Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6820408C15Rik |
T |
A |
2: 152,282,808 (GRCm39) |
I221K |
possibly damaging |
Het |
Abhd16a |
T |
A |
17: 35,321,318 (GRCm39) |
S498T |
probably benign |
Het |
Adamts18 |
G |
A |
8: 114,463,357 (GRCm39) |
R830* |
probably null |
Het |
Ankrd27 |
A |
G |
7: 35,332,417 (GRCm39) |
D848G |
probably benign |
Het |
Art3 |
A |
G |
5: 92,551,478 (GRCm39) |
Y279C |
probably damaging |
Het |
Atp2c2 |
A |
G |
8: 120,481,002 (GRCm39) |
T797A |
probably benign |
Het |
Ccdc121rt1 |
A |
T |
1: 181,338,829 (GRCm39) |
V41E |
possibly damaging |
Het |
Ccdc122 |
A |
T |
14: 77,305,381 (GRCm39) |
I12F |
possibly damaging |
Het |
Ccdc154 |
T |
C |
17: 25,389,888 (GRCm39) |
L508P |
probably damaging |
Het |
Cdk5r2 |
A |
G |
1: 74,894,831 (GRCm39) |
D192G |
probably damaging |
Het |
Cgn |
C |
T |
3: 94,685,564 (GRCm39) |
A320T |
probably benign |
Het |
Cklf |
A |
G |
8: 104,988,184 (GRCm39) |
K106E |
probably benign |
Het |
Clec12a |
C |
A |
6: 129,330,628 (GRCm39) |
T70K |
probably benign |
Het |
Clock |
A |
G |
5: 76,402,258 (GRCm39) |
V134A |
possibly damaging |
Het |
CN725425 |
G |
A |
15: 91,129,904 (GRCm39) |
A256T |
possibly damaging |
Het |
Csf1r |
A |
T |
18: 61,262,119 (GRCm39) |
I792F |
probably damaging |
Het |
Csn1s1 |
T |
G |
5: 87,821,120 (GRCm39) |
S33A |
probably benign |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
D5Ertd579e |
A |
G |
5: 36,830,249 (GRCm39) |
V25A |
probably benign |
Het |
D630045J12Rik |
C |
T |
6: 38,125,302 (GRCm39) |
V1571M |
possibly damaging |
Het |
Ddx5 |
C |
A |
11: 106,675,833 (GRCm39) |
V286L |
possibly damaging |
Het |
Deup1 |
G |
A |
9: 15,523,310 (GRCm39) |
Q58* |
probably null |
Het |
Dnhd1 |
T |
G |
7: 105,362,840 (GRCm39) |
L3801V |
probably benign |
Het |
Dph2 |
T |
A |
4: 117,748,527 (GRCm39) |
D82V |
probably damaging |
Het |
Ercc6 |
A |
G |
14: 32,296,859 (GRCm39) |
D1283G |
probably damaging |
Het |
Evi5l |
G |
T |
8: 4,255,406 (GRCm39) |
V477L |
probably benign |
Het |
Fam91a1 |
A |
G |
15: 58,303,059 (GRCm39) |
T323A |
probably benign |
Het |
Fanca |
G |
A |
8: 124,035,261 (GRCm39) |
T228M |
probably damaging |
Het |
Fat4 |
T |
G |
3: 39,037,195 (GRCm39) |
S3616A |
probably benign |
Het |
Fbxo16 |
G |
T |
14: 65,558,746 (GRCm39) |
A302S |
probably benign |
Het |
Fkbp5 |
T |
C |
17: 28,647,343 (GRCm39) |
E164G |
probably damaging |
Het |
Fpr-rs3 |
T |
C |
17: 20,844,211 (GRCm39) |
Y310C |
possibly damaging |
Het |
Fsip2 |
T |
C |
2: 82,815,169 (GRCm39) |
I3634T |
probably benign |
Het |
Gm6327 |
T |
C |
16: 12,578,845 (GRCm39) |
|
noncoding transcript |
Het |
Gnl3 |
A |
T |
14: 30,735,462 (GRCm39) |
N411K |
possibly damaging |
Het |
Golga1 |
A |
T |
2: 38,929,118 (GRCm39) |
D308E |
probably damaging |
Het |
Gpbar1 |
TACCAC |
TAC |
1: 74,318,704 (GRCm39) |
|
probably benign |
Het |
Gsap |
A |
T |
5: 21,459,037 (GRCm39) |
T501S |
probably benign |
Het |
Helq |
A |
G |
5: 100,940,737 (GRCm39) |
|
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,234,108 (GRCm39) |
H291R |
probably benign |
Het |
Htt |
A |
T |
5: 34,970,367 (GRCm39) |
D505V |
probably damaging |
Het |
Ildr1 |
C |
T |
16: 36,528,660 (GRCm39) |
T35I |
probably benign |
Het |
Iqgap2 |
A |
G |
13: 95,794,305 (GRCm39) |
|
probably null |
Het |
Kansl1 |
C |
T |
11: 104,315,147 (GRCm39) |
R297H |
probably damaging |
Het |
Kat2b-ps |
T |
C |
5: 93,539,644 (GRCm39) |
|
noncoding transcript |
Het |
Kbtbd2 |
A |
G |
6: 56,758,943 (GRCm39) |
F60S |
probably benign |
Het |
Kcnt2 |
A |
T |
1: 140,537,388 (GRCm39) |
S1116C |
probably damaging |
Het |
Krt9 |
C |
T |
11: 100,079,538 (GRCm39) |
G618E |
unknown |
Het |
Lsm5 |
A |
T |
6: 56,680,309 (GRCm39) |
D44E |
probably damaging |
Het |
Mdn1 |
A |
G |
4: 32,734,418 (GRCm39) |
D3275G |
probably benign |
Het |
Mindy2 |
A |
T |
9: 70,512,453 (GRCm39) |
V599E |
possibly damaging |
Het |
Nelfa |
A |
G |
5: 34,059,162 (GRCm39) |
V231A |
probably benign |
Het |
Nepro |
T |
C |
16: 44,555,156 (GRCm39) |
Y411H |
probably benign |
Het |
Nes |
T |
A |
3: 87,882,983 (GRCm39) |
L414Q |
probably damaging |
Het |
Neurl2 |
T |
A |
2: 164,675,122 (GRCm39) |
|
probably null |
Het |
Nkx1-1 |
G |
T |
5: 33,588,410 (GRCm39) |
Q293K |
possibly damaging |
Het |
Nphp3 |
C |
T |
9: 103,909,198 (GRCm39) |
H803Y |
probably benign |
Het |
Obscn |
A |
G |
11: 59,023,292 (GRCm39) |
V695A |
probably damaging |
Het |
Or10v5 |
A |
G |
19: 11,806,300 (GRCm39) |
L30P |
probably benign |
Het |
Or12d15 |
G |
A |
17: 37,693,910 (GRCm39) |
A151T |
probably damaging |
Het |
Or2f1 |
T |
C |
6: 42,721,621 (GRCm39) |
S217P |
probably damaging |
Het |
Or2t48 |
T |
C |
11: 58,419,903 (GRCm39) |
E303G |
probably benign |
Het |
Or4c106 |
T |
C |
2: 88,682,516 (GRCm39) |
V74A |
possibly damaging |
Het |
Or4f17-ps1 |
T |
A |
2: 111,357,969 (GRCm39) |
F103L |
probably damaging |
Het |
Or4p7 |
T |
A |
2: 88,221,674 (GRCm39) |
L28I |
probably benign |
Het |
Or7g35 |
A |
G |
9: 19,496,504 (GRCm39) |
T224A |
probably benign |
Het |
Or8d2b |
A |
G |
9: 38,789,400 (GRCm39) |
*309W |
probably null |
Het |
Orai3 |
T |
A |
7: 127,373,348 (GRCm39) |
L283Q |
probably damaging |
Het |
Pcdhb13 |
A |
T |
18: 37,576,237 (GRCm39) |
D205V |
probably benign |
Het |
Pdlim5 |
G |
A |
3: 142,017,740 (GRCm39) |
|
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,375,734 (GRCm39) |
V1467A |
probably damaging |
Het |
Pgm3 |
A |
G |
9: 86,444,732 (GRCm39) |
S268P |
probably benign |
Het |
Piezo2 |
A |
T |
18: 63,207,751 (GRCm39) |
I1420N |
probably damaging |
Het |
Pigp |
C |
A |
16: 94,160,006 (GRCm39) |
G134V |
probably benign |
Het |
Pik3c2g |
T |
C |
6: 139,789,657 (GRCm39) |
Y385H |
possibly damaging |
Het |
Pnliprp2 |
G |
A |
19: 58,754,750 (GRCm39) |
E265K |
probably benign |
Het |
Psmd13 |
T |
A |
7: 140,466,766 (GRCm39) |
Y117* |
probably null |
Het |
Pum1 |
T |
G |
4: 130,396,448 (GRCm39) |
S68A |
probably benign |
Het |
Rnf167 |
T |
A |
11: 70,540,701 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
T |
C |
11: 119,318,983 (GRCm39) |
V1148A |
possibly damaging |
Het |
Rnf216 |
T |
C |
5: 143,076,071 (GRCm39) |
E271G |
probably benign |
Het |
Ros1 |
A |
T |
10: 52,031,087 (GRCm39) |
I506N |
probably damaging |
Het |
Rpl37 |
G |
A |
15: 5,147,128 (GRCm39) |
R56Q |
possibly damaging |
Het |
Rpl41 |
A |
C |
10: 128,384,576 (GRCm39) |
|
probably benign |
Het |
Rttn |
A |
T |
18: 89,060,292 (GRCm39) |
H998L |
probably damaging |
Het |
Sacs |
G |
T |
14: 61,450,571 (GRCm39) |
A4206S |
probably damaging |
Het |
Slc22a14 |
CTTTCCTGAA |
C |
9: 119,003,101 (GRCm39) |
|
probably benign |
Het |
Slc36a3 |
T |
C |
11: 55,037,630 (GRCm39) |
|
probably benign |
Het |
Slc39a3 |
A |
T |
10: 80,866,796 (GRCm39) |
W317R |
probably damaging |
Het |
Snd1 |
C |
A |
6: 28,884,250 (GRCm39) |
Y766* |
probably null |
Het |
Snrpd1 |
T |
C |
18: 10,626,835 (GRCm39) |
V34A |
probably benign |
Het |
Spire2 |
T |
A |
8: 124,083,583 (GRCm39) |
I189N |
probably damaging |
Het |
Stard6 |
A |
C |
18: 70,631,631 (GRCm39) |
D74A |
possibly damaging |
Het |
Sufu |
C |
T |
19: 46,463,991 (GRCm39) |
T401I |
possibly damaging |
Het |
Taar7b |
T |
A |
10: 23,876,243 (GRCm39) |
F136Y |
probably benign |
Het |
Taf6 |
G |
A |
5: 138,181,465 (GRCm39) |
Q156* |
probably null |
Het |
Tcp11l2 |
A |
G |
10: 84,427,027 (GRCm39) |
I164V |
probably damaging |
Het |
Tead4 |
T |
C |
6: 128,247,950 (GRCm39) |
D29G |
probably damaging |
Het |
Tns4 |
G |
T |
11: 98,966,039 (GRCm39) |
P448Q |
probably damaging |
Het |
Trappc9 |
G |
T |
15: 72,808,905 (GRCm39) |
N540K |
probably damaging |
Het |
Trbv28 |
C |
T |
6: 41,248,788 (GRCm39) |
S106F |
probably damaging |
Het |
Usp16 |
T |
A |
16: 87,277,802 (GRCm39) |
M684K |
probably damaging |
Het |
Usp45 |
A |
T |
4: 21,815,372 (GRCm39) |
T362S |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,836,961 (GRCm39) |
M2861K |
probably benign |
Het |
Vps8 |
T |
C |
16: 21,278,536 (GRCm39) |
S267P |
probably damaging |
Het |
Wdfy3 |
C |
T |
5: 102,090,985 (GRCm39) |
D532N |
probably benign |
Het |
Zbtb34 |
T |
A |
2: 33,301,626 (GRCm39) |
Q305L |
probably benign |
Het |
Zfp267 |
C |
T |
3: 36,218,285 (GRCm39) |
R102C |
possibly damaging |
Het |
Zfp352 |
T |
A |
4: 90,112,376 (GRCm39) |
V172E |
probably benign |
Het |
Zfp454 |
T |
C |
11: 50,764,950 (GRCm39) |
N161D |
probably benign |
Het |
Zfp804b |
A |
T |
5: 6,821,198 (GRCm39) |
S622T |
probably damaging |
Het |
Zswim4 |
G |
T |
8: 84,938,852 (GRCm39) |
A1010D |
probably benign |
Het |
|
Other mutations in Ptprq |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Ptprq
|
APN |
10 |
107,412,790 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00537:Ptprq
|
APN |
10 |
107,546,383 (GRCm39) |
missense |
probably benign |
0.07 |
IGL00547:Ptprq
|
APN |
10 |
107,554,402 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00586:Ptprq
|
APN |
10 |
107,443,983 (GRCm39) |
splice site |
probably benign |
|
IGL00648:Ptprq
|
APN |
10 |
107,482,577 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01123:Ptprq
|
APN |
10 |
107,522,079 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01343:Ptprq
|
APN |
10 |
107,474,700 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01348:Ptprq
|
APN |
10 |
107,547,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01433:Ptprq
|
APN |
10 |
107,412,741 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01510:Ptprq
|
APN |
10 |
107,547,909 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01535:Ptprq
|
APN |
10 |
107,535,457 (GRCm39) |
missense |
probably benign |
|
IGL01631:Ptprq
|
APN |
10 |
107,479,399 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01633:Ptprq
|
APN |
10 |
107,535,584 (GRCm39) |
splice site |
probably benign |
|
IGL01702:Ptprq
|
APN |
10 |
107,353,727 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01733:Ptprq
|
APN |
10 |
107,498,460 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01806:Ptprq
|
APN |
10 |
107,535,469 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01832:Ptprq
|
APN |
10 |
107,401,700 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01961:Ptprq
|
APN |
10 |
107,479,515 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02108:Ptprq
|
APN |
10 |
107,482,478 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02120:Ptprq
|
APN |
10 |
107,503,333 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02160:Ptprq
|
APN |
10 |
107,489,426 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02178:Ptprq
|
APN |
10 |
107,522,180 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02249:Ptprq
|
APN |
10 |
107,418,220 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02267:Ptprq
|
APN |
10 |
107,482,419 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02527:Ptprq
|
APN |
10 |
107,522,424 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02529:Ptprq
|
APN |
10 |
107,471,226 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02542:Ptprq
|
APN |
10 |
107,498,416 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02582:Ptprq
|
APN |
10 |
107,479,860 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02708:Ptprq
|
APN |
10 |
107,488,561 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02894:Ptprq
|
APN |
10 |
107,503,285 (GRCm39) |
missense |
probably benign |
|
IGL02903:Ptprq
|
APN |
10 |
107,502,447 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02951:Ptprq
|
APN |
10 |
107,503,321 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02982:Ptprq
|
APN |
10 |
107,422,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03000:Ptprq
|
APN |
10 |
107,378,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03024:Ptprq
|
APN |
10 |
107,521,427 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03240:Ptprq
|
APN |
10 |
107,524,368 (GRCm39) |
missense |
probably benign |
|
P0043:Ptprq
|
UTSW |
10 |
107,416,086 (GRCm39) |
missense |
probably benign |
0.03 |
PIT4812001:Ptprq
|
UTSW |
10 |
107,502,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R0200:Ptprq
|
UTSW |
10 |
107,521,018 (GRCm39) |
missense |
probably benign |
|
R0268:Ptprq
|
UTSW |
10 |
107,541,409 (GRCm39) |
missense |
probably benign |
|
R0276:Ptprq
|
UTSW |
10 |
107,378,596 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0279:Ptprq
|
UTSW |
10 |
107,444,278 (GRCm39) |
missense |
probably damaging |
0.96 |
R0335:Ptprq
|
UTSW |
10 |
107,544,589 (GRCm39) |
missense |
probably benign |
|
R0344:Ptprq
|
UTSW |
10 |
107,541,443 (GRCm39) |
missense |
probably benign |
|
R0357:Ptprq
|
UTSW |
10 |
107,522,060 (GRCm39) |
splice site |
probably benign |
|
R0454:Ptprq
|
UTSW |
10 |
107,418,391 (GRCm39) |
nonsense |
probably null |
|
R0479:Ptprq
|
UTSW |
10 |
107,479,855 (GRCm39) |
nonsense |
probably null |
|
R0491:Ptprq
|
UTSW |
10 |
107,444,036 (GRCm39) |
missense |
probably damaging |
0.98 |
R0519:Ptprq
|
UTSW |
10 |
107,374,781 (GRCm39) |
splice site |
probably benign |
|
R0523:Ptprq
|
UTSW |
10 |
107,416,081 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0553:Ptprq
|
UTSW |
10 |
107,546,488 (GRCm39) |
missense |
probably benign |
0.33 |
R0746:Ptprq
|
UTSW |
10 |
107,353,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R0755:Ptprq
|
UTSW |
10 |
107,418,400 (GRCm39) |
missense |
probably benign |
0.09 |
R1434:Ptprq
|
UTSW |
10 |
107,422,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Ptprq
|
UTSW |
10 |
107,498,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Ptprq
|
UTSW |
10 |
107,554,435 (GRCm39) |
missense |
probably damaging |
0.97 |
R1470:Ptprq
|
UTSW |
10 |
107,554,435 (GRCm39) |
missense |
probably damaging |
0.97 |
R1558:Ptprq
|
UTSW |
10 |
107,479,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R1567:Ptprq
|
UTSW |
10 |
107,401,748 (GRCm39) |
missense |
probably benign |
0.13 |
R1711:Ptprq
|
UTSW |
10 |
107,370,560 (GRCm39) |
nonsense |
probably null |
|
R1720:Ptprq
|
UTSW |
10 |
107,522,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R1746:Ptprq
|
UTSW |
10 |
107,474,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R1776:Ptprq
|
UTSW |
10 |
107,520,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Ptprq
|
UTSW |
10 |
107,554,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Ptprq
|
UTSW |
10 |
107,479,860 (GRCm39) |
missense |
probably benign |
0.19 |
R1944:Ptprq
|
UTSW |
10 |
107,418,249 (GRCm39) |
missense |
probably benign |
0.23 |
R1945:Ptprq
|
UTSW |
10 |
107,418,249 (GRCm39) |
missense |
probably benign |
0.23 |
R2006:Ptprq
|
UTSW |
10 |
107,502,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Ptprq
|
UTSW |
10 |
107,503,283 (GRCm39) |
missense |
probably damaging |
0.96 |
R2015:Ptprq
|
UTSW |
10 |
107,503,283 (GRCm39) |
missense |
probably damaging |
0.96 |
R2097:Ptprq
|
UTSW |
10 |
107,489,354 (GRCm39) |
missense |
probably benign |
0.05 |
R2172:Ptprq
|
UTSW |
10 |
107,426,855 (GRCm39) |
nonsense |
probably null |
|
R2174:Ptprq
|
UTSW |
10 |
107,541,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R2248:Ptprq
|
UTSW |
10 |
107,478,931 (GRCm39) |
splice site |
probably null |
|
R2404:Ptprq
|
UTSW |
10 |
107,522,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R3423:Ptprq
|
UTSW |
10 |
107,418,337 (GRCm39) |
missense |
probably damaging |
0.99 |
R3683:Ptprq
|
UTSW |
10 |
107,544,489 (GRCm39) |
missense |
probably benign |
0.01 |
R3875:Ptprq
|
UTSW |
10 |
107,520,965 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3945:Ptprq
|
UTSW |
10 |
107,522,253 (GRCm39) |
splice site |
probably benign |
|
R3946:Ptprq
|
UTSW |
10 |
107,522,253 (GRCm39) |
splice site |
probably benign |
|
R3974:Ptprq
|
UTSW |
10 |
107,547,923 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3982:Ptprq
|
UTSW |
10 |
107,379,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R4105:Ptprq
|
UTSW |
10 |
107,408,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R4118:Ptprq
|
UTSW |
10 |
107,547,781 (GRCm39) |
missense |
probably benign |
0.37 |
R4175:Ptprq
|
UTSW |
10 |
107,547,778 (GRCm39) |
missense |
probably benign |
|
R4231:Ptprq
|
UTSW |
10 |
107,522,144 (GRCm39) |
nonsense |
probably null |
|
R4356:Ptprq
|
UTSW |
10 |
107,444,225 (GRCm39) |
missense |
probably damaging |
0.99 |
R4435:Ptprq
|
UTSW |
10 |
107,520,916 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4678:Ptprq
|
UTSW |
10 |
107,521,043 (GRCm39) |
missense |
probably benign |
0.19 |
R4679:Ptprq
|
UTSW |
10 |
107,521,043 (GRCm39) |
missense |
probably benign |
0.19 |
R4745:Ptprq
|
UTSW |
10 |
107,360,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Ptprq
|
UTSW |
10 |
107,524,288 (GRCm39) |
missense |
probably benign |
|
R4778:Ptprq
|
UTSW |
10 |
107,426,883 (GRCm39) |
missense |
probably benign |
0.15 |
R4808:Ptprq
|
UTSW |
10 |
107,554,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R4809:Ptprq
|
UTSW |
10 |
107,399,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R4818:Ptprq
|
UTSW |
10 |
107,546,442 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4845:Ptprq
|
UTSW |
10 |
107,489,393 (GRCm39) |
missense |
probably benign |
0.00 |
R4901:Ptprq
|
UTSW |
10 |
107,524,275 (GRCm39) |
missense |
probably benign |
0.01 |
R4942:Ptprq
|
UTSW |
10 |
107,524,290 (GRCm39) |
missense |
probably benign |
0.01 |
R4946:Ptprq
|
UTSW |
10 |
107,361,595 (GRCm39) |
missense |
probably benign |
|
R4959:Ptprq
|
UTSW |
10 |
107,522,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R5007:Ptprq
|
UTSW |
10 |
107,444,137 (GRCm39) |
missense |
probably benign |
0.00 |
R5053:Ptprq
|
UTSW |
10 |
107,399,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Ptprq
|
UTSW |
10 |
107,370,540 (GRCm39) |
missense |
probably benign |
0.37 |
R5090:Ptprq
|
UTSW |
10 |
107,361,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R5158:Ptprq
|
UTSW |
10 |
107,370,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5163:Ptprq
|
UTSW |
10 |
107,360,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R5222:Ptprq
|
UTSW |
10 |
107,498,425 (GRCm39) |
missense |
probably damaging |
0.96 |
R5244:Ptprq
|
UTSW |
10 |
107,422,556 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5249:Ptprq
|
UTSW |
10 |
107,535,496 (GRCm39) |
missense |
probably damaging |
0.99 |
R5503:Ptprq
|
UTSW |
10 |
107,524,189 (GRCm39) |
splice site |
probably null |
|
R5508:Ptprq
|
UTSW |
10 |
107,522,092 (GRCm39) |
missense |
probably benign |
0.00 |
R5601:Ptprq
|
UTSW |
10 |
107,444,291 (GRCm39) |
missense |
probably benign |
|
R5722:Ptprq
|
UTSW |
10 |
107,522,226 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5819:Ptprq
|
UTSW |
10 |
107,555,744 (GRCm39) |
start gained |
probably benign |
|
R5862:Ptprq
|
UTSW |
10 |
107,401,739 (GRCm39) |
missense |
probably benign |
0.02 |
R5891:Ptprq
|
UTSW |
10 |
107,412,756 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5916:Ptprq
|
UTSW |
10 |
107,359,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R6054:Ptprq
|
UTSW |
10 |
107,418,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R6058:Ptprq
|
UTSW |
10 |
107,471,135 (GRCm39) |
missense |
probably benign |
0.00 |
R6075:Ptprq
|
UTSW |
10 |
107,361,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R6101:Ptprq
|
UTSW |
10 |
107,416,127 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6189:Ptprq
|
UTSW |
10 |
107,353,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Ptprq
|
UTSW |
10 |
107,471,199 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6351:Ptprq
|
UTSW |
10 |
107,544,529 (GRCm39) |
missense |
probably damaging |
0.99 |
R6394:Ptprq
|
UTSW |
10 |
107,478,804 (GRCm39) |
nonsense |
probably null |
|
R6449:Ptprq
|
UTSW |
10 |
107,541,444 (GRCm39) |
missense |
probably benign |
0.00 |
R6526:Ptprq
|
UTSW |
10 |
107,378,514 (GRCm39) |
nonsense |
probably null |
|
R6544:Ptprq
|
UTSW |
10 |
107,444,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R6609:Ptprq
|
UTSW |
10 |
107,408,829 (GRCm39) |
missense |
probably damaging |
0.99 |
R6862:Ptprq
|
UTSW |
10 |
107,522,086 (GRCm39) |
missense |
probably damaging |
0.96 |
R6874:Ptprq
|
UTSW |
10 |
107,554,460 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6892:Ptprq
|
UTSW |
10 |
107,411,865 (GRCm39) |
missense |
probably benign |
0.00 |
R7082:Ptprq
|
UTSW |
10 |
107,544,591 (GRCm39) |
missense |
probably benign |
0.10 |
R7210:Ptprq
|
UTSW |
10 |
107,521,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R7253:Ptprq
|
UTSW |
10 |
107,444,134 (GRCm39) |
missense |
probably benign |
0.30 |
R7293:Ptprq
|
UTSW |
10 |
107,471,367 (GRCm39) |
nonsense |
probably null |
|
R7445:Ptprq
|
UTSW |
10 |
107,426,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7632:Ptprq
|
UTSW |
10 |
107,547,783 (GRCm39) |
missense |
probably benign |
0.32 |
R7685:Ptprq
|
UTSW |
10 |
107,479,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R7703:Ptprq
|
UTSW |
10 |
107,480,007 (GRCm39) |
missense |
probably benign |
0.01 |
R7774:Ptprq
|
UTSW |
10 |
107,479,530 (GRCm39) |
missense |
probably damaging |
0.96 |
R7897:Ptprq
|
UTSW |
10 |
107,546,484 (GRCm39) |
missense |
probably benign |
0.21 |
R7936:Ptprq
|
UTSW |
10 |
107,488,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R7983:Ptprq
|
UTSW |
10 |
107,444,272 (GRCm39) |
nonsense |
probably null |
|
R8023:Ptprq
|
UTSW |
10 |
107,488,477 (GRCm39) |
nonsense |
probably null |
|
R8071:Ptprq
|
UTSW |
10 |
107,479,896 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8084:Ptprq
|
UTSW |
10 |
107,444,294 (GRCm39) |
missense |
probably benign |
|
R8086:Ptprq
|
UTSW |
10 |
107,482,500 (GRCm39) |
nonsense |
probably null |
|
R8169:Ptprq
|
UTSW |
10 |
107,418,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R8223:Ptprq
|
UTSW |
10 |
107,535,499 (GRCm39) |
missense |
probably benign |
0.00 |
R8235:Ptprq
|
UTSW |
10 |
107,541,351 (GRCm39) |
missense |
probably benign |
0.32 |
R8235:Ptprq
|
UTSW |
10 |
107,418,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R8278:Ptprq
|
UTSW |
10 |
107,522,239 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8710:Ptprq
|
UTSW |
10 |
107,411,919 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8828:Ptprq
|
UTSW |
10 |
107,482,513 (GRCm39) |
missense |
probably benign |
|
R8830:Ptprq
|
UTSW |
10 |
107,422,556 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8869:Ptprq
|
UTSW |
10 |
107,535,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R9012:Ptprq
|
UTSW |
10 |
107,489,411 (GRCm39) |
missense |
probably benign |
0.09 |
R9072:Ptprq
|
UTSW |
10 |
107,401,736 (GRCm39) |
missense |
|
|
R9153:Ptprq
|
UTSW |
10 |
107,416,126 (GRCm39) |
missense |
probably damaging |
0.98 |
R9202:Ptprq
|
UTSW |
10 |
107,522,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R9252:Ptprq
|
UTSW |
10 |
107,522,247 (GRCm39) |
missense |
probably benign |
0.12 |
R9306:Ptprq
|
UTSW |
10 |
107,422,599 (GRCm39) |
missense |
probably benign |
0.00 |
R9492:Ptprq
|
UTSW |
10 |
107,478,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R9519:Ptprq
|
UTSW |
10 |
107,520,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R9581:Ptprq
|
UTSW |
10 |
107,547,771 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9593:Ptprq
|
UTSW |
10 |
107,524,254 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9621:Ptprq
|
UTSW |
10 |
107,378,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R9732:Ptprq
|
UTSW |
10 |
107,412,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R9743:Ptprq
|
UTSW |
10 |
107,520,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R9771:Ptprq
|
UTSW |
10 |
107,521,085 (GRCm39) |
missense |
probably damaging |
0.99 |
R9788:Ptprq
|
UTSW |
10 |
107,401,751 (GRCm39) |
missense |
probably benign |
0.24 |
Z1088:Ptprq
|
UTSW |
10 |
107,535,533 (GRCm39) |
missense |
possibly damaging |
0.56 |
Z1176:Ptprq
|
UTSW |
10 |
107,361,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|