Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadac |
T |
A |
3: 59,944,737 (GRCm39) |
D136E |
probably damaging |
Het |
Agrn |
C |
T |
4: 156,263,675 (GRCm39) |
G173R |
probably damaging |
Het |
Apob |
T |
C |
12: 8,065,475 (GRCm39) |
F4115S |
possibly damaging |
Het |
Bsn |
T |
A |
9: 107,992,323 (GRCm39) |
D1143V |
probably damaging |
Het |
Cacna2d2 |
T |
C |
9: 107,390,479 (GRCm39) |
V317A |
probably damaging |
Het |
Cdh1 |
G |
A |
8: 107,388,635 (GRCm39) |
V564I |
probably benign |
Het |
Ces2a |
A |
T |
8: 105,466,822 (GRCm39) |
I65F |
probably benign |
Het |
Commd8 |
A |
G |
5: 72,322,765 (GRCm39) |
W51R |
probably damaging |
Het |
Cyb561d1 |
A |
T |
3: 108,106,720 (GRCm39) |
H166Q |
probably damaging |
Het |
Dcun1d4 |
T |
A |
5: 73,638,618 (GRCm39) |
|
probably benign |
Het |
Dgkd |
A |
G |
1: 87,855,540 (GRCm39) |
|
probably benign |
Het |
Dipk2b |
A |
G |
X: 18,289,926 (GRCm39) |
S179P |
possibly damaging |
Het |
Dnajc28 |
T |
C |
16: 91,413,200 (GRCm39) |
N372S |
probably benign |
Het |
Ecpas |
A |
T |
4: 58,830,332 (GRCm39) |
|
probably null |
Het |
Eid1 |
A |
G |
2: 125,515,344 (GRCm39) |
D78G |
possibly damaging |
Het |
Emid1 |
T |
A |
11: 5,094,331 (GRCm39) |
Q60L |
probably damaging |
Het |
Fam135a |
A |
T |
1: 24,067,878 (GRCm39) |
V801E |
probably benign |
Het |
Foxh1 |
A |
G |
15: 76,552,820 (GRCm39) |
V298A |
probably benign |
Het |
Foxn4 |
T |
C |
5: 114,393,662 (GRCm39) |
T486A |
probably damaging |
Het |
Gpc6 |
A |
T |
14: 118,125,932 (GRCm39) |
|
probably null |
Het |
Grid2ip |
C |
T |
5: 143,371,847 (GRCm39) |
P690L |
probably benign |
Het |
H2bc9 |
T |
C |
13: 23,727,162 (GRCm39) |
K121E |
possibly damaging |
Het |
Hdhd2 |
C |
T |
18: 77,052,866 (GRCm39) |
T172M |
probably benign |
Het |
Hr |
A |
T |
14: 70,795,547 (GRCm39) |
D393V |
probably benign |
Het |
Ido2 |
T |
C |
8: 25,025,268 (GRCm39) |
Y253C |
probably damaging |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Klra10 |
A |
G |
6: 130,246,264 (GRCm39) |
V237A |
probably benign |
Het |
Klre1 |
A |
G |
6: 129,562,593 (GRCm39) |
K206R |
probably benign |
Het |
Lama2 |
T |
C |
10: 26,862,793 (GRCm39) |
D2990G |
probably benign |
Het |
Magi3 |
G |
A |
3: 103,928,382 (GRCm39) |
|
probably benign |
Het |
Mamdc2 |
A |
T |
19: 23,281,267 (GRCm39) |
|
probably benign |
Het |
Med23 |
T |
G |
10: 24,750,499 (GRCm39) |
S109A |
probably benign |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Mtss2 |
A |
G |
8: 111,455,362 (GRCm39) |
K92E |
possibly damaging |
Het |
Mybphl |
A |
G |
3: 108,272,317 (GRCm39) |
E2G |
probably damaging |
Het |
Naip6 |
A |
G |
13: 100,420,067 (GRCm39) |
V1401A |
possibly damaging |
Het |
Ncapg2 |
A |
G |
12: 116,393,296 (GRCm39) |
E500G |
probably damaging |
Het |
Nlrp12 |
T |
C |
7: 3,282,575 (GRCm39) |
I775V |
probably benign |
Het |
Nr4a2 |
T |
A |
2: 57,002,018 (GRCm39) |
D145V |
possibly damaging |
Het |
Ntmt1 |
C |
A |
2: 30,710,472 (GRCm39) |
N58K |
probably benign |
Het |
P2ry13 |
T |
C |
3: 59,117,449 (GRCm39) |
M110V |
probably damaging |
Het |
P2ry14 |
T |
C |
3: 59,022,992 (GRCm39) |
N165S |
probably damaging |
Het |
Plch2 |
T |
C |
4: 155,077,461 (GRCm39) |
E423G |
probably benign |
Het |
Polq |
C |
A |
16: 36,882,515 (GRCm39) |
Q1560K |
possibly damaging |
Het |
Prrc1 |
G |
T |
18: 57,514,718 (GRCm39) |
D312Y |
probably damaging |
Het |
Ptprm |
A |
T |
17: 67,032,846 (GRCm39) |
|
probably null |
Het |
Ripk2 |
A |
T |
4: 16,152,011 (GRCm39) |
S183T |
possibly damaging |
Het |
Robo1 |
T |
A |
16: 72,775,660 (GRCm39) |
F728L |
probably benign |
Het |
Rttn |
A |
G |
18: 89,082,295 (GRCm39) |
N1407S |
probably benign |
Het |
Sec14l1 |
A |
T |
11: 117,047,314 (GRCm39) |
H664L |
probably damaging |
Het |
Slc10a7 |
G |
A |
8: 79,236,264 (GRCm39) |
G21S |
probably benign |
Het |
Slc35a3 |
T |
C |
3: 116,467,285 (GRCm39) |
K325E |
possibly damaging |
Het |
Spag17 |
C |
A |
3: 99,969,182 (GRCm39) |
|
probably null |
Het |
Spesp1 |
A |
T |
9: 62,180,834 (GRCm39) |
L25M |
probably damaging |
Het |
St6galnac1 |
G |
A |
11: 116,658,673 (GRCm39) |
Q264* |
probably null |
Het |
Tbc1d14 |
A |
G |
5: 36,700,561 (GRCm39) |
L269P |
possibly damaging |
Het |
Tgfbr3l |
A |
G |
8: 4,300,506 (GRCm39) |
E228G |
probably benign |
Het |
Tlr5 |
T |
A |
1: 182,802,600 (GRCm39) |
S635T |
possibly damaging |
Het |
Tmem233 |
G |
C |
5: 116,189,517 (GRCm39) |
|
probably benign |
Het |
Tnfsf13b |
A |
T |
8: 10,057,306 (GRCm39) |
R125S |
probably benign |
Het |
Tymp |
A |
T |
15: 89,258,011 (GRCm39) |
V378D |
probably damaging |
Het |
Vmn1r38 |
G |
T |
6: 66,753,433 (GRCm39) |
Q228K |
probably benign |
Het |
Vmn2r18 |
T |
C |
5: 151,510,127 (GRCm39) |
E82G |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,828,229 (GRCm39) |
V1461A |
possibly damaging |
Het |
Xrn1 |
A |
G |
9: 95,888,765 (GRCm39) |
D948G |
possibly damaging |
Het |
Zfp280d |
C |
A |
9: 72,209,052 (GRCm39) |
|
probably benign |
Het |
Zfp418 |
G |
A |
7: 7,185,807 (GRCm39) |
R590K |
probably benign |
Het |
|
Other mutations in Cep250 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Cep250
|
APN |
2 |
155,833,249 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01077:Cep250
|
APN |
2 |
155,804,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01084:Cep250
|
APN |
2 |
155,840,313 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01400:Cep250
|
APN |
2 |
155,840,211 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01570:Cep250
|
APN |
2 |
155,809,583 (GRCm39) |
splice site |
probably benign |
|
IGL01583:Cep250
|
APN |
2 |
155,818,069 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01590:Cep250
|
APN |
2 |
155,834,237 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01647:Cep250
|
APN |
2 |
155,825,296 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01959:Cep250
|
APN |
2 |
155,825,279 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02066:Cep250
|
APN |
2 |
155,818,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02219:Cep250
|
APN |
2 |
155,833,514 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02322:Cep250
|
APN |
2 |
155,832,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02728:Cep250
|
APN |
2 |
155,825,198 (GRCm39) |
unclassified |
probably benign |
|
IGL02955:Cep250
|
APN |
2 |
155,817,676 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03369:Cep250
|
APN |
2 |
155,832,191 (GRCm39) |
missense |
probably benign |
0.00 |
R0366:Cep250
|
UTSW |
2 |
155,830,321 (GRCm39) |
missense |
probably benign |
0.00 |
R0403:Cep250
|
UTSW |
2 |
155,834,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R0441:Cep250
|
UTSW |
2 |
155,813,924 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0482:Cep250
|
UTSW |
2 |
155,806,894 (GRCm39) |
splice site |
probably benign |
|
R0507:Cep250
|
UTSW |
2 |
155,834,452 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0614:Cep250
|
UTSW |
2 |
155,812,017 (GRCm39) |
nonsense |
probably null |
|
R0855:Cep250
|
UTSW |
2 |
155,806,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Cep250
|
UTSW |
2 |
155,806,209 (GRCm39) |
splice site |
probably benign |
|
R1137:Cep250
|
UTSW |
2 |
155,832,760 (GRCm39) |
missense |
probably benign |
0.05 |
R1270:Cep250
|
UTSW |
2 |
155,832,601 (GRCm39) |
missense |
probably benign |
0.01 |
R1313:Cep250
|
UTSW |
2 |
155,813,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R1313:Cep250
|
UTSW |
2 |
155,813,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R1470:Cep250
|
UTSW |
2 |
155,832,995 (GRCm39) |
missense |
probably damaging |
0.99 |
R1470:Cep250
|
UTSW |
2 |
155,832,995 (GRCm39) |
missense |
probably damaging |
0.99 |
R1703:Cep250
|
UTSW |
2 |
155,807,466 (GRCm39) |
missense |
probably benign |
0.23 |
R1705:Cep250
|
UTSW |
2 |
155,805,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1740:Cep250
|
UTSW |
2 |
155,815,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R1796:Cep250
|
UTSW |
2 |
155,834,107 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1897:Cep250
|
UTSW |
2 |
155,818,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R1900:Cep250
|
UTSW |
2 |
155,827,294 (GRCm39) |
critical splice donor site |
probably null |
|
R1958:Cep250
|
UTSW |
2 |
155,818,301 (GRCm39) |
splice site |
probably null |
|
R1974:Cep250
|
UTSW |
2 |
155,831,424 (GRCm39) |
missense |
probably damaging |
0.96 |
R2015:Cep250
|
UTSW |
2 |
155,823,373 (GRCm39) |
missense |
probably damaging |
0.96 |
R2033:Cep250
|
UTSW |
2 |
155,812,812 (GRCm39) |
missense |
probably damaging |
0.99 |
R2224:Cep250
|
UTSW |
2 |
155,833,737 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2278:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2332:Cep250
|
UTSW |
2 |
155,832,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R2364:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2366:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2367:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R2385:Cep250
|
UTSW |
2 |
155,816,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R2830:Cep250
|
UTSW |
2 |
155,825,236 (GRCm39) |
missense |
probably benign |
0.00 |
R2895:Cep250
|
UTSW |
2 |
155,834,042 (GRCm39) |
missense |
probably benign |
0.00 |
R2965:Cep250
|
UTSW |
2 |
155,836,798 (GRCm39) |
missense |
probably benign |
0.44 |
R2966:Cep250
|
UTSW |
2 |
155,836,798 (GRCm39) |
missense |
probably benign |
0.44 |
R3016:Cep250
|
UTSW |
2 |
155,833,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R3052:Cep250
|
UTSW |
2 |
155,832,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R3424:Cep250
|
UTSW |
2 |
155,823,381 (GRCm39) |
missense |
probably benign |
0.02 |
R3930:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4085:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4087:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4090:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4110:Cep250
|
UTSW |
2 |
155,834,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4355:Cep250
|
UTSW |
2 |
155,833,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R4601:Cep250
|
UTSW |
2 |
155,803,973 (GRCm39) |
missense |
probably benign |
0.10 |
R4721:Cep250
|
UTSW |
2 |
155,812,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Cep250
|
UTSW |
2 |
155,830,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5053:Cep250
|
UTSW |
2 |
155,804,848 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5090:Cep250
|
UTSW |
2 |
155,818,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R5744:Cep250
|
UTSW |
2 |
155,823,394 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5775:Cep250
|
UTSW |
2 |
155,811,294 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5986:Cep250
|
UTSW |
2 |
155,821,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R6112:Cep250
|
UTSW |
2 |
155,836,503 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6152:Cep250
|
UTSW |
2 |
155,823,358 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6823:Cep250
|
UTSW |
2 |
155,823,379 (GRCm39) |
missense |
probably benign |
0.02 |
R6859:Cep250
|
UTSW |
2 |
155,834,446 (GRCm39) |
missense |
probably benign |
0.24 |
R6900:Cep250
|
UTSW |
2 |
155,838,190 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7107:Cep250
|
UTSW |
2 |
155,837,314 (GRCm39) |
missense |
probably benign |
0.00 |
R7131:Cep250
|
UTSW |
2 |
155,806,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R7178:Cep250
|
UTSW |
2 |
155,815,375 (GRCm39) |
nonsense |
probably null |
|
R7241:Cep250
|
UTSW |
2 |
155,833,472 (GRCm39) |
missense |
probably benign |
0.20 |
R7264:Cep250
|
UTSW |
2 |
155,821,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R7290:Cep250
|
UTSW |
2 |
155,834,682 (GRCm39) |
missense |
probably benign |
0.03 |
R7367:Cep250
|
UTSW |
2 |
155,811,227 (GRCm39) |
missense |
probably benign |
0.00 |
R7397:Cep250
|
UTSW |
2 |
155,823,331 (GRCm39) |
missense |
probably damaging |
0.99 |
R7768:Cep250
|
UTSW |
2 |
155,827,929 (GRCm39) |
missense |
|
|
R7823:Cep250
|
UTSW |
2 |
155,807,336 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8152:Cep250
|
UTSW |
2 |
155,811,227 (GRCm39) |
missense |
probably benign |
0.00 |
R8331:Cep250
|
UTSW |
2 |
155,832,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R8559:Cep250
|
UTSW |
2 |
155,834,656 (GRCm39) |
missense |
probably damaging |
0.99 |
R8972:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8973:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8974:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8975:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R8976:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9072:Cep250
|
UTSW |
2 |
155,834,035 (GRCm39) |
missense |
probably benign |
0.01 |
R9123:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9127:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9128:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9167:Cep250
|
UTSW |
2 |
155,828,920 (GRCm39) |
missense |
|
|
R9189:Cep250
|
UTSW |
2 |
155,818,350 (GRCm39) |
missense |
probably benign |
0.00 |
R9198:Cep250
|
UTSW |
2 |
155,830,354 (GRCm39) |
critical splice donor site |
probably null |
|
R9227:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9228:Cep250
|
UTSW |
2 |
155,812,042 (GRCm39) |
missense |
unknown |
|
R9292:Cep250
|
UTSW |
2 |
155,832,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R9516:Cep250
|
UTSW |
2 |
155,833,459 (GRCm39) |
missense |
probably benign |
0.00 |
R9723:Cep250
|
UTSW |
2 |
155,823,337 (GRCm39) |
missense |
probably benign |
0.00 |
R9760:Cep250
|
UTSW |
2 |
155,818,473 (GRCm39) |
missense |
probably benign |
0.02 |
X0061:Cep250
|
UTSW |
2 |
155,803,905 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Cep250
|
UTSW |
2 |
155,818,387 (GRCm39) |
missense |
probably benign |
0.03 |
|