Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank1 |
T |
A |
8: 23,586,200 (GRCm39) |
N427K |
probably damaging |
Het |
Ano10 |
C |
T |
9: 122,090,408 (GRCm39) |
E302K |
probably damaging |
Het |
Arl3 |
T |
A |
19: 46,530,785 (GRCm39) |
|
probably benign |
Het |
Clec14a |
T |
A |
12: 58,314,934 (GRCm39) |
E229D |
probably benign |
Het |
Ctbp1 |
T |
C |
5: 33,424,312 (GRCm39) |
D26G |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,848,382 (GRCm39) |
D1799G |
probably benign |
Het |
Il20ra |
G |
A |
10: 19,635,253 (GRCm39) |
G498D |
possibly damaging |
Het |
Kcnu1 |
T |
G |
8: 26,427,727 (GRCm39) |
L348R |
possibly damaging |
Het |
Lrpprc |
A |
T |
17: 85,033,998 (GRCm39) |
L999* |
probably null |
Het |
Myt1 |
T |
G |
2: 181,457,410 (GRCm39) |
|
probably benign |
Het |
N4bp2 |
C |
T |
5: 65,955,477 (GRCm39) |
T467M |
probably damaging |
Het |
Nup98 |
T |
C |
7: 101,832,693 (GRCm39) |
T355A |
probably benign |
Het |
Ocstamp |
A |
T |
2: 165,239,256 (GRCm39) |
V310E |
possibly damaging |
Het |
Or4k39 |
T |
G |
2: 111,238,838 (GRCm39) |
|
noncoding transcript |
Het |
Or8b3 |
T |
C |
9: 38,314,382 (GRCm39) |
F71L |
possibly damaging |
Het |
Plcb1 |
C |
A |
2: 134,628,479 (GRCm39) |
H9Q |
probably damaging |
Het |
Plxna4 |
T |
A |
6: 32,192,576 (GRCm39) |
Q795L |
probably benign |
Het |
Pms1 |
A |
G |
1: 53,246,568 (GRCm39) |
S324P |
probably damaging |
Het |
Pnldc1 |
G |
T |
17: 13,124,425 (GRCm39) |
H143Q |
probably benign |
Het |
Ppp1r12b |
A |
G |
1: 134,800,543 (GRCm39) |
|
probably null |
Het |
Ryr3 |
A |
G |
2: 112,779,502 (GRCm39) |
F250L |
probably benign |
Het |
Scgn |
T |
C |
13: 24,137,948 (GRCm39) |
D241G |
possibly damaging |
Het |
St8sia4 |
T |
C |
1: 95,588,617 (GRCm39) |
I73V |
possibly damaging |
Het |
Tle3 |
T |
A |
9: 61,320,332 (GRCm39) |
C595S |
probably damaging |
Het |
Tmem209 |
T |
C |
6: 30,497,944 (GRCm39) |
Y117C |
probably damaging |
Het |
Tshr |
T |
A |
12: 91,504,766 (GRCm39) |
I568N |
probably damaging |
Het |
Ttll10 |
C |
T |
4: 156,131,937 (GRCm39) |
D22N |
probably benign |
Het |
Ttn |
A |
T |
2: 76,640,202 (GRCm39) |
V13802E |
probably damaging |
Het |
|
Other mutations in Flt3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Flt3
|
APN |
5 |
147,291,686 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01083:Flt3
|
APN |
5 |
147,291,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01749:Flt3
|
APN |
5 |
147,294,838 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01765:Flt3
|
APN |
5 |
147,294,788 (GRCm39) |
missense |
probably benign |
|
IGL02490:Flt3
|
APN |
5 |
147,268,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02631:Flt3
|
APN |
5 |
147,281,362 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03117:Flt3
|
APN |
5 |
147,293,020 (GRCm39) |
missense |
probably benign |
|
flick
|
UTSW |
5 |
147,278,048 (GRCm39) |
missense |
probably damaging |
1.00 |
warmflash
|
UTSW |
5 |
147,303,728 (GRCm39) |
critical splice donor site |
probably null |
|
R0070:Flt3
|
UTSW |
5 |
147,309,536 (GRCm39) |
splice site |
probably benign |
|
R0070:Flt3
|
UTSW |
5 |
147,309,536 (GRCm39) |
splice site |
probably benign |
|
R0320:Flt3
|
UTSW |
5 |
147,306,389 (GRCm39) |
splice site |
probably benign |
|
R0347:Flt3
|
UTSW |
5 |
147,294,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R0512:Flt3
|
UTSW |
5 |
147,278,080 (GRCm39) |
nonsense |
probably null |
|
R0968:Flt3
|
UTSW |
5 |
147,278,037 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1180:Flt3
|
UTSW |
5 |
147,278,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R1266:Flt3
|
UTSW |
5 |
147,293,670 (GRCm39) |
missense |
probably benign |
0.00 |
R1562:Flt3
|
UTSW |
5 |
147,281,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Flt3
|
UTSW |
5 |
147,303,865 (GRCm39) |
nonsense |
probably null |
|
R2000:Flt3
|
UTSW |
5 |
147,278,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R2021:Flt3
|
UTSW |
5 |
147,306,300 (GRCm39) |
missense |
probably damaging |
0.98 |
R2079:Flt3
|
UTSW |
5 |
147,291,893 (GRCm39) |
missense |
probably damaging |
0.97 |
R2261:Flt3
|
UTSW |
5 |
147,284,873 (GRCm39) |
missense |
probably benign |
0.00 |
R2263:Flt3
|
UTSW |
5 |
147,284,873 (GRCm39) |
missense |
probably benign |
0.00 |
R3087:Flt3
|
UTSW |
5 |
147,284,856 (GRCm39) |
missense |
probably benign |
0.15 |
R3727:Flt3
|
UTSW |
5 |
147,291,733 (GRCm39) |
missense |
probably damaging |
0.96 |
R3939:Flt3
|
UTSW |
5 |
147,293,053 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4469:Flt3
|
UTSW |
5 |
147,312,454 (GRCm39) |
splice site |
silent |
|
R4527:Flt3
|
UTSW |
5 |
147,293,163 (GRCm39) |
missense |
probably benign |
0.37 |
R4592:Flt3
|
UTSW |
5 |
147,291,509 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4655:Flt3
|
UTSW |
5 |
147,286,403 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4686:Flt3
|
UTSW |
5 |
147,313,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R4867:Flt3
|
UTSW |
5 |
147,271,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4897:Flt3
|
UTSW |
5 |
147,306,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R4941:Flt3
|
UTSW |
5 |
147,293,185 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5254:Flt3
|
UTSW |
5 |
147,312,500 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5325:Flt3
|
UTSW |
5 |
147,312,459 (GRCm39) |
missense |
probably benign |
0.00 |
R5395:Flt3
|
UTSW |
5 |
147,291,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R5445:Flt3
|
UTSW |
5 |
147,291,905 (GRCm39) |
nonsense |
probably null |
|
R5469:Flt3
|
UTSW |
5 |
147,291,893 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5556:Flt3
|
UTSW |
5 |
147,269,807 (GRCm39) |
splice site |
probably null |
|
R5660:Flt3
|
UTSW |
5 |
147,306,291 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5879:Flt3
|
UTSW |
5 |
147,271,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R5885:Flt3
|
UTSW |
5 |
147,286,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R6554:Flt3
|
UTSW |
5 |
147,312,545 (GRCm39) |
missense |
probably damaging |
0.99 |
R6813:Flt3
|
UTSW |
5 |
147,291,653 (GRCm39) |
missense |
probably damaging |
0.97 |
R7451:Flt3
|
UTSW |
5 |
147,286,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R7469:Flt3
|
UTSW |
5 |
147,268,084 (GRCm39) |
missense |
probably benign |
0.18 |
R7537:Flt3
|
UTSW |
5 |
147,271,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R7605:Flt3
|
UTSW |
5 |
147,286,386 (GRCm39) |
missense |
probably benign |
0.01 |
R7651:Flt3
|
UTSW |
5 |
147,291,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Flt3
|
UTSW |
5 |
147,271,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R8051:Flt3
|
UTSW |
5 |
147,295,765 (GRCm39) |
intron |
probably benign |
|
R8236:Flt3
|
UTSW |
5 |
147,293,670 (GRCm39) |
missense |
probably benign |
0.00 |
R8305:Flt3
|
UTSW |
5 |
147,284,864 (GRCm39) |
missense |
probably damaging |
0.96 |
R8337:Flt3
|
UTSW |
5 |
147,269,698 (GRCm39) |
critical splice donor site |
probably null |
|
R8680:Flt3
|
UTSW |
5 |
147,320,265 (GRCm39) |
missense |
probably benign |
0.13 |
R8682:Flt3
|
UTSW |
5 |
147,320,265 (GRCm39) |
missense |
probably benign |
0.13 |
R8697:Flt3
|
UTSW |
5 |
147,294,811 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8824:Flt3
|
UTSW |
5 |
147,271,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R8959:Flt3
|
UTSW |
5 |
147,303,774 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9235:Flt3
|
UTSW |
5 |
147,320,202 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9324:Flt3
|
UTSW |
5 |
147,313,790 (GRCm39) |
missense |
probably benign |
0.27 |
R9544:Flt3
|
UTSW |
5 |
147,291,442 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9570:Flt3
|
UTSW |
5 |
147,309,424 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9622:Flt3
|
UTSW |
5 |
147,303,841 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9668:Flt3
|
UTSW |
5 |
147,293,694 (GRCm39) |
missense |
probably benign |
0.13 |
X0018:Flt3
|
UTSW |
5 |
147,303,876 (GRCm39) |
missense |
possibly damaging |
0.54 |
Z1088:Flt3
|
UTSW |
5 |
147,286,374 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Flt3
|
UTSW |
5 |
147,320,211 (GRCm39) |
missense |
probably benign |
0.27 |
Z31818:Flt3
|
UTSW |
5 |
147,303,728 (GRCm39) |
critical splice donor site |
probably null |
|
|