Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
C |
T |
1: 183,765,624 (GRCm39) |
R145H |
probably damaging |
Het |
Adam26a |
C |
T |
8: 44,021,439 (GRCm39) |
V684I |
probably benign |
Het |
Alk |
T |
C |
17: 72,910,195 (GRCm39) |
I170M |
probably benign |
Het |
Apc2 |
T |
C |
10: 80,151,239 (GRCm39) |
Y2069H |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,401,992 (GRCm39) |
T1219A |
probably damaging |
Het |
Bnip1 |
T |
C |
17: 27,008,679 (GRCm39) |
S94P |
probably benign |
Het |
Col25a1 |
T |
A |
3: 130,378,375 (GRCm39) |
D609E |
probably damaging |
Het |
Cplane1 |
T |
A |
15: 8,276,669 (GRCm39) |
V2771E |
unknown |
Het |
Cyp2g1 |
A |
G |
7: 26,514,216 (GRCm39) |
K274R |
probably benign |
Het |
D5Ertd579e |
G |
A |
5: 36,771,101 (GRCm39) |
T1098I |
probably damaging |
Het |
Ddx39a |
T |
A |
8: 84,446,452 (GRCm39) |
C74S |
possibly damaging |
Het |
E2f3 |
C |
T |
13: 30,169,543 (GRCm39) |
A37T |
probably benign |
Het |
Emilin2 |
A |
G |
17: 71,580,815 (GRCm39) |
M637T |
probably benign |
Het |
Exosc7 |
T |
C |
9: 122,948,358 (GRCm39) |
L93P |
probably benign |
Het |
F2 |
T |
C |
2: 91,460,545 (GRCm39) |
E316G |
probably benign |
Het |
Fat4 |
A |
C |
3: 39,053,258 (GRCm39) |
Q4084P |
probably benign |
Het |
Flywch1 |
T |
C |
17: 23,981,344 (GRCm39) |
K160E |
probably benign |
Het |
Foxi2 |
A |
G |
7: 135,013,459 (GRCm39) |
T230A |
probably benign |
Het |
Fthl17a |
A |
G |
X: 84,313,679 (GRCm39) |
N154S |
possibly damaging |
Het |
Hykk |
G |
A |
9: 54,844,601 (GRCm39) |
R222Q |
probably damaging |
Het |
Il18rap |
T |
A |
1: 40,582,150 (GRCm39) |
V357E |
probably damaging |
Het |
Ing4 |
A |
G |
6: 125,020,923 (GRCm39) |
E15G |
probably damaging |
Het |
Irak1 |
T |
C |
X: 73,060,189 (GRCm39) |
D679G |
probably damaging |
Het |
Itga1 |
T |
C |
13: 115,143,568 (GRCm39) |
E321G |
probably benign |
Het |
Nudt1 |
T |
A |
5: 140,321,076 (GRCm39) |
|
probably null |
Het |
Nup58 |
A |
G |
14: 60,480,931 (GRCm39) |
F138S |
probably damaging |
Het |
Or10al6 |
A |
T |
17: 38,082,804 (GRCm39) |
M87L |
probably damaging |
Het |
Or2a5 |
G |
T |
6: 42,873,532 (GRCm39) |
W49L |
probably benign |
Het |
Pllp |
T |
C |
8: 95,406,103 (GRCm39) |
Y60C |
probably damaging |
Het |
Pnpla7 |
T |
C |
2: 24,887,267 (GRCm39) |
V37A |
probably damaging |
Het |
Poglut3 |
T |
G |
9: 53,302,011 (GRCm39) |
L32R |
probably damaging |
Het |
Psme4 |
A |
G |
11: 30,757,797 (GRCm39) |
H310R |
possibly damaging |
Het |
Rasl10b |
G |
A |
11: 83,308,665 (GRCm39) |
|
probably null |
Het |
Sash1 |
C |
T |
10: 8,605,673 (GRCm39) |
V906M |
probably benign |
Het |
Scn1a |
A |
T |
2: 66,130,128 (GRCm39) |
I1212K |
probably damaging |
Het |
Stbd1 |
A |
T |
5: 92,752,989 (GRCm39) |
S160C |
probably benign |
Het |
Tex29 |
T |
C |
8: 11,904,157 (GRCm39) |
V99A |
probably benign |
Het |
Tg |
A |
T |
15: 66,596,993 (GRCm39) |
N79I |
probably damaging |
Het |
Tie1 |
T |
C |
4: 118,339,860 (GRCm39) |
D389G |
probably damaging |
Het |
Vmn1r178 |
A |
G |
7: 23,593,452 (GRCm39) |
T167A |
possibly damaging |
Het |
Xkr4 |
C |
T |
1: 3,740,968 (GRCm39) |
G202S |
possibly damaging |
Het |
|
Other mutations in Cftr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00901:Cftr
|
APN |
6 |
18,268,429 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01082:Cftr
|
APN |
6 |
18,226,102 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01113:Cftr
|
APN |
6 |
18,270,252 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01383:Cftr
|
APN |
6 |
18,226,040 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01595:Cftr
|
APN |
6 |
18,198,238 (GRCm39) |
splice site |
probably benign |
|
IGL01820:Cftr
|
APN |
6 |
18,226,138 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02223:Cftr
|
APN |
6 |
18,221,481 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02249:Cftr
|
APN |
6 |
18,277,870 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02439:Cftr
|
APN |
6 |
18,258,237 (GRCm39) |
nonsense |
probably null |
|
IGL02537:Cftr
|
APN |
6 |
18,274,596 (GRCm39) |
missense |
probably benign |
0.31 |
IGL03234:Cftr
|
APN |
6 |
18,225,987 (GRCm39) |
missense |
probably damaging |
0.96 |
BB004:Cftr
|
UTSW |
6 |
18,267,970 (GRCm39) |
missense |
possibly damaging |
0.81 |
BB014:Cftr
|
UTSW |
6 |
18,267,970 (GRCm39) |
missense |
possibly damaging |
0.81 |
PIT4453001:Cftr
|
UTSW |
6 |
18,214,105 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4520001:Cftr
|
UTSW |
6 |
18,277,842 (GRCm39) |
missense |
probably benign |
0.01 |
R0114:Cftr
|
UTSW |
6 |
18,282,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R0329:Cftr
|
UTSW |
6 |
18,226,096 (GRCm39) |
missense |
probably null |
1.00 |
R0330:Cftr
|
UTSW |
6 |
18,226,096 (GRCm39) |
missense |
probably null |
1.00 |
R0331:Cftr
|
UTSW |
6 |
18,235,225 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0480:Cftr
|
UTSW |
6 |
18,274,517 (GRCm39) |
splice site |
probably benign |
|
R0612:Cftr
|
UTSW |
6 |
18,198,125 (GRCm39) |
missense |
probably benign |
0.01 |
R0633:Cftr
|
UTSW |
6 |
18,305,979 (GRCm39) |
missense |
probably damaging |
0.99 |
R1559:Cftr
|
UTSW |
6 |
18,225,936 (GRCm39) |
missense |
probably benign |
0.01 |
R1629:Cftr
|
UTSW |
6 |
18,226,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R1636:Cftr
|
UTSW |
6 |
18,226,156 (GRCm39) |
missense |
probably damaging |
0.99 |
R1860:Cftr
|
UTSW |
6 |
18,268,288 (GRCm39) |
missense |
probably benign |
0.00 |
R2043:Cftr
|
UTSW |
6 |
18,320,934 (GRCm39) |
missense |
probably benign |
|
R2211:Cftr
|
UTSW |
6 |
18,214,279 (GRCm39) |
missense |
probably null |
0.13 |
R4737:Cftr
|
UTSW |
6 |
18,299,882 (GRCm39) |
missense |
probably benign |
0.19 |
R4793:Cftr
|
UTSW |
6 |
18,226,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Cftr
|
UTSW |
6 |
18,320,974 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4984:Cftr
|
UTSW |
6 |
18,235,198 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4999:Cftr
|
UTSW |
6 |
18,221,613 (GRCm39) |
missense |
probably benign |
0.17 |
R5045:Cftr
|
UTSW |
6 |
18,230,080 (GRCm39) |
missense |
probably benign |
0.20 |
R5183:Cftr
|
UTSW |
6 |
18,299,832 (GRCm39) |
missense |
probably damaging |
0.99 |
R5197:Cftr
|
UTSW |
6 |
18,255,413 (GRCm39) |
missense |
probably benign |
0.00 |
R5288:Cftr
|
UTSW |
6 |
18,226,128 (GRCm39) |
nonsense |
probably null |
|
R5337:Cftr
|
UTSW |
6 |
18,319,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R5549:Cftr
|
UTSW |
6 |
18,227,953 (GRCm39) |
missense |
probably benign |
0.00 |
R5596:Cftr
|
UTSW |
6 |
18,268,095 (GRCm39) |
missense |
probably benign |
0.00 |
R5651:Cftr
|
UTSW |
6 |
18,255,364 (GRCm39) |
splice site |
probably null |
|
R5660:Cftr
|
UTSW |
6 |
18,313,686 (GRCm39) |
missense |
probably benign |
0.22 |
R5941:Cftr
|
UTSW |
6 |
18,313,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R6221:Cftr
|
UTSW |
6 |
18,282,500 (GRCm39) |
missense |
probably benign |
0.00 |
R6222:Cftr
|
UTSW |
6 |
18,282,500 (GRCm39) |
missense |
probably benign |
0.00 |
R6229:Cftr
|
UTSW |
6 |
18,220,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R6256:Cftr
|
UTSW |
6 |
18,274,660 (GRCm39) |
missense |
probably damaging |
0.96 |
R6257:Cftr
|
UTSW |
6 |
18,282,500 (GRCm39) |
missense |
probably benign |
0.00 |
R6412:Cftr
|
UTSW |
6 |
18,285,603 (GRCm39) |
missense |
probably damaging |
0.97 |
R6459:Cftr
|
UTSW |
6 |
18,258,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R6558:Cftr
|
UTSW |
6 |
18,222,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R6724:Cftr
|
UTSW |
6 |
18,255,973 (GRCm39) |
nonsense |
probably null |
|
R6787:Cftr
|
UTSW |
6 |
18,274,607 (GRCm39) |
nonsense |
probably null |
|
R6861:Cftr
|
UTSW |
6 |
18,268,107 (GRCm39) |
missense |
probably benign |
0.00 |
R6888:Cftr
|
UTSW |
6 |
18,313,729 (GRCm39) |
critical splice donor site |
probably null |
|
R7084:Cftr
|
UTSW |
6 |
18,226,137 (GRCm39) |
missense |
probably benign |
0.17 |
R7105:Cftr
|
UTSW |
6 |
18,318,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Cftr
|
UTSW |
6 |
18,319,012 (GRCm39) |
missense |
probably damaging |
0.97 |
R7359:Cftr
|
UTSW |
6 |
18,221,623 (GRCm39) |
missense |
probably benign |
0.00 |
R7466:Cftr
|
UTSW |
6 |
18,227,972 (GRCm39) |
missense |
probably benign |
|
R7502:Cftr
|
UTSW |
6 |
18,214,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R7748:Cftr
|
UTSW |
6 |
18,277,888 (GRCm39) |
critical splice donor site |
probably null |
|
R7808:Cftr
|
UTSW |
6 |
18,204,204 (GRCm39) |
missense |
probably benign |
|
R7817:Cftr
|
UTSW |
6 |
18,267,967 (GRCm39) |
missense |
probably damaging |
0.97 |
R7927:Cftr
|
UTSW |
6 |
18,267,970 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7968:Cftr
|
UTSW |
6 |
18,226,048 (GRCm39) |
missense |
probably benign |
0.00 |
R7995:Cftr
|
UTSW |
6 |
18,214,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Cftr
|
UTSW |
6 |
18,258,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R8210:Cftr
|
UTSW |
6 |
18,220,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8548:Cftr
|
UTSW |
6 |
18,273,698 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8712:Cftr
|
UTSW |
6 |
18,274,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R8737:Cftr
|
UTSW |
6 |
18,319,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R8926:Cftr
|
UTSW |
6 |
18,268,003 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8979:Cftr
|
UTSW |
6 |
18,227,947 (GRCm39) |
missense |
probably benign |
0.10 |
R8996:Cftr
|
UTSW |
6 |
18,255,945 (GRCm39) |
nonsense |
probably null |
|
R9087:Cftr
|
UTSW |
6 |
18,214,180 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9115:Cftr
|
UTSW |
6 |
18,235,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R9406:Cftr
|
UTSW |
6 |
18,299,866 (GRCm39) |
missense |
probably benign |
0.00 |
R9689:Cftr
|
UTSW |
6 |
18,313,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R9700:Cftr
|
UTSW |
6 |
18,268,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R9747:Cftr
|
UTSW |
6 |
18,285,636 (GRCm39) |
missense |
possibly damaging |
0.52 |
|