Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
C |
T |
16: 8,400,676 (GRCm39) |
R92C |
probably damaging |
Het |
Adam29 |
C |
A |
8: 56,324,589 (GRCm39) |
V622L |
possibly damaging |
Het |
Bzw2 |
T |
C |
12: 36,157,502 (GRCm39) |
H321R |
probably benign |
Het |
C2cd2 |
C |
T |
16: 97,671,432 (GRCm39) |
R489Q |
probably damaging |
Het |
Cdh23 |
G |
A |
10: 60,359,339 (GRCm39) |
T253I |
possibly damaging |
Het |
Col4a3 |
T |
G |
1: 82,638,608 (GRCm39) |
|
probably null |
Het |
D630039A03Rik |
T |
C |
4: 57,910,309 (GRCm39) |
T168A |
possibly damaging |
Het |
Dnajc19 |
A |
G |
3: 34,132,914 (GRCm39) |
L97P |
possibly damaging |
Het |
Dpep2 |
A |
T |
8: 106,711,776 (GRCm39) |
H550Q |
probably benign |
Het |
Dvl2 |
C |
A |
11: 69,895,626 (GRCm39) |
|
probably null |
Het |
Fam234b |
A |
G |
6: 135,204,149 (GRCm39) |
|
probably null |
Het |
Fxyd5 |
A |
G |
7: 30,739,613 (GRCm39) |
V32A |
possibly damaging |
Het |
Itprid1 |
C |
A |
6: 55,944,710 (GRCm39) |
S477* |
probably null |
Het |
Mak16 |
A |
T |
8: 31,650,557 (GRCm39) |
S251T |
probably benign |
Het |
Med10 |
T |
C |
13: 69,963,747 (GRCm39) |
V116A |
probably benign |
Het |
Mycbp2 |
G |
A |
14: 103,392,343 (GRCm39) |
R50* |
probably null |
Het |
Nckap5 |
G |
A |
1: 125,909,305 (GRCm39) |
P272L |
probably damaging |
Het |
Nrxn2 |
T |
A |
19: 6,531,783 (GRCm39) |
V749E |
probably damaging |
Het |
Or51e2 |
A |
C |
7: 102,391,355 (GRCm39) |
V285G |
probably damaging |
Het |
Or5al1 |
C |
A |
2: 85,990,219 (GRCm39) |
R165L |
probably benign |
Het |
Osbpl9 |
T |
C |
4: 108,929,176 (GRCm39) |
Y417C |
probably damaging |
Het |
Otop1 |
G |
A |
5: 38,445,327 (GRCm39) |
A162T |
probably damaging |
Het |
Patl1 |
C |
A |
19: 11,917,054 (GRCm39) |
P634T |
probably damaging |
Het |
Ppl |
A |
T |
16: 4,930,936 (GRCm39) |
S28T |
probably benign |
Het |
Prkar2b |
C |
T |
12: 32,013,016 (GRCm39) |
G367R |
probably damaging |
Het |
Rbl2 |
G |
A |
8: 91,828,826 (GRCm39) |
V576I |
probably damaging |
Het |
Rgl3 |
C |
T |
9: 21,899,559 (GRCm39) |
A53T |
probably benign |
Het |
Rp1 |
T |
A |
1: 4,415,533 (GRCm39) |
I1860F |
possibly damaging |
Het |
Sbno2 |
A |
T |
10: 79,896,475 (GRCm39) |
D877E |
probably damaging |
Het |
Sectm1b |
C |
T |
11: 120,946,761 (GRCm39) |
V45I |
probably damaging |
Het |
Sfmbt2 |
G |
A |
2: 10,582,763 (GRCm39) |
V741I |
probably benign |
Het |
Sugt1 |
T |
A |
14: 79,847,723 (GRCm39) |
L191* |
probably null |
Het |
Tcf21 |
A |
T |
10: 22,693,709 (GRCm39) |
V156E |
possibly damaging |
Het |
Tep1 |
T |
A |
14: 51,071,506 (GRCm39) |
R2046S |
possibly damaging |
Het |
Tmem181a |
T |
C |
17: 6,347,531 (GRCm39) |
F241S |
probably damaging |
Het |
Traf6 |
G |
A |
2: 101,527,138 (GRCm39) |
C296Y |
probably benign |
Het |
Trim40 |
A |
G |
17: 37,200,070 (GRCm39) |
S3P |
probably benign |
Het |
Ttll2 |
A |
T |
17: 7,619,130 (GRCm39) |
Y266N |
probably damaging |
Het |
Vps54 |
A |
G |
11: 21,225,071 (GRCm39) |
N177S |
probably null |
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 |
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 |
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 |
|