Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
G |
A |
1: 71,353,273 (GRCm39) |
S723F |
probably damaging |
Het |
Cacng5 |
C |
T |
11: 107,772,531 (GRCm39) |
V106I |
probably benign |
Het |
Ccdc116 |
A |
G |
16: 16,959,856 (GRCm39) |
S278P |
probably damaging |
Het |
Cep152 |
A |
T |
2: 125,411,465 (GRCm39) |
|
probably benign |
Het |
Dsc2 |
A |
T |
18: 20,176,849 (GRCm39) |
N399K |
probably damaging |
Het |
Eif3d |
T |
C |
15: 77,843,943 (GRCm39) |
T468A |
probably damaging |
Het |
Fam110b |
C |
T |
4: 5,799,461 (GRCm39) |
A293V |
possibly damaging |
Het |
Flrt1 |
T |
C |
19: 7,073,339 (GRCm39) |
T403A |
probably benign |
Het |
H3c6 |
A |
G |
13: 23,746,548 (GRCm39) |
|
probably benign |
Het |
Ift140 |
T |
A |
17: 25,267,429 (GRCm39) |
V609E |
possibly damaging |
Het |
Klb |
G |
A |
5: 65,533,283 (GRCm39) |
V531I |
possibly damaging |
Het |
Krt73 |
T |
C |
15: 101,707,372 (GRCm39) |
|
probably null |
Het |
Mcm2 |
A |
G |
6: 88,864,859 (GRCm39) |
V539A |
probably benign |
Het |
Myb |
A |
G |
10: 21,028,843 (GRCm39) |
V85A |
probably damaging |
Het |
Ndufs1 |
T |
C |
1: 63,203,976 (GRCm39) |
E102G |
probably damaging |
Het |
Nr5a2 |
C |
A |
1: 136,773,206 (GRCm39) |
A499S |
probably benign |
Het |
Opa1 |
A |
T |
16: 29,436,933 (GRCm39) |
|
probably benign |
Het |
Or14j5 |
T |
A |
17: 38,161,514 (GRCm39) |
S10R |
probably benign |
Het |
Or4a47 |
A |
T |
2: 89,674,407 (GRCm39) |
|
probably benign |
Het |
Or4c11b |
T |
C |
2: 88,625,637 (GRCm39) |
F304L |
probably benign |
Het |
Pcnx1 |
G |
A |
12: 82,037,372 (GRCm39) |
E1877K |
possibly damaging |
Het |
Sel1l |
A |
G |
12: 91,778,682 (GRCm39) |
V711A |
probably benign |
Het |
Slc22a16 |
A |
G |
10: 40,449,860 (GRCm39) |
T120A |
probably benign |
Het |
Slc26a1 |
G |
T |
5: 108,819,744 (GRCm39) |
T485N |
possibly damaging |
Het |
Sp100 |
T |
C |
1: 85,597,741 (GRCm39) |
V201A |
possibly damaging |
Het |
Spz1 |
T |
G |
13: 92,712,029 (GRCm39) |
K149T |
probably damaging |
Het |
Stxbp5l |
A |
G |
16: 37,024,940 (GRCm39) |
S553P |
possibly damaging |
Het |
Szt2 |
A |
G |
4: 118,254,821 (GRCm39) |
S290P |
probably damaging |
Het |
Tbc1d10c |
A |
G |
19: 4,239,026 (GRCm39) |
Y165H |
probably damaging |
Het |
Tnxb |
C |
A |
17: 34,933,584 (GRCm39) |
Q2335K |
probably damaging |
Het |
Trim33 |
T |
C |
3: 103,234,175 (GRCm39) |
I471T |
possibly damaging |
Het |
Vsig10 |
A |
G |
5: 117,472,970 (GRCm39) |
I188V |
probably benign |
Het |
Zfp109 |
A |
T |
7: 23,933,784 (GRCm39) |
L45Q |
probably 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 |
|
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 |
R0830:Cftr
|
UTSW |
6 |
18,270,224 (GRCm39) |
missense |
probably benign |
0.02 |
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 |
|