Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
A |
5: 8,863,581 (GRCm39) |
S179T |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,988,223 (GRCm39) |
E3169G |
possibly damaging |
Het |
Ccdc82 |
G |
A |
9: 13,251,704 (GRCm39) |
|
probably benign |
Het |
Ccng1 |
A |
G |
11: 40,644,660 (GRCm39) |
L79P |
probably damaging |
Het |
Cd2ap |
G |
A |
17: 43,127,463 (GRCm39) |
Q377* |
probably null |
Het |
Celf1 |
A |
G |
2: 90,843,086 (GRCm39) |
E411G |
probably damaging |
Het |
Cemip2 |
A |
G |
19: 21,829,598 (GRCm39) |
T1236A |
probably benign |
Het |
Cps1 |
A |
G |
1: 67,207,437 (GRCm39) |
Y582C |
probably damaging |
Het |
Efhb |
A |
G |
17: 53,769,808 (GRCm39) |
L167S |
possibly damaging |
Het |
Erc2 |
A |
G |
14: 28,197,599 (GRCm39) |
|
probably benign |
Het |
Hs3st1 |
G |
A |
5: 39,772,256 (GRCm39) |
T129I |
probably damaging |
Het |
Irs4 |
T |
C |
X: 140,507,059 (GRCm39) |
E379G |
probably damaging |
Het |
Kcnmb2 |
T |
C |
3: 32,252,450 (GRCm39) |
V217A |
probably damaging |
Het |
Mib1 |
T |
A |
18: 10,798,409 (GRCm39) |
C757S |
possibly damaging |
Het |
Mtmr4 |
G |
A |
11: 87,488,088 (GRCm39) |
V24M |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,971,795 (GRCm39) |
|
probably benign |
Het |
Or12d13 |
A |
T |
17: 37,648,117 (GRCm39) |
L2* |
probably null |
Het |
Or5b119 |
T |
A |
19: 13,457,494 (GRCm39) |
I23F |
possibly damaging |
Het |
Pirb |
T |
C |
7: 3,720,662 (GRCm39) |
K279E |
possibly damaging |
Het |
Pmp22 |
T |
C |
11: 63,025,301 (GRCm39) |
S45P |
probably benign |
Het |
Pth2r |
A |
T |
1: 65,361,206 (GRCm39) |
I52F |
probably damaging |
Het |
Reck |
A |
G |
4: 43,930,261 (GRCm39) |
T612A |
probably benign |
Het |
Rtn4rl2 |
A |
G |
2: 84,710,730 (GRCm39) |
|
probably null |
Het |
Sis |
A |
G |
3: 72,835,985 (GRCm39) |
I868T |
probably damaging |
Het |
Slc23a3 |
A |
G |
1: 75,106,040 (GRCm39) |
|
probably null |
Het |
Slc4a1 |
A |
T |
11: 102,247,947 (GRCm39) |
V349E |
probably benign |
Het |
Thsd7a |
C |
T |
6: 12,555,225 (GRCm39) |
G220S |
probably benign |
Het |
Tle4 |
G |
A |
19: 14,445,577 (GRCm39) |
T223I |
probably benign |
Het |
Tor3a |
T |
A |
1: 156,497,124 (GRCm39) |
L140F |
probably damaging |
Het |
Vcf2 |
T |
C |
X: 149,203,357 (GRCm39) |
Q39R |
probably benign |
Het |
Vmn2r86 |
A |
G |
10: 130,291,594 (GRCm39) |
M57T |
probably benign |
Het |
Zfp512 |
G |
T |
5: 31,630,184 (GRCm39) |
R222L |
probably damaging |
Het |
|
Other mutations in Megf10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00425:Megf10
|
APN |
18 |
57,373,700 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00736:Megf10
|
APN |
18 |
57,425,782 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01631:Megf10
|
APN |
18 |
57,392,869 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02488:Megf10
|
APN |
18 |
57,425,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02747:Megf10
|
APN |
18 |
57,423,565 (GRCm39) |
missense |
probably benign |
0.43 |
IGL03298:Megf10
|
APN |
18 |
57,416,910 (GRCm39) |
nonsense |
probably null |
|
deep
|
UTSW |
18 |
57,395,203 (GRCm39) |
missense |
probably damaging |
1.00 |
megalodon
|
UTSW |
18 |
57,421,048 (GRCm39) |
nonsense |
probably null |
|
sharkie
|
UTSW |
18 |
57,324,257 (GRCm39) |
nonsense |
probably null |
|
IGL03046:Megf10
|
UTSW |
18 |
57,421,055 (GRCm39) |
missense |
possibly damaging |
0.95 |
PIT4696001:Megf10
|
UTSW |
18 |
57,410,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R0020:Megf10
|
UTSW |
18 |
57,420,965 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0020:Megf10
|
UTSW |
18 |
57,420,965 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0115:Megf10
|
UTSW |
18 |
57,392,874 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0455:Megf10
|
UTSW |
18 |
57,386,054 (GRCm39) |
missense |
probably benign |
0.34 |
R0602:Megf10
|
UTSW |
18 |
57,395,172 (GRCm39) |
missense |
probably damaging |
0.98 |
R0630:Megf10
|
UTSW |
18 |
57,421,067 (GRCm39) |
missense |
probably benign |
0.14 |
R0652:Megf10
|
UTSW |
18 |
57,410,796 (GRCm39) |
missense |
probably benign |
0.00 |
R0658:Megf10
|
UTSW |
18 |
57,385,968 (GRCm39) |
missense |
probably benign |
0.00 |
R0761:Megf10
|
UTSW |
18 |
57,421,048 (GRCm39) |
nonsense |
probably null |
|
R1013:Megf10
|
UTSW |
18 |
57,394,291 (GRCm39) |
missense |
probably benign |
0.00 |
R1130:Megf10
|
UTSW |
18 |
57,395,078 (GRCm39) |
missense |
probably benign |
0.06 |
R1451:Megf10
|
UTSW |
18 |
57,385,931 (GRCm39) |
missense |
probably damaging |
0.97 |
R1699:Megf10
|
UTSW |
18 |
57,410,802 (GRCm39) |
splice site |
probably null |
|
R1729:Megf10
|
UTSW |
18 |
57,373,864 (GRCm39) |
critical splice donor site |
probably null |
|
R1784:Megf10
|
UTSW |
18 |
57,373,864 (GRCm39) |
critical splice donor site |
probably null |
|
R1870:Megf10
|
UTSW |
18 |
57,324,257 (GRCm39) |
nonsense |
probably null |
|
R1961:Megf10
|
UTSW |
18 |
57,345,426 (GRCm39) |
missense |
probably damaging |
0.97 |
R2094:Megf10
|
UTSW |
18 |
57,414,785 (GRCm39) |
nonsense |
probably null |
|
R2213:Megf10
|
UTSW |
18 |
57,421,081 (GRCm39) |
nonsense |
probably null |
|
R2853:Megf10
|
UTSW |
18 |
57,427,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R3772:Megf10
|
UTSW |
18 |
57,416,934 (GRCm39) |
missense |
probably benign |
0.39 |
R3774:Megf10
|
UTSW |
18 |
57,410,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R3775:Megf10
|
UTSW |
18 |
57,410,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R3776:Megf10
|
UTSW |
18 |
57,410,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R3911:Megf10
|
UTSW |
18 |
57,422,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R3966:Megf10
|
UTSW |
18 |
57,313,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R4043:Megf10
|
UTSW |
18 |
57,392,870 (GRCm39) |
missense |
probably damaging |
0.98 |
R4131:Megf10
|
UTSW |
18 |
57,313,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R4598:Megf10
|
UTSW |
18 |
57,322,675 (GRCm39) |
critical splice donor site |
probably null |
|
R4598:Megf10
|
UTSW |
18 |
57,420,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R4726:Megf10
|
UTSW |
18 |
57,420,864 (GRCm39) |
missense |
probably benign |
0.32 |
R4765:Megf10
|
UTSW |
18 |
57,420,866 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4874:Megf10
|
UTSW |
18 |
57,426,930 (GRCm39) |
missense |
probably benign |
0.00 |
R4928:Megf10
|
UTSW |
18 |
57,373,745 (GRCm39) |
missense |
probably benign |
|
R5412:Megf10
|
UTSW |
18 |
57,324,219 (GRCm39) |
missense |
probably damaging |
0.99 |
R5901:Megf10
|
UTSW |
18 |
57,410,180 (GRCm39) |
missense |
probably benign |
0.11 |
R6015:Megf10
|
UTSW |
18 |
57,386,100 (GRCm39) |
missense |
probably benign |
0.01 |
R6036:Megf10
|
UTSW |
18 |
57,375,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R6036:Megf10
|
UTSW |
18 |
57,375,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R6041:Megf10
|
UTSW |
18 |
57,313,621 (GRCm39) |
missense |
probably benign |
|
R6369:Megf10
|
UTSW |
18 |
57,394,259 (GRCm39) |
missense |
probably benign |
0.06 |
R6479:Megf10
|
UTSW |
18 |
57,379,642 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6489:Megf10
|
UTSW |
18 |
57,424,879 (GRCm39) |
missense |
probably benign |
0.01 |
R7228:Megf10
|
UTSW |
18 |
57,322,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R7296:Megf10
|
UTSW |
18 |
57,408,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R7437:Megf10
|
UTSW |
18 |
57,395,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R7461:Megf10
|
UTSW |
18 |
57,385,925 (GRCm39) |
missense |
probably damaging |
0.98 |
R7488:Megf10
|
UTSW |
18 |
57,324,187 (GRCm39) |
missense |
probably damaging |
0.99 |
R7492:Megf10
|
UTSW |
18 |
57,424,866 (GRCm39) |
missense |
probably benign |
0.00 |
R7542:Megf10
|
UTSW |
18 |
57,322,642 (GRCm39) |
missense |
probably benign |
0.07 |
R7636:Megf10
|
UTSW |
18 |
57,410,061 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7646:Megf10
|
UTSW |
18 |
57,427,071 (GRCm39) |
unclassified |
probably benign |
|
R7650:Megf10
|
UTSW |
18 |
57,427,071 (GRCm39) |
unclassified |
probably benign |
|
R7713:Megf10
|
UTSW |
18 |
57,427,071 (GRCm39) |
unclassified |
probably benign |
|
R7714:Megf10
|
UTSW |
18 |
57,427,071 (GRCm39) |
unclassified |
probably benign |
|
R7716:Megf10
|
UTSW |
18 |
57,427,071 (GRCm39) |
unclassified |
probably benign |
|
R7796:Megf10
|
UTSW |
18 |
57,410,731 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7915:Megf10
|
UTSW |
18 |
57,373,807 (GRCm39) |
missense |
probably benign |
0.05 |
R8221:Megf10
|
UTSW |
18 |
57,416,893 (GRCm39) |
missense |
probably benign |
0.00 |
R8527:Megf10
|
UTSW |
18 |
57,425,790 (GRCm39) |
missense |
probably benign |
0.00 |
R8559:Megf10
|
UTSW |
18 |
57,373,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R9117:Megf10
|
UTSW |
18 |
57,392,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9337:Megf10
|
UTSW |
18 |
57,394,252 (GRCm39) |
nonsense |
probably null |
|
R9481:Megf10
|
UTSW |
18 |
57,395,090 (GRCm39) |
missense |
probably benign |
0.38 |
R9644:Megf10
|
UTSW |
18 |
57,375,773 (GRCm39) |
missense |
probably benign |
|
RF003:Megf10
|
UTSW |
18 |
57,427,099 (GRCm39) |
unclassified |
probably benign |
|
Z1176:Megf10
|
UTSW |
18 |
57,410,766 (GRCm39) |
missense |
probably damaging |
0.96 |
|