Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf3 |
G |
A |
5: 30,404,489 (GRCm39) |
H316Y |
possibly damaging |
Het |
Adgrf5 |
A |
G |
17: 43,739,477 (GRCm39) |
Y72C |
possibly damaging |
Het |
Ak5 |
T |
A |
3: 152,366,274 (GRCm39) |
L42F |
probably damaging |
Het |
Alas1 |
T |
C |
9: 106,118,489 (GRCm39) |
E211G |
probably damaging |
Het |
Alkbh1 |
C |
T |
12: 87,490,520 (GRCm39) |
|
probably benign |
Het |
Als2cl |
T |
C |
9: 110,714,506 (GRCm39) |
V118A |
probably benign |
Het |
Ano1 |
G |
C |
7: 144,165,127 (GRCm39) |
L641V |
probably damaging |
Het |
Arfgef1 |
C |
T |
1: 10,258,977 (GRCm39) |
|
probably null |
Het |
Atf6b |
A |
T |
17: 34,867,549 (GRCm39) |
|
probably null |
Het |
Atf7ip |
T |
G |
6: 136,586,346 (GRCm39) |
|
probably benign |
Het |
Atp2b4 |
G |
T |
1: 133,654,275 (GRCm39) |
Q777K |
probably benign |
Het |
Baz2a |
T |
A |
10: 127,949,447 (GRCm39) |
S347R |
probably damaging |
Het |
C2cd3 |
T |
C |
7: 100,104,700 (GRCm39) |
|
probably benign |
Het |
Cage1 |
A |
G |
13: 38,207,356 (GRCm39) |
V163A |
probably benign |
Het |
Cdh12 |
T |
A |
15: 21,583,826 (GRCm39) |
N555K |
probably benign |
Het |
Cenpj |
G |
A |
14: 56,801,412 (GRCm39) |
P187L |
possibly damaging |
Het |
Cep112 |
T |
A |
11: 108,410,087 (GRCm39) |
|
probably null |
Het |
Cfap54 |
A |
T |
10: 92,778,841 (GRCm39) |
|
probably benign |
Het |
Cgref1 |
T |
G |
5: 31,090,989 (GRCm39) |
D275A |
possibly damaging |
Het |
Clgn |
A |
C |
8: 84,126,607 (GRCm39) |
N103H |
probably benign |
Het |
Corin |
A |
G |
5: 72,473,394 (GRCm39) |
V905A |
possibly damaging |
Het |
Csta1 |
A |
C |
16: 35,942,692 (GRCm39) |
D72E |
probably benign |
Het |
Cul5 |
A |
T |
9: 53,578,456 (GRCm39) |
L44Q |
probably damaging |
Het |
Dmbt1 |
G |
A |
7: 130,707,900 (GRCm39) |
A1381T |
possibly damaging |
Het |
Dync1i2 |
G |
A |
2: 71,080,197 (GRCm39) |
|
probably null |
Het |
Enoph1 |
A |
G |
5: 100,207,078 (GRCm39) |
D55G |
probably damaging |
Het |
Fat4 |
T |
A |
3: 38,945,319 (GRCm39) |
M1404K |
possibly damaging |
Het |
Fhip2b |
A |
G |
14: 70,822,489 (GRCm39) |
V744A |
possibly damaging |
Het |
Foxi2 |
G |
T |
7: 135,012,406 (GRCm39) |
G98V |
probably damaging |
Het |
Galr2 |
T |
C |
11: 116,173,765 (GRCm39) |
S132P |
probably damaging |
Het |
Gcm2 |
T |
C |
13: 41,263,430 (GRCm39) |
M1V |
probably null |
Het |
Gm15446 |
C |
T |
5: 110,090,362 (GRCm39) |
H205Y |
probably damaging |
Het |
Gm21775 |
T |
A |
Y: 10,553,910 (GRCm39) |
I153N |
probably benign |
Het |
Grip1 |
A |
G |
10: 119,874,603 (GRCm39) |
K789R |
possibly damaging |
Het |
Gsk3b |
T |
A |
16: 38,008,271 (GRCm39) |
D192E |
probably benign |
Het |
Herc2 |
T |
A |
7: 55,813,645 (GRCm39) |
H2625Q |
probably damaging |
Het |
Hoxc9 |
A |
G |
15: 102,892,555 (GRCm39) |
D256G |
probably benign |
Het |
Il7 |
A |
T |
3: 7,638,975 (GRCm39) |
N130K |
probably damaging |
Het |
Irf2 |
A |
T |
8: 47,260,380 (GRCm39) |
N104I |
probably damaging |
Het |
Kat6a |
A |
G |
8: 23,429,321 (GRCm39) |
N1559D |
possibly damaging |
Het |
Kcnq4 |
G |
T |
4: 120,555,199 (GRCm39) |
F661L |
probably benign |
Het |
Kdm5b |
T |
A |
1: 134,540,952 (GRCm39) |
D681E |
probably benign |
Het |
Khdrbs1 |
T |
C |
4: 129,619,514 (GRCm39) |
E209G |
probably damaging |
Het |
Lama3 |
A |
T |
18: 12,661,390 (GRCm39) |
R2116S |
probably damaging |
Het |
Mir124-2hg |
C |
A |
3: 17,839,877 (GRCm39) |
E65* |
probably null |
Het |
Mphosph10 |
T |
A |
7: 64,026,499 (GRCm39) |
L650F |
probably damaging |
Het |
Mrpl48 |
T |
C |
7: 100,198,540 (GRCm39) |
E204G |
probably damaging |
Het |
Msl3l2 |
T |
A |
10: 55,992,040 (GRCm39) |
L255Q |
probably damaging |
Het |
Mx1 |
T |
A |
16: 97,255,379 (GRCm39) |
K225* |
probably null |
Het |
Nid1 |
A |
C |
13: 13,675,058 (GRCm39) |
H926P |
probably benign |
Het |
Nlrp9a |
T |
A |
7: 26,256,787 (GRCm39) |
I46K |
possibly damaging |
Het |
Nop2 |
T |
A |
6: 125,116,823 (GRCm39) |
M359K |
probably null |
Het |
Nox1 |
T |
C |
X: 132,995,993 (GRCm39) |
|
probably benign |
Het |
Ogdhl |
G |
A |
14: 32,054,841 (GRCm39) |
R263K |
probably damaging |
Het |
Or14c40 |
A |
T |
7: 86,313,591 (GRCm39) |
K240N |
probably damaging |
Het |
Or2y16 |
T |
A |
11: 49,335,278 (GRCm39) |
V200E |
probably damaging |
Het |
Pbsn |
T |
C |
X: 76,891,582 (GRCm39) |
K72E |
probably damaging |
Het |
Pde12 |
T |
C |
14: 26,390,035 (GRCm39) |
I225V |
probably benign |
Het |
Ppt2 |
A |
T |
17: 34,841,818 (GRCm39) |
|
probably benign |
Het |
Prl3a1 |
A |
G |
13: 27,454,127 (GRCm39) |
D35G |
probably benign |
Het |
Prss3b |
G |
A |
6: 41,009,315 (GRCm39) |
T173I |
probably benign |
Het |
Ptprk |
T |
A |
10: 28,442,599 (GRCm39) |
I893N |
probably damaging |
Het |
Ptprz1 |
T |
C |
6: 22,986,322 (GRCm39) |
|
probably benign |
Het |
Rab3c |
A |
G |
13: 110,397,050 (GRCm39) |
V72A |
probably damaging |
Het |
Rbms2 |
A |
G |
10: 127,973,387 (GRCm39) |
S251P |
probably benign |
Het |
Rfwd3 |
A |
G |
8: 112,024,127 (GRCm39) |
V65A |
probably benign |
Het |
Rps6kl1 |
T |
A |
12: 85,186,397 (GRCm39) |
Y211F |
probably benign |
Het |
Saal1 |
T |
C |
7: 46,348,880 (GRCm39) |
Q317R |
probably damaging |
Het |
Scg3 |
T |
C |
9: 75,572,998 (GRCm39) |
D311G |
probably damaging |
Het |
Sdk2 |
C |
A |
11: 113,745,158 (GRCm39) |
M712I |
probably damaging |
Het |
Serinc2 |
T |
G |
4: 130,154,578 (GRCm39) |
Y158S |
probably damaging |
Het |
Serpinb9c |
A |
T |
13: 33,340,854 (GRCm39) |
C81* |
probably null |
Het |
Sgpp2 |
T |
A |
1: 78,393,588 (GRCm39) |
L197Q |
probably damaging |
Het |
Shroom3 |
A |
T |
5: 92,831,643 (GRCm39) |
T40S |
probably damaging |
Het |
Sik1 |
A |
G |
17: 32,067,771 (GRCm39) |
S435P |
probably benign |
Het |
Slc7a3 |
A |
G |
X: 100,124,373 (GRCm39) |
V464A |
probably benign |
Het |
Snd1 |
T |
C |
6: 28,745,206 (GRCm39) |
F517S |
probably damaging |
Het |
Spata13 |
A |
C |
14: 60,997,040 (GRCm39) |
I1165L |
possibly damaging |
Het |
St8sia5 |
A |
T |
18: 77,342,459 (GRCm39) |
I390F |
probably damaging |
Het |
Stat5b |
A |
T |
11: 100,678,158 (GRCm39) |
S652T |
probably benign |
Het |
Stom |
A |
G |
2: 35,206,037 (GRCm39) |
S231P |
probably damaging |
Het |
Sult1b1 |
A |
G |
5: 87,682,892 (GRCm39) |
Y18H |
probably damaging |
Het |
Tgm4 |
T |
C |
9: 122,890,835 (GRCm39) |
I54T |
probably damaging |
Het |
Tmem176b |
G |
A |
6: 48,813,267 (GRCm39) |
T64I |
probably damaging |
Het |
Tmem87a |
A |
T |
2: 120,199,773 (GRCm39) |
I457N |
probably damaging |
Het |
Trim12c |
A |
G |
7: 103,997,398 (GRCm39) |
F53L |
possibly damaging |
Het |
Ttc6 |
T |
A |
12: 57,784,479 (GRCm39) |
D1849E |
probably benign |
Het |
Ubap2l |
A |
T |
3: 89,938,683 (GRCm39) |
|
probably benign |
Het |
Ush2a |
T |
G |
1: 188,113,746 (GRCm39) |
|
probably null |
Het |
Usp17la |
A |
C |
7: 104,510,378 (GRCm39) |
T328P |
probably damaging |
Het |
Ust |
A |
G |
10: 8,083,330 (GRCm39) |
Y349H |
probably damaging |
Het |
V1rd19 |
A |
T |
7: 23,703,259 (GRCm39) |
M242L |
probably benign |
Het |
Vmn1r33 |
T |
A |
6: 66,589,186 (GRCm39) |
M123L |
probably benign |
Het |
Vps13c |
A |
T |
9: 67,768,115 (GRCm39) |
K111N |
probably damaging |
Het |
Vwa3a |
A |
G |
7: 120,358,172 (GRCm39) |
D81G |
probably damaging |
Het |
Zfp318 |
G |
A |
17: 46,707,950 (GRCm39) |
R336Q |
probably damaging |
Het |
Zfp609 |
A |
G |
9: 65,611,716 (GRCm39) |
S416P |
possibly damaging |
Het |
|
Other mutations in Nf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00225:Nf1
|
APN |
11 |
79,286,731 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00801:Nf1
|
APN |
11 |
79,319,526 (GRCm39) |
splice site |
probably benign |
|
IGL00823:Nf1
|
APN |
11 |
79,456,343 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00945:Nf1
|
APN |
11 |
79,360,629 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00960:Nf1
|
APN |
11 |
79,335,947 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01118:Nf1
|
APN |
11 |
79,437,812 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01604:Nf1
|
APN |
11 |
79,332,535 (GRCm39) |
splice site |
probably benign |
|
IGL01637:Nf1
|
APN |
11 |
79,437,946 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01659:Nf1
|
APN |
11 |
79,450,275 (GRCm39) |
missense |
probably benign |
|
IGL01764:Nf1
|
APN |
11 |
79,275,013 (GRCm39) |
missense |
probably benign |
|
IGL01772:Nf1
|
APN |
11 |
79,281,075 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02047:Nf1
|
APN |
11 |
79,316,361 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02052:Nf1
|
APN |
11 |
79,303,553 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02071:Nf1
|
APN |
11 |
79,334,947 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02312:Nf1
|
APN |
11 |
79,335,474 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02341:Nf1
|
APN |
11 |
79,455,752 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02390:Nf1
|
APN |
11 |
79,456,761 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02390:Nf1
|
APN |
11 |
79,302,502 (GRCm39) |
splice site |
probably benign |
|
IGL02475:Nf1
|
APN |
11 |
79,426,493 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02567:Nf1
|
APN |
11 |
79,437,969 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02571:Nf1
|
APN |
11 |
79,319,453 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Nf1
|
APN |
11 |
79,335,424 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02664:Nf1
|
APN |
11 |
79,335,425 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02992:Nf1
|
APN |
11 |
79,325,759 (GRCm39) |
splice site |
probably benign |
|
IGL03006:Nf1
|
APN |
11 |
79,436,257 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03216:Nf1
|
APN |
11 |
79,455,721 (GRCm39) |
missense |
probably benign |
0.17 |
Diesel
|
UTSW |
11 |
79,447,549 (GRCm39) |
missense |
probably damaging |
0.96 |
Eyecandy
|
UTSW |
11 |
79,436,291 (GRCm39) |
missense |
probably damaging |
1.00 |
Franklin
|
UTSW |
11 |
79,364,146 (GRCm39) |
splice site |
probably null |
|
Gasoline
|
UTSW |
11 |
79,447,615 (GRCm39) |
missense |
probably benign |
0.17 |
hancock
|
UTSW |
11 |
79,427,676 (GRCm39) |
missense |
probably benign |
|
independence
|
UTSW |
11 |
79,345,136 (GRCm39) |
intron |
probably benign |
|
jackson
|
UTSW |
11 |
79,338,398 (GRCm39) |
missense |
probably damaging |
1.00 |
Jefferson
|
UTSW |
11 |
79,337,690 (GRCm39) |
missense |
probably damaging |
1.00 |
Phyletic_dwarf
|
UTSW |
11 |
79,345,015 (GRCm39) |
missense |
probably damaging |
1.00 |
responsibility
|
UTSW |
11 |
79,456,801 (GRCm39) |
missense |
probably damaging |
0.99 |
weepy
|
UTSW |
11 |
79,437,812 (GRCm39) |
missense |
probably damaging |
1.00 |
C9142:Nf1
|
UTSW |
11 |
79,447,557 (GRCm39) |
missense |
probably damaging |
0.98 |
I2289:Nf1
|
UTSW |
11 |
79,438,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Nf1
|
UTSW |
11 |
79,362,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Nf1
|
UTSW |
11 |
79,362,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R0081:Nf1
|
UTSW |
11 |
79,344,805 (GRCm39) |
splice site |
probably benign |
|
R0115:Nf1
|
UTSW |
11 |
79,359,702 (GRCm39) |
critical splice donor site |
probably null |
|
R0144:Nf1
|
UTSW |
11 |
79,437,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R0196:Nf1
|
UTSW |
11 |
79,469,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R0196:Nf1
|
UTSW |
11 |
79,359,595 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0217:Nf1
|
UTSW |
11 |
79,319,400 (GRCm39) |
splice site |
probably benign |
|
R0238:Nf1
|
UTSW |
11 |
79,309,400 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0238:Nf1
|
UTSW |
11 |
79,309,400 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0239:Nf1
|
UTSW |
11 |
79,309,400 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0239:Nf1
|
UTSW |
11 |
79,309,400 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0255:Nf1
|
UTSW |
11 |
79,299,525 (GRCm39) |
splice site |
probably null |
|
R0362:Nf1
|
UTSW |
11 |
79,427,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R0364:Nf1
|
UTSW |
11 |
79,332,783 (GRCm39) |
nonsense |
probably null |
|
R0464:Nf1
|
UTSW |
11 |
79,447,615 (GRCm39) |
missense |
probably benign |
0.17 |
R0511:Nf1
|
UTSW |
11 |
79,329,595 (GRCm39) |
missense |
probably benign |
0.01 |
R0549:Nf1
|
UTSW |
11 |
79,359,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R0585:Nf1
|
UTSW |
11 |
79,459,527 (GRCm39) |
missense |
probably damaging |
0.99 |
R0636:Nf1
|
UTSW |
11 |
79,426,529 (GRCm39) |
missense |
probably damaging |
0.99 |
R0924:Nf1
|
UTSW |
11 |
79,344,692 (GRCm39) |
missense |
probably damaging |
0.98 |
R0942:Nf1
|
UTSW |
11 |
79,329,537 (GRCm39) |
missense |
probably benign |
0.00 |
R1022:Nf1
|
UTSW |
11 |
79,437,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R1024:Nf1
|
UTSW |
11 |
79,437,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R1350:Nf1
|
UTSW |
11 |
79,303,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R1365:Nf1
|
UTSW |
11 |
79,438,711 (GRCm39) |
splice site |
probably null |
|
R1395:Nf1
|
UTSW |
11 |
79,426,809 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1467:Nf1
|
UTSW |
11 |
79,319,452 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1467:Nf1
|
UTSW |
11 |
79,319,452 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1477:Nf1
|
UTSW |
11 |
79,286,685 (GRCm39) |
nonsense |
probably null |
|
R1508:Nf1
|
UTSW |
11 |
79,331,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Nf1
|
UTSW |
11 |
79,281,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Nf1
|
UTSW |
11 |
79,331,749 (GRCm39) |
missense |
probably benign |
0.01 |
R1680:Nf1
|
UTSW |
11 |
79,441,824 (GRCm39) |
nonsense |
probably null |
|
R1704:Nf1
|
UTSW |
11 |
79,354,127 (GRCm39) |
splice site |
probably null |
|
R1707:Nf1
|
UTSW |
11 |
79,426,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1741:Nf1
|
UTSW |
11 |
79,334,757 (GRCm39) |
missense |
probably benign |
|
R1761:Nf1
|
UTSW |
11 |
79,275,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R1800:Nf1
|
UTSW |
11 |
79,444,794 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1873:Nf1
|
UTSW |
11 |
79,437,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R1966:Nf1
|
UTSW |
11 |
79,302,390 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1967:Nf1
|
UTSW |
11 |
79,303,571 (GRCm39) |
missense |
probably damaging |
0.96 |
R1970:Nf1
|
UTSW |
11 |
79,444,787 (GRCm39) |
missense |
probably benign |
0.08 |
R2105:Nf1
|
UTSW |
11 |
79,360,652 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2151:Nf1
|
UTSW |
11 |
79,338,396 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2211:Nf1
|
UTSW |
11 |
79,334,890 (GRCm39) |
missense |
probably benign |
0.39 |
R2497:Nf1
|
UTSW |
11 |
79,334,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R2899:Nf1
|
UTSW |
11 |
79,303,584 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3086:Nf1
|
UTSW |
11 |
79,437,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R3120:Nf1
|
UTSW |
11 |
79,455,725 (GRCm39) |
missense |
probably damaging |
0.99 |
R3744:Nf1
|
UTSW |
11 |
79,439,573 (GRCm39) |
missense |
probably benign |
0.23 |
R3801:Nf1
|
UTSW |
11 |
79,450,347 (GRCm39) |
missense |
probably null |
0.98 |
R3804:Nf1
|
UTSW |
11 |
79,450,347 (GRCm39) |
missense |
probably null |
0.98 |
R4212:Nf1
|
UTSW |
11 |
79,360,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R4298:Nf1
|
UTSW |
11 |
79,275,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R4578:Nf1
|
UTSW |
11 |
79,336,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R4579:Nf1
|
UTSW |
11 |
79,359,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R4587:Nf1
|
UTSW |
11 |
79,426,863 (GRCm39) |
critical splice donor site |
probably null |
|
R4793:Nf1
|
UTSW |
11 |
79,338,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Nf1
|
UTSW |
11 |
79,437,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R4863:Nf1
|
UTSW |
11 |
79,300,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Nf1
|
UTSW |
11 |
79,456,379 (GRCm39) |
critical splice donor site |
probably null |
|
R4971:Nf1
|
UTSW |
11 |
79,335,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R5034:Nf1
|
UTSW |
11 |
79,334,976 (GRCm39) |
missense |
probably damaging |
0.98 |
R5036:Nf1
|
UTSW |
11 |
79,337,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5207:Nf1
|
UTSW |
11 |
79,345,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R5348:Nf1
|
UTSW |
11 |
79,455,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Nf1
|
UTSW |
11 |
79,364,282 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5444:Nf1
|
UTSW |
11 |
79,334,785 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5533:Nf1
|
UTSW |
11 |
79,336,615 (GRCm39) |
missense |
probably damaging |
0.99 |
R5918:Nf1
|
UTSW |
11 |
79,460,048 (GRCm39) |
intron |
probably benign |
|
R5978:Nf1
|
UTSW |
11 |
79,431,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R6140:Nf1
|
UTSW |
11 |
79,364,146 (GRCm39) |
splice site |
probably null |
|
R6195:Nf1
|
UTSW |
11 |
79,456,801 (GRCm39) |
missense |
probably damaging |
0.99 |
R6216:Nf1
|
UTSW |
11 |
79,302,433 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6233:Nf1
|
UTSW |
11 |
79,456,801 (GRCm39) |
missense |
probably damaging |
0.99 |
R6257:Nf1
|
UTSW |
11 |
79,440,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R6258:Nf1
|
UTSW |
11 |
79,456,581 (GRCm39) |
splice site |
probably null |
|
R6756:Nf1
|
UTSW |
11 |
79,335,413 (GRCm39) |
splice site |
probably null |
|
R6878:Nf1
|
UTSW |
11 |
79,325,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R6959:Nf1
|
UTSW |
11 |
79,440,294 (GRCm39) |
missense |
probably damaging |
0.98 |
R7007:Nf1
|
UTSW |
11 |
79,337,849 (GRCm39) |
splice site |
probably null |
|
R7066:Nf1
|
UTSW |
11 |
79,447,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R7099:Nf1
|
UTSW |
11 |
79,461,156 (GRCm39) |
missense |
probably benign |
0.08 |
R7213:Nf1
|
UTSW |
11 |
79,360,645 (GRCm39) |
missense |
probably benign |
0.23 |
R7326:Nf1
|
UTSW |
11 |
79,455,769 (GRCm39) |
missense |
probably benign |
|
R7348:Nf1
|
UTSW |
11 |
79,427,676 (GRCm39) |
missense |
probably benign |
|
R7380:Nf1
|
UTSW |
11 |
79,437,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R7407:Nf1
|
UTSW |
11 |
79,338,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7412:Nf1
|
UTSW |
11 |
79,364,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R7545:Nf1
|
UTSW |
11 |
79,300,350 (GRCm39) |
missense |
probably benign |
|
R7567:Nf1
|
UTSW |
11 |
79,438,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R7574:Nf1
|
UTSW |
11 |
79,299,595 (GRCm39) |
missense |
probably null |
0.99 |
R7616:Nf1
|
UTSW |
11 |
79,275,092 (GRCm39) |
missense |
probably damaging |
0.97 |
R7713:Nf1
|
UTSW |
11 |
79,316,432 (GRCm39) |
missense |
probably benign |
|
R7737:Nf1
|
UTSW |
11 |
79,436,314 (GRCm39) |
missense |
probably benign |
0.33 |
R7869:Nf1
|
UTSW |
11 |
79,309,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R7905:Nf1
|
UTSW |
11 |
79,437,938 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8232:Nf1
|
UTSW |
11 |
79,469,157 (GRCm39) |
missense |
probably damaging |
0.96 |
R8244:Nf1
|
UTSW |
11 |
79,331,750 (GRCm39) |
missense |
probably benign |
|
R8397:Nf1
|
UTSW |
11 |
79,438,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R8436:Nf1
|
UTSW |
11 |
79,349,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R8492:Nf1
|
UTSW |
11 |
79,299,248 (GRCm39) |
missense |
probably benign |
0.06 |
R8719:Nf1
|
UTSW |
11 |
79,281,119 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8735:Nf1
|
UTSW |
11 |
79,345,136 (GRCm39) |
intron |
probably benign |
|
R8795:Nf1
|
UTSW |
11 |
79,316,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R8797:Nf1
|
UTSW |
11 |
79,366,711 (GRCm39) |
critical splice donor site |
probably benign |
|
R8809:Nf1
|
UTSW |
11 |
79,437,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R8812:Nf1
|
UTSW |
11 |
79,437,180 (GRCm39) |
missense |
probably damaging |
0.96 |
R8815:Nf1
|
UTSW |
11 |
79,332,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R8828:Nf1
|
UTSW |
11 |
79,286,679 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8894:Nf1
|
UTSW |
11 |
79,336,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Nf1
|
UTSW |
11 |
79,364,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R9103:Nf1
|
UTSW |
11 |
79,450,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R9142:Nf1
|
UTSW |
11 |
79,366,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R9142:Nf1
|
UTSW |
11 |
79,362,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R9170:Nf1
|
UTSW |
11 |
79,436,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R9201:Nf1
|
UTSW |
11 |
79,461,156 (GRCm39) |
missense |
probably benign |
0.08 |
R9267:Nf1
|
UTSW |
11 |
79,331,716 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9309:Nf1
|
UTSW |
11 |
79,359,595 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9340:Nf1
|
UTSW |
11 |
79,447,629 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9398:Nf1
|
UTSW |
11 |
79,438,018 (GRCm39) |
missense |
probably damaging |
0.99 |
R9471:Nf1
|
UTSW |
11 |
79,436,195 (GRCm39) |
missense |
probably damaging |
0.99 |
R9630:Nf1
|
UTSW |
11 |
79,302,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R9664:Nf1
|
UTSW |
11 |
79,334,733 (GRCm39) |
missense |
probably damaging |
1.00 |
X0052:Nf1
|
UTSW |
11 |
79,450,242 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Nf1
|
UTSW |
11 |
79,455,751 (GRCm39) |
missense |
probably benign |
0.00 |
|