Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930524J08Rik |
T |
C |
5: 100,127,068 (GRCm39) |
|
probably benign |
Het |
Ahsg |
T |
A |
16: 22,716,913 (GRCm39) |
N158K |
probably benign |
Het |
Arhgef10 |
T |
C |
8: 15,004,774 (GRCm39) |
M430T |
probably benign |
Het |
Becn2 |
C |
T |
1: 175,749,179 (GRCm39) |
T415M |
probably damaging |
Het |
Bmper |
T |
A |
9: 23,384,759 (GRCm39) |
M588K |
probably damaging |
Het |
Btla |
A |
T |
16: 45,070,782 (GRCm39) |
D247V |
probably damaging |
Het |
Cap2 |
T |
A |
13: 46,684,559 (GRCm39) |
|
probably null |
Het |
Col4a4 |
A |
G |
1: 82,463,300 (GRCm39) |
|
probably null |
Het |
Copg1 |
C |
T |
6: 87,889,217 (GRCm39) |
T853M |
probably damaging |
Het |
Ddb2 |
C |
T |
2: 91,042,926 (GRCm39) |
V353M |
probably damaging |
Het |
Dip2b |
A |
G |
15: 100,087,985 (GRCm39) |
D973G |
possibly damaging |
Het |
Dscam |
G |
A |
16: 96,519,364 (GRCm39) |
T791I |
probably benign |
Het |
Dtd2 |
T |
A |
12: 52,046,643 (GRCm39) |
L65F |
probably damaging |
Het |
Fer1l6 |
C |
T |
15: 58,494,331 (GRCm39) |
P1175S |
probably benign |
Het |
Fzd6 |
A |
T |
15: 38,894,510 (GRCm39) |
R225S |
probably benign |
Het |
Glce |
A |
G |
9: 61,967,793 (GRCm39) |
S453P |
probably damaging |
Het |
Gm4787 |
G |
A |
12: 81,424,805 (GRCm39) |
T451I |
probably benign |
Het |
Igkv8-18 |
C |
T |
6: 70,333,133 (GRCm39) |
T25I |
probably benign |
Het |
Ikzf2 |
A |
G |
1: 69,617,059 (GRCm39) |
V96A |
probably benign |
Het |
Ilkap |
T |
C |
1: 91,318,863 (GRCm39) |
T38A |
probably benign |
Het |
Lpin3 |
A |
G |
2: 160,739,250 (GRCm39) |
T353A |
probably benign |
Het |
Mfsd8 |
A |
T |
3: 40,776,484 (GRCm39) |
N389K |
probably benign |
Het |
Mttp |
A |
T |
3: 137,830,874 (GRCm39) |
V65D |
probably damaging |
Het |
Ndufaf4 |
A |
T |
4: 24,898,636 (GRCm39) |
D64V |
probably damaging |
Het |
Nfe2l2 |
T |
C |
2: 75,507,462 (GRCm39) |
T213A |
probably benign |
Het |
Nkain4 |
A |
G |
2: 180,584,995 (GRCm39) |
L73P |
probably damaging |
Het |
Nwd1 |
T |
A |
8: 73,419,745 (GRCm39) |
S977T |
probably damaging |
Het |
Or1l4 |
T |
A |
2: 37,092,006 (GRCm39) |
V251D |
probably benign |
Het |
Or2y1d |
T |
G |
11: 49,322,035 (GRCm39) |
L244R |
probably damaging |
Het |
Or4b12 |
T |
C |
2: 90,096,308 (GRCm39) |
I155M |
probably benign |
Het |
Or5k1 |
G |
A |
16: 58,617,424 (GRCm39) |
P262S |
possibly damaging |
Het |
Pdgfra |
T |
C |
5: 75,334,156 (GRCm39) |
S410P |
probably benign |
Het |
Phldb1 |
T |
C |
9: 44,627,078 (GRCm39) |
M456V |
probably damaging |
Het |
Pi16 |
C |
T |
17: 29,545,870 (GRCm39) |
T216I |
probably damaging |
Het |
Plekha2 |
C |
A |
8: 25,549,254 (GRCm39) |
A177S |
probably benign |
Het |
Pramel29 |
A |
G |
4: 143,936,192 (GRCm39) |
S23P |
probably benign |
Het |
Prss16 |
C |
T |
13: 22,187,221 (GRCm39) |
V450I |
possibly damaging |
Het |
Rab3gap2 |
T |
A |
1: 185,009,402 (GRCm39) |
L1086H |
probably damaging |
Het |
Rab3gap2 |
C |
T |
1: 184,954,096 (GRCm39) |
P56L |
probably benign |
Het |
Rgs21 |
A |
G |
1: 144,412,680 (GRCm39) |
V48A |
probably benign |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,325,512 (GRCm39) |
|
probably null |
Het |
Slc4a2 |
G |
T |
5: 24,639,836 (GRCm39) |
V506L |
probably damaging |
Het |
Sptbn5 |
C |
G |
2: 119,916,048 (GRCm39) |
|
probably benign |
Het |
Steap2 |
C |
T |
5: 5,723,681 (GRCm39) |
V400I |
probably benign |
Het |
Syne2 |
G |
A |
12: 75,997,733 (GRCm39) |
G2236D |
probably benign |
Het |
Tespa1 |
T |
C |
10: 130,190,624 (GRCm39) |
S84P |
probably damaging |
Het |
Tlx2 |
G |
A |
6: 83,046,807 (GRCm39) |
A85V |
possibly damaging |
Het |
Tm4sf1 |
A |
T |
3: 57,200,508 (GRCm39) |
F65I |
probably benign |
Het |
Tmprss13 |
A |
G |
9: 45,256,253 (GRCm39) |
I456V |
probably damaging |
Het |
Tpte |
C |
T |
8: 22,817,764 (GRCm39) |
S250F |
probably damaging |
Het |
Trim24 |
T |
C |
6: 37,942,536 (GRCm39) |
F946S |
probably benign |
Het |
Vmn2r10 |
A |
T |
5: 109,146,910 (GRCm39) |
Y459* |
probably null |
Het |
Vps54 |
T |
A |
11: 21,214,864 (GRCm39) |
I112N |
probably damaging |
Het |
Vwa1 |
A |
G |
4: 155,858,922 (GRCm39) |
L13P |
probably damaging |
Het |
Zfp648 |
C |
A |
1: 154,079,963 (GRCm39) |
Q41K |
probably benign |
Het |
|
Other mutations in Chd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00232:Chd2
|
APN |
7 |
73,118,325 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00535:Chd2
|
APN |
7 |
73,190,576 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00961:Chd2
|
APN |
7 |
73,093,997 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01092:Chd2
|
APN |
7 |
73,091,434 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02035:Chd2
|
APN |
7 |
73,091,375 (GRCm39) |
splice site |
probably null |
|
IGL02083:Chd2
|
APN |
7 |
73,130,816 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02205:Chd2
|
APN |
7 |
73,091,465 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02243:Chd2
|
APN |
7 |
73,147,456 (GRCm39) |
splice site |
probably null |
|
IGL02385:Chd2
|
APN |
7 |
73,085,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02552:Chd2
|
APN |
7 |
73,097,068 (GRCm39) |
unclassified |
probably benign |
|
IGL02590:Chd2
|
APN |
7 |
73,102,948 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02684:Chd2
|
APN |
7 |
73,125,097 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02731:Chd2
|
APN |
7 |
73,143,204 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03272:Chd2
|
APN |
7 |
73,102,914 (GRCm39) |
missense |
possibly damaging |
0.94 |
1mM(1):Chd2
|
UTSW |
7 |
73,151,852 (GRCm39) |
missense |
possibly damaging |
0.65 |
A4554:Chd2
|
UTSW |
7 |
73,130,716 (GRCm39) |
missense |
probably benign |
|
F6893:Chd2
|
UTSW |
7 |
73,157,620 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0012:Chd2
|
UTSW |
7 |
73,105,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Chd2
|
UTSW |
7 |
73,105,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Chd2
|
UTSW |
7 |
73,134,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R0763:Chd2
|
UTSW |
7 |
73,097,022 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0973:Chd2
|
UTSW |
7 |
73,128,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Chd2
|
UTSW |
7 |
73,128,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0974:Chd2
|
UTSW |
7 |
73,128,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R1223:Chd2
|
UTSW |
7 |
73,134,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R1435:Chd2
|
UTSW |
7 |
73,102,884 (GRCm39) |
missense |
probably damaging |
0.99 |
R1527:Chd2
|
UTSW |
7 |
73,140,362 (GRCm39) |
nonsense |
probably null |
|
R1599:Chd2
|
UTSW |
7 |
73,122,799 (GRCm39) |
missense |
probably benign |
0.05 |
R1657:Chd2
|
UTSW |
7 |
73,130,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R1932:Chd2
|
UTSW |
7 |
73,104,193 (GRCm39) |
missense |
probably damaging |
0.99 |
R2110:Chd2
|
UTSW |
7 |
73,079,735 (GRCm39) |
missense |
probably benign |
0.00 |
R2202:Chd2
|
UTSW |
7 |
73,128,416 (GRCm39) |
missense |
probably benign |
0.00 |
R2383:Chd2
|
UTSW |
7 |
73,153,168 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2393:Chd2
|
UTSW |
7 |
73,157,631 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3699:Chd2
|
UTSW |
7 |
73,118,238 (GRCm39) |
missense |
probably benign |
0.35 |
R3713:Chd2
|
UTSW |
7 |
73,121,538 (GRCm39) |
unclassified |
probably benign |
|
R3788:Chd2
|
UTSW |
7 |
73,096,878 (GRCm39) |
unclassified |
probably benign |
|
R3826:Chd2
|
UTSW |
7 |
73,141,163 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3828:Chd2
|
UTSW |
7 |
73,141,163 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3830:Chd2
|
UTSW |
7 |
73,141,163 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3966:Chd2
|
UTSW |
7 |
73,114,143 (GRCm39) |
splice site |
probably benign |
|
R4093:Chd2
|
UTSW |
7 |
73,150,764 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4431:Chd2
|
UTSW |
7 |
73,085,709 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4461:Chd2
|
UTSW |
7 |
73,190,622 (GRCm39) |
intron |
probably benign |
|
R4782:Chd2
|
UTSW |
7 |
73,134,184 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4791:Chd2
|
UTSW |
7 |
73,118,325 (GRCm39) |
missense |
probably benign |
0.13 |
R4792:Chd2
|
UTSW |
7 |
73,118,325 (GRCm39) |
missense |
probably benign |
0.13 |
R4799:Chd2
|
UTSW |
7 |
73,134,184 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4832:Chd2
|
UTSW |
7 |
73,151,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Chd2
|
UTSW |
7 |
73,130,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R5071:Chd2
|
UTSW |
7 |
73,079,437 (GRCm39) |
missense |
probably benign |
0.03 |
R5328:Chd2
|
UTSW |
7 |
73,113,429 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5444:Chd2
|
UTSW |
7 |
73,122,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R5643:Chd2
|
UTSW |
7 |
73,134,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R5666:Chd2
|
UTSW |
7 |
73,091,465 (GRCm39) |
missense |
probably benign |
0.01 |
R5706:Chd2
|
UTSW |
7 |
73,141,105 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5825:Chd2
|
UTSW |
7 |
73,134,350 (GRCm39) |
splice site |
probably null |
|
R5834:Chd2
|
UTSW |
7 |
73,128,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R5920:Chd2
|
UTSW |
7 |
73,187,060 (GRCm39) |
missense |
probably damaging |
0.97 |
R6051:Chd2
|
UTSW |
7 |
73,085,590 (GRCm39) |
missense |
probably benign |
0.00 |
R6179:Chd2
|
UTSW |
7 |
73,094,071 (GRCm39) |
missense |
probably damaging |
0.98 |
R6229:Chd2
|
UTSW |
7 |
73,101,471 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6267:Chd2
|
UTSW |
7 |
73,113,419 (GRCm39) |
missense |
probably damaging |
0.99 |
R6310:Chd2
|
UTSW |
7 |
73,102,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R6439:Chd2
|
UTSW |
7 |
73,130,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6444:Chd2
|
UTSW |
7 |
73,150,785 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6529:Chd2
|
UTSW |
7 |
73,153,191 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6611:Chd2
|
UTSW |
7 |
73,143,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R6661:Chd2
|
UTSW |
7 |
73,140,230 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6782:Chd2
|
UTSW |
7 |
73,125,127 (GRCm39) |
nonsense |
probably null |
|
R6860:Chd2
|
UTSW |
7 |
73,147,558 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6955:Chd2
|
UTSW |
7 |
73,125,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6984:Chd2
|
UTSW |
7 |
73,134,159 (GRCm39) |
nonsense |
probably null |
|
R7095:Chd2
|
UTSW |
7 |
73,121,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Chd2
|
UTSW |
7 |
73,119,418 (GRCm39) |
missense |
probably benign |
0.00 |
R7179:Chd2
|
UTSW |
7 |
73,125,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R7500:Chd2
|
UTSW |
7 |
73,101,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R7615:Chd2
|
UTSW |
7 |
73,091,390 (GRCm39) |
missense |
probably damaging |
0.97 |
R7646:Chd2
|
UTSW |
7 |
73,085,521 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7764:Chd2
|
UTSW |
7 |
73,121,567 (GRCm39) |
missense |
probably null |
1.00 |
R7898:Chd2
|
UTSW |
7 |
73,169,223 (GRCm39) |
critical splice donor site |
probably null |
|
R7935:Chd2
|
UTSW |
7 |
73,149,373 (GRCm39) |
missense |
probably benign |
0.01 |
R8033:Chd2
|
UTSW |
7 |
73,085,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R8070:Chd2
|
UTSW |
7 |
73,101,506 (GRCm39) |
missense |
probably benign |
|
R8071:Chd2
|
UTSW |
7 |
73,187,132 (GRCm39) |
missense |
probably benign |
|
R8188:Chd2
|
UTSW |
7 |
73,079,504 (GRCm39) |
nonsense |
probably null |
|
R8196:Chd2
|
UTSW |
7 |
73,118,285 (GRCm39) |
missense |
probably benign |
0.00 |
R8258:Chd2
|
UTSW |
7 |
73,085,532 (GRCm39) |
missense |
probably benign |
0.11 |
R8259:Chd2
|
UTSW |
7 |
73,085,532 (GRCm39) |
missense |
probably benign |
0.11 |
R8357:Chd2
|
UTSW |
7 |
73,096,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R8457:Chd2
|
UTSW |
7 |
73,096,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R8778:Chd2
|
UTSW |
7 |
73,079,483 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8816:Chd2
|
UTSW |
7 |
73,140,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R8875:Chd2
|
UTSW |
7 |
73,151,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R8935:Chd2
|
UTSW |
7 |
73,153,210 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9005:Chd2
|
UTSW |
7 |
73,134,294 (GRCm39) |
missense |
probably damaging |
0.98 |
R9009:Chd2
|
UTSW |
7 |
73,143,192 (GRCm39) |
missense |
probably benign |
0.39 |
R9009:Chd2
|
UTSW |
7 |
73,140,402 (GRCm39) |
missense |
probably benign |
0.12 |
R9021:Chd2
|
UTSW |
7 |
73,091,393 (GRCm39) |
missense |
probably benign |
0.03 |
R9038:Chd2
|
UTSW |
7 |
73,105,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R9064:Chd2
|
UTSW |
7 |
73,143,279 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9383:Chd2
|
UTSW |
7 |
73,098,918 (GRCm39) |
missense |
probably null |
1.00 |
R9501:Chd2
|
UTSW |
7 |
73,130,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R9501:Chd2
|
UTSW |
7 |
73,091,481 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9550:Chd2
|
UTSW |
7 |
73,119,439 (GRCm39) |
missense |
probably damaging |
0.99 |
R9583:Chd2
|
UTSW |
7 |
73,130,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R9665:Chd2
|
UTSW |
7 |
73,079,555 (GRCm39) |
missense |
probably benign |
0.00 |
RF009:Chd2
|
UTSW |
7 |
73,169,410 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0025:Chd2
|
UTSW |
7 |
73,157,585 (GRCm39) |
missense |
probably benign |
0.11 |
Z1177:Chd2
|
UTSW |
7 |
73,118,334 (GRCm39) |
missense |
possibly damaging |
0.48 |
|