Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
T |
3: 137,773,811 (GRCm39) |
Y1000F |
probably damaging |
Het |
1700018B08Rik |
A |
G |
8: 122,262,160 (GRCm39) |
|
probably null |
Het |
Aadat |
T |
C |
8: 60,982,467 (GRCm39) |
F245L |
probably damaging |
Het |
Adcy10 |
T |
G |
1: 165,403,227 (GRCm39) |
L1575W |
probably damaging |
Het |
Anks4b |
A |
T |
7: 119,782,231 (GRCm39) |
T421S |
probably damaging |
Het |
Anpep |
A |
T |
7: 79,475,097 (GRCm39) |
I155N |
probably damaging |
Het |
Arnt |
T |
C |
3: 95,397,932 (GRCm39) |
F572L |
probably damaging |
Het |
Brip1 |
G |
A |
11: 86,039,362 (GRCm39) |
Q391* |
probably null |
Het |
Brpf3 |
C |
A |
17: 29,042,970 (GRCm39) |
H1004N |
probably benign |
Het |
Cand2 |
T |
A |
6: 115,768,250 (GRCm39) |
V465D |
possibly damaging |
Het |
Catsperd |
A |
T |
17: 56,962,175 (GRCm39) |
K450* |
probably null |
Het |
Ccdc137 |
T |
C |
11: 120,351,009 (GRCm39) |
L137P |
probably damaging |
Het |
Cic |
T |
C |
7: 24,990,107 (GRCm39) |
S1905P |
probably damaging |
Het |
Csmd3 |
C |
T |
15: 47,507,601 (GRCm39) |
G2971S |
probably damaging |
Het |
Dmxl2 |
A |
G |
9: 54,379,496 (GRCm39) |
Y183H |
probably damaging |
Het |
Drosha |
T |
C |
15: 12,834,396 (GRCm39) |
Y167H |
unknown |
Het |
E330034G19Rik |
A |
G |
14: 24,358,310 (GRCm39) |
K214R |
unknown |
Het |
Fam180a |
T |
G |
6: 35,290,765 (GRCm39) |
I73L |
possibly damaging |
Het |
Fbxo28 |
G |
T |
1: 182,168,986 (GRCm39) |
H51N |
probably benign |
Het |
Gm12728 |
T |
G |
4: 105,647,533 (GRCm39) |
|
probably null |
Het |
Gm973 |
T |
C |
1: 59,591,620 (GRCm39) |
C335R |
possibly damaging |
Het |
Gpx8 |
A |
G |
13: 113,179,770 (GRCm39) |
V177A |
probably damaging |
Het |
Hdlbp |
A |
G |
1: 93,340,083 (GRCm39) |
|
probably null |
Het |
Htt |
T |
G |
5: 35,034,444 (GRCm39) |
Y1972D |
probably null |
Het |
Igkv6-14 |
T |
C |
6: 70,412,116 (GRCm39) |
Y56C |
possibly damaging |
Het |
Kcnma1 |
A |
G |
14: 23,576,602 (GRCm39) |
|
probably null |
Het |
Klc1 |
T |
C |
12: 111,754,019 (GRCm39) |
S105P |
probably damaging |
Het |
Klhl20 |
T |
C |
1: 160,921,266 (GRCm39) |
D63G |
possibly damaging |
Het |
Lamc3 |
A |
G |
2: 31,798,701 (GRCm39) |
D469G |
probably damaging |
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Mboat4 |
G |
A |
8: 34,591,865 (GRCm39) |
R434H |
probably benign |
Het |
Mttp |
T |
C |
3: 137,821,043 (GRCm39) |
K270E |
possibly damaging |
Het |
Muc5ac |
G |
A |
7: 141,347,035 (GRCm39) |
C337Y |
possibly damaging |
Het |
Nars1 |
A |
G |
18: 64,634,471 (GRCm39) |
V484A |
probably damaging |
Het |
Noxa1 |
G |
T |
2: 24,981,844 (GRCm39) |
|
probably null |
Het |
Or14c45 |
A |
G |
7: 86,176,522 (GRCm39) |
T186A |
probably benign |
Het |
Or7g18 |
T |
A |
9: 18,786,821 (GRCm39) |
L63H |
probably damaging |
Het |
Osbpl7 |
G |
A |
11: 96,941,584 (GRCm39) |
G36S |
probably damaging |
Het |
P4htm |
C |
T |
9: 108,460,812 (GRCm39) |
G220D |
probably benign |
Het |
Pcdhga7 |
A |
G |
18: 37,848,199 (GRCm39) |
I69V |
probably benign |
Het |
Pla2g4e |
C |
T |
2: 120,015,795 (GRCm39) |
E250K |
possibly damaging |
Het |
Plcd4 |
A |
G |
1: 74,604,994 (GRCm39) |
|
probably benign |
Het |
Ppfia3 |
C |
A |
7: 45,008,231 (GRCm39) |
G213V |
possibly damaging |
Het |
Ppp1r1a |
A |
G |
15: 103,441,513 (GRCm39) |
S67P |
probably damaging |
Het |
Prss43 |
T |
C |
9: 110,657,680 (GRCm39) |
F193S |
probably benign |
Het |
Rfx1 |
A |
G |
8: 84,822,117 (GRCm39) |
Y872C |
probably damaging |
Het |
Rhot1 |
T |
A |
11: 80,132,921 (GRCm39) |
N218K |
probably benign |
Het |
Sall1 |
A |
G |
8: 89,757,021 (GRCm39) |
F1028L |
probably damaging |
Het |
Siglec1 |
G |
A |
2: 130,919,997 (GRCm39) |
Q845* |
probably null |
Het |
Slc38a9 |
C |
T |
13: 112,838,060 (GRCm39) |
T275I |
possibly damaging |
Het |
Slc39a4 |
A |
T |
15: 76,497,470 (GRCm39) |
S481T |
probably damaging |
Het |
Ssr1 |
A |
T |
13: 38,169,998 (GRCm39) |
N191K |
probably damaging |
Het |
Tenm4 |
A |
T |
7: 96,544,757 (GRCm39) |
S2258C |
probably damaging |
Het |
Tm7sf3 |
T |
G |
6: 146,507,645 (GRCm39) |
R472S |
possibly damaging |
Het |
Tmprss11a |
G |
A |
5: 86,576,494 (GRCm39) |
T119M |
probably benign |
Het |
Traip |
C |
T |
9: 107,838,240 (GRCm39) |
R142* |
probably null |
Het |
Utrn |
T |
C |
10: 12,626,214 (GRCm39) |
N100D |
probably damaging |
Het |
Vmn1r74 |
T |
C |
7: 11,581,575 (GRCm39) |
S292P |
probably benign |
Het |
Vmn2r71 |
A |
T |
7: 85,273,108 (GRCm39) |
I641F |
probably damaging |
Het |
Vmn2r9 |
T |
A |
5: 108,996,912 (GRCm39) |
Y119F |
possibly damaging |
Het |
Vmn2r98 |
A |
G |
17: 19,285,510 (GRCm39) |
N110S |
probably damaging |
Het |
Vwce |
A |
G |
19: 10,642,057 (GRCm39) |
T928A |
probably benign |
Het |
Zfp608 |
T |
A |
18: 55,121,337 (GRCm39) |
K83N |
probably damaging |
Het |
Zfp808 |
A |
G |
13: 62,320,982 (GRCm39) |
H737R |
probably benign |
Het |
Zswim4 |
T |
C |
8: 84,940,714 (GRCm39) |
N795S |
probably benign |
Het |
|
Other mutations in Card10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02061:Card10
|
APN |
15 |
78,662,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02804:Card10
|
APN |
15 |
78,686,649 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4366001:Card10
|
UTSW |
15 |
78,671,631 (GRCm39) |
missense |
probably benign |
0.14 |
R0529:Card10
|
UTSW |
15 |
78,664,675 (GRCm39) |
critical splice donor site |
probably null |
|
R0571:Card10
|
UTSW |
15 |
78,671,601 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1118:Card10
|
UTSW |
15 |
78,686,643 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1444:Card10
|
UTSW |
15 |
78,672,041 (GRCm39) |
splice site |
probably benign |
|
R1632:Card10
|
UTSW |
15 |
78,675,420 (GRCm39) |
nonsense |
probably null |
|
R1669:Card10
|
UTSW |
15 |
78,678,153 (GRCm39) |
missense |
probably benign |
0.20 |
R1862:Card10
|
UTSW |
15 |
78,664,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1863:Card10
|
UTSW |
15 |
78,664,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1997:Card10
|
UTSW |
15 |
78,678,175 (GRCm39) |
missense |
probably damaging |
0.99 |
R2046:Card10
|
UTSW |
15 |
78,671,673 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2084:Card10
|
UTSW |
15 |
78,677,171 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2509:Card10
|
UTSW |
15 |
78,664,473 (GRCm39) |
missense |
probably benign |
0.00 |
R2511:Card10
|
UTSW |
15 |
78,664,473 (GRCm39) |
missense |
probably benign |
0.00 |
R4274:Card10
|
UTSW |
15 |
78,664,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R4887:Card10
|
UTSW |
15 |
78,665,724 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4970:Card10
|
UTSW |
15 |
78,686,580 (GRCm39) |
critical splice donor site |
probably null |
|
R5098:Card10
|
UTSW |
15 |
78,660,917 (GRCm39) |
missense |
probably benign |
0.37 |
R5112:Card10
|
UTSW |
15 |
78,686,580 (GRCm39) |
critical splice donor site |
probably null |
|
R5243:Card10
|
UTSW |
15 |
78,664,872 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5256:Card10
|
UTSW |
15 |
78,662,451 (GRCm39) |
missense |
probably damaging |
0.98 |
R5985:Card10
|
UTSW |
15 |
78,675,411 (GRCm39) |
missense |
probably benign |
0.01 |
R6089:Card10
|
UTSW |
15 |
78,686,614 (GRCm39) |
missense |
probably benign |
0.02 |
R6357:Card10
|
UTSW |
15 |
78,683,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R6545:Card10
|
UTSW |
15 |
78,661,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R6865:Card10
|
UTSW |
15 |
78,686,822 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6907:Card10
|
UTSW |
15 |
78,671,671 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7913:Card10
|
UTSW |
15 |
78,665,303 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8258:Card10
|
UTSW |
15 |
78,660,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R8259:Card10
|
UTSW |
15 |
78,660,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Card10
|
UTSW |
15 |
78,673,036 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9661:Card10
|
UTSW |
15 |
78,683,318 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Card10
|
UTSW |
15 |
78,679,528 (GRCm39) |
missense |
probably benign |
0.28 |
|