Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
A |
T |
12: 72,954,654 (GRCm39) |
S206T |
probably benign |
Het |
Aasdh |
A |
T |
5: 77,036,696 (GRCm39) |
|
probably null |
Het |
Adam10 |
G |
T |
9: 70,668,884 (GRCm39) |
C400F |
probably damaging |
Het |
Ankle2 |
A |
T |
5: 110,398,635 (GRCm39) |
R561S |
probably null |
Het |
Arhgef5 |
C |
T |
6: 43,251,895 (GRCm39) |
T882I |
probably damaging |
Het |
Arpc1a |
A |
T |
5: 145,032,936 (GRCm39) |
K82* |
probably null |
Het |
Card11 |
C |
A |
5: 140,863,837 (GRCm39) |
R967L |
probably benign |
Het |
Ccdc82 |
G |
T |
9: 13,251,601 (GRCm39) |
|
probably benign |
Het |
Cebpz |
T |
C |
17: 79,227,392 (GRCm39) |
D1026G |
probably damaging |
Het |
Clcn2 |
C |
A |
16: 20,528,408 (GRCm39) |
|
probably benign |
Het |
Csf3 |
G |
C |
11: 98,593,273 (GRCm39) |
G130A |
probably damaging |
Het |
Cul2 |
T |
A |
18: 3,434,946 (GRCm39) |
S737T |
probably damaging |
Het |
Cyp1a2 |
G |
A |
9: 57,584,543 (GRCm39) |
H504Y |
probably benign |
Het |
Cyp3a44 |
G |
A |
5: 145,716,396 (GRCm39) |
P398L |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 30,960,147 (GRCm39) |
I2206T |
probably damaging |
Het |
Efr3a |
G |
A |
15: 65,701,679 (GRCm39) |
V198I |
probably benign |
Het |
Epb41l5 |
A |
T |
1: 119,547,931 (GRCm39) |
D157E |
possibly damaging |
Het |
Ercc8 |
T |
C |
13: 108,295,343 (GRCm39) |
S6P |
probably damaging |
Het |
Faxc |
T |
C |
4: 21,931,672 (GRCm39) |
S37P |
probably benign |
Het |
Fbxl19 |
T |
A |
7: 127,349,187 (GRCm39) |
I119K |
probably damaging |
Het |
Frmd4b |
A |
G |
6: 97,302,437 (GRCm39) |
V195A |
possibly damaging |
Het |
Fut9 |
A |
T |
4: 25,619,925 (GRCm39) |
S296R |
probably benign |
Het |
Gas6 |
T |
C |
8: 13,533,674 (GRCm39) |
N112D |
probably benign |
Het |
H2-Q1 |
T |
C |
17: 35,540,028 (GRCm39) |
L99P |
probably damaging |
Het |
Helq |
A |
T |
5: 100,940,561 (GRCm39) |
I346N |
probably damaging |
Het |
Hepacam |
A |
G |
9: 37,278,976 (GRCm39) |
K2E |
possibly damaging |
Het |
Itgae |
T |
C |
11: 73,009,322 (GRCm39) |
M502T |
possibly damaging |
Het |
Kmt2a |
G |
A |
9: 44,729,704 (GRCm39) |
|
probably benign |
Het |
Lhx9 |
ACC |
ACCC |
1: 138,769,544 (GRCm39) |
|
probably null |
Het |
Macf1 |
A |
T |
4: 123,277,015 (GRCm39) |
|
probably null |
Het |
Mgat4a |
T |
A |
1: 37,503,515 (GRCm39) |
K220* |
probably null |
Het |
Or2t43 |
T |
C |
11: 58,457,476 (GRCm39) |
R232G |
possibly damaging |
Het |
Or4c104 |
T |
C |
2: 88,586,255 (GRCm39) |
I255V |
possibly damaging |
Het |
Or5b3 |
G |
A |
19: 13,388,514 (GRCm39) |
V194I |
probably benign |
Het |
Pex5 |
A |
T |
6: 124,391,340 (GRCm39) |
M18K |
probably damaging |
Het |
Phlda3 |
T |
C |
1: 135,694,562 (GRCm39) |
*126Q |
probably null |
Het |
Plxna1 |
G |
T |
6: 89,297,597 (GRCm39) |
D1862E |
probably benign |
Het |
Pold4 |
A |
T |
19: 4,282,164 (GRCm39) |
I7F |
possibly damaging |
Het |
Prkaa1 |
A |
T |
15: 5,173,432 (GRCm39) |
I19F |
possibly damaging |
Het |
Prl7d1 |
T |
G |
13: 27,894,125 (GRCm39) |
E148A |
probably benign |
Het |
Prr14l |
A |
T |
5: 32,985,892 (GRCm39) |
V1201E |
possibly damaging |
Het |
Rab3gap1 |
T |
C |
1: 127,858,158 (GRCm39) |
C510R |
probably damaging |
Het |
Rhbdf1 |
C |
T |
11: 32,159,970 (GRCm39) |
R802H |
probably damaging |
Het |
Rpl18a |
A |
C |
8: 71,348,836 (GRCm39) |
F47V |
probably damaging |
Het |
Sema5b |
C |
A |
16: 35,448,377 (GRCm39) |
|
probably null |
Het |
Sspo |
G |
A |
6: 48,442,459 (GRCm39) |
G1985R |
probably benign |
Het |
Tcaf2 |
C |
T |
6: 42,606,452 (GRCm39) |
A501T |
probably benign |
Het |
Tcerg1 |
A |
G |
18: 42,681,542 (GRCm39) |
D563G |
probably damaging |
Het |
Tdh |
G |
A |
14: 63,733,281 (GRCm39) |
T155M |
probably damaging |
Het |
Tenm2 |
T |
C |
11: 35,937,711 (GRCm39) |
N1654S |
probably benign |
Het |
Tlr5 |
A |
T |
1: 182,800,609 (GRCm39) |
|
probably benign |
Het |
Tns1 |
G |
T |
1: 74,041,482 (GRCm39) |
C136* |
probably null |
Het |
Tomm5 |
A |
T |
4: 45,106,443 (GRCm39) |
|
probably null |
Het |
Trio |
A |
T |
15: 27,889,394 (GRCm39) |
F512I |
probably damaging |
Het |
Ttll5 |
A |
T |
12: 85,930,102 (GRCm39) |
|
probably null |
Het |
Upp1 |
T |
A |
11: 9,081,707 (GRCm39) |
H81Q |
probably benign |
Het |
Usp42 |
A |
G |
5: 143,713,562 (GRCm39) |
S71P |
probably damaging |
Het |
Vamp5 |
G |
A |
6: 72,357,424 (GRCm39) |
|
probably benign |
Het |
Zap70 |
A |
G |
1: 36,817,471 (GRCm39) |
Y238C |
probably damaging |
Het |
Zfp398 |
A |
G |
6: 47,843,265 (GRCm39) |
D307G |
probably damaging |
Het |
|
Other mutations in Cit |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00321:Cit
|
APN |
5 |
115,984,524 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00482:Cit
|
APN |
5 |
116,076,814 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01317:Cit
|
APN |
5 |
116,046,775 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01335:Cit
|
APN |
5 |
116,046,889 (GRCm39) |
splice site |
probably benign |
|
IGL01415:Cit
|
APN |
5 |
116,079,962 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01447:Cit
|
APN |
5 |
116,011,902 (GRCm39) |
splice site |
probably benign |
|
IGL01537:Cit
|
APN |
5 |
116,071,913 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01621:Cit
|
APN |
5 |
116,130,662 (GRCm39) |
splice site |
probably benign |
|
IGL02010:Cit
|
APN |
5 |
116,014,006 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02538:Cit
|
APN |
5 |
116,125,048 (GRCm39) |
nonsense |
probably null |
|
IGL02607:Cit
|
APN |
5 |
115,997,268 (GRCm39) |
missense |
probably benign |
|
IGL02720:Cit
|
APN |
5 |
116,133,511 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02725:Cit
|
APN |
5 |
116,123,532 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02967:Cit
|
APN |
5 |
116,083,896 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02973:Cit
|
APN |
5 |
116,144,058 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03383:Cit
|
APN |
5 |
116,011,904 (GRCm39) |
splice site |
probably benign |
|
PIT4514001:Cit
|
UTSW |
5 |
116,135,913 (GRCm39) |
critical splice donor site |
probably null |
|
R0206:Cit
|
UTSW |
5 |
116,132,089 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0206:Cit
|
UTSW |
5 |
116,132,089 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0226:Cit
|
UTSW |
5 |
116,122,899 (GRCm39) |
missense |
probably damaging |
0.99 |
R0320:Cit
|
UTSW |
5 |
116,117,504 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0401:Cit
|
UTSW |
5 |
116,123,538 (GRCm39) |
missense |
probably benign |
0.06 |
R0480:Cit
|
UTSW |
5 |
116,071,452 (GRCm39) |
splice site |
probably benign |
|
R0609:Cit
|
UTSW |
5 |
116,012,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R0737:Cit
|
UTSW |
5 |
116,084,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R1238:Cit
|
UTSW |
5 |
115,989,280 (GRCm39) |
missense |
probably benign |
0.30 |
R1503:Cit
|
UTSW |
5 |
116,011,959 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1551:Cit
|
UTSW |
5 |
116,083,901 (GRCm39) |
missense |
probably benign |
0.00 |
R1602:Cit
|
UTSW |
5 |
116,135,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R1720:Cit
|
UTSW |
5 |
116,105,956 (GRCm39) |
missense |
probably damaging |
0.98 |
R1854:Cit
|
UTSW |
5 |
116,011,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1886:Cit
|
UTSW |
5 |
116,071,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R2024:Cit
|
UTSW |
5 |
116,143,899 (GRCm39) |
missense |
probably damaging |
0.97 |
R2024:Cit
|
UTSW |
5 |
116,085,983 (GRCm39) |
missense |
probably damaging |
0.97 |
R2048:Cit
|
UTSW |
5 |
116,024,872 (GRCm39) |
splice site |
probably null |
|
R2128:Cit
|
UTSW |
5 |
116,123,566 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2192:Cit
|
UTSW |
5 |
116,106,068 (GRCm39) |
missense |
probably benign |
0.00 |
R2244:Cit
|
UTSW |
5 |
116,064,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R2518:Cit
|
UTSW |
5 |
116,125,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R2679:Cit
|
UTSW |
5 |
116,107,174 (GRCm39) |
missense |
probably benign |
0.00 |
R2898:Cit
|
UTSW |
5 |
116,012,037 (GRCm39) |
splice site |
probably null |
|
R2908:Cit
|
UTSW |
5 |
116,119,735 (GRCm39) |
missense |
probably benign |
0.00 |
R3079:Cit
|
UTSW |
5 |
116,063,545 (GRCm39) |
missense |
probably damaging |
0.97 |
R3779:Cit
|
UTSW |
5 |
115,997,400 (GRCm39) |
missense |
probably benign |
0.01 |
R4081:Cit
|
UTSW |
5 |
116,086,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R4494:Cit
|
UTSW |
5 |
116,012,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Cit
|
UTSW |
5 |
116,132,146 (GRCm39) |
missense |
probably benign |
0.01 |
R4757:Cit
|
UTSW |
5 |
116,135,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R4788:Cit
|
UTSW |
5 |
116,071,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R4816:Cit
|
UTSW |
5 |
116,046,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Cit
|
UTSW |
5 |
116,126,182 (GRCm39) |
intron |
probably benign |
|
R4899:Cit
|
UTSW |
5 |
116,001,087 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4928:Cit
|
UTSW |
5 |
116,123,856 (GRCm39) |
missense |
probably benign |
0.00 |
R5073:Cit
|
UTSW |
5 |
116,084,902 (GRCm39) |
missense |
probably benign |
0.24 |
R5151:Cit
|
UTSW |
5 |
116,117,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R5154:Cit
|
UTSW |
5 |
116,126,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R5222:Cit
|
UTSW |
5 |
116,090,602 (GRCm39) |
missense |
probably benign |
0.03 |
R5814:Cit
|
UTSW |
5 |
116,117,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Cit
|
UTSW |
5 |
116,063,598 (GRCm39) |
intron |
probably benign |
|
R5946:Cit
|
UTSW |
5 |
116,135,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R6051:Cit
|
UTSW |
5 |
115,984,464 (GRCm39) |
missense |
probably benign |
|
R6289:Cit
|
UTSW |
5 |
116,144,385 (GRCm39) |
makesense |
probably null |
|
R6298:Cit
|
UTSW |
5 |
116,086,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R6362:Cit
|
UTSW |
5 |
116,024,735 (GRCm39) |
missense |
probably benign |
0.01 |
R6545:Cit
|
UTSW |
5 |
115,984,493 (GRCm39) |
missense |
probably null |
0.00 |
R6761:Cit
|
UTSW |
5 |
116,046,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Cit
|
UTSW |
5 |
116,064,585 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6814:Cit
|
UTSW |
5 |
116,023,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R6845:Cit
|
UTSW |
5 |
116,122,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R6983:Cit
|
UTSW |
5 |
116,132,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7164:Cit
|
UTSW |
5 |
116,123,846 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7359:Cit
|
UTSW |
5 |
116,064,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R7597:Cit
|
UTSW |
5 |
116,024,740 (GRCm39) |
nonsense |
probably null |
|
R7729:Cit
|
UTSW |
5 |
116,122,881 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7763:Cit
|
UTSW |
5 |
116,125,060 (GRCm39) |
missense |
probably benign |
0.01 |
R7786:Cit
|
UTSW |
5 |
116,001,077 (GRCm39) |
missense |
probably benign |
0.00 |
R7799:Cit
|
UTSW |
5 |
116,001,027 (GRCm39) |
missense |
probably benign |
0.00 |
R8060:Cit
|
UTSW |
5 |
116,046,786 (GRCm39) |
missense |
probably benign |
0.00 |
R8068:Cit
|
UTSW |
5 |
116,120,294 (GRCm39) |
missense |
probably benign |
0.03 |
R8068:Cit
|
UTSW |
5 |
116,090,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Cit
|
UTSW |
5 |
116,107,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R8177:Cit
|
UTSW |
5 |
116,126,218 (GRCm39) |
missense |
probably benign |
0.18 |
R8178:Cit
|
UTSW |
5 |
116,107,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R8265:Cit
|
UTSW |
5 |
116,126,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R8359:Cit
|
UTSW |
5 |
116,122,603 (GRCm39) |
splice site |
probably null |
|
R8397:Cit
|
UTSW |
5 |
116,024,856 (GRCm39) |
missense |
probably benign |
|
R8489:Cit
|
UTSW |
5 |
116,083,962 (GRCm39) |
critical splice donor site |
probably null |
|
R8784:Cit
|
UTSW |
5 |
115,984,442 (GRCm39) |
nonsense |
probably null |
|
R8798:Cit
|
UTSW |
5 |
116,107,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R8882:Cit
|
UTSW |
5 |
116,001,089 (GRCm39) |
missense |
probably benign |
0.04 |
R8984:Cit
|
UTSW |
5 |
116,064,534 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9091:Cit
|
UTSW |
5 |
115,984,161 (GRCm39) |
intron |
probably benign |
|
R9127:Cit
|
UTSW |
5 |
116,074,896 (GRCm39) |
nonsense |
probably null |
|
R9204:Cit
|
UTSW |
5 |
116,126,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R9212:Cit
|
UTSW |
5 |
116,013,952 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9279:Cit
|
UTSW |
5 |
116,065,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Cit
|
UTSW |
5 |
116,123,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Cit
|
UTSW |
5 |
116,084,914 (GRCm39) |
missense |
probably benign |
0.04 |
R9520:Cit
|
UTSW |
5 |
116,079,954 (GRCm39) |
nonsense |
probably null |
|
Z1088:Cit
|
UTSW |
5 |
116,123,592 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1176:Cit
|
UTSW |
5 |
116,124,662 (GRCm39) |
missense |
probably damaging |
1.00 |
|