Other mutations in this stock |
Total: 18 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,135,050 (GRCm39) |
E245G |
probably damaging |
Het |
Bach2 |
A |
G |
4: 32,580,261 (GRCm39) |
T829A |
probably damaging |
Het |
Car1 |
T |
A |
3: 14,832,519 (GRCm39) |
H205L |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,225,807 (GRCm39) |
T3094A |
probably benign |
Het |
Dctn2 |
G |
A |
10: 127,117,286 (GRCm39) |
R380H |
possibly damaging |
Het |
Gm5263 |
T |
G |
1: 146,296,302 (GRCm39) |
|
noncoding transcript |
Het |
Hook2 |
T |
C |
8: 85,719,865 (GRCm39) |
|
probably null |
Het |
Iqsec1 |
G |
A |
6: 90,657,486 (GRCm39) |
R571C |
probably benign |
Het |
Lig3 |
T |
G |
11: 82,680,693 (GRCm39) |
L421R |
probably damaging |
Het |
Mtcl2 |
G |
T |
2: 156,863,461 (GRCm39) |
|
probably benign |
Het |
Nipbl |
A |
G |
15: 8,391,305 (GRCm39) |
V223A |
probably benign |
Het |
Or2n1 |
G |
T |
17: 38,486,577 (GRCm39) |
V201L |
probably benign |
Het |
Or2y12 |
A |
T |
11: 49,426,944 (GRCm39) |
R311W |
probably damaging |
Het |
Or8b48 |
C |
T |
9: 38,492,809 (GRCm39) |
P79S |
probably damaging |
Het |
Reln |
C |
A |
5: 22,549,244 (GRCm39) |
E55* |
probably null |
Het |
Tlr1 |
A |
T |
5: 65,083,290 (GRCm39) |
L429* |
probably null |
Het |
Ttc22 |
A |
G |
4: 106,495,800 (GRCm39) |
T385A |
probably benign |
Het |
Vmn1r48 |
A |
G |
6: 90,012,934 (GRCm39) |
V297A |
possibly 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 |
IGL01765:Flt3
|
APN |
5 |
147,294,788 (GRCm39) |
missense |
probably benign |
|
IGL02109:Flt3
|
APN |
5 |
147,287,491 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|
|