3
|
APN |
8 |
81,339,723 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02140:Frem3
|
APN |
8 |
81,340,736 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03090:Frem3
|
APN |
8 |
81,344,858 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03102:Frem3
|
APN |
8 |
81,339,661 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03116:Frem3
|
APN |
8 |
81,339,435 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03165:Frem3
|
APN |
8 |
81,339,158 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03224:Frem3
|
APN |
8 |
81,340,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03401:Frem3
|
APN |
8 |
81,341,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03403:Frem3
|
APN |
8 |
81,337,719 (GRCm39) |
missense |
probably benign |
0.04 |
FR4340:Frem3
|
UTSW |
8 |
81,341,870 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Frem3
|
UTSW |
8 |
81,341,870 (GRCm39) |
small insertion |
probably benign |
|
IGL02991:Frem3
|
UTSW |
8 |
81,395,511 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03052:Frem3
|
UTSW |
8 |
81,341,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Frem3
|
UTSW |
8 |
81,342,507 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0647:Frem3
|
UTSW |
8 |
81,341,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Frem3
|
UTSW |
8 |
81,340,581 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0766:Frem3
|
UTSW |
8 |
81,341,951 (GRCm39) |
missense |
probably benign |
|
R0834:Frem3
|
UTSW |
8 |
81,413,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R0909:Frem3
|
UTSW |
8 |
81,390,035 (GRCm39) |
missense |
probably benign |
0.45 |
R1033:Frem3
|
UTSW |
8 |
81,421,786 (GRCm39) |
missense |
probably benign |
0.00 |
R1144:Frem3
|
UTSW |
8 |
81,338,513 (GRCm39) |
missense |
probably benign |
0.01 |
R1312:Frem3
|
UTSW |
8 |
81,341,951 (GRCm39) |
missense |
probably benign |
|
R1330:Frem3
|
UTSW |
8 |
81,395,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R1355:Frem3
|
UTSW |
8 |
81,417,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R1390:Frem3
|
UTSW |
8 |
81,417,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R1413:Frem3
|
UTSW |
8 |
81,395,430 (GRCm39) |
missense |
probably benign |
|
R1470:Frem3
|
UTSW |
8 |
81,337,820 (GRCm39) |
missense |
probably benign |
0.05 |
R1470:Frem3
|
UTSW |
8 |
81,337,820 (GRCm39) |
missense |
probably benign |
0.05 |
R1503:Frem3
|
UTSW |
8 |
81,413,647 (GRCm39) |
missense |
probably damaging |
0.99 |
R1538:Frem3
|
UTSW |
8 |
81,339,764 (GRCm39) |
missense |
probably benign |
0.00 |
R1538:Frem3
|
UTSW |
8 |
81,339,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1612:Frem3
|
UTSW |
8 |
81,341,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Frem3
|
UTSW |
8 |
81,339,741 (GRCm39) |
missense |
probably benign |
0.03 |
R1872:Frem3
|
UTSW |
8 |
81,339,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R1879:Frem3
|
UTSW |
8 |
81,338,567 (GRCm39) |
nonsense |
probably null |
|
R1886:Frem3
|
UTSW |
8 |
81,340,514 (GRCm39) |
missense |
probably benign |
0.00 |
R1933:Frem3
|
UTSW |
8 |
81,339,519 (GRCm39) |
missense |
probably benign |
0.00 |
R2027:Frem3
|
UTSW |
8 |
81,421,966 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2040:Frem3
|
UTSW |
8 |
81,342,455 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2050:Frem3
|
UTSW |
8 |
81,341,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R2079:Frem3
|
UTSW |
8 |
81,341,732 (GRCm39) |
missense |
probably benign |
0.03 |
R2099:Frem3
|
UTSW |
8 |
81,342,488 (GRCm39) |
missense |
probably benign |
0.06 |
R2120:Frem3
|
UTSW |
8 |
81,342,086 (GRCm39) |
missense |
probably benign |
0.20 |
R2842:Frem3
|
UTSW |
8 |
81,395,978 (GRCm39) |
splice site |
probably null |
|
R2845:Frem3
|
UTSW |
8 |
81,339,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R3015:Frem3
|
UTSW |
8 |
81,417,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R3442:Frem3
|
UTSW |
8 |
81,339,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R3724:Frem3
|
UTSW |
8 |
81,341,900 (GRCm39) |
missense |
probably benign |
0.06 |
R3730:Frem3
|
UTSW |
8 |
81,342,545 (GRCm39) |
missense |
probably damaging |
0.99 |
R3939:Frem3
|
UTSW |
8 |
81,341,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3940:Frem3
|
UTSW |
8 |
81,341,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3941:Frem3
|
UTSW |
8 |
81,341,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4089:Frem3
|
UTSW |
8 |
81,341,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R4282:Frem3
|
UTSW |
8 |
81,340,770 (GRCm39) |
missense |
probably benign |
0.00 |
R4437:Frem3
|
UTSW |
8 |
81,339,236 (GRCm39) |
missense |
probably benign |
0.30 |
R4480:Frem3
|
UTSW |
8 |
81,337,986 (GRCm39) |
missense |
probably benign |
0.10 |
R4575:Frem3
|
UTSW |
8 |
81,342,704 (GRCm39) |
missense |
probably benign |
0.17 |
R4583:Frem3
|
UTSW |
8 |
81,340,143 (GRCm39) |
missense |
probably benign |
0.03 |
R4620:Frem3
|
UTSW |
8 |
81,395,586 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4621:Frem3
|
UTSW |
8 |
81,395,820 (GRCm39) |
splice site |
probably null |
|
R4644:Frem3
|
UTSW |
8 |
81,340,356 (GRCm39) |
missense |
probably benign |
0.33 |
R4667:Frem3
|
UTSW |
8 |
81,390,049 (GRCm39) |
missense |
probably damaging |
0.97 |
R4748:Frem3
|
UTSW |
8 |
81,338,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Frem3
|
UTSW |
8 |
81,340,587 (GRCm39) |
missense |
probably benign |
0.25 |
R4836:Frem3
|
UTSW |
8 |
81,390,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R4867:Frem3
|
UTSW |
8 |
81,339,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Frem3
|
UTSW |
8 |
81,339,765 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5030:Frem3
|
UTSW |
8 |
81,339,876 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5035:Frem3
|
UTSW |
8 |
81,342,543 (GRCm39) |
missense |
probably damaging |
0.97 |
R5172:Frem3
|
UTSW |
8 |
81,339,195 (GRCm39) |
missense |
probably benign |
0.44 |
R5289:Frem3
|
UTSW |
8 |
81,338,948 (GRCm39) |
missense |
probably benign |
0.00 |
R5492:Frem3
|
UTSW |
8 |
81,339,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Frem3
|
UTSW |
8 |
81,339,323 (GRCm39) |
missense |
probably benign |
0.00 |
R5685:Frem3
|
UTSW |
8 |
81,421,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R5723:Frem3
|
UTSW |
8 |
81,340,026 (GRCm39) |
missense |
probably benign |
0.02 |
R5743:Frem3
|
UTSW |
8 |
81,342,407 (GRCm39) |
missense |
probably damaging |
0.98 |
R5889:Frem3
|
UTSW |
8 |
81,340,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Frem3
|
UTSW |
8 |
81,340,062 (GRCm39) |
missense |
probably benign |
0.03 |
R6057:Frem3
|
UTSW |
8 |
81,342,216 (GRCm39) |
missense |
probably damaging |
0.99 |
R6137:Frem3
|
UTSW |
8 |
81,341,676 (GRCm39) |
missense |
probably benign |
|
R6264:Frem3
|
UTSW |
8 |
81,341,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R6339:Frem3
|
UTSW |
8 |
81,339,644 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6418:Frem3
|
UTSW |
8 |
81,337,781 (GRCm39) |
missense |
probably benign |
0.08 |
R6680:Frem3
|
UTSW |
8 |
81,395,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6773:Frem3
|
UTSW |
8 |
81,338,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R6838:Frem3
|
UTSW |
8 |
81,338,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R6928:Frem3
|
UTSW |
8 |
81,337,911 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6939:Frem3
|
UTSW |
8 |
81,341,774 (GRCm39) |
missense |
probably benign |
0.23 |
R6995:Frem3
|
UTSW |
8 |
81,339,208 (GRCm39) |
missense |
probably damaging |
0.98 |
R7112:Frem3
|
UTSW |
8 |
81,338,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7155:Frem3
|
UTSW |
8 |
81,342,668 (GRCm39) |
missense |
probably benign |
0.01 |
R7235:Frem3
|
UTSW |
8 |
81,417,354 (GRCm39) |
missense |
probably benign |
0.00 |
R7282:Frem3
|
UTSW |
8 |
81,338,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7403:Frem3
|
UTSW |
8 |
81,342,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Frem3
|
UTSW |
8 |
81,342,392 (GRCm39) |
missense |
probably benign |
0.00 |
R7485:Frem3
|
UTSW |
8 |
81,339,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Frem3
|
UTSW |
8 |
81,338,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R7858:Frem3
|
UTSW |
8 |
81,338,350 (GRCm39) |
nonsense |
probably null |
|
R7976:Frem3
|
UTSW |
8 |
81,338,231 (GRCm39) |
nonsense |
probably null |
|
R8171:Frem3
|
UTSW |
8 |
81,341,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8185:Frem3
|
UTSW |
8 |
81,338,933 (GRCm39) |
nonsense |
probably null |
|
R8306:Frem3
|
UTSW |
8 |
81,338,840 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8478:Frem3
|
UTSW |
8 |
81,338,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8518:Frem3
|
UTSW |
8 |
81,339,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:Frem3
|
UTSW |
8 |
81,342,851 (GRCm39) |
missense |
probably benign |
0.02 |
R8794:Frem3
|
UTSW |
8 |
81,338,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R8806:Frem3
|
UTSW |
8 |
81,390,064 (GRCm39) |
missense |
probably benign |
0.30 |
R8833:Frem3
|
UTSW |
8 |
81,339,401 (GRCm39) |
missense |
probably benign |
0.29 |
R8879:Frem3
|
UTSW |
8 |
81,339,777 (GRCm39) |
missense |
probably damaging |
0.98 |
R8897:Frem3
|
UTSW |
8 |
81,339,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R8983:Frem3
|
UTSW |
8 |
81,395,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R9207:Frem3
|
UTSW |
8 |
81,340,071 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9277:Frem3
|
UTSW |
8 |
81,417,402 (GRCm39) |
missense |
probably damaging |
0.96 |
R9536:Frem3
|
UTSW |
8 |
81,342,048 (GRCm39) |
missense |
probably benign |
0.00 |
R9596:Frem3
|
UTSW |
8 |
81,341,951 (GRCm39) |
missense |
probably benign |
|
R9649:Frem3
|
UTSW |
8 |
81,341,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R9671:Frem3
|
UTSW |
8 |
81,339,134 (GRCm39) |
missense |
probably benign |
0.00 |
R9723:Frem3
|
UTSW |
8 |
81,341,352 (GRCm39) |
missense |
probably benign |
|
R9790:Frem3
|
UTSW |
8 |
81,339,890 (GRCm39) |
missense |
probably benign |
0.01 |
R9791:Frem3
|
UTSW |
8 |
81,339,890 (GRCm39) |
missense |
probably benign |
0.01 |
RF030:Frem3
|
UTSW |
8 |
81,341,867 (GRCm39) |
small insertion |
probably benign |
|
RF034:Frem3
|
UTSW |
8 |
81,341,867 (GRCm39) |
small insertion |
probably benign |
|
RF042:Frem3
|
UTSW |
8 |
81,341,867 (GRCm39) |
small insertion |
probably benign |
|
X0024:Frem3
|
UTSW |
8 |
81,339,710 (GRCm39) |
missense |
possibly damaging |
0.76 |
X0027:Frem3
|
UTSW |
8 |
81,339,017 (GRCm39) |
nonsense |
probably null |
|
Z1088:Frem3
|
UTSW |
8 |
81,342,055 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:Frem3
|
UTSW |
8 |
81,342,060 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Frem3
|
UTSW |
8 |
81,338,132 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Frem3
|
UTSW |
8 |
81,342,758 (GRCm39) |
missense |
possibly damaging |
0.81 |
|