Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
A |
G |
8: 25,118,171 (GRCm39) |
S34P |
probably damaging |
Het |
Adam23 |
T |
A |
1: 63,612,288 (GRCm39) |
|
probably benign |
Het |
Adcy10 |
A |
T |
1: 165,345,781 (GRCm39) |
I277F |
probably damaging |
Het |
Arfgef3 |
A |
T |
10: 18,467,993 (GRCm39) |
S1736T |
possibly damaging |
Het |
Arhgap21 |
A |
T |
2: 20,886,451 (GRCm39) |
M242K |
possibly damaging |
Het |
Arhgef18 |
T |
C |
8: 3,437,680 (GRCm39) |
S268P |
possibly damaging |
Het |
Astn1 |
A |
G |
1: 158,484,876 (GRCm39) |
R4G |
probably benign |
Het |
AU041133 |
G |
A |
10: 81,986,755 (GRCm39) |
C135Y |
probably damaging |
Het |
Cdc42bpb |
A |
G |
12: 111,268,288 (GRCm39) |
V53A |
probably benign |
Het |
Cdh23 |
T |
C |
10: 60,301,783 (GRCm39) |
D428G |
possibly damaging |
Het |
Cebpa |
T |
C |
7: 34,819,891 (GRCm39) |
S350P |
probably damaging |
Het |
Cftr |
A |
G |
6: 18,214,279 (GRCm39) |
M152V |
probably null |
Het |
Cpa4 |
A |
G |
6: 30,583,649 (GRCm39) |
N255S |
possibly damaging |
Het |
Ddx51 |
T |
A |
5: 110,803,634 (GRCm39) |
D343E |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,518,932 (GRCm39) |
I2942V |
probably benign |
Het |
Dnajc1 |
G |
T |
2: 18,397,286 (GRCm39) |
A9E |
probably damaging |
Het |
Dpysl5 |
G |
A |
5: 30,948,941 (GRCm39) |
D399N |
probably damaging |
Het |
Edem3 |
A |
G |
1: 151,680,453 (GRCm39) |
D526G |
possibly damaging |
Het |
Emc10 |
G |
A |
7: 44,142,616 (GRCm39) |
R109W |
probably damaging |
Het |
Etaa1 |
G |
A |
11: 17,902,686 (GRCm39) |
Q84* |
probably null |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fam149a |
G |
A |
8: 45,794,046 (GRCm39) |
T674I |
probably damaging |
Het |
Fam98a |
A |
G |
17: 75,845,940 (GRCm39) |
|
probably null |
Het |
Fat4 |
A |
G |
3: 38,945,676 (GRCm39) |
N1523S |
possibly damaging |
Het |
Fbxw10 |
A |
G |
11: 62,758,361 (GRCm39) |
T529A |
probably damaging |
Het |
Gzf1 |
C |
T |
2: 148,526,870 (GRCm39) |
A447V |
probably damaging |
Het |
Hap1 |
G |
A |
11: 100,245,550 (GRCm39) |
T138M |
probably benign |
Het |
Hic1 |
T |
A |
11: 75,060,210 (GRCm39) |
R46W |
possibly damaging |
Het |
Id4 |
T |
A |
13: 48,415,278 (GRCm39) |
L102Q |
probably damaging |
Het |
Il3ra |
T |
C |
14: 14,355,029 (GRCm38) |
C271R |
probably benign |
Het |
Ints4 |
T |
C |
7: 97,158,957 (GRCm39) |
I443T |
possibly damaging |
Het |
Lmln |
A |
G |
16: 32,930,148 (GRCm39) |
E535G |
probably benign |
Het |
Lrrtm4 |
A |
G |
6: 79,999,623 (GRCm39) |
H345R |
probably benign |
Het |
Ltbp3 |
T |
C |
19: 5,803,990 (GRCm39) |
I834T |
possibly damaging |
Het |
Mnd1 |
C |
A |
3: 84,041,416 (GRCm39) |
C62F |
probably benign |
Het |
Ms4a18 |
C |
A |
19: 10,974,669 (GRCm39) |
V341L |
probably benign |
Het |
Nbr1 |
T |
C |
11: 101,458,090 (GRCm39) |
|
probably null |
Het |
Notch3 |
T |
A |
17: 32,366,952 (GRCm39) |
H861L |
probably benign |
Het |
Nup58 |
A |
G |
14: 60,470,089 (GRCm39) |
F341L |
probably damaging |
Het |
Ogfod2 |
C |
A |
5: 124,250,843 (GRCm39) |
|
probably null |
Het |
Oit3 |
T |
C |
10: 59,263,892 (GRCm39) |
D414G |
probably damaging |
Het |
Or6c5c |
A |
T |
10: 129,298,809 (GRCm39) |
K88M |
probably damaging |
Het |
Or6c6c |
A |
G |
10: 129,541,320 (GRCm39) |
H191R |
probably benign |
Het |
Or8k32 |
T |
C |
2: 86,368,857 (GRCm39) |
Y132C |
probably damaging |
Het |
Or9q2 |
T |
A |
19: 13,772,733 (GRCm39) |
M81L |
probably benign |
Het |
Pals1 |
A |
T |
12: 78,844,022 (GRCm39) |
K75N |
possibly damaging |
Het |
Pcbp4 |
C |
A |
9: 106,337,933 (GRCm39) |
H74Q |
probably benign |
Het |
Pip5k1b |
A |
T |
19: 24,356,214 (GRCm39) |
D241E |
probably damaging |
Het |
Plcb2 |
T |
C |
2: 118,554,015 (GRCm39) |
D102G |
probably benign |
Het |
Plekha5 |
G |
A |
6: 140,471,587 (GRCm39) |
E4K |
possibly damaging |
Het |
Ppargc1a |
A |
C |
5: 51,631,601 (GRCm39) |
S343A |
possibly damaging |
Het |
Ppwd1 |
G |
A |
13: 104,343,650 (GRCm39) |
S585L |
probably benign |
Het |
Rarg |
T |
C |
15: 102,147,959 (GRCm39) |
N284S |
probably benign |
Het |
Rnpepl1 |
C |
T |
1: 92,844,102 (GRCm39) |
L278F |
probably damaging |
Het |
Rp1 |
A |
C |
1: 4,418,362 (GRCm39) |
S917A |
probably damaging |
Het |
Rsf1 |
ATGGCG |
ATGGCGAGGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Rsph3b |
T |
C |
17: 7,209,139 (GRCm39) |
S189G |
probably benign |
Het |
Sec31b |
A |
T |
19: 44,511,589 (GRCm39) |
L604Q |
probably damaging |
Het |
Sema6b |
T |
A |
17: 56,431,741 (GRCm39) |
I641F |
probably benign |
Het |
Slc35f5 |
A |
T |
1: 125,507,001 (GRCm39) |
I309F |
possibly damaging |
Het |
Smarca4 |
A |
G |
9: 21,597,325 (GRCm39) |
E1360G |
probably damaging |
Het |
Spata31d1c |
T |
C |
13: 65,183,753 (GRCm39) |
S432P |
probably benign |
Het |
Spsb3 |
T |
C |
17: 25,109,911 (GRCm39) |
|
probably null |
Het |
Sptbn4 |
T |
C |
7: 27,067,034 (GRCm39) |
D1960G |
probably damaging |
Het |
Srgap1 |
A |
G |
10: 121,689,645 (GRCm39) |
V345A |
possibly damaging |
Het |
Tiam2 |
C |
A |
17: 3,465,193 (GRCm39) |
C307* |
probably null |
Het |
Trim43b |
T |
A |
9: 88,967,302 (GRCm39) |
T444S |
possibly damaging |
Het |
Trmt13 |
A |
G |
3: 116,388,403 (GRCm39) |
I11T |
probably benign |
Het |
Ylpm1 |
A |
T |
12: 85,091,152 (GRCm39) |
R1073* |
probably null |
Het |
Zfp524 |
T |
C |
7: 5,020,918 (GRCm39) |
S149P |
probably damaging |
Het |
Zfp777 |
T |
C |
6: 48,020,819 (GRCm39) |
I312V |
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 |
R2059:Nf1
|
UTSW |
11 |
79,447,549 (GRCm39) |
missense |
probably damaging |
0.96 |
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 |
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 |
|