Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931440F15Rik |
A |
G |
11: 29,824,755 |
L234P |
probably damaging |
Het |
9230110C19Rik |
T |
C |
9: 8,042,431 |
Y57C |
probably damaging |
Het |
Abca13 |
T |
C |
11: 9,290,969 |
L944P |
probably damaging |
Het |
Akap13 |
A |
G |
7: 75,723,895 |
S1885G |
probably damaging |
Het |
Aqp3 |
A |
G |
4: 41,093,632 |
Y261H |
probably damaging |
Het |
Arap2 |
A |
T |
5: 62,635,962 |
N1380K |
probably damaging |
Het |
Arntl2 |
T |
A |
6: 146,809,666 |
M56K |
probably benign |
Het |
Barx2 |
T |
C |
9: 31,846,845 |
I266V |
unknown |
Het |
BC034090 |
C |
T |
1: 155,232,521 |
R360H |
probably benign |
Het |
Ccnb2 |
T |
C |
9: 70,418,907 |
K52E |
probably damaging |
Het |
Ccp110 |
G |
A |
7: 118,729,997 |
V868I |
possibly damaging |
Het |
Cyld |
G |
T |
8: 88,707,290 |
V236F |
probably damaging |
Het |
Dst |
T |
C |
1: 34,169,329 |
|
probably benign |
Het |
Ehmt1 |
G |
T |
2: 24,838,818 |
A637E |
possibly damaging |
Het |
Erlin1 |
G |
T |
19: 44,069,319 |
Y22* |
probably null |
Het |
Ezh1 |
A |
T |
11: 101,199,302 |
M539K |
possibly damaging |
Het |
Fam160b1 |
A |
G |
19: 57,381,345 |
E440G |
probably benign |
Het |
Fancc |
A |
T |
13: 63,400,245 |
I80N |
probably damaging |
Het |
Fat1 |
G |
A |
8: 45,050,940 |
S4447N |
probably benign |
Het |
Iqgap1 |
C |
T |
7: 80,759,844 |
V248I |
probably benign |
Het |
Itch |
T |
C |
2: 155,213,023 |
I749T |
probably damaging |
Het |
Kcna10 |
T |
A |
3: 107,195,514 |
M487K |
probably benign |
Het |
Krt83 |
A |
T |
15: 101,488,211 |
L223Q |
probably benign |
Het |
Mtmr2 |
T |
C |
9: 13,785,916 |
I84T |
probably benign |
Het |
Myocd |
G |
A |
11: 65,187,154 |
T477M |
probably damaging |
Het |
Nfic |
A |
T |
10: 81,408,220 |
V240E |
possibly damaging |
Het |
Olfr463 |
A |
G |
11: 87,893,621 |
I101T |
possibly damaging |
Het |
Prkdc |
A |
T |
16: 15,790,466 |
Y3044F |
probably benign |
Het |
Prkg1 |
A |
G |
19: 30,571,622 |
I636T |
probably benign |
Het |
Ptpru |
A |
G |
4: 131,808,235 |
V477A |
probably benign |
Het |
Rab7b |
T |
A |
1: 131,698,591 |
M119K |
possibly damaging |
Het |
Sec61a1 |
T |
C |
6: 88,506,940 |
|
probably benign |
Het |
Sectm1b |
A |
G |
11: 121,055,973 |
V32A |
probably benign |
Het |
Shroom2 |
A |
G |
X: 152,623,223 |
S1034P |
probably benign |
Het |
Sipa1l3 |
A |
T |
7: 29,386,108 |
I688N |
probably damaging |
Het |
Slc24a1 |
T |
C |
9: 64,928,019 |
Y942C |
probably damaging |
Het |
Smg1 |
C |
T |
7: 118,210,794 |
R139K |
possibly damaging |
Het |
Stt3b |
G |
A |
9: 115,251,847 |
T574I |
probably benign |
Het |
Thoc2 |
A |
G |
X: 41,879,891 |
I76T |
possibly damaging |
Het |
Tpm3 |
C |
T |
3: 90,087,717 |
T180M |
probably damaging |
Het |
Uqcrfs1 |
C |
A |
13: 30,540,925 |
V211F |
probably benign |
Het |
Usp47 |
A |
G |
7: 112,074,783 |
S418G |
probably benign |
Het |
Usp5 |
T |
C |
6: 124,829,353 |
T15A |
probably benign |
Het |
Vps13c |
T |
C |
9: 67,860,865 |
L122P |
probably damaging |
Het |
Zfp677 |
A |
T |
17: 21,397,668 |
E329V |
probably benign |
Het |
Zfyve16 |
A |
T |
13: 92,516,538 |
N846K |
possibly damaging |
Het |
Zp1 |
G |
T |
19: 10,918,777 |
P195T |
probably damaging |
Het |
|
Other mutations in Frem3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01019:Frem3
|
APN |
8 |
80,615,134 (GRCm38) |
missense |
probably benign |
0.02 |
IGL01470:Frem3
|
APN |
8 |
80,614,315 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01609:Frem3
|
APN |
8 |
80,612,704 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01622:Frem3
|
APN |
8 |
80,613,915 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01623:Frem3
|
APN |
8 |
80,613,915 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01751:Frem3
|
APN |
8 |
80,615,743 (GRCm38) |
missense |
probably benign |
0.33 |
IGL02037:Frem3
|
APN |
8 |
80,611,489 (GRCm38) |
missense |
probably benign |
0.31 |
IGL02039:Frem3
|
APN |
8 |
80,612,971 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02084:Frem3
|
APN |
8 |
80,612,443 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL02124:Frem3
|
APN |
8 |
80,613,094 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02140:Frem3
|
APN |
8 |
80,614,107 (GRCm38) |
missense |
possibly damaging |
0.84 |
IGL02836:Frem3
|
APN |
8 |
80,614,381 (GRCm38) |
missense |
probably benign |
|
IGL03090:Frem3
|
APN |
8 |
80,618,229 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03102:Frem3
|
APN |
8 |
80,613,032 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL03116:Frem3
|
APN |
8 |
80,612,806 (GRCm38) |
missense |
possibly damaging |
0.84 |
IGL03165:Frem3
|
APN |
8 |
80,612,529 (GRCm38) |
missense |
probably benign |
0.26 |
IGL03224:Frem3
|
APN |
8 |
80,613,463 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03401:Frem3
|
APN |
8 |
80,614,541 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03403:Frem3
|
APN |
8 |
80,611,090 (GRCm38) |
missense |
probably benign |
0.04 |
FR4340:Frem3
|
UTSW |
8 |
80,615,241 (GRCm38) |
small insertion |
probably benign |
|
FR4976:Frem3
|
UTSW |
8 |
80,615,241 (GRCm38) |
small insertion |
probably benign |
|
IGL02991:Frem3
|
UTSW |
8 |
80,668,882 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03052:Frem3
|
UTSW |
8 |
80,614,530 (GRCm38) |
missense |
probably damaging |
1.00 |
R0089:Frem3
|
UTSW |
8 |
80,615,878 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0647:Frem3
|
UTSW |
8 |
80,615,185 (GRCm38) |
missense |
probably damaging |
1.00 |
R0690:Frem3
|
UTSW |
8 |
80,613,952 (GRCm38) |
missense |
possibly damaging |
0.84 |
R0766:Frem3
|
UTSW |
8 |
80,615,322 (GRCm38) |
missense |
probably benign |
|
R0834:Frem3
|
UTSW |
8 |
80,687,008 (GRCm38) |
missense |
probably damaging |
1.00 |
R0909:Frem3
|
UTSW |
8 |
80,663,406 (GRCm38) |
missense |
probably benign |
0.45 |
R1033:Frem3
|
UTSW |
8 |
80,695,157 (GRCm38) |
missense |
probably benign |
0.00 |
R1144:Frem3
|
UTSW |
8 |
80,611,884 (GRCm38) |
missense |
probably benign |
0.01 |
R1312:Frem3
|
UTSW |
8 |
80,615,322 (GRCm38) |
missense |
probably benign |
|
R1330:Frem3
|
UTSW |
8 |
80,668,839 (GRCm38) |
missense |
probably damaging |
0.99 |
R1355:Frem3
|
UTSW |
8 |
80,690,702 (GRCm38) |
missense |
probably damaging |
1.00 |
R1390:Frem3
|
UTSW |
8 |
80,690,773 (GRCm38) |
missense |
probably damaging |
0.99 |
R1413:Frem3
|
UTSW |
8 |
80,668,801 (GRCm38) |
missense |
probably benign |
|
R1470:Frem3
|
UTSW |
8 |
80,611,191 (GRCm38) |
missense |
probably benign |
0.05 |
R1470:Frem3
|
UTSW |
8 |
80,611,191 (GRCm38) |
missense |
probably benign |
0.05 |
R1503:Frem3
|
UTSW |
8 |
80,687,018 (GRCm38) |
missense |
probably damaging |
0.99 |
R1538:Frem3
|
UTSW |
8 |
80,613,135 (GRCm38) |
missense |
probably benign |
0.00 |
R1538:Frem3
|
UTSW |
8 |
80,612,710 (GRCm38) |
missense |
probably damaging |
1.00 |
R1612:Frem3
|
UTSW |
8 |
80,614,861 (GRCm38) |
missense |
probably damaging |
1.00 |
R1793:Frem3
|
UTSW |
8 |
80,613,112 (GRCm38) |
missense |
probably benign |
0.03 |
R1872:Frem3
|
UTSW |
8 |
80,612,576 (GRCm38) |
missense |
probably damaging |
1.00 |
R1879:Frem3
|
UTSW |
8 |
80,611,938 (GRCm38) |
nonsense |
probably null |
|
R1886:Frem3
|
UTSW |
8 |
80,613,885 (GRCm38) |
missense |
probably benign |
0.00 |
R1933:Frem3
|
UTSW |
8 |
80,612,890 (GRCm38) |
missense |
probably benign |
0.00 |
R2027:Frem3
|
UTSW |
8 |
80,695,337 (GRCm38) |
missense |
possibly damaging |
0.75 |
R2040:Frem3
|
UTSW |
8 |
80,615,826 (GRCm38) |
missense |
possibly damaging |
0.92 |
R2050:Frem3
|
UTSW |
8 |
80,614,891 (GRCm38) |
missense |
probably damaging |
1.00 |
R2079:Frem3
|
UTSW |
8 |
80,615,103 (GRCm38) |
missense |
probably benign |
0.03 |
R2099:Frem3
|
UTSW |
8 |
80,615,859 (GRCm38) |
missense |
probably benign |
0.06 |
R2120:Frem3
|
UTSW |
8 |
80,615,457 (GRCm38) |
missense |
probably benign |
0.20 |
R2842:Frem3
|
UTSW |
8 |
80,669,349 (GRCm38) |
splice site |
probably null |
|
R2845:Frem3
|
UTSW |
8 |
80,613,220 (GRCm38) |
missense |
probably damaging |
1.00 |
R3015:Frem3
|
UTSW |
8 |
80,690,773 (GRCm38) |
missense |
probably damaging |
0.99 |
R3442:Frem3
|
UTSW |
8 |
80,613,040 (GRCm38) |
missense |
probably damaging |
1.00 |
R3724:Frem3
|
UTSW |
8 |
80,615,271 (GRCm38) |
missense |
probably benign |
0.06 |
R3730:Frem3
|
UTSW |
8 |
80,615,916 (GRCm38) |
missense |
probably damaging |
0.99 |
R3939:Frem3
|
UTSW |
8 |
80,615,020 (GRCm38) |
missense |
possibly damaging |
0.84 |
R3940:Frem3
|
UTSW |
8 |
80,615,020 (GRCm38) |
missense |
possibly damaging |
0.84 |
R3941:Frem3
|
UTSW |
8 |
80,615,020 (GRCm38) |
missense |
possibly damaging |
0.84 |
R4089:Frem3
|
UTSW |
8 |
80,615,173 (GRCm38) |
missense |
probably damaging |
1.00 |
R4282:Frem3
|
UTSW |
8 |
80,614,141 (GRCm38) |
missense |
probably benign |
0.00 |
R4437:Frem3
|
UTSW |
8 |
80,612,607 (GRCm38) |
missense |
probably benign |
0.30 |
R4480:Frem3
|
UTSW |
8 |
80,611,357 (GRCm38) |
missense |
probably benign |
0.10 |
R4575:Frem3
|
UTSW |
8 |
80,616,075 (GRCm38) |
missense |
probably benign |
0.17 |
R4583:Frem3
|
UTSW |
8 |
80,613,514 (GRCm38) |
missense |
probably benign |
0.03 |
R4620:Frem3
|
UTSW |
8 |
80,668,957 (GRCm38) |
missense |
possibly damaging |
0.82 |
R4621:Frem3
|
UTSW |
8 |
80,669,191 (GRCm38) |
splice site |
probably null |
|
R4644:Frem3
|
UTSW |
8 |
80,613,727 (GRCm38) |
missense |
probably benign |
0.33 |
R4667:Frem3
|
UTSW |
8 |
80,663,420 (GRCm38) |
missense |
probably damaging |
0.97 |
R4748:Frem3
|
UTSW |
8 |
80,611,459 (GRCm38) |
missense |
probably damaging |
1.00 |
R4823:Frem3
|
UTSW |
8 |
80,613,958 (GRCm38) |
missense |
probably benign |
0.25 |
R4836:Frem3
|
UTSW |
8 |
80,663,397 (GRCm38) |
missense |
probably damaging |
0.99 |
R4867:Frem3
|
UTSW |
8 |
80,613,283 (GRCm38) |
missense |
probably damaging |
1.00 |
R4921:Frem3
|
UTSW |
8 |
80,613,136 (GRCm38) |
missense |
possibly damaging |
0.83 |
R5030:Frem3
|
UTSW |
8 |
80,613,247 (GRCm38) |
missense |
possibly damaging |
0.89 |
R5035:Frem3
|
UTSW |
8 |
80,615,914 (GRCm38) |
missense |
probably damaging |
0.97 |
R5172:Frem3
|
UTSW |
8 |
80,612,566 (GRCm38) |
missense |
probably benign |
0.44 |
R5289:Frem3
|
UTSW |
8 |
80,612,319 (GRCm38) |
missense |
probably benign |
0.00 |
R5492:Frem3
|
UTSW |
8 |
80,612,677 (GRCm38) |
missense |
probably damaging |
1.00 |
R5655:Frem3
|
UTSW |
8 |
80,612,694 (GRCm38) |
missense |
probably benign |
0.00 |
R5685:Frem3
|
UTSW |
8 |
80,695,303 (GRCm38) |
missense |
probably damaging |
1.00 |
R5723:Frem3
|
UTSW |
8 |
80,613,397 (GRCm38) |
missense |
probably benign |
0.02 |
R5743:Frem3
|
UTSW |
8 |
80,615,778 (GRCm38) |
missense |
probably damaging |
0.98 |
R5889:Frem3
|
UTSW |
8 |
80,614,288 (GRCm38) |
missense |
probably damaging |
1.00 |
R6048:Frem3
|
UTSW |
8 |
80,613,433 (GRCm38) |
missense |
probably benign |
0.03 |
R6057:Frem3
|
UTSW |
8 |
80,615,587 (GRCm38) |
missense |
probably damaging |
0.99 |
R6137:Frem3
|
UTSW |
8 |
80,615,047 (GRCm38) |
missense |
probably benign |
|
R6264:Frem3
|
UTSW |
8 |
80,615,203 (GRCm38) |
missense |
probably damaging |
1.00 |
R6339:Frem3
|
UTSW |
8 |
80,613,015 (GRCm38) |
missense |
possibly damaging |
0.84 |
R6418:Frem3
|
UTSW |
8 |
80,611,152 (GRCm38) |
missense |
probably benign |
0.08 |
R6680:Frem3
|
UTSW |
8 |
80,669,320 (GRCm38) |
missense |
probably damaging |
1.00 |
R6773:Frem3
|
UTSW |
8 |
80,611,815 (GRCm38) |
missense |
probably damaging |
1.00 |
R6838:Frem3
|
UTSW |
8 |
80,612,031 (GRCm38) |
missense |
probably damaging |
1.00 |
R6928:Frem3
|
UTSW |
8 |
80,611,282 (GRCm38) |
missense |
possibly damaging |
0.48 |
R6939:Frem3
|
UTSW |
8 |
80,615,145 (GRCm38) |
missense |
probably benign |
0.23 |
R6995:Frem3
|
UTSW |
8 |
80,612,579 (GRCm38) |
missense |
probably damaging |
0.98 |
R7112:Frem3
|
UTSW |
8 |
80,612,031 (GRCm38) |
missense |
probably damaging |
1.00 |
R7155:Frem3
|
UTSW |
8 |
80,616,039 (GRCm38) |
missense |
probably benign |
0.01 |
R7235:Frem3
|
UTSW |
8 |
80,690,725 (GRCm38) |
missense |
probably benign |
0.00 |
R7282:Frem3
|
UTSW |
8 |
80,612,031 (GRCm38) |
missense |
probably damaging |
1.00 |
R7403:Frem3
|
UTSW |
8 |
80,616,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R7422:Frem3
|
UTSW |
8 |
80,615,763 (GRCm38) |
missense |
probably benign |
0.00 |
R7485:Frem3
|
UTSW |
8 |
80,613,336 (GRCm38) |
missense |
probably damaging |
1.00 |
R7516:Frem3
|
UTSW |
8 |
80,612,083 (GRCm38) |
missense |
probably damaging |
0.99 |
R7858:Frem3
|
UTSW |
8 |
80,611,721 (GRCm38) |
nonsense |
probably null |
|
R7976:Frem3
|
UTSW |
8 |
80,611,602 (GRCm38) |
nonsense |
probably null |
|
R8171:Frem3
|
UTSW |
8 |
80,615,240 (GRCm38) |
missense |
probably damaging |
1.00 |
R8185:Frem3
|
UTSW |
8 |
80,612,304 (GRCm38) |
nonsense |
probably null |
|
R8306:Frem3
|
UTSW |
8 |
80,612,211 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8478:Frem3
|
UTSW |
8 |
80,611,558 (GRCm38) |
missense |
probably damaging |
1.00 |
R8518:Frem3
|
UTSW |
8 |
80,612,595 (GRCm38) |
missense |
probably damaging |
1.00 |
R8794:Frem3
|
UTSW |
8 |
80,616,222 (GRCm38) |
missense |
probably benign |
0.02 |
R8794:Frem3
|
UTSW |
8 |
80,612,278 (GRCm38) |
missense |
probably damaging |
1.00 |
R8806:Frem3
|
UTSW |
8 |
80,663,435 (GRCm38) |
missense |
probably benign |
0.30 |
R8833:Frem3
|
UTSW |
8 |
80,612,772 (GRCm38) |
missense |
probably benign |
0.29 |
R8879:Frem3
|
UTSW |
8 |
80,613,148 (GRCm38) |
missense |
probably damaging |
0.98 |
R8897:Frem3
|
UTSW |
8 |
80,612,790 (GRCm38) |
missense |
probably damaging |
1.00 |
R8983:Frem3
|
UTSW |
8 |
80,669,246 (GRCm38) |
missense |
probably damaging |
1.00 |
R9207:Frem3
|
UTSW |
8 |
80,613,442 (GRCm38) |
missense |
possibly damaging |
0.73 |
R9277:Frem3
|
UTSW |
8 |
80,690,773 (GRCm38) |
missense |
probably damaging |
0.96 |
R9536:Frem3
|
UTSW |
8 |
80,615,419 (GRCm38) |
missense |
probably benign |
0.00 |
R9596:Frem3
|
UTSW |
8 |
80,615,322 (GRCm38) |
missense |
probably benign |
|
R9649:Frem3
|
UTSW |
8 |
80,614,516 (GRCm38) |
missense |
probably damaging |
1.00 |
R9671:Frem3
|
UTSW |
8 |
80,612,505 (GRCm38) |
missense |
probably benign |
0.00 |
R9723:Frem3
|
UTSW |
8 |
80,614,723 (GRCm38) |
missense |
probably benign |
|
R9790:Frem3
|
UTSW |
8 |
80,613,261 (GRCm38) |
missense |
probably benign |
0.01 |
R9791:Frem3
|
UTSW |
8 |
80,613,261 (GRCm38) |
missense |
probably benign |
0.01 |
RF030:Frem3
|
UTSW |
8 |
80,615,238 (GRCm38) |
small insertion |
probably benign |
|
RF034:Frem3
|
UTSW |
8 |
80,615,238 (GRCm38) |
small insertion |
probably benign |
|
RF042:Frem3
|
UTSW |
8 |
80,615,238 (GRCm38) |
small insertion |
probably benign |
|
X0024:Frem3
|
UTSW |
8 |
80,613,081 (GRCm38) |
missense |
possibly damaging |
0.76 |
X0027:Frem3
|
UTSW |
8 |
80,612,388 (GRCm38) |
nonsense |
probably null |
|
Z1088:Frem3
|
UTSW |
8 |
80,615,426 (GRCm38) |
missense |
probably benign |
0.04 |
Z1176:Frem3
|
UTSW |
8 |
80,615,431 (GRCm38) |
missense |
probably benign |
0.03 |
Z1176:Frem3
|
UTSW |
8 |
80,611,503 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1177:Frem3
|
UTSW |
8 |
80,616,129 (GRCm38) |
missense |
possibly damaging |
0.81 |
|