Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700066M21Rik |
A |
T |
1: 57,421,943 (GRCm39) |
Q106H |
probably damaging |
Het |
Acad9 |
T |
C |
3: 36,139,590 (GRCm39) |
C397R |
probably damaging |
Het |
Ankfn1 |
T |
G |
11: 89,282,602 (GRCm39) |
R348S |
probably damaging |
Het |
Ankrd61 |
A |
G |
5: 143,831,336 (GRCm39) |
C28R |
probably benign |
Het |
Ano5 |
C |
T |
7: 51,194,548 (GRCm39) |
R94* |
probably null |
Het |
Apela |
A |
T |
8: 65,489,590 (GRCm39) |
F10I |
unknown |
Het |
Arhgap31 |
T |
C |
16: 38,429,790 (GRCm39) |
S362G |
probably benign |
Het |
Arhgef18 |
C |
A |
8: 3,430,410 (GRCm39) |
H94Q |
probably benign |
Het |
Astn2 |
A |
T |
4: 65,830,834 (GRCm39) |
L585Q |
possibly damaging |
Het |
Atf3 |
G |
T |
1: 190,909,564 (GRCm39) |
A35D |
probably benign |
Het |
Atp10b |
A |
T |
11: 43,093,978 (GRCm39) |
R507S |
possibly damaging |
Het |
Brip1 |
A |
C |
11: 86,080,598 (GRCm39) |
V156G |
probably benign |
Het |
Ccdc27 |
T |
A |
4: 154,111,205 (GRCm39) |
M636L |
probably benign |
Het |
Ceacam5 |
T |
A |
7: 17,493,285 (GRCm39) |
N769K |
possibly damaging |
Het |
Cklf |
C |
T |
8: 104,977,560 (GRCm39) |
|
probably benign |
Het |
Cpeb4 |
G |
A |
11: 31,870,546 (GRCm39) |
V474M |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,673,834 (GRCm39) |
C1091* |
probably null |
Het |
Eef1akmt4 |
T |
A |
16: 20,437,288 (GRCm39) |
I210N |
possibly damaging |
Het |
Fbxo38 |
A |
T |
18: 62,666,587 (GRCm39) |
H195Q |
probably damaging |
Het |
Fbxw14 |
G |
A |
9: 109,105,305 (GRCm39) |
R287* |
probably null |
Het |
Fes |
A |
G |
7: 80,033,619 (GRCm39) |
S211P |
possibly damaging |
Het |
Fry |
G |
T |
5: 150,317,603 (GRCm39) |
R861L |
possibly damaging |
Het |
Galnt12 |
A |
G |
4: 47,113,908 (GRCm39) |
|
probably benign |
Het |
Gm14226 |
G |
A |
2: 154,866,538 (GRCm39) |
W165* |
probably null |
Het |
Gm40460 |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
7: 141,794,171 (GRCm39) |
|
probably benign |
Het |
Gm40460 |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,554 (GRCm39) |
|
probably benign |
Het |
Gprc6a |
A |
G |
10: 51,497,079 (GRCm39) |
V488A |
probably benign |
Het |
Haus8 |
A |
T |
8: 71,705,910 (GRCm39) |
|
probably benign |
Het |
Helb |
A |
T |
10: 119,948,692 (GRCm39) |
C26S |
possibly damaging |
Het |
Icam1 |
A |
T |
9: 20,937,862 (GRCm39) |
I300F |
probably benign |
Het |
Ip6k1 |
A |
G |
9: 107,918,211 (GRCm39) |
N181S |
probably benign |
Het |
Itga2b |
C |
A |
11: 102,351,687 (GRCm39) |
R546L |
possibly damaging |
Het |
Kif27 |
A |
T |
13: 58,476,818 (GRCm39) |
Y611N |
probably damaging |
Het |
Lpcat2 |
A |
G |
8: 93,640,979 (GRCm39) |
I475V |
possibly damaging |
Het |
Lrit2 |
A |
G |
14: 36,794,487 (GRCm39) |
K517R |
probably benign |
Het |
Lrp1b |
A |
T |
2: 40,555,171 (GRCm39) |
I4085N |
|
Het |
Lrrc32 |
T |
A |
7: 98,148,242 (GRCm39) |
S341T |
probably damaging |
Het |
Lrrn2 |
T |
A |
1: 132,866,831 (GRCm39) |
I632K |
possibly damaging |
Het |
Mettl22 |
A |
G |
16: 8,300,178 (GRCm39) |
Q194R |
probably benign |
Het |
Mfhas1 |
T |
A |
8: 36,057,394 (GRCm39) |
V623E |
probably damaging |
Het |
Mitd1 |
T |
C |
1: 37,929,315 (GRCm39) |
D26G |
probably damaging |
Het |
Myo1a |
C |
T |
10: 127,546,043 (GRCm39) |
T222M |
probably benign |
Het |
Naf1 |
A |
G |
8: 67,317,333 (GRCm39) |
K275R |
possibly damaging |
Het |
Or12k7 |
G |
T |
2: 36,958,429 (GRCm39) |
M37I |
probably benign |
Het |
Or52a5 |
A |
G |
7: 103,427,063 (GRCm39) |
L163P |
possibly damaging |
Het |
Or5ac16 |
T |
A |
16: 59,022,264 (GRCm39) |
H175L |
possibly damaging |
Het |
Or9r3 |
T |
A |
10: 129,947,808 (GRCm39) |
I284F |
probably damaging |
Het |
Pappa |
A |
G |
4: 65,099,347 (GRCm39) |
H622R |
probably benign |
Het |
Pcdhb4 |
A |
T |
18: 37,442,055 (GRCm39) |
Y455F |
probably damaging |
Het |
Pepd |
A |
G |
7: 34,671,116 (GRCm39) |
Y220C |
probably damaging |
Het |
Pias3 |
T |
C |
3: 96,607,381 (GRCm39) |
I172T |
probably damaging |
Het |
Polq |
T |
A |
16: 36,853,893 (GRCm39) |
H415Q |
probably damaging |
Het |
Pp2d1 |
A |
T |
17: 53,814,897 (GRCm39) |
M609K |
probably benign |
Het |
Ppm1m |
G |
A |
9: 106,076,237 (GRCm39) |
|
probably benign |
Het |
Prss22 |
T |
A |
17: 24,215,662 (GRCm39) |
T87S |
probably benign |
Het |
Ptprf |
C |
A |
4: 118,095,125 (GRCm39) |
V254L |
possibly damaging |
Het |
Ripply3 |
A |
G |
16: 94,136,723 (GRCm39) |
E128G |
possibly damaging |
Het |
Rrm2 |
A |
C |
12: 24,760,470 (GRCm39) |
I185L |
possibly damaging |
Het |
Sbsn |
T |
A |
7: 30,454,227 (GRCm39) |
|
probably benign |
Het |
Sdc3 |
T |
A |
4: 130,546,336 (GRCm39) |
S232T |
probably benign |
Het |
Slx4 |
G |
C |
16: 3,803,458 (GRCm39) |
P1119A |
probably benign |
Het |
Smc5 |
C |
T |
19: 23,221,422 (GRCm39) |
R369Q |
probably damaging |
Het |
Speer4a3 |
A |
G |
5: 26,158,191 (GRCm39) |
S54P |
probably damaging |
Het |
Spns1 |
G |
A |
7: 125,971,593 (GRCm39) |
S319F |
possibly damaging |
Het |
Sptbn4 |
G |
A |
7: 27,106,657 (GRCm39) |
Q924* |
probably null |
Het |
Srcap |
G |
C |
7: 127,158,037 (GRCm39) |
D2638H |
unknown |
Het |
Srsf12 |
T |
C |
4: 33,226,045 (GRCm39) |
S103P |
possibly damaging |
Het |
Tanc1 |
A |
G |
2: 59,621,185 (GRCm39) |
T335A |
possibly damaging |
Het |
Them4 |
C |
T |
3: 94,231,610 (GRCm39) |
T149I |
probably damaging |
Het |
Trpc7 |
T |
C |
13: 56,970,312 (GRCm39) |
Y424C |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,628,364 (GRCm39) |
D14599N |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,698,244 (GRCm39) |
L186H |
|
Het |
Usp17lc |
T |
C |
7: 103,067,524 (GRCm39) |
F273S |
probably benign |
Het |
Vwa5b2 |
T |
C |
16: 20,419,516 (GRCm39) |
S620P |
probably 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 |
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 |
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 |
|