Other mutations in this stock |
Total: 147 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900092C05Rik |
A |
G |
7: 12,288,625 (GRCm39) |
E146G |
probably benign |
Het |
Abca4 |
G |
A |
3: 121,950,081 (GRCm39) |
G594S |
probably damaging |
Het |
Acacb |
T |
C |
5: 114,338,362 (GRCm39) |
Y726H |
probably damaging |
Het |
Adam20 |
T |
A |
8: 41,248,517 (GRCm39) |
M209K |
probably benign |
Het |
Adam29 |
A |
G |
8: 56,326,310 (GRCm39) |
V48A |
probably damaging |
Het |
Adss2 |
A |
G |
1: 177,595,253 (GRCm39) |
V429A |
possibly damaging |
Het |
Aff1 |
T |
C |
5: 103,976,320 (GRCm39) |
S481P |
probably damaging |
Het |
Akr1c19 |
G |
A |
13: 4,288,459 (GRCm39) |
A146T |
probably benign |
Het |
Ankhd1 |
G |
T |
18: 36,773,333 (GRCm39) |
V59F |
probably damaging |
Het |
Ankmy1 |
T |
G |
1: 92,816,397 (GRCm39) |
Y239S |
probably damaging |
Het |
Ankrd24 |
G |
T |
10: 81,474,142 (GRCm39) |
C19F |
probably damaging |
Het |
Apaf1 |
T |
C |
10: 90,845,065 (GRCm39) |
H1002R |
probably damaging |
Het |
Apc2 |
T |
C |
10: 80,149,935 (GRCm39) |
I1663T |
probably benign |
Het |
Apcdd1 |
A |
G |
18: 63,084,967 (GRCm39) |
N388S |
possibly damaging |
Het |
Arap2 |
G |
A |
5: 62,763,474 (GRCm39) |
P1557S |
possibly damaging |
Het |
Armc2 |
T |
A |
10: 41,798,691 (GRCm39) |
H706L |
probably benign |
Het |
Arrb1 |
T |
C |
7: 99,237,403 (GRCm39) |
|
probably null |
Het |
Atl3 |
T |
C |
19: 7,507,031 (GRCm39) |
|
probably null |
Het |
B9d2 |
A |
G |
7: 25,382,757 (GRCm39) |
T44A |
probably damaging |
Het |
Btbd3 |
C |
T |
2: 138,125,736 (GRCm39) |
R307W |
possibly damaging |
Het |
C1galt1 |
T |
C |
6: 7,871,193 (GRCm39) |
I343T |
probably benign |
Het |
Cacna1a |
A |
G |
8: 85,356,460 (GRCm39) |
D1901G |
probably damaging |
Het |
Ccdc42 |
C |
T |
11: 68,488,536 (GRCm39) |
Q312* |
probably null |
Het |
Cdh18 |
T |
C |
15: 23,410,876 (GRCm39) |
Y454H |
probably benign |
Het |
Celf5 |
G |
A |
10: 81,301,839 (GRCm39) |
T317I |
probably damaging |
Het |
Celsr2 |
A |
T |
3: 108,311,211 (GRCm39) |
|
probably null |
Het |
Cenpf |
A |
T |
1: 189,414,660 (GRCm39) |
|
probably null |
Het |
Cep350 |
T |
C |
1: 155,747,794 (GRCm39) |
D2042G |
probably damaging |
Het |
Chd3 |
T |
C |
11: 69,235,184 (GRCm39) |
D2054G |
probably damaging |
Het |
Chgb |
A |
G |
2: 132,635,255 (GRCm39) |
H399R |
probably benign |
Het |
Clp1 |
C |
T |
2: 84,555,935 (GRCm39) |
A182T |
possibly damaging |
Het |
Col15a1 |
A |
G |
4: 47,282,654 (GRCm39) |
N777S |
probably damaging |
Het |
Coq6 |
A |
G |
12: 84,415,412 (GRCm39) |
D145G |
possibly damaging |
Het |
Csf2rb2 |
T |
C |
15: 78,172,108 (GRCm39) |
Y325C |
probably benign |
Het |
Ctnna2 |
T |
C |
6: 76,879,413 (GRCm39) |
T824A |
probably benign |
Het |
Cyp4x1 |
T |
A |
4: 114,970,023 (GRCm39) |
D368V |
probably damaging |
Het |
D430041D05Rik |
C |
T |
2: 104,063,790 (GRCm39) |
R1354H |
probably damaging |
Het |
D6Ertd527e |
A |
C |
6: 87,088,887 (GRCm39) |
D350A |
unknown |
Het |
Ddx24 |
A |
G |
12: 103,385,326 (GRCm39) |
Y426H |
possibly damaging |
Het |
Dexi |
G |
T |
16: 10,360,426 (GRCm39) |
Y43* |
probably null |
Het |
Dgka |
A |
G |
10: 128,556,338 (GRCm39) |
|
probably null |
Het |
Dhx38 |
A |
T |
8: 110,285,575 (GRCm39) |
D419E |
probably benign |
Het |
Dlg1 |
G |
A |
16: 31,656,992 (GRCm39) |
V596I |
possibly damaging |
Het |
Dlg1 |
C |
A |
16: 31,484,398 (GRCm39) |
Q9K |
probably benign |
Het |
Dnah11 |
A |
C |
12: 118,046,246 (GRCm39) |
W1731G |
probably damaging |
Het |
Dnhd1 |
T |
A |
7: 105,369,995 (GRCm39) |
N4473K |
probably benign |
Het |
Dync2h1 |
A |
C |
9: 7,051,480 (GRCm39) |
S3152A |
probably benign |
Het |
Egfl7 |
C |
T |
2: 26,479,452 (GRCm39) |
T68I |
probably damaging |
Het |
Eif2a |
G |
A |
3: 58,463,073 (GRCm39) |
|
probably null |
Het |
Emb |
G |
A |
13: 117,369,286 (GRCm39) |
V56I |
possibly damaging |
Het |
Enpp4 |
A |
T |
17: 44,410,386 (GRCm39) |
C397S |
probably damaging |
Het |
Entpd3 |
A |
G |
9: 120,386,471 (GRCm39) |
T151A |
possibly damaging |
Het |
Ero1b |
A |
G |
13: 12,589,747 (GRCm39) |
D50G |
probably damaging |
Het |
Fam219a |
A |
G |
4: 41,520,242 (GRCm39) |
*169Q |
probably null |
Het |
Fga |
G |
A |
3: 82,935,869 (GRCm39) |
G32E |
probably damaging |
Het |
Fkbpl |
T |
C |
17: 34,864,333 (GRCm39) |
F34L |
probably benign |
Het |
Fsd2 |
T |
A |
7: 81,194,765 (GRCm39) |
D466V |
probably damaging |
Het |
Gja1 |
A |
G |
10: 56,264,166 (GRCm39) |
Y175C |
possibly damaging |
Het |
Gm5478 |
T |
A |
15: 101,553,059 (GRCm39) |
I338F |
probably damaging |
Het |
Greb1 |
T |
A |
12: 16,732,194 (GRCm39) |
Y1589F |
probably damaging |
Het |
Grk3 |
C |
T |
5: 113,067,919 (GRCm39) |
E537K |
probably damaging |
Het |
H2-K2 |
G |
T |
17: 34,218,474 (GRCm39) |
D127E |
probably damaging |
Het |
Hcrtr2 |
A |
G |
9: 76,137,966 (GRCm39) |
L383P |
probably benign |
Het |
Hmcn1 |
C |
T |
1: 150,514,651 (GRCm39) |
V3574M |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,197,921 (GRCm39) |
|
probably null |
Het |
Il1r2 |
A |
G |
1: 40,144,615 (GRCm39) |
K101E |
probably benign |
Het |
Itga11 |
A |
T |
9: 62,681,653 (GRCm39) |
H1054L |
probably benign |
Het |
Kif13a |
A |
T |
13: 46,956,187 (GRCm39) |
V539D |
probably damaging |
Het |
Kifc1 |
G |
A |
17: 34,105,621 (GRCm39) |
T62I |
probably damaging |
Het |
Klhl28 |
A |
G |
12: 64,998,529 (GRCm39) |
Y322H |
probably damaging |
Het |
Klhl6 |
C |
A |
16: 19,775,764 (GRCm39) |
D265Y |
possibly damaging |
Het |
Krt86 |
T |
A |
15: 101,377,412 (GRCm39) |
C479S |
unknown |
Het |
Lama2 |
C |
T |
10: 27,065,127 (GRCm39) |
R1179H |
probably benign |
Het |
Lce6a |
A |
T |
3: 92,527,635 (GRCm39) |
H57Q |
probably benign |
Het |
Lcn11 |
T |
C |
2: 25,669,305 (GRCm39) |
V154A |
probably benign |
Het |
Lnpep |
A |
T |
17: 17,758,816 (GRCm39) |
F843I |
probably damaging |
Het |
Lrrc49 |
C |
T |
9: 60,573,640 (GRCm39) |
V281I |
probably benign |
Het |
Lrrtm1 |
C |
A |
6: 77,221,611 (GRCm39) |
A356E |
probably damaging |
Het |
Map3k1 |
A |
C |
13: 111,900,044 (GRCm39) |
H493Q |
probably benign |
Het |
Mcm4 |
A |
T |
16: 15,449,979 (GRCm39) |
|
probably null |
Het |
Mdn1 |
C |
T |
4: 32,712,014 (GRCm39) |
P1844L |
probably damaging |
Het |
Mdn1 |
T |
A |
4: 32,732,829 (GRCm39) |
D3076E |
probably benign |
Het |
Med6 |
A |
T |
12: 81,635,798 (GRCm39) |
L27H |
probably damaging |
Het |
Mrtfb |
A |
G |
16: 13,199,465 (GRCm39) |
E106G |
probably damaging |
Het |
Myo7a |
T |
A |
7: 97,721,153 (GRCm39) |
T1271S |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,829,076 (GRCm39) |
M2376K |
probably benign |
Het |
Nell2 |
G |
A |
15: 95,127,095 (GRCm39) |
T760I |
probably benign |
Het |
Neurod6 |
C |
T |
6: 55,656,572 (GRCm39) |
A22T |
probably benign |
Het |
Nlrp10 |
T |
C |
7: 108,523,492 (GRCm39) |
K663E |
probably benign |
Het |
Nopchap1 |
T |
C |
10: 83,197,961 (GRCm39) |
S56P |
probably benign |
Het |
Npr3 |
T |
A |
15: 11,845,368 (GRCm39) |
K501N |
probably benign |
Het |
Nr2f2 |
C |
A |
7: 70,004,460 (GRCm39) |
R264L |
probably damaging |
Het |
Nup35 |
T |
A |
2: 80,472,984 (GRCm39) |
M19K |
probably benign |
Het |
Oacyl |
A |
T |
18: 65,880,962 (GRCm39) |
Q592L |
possibly damaging |
Het |
Or10a4 |
T |
A |
7: 106,696,933 (GRCm39) |
I87K |
probably benign |
Het |
Or1ad6 |
C |
A |
11: 50,860,670 (GRCm39) |
A275D |
possibly damaging |
Het |
Or2v1 |
C |
G |
11: 49,025,549 (GRCm39) |
H177D |
probably damaging |
Het |
Or4a71 |
A |
G |
2: 89,358,451 (GRCm39) |
V101A |
possibly damaging |
Het |
Or5af1 |
T |
A |
11: 58,722,798 (GRCm39) |
S273T |
probably damaging |
Het |
Or5b105 |
G |
A |
19: 13,080,642 (GRCm39) |
R3C |
possibly damaging |
Het |
Or5b122 |
T |
A |
19: 13,563,534 (GRCm39) |
Y289N |
probably damaging |
Het |
Or5p51 |
A |
G |
7: 107,444,776 (GRCm39) |
S55P |
probably damaging |
Het |
Or6c76b |
T |
G |
10: 129,693,070 (GRCm39) |
S228A |
possibly damaging |
Het |
Or8k25 |
T |
A |
2: 86,243,514 (GRCm39) |
N294I |
probably damaging |
Het |
Or9k7 |
T |
C |
10: 130,046,939 (GRCm39) |
E20G |
probably benign |
Het |
Patl2 |
T |
C |
2: 121,957,150 (GRCm39) |
Y128C |
probably benign |
Het |
Pcdhac2 |
A |
G |
18: 37,278,942 (GRCm39) |
I641V |
probably benign |
Het |
Polr2b |
T |
C |
5: 77,461,006 (GRCm39) |
|
probably benign |
Het |
Pot1b |
A |
T |
17: 55,972,765 (GRCm39) |
I469N |
probably damaging |
Het |
Prdm11 |
G |
T |
2: 92,844,130 (GRCm39) |
D33E |
possibly damaging |
Het |
Prkdc |
A |
G |
16: 15,589,921 (GRCm39) |
S2595G |
probably damaging |
Het |
Prrc1 |
G |
A |
18: 57,507,622 (GRCm39) |
V259I |
possibly damaging |
Het |
Prrc2b |
G |
T |
2: 32,103,882 (GRCm39) |
R1120L |
probably damaging |
Het |
Prss38 |
T |
C |
11: 59,266,369 (GRCm39) |
S30G |
possibly damaging |
Het |
Raph1 |
A |
T |
1: 60,565,028 (GRCm39) |
L153Q |
probably damaging |
Het |
Reck |
A |
G |
4: 43,940,719 (GRCm39) |
T843A |
probably benign |
Het |
Rgs7bp |
T |
C |
13: 105,103,610 (GRCm39) |
N164D |
probably benign |
Het |
Rpusd4 |
C |
A |
9: 35,179,289 (GRCm39) |
A35D |
possibly damaging |
Het |
Setd1b |
T |
C |
5: 123,298,014 (GRCm39) |
|
probably benign |
Het |
Siglec15 |
G |
T |
18: 78,089,352 (GRCm39) |
D297E |
probably benign |
Het |
Skint7 |
T |
A |
4: 111,834,656 (GRCm39) |
C13* |
probably null |
Het |
Slc5a12 |
A |
G |
2: 110,463,088 (GRCm39) |
M395V |
probably benign |
Het |
Sohlh2 |
C |
A |
3: 55,115,104 (GRCm39) |
S363Y |
probably damaging |
Het |
Srgap3 |
A |
T |
6: 112,700,080 (GRCm39) |
V966E |
probably damaging |
Het |
Stk4 |
C |
T |
2: 163,940,462 (GRCm39) |
P266L |
probably damaging |
Het |
Stxbp5l |
G |
A |
16: 36,962,794 (GRCm39) |
H754Y |
probably benign |
Het |
Synpo2l |
A |
T |
14: 20,710,748 (GRCm39) |
M624K |
probably damaging |
Het |
Tas2r136 |
T |
C |
6: 132,754,375 (GRCm39) |
I251V |
probably benign |
Het |
Tecpr1 |
C |
T |
5: 144,149,408 (GRCm39) |
V340M |
probably damaging |
Het |
Tecta |
C |
T |
9: 42,299,501 (GRCm39) |
G196S |
probably damaging |
Het |
Tex55 |
A |
C |
16: 38,648,726 (GRCm39) |
S128A |
probably benign |
Het |
Thsd7a |
T |
A |
6: 12,331,541 (GRCm39) |
|
probably null |
Het |
Timeless |
T |
C |
10: 128,082,203 (GRCm39) |
V577A |
probably benign |
Het |
Tln1 |
A |
T |
4: 43,553,071 (GRCm39) |
V340E |
probably damaging |
Het |
Tmem132c |
T |
A |
5: 127,640,617 (GRCm39) |
Y929* |
probably null |
Het |
Tmprss7 |
C |
T |
16: 45,489,914 (GRCm39) |
R436Q |
probably damaging |
Het |
Tnik |
A |
C |
3: 28,704,308 (GRCm39) |
K989T |
probably damaging |
Het |
Tnxb |
T |
A |
17: 34,890,892 (GRCm39) |
Y412N |
probably damaging |
Het |
Trmt44 |
A |
G |
5: 35,726,103 (GRCm39) |
|
probably null |
Het |
Trpm6 |
C |
A |
19: 18,849,585 (GRCm39) |
T1704N |
probably benign |
Het |
Ttc22 |
T |
C |
4: 106,496,510 (GRCm39) |
V520A |
possibly damaging |
Het |
Ttc3 |
T |
A |
16: 94,257,644 (GRCm39) |
Y1650* |
probably null |
Het |
Vmn2r24 |
A |
G |
6: 123,763,893 (GRCm39) |
T257A |
probably benign |
Het |
Xab2 |
A |
C |
8: 3,663,605 (GRCm39) |
N408K |
probably benign |
Het |
Zbtb42 |
A |
T |
12: 112,647,061 (GRCm39) |
Y412F |
probably benign |
Het |
Zfp282 |
A |
G |
6: 47,857,303 (GRCm39) |
N179D |
probably damaging |
Het |
Zfp62 |
C |
A |
11: 49,106,227 (GRCm39) |
T106K |
probably benign |
Het |
|
Other mutations in Tsc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Tsc2
|
APN |
17 |
24,827,081 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00985:Tsc2
|
APN |
17 |
24,816,105 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01386:Tsc2
|
APN |
17 |
24,832,259 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01468:Tsc2
|
APN |
17 |
24,840,071 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01530:Tsc2
|
APN |
17 |
24,841,636 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02390:Tsc2
|
APN |
17 |
24,819,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02398:Tsc2
|
APN |
17 |
24,840,703 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02741:Tsc2
|
APN |
17 |
24,848,943 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03191:Tsc2
|
APN |
17 |
24,847,028 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03372:Tsc2
|
APN |
17 |
24,838,444 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03412:Tsc2
|
APN |
17 |
24,816,042 (GRCm39) |
missense |
probably damaging |
0.98 |
Twitch
|
UTSW |
17 |
24,815,716 (GRCm39) |
splice site |
probably null |
|
PIT4515001:Tsc2
|
UTSW |
17 |
24,840,121 (GRCm39) |
missense |
probably benign |
0.15 |
R0025:Tsc2
|
UTSW |
17 |
24,849,978 (GRCm39) |
splice site |
probably benign |
|
R0025:Tsc2
|
UTSW |
17 |
24,849,978 (GRCm39) |
splice site |
probably benign |
|
R0138:Tsc2
|
UTSW |
17 |
24,818,600 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0540:Tsc2
|
UTSW |
17 |
24,840,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R0570:Tsc2
|
UTSW |
17 |
24,845,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0826:Tsc2
|
UTSW |
17 |
24,815,932 (GRCm39) |
missense |
probably benign |
0.04 |
R1430:Tsc2
|
UTSW |
17 |
24,817,997 (GRCm39) |
critical splice donor site |
probably null |
|
R1440:Tsc2
|
UTSW |
17 |
24,833,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Tsc2
|
UTSW |
17 |
24,827,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Tsc2
|
UTSW |
17 |
24,827,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R1541:Tsc2
|
UTSW |
17 |
24,850,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R1717:Tsc2
|
UTSW |
17 |
24,816,042 (GRCm39) |
missense |
probably damaging |
0.98 |
R1799:Tsc2
|
UTSW |
17 |
24,823,382 (GRCm39) |
missense |
probably benign |
|
R2030:Tsc2
|
UTSW |
17 |
24,842,444 (GRCm39) |
splice site |
probably benign |
|
R2147:Tsc2
|
UTSW |
17 |
24,840,116 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2888:Tsc2
|
UTSW |
17 |
24,850,969 (GRCm39) |
critical splice donor site |
probably null |
|
R3609:Tsc2
|
UTSW |
17 |
24,841,524 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3610:Tsc2
|
UTSW |
17 |
24,841,524 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3811:Tsc2
|
UTSW |
17 |
24,848,011 (GRCm39) |
missense |
probably benign |
0.09 |
R3895:Tsc2
|
UTSW |
17 |
24,818,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R3962:Tsc2
|
UTSW |
17 |
24,840,140 (GRCm39) |
splice site |
probably benign |
|
R3971:Tsc2
|
UTSW |
17 |
24,842,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R4018:Tsc2
|
UTSW |
17 |
24,844,255 (GRCm39) |
missense |
probably damaging |
0.99 |
R4184:Tsc2
|
UTSW |
17 |
24,850,990 (GRCm39) |
missense |
probably benign |
0.43 |
R4435:Tsc2
|
UTSW |
17 |
24,818,687 (GRCm39) |
missense |
probably benign |
0.01 |
R4437:Tsc2
|
UTSW |
17 |
24,818,687 (GRCm39) |
missense |
probably benign |
0.01 |
R4474:Tsc2
|
UTSW |
17 |
24,816,238 (GRCm39) |
missense |
probably damaging |
0.98 |
R4703:Tsc2
|
UTSW |
17 |
24,823,883 (GRCm39) |
missense |
probably benign |
0.13 |
R4731:Tsc2
|
UTSW |
17 |
24,822,249 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4732:Tsc2
|
UTSW |
17 |
24,822,249 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4733:Tsc2
|
UTSW |
17 |
24,822,249 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4817:Tsc2
|
UTSW |
17 |
24,815,716 (GRCm39) |
splice site |
probably null |
|
R4890:Tsc2
|
UTSW |
17 |
24,819,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R4922:Tsc2
|
UTSW |
17 |
24,819,343 (GRCm39) |
missense |
probably benign |
0.22 |
R5119:Tsc2
|
UTSW |
17 |
24,822,254 (GRCm39) |
missense |
probably benign |
0.00 |
R5393:Tsc2
|
UTSW |
17 |
24,819,370 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5785:Tsc2
|
UTSW |
17 |
24,818,861 (GRCm39) |
splice site |
probably null |
|
R5838:Tsc2
|
UTSW |
17 |
24,832,190 (GRCm39) |
missense |
probably benign |
0.01 |
R5857:Tsc2
|
UTSW |
17 |
24,818,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R5911:Tsc2
|
UTSW |
17 |
24,819,361 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5988:Tsc2
|
UTSW |
17 |
24,839,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R6275:Tsc2
|
UTSW |
17 |
24,819,394 (GRCm39) |
missense |
probably benign |
0.00 |
R6290:Tsc2
|
UTSW |
17 |
24,815,884 (GRCm39) |
missense |
probably benign |
0.04 |
R6371:Tsc2
|
UTSW |
17 |
24,845,688 (GRCm39) |
missense |
probably benign |
0.00 |
R6467:Tsc2
|
UTSW |
17 |
24,828,101 (GRCm39) |
missense |
probably benign |
0.04 |
R6577:Tsc2
|
UTSW |
17 |
24,829,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R6728:Tsc2
|
UTSW |
17 |
24,840,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R6918:Tsc2
|
UTSW |
17 |
24,832,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R6995:Tsc2
|
UTSW |
17 |
24,847,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R7026:Tsc2
|
UTSW |
17 |
24,845,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R7136:Tsc2
|
UTSW |
17 |
24,832,254 (GRCm39) |
missense |
probably benign |
0.00 |
R7236:Tsc2
|
UTSW |
17 |
24,842,568 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7243:Tsc2
|
UTSW |
17 |
24,818,604 (GRCm39) |
missense |
probably benign |
0.02 |
R7249:Tsc2
|
UTSW |
17 |
24,826,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R7450:Tsc2
|
UTSW |
17 |
24,819,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R7522:Tsc2
|
UTSW |
17 |
24,849,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7529:Tsc2
|
UTSW |
17 |
24,816,922 (GRCm39) |
missense |
probably damaging |
0.98 |
R7637:Tsc2
|
UTSW |
17 |
24,826,466 (GRCm39) |
missense |
probably benign |
0.13 |
R7781:Tsc2
|
UTSW |
17 |
24,827,089 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8005:Tsc2
|
UTSW |
17 |
24,818,570 (GRCm39) |
missense |
probably damaging |
0.98 |
R8262:Tsc2
|
UTSW |
17 |
24,833,340 (GRCm39) |
missense |
probably benign |
0.06 |
R8268:Tsc2
|
UTSW |
17 |
24,818,984 (GRCm39) |
missense |
probably benign |
0.44 |
R8400:Tsc2
|
UTSW |
17 |
24,823,961 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9020:Tsc2
|
UTSW |
17 |
24,845,691 (GRCm39) |
missense |
probably damaging |
0.99 |
R9039:Tsc2
|
UTSW |
17 |
24,826,489 (GRCm39) |
missense |
probably benign |
0.01 |
R9065:Tsc2
|
UTSW |
17 |
24,822,164 (GRCm39) |
missense |
probably benign |
0.39 |
R9123:Tsc2
|
UTSW |
17 |
24,823,802 (GRCm39) |
missense |
probably null |
0.40 |
R9125:Tsc2
|
UTSW |
17 |
24,823,802 (GRCm39) |
missense |
probably null |
0.40 |
R9186:Tsc2
|
UTSW |
17 |
24,823,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R9390:Tsc2
|
UTSW |
17 |
24,823,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R9542:Tsc2
|
UTSW |
17 |
24,819,308 (GRCm39) |
critical splice donor site |
probably null |
|
R9721:Tsc2
|
UTSW |
17 |
24,818,616 (GRCm39) |
nonsense |
probably null |
|
Z1177:Tsc2
|
UTSW |
17 |
24,839,753 (GRCm39) |
missense |
possibly damaging |
0.61 |
|