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 |
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 |
Tsc2 |
A |
T |
17: 24,840,686 (GRCm39) |
V391E |
probably damaging |
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 Prkdc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Prkdc
|
APN |
16 |
15,515,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00225:Prkdc
|
APN |
16 |
15,627,508 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL00481:Prkdc
|
APN |
16 |
15,608,330 (GRCm39) |
missense |
probably benign |
0.41 |
IGL00488:Prkdc
|
APN |
16 |
15,593,711 (GRCm39) |
splice site |
probably null |
|
IGL00489:Prkdc
|
APN |
16 |
15,617,790 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL00579:Prkdc
|
APN |
16 |
15,482,103 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00587:Prkdc
|
APN |
16 |
15,470,222 (GRCm39) |
splice site |
probably benign |
|
IGL00666:Prkdc
|
APN |
16 |
15,554,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00675:Prkdc
|
APN |
16 |
15,605,022 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00708:Prkdc
|
APN |
16 |
15,597,290 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00725:Prkdc
|
APN |
16 |
15,634,503 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00818:Prkdc
|
APN |
16 |
15,577,618 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00917:Prkdc
|
APN |
16 |
15,557,428 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00990:Prkdc
|
APN |
16 |
15,519,979 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01126:Prkdc
|
APN |
16 |
15,487,185 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01141:Prkdc
|
APN |
16 |
15,544,568 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01306:Prkdc
|
APN |
16 |
15,485,595 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01326:Prkdc
|
APN |
16 |
15,647,556 (GRCm39) |
missense |
probably benign |
|
IGL01335:Prkdc
|
APN |
16 |
15,634,760 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01419:Prkdc
|
APN |
16 |
15,653,030 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01434:Prkdc
|
APN |
16 |
15,531,451 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01554:Prkdc
|
APN |
16 |
15,470,166 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01671:Prkdc
|
APN |
16 |
15,485,609 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01871:Prkdc
|
APN |
16 |
15,600,951 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01874:Prkdc
|
APN |
16 |
15,552,858 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01930:Prkdc
|
APN |
16 |
15,516,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01984:Prkdc
|
APN |
16 |
15,526,643 (GRCm39) |
missense |
probably benign |
|
IGL02121:Prkdc
|
APN |
16 |
15,535,048 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02152:Prkdc
|
APN |
16 |
15,487,149 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02172:Prkdc
|
APN |
16 |
15,627,623 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02336:Prkdc
|
APN |
16 |
15,603,843 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02336:Prkdc
|
APN |
16 |
15,603,842 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02393:Prkdc
|
APN |
16 |
15,634,622 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02406:Prkdc
|
APN |
16 |
15,488,399 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02500:Prkdc
|
APN |
16 |
15,532,146 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02568:Prkdc
|
APN |
16 |
15,544,406 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02579:Prkdc
|
APN |
16 |
15,488,465 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02652:Prkdc
|
APN |
16 |
15,600,951 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02661:Prkdc
|
APN |
16 |
15,587,689 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02685:Prkdc
|
APN |
16 |
15,653,907 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02741:Prkdc
|
APN |
16 |
15,570,590 (GRCm39) |
splice site |
probably benign |
|
IGL02803:Prkdc
|
APN |
16 |
15,651,530 (GRCm39) |
splice site |
probably benign |
|
IGL02866:Prkdc
|
APN |
16 |
15,649,191 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02882:Prkdc
|
APN |
16 |
15,469,383 (GRCm39) |
nonsense |
probably null |
|
IGL02989:Prkdc
|
APN |
16 |
15,617,880 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03053:Prkdc
|
APN |
16 |
15,652,030 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03071:Prkdc
|
APN |
16 |
15,617,848 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03091:Prkdc
|
APN |
16 |
15,523,174 (GRCm39) |
splice site |
probably benign |
|
IGL03100:Prkdc
|
APN |
16 |
15,531,499 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03128:Prkdc
|
APN |
16 |
15,518,608 (GRCm39) |
splice site |
probably benign |
|
IGL03168:Prkdc
|
APN |
16 |
15,652,030 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03204:Prkdc
|
APN |
16 |
15,587,665 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03390:Prkdc
|
APN |
16 |
15,488,490 (GRCm39) |
nonsense |
probably null |
|
anhimid
|
UTSW |
16 |
15,543,325 (GRCm39) |
critical splice donor site |
probably null |
|
anhinga
|
UTSW |
16 |
15,526,796 (GRCm39) |
critical splice donor site |
probably null |
|
Bushtit
|
UTSW |
16 |
15,570,628 (GRCm39) |
missense |
probably damaging |
0.97 |
clover
|
UTSW |
16 |
15,520,020 (GRCm39) |
splice site |
probably benign |
|
crackle
|
UTSW |
16 |
15,603,914 (GRCm39) |
critical splice donor site |
probably null |
|
Daffy
|
UTSW |
16 |
15,647,561 (GRCm39) |
missense |
possibly damaging |
0.86 |
darter
|
UTSW |
16 |
15,591,477 (GRCm39) |
missense |
possibly damaging |
0.93 |
Elmer_fudd
|
UTSW |
16 |
15,625,922 (GRCm39) |
missense |
probably benign |
0.01 |
envenomation
|
UTSW |
16 |
15,653,091 (GRCm39) |
nonsense |
probably null |
|
hobgoblin
|
UTSW |
16 |
15,633,850 (GRCm39) |
missense |
probably damaging |
1.00 |
Incubus
|
UTSW |
16 |
15,490,191 (GRCm39) |
missense |
probably damaging |
1.00 |
liming
|
UTSW |
16 |
15,570,693 (GRCm39) |
nonsense |
probably null |
|
newt
|
UTSW |
16 |
15,545,590 (GRCm39) |
missense |
probably benign |
0.04 |
ornithorhynchus
|
UTSW |
16 |
15,634,523 (GRCm39) |
critical splice donor site |
probably null |
|
primitive
|
UTSW |
16 |
15,653,022 (GRCm39) |
frame shift |
probably null |
|
roadrunner
|
UTSW |
16 |
15,651,751 (GRCm39) |
missense |
probably damaging |
1.00 |
Schreier
|
UTSW |
16 |
15,488,392 (GRCm39) |
missense |
probably benign |
0.00 |
screamer
|
UTSW |
16 |
15,649,146 (GRCm39) |
nonsense |
probably null |
|
Screamer10
|
UTSW |
16 |
15,585,889 (GRCm39) |
missense |
probably damaging |
0.98 |
screamer2
|
UTSW |
16 |
15,470,416 (GRCm39) |
critical splice donor site |
probably null |
|
screamer3
|
UTSW |
16 |
15,558,196 (GRCm39) |
critical splice donor site |
probably null |
|
screamer4
|
UTSW |
16 |
15,600,943 (GRCm39) |
missense |
probably benign |
0.00 |
screamer5
|
UTSW |
16 |
15,505,268 (GRCm39) |
missense |
probably benign |
|
screamer6
|
UTSW |
16 |
15,577,469 (GRCm39) |
missense |
probably damaging |
1.00 |
screamer7
|
UTSW |
16 |
15,472,681 (GRCm39) |
splice site |
probably null |
|
Screamer8
|
UTSW |
16 |
15,537,297 (GRCm39) |
missense |
probably benign |
0.00 |
Screamer9
|
UTSW |
16 |
15,552,786 (GRCm39) |
missense |
probably benign |
0.01 |
Tweetie
|
UTSW |
16 |
15,535,665 (GRCm39) |
missense |
probably damaging |
1.00 |
updock
|
UTSW |
16 |
15,612,958 (GRCm39) |
missense |
probably benign |
|
ANU23:Prkdc
|
UTSW |
16 |
15,485,595 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0008:Prkdc
|
UTSW |
16 |
15,526,565 (GRCm39) |
splice site |
probably benign |
|
R0018:Prkdc
|
UTSW |
16 |
15,544,406 (GRCm39) |
missense |
probably benign |
0.03 |
R0018:Prkdc
|
UTSW |
16 |
15,544,406 (GRCm39) |
missense |
probably benign |
0.03 |
R0069:Prkdc
|
UTSW |
16 |
15,544,368 (GRCm39) |
missense |
probably benign |
0.03 |
R0125:Prkdc
|
UTSW |
16 |
15,516,871 (GRCm39) |
missense |
probably damaging |
0.98 |
R0131:Prkdc
|
UTSW |
16 |
15,531,517 (GRCm39) |
missense |
probably benign |
0.09 |
R0131:Prkdc
|
UTSW |
16 |
15,531,517 (GRCm39) |
missense |
probably benign |
0.09 |
R0132:Prkdc
|
UTSW |
16 |
15,531,517 (GRCm39) |
missense |
probably benign |
0.09 |
R0137:Prkdc
|
UTSW |
16 |
15,558,196 (GRCm39) |
critical splice donor site |
probably null |
|
R0334:Prkdc
|
UTSW |
16 |
15,554,663 (GRCm39) |
missense |
probably benign |
0.00 |
R0373:Prkdc
|
UTSW |
16 |
15,609,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R0485:Prkdc
|
UTSW |
16 |
15,651,604 (GRCm39) |
missense |
probably damaging |
0.97 |
R0511:Prkdc
|
UTSW |
16 |
15,649,146 (GRCm39) |
nonsense |
probably null |
|
R0538:Prkdc
|
UTSW |
16 |
15,651,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R0595:Prkdc
|
UTSW |
16 |
15,625,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Prkdc
|
UTSW |
16 |
15,508,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R0630:Prkdc
|
UTSW |
16 |
15,628,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R0694:Prkdc
|
UTSW |
16 |
15,586,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R0702:Prkdc
|
UTSW |
16 |
15,603,835 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0965:Prkdc
|
UTSW |
16 |
15,647,580 (GRCm39) |
missense |
probably benign |
|
R1027:Prkdc
|
UTSW |
16 |
15,468,576 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1029:Prkdc
|
UTSW |
16 |
15,472,613 (GRCm39) |
splice site |
probably benign |
|
R1033:Prkdc
|
UTSW |
16 |
15,585,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R1067:Prkdc
|
UTSW |
16 |
15,570,646 (GRCm39) |
missense |
probably damaging |
0.99 |
R1116:Prkdc
|
UTSW |
16 |
15,600,943 (GRCm39) |
missense |
probably benign |
0.00 |
R1187:Prkdc
|
UTSW |
16 |
15,577,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R1226:Prkdc
|
UTSW |
16 |
15,491,861 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1279:Prkdc
|
UTSW |
16 |
15,508,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R1304:Prkdc
|
UTSW |
16 |
15,577,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R1314:Prkdc
|
UTSW |
16 |
15,482,091 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1351:Prkdc
|
UTSW |
16 |
15,485,564 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1509:Prkdc
|
UTSW |
16 |
15,549,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Prkdc
|
UTSW |
16 |
15,505,268 (GRCm39) |
missense |
probably benign |
|
R1531:Prkdc
|
UTSW |
16 |
15,589,970 (GRCm39) |
missense |
probably benign |
0.01 |
R1579:Prkdc
|
UTSW |
16 |
15,493,192 (GRCm39) |
missense |
probably benign |
0.00 |
R1669:Prkdc
|
UTSW |
16 |
15,551,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R1682:Prkdc
|
UTSW |
16 |
15,494,853 (GRCm39) |
missense |
probably benign |
0.19 |
R1713:Prkdc
|
UTSW |
16 |
15,612,958 (GRCm39) |
missense |
probably benign |
|
R1762:Prkdc
|
UTSW |
16 |
15,455,825 (GRCm39) |
missense |
probably benign |
|
R1789:Prkdc
|
UTSW |
16 |
15,557,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Prkdc
|
UTSW |
16 |
15,577,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R1848:Prkdc
|
UTSW |
16 |
15,625,922 (GRCm39) |
missense |
probably benign |
0.01 |
R1887:Prkdc
|
UTSW |
16 |
15,647,499 (GRCm39) |
missense |
probably benign |
0.00 |
R1891:Prkdc
|
UTSW |
16 |
15,543,300 (GRCm39) |
missense |
probably benign |
0.02 |
R1921:Prkdc
|
UTSW |
16 |
15,532,079 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1922:Prkdc
|
UTSW |
16 |
15,532,130 (GRCm39) |
missense |
probably benign |
0.00 |
R1929:Prkdc
|
UTSW |
16 |
15,472,681 (GRCm39) |
splice site |
probably null |
|
R1939:Prkdc
|
UTSW |
16 |
15,653,777 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2021:Prkdc
|
UTSW |
16 |
15,494,873 (GRCm39) |
missense |
probably benign |
0.00 |
R2033:Prkdc
|
UTSW |
16 |
15,505,216 (GRCm39) |
splice site |
probably benign |
|
R2056:Prkdc
|
UTSW |
16 |
15,545,469 (GRCm39) |
missense |
probably benign |
0.03 |
R2057:Prkdc
|
UTSW |
16 |
15,545,469 (GRCm39) |
missense |
probably benign |
0.03 |
R2058:Prkdc
|
UTSW |
16 |
15,545,469 (GRCm39) |
missense |
probably benign |
0.03 |
R2082:Prkdc
|
UTSW |
16 |
15,533,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Prkdc
|
UTSW |
16 |
15,505,254 (GRCm39) |
missense |
probably benign |
0.01 |
R2124:Prkdc
|
UTSW |
16 |
15,537,297 (GRCm39) |
missense |
probably benign |
0.00 |
R2164:Prkdc
|
UTSW |
16 |
15,523,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Prkdc
|
UTSW |
16 |
15,552,786 (GRCm39) |
missense |
probably benign |
0.01 |
R2191:Prkdc
|
UTSW |
16 |
15,516,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R2270:Prkdc
|
UTSW |
16 |
15,472,681 (GRCm39) |
splice site |
probably null |
|
R2271:Prkdc
|
UTSW |
16 |
15,472,681 (GRCm39) |
splice site |
probably null |
|
R2272:Prkdc
|
UTSW |
16 |
15,472,681 (GRCm39) |
splice site |
probably null |
|
R2356:Prkdc
|
UTSW |
16 |
15,502,068 (GRCm39) |
missense |
probably benign |
|
R2852:Prkdc
|
UTSW |
16 |
15,470,416 (GRCm39) |
critical splice donor site |
probably null |
|
R3115:Prkdc
|
UTSW |
16 |
15,482,222 (GRCm39) |
missense |
probably benign |
0.01 |
R3116:Prkdc
|
UTSW |
16 |
15,482,222 (GRCm39) |
missense |
probably benign |
0.01 |
R3499:Prkdc
|
UTSW |
16 |
15,585,889 (GRCm39) |
missense |
probably damaging |
0.98 |
R3687:Prkdc
|
UTSW |
16 |
15,617,831 (GRCm39) |
missense |
probably benign |
|
R3834:Prkdc
|
UTSW |
16 |
15,609,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3835:Prkdc
|
UTSW |
16 |
15,609,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R3961:Prkdc
|
UTSW |
16 |
15,647,475 (GRCm39) |
splice site |
probably null |
|
R4151:Prkdc
|
UTSW |
16 |
15,634,637 (GRCm39) |
missense |
probably benign |
|
R4233:Prkdc
|
UTSW |
16 |
15,653,783 (GRCm39) |
missense |
probably benign |
0.11 |
R4281:Prkdc
|
UTSW |
16 |
15,623,963 (GRCm39) |
splice site |
probably null |
|
R4296:Prkdc
|
UTSW |
16 |
15,555,769 (GRCm39) |
missense |
probably damaging |
0.99 |
R4344:Prkdc
|
UTSW |
16 |
15,585,886 (GRCm39) |
missense |
probably damaging |
0.98 |
R4424:Prkdc
|
UTSW |
16 |
15,653,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R4424:Prkdc
|
UTSW |
16 |
15,591,603 (GRCm39) |
missense |
probably damaging |
0.98 |
R4497:Prkdc
|
UTSW |
16 |
15,518,517 (GRCm39) |
missense |
probably benign |
0.43 |
R4549:Prkdc
|
UTSW |
16 |
15,554,734 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4594:Prkdc
|
UTSW |
16 |
15,585,830 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4603:Prkdc
|
UTSW |
16 |
15,628,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R4615:Prkdc
|
UTSW |
16 |
15,480,938 (GRCm39) |
missense |
probably damaging |
0.99 |
R4648:Prkdc
|
UTSW |
16 |
15,634,638 (GRCm39) |
missense |
probably benign |
0.05 |
R4662:Prkdc
|
UTSW |
16 |
15,551,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R4680:Prkdc
|
UTSW |
16 |
15,589,894 (GRCm39) |
missense |
probably benign |
0.00 |
R4700:Prkdc
|
UTSW |
16 |
15,519,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Prkdc
|
UTSW |
16 |
15,628,701 (GRCm39) |
missense |
probably benign |
0.32 |
R4720:Prkdc
|
UTSW |
16 |
15,485,579 (GRCm39) |
missense |
probably benign |
|
R4785:Prkdc
|
UTSW |
16 |
15,466,840 (GRCm39) |
missense |
probably benign |
0.21 |
R4822:Prkdc
|
UTSW |
16 |
15,468,576 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4829:Prkdc
|
UTSW |
16 |
15,519,939 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4981:Prkdc
|
UTSW |
16 |
15,496,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R4989:Prkdc
|
UTSW |
16 |
15,491,861 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5059:Prkdc
|
UTSW |
16 |
15,655,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Prkdc
|
UTSW |
16 |
15,589,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R5115:Prkdc
|
UTSW |
16 |
15,608,444 (GRCm39) |
missense |
probably benign |
|
R5151:Prkdc
|
UTSW |
16 |
15,533,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R5165:Prkdc
|
UTSW |
16 |
15,496,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R5215:Prkdc
|
UTSW |
16 |
15,589,985 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5270:Prkdc
|
UTSW |
16 |
15,552,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R5278:Prkdc
|
UTSW |
16 |
15,532,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5351:Prkdc
|
UTSW |
16 |
15,649,176 (GRCm39) |
missense |
probably benign |
0.03 |
R5416:Prkdc
|
UTSW |
16 |
15,623,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R5418:Prkdc
|
UTSW |
16 |
15,612,961 (GRCm39) |
missense |
probably benign |
0.20 |
R5437:Prkdc
|
UTSW |
16 |
15,587,739 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5452:Prkdc
|
UTSW |
16 |
15,586,501 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5518:Prkdc
|
UTSW |
16 |
15,496,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R5538:Prkdc
|
UTSW |
16 |
15,469,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R5589:Prkdc
|
UTSW |
16 |
15,524,655 (GRCm39) |
missense |
probably benign |
0.02 |
R5618:Prkdc
|
UTSW |
16 |
15,627,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R5640:Prkdc
|
UTSW |
16 |
15,647,633 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5661:Prkdc
|
UTSW |
16 |
15,628,634 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5771:Prkdc
|
UTSW |
16 |
15,482,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Prkdc
|
UTSW |
16 |
15,597,252 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5783:Prkdc
|
UTSW |
16 |
15,535,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R5792:Prkdc
|
UTSW |
16 |
15,634,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5797:Prkdc
|
UTSW |
16 |
15,555,698 (GRCm39) |
nonsense |
probably null |
|
R5826:Prkdc
|
UTSW |
16 |
15,551,962 (GRCm39) |
missense |
probably benign |
|
R5883:Prkdc
|
UTSW |
16 |
15,533,778 (GRCm39) |
missense |
probably benign |
|
R5895:Prkdc
|
UTSW |
16 |
15,570,693 (GRCm39) |
nonsense |
probably null |
|
R5998:Prkdc
|
UTSW |
16 |
15,601,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Prkdc
|
UTSW |
16 |
15,647,561 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6120:Prkdc
|
UTSW |
16 |
15,557,335 (GRCm39) |
missense |
probably benign |
0.00 |
R6145:Prkdc
|
UTSW |
16 |
15,589,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Prkdc
|
UTSW |
16 |
15,608,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R6293:Prkdc
|
UTSW |
16 |
15,605,019 (GRCm39) |
missense |
probably benign |
0.00 |
R6321:Prkdc
|
UTSW |
16 |
15,532,783 (GRCm39) |
missense |
probably benign |
|
R6376:Prkdc
|
UTSW |
16 |
15,587,749 (GRCm39) |
missense |
probably benign |
0.06 |
R6387:Prkdc
|
UTSW |
16 |
15,516,679 (GRCm39) |
missense |
probably benign |
0.01 |
R6406:Prkdc
|
UTSW |
16 |
15,535,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R6469:Prkdc
|
UTSW |
16 |
15,612,939 (GRCm39) |
missense |
probably benign |
0.10 |
R6486:Prkdc
|
UTSW |
16 |
15,570,628 (GRCm39) |
missense |
probably damaging |
0.97 |
R6665:Prkdc
|
UTSW |
16 |
15,603,914 (GRCm39) |
critical splice donor site |
probably null |
|
R6703:Prkdc
|
UTSW |
16 |
15,488,392 (GRCm39) |
missense |
probably benign |
0.00 |
R6774:Prkdc
|
UTSW |
16 |
15,543,325 (GRCm39) |
critical splice donor site |
probably null |
|
R6854:Prkdc
|
UTSW |
16 |
15,469,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R6878:Prkdc
|
UTSW |
16 |
15,594,936 (GRCm39) |
missense |
probably benign |
0.31 |
R6882:Prkdc
|
UTSW |
16 |
15,626,020 (GRCm39) |
missense |
probably benign |
0.33 |
R6882:Prkdc
|
UTSW |
16 |
15,601,127 (GRCm39) |
critical splice donor site |
probably null |
|
R6949:Prkdc
|
UTSW |
16 |
15,617,853 (GRCm39) |
missense |
probably benign |
|
R6950:Prkdc
|
UTSW |
16 |
15,633,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Prkdc
|
UTSW |
16 |
15,587,830 (GRCm39) |
missense |
probably benign |
0.00 |
R7064:Prkdc
|
UTSW |
16 |
15,608,317 (GRCm39) |
missense |
probably benign |
0.00 |
R7097:Prkdc
|
UTSW |
16 |
15,507,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R7201:Prkdc
|
UTSW |
16 |
15,516,667 (GRCm39) |
missense |
probably benign |
0.12 |
R7235:Prkdc
|
UTSW |
16 |
15,532,127 (GRCm39) |
missense |
probably benign |
|
R7283:Prkdc
|
UTSW |
16 |
15,535,628 (GRCm39) |
missense |
probably benign |
0.00 |
R7401:Prkdc
|
UTSW |
16 |
15,466,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R7525:Prkdc
|
UTSW |
16 |
15,490,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R7647:Prkdc
|
UTSW |
16 |
15,555,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Prkdc
|
UTSW |
16 |
15,649,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R7803:Prkdc
|
UTSW |
16 |
15,623,960 (GRCm39) |
missense |
probably null |
0.05 |
R7858:Prkdc
|
UTSW |
16 |
15,507,141 (GRCm39) |
missense |
probably benign |
0.11 |
R7872:Prkdc
|
UTSW |
16 |
15,532,870 (GRCm39) |
missense |
probably benign |
0.05 |
R7896:Prkdc
|
UTSW |
16 |
15,526,767 (GRCm39) |
missense |
probably damaging |
0.97 |
R8032:Prkdc
|
UTSW |
16 |
15,597,315 (GRCm39) |
missense |
probably benign |
0.00 |
R8055:Prkdc
|
UTSW |
16 |
15,634,749 (GRCm39) |
missense |
probably benign |
0.09 |
R8153:Prkdc
|
UTSW |
16 |
15,482,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R8281:Prkdc
|
UTSW |
16 |
15,523,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8302:Prkdc
|
UTSW |
16 |
15,653,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R8322:Prkdc
|
UTSW |
16 |
15,532,005 (GRCm39) |
splice site |
probably benign |
|
R8401:Prkdc
|
UTSW |
16 |
15,591,477 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8440:Prkdc
|
UTSW |
16 |
15,653,022 (GRCm39) |
frame shift |
probably null |
|
R8458:Prkdc
|
UTSW |
16 |
15,608,540 (GRCm39) |
critical splice donor site |
probably null |
|
R8472:Prkdc
|
UTSW |
16 |
15,469,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R8478:Prkdc
|
UTSW |
16 |
15,466,788 (GRCm39) |
missense |
probably benign |
0.00 |
R8515:Prkdc
|
UTSW |
16 |
15,482,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R8546:Prkdc
|
UTSW |
16 |
15,480,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R8678:Prkdc
|
UTSW |
16 |
15,526,796 (GRCm39) |
critical splice donor site |
probably null |
|
R8739:Prkdc
|
UTSW |
16 |
15,626,068 (GRCm39) |
missense |
probably benign |
0.01 |
R8749:Prkdc
|
UTSW |
16 |
15,601,029 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8836:Prkdc
|
UTSW |
16 |
15,545,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R8904:Prkdc
|
UTSW |
16 |
15,545,590 (GRCm39) |
missense |
probably benign |
0.04 |
R8952:Prkdc
|
UTSW |
16 |
15,491,624 (GRCm39) |
intron |
probably benign |
|
R8971:Prkdc
|
UTSW |
16 |
15,493,229 (GRCm39) |
missense |
probably null |
0.99 |
R8974:Prkdc
|
UTSW |
16 |
15,617,726 (GRCm39) |
splice site |
probably null |
|
R9052:Prkdc
|
UTSW |
16 |
15,508,160 (GRCm39) |
missense |
probably benign |
0.05 |
R9069:Prkdc
|
UTSW |
16 |
15,653,091 (GRCm39) |
nonsense |
probably null |
|
R9200:Prkdc
|
UTSW |
16 |
15,523,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R9235:Prkdc
|
UTSW |
16 |
15,651,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R9278:Prkdc
|
UTSW |
16 |
15,634,523 (GRCm39) |
critical splice donor site |
probably null |
|
R9309:Prkdc
|
UTSW |
16 |
15,526,792 (GRCm39) |
nonsense |
probably null |
|
R9386:Prkdc
|
UTSW |
16 |
15,496,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R9452:Prkdc
|
UTSW |
16 |
15,485,465 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9500:Prkdc
|
UTSW |
16 |
15,657,079 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9608:Prkdc
|
UTSW |
16 |
15,548,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R9608:Prkdc
|
UTSW |
16 |
15,548,334 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9636:Prkdc
|
UTSW |
16 |
15,548,341 (GRCm39) |
missense |
probably benign |
0.19 |
R9656:Prkdc
|
UTSW |
16 |
15,617,818 (GRCm39) |
missense |
probably benign |
0.00 |
R9674:Prkdc
|
UTSW |
16 |
15,533,819 (GRCm39) |
missense |
probably damaging |
0.98 |
R9760:Prkdc
|
UTSW |
16 |
15,657,044 (GRCm39) |
nonsense |
probably null |
|
X0023:Prkdc
|
UTSW |
16 |
15,558,142 (GRCm39) |
missense |
probably benign |
|
Z1176:Prkdc
|
UTSW |
16 |
15,505,286 (GRCm39) |
nonsense |
probably null |
|
|