Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
C |
A |
1: 179,596,626 (GRCm39) |
S1056I |
possibly damaging |
Het |
Ajm1 |
A |
G |
2: 25,468,577 (GRCm39) |
Y445H |
possibly damaging |
Het |
Akap13 |
T |
A |
7: 75,259,606 (GRCm39) |
D743E |
probably benign |
Het |
Alas1 |
T |
A |
9: 106,118,513 (GRCm39) |
H203L |
probably benign |
Het |
Ankfn1 |
G |
A |
11: 89,429,279 (GRCm39) |
T35I |
possibly damaging |
Het |
Ankrd11 |
C |
T |
8: 123,622,718 (GRCm39) |
R378K |
probably damaging |
Het |
Arap1 |
G |
A |
7: 101,057,324 (GRCm39) |
R1355Q |
possibly damaging |
Het |
Cabp7 |
T |
A |
11: 4,696,640 (GRCm39) |
I30F |
possibly damaging |
Het |
Ccdc113 |
T |
C |
8: 96,267,584 (GRCm39) |
|
probably null |
Het |
Cdh1 |
ACTCGAAATGATGTGGCTC |
ACTC |
8: 107,392,870 (GRCm39) |
|
probably benign |
Het |
Cep85 |
G |
T |
4: 133,859,715 (GRCm39) |
H651Q |
probably benign |
Het |
Cfap43 |
T |
A |
19: 47,804,399 (GRCm39) |
I266L |
probably benign |
Het |
Crybg3 |
T |
C |
16: 59,315,123 (GRCm39) |
T1179A |
probably benign |
Het |
Crybg3 |
A |
G |
16: 59,376,715 (GRCm39) |
V1513A |
probably benign |
Het |
Csmd2 |
G |
T |
4: 128,369,582 (GRCm39) |
V1905L |
|
Het |
D630003M21Rik |
T |
C |
2: 158,059,447 (GRCm39) |
E151G |
probably damaging |
Het |
Dnah10 |
A |
T |
5: 124,866,828 (GRCm39) |
Y2306F |
probably damaging |
Het |
Dpy19l4 |
A |
T |
4: 11,304,674 (GRCm39) |
|
probably benign |
Het |
Dsc1 |
G |
T |
18: 20,243,225 (GRCm39) |
T76K |
probably benign |
Het |
Egfem1 |
A |
C |
3: 29,744,561 (GRCm39) |
*591C |
probably null |
Het |
Elapor2 |
T |
A |
5: 9,496,979 (GRCm39) |
H814Q |
possibly damaging |
Het |
Epha8 |
G |
T |
4: 136,665,897 (GRCm39) |
L420M |
probably damaging |
Het |
Fn1 |
T |
C |
1: 71,641,777 (GRCm39) |
|
probably benign |
Het |
Fsd2 |
T |
C |
7: 81,209,354 (GRCm39) |
T163A |
probably benign |
Het |
Gm45844 |
A |
G |
7: 7,281,094 (GRCm39) |
|
probably benign |
Het |
Grid1 |
T |
A |
14: 35,302,723 (GRCm39) |
V996D |
probably benign |
Het |
Hepacam2 |
C |
A |
6: 3,467,623 (GRCm39) |
|
probably null |
Het |
Hira |
A |
G |
16: 18,716,537 (GRCm39) |
T101A |
probably benign |
Het |
Ighv8-9 |
T |
A |
12: 115,432,204 (GRCm39) |
T36S |
possibly damaging |
Het |
Lama5 |
A |
T |
2: 179,843,832 (GRCm39) |
C413S |
probably damaging |
Het |
Lpcat2b |
G |
T |
5: 107,580,913 (GRCm39) |
V81L |
probably benign |
Het |
Map1b |
C |
G |
13: 99,568,624 (GRCm39) |
E1366Q |
unknown |
Het |
Marchf4 |
C |
A |
1: 72,574,035 (GRCm39) |
A88S |
probably benign |
Het |
Mbnl2 |
A |
G |
14: 120,633,974 (GRCm39) |
T324A |
probably benign |
Het |
Mipol1 |
T |
A |
12: 57,507,651 (GRCm39) |
M387K |
probably benign |
Het |
Mtor |
T |
C |
4: 148,623,356 (GRCm39) |
S2069P |
probably damaging |
Het |
Mycbp2 |
T |
A |
14: 103,393,781 (GRCm39) |
T2927S |
probably benign |
Het |
Nfatc1 |
A |
T |
18: 80,741,180 (GRCm39) |
N273K |
possibly damaging |
Het |
Or10p22 |
T |
C |
10: 128,826,317 (GRCm39) |
C179R |
probably damaging |
Het |
Or2i1 |
T |
A |
17: 37,507,861 (GRCm39) |
T258S |
probably damaging |
Het |
Or5k15 |
T |
A |
16: 58,709,750 (GRCm39) |
T278S |
possibly damaging |
Het |
Or5v1 |
A |
T |
17: 37,809,583 (GRCm39) |
I14F |
probably damaging |
Het |
Or7a36 |
A |
G |
10: 78,820,547 (GRCm39) |
K308E |
|
Het |
Or8b49 |
A |
T |
9: 38,505,662 (GRCm39) |
L48F |
probably damaging |
Het |
Parp16 |
A |
G |
9: 65,133,396 (GRCm39) |
D79G |
probably benign |
Het |
Ppp4r3b |
T |
C |
11: 29,144,598 (GRCm39) |
V316A |
probably benign |
Het |
Ptcd2 |
G |
A |
13: 99,476,505 (GRCm39) |
T78I |
probably damaging |
Het |
Rbpjl |
A |
G |
2: 164,250,313 (GRCm39) |
Y155C |
probably damaging |
Het |
Slc5a7 |
G |
T |
17: 54,591,258 (GRCm39) |
Q225K |
possibly damaging |
Het |
Stom |
T |
C |
2: 35,205,937 (GRCm39) |
N264S |
probably damaging |
Het |
Tbc1d2b |
C |
T |
9: 90,108,190 (GRCm39) |
E454K |
probably damaging |
Het |
Tmem209 |
C |
T |
6: 30,489,365 (GRCm39) |
C495Y |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,953,099 (GRCm39) |
D647G |
probably damaging |
Het |
Vmn2r44 |
A |
T |
7: 8,381,101 (GRCm39) |
V264E |
probably damaging |
Het |
Wscd2 |
A |
T |
5: 113,715,401 (GRCm39) |
I414F |
possibly damaging |
Het |
Xkr5 |
A |
G |
8: 18,983,787 (GRCm39) |
V585A |
probably benign |
Het |
Zfp456 |
G |
A |
13: 67,514,603 (GRCm39) |
R368C |
probably benign |
Het |
Zscan18 |
G |
A |
7: 12,509,120 (GRCm39) |
Q127* |
probably null |
Het |
|
Other mutations in Ccdc162 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01013:Ccdc162
|
APN |
10 |
41,457,335 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01366:Ccdc162
|
APN |
10 |
41,456,302 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01924:Ccdc162
|
APN |
10 |
41,445,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02504:Ccdc162
|
APN |
10 |
41,428,384 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02678:Ccdc162
|
APN |
10 |
41,437,151 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02955:Ccdc162
|
APN |
10 |
41,437,123 (GRCm39) |
missense |
probably damaging |
1.00 |
beeswax
|
UTSW |
10 |
41,437,222 (GRCm39) |
missense |
possibly damaging |
0.57 |
honeycomb
|
UTSW |
10 |
41,520,637 (GRCm39) |
missense |
probably benign |
0.35 |
FR4304:Ccdc162
|
UTSW |
10 |
41,432,117 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0432:Ccdc162
|
UTSW |
10 |
41,417,856 (GRCm39) |
missense |
probably benign |
0.01 |
R0585:Ccdc162
|
UTSW |
10 |
41,462,375 (GRCm39) |
missense |
probably benign |
0.03 |
R0645:Ccdc162
|
UTSW |
10 |
41,462,407 (GRCm39) |
splice site |
probably benign |
|
R0731:Ccdc162
|
UTSW |
10 |
41,455,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R1426:Ccdc162
|
UTSW |
10 |
41,429,178 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1447:Ccdc162
|
UTSW |
10 |
41,456,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R1712:Ccdc162
|
UTSW |
10 |
41,415,427 (GRCm39) |
missense |
probably benign |
0.35 |
R2138:Ccdc162
|
UTSW |
10 |
41,457,293 (GRCm39) |
missense |
probably benign |
0.15 |
R2351:Ccdc162
|
UTSW |
10 |
41,431,968 (GRCm39) |
critical splice donor site |
probably null |
|
R2394:Ccdc162
|
UTSW |
10 |
41,445,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R2431:Ccdc162
|
UTSW |
10 |
41,445,841 (GRCm39) |
missense |
probably benign |
|
R2571:Ccdc162
|
UTSW |
10 |
41,428,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R2873:Ccdc162
|
UTSW |
10 |
41,531,095 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2926:Ccdc162
|
UTSW |
10 |
41,437,203 (GRCm39) |
start gained |
probably benign |
|
R2999:Ccdc162
|
UTSW |
10 |
41,456,286 (GRCm39) |
missense |
probably benign |
0.00 |
R3412:Ccdc162
|
UTSW |
10 |
41,415,545 (GRCm39) |
splice site |
probably benign |
|
R3712:Ccdc162
|
UTSW |
10 |
41,463,375 (GRCm39) |
missense |
probably benign |
|
R3736:Ccdc162
|
UTSW |
10 |
41,465,564 (GRCm39) |
splice site |
probably null |
|
R4112:Ccdc162
|
UTSW |
10 |
41,532,324 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4557:Ccdc162
|
UTSW |
10 |
41,463,384 (GRCm39) |
missense |
probably benign |
0.01 |
R4580:Ccdc162
|
UTSW |
10 |
41,437,136 (GRCm39) |
missense |
probably benign |
0.02 |
R4685:Ccdc162
|
UTSW |
10 |
41,557,682 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4837:Ccdc162
|
UTSW |
10 |
41,549,863 (GRCm39) |
missense |
probably benign |
0.00 |
R5155:Ccdc162
|
UTSW |
10 |
41,455,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5155:Ccdc162
|
UTSW |
10 |
41,429,576 (GRCm39) |
splice site |
probably null |
|
R5645:Ccdc162
|
UTSW |
10 |
41,428,352 (GRCm39) |
missense |
probably benign |
0.06 |
R5656:Ccdc162
|
UTSW |
10 |
41,445,930 (GRCm39) |
missense |
probably benign |
0.26 |
R5682:Ccdc162
|
UTSW |
10 |
41,432,799 (GRCm39) |
nonsense |
probably null |
|
R5808:Ccdc162
|
UTSW |
10 |
41,531,500 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5909:Ccdc162
|
UTSW |
10 |
41,437,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Ccdc162
|
UTSW |
10 |
41,437,159 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6057:Ccdc162
|
UTSW |
10 |
41,510,037 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6211:Ccdc162
|
UTSW |
10 |
41,506,141 (GRCm39) |
nonsense |
probably null |
|
R6264:Ccdc162
|
UTSW |
10 |
41,570,464 (GRCm39) |
missense |
probably benign |
0.31 |
R6329:Ccdc162
|
UTSW |
10 |
41,539,147 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6349:Ccdc162
|
UTSW |
10 |
41,570,396 (GRCm39) |
missense |
probably damaging |
0.97 |
R6398:Ccdc162
|
UTSW |
10 |
41,503,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R6453:Ccdc162
|
UTSW |
10 |
41,426,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R6602:Ccdc162
|
UTSW |
10 |
41,491,976 (GRCm39) |
missense |
probably benign |
0.00 |
R6627:Ccdc162
|
UTSW |
10 |
41,539,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6722:Ccdc162
|
UTSW |
10 |
41,520,637 (GRCm39) |
missense |
probably benign |
0.35 |
R6750:Ccdc162
|
UTSW |
10 |
41,437,222 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6968:Ccdc162
|
UTSW |
10 |
41,549,840 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6970:Ccdc162
|
UTSW |
10 |
41,491,954 (GRCm39) |
missense |
probably benign |
0.03 |
R6989:Ccdc162
|
UTSW |
10 |
41,457,349 (GRCm39) |
missense |
probably damaging |
0.99 |
R7008:Ccdc162
|
UTSW |
10 |
41,428,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R7135:Ccdc162
|
UTSW |
10 |
41,549,855 (GRCm39) |
missense |
probably benign |
0.00 |
R7139:Ccdc162
|
UTSW |
10 |
41,542,717 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7224:Ccdc162
|
UTSW |
10 |
41,437,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R7230:Ccdc162
|
UTSW |
10 |
41,554,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R7256:Ccdc162
|
UTSW |
10 |
41,431,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R7261:Ccdc162
|
UTSW |
10 |
41,437,136 (GRCm39) |
missense |
probably benign |
0.02 |
R7390:Ccdc162
|
UTSW |
10 |
41,510,044 (GRCm39) |
missense |
probably benign |
|
R7712:Ccdc162
|
UTSW |
10 |
41,503,223 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7726:Ccdc162
|
UTSW |
10 |
41,429,071 (GRCm39) |
missense |
probably benign |
0.00 |
R7754:Ccdc162
|
UTSW |
10 |
41,463,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R7764:Ccdc162
|
UTSW |
10 |
41,566,109 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8053:Ccdc162
|
UTSW |
10 |
41,520,577 (GRCm39) |
missense |
probably benign |
|
R8088:Ccdc162
|
UTSW |
10 |
41,499,410 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8094:Ccdc162
|
UTSW |
10 |
41,488,864 (GRCm39) |
missense |
probably benign |
0.02 |
R8097:Ccdc162
|
UTSW |
10 |
41,510,115 (GRCm39) |
missense |
probably benign |
0.03 |
R8321:Ccdc162
|
UTSW |
10 |
41,510,029 (GRCm39) |
missense |
probably damaging |
0.98 |
R8377:Ccdc162
|
UTSW |
10 |
41,457,306 (GRCm39) |
missense |
probably benign |
0.08 |
R8399:Ccdc162
|
UTSW |
10 |
41,415,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R8669:Ccdc162
|
UTSW |
10 |
41,428,352 (GRCm39) |
missense |
probably benign |
0.06 |
R8772:Ccdc162
|
UTSW |
10 |
41,506,033 (GRCm39) |
missense |
probably damaging |
0.99 |
R8810:Ccdc162
|
UTSW |
10 |
41,542,737 (GRCm39) |
missense |
probably benign |
0.41 |
R8903:Ccdc162
|
UTSW |
10 |
41,531,440 (GRCm39) |
critical splice donor site |
probably null |
|
R8950:Ccdc162
|
UTSW |
10 |
41,474,507 (GRCm39) |
missense |
probably benign |
0.00 |
R8960:Ccdc162
|
UTSW |
10 |
41,429,178 (GRCm39) |
missense |
probably damaging |
0.96 |
R8985:Ccdc162
|
UTSW |
10 |
41,432,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R9071:Ccdc162
|
UTSW |
10 |
41,457,174 (GRCm39) |
nonsense |
probably null |
|
R9254:Ccdc162
|
UTSW |
10 |
41,488,944 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9297:Ccdc162
|
UTSW |
10 |
41,506,110 (GRCm39) |
missense |
probably benign |
|
R9318:Ccdc162
|
UTSW |
10 |
41,506,110 (GRCm39) |
missense |
probably benign |
|
R9518:Ccdc162
|
UTSW |
10 |
41,465,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R9525:Ccdc162
|
UTSW |
10 |
41,559,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R9539:Ccdc162
|
UTSW |
10 |
41,463,407 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9638:Ccdc162
|
UTSW |
10 |
41,437,159 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Ccdc162
|
UTSW |
10 |
41,530,993 (GRCm39) |
missense |
possibly damaging |
0.84 |
Z1176:Ccdc162
|
UTSW |
10 |
41,481,104 (GRCm39) |
missense |
possibly damaging |
0.84 |
Z1176:Ccdc162
|
UTSW |
10 |
41,429,127 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Ccdc162
|
UTSW |
10 |
41,566,088 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Ccdc162
|
UTSW |
10 |
41,559,191 (GRCm39) |
missense |
probably benign |
0.00 |
|