Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
T |
C |
10: 87,061,907 (GRCm39) |
F119S |
probably damaging |
Het |
Abca13 |
C |
A |
11: 9,531,545 (GRCm39) |
Q4591K |
probably damaging |
Het |
Anapc1 |
A |
T |
2: 128,476,631 (GRCm39) |
M1329K |
probably damaging |
Het |
Aoah |
A |
T |
13: 21,163,710 (GRCm39) |
K338* |
probably null |
Het |
Ascc3 |
A |
T |
10: 50,521,154 (GRCm39) |
T416S |
probably benign |
Het |
Baz2a |
A |
G |
10: 127,950,508 (GRCm39) |
T484A |
possibly damaging |
Het |
Btnl6 |
T |
C |
17: 34,727,477 (GRCm39) |
N351S |
probably benign |
Het |
Cacna1s |
T |
G |
1: 136,046,544 (GRCm39) |
I1772S |
possibly damaging |
Het |
Ccdc8 |
A |
G |
7: 16,729,582 (GRCm39) |
D357G |
unknown |
Het |
Ccna1 |
T |
C |
3: 54,958,049 (GRCm39) |
E152G |
probably damaging |
Het |
Cct4 |
A |
G |
11: 22,949,073 (GRCm39) |
D273G |
probably damaging |
Het |
Cd9 |
A |
G |
6: 125,440,703 (GRCm39) |
V96A |
probably damaging |
Het |
Cdc5l |
G |
A |
17: 45,726,610 (GRCm39) |
R321W |
probably damaging |
Het |
Cdh20 |
T |
C |
1: 109,922,036 (GRCm39) |
S43P |
probably benign |
Het |
Cep95 |
G |
A |
11: 106,702,097 (GRCm39) |
V365M |
probably benign |
Het |
Ces1c |
T |
C |
8: 93,854,152 (GRCm39) |
T128A |
probably benign |
Het |
Chil5 |
A |
G |
3: 105,926,583 (GRCm39) |
V82A |
probably damaging |
Het |
Clmn |
T |
C |
12: 104,748,023 (GRCm39) |
D508G |
probably benign |
Het |
Cog8 |
A |
T |
8: 107,775,777 (GRCm39) |
|
probably benign |
Het |
Cst3 |
A |
T |
2: 148,717,089 (GRCm39) |
V70E |
probably damaging |
Het |
Ctcf |
A |
G |
8: 106,390,671 (GRCm39) |
T93A |
possibly damaging |
Het |
Ctsk |
C |
A |
3: 95,416,188 (GRCm39) |
N315K |
probably benign |
Het |
Cyp2j12 |
G |
T |
4: 96,029,262 (GRCm39) |
D6E |
probably benign |
Het |
Dhx34 |
A |
G |
7: 15,939,917 (GRCm39) |
V655A |
probably benign |
Het |
Dock10 |
T |
C |
1: 80,583,593 (GRCm39) |
Y203C |
probably damaging |
Het |
Dok7 |
A |
T |
5: 35,221,678 (GRCm39) |
D26V |
probably damaging |
Het |
Epha8 |
G |
A |
4: 136,667,597 (GRCm39) |
H295Y |
probably damaging |
Het |
Esf1 |
A |
G |
2: 139,990,843 (GRCm39) |
|
probably benign |
Het |
Fam83c |
A |
G |
2: 155,671,672 (GRCm39) |
S588P |
probably benign |
Het |
Fat3 |
G |
A |
9: 15,881,002 (GRCm39) |
|
probably benign |
Het |
Fhdc1 |
T |
C |
3: 84,360,817 (GRCm39) |
|
probably benign |
Het |
Frmd4b |
A |
G |
6: 97,285,047 (GRCm39) |
V338A |
probably damaging |
Het |
Fsd1l |
A |
G |
4: 53,694,727 (GRCm39) |
T394A |
probably damaging |
Het |
Gbf1 |
A |
G |
19: 46,242,549 (GRCm39) |
|
probably benign |
Het |
Glg1 |
G |
T |
8: 111,886,490 (GRCm39) |
Q1101K |
possibly damaging |
Het |
Glt8d2 |
T |
A |
10: 82,487,361 (GRCm39) |
|
probably null |
Het |
Gm19345 |
T |
C |
7: 19,588,855 (GRCm39) |
|
probably benign |
Het |
Gpr179 |
A |
T |
11: 97,226,892 (GRCm39) |
D1754E |
probably benign |
Het |
Hydin |
A |
G |
8: 111,291,650 (GRCm39) |
T3381A |
probably benign |
Het |
Igkv12-41 |
G |
A |
6: 69,835,822 (GRCm39) |
T16I |
possibly damaging |
Het |
Insl5 |
A |
G |
4: 102,875,313 (GRCm39) |
*146Q |
probably null |
Het |
Iqce |
A |
T |
5: 140,651,957 (GRCm39) |
I655N |
possibly damaging |
Het |
Irf2bp1 |
G |
A |
7: 18,738,927 (GRCm39) |
R189H |
possibly damaging |
Het |
Itprid2 |
T |
A |
2: 79,490,810 (GRCm39) |
L976Q |
probably damaging |
Het |
Itsn1 |
C |
T |
16: 91,602,978 (GRCm39) |
|
probably benign |
Het |
Kansl3 |
A |
T |
1: 36,384,050 (GRCm39) |
I724N |
probably benign |
Het |
Kcna4 |
T |
C |
2: 107,126,907 (GRCm39) |
I547T |
probably damaging |
Het |
Klk1b4 |
A |
T |
7: 43,860,158 (GRCm39) |
I91F |
probably benign |
Het |
Lmbr1 |
A |
G |
5: 29,457,753 (GRCm39) |
S282P |
probably damaging |
Het |
Lrrc17 |
G |
A |
5: 21,765,967 (GRCm39) |
A150T |
probably benign |
Het |
Lrrc2 |
A |
G |
9: 110,809,966 (GRCm39) |
E334G |
possibly damaging |
Het |
Lrrc7 |
G |
A |
3: 157,866,475 (GRCm39) |
Q1077* |
probably null |
Het |
Mapk8 |
A |
T |
14: 33,109,264 (GRCm39) |
|
probably benign |
Het |
Mast1 |
T |
A |
8: 85,638,650 (GRCm39) |
T1560S |
probably benign |
Het |
Mdh1b |
C |
A |
1: 63,758,777 (GRCm39) |
A272S |
probably damaging |
Het |
Myo15b |
T |
C |
11: 115,777,109 (GRCm39) |
Y912H |
probably damaging |
Het |
Nme7 |
T |
A |
1: 164,172,944 (GRCm39) |
D218E |
probably damaging |
Het |
Nsun7 |
T |
A |
5: 66,446,751 (GRCm39) |
|
probably benign |
Het |
Nxpe2 |
A |
G |
9: 48,251,870 (GRCm39) |
|
probably null |
Het |
Or1e34 |
A |
G |
11: 73,778,655 (GRCm39) |
V181A |
probably benign |
Het |
Or2ag16 |
G |
A |
7: 106,352,196 (GRCm39) |
T133I |
probably benign |
Het |
Or2n1c |
T |
G |
17: 38,519,286 (GRCm39) |
I50R |
probably benign |
Het |
Or5p53 |
T |
A |
7: 107,533,375 (GRCm39) |
V216D |
probably damaging |
Het |
P2ry1 |
T |
C |
3: 60,910,951 (GRCm39) |
V30A |
probably benign |
Het |
Pgm2 |
T |
A |
5: 64,269,386 (GRCm39) |
I491N |
possibly damaging |
Het |
Pkd1l3 |
A |
T |
8: 110,365,386 (GRCm39) |
D1169V |
probably damaging |
Het |
Poldip2 |
T |
A |
11: 78,403,189 (GRCm39) |
S18T |
probably benign |
Het |
Prg4 |
C |
T |
1: 150,331,558 (GRCm39) |
|
probably benign |
Het |
Prkab2 |
T |
A |
3: 97,574,728 (GRCm39) |
Y241* |
probably null |
Het |
Prmt7 |
A |
G |
8: 106,953,839 (GRCm39) |
|
probably benign |
Het |
Proser3 |
T |
A |
7: 30,245,842 (GRCm39) |
R80W |
probably damaging |
Het |
Prr12 |
A |
G |
7: 44,699,415 (GRCm39) |
|
probably benign |
Het |
Psmd1 |
A |
T |
1: 86,006,304 (GRCm39) |
L223F |
probably damaging |
Het |
Rab13 |
A |
G |
3: 90,131,088 (GRCm39) |
|
probably benign |
Het |
Rgl1 |
C |
T |
1: 152,428,347 (GRCm39) |
C294Y |
probably damaging |
Het |
Rpl21-ps4 |
C |
A |
14: 11,227,556 (GRCm38) |
|
noncoding transcript |
Het |
Rusc2 |
T |
C |
4: 43,423,954 (GRCm39) |
V1036A |
probably damaging |
Het |
Sae1 |
T |
A |
7: 16,104,247 (GRCm39) |
K121* |
probably null |
Het |
Sap130 |
C |
T |
18: 31,813,559 (GRCm39) |
P539S |
probably damaging |
Het |
Saxo4 |
C |
T |
19: 10,452,418 (GRCm39) |
R364Q |
probably damaging |
Het |
Scube2 |
A |
G |
7: 109,424,079 (GRCm39) |
L475P |
probably damaging |
Het |
Sec16a |
T |
C |
2: 26,321,198 (GRCm39) |
D1298G |
probably damaging |
Het |
Serpinb9b |
T |
C |
13: 33,222,003 (GRCm39) |
F206L |
probably benign |
Het |
Sh3bp1 |
T |
A |
15: 78,788,534 (GRCm39) |
Y202* |
probably null |
Het |
Shprh |
T |
A |
10: 11,062,135 (GRCm39) |
C1177S |
possibly damaging |
Het |
Slc27a6 |
T |
C |
18: 58,742,937 (GRCm39) |
Y542H |
possibly damaging |
Het |
Slc41a1 |
T |
C |
1: 131,771,650 (GRCm39) |
|
probably benign |
Het |
Slc46a1 |
T |
C |
11: 78,361,625 (GRCm39) |
F424L |
probably damaging |
Het |
Slc66a2 |
C |
T |
18: 80,306,733 (GRCm39) |
A101V |
probably benign |
Het |
Slc6a12 |
G |
A |
6: 121,333,877 (GRCm39) |
V238I |
probably damaging |
Het |
Slc6a20a |
A |
G |
9: 123,493,686 (GRCm39) |
V65A |
probably damaging |
Het |
Slc9c1 |
T |
A |
16: 45,374,663 (GRCm39) |
S343T |
probably benign |
Het |
Spcs3 |
C |
A |
8: 54,981,415 (GRCm39) |
R60I |
probably benign |
Het |
Tbc1d16 |
C |
A |
11: 119,038,401 (GRCm39) |
R764L |
possibly damaging |
Het |
Tcaf2 |
A |
T |
6: 42,619,838 (GRCm39) |
V63E |
possibly damaging |
Het |
Tmc1 |
G |
T |
19: 20,766,951 (GRCm39) |
A750E |
possibly damaging |
Het |
Tmem273 |
A |
G |
14: 32,530,320 (GRCm39) |
K83E |
possibly damaging |
Het |
Tmem81 |
C |
G |
1: 132,435,567 (GRCm39) |
I124M |
probably damaging |
Het |
Tmx3 |
T |
C |
18: 90,558,130 (GRCm39) |
I394T |
probably damaging |
Het |
Trank1 |
G |
A |
9: 111,195,092 (GRCm39) |
E1039K |
possibly damaging |
Het |
Trpc4ap |
A |
G |
2: 155,499,866 (GRCm39) |
|
probably benign |
Het |
Tsen54 |
T |
C |
11: 115,706,234 (GRCm39) |
C123R |
probably damaging |
Het |
Ubtd1 |
A |
G |
19: 42,020,373 (GRCm39) |
D39G |
possibly damaging |
Het |
Vmn1r181 |
A |
T |
7: 23,683,759 (GRCm39) |
M75L |
probably benign |
Het |
Zc3h7a |
T |
C |
16: 10,958,601 (GRCm39) |
T847A |
probably damaging |
Het |
Zc3hav1 |
A |
G |
6: 38,313,485 (GRCm39) |
C187R |
probably damaging |
Het |
Zfp692 |
G |
A |
11: 58,201,229 (GRCm39) |
|
probably benign |
Het |
Zmiz1 |
G |
A |
14: 25,654,919 (GRCm39) |
|
probably benign |
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 |
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 |
|