Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700061I17Rik |
G |
T |
3: 116,861,385 (GRCm39) |
|
noncoding transcript |
Het |
2300003K06Rik |
G |
T |
11: 99,728,793 (GRCm39) |
Q17K |
probably benign |
Het |
Abca16 |
T |
C |
7: 120,119,256 (GRCm39) |
V999A |
probably benign |
Het |
Actn3 |
C |
T |
19: 4,915,483 (GRCm39) |
|
probably benign |
Het |
Agap2 |
T |
A |
10: 126,926,981 (GRCm39) |
|
probably benign |
Het |
Ago3 |
C |
A |
4: 126,265,580 (GRCm39) |
R278L |
probably benign |
Het |
Aldh1a2 |
T |
C |
9: 71,192,492 (GRCm39) |
V449A |
possibly damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Aplnr |
A |
G |
2: 84,967,353 (GRCm39) |
Y126C |
probably damaging |
Het |
Apob |
T |
C |
12: 8,066,084 (GRCm39) |
I4351T |
possibly damaging |
Het |
Ash1l |
T |
C |
3: 88,914,659 (GRCm39) |
L1763P |
probably benign |
Het |
Aspn |
T |
C |
13: 49,710,849 (GRCm39) |
S165P |
possibly damaging |
Het |
Atg13 |
A |
T |
2: 91,510,335 (GRCm39) |
V349E |
probably damaging |
Het |
Atp1b2 |
T |
A |
11: 69,493,309 (GRCm39) |
|
probably null |
Het |
B3glct |
A |
T |
5: 149,677,604 (GRCm39) |
D411V |
probably damaging |
Het |
Bcar3 |
A |
T |
3: 122,316,840 (GRCm39) |
I255F |
probably damaging |
Het |
Cacna1b |
G |
A |
2: 24,608,148 (GRCm39) |
|
probably benign |
Het |
Cep164 |
T |
G |
9: 45,690,198 (GRCm39) |
E675A |
possibly damaging |
Het |
Chd1l |
C |
T |
3: 97,490,047 (GRCm39) |
E503K |
probably benign |
Het |
Chst8 |
C |
A |
7: 34,447,593 (GRCm39) |
M8I |
possibly damaging |
Het |
Clec4n |
A |
G |
6: 123,212,475 (GRCm39) |
E67G |
probably benign |
Het |
Cobll1 |
A |
T |
2: 64,929,480 (GRCm39) |
D653E |
probably damaging |
Het |
Col9a1 |
T |
C |
1: 24,276,579 (GRCm39) |
|
probably null |
Het |
Crip2 |
T |
C |
12: 113,107,124 (GRCm39) |
L30P |
probably damaging |
Het |
Ctbp1 |
C |
T |
5: 33,418,407 (GRCm39) |
V22I |
probably benign |
Het |
Cwc22 |
T |
C |
2: 77,747,521 (GRCm39) |
|
probably benign |
Het |
Cyp4a32 |
C |
A |
4: 115,460,147 (GRCm39) |
Y119* |
probably null |
Het |
Dido1 |
G |
T |
2: 180,313,263 (GRCm39) |
A463E |
possibly damaging |
Het |
Dnah7a |
G |
A |
1: 53,567,956 (GRCm39) |
P1880L |
probably benign |
Het |
Dock2 |
T |
A |
11: 34,189,705 (GRCm39) |
T1489S |
probably benign |
Het |
Dsp |
A |
G |
13: 38,375,907 (GRCm39) |
T1231A |
probably damaging |
Het |
Eif2ak1 |
G |
T |
5: 143,810,717 (GRCm39) |
|
probably benign |
Het |
Entrep1 |
G |
A |
19: 23,998,998 (GRCm39) |
T140M |
probably damaging |
Het |
Epc1 |
A |
T |
18: 6,452,360 (GRCm39) |
M233K |
probably damaging |
Het |
Gigyf2 |
A |
G |
1: 87,371,360 (GRCm39) |
|
probably benign |
Het |
Greb1 |
T |
G |
12: 16,757,852 (GRCm39) |
H58P |
probably damaging |
Het |
Gtpbp1 |
T |
C |
15: 79,597,649 (GRCm39) |
I348T |
possibly damaging |
Het |
Hck |
A |
T |
2: 152,970,192 (GRCm39) |
N64Y |
probably benign |
Het |
Herc2 |
T |
C |
7: 55,818,744 (GRCm39) |
S2812P |
probably damaging |
Het |
Inpp4b |
T |
A |
8: 82,679,463 (GRCm39) |
|
probably null |
Het |
Kcnq5 |
A |
C |
1: 21,475,248 (GRCm39) |
S473A |
probably benign |
Het |
Lrat |
T |
G |
3: 82,810,676 (GRCm39) |
D115A |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,814,639 (GRCm39) |
I1131M |
possibly damaging |
Het |
Man2a2 |
T |
C |
7: 80,018,310 (GRCm39) |
D160G |
probably benign |
Het |
Marf1 |
C |
T |
16: 13,933,688 (GRCm39) |
D1567N |
probably benign |
Het |
Mars1 |
T |
C |
10: 127,133,857 (GRCm39) |
D680G |
possibly damaging |
Het |
Mat1a |
T |
C |
14: 40,843,797 (GRCm39) |
S339P |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,042,081 (GRCm39) |
S1300P |
probably damaging |
Het |
Mga |
T |
C |
2: 119,733,179 (GRCm39) |
L9S |
probably damaging |
Het |
Mllt6 |
T |
C |
11: 97,563,277 (GRCm39) |
|
probably benign |
Het |
Mrpl37 |
A |
G |
4: 106,921,692 (GRCm39) |
L179P |
probably benign |
Het |
Mtnr1a |
G |
T |
8: 45,540,782 (GRCm39) |
V248L |
probably benign |
Het |
Mylk |
T |
C |
16: 34,635,835 (GRCm39) |
S19P |
possibly damaging |
Het |
Or11g1 |
A |
G |
14: 50,651,858 (GRCm39) |
T286A |
probably damaging |
Het |
Pacc1 |
A |
G |
1: 191,080,559 (GRCm39) |
|
probably benign |
Het |
Parp8 |
A |
T |
13: 117,161,886 (GRCm39) |
|
probably null |
Het |
Pcnx2 |
T |
C |
8: 126,479,023 (GRCm39) |
D2075G |
probably damaging |
Het |
Pigo |
A |
T |
4: 43,021,460 (GRCm39) |
I494K |
probably benign |
Het |
Pkd1l1 |
A |
T |
11: 8,820,313 (GRCm39) |
D1217E |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,369,040 (GRCm39) |
V895A |
probably benign |
Het |
Plcb4 |
A |
T |
2: 135,842,109 (GRCm39) |
H1031L |
possibly damaging |
Het |
Plxnb1 |
A |
G |
9: 108,937,989 (GRCm39) |
K1245R |
probably null |
Het |
Pold1 |
C |
T |
7: 44,192,181 (GRCm39) |
|
probably benign |
Het |
Ptprz1 |
A |
G |
6: 23,050,473 (GRCm39) |
D1398G |
probably damaging |
Het |
Pygm |
G |
A |
19: 6,439,917 (GRCm39) |
A364T |
probably benign |
Het |
Rbl1 |
T |
C |
2: 157,035,018 (GRCm39) |
N354S |
probably benign |
Het |
Scgb2b19 |
C |
T |
7: 32,979,037 (GRCm39) |
|
probably null |
Het |
Slc26a8 |
C |
T |
17: 28,867,187 (GRCm39) |
V545M |
possibly damaging |
Het |
Slc27a1 |
T |
A |
8: 72,036,757 (GRCm39) |
|
probably null |
Het |
Smpd1 |
A |
G |
7: 105,205,881 (GRCm39) |
D416G |
possibly damaging |
Het |
Sorbs3 |
A |
G |
14: 70,431,095 (GRCm39) |
V284A |
probably benign |
Het |
Stfa2l1 |
T |
C |
16: 35,982,154 (GRCm39) |
V75A |
probably damaging |
Het |
Syndig1 |
A |
G |
2: 149,772,841 (GRCm39) |
D166G |
probably damaging |
Het |
Tcp10a |
G |
A |
17: 7,593,406 (GRCm39) |
|
probably null |
Het |
Themis2 |
T |
A |
4: 132,510,212 (GRCm39) |
I663F |
possibly damaging |
Het |
Thrap3 |
T |
C |
4: 126,070,129 (GRCm39) |
Q586R |
probably damaging |
Het |
Tinag |
C |
A |
9: 76,952,798 (GRCm39) |
C62F |
probably damaging |
Het |
Tmod1 |
T |
C |
4: 46,090,884 (GRCm39) |
Y146H |
probably damaging |
Het |
Tmprss4 |
T |
A |
9: 45,095,683 (GRCm39) |
I54F |
possibly damaging |
Het |
Tnks |
A |
C |
8: 35,301,757 (GRCm39) |
|
probably benign |
Het |
Trim43a |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
9: 88,465,042 (GRCm39) |
|
probably benign |
Het |
Trpc6 |
A |
G |
9: 8,680,538 (GRCm39) |
E844G |
probably benign |
Het |
Ubtd2 |
C |
T |
11: 32,466,125 (GRCm39) |
R115W |
probably damaging |
Het |
Ubxn6 |
T |
C |
17: 56,376,042 (GRCm39) |
D373G |
probably benign |
Het |
Upf1 |
T |
A |
8: 70,794,174 (GRCm39) |
Q244L |
probably benign |
Het |
Usp33 |
A |
G |
3: 152,074,271 (GRCm39) |
I372M |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,301,629 (GRCm39) |
E351G |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,554,318 (GRCm39) |
|
probably benign |
Het |
Vmn1r78 |
A |
G |
7: 11,886,508 (GRCm39) |
K40E |
possibly damaging |
Het |
Vmn2r7 |
T |
A |
3: 64,632,223 (GRCm39) |
M80L |
probably benign |
Het |
Vps13a |
G |
T |
19: 16,678,602 (GRCm39) |
Y1126* |
probably null |
Het |
Wfdc11 |
T |
C |
2: 164,506,366 (GRCm39) |
N60S |
probably benign |
Het |
Wnk2 |
C |
T |
13: 49,224,586 (GRCm39) |
D992N |
probably damaging |
Het |
Zpbp2 |
C |
A |
11: 98,444,670 (GRCm39) |
T66K |
probably damaging |
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 |
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 |
R4973: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 |
|