Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210017I01Rik |
A |
G |
3: 92,512,382 (GRCm39) |
I59T |
unknown |
Het |
Aspm |
C |
T |
1: 139,406,389 (GRCm39) |
Q1759* |
probably null |
Het |
Atn1 |
A |
T |
6: 124,724,861 (GRCm39) |
I124K |
unknown |
Het |
Catsper2 |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
2: 121,228,053 (GRCm39) |
|
probably benign |
Het |
Ccdc88c |
C |
T |
12: 100,911,198 (GRCm39) |
V879M |
probably benign |
Het |
Cd300c |
A |
G |
11: 114,850,609 (GRCm39) |
C65R |
possibly damaging |
Het |
Cd69 |
A |
T |
6: 129,247,005 (GRCm39) |
S112T |
possibly damaging |
Het |
Cdh19 |
T |
C |
1: 110,821,137 (GRCm39) |
T534A |
probably benign |
Het |
Cdk5rap2 |
T |
A |
4: 70,210,145 (GRCm39) |
D701V |
probably damaging |
Het |
D130052B06Rik |
A |
G |
11: 33,573,874 (GRCm39) |
H157R |
possibly damaging |
Het |
Dpf1 |
T |
A |
7: 29,011,052 (GRCm39) |
F150L |
probably benign |
Het |
Dsg1c |
T |
C |
18: 20,416,166 (GRCm39) |
L689P |
probably damaging |
Het |
Dstyk |
G |
A |
1: 132,381,861 (GRCm39) |
M538I |
probably benign |
Het |
E4f1 |
T |
A |
17: 24,663,299 (GRCm39) |
I669F |
probably damaging |
Het |
Gm7138 |
T |
C |
10: 77,612,589 (GRCm39) |
T64A |
unknown |
Het |
Gnai2 |
A |
C |
9: 107,492,972 (GRCm39) |
D310E |
|
Het |
Iqca1 |
A |
G |
1: 89,998,272 (GRCm39) |
V567A |
possibly damaging |
Het |
Lamc1 |
A |
G |
1: 153,110,396 (GRCm39) |
V1093A |
possibly damaging |
Het |
Mfap3 |
A |
G |
11: 57,420,582 (GRCm39) |
K188E |
probably damaging |
Het |
N4bp2 |
T |
A |
5: 65,951,888 (GRCm39) |
V431D |
probably damaging |
Het |
Notch4 |
A |
G |
17: 34,795,445 (GRCm39) |
T792A |
probably benign |
Het |
Ntn4 |
A |
G |
10: 93,581,603 (GRCm39) |
H592R |
probably damaging |
Het |
Ofcc1 |
A |
G |
13: 40,362,317 (GRCm39) |
C202R |
probably benign |
Het |
Or10j2 |
T |
C |
1: 173,098,561 (GRCm39) |
I273T |
probably benign |
Het |
Or2a7 |
A |
G |
6: 43,151,435 (GRCm39) |
K172E |
probably benign |
Het |
Or5p55 |
T |
C |
7: 107,567,395 (GRCm39) |
S264P |
probably benign |
Het |
Or5p72 |
A |
G |
7: 108,022,140 (GRCm39) |
M121V |
probably damaging |
Het |
Or8b55 |
A |
G |
9: 38,727,009 (GRCm39) |
D70G |
probably benign |
Het |
Or8g24 |
A |
T |
9: 38,989,906 (GRCm39) |
M45K |
probably damaging |
Het |
Parpbp |
G |
A |
10: 87,960,802 (GRCm39) |
T228I |
probably damaging |
Het |
Pcdhgb8 |
G |
A |
18: 37,896,756 (GRCm39) |
V609M |
probably damaging |
Het |
Pla2g4d |
T |
C |
2: 120,100,830 (GRCm39) |
N543S |
probably damaging |
Het |
Puf60 |
A |
G |
15: 75,944,388 (GRCm39) |
|
probably benign |
Het |
Rbm6 |
A |
T |
9: 107,730,095 (GRCm39) |
D184E |
probably damaging |
Het |
Rnase9 |
A |
C |
14: 51,276,436 (GRCm39) |
S181A |
probably benign |
Het |
Rnpc3 |
T |
A |
3: 113,410,480 (GRCm39) |
R270S |
probably damaging |
Het |
Rundc1 |
T |
C |
11: 101,322,374 (GRCm39) |
|
probably null |
Het |
Ryr1 |
T |
C |
7: 28,751,440 (GRCm39) |
S3715G |
possibly damaging |
Het |
Scn3a |
A |
T |
2: 65,299,386 (GRCm39) |
D1373E |
possibly damaging |
Het |
Serpina3k |
T |
G |
12: 104,306,861 (GRCm39) |
I31S |
probably benign |
Het |
Sipa1l2 |
A |
G |
8: 126,196,599 (GRCm39) |
F712L |
probably damaging |
Het |
Slc22a29 |
A |
G |
19: 8,138,875 (GRCm39) |
V529A |
probably damaging |
Het |
Tdrd3 |
A |
G |
14: 87,696,239 (GRCm39) |
N58S |
probably benign |
Het |
Tmc2 |
C |
T |
2: 130,076,724 (GRCm39) |
T350I |
possibly damaging |
Het |
Tpst2 |
T |
C |
5: 112,455,544 (GRCm39) |
C28R |
probably benign |
Het |
Trbv21 |
A |
T |
6: 41,179,892 (GRCm39) |
K69N |
probably benign |
Het |
Trpm2 |
A |
G |
10: 77,771,710 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,679,334 (GRCm39) |
V10796A |
unknown |
Het |
Ush2a |
A |
G |
1: 188,643,858 (GRCm39) |
T4407A |
possibly damaging |
Het |
Vmn2r95 |
A |
G |
17: 18,672,225 (GRCm39) |
H726R |
probably benign |
Het |
Zfp777 |
A |
G |
6: 48,021,383 (GRCm39) |
S80P |
probably benign |
Het |
|
Other mutations in Iqgap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Iqgap1
|
APN |
7 |
80,409,592 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00984:Iqgap1
|
APN |
7 |
80,376,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01570:Iqgap1
|
APN |
7 |
80,372,809 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01738:Iqgap1
|
APN |
7 |
80,373,648 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02141:Iqgap1
|
APN |
7 |
80,387,869 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02336:Iqgap1
|
APN |
7 |
80,402,041 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02416:Iqgap1
|
APN |
7 |
80,375,786 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02597:Iqgap1
|
APN |
7 |
80,373,633 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02662:Iqgap1
|
APN |
7 |
80,392,827 (GRCm39) |
missense |
probably benign |
|
IGL03157:Iqgap1
|
APN |
7 |
80,401,636 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03189:Iqgap1
|
APN |
7 |
80,363,590 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03216:Iqgap1
|
APN |
7 |
80,392,836 (GRCm39) |
missense |
probably benign |
0.33 |
R0024:Iqgap1
|
UTSW |
7 |
80,401,687 (GRCm39) |
missense |
probably benign |
|
R0126:Iqgap1
|
UTSW |
7 |
80,388,070 (GRCm39) |
missense |
probably benign |
0.00 |
R0144:Iqgap1
|
UTSW |
7 |
80,401,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Iqgap1
|
UTSW |
7 |
80,401,678 (GRCm39) |
missense |
probably benign |
0.01 |
R0376:Iqgap1
|
UTSW |
7 |
80,373,627 (GRCm39) |
missense |
probably benign |
0.01 |
R0650:Iqgap1
|
UTSW |
7 |
80,386,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Iqgap1
|
UTSW |
7 |
80,386,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R0741:Iqgap1
|
UTSW |
7 |
80,370,735 (GRCm39) |
missense |
probably benign |
0.03 |
R0751:Iqgap1
|
UTSW |
7 |
80,375,321 (GRCm39) |
unclassified |
probably benign |
|
R1067:Iqgap1
|
UTSW |
7 |
80,373,576 (GRCm39) |
missense |
probably benign |
0.01 |
R1389:Iqgap1
|
UTSW |
7 |
80,409,504 (GRCm39) |
critical splice donor site |
probably null |
|
R1473:Iqgap1
|
UTSW |
7 |
80,383,759 (GRCm39) |
missense |
probably benign |
0.00 |
R1613:Iqgap1
|
UTSW |
7 |
80,418,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R1842:Iqgap1
|
UTSW |
7 |
80,410,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Iqgap1
|
UTSW |
7 |
80,393,576 (GRCm39) |
missense |
probably benign |
|
R2062:Iqgap1
|
UTSW |
7 |
80,373,727 (GRCm39) |
nonsense |
probably null |
|
R2149:Iqgap1
|
UTSW |
7 |
80,412,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Iqgap1
|
UTSW |
7 |
80,409,651 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2153:Iqgap1
|
UTSW |
7 |
80,401,701 (GRCm39) |
missense |
probably benign |
0.00 |
R3160:Iqgap1
|
UTSW |
7 |
80,402,086 (GRCm39) |
missense |
probably benign |
|
R3162:Iqgap1
|
UTSW |
7 |
80,402,086 (GRCm39) |
missense |
probably benign |
|
R3605:Iqgap1
|
UTSW |
7 |
80,373,537 (GRCm39) |
missense |
probably benign |
0.02 |
R3709:Iqgap1
|
UTSW |
7 |
80,366,835 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3935:Iqgap1
|
UTSW |
7 |
80,393,585 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3979:Iqgap1
|
UTSW |
7 |
80,409,682 (GRCm39) |
missense |
probably damaging |
0.98 |
R4545:Iqgap1
|
UTSW |
7 |
80,412,315 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4787:Iqgap1
|
UTSW |
7 |
80,385,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R4925:Iqgap1
|
UTSW |
7 |
80,415,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Iqgap1
|
UTSW |
7 |
80,373,524 (GRCm39) |
splice site |
probably null |
|
R5037:Iqgap1
|
UTSW |
7 |
80,383,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R5158:Iqgap1
|
UTSW |
7 |
80,392,816 (GRCm39) |
missense |
probably benign |
0.02 |
R5183:Iqgap1
|
UTSW |
7 |
80,372,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R5262:Iqgap1
|
UTSW |
7 |
80,376,490 (GRCm39) |
missense |
probably benign |
0.00 |
R5271:Iqgap1
|
UTSW |
7 |
80,383,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R5289:Iqgap1
|
UTSW |
7 |
80,388,472 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5359:Iqgap1
|
UTSW |
7 |
80,416,707 (GRCm39) |
missense |
probably benign |
0.00 |
R5423:Iqgap1
|
UTSW |
7 |
80,449,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R5843:Iqgap1
|
UTSW |
7 |
80,375,828 (GRCm39) |
missense |
probably benign |
0.03 |
R5849:Iqgap1
|
UTSW |
7 |
80,452,906 (GRCm39) |
missense |
probably benign |
|
R6164:Iqgap1
|
UTSW |
7 |
80,458,854 (GRCm39) |
missense |
unknown |
|
R6315:Iqgap1
|
UTSW |
7 |
80,449,638 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6335:Iqgap1
|
UTSW |
7 |
80,377,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R6488:Iqgap1
|
UTSW |
7 |
80,380,074 (GRCm39) |
missense |
probably benign |
0.00 |
R6723:Iqgap1
|
UTSW |
7 |
80,373,570 (GRCm39) |
missense |
probably benign |
0.01 |
R6800:Iqgap1
|
UTSW |
7 |
80,378,729 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6815:Iqgap1
|
UTSW |
7 |
80,416,632 (GRCm39) |
critical splice donor site |
probably null |
|
R7386:Iqgap1
|
UTSW |
7 |
80,375,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R7387:Iqgap1
|
UTSW |
7 |
80,370,738 (GRCm39) |
missense |
probably benign |
0.03 |
R7410:Iqgap1
|
UTSW |
7 |
80,372,778 (GRCm39) |
nonsense |
probably null |
|
R7429:Iqgap1
|
UTSW |
7 |
80,401,188 (GRCm39) |
missense |
probably benign |
0.00 |
R7452:Iqgap1
|
UTSW |
7 |
80,410,577 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7615:Iqgap1
|
UTSW |
7 |
80,401,094 (GRCm39) |
missense |
probably benign |
|
R7615:Iqgap1
|
UTSW |
7 |
80,379,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R7726:Iqgap1
|
UTSW |
7 |
80,407,204 (GRCm39) |
missense |
probably benign |
0.37 |
R7783:Iqgap1
|
UTSW |
7 |
80,458,807 (GRCm39) |
missense |
probably benign |
0.01 |
R7785:Iqgap1
|
UTSW |
7 |
80,387,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R7862:Iqgap1
|
UTSW |
7 |
80,393,636 (GRCm39) |
missense |
probably benign |
0.04 |
R8270:Iqgap1
|
UTSW |
7 |
80,379,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R8556:Iqgap1
|
UTSW |
7 |
80,375,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R8932:Iqgap1
|
UTSW |
7 |
80,401,141 (GRCm39) |
missense |
probably benign |
|
R9520:Iqgap1
|
UTSW |
7 |
80,393,869 (GRCm39) |
missense |
probably benign |
|
R9533:Iqgap1
|
UTSW |
7 |
80,383,929 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9536:Iqgap1
|
UTSW |
7 |
80,458,840 (GRCm39) |
missense |
|
|
R9730:Iqgap1
|
UTSW |
7 |
80,401,124 (GRCm39) |
missense |
possibly damaging |
0.63 |
RF004:Iqgap1
|
UTSW |
7 |
80,370,623 (GRCm39) |
missense |
probably benign |
|
RF063:Iqgap1
|
UTSW |
7 |
80,373,499 (GRCm39) |
frame shift |
probably null |
|
X0064:Iqgap1
|
UTSW |
7 |
80,370,679 (GRCm39) |
nonsense |
probably null |
|
X0067:Iqgap1
|
UTSW |
7 |
80,416,651 (GRCm39) |
missense |
probably benign |
|
Z1176:Iqgap1
|
UTSW |
7 |
80,418,057 (GRCm39) |
missense |
probably benign |
0.00 |
|