Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730061H03Rik |
A |
T |
14: 55,797,638 (GRCm39) |
|
probably benign |
Het |
Acin1 |
A |
G |
14: 54,889,292 (GRCm39) |
M1T |
probably null |
Het |
Akp3 |
G |
A |
1: 87,055,593 (GRCm39) |
G547R |
unknown |
Het |
Aldh1a1 |
A |
G |
19: 20,595,358 (GRCm39) |
M96V |
probably benign |
Het |
Ankfn1 |
T |
A |
11: 89,282,913 (GRCm39) |
M245L |
probably benign |
Het |
Arhgap19 |
T |
C |
19: 41,769,614 (GRCm39) |
K54E |
probably damaging |
Het |
Atp1a2 |
T |
C |
1: 172,116,948 (GRCm39) |
Q223R |
probably benign |
Het |
Atp8a2 |
C |
T |
14: 60,247,330 (GRCm39) |
V557I |
possibly damaging |
Het |
AU041133 |
A |
T |
10: 81,986,724 (GRCm39) |
K126* |
probably null |
Het |
Axin1 |
T |
A |
17: 26,401,480 (GRCm39) |
Y351N |
possibly damaging |
Het |
Baiap2l1 |
T |
C |
5: 144,221,367 (GRCm39) |
K176E |
probably damaging |
Het |
Baz2a |
C |
T |
10: 127,955,560 (GRCm39) |
T848I |
possibly damaging |
Het |
Bbs2 |
A |
C |
8: 94,808,708 (GRCm39) |
V333G |
probably benign |
Het |
BC051019 |
G |
A |
7: 109,315,302 (GRCm39) |
Q318* |
probably null |
Het |
Bltp1 |
T |
C |
3: 37,000,513 (GRCm39) |
S1231P |
probably damaging |
Het |
Cdc37 |
C |
T |
9: 21,051,160 (GRCm39) |
D362N |
probably damaging |
Het |
Cep170 |
A |
T |
1: 176,583,319 (GRCm39) |
V1020E |
probably damaging |
Het |
Chrm4 |
T |
C |
2: 91,758,747 (GRCm39) |
V385A |
probably benign |
Het |
Cntrl |
G |
A |
2: 35,035,151 (GRCm39) |
S373N |
probably damaging |
Het |
Col23a1 |
G |
A |
11: 51,467,706 (GRCm39) |
G19D |
probably damaging |
Het |
Cyb5r4 |
G |
T |
9: 86,911,625 (GRCm39) |
A100S |
probably damaging |
Het |
Dctn1 |
C |
T |
6: 83,166,059 (GRCm39) |
P115S |
probably damaging |
Het |
Dhrs2 |
C |
T |
14: 55,472,247 (GRCm39) |
T46M |
probably damaging |
Het |
Disp2 |
T |
C |
2: 118,620,243 (GRCm39) |
F325S |
probably benign |
Het |
Dnah11 |
T |
G |
12: 117,918,564 (GRCm39) |
T3456P |
possibly damaging |
Het |
Dnah11 |
C |
A |
12: 118,162,360 (GRCm39) |
V70F |
probably benign |
Het |
Duoxa1 |
T |
A |
2: 122,135,161 (GRCm39) |
T195S |
probably benign |
Het |
Dync2i1 |
T |
C |
12: 116,175,412 (GRCm39) |
I922V |
probably benign |
Het |
Eif2ak1 |
T |
A |
5: 143,821,742 (GRCm39) |
F353I |
possibly damaging |
Het |
Esam |
A |
G |
9: 37,447,998 (GRCm39) |
T211A |
probably damaging |
Het |
Faf1 |
A |
G |
4: 109,819,036 (GRCm39) |
N636S |
probably benign |
Het |
Fbxo25 |
A |
G |
8: 13,985,219 (GRCm39) |
Y305C |
probably benign |
Het |
Fchsd1 |
C |
T |
18: 38,101,803 (GRCm39) |
|
probably null |
Het |
Fdxacb1 |
T |
A |
9: 50,683,025 (GRCm39) |
D329E |
possibly damaging |
Het |
Gvin2 |
A |
T |
7: 105,545,892 (GRCm39) |
F2387I |
possibly damaging |
Het |
Hbq1b |
A |
T |
11: 32,237,104 (GRCm39) |
|
probably null |
Het |
Hmcn2 |
T |
A |
2: 31,343,172 (GRCm39) |
V4566E |
probably damaging |
Het |
Igkv6-29 |
G |
A |
6: 70,116,053 (GRCm39) |
T5I |
probably benign |
Het |
Itfg1 |
A |
T |
8: 86,452,834 (GRCm39) |
D511E |
possibly damaging |
Het |
Jmjd1c |
C |
T |
10: 66,932,378 (GRCm39) |
|
probably benign |
Het |
Kat6b |
T |
A |
14: 21,687,661 (GRCm39) |
M570K |
probably damaging |
Het |
Kdm4d |
T |
A |
9: 14,375,591 (GRCm39) |
K89M |
probably damaging |
Het |
Krt19 |
A |
T |
11: 100,032,965 (GRCm39) |
D194E |
possibly damaging |
Het |
Lamc1 |
A |
T |
1: 153,123,196 (GRCm39) |
Y665N |
possibly damaging |
Het |
Lct |
A |
T |
1: 128,221,872 (GRCm39) |
S1556T |
possibly damaging |
Het |
Macf1 |
A |
G |
4: 123,263,719 (GRCm39) |
L4924P |
probably damaging |
Het |
Mef2c |
G |
A |
13: 83,804,472 (GRCm39) |
|
probably null |
Het |
Mff |
G |
A |
1: 82,728,326 (GRCm39) |
|
probably null |
Het |
Mycbp2 |
A |
T |
14: 103,412,230 (GRCm39) |
L2581Q |
probably damaging |
Het |
Mylk |
G |
C |
16: 34,699,845 (GRCm39) |
E403Q |
possibly damaging |
Het |
Nos3 |
T |
A |
5: 24,572,295 (GRCm39) |
L123M |
probably damaging |
Het |
Ntn5 |
C |
T |
7: 45,335,952 (GRCm39) |
P128S |
probably benign |
Het |
Nudt9 |
T |
C |
5: 104,212,920 (GRCm39) |
V331A |
probably damaging |
Het |
Or2y3 |
A |
T |
17: 38,393,085 (GRCm39) |
Y261* |
probably null |
Het |
Or7g34 |
T |
C |
9: 19,478,415 (GRCm39) |
I88M |
possibly damaging |
Het |
Pcdh7 |
A |
T |
5: 57,877,664 (GRCm39) |
K406N |
possibly damaging |
Het |
Pkdrej |
T |
A |
15: 85,700,336 (GRCm39) |
I1867L |
probably benign |
Het |
Plppr4 |
C |
T |
3: 117,116,319 (GRCm39) |
G455R |
possibly damaging |
Het |
Pramel11 |
A |
G |
4: 143,624,299 (GRCm39) |
V66A |
probably damaging |
Het |
Prkag2 |
G |
C |
5: 25,152,629 (GRCm39) |
S158R |
probably benign |
Het |
Rasl12 |
A |
G |
9: 65,318,241 (GRCm39) |
K202E |
probably benign |
Het |
Rb1 |
A |
C |
14: 73,434,653 (GRCm39) |
*922G |
probably null |
Het |
Rsf1 |
C |
T |
7: 97,229,174 (GRCm39) |
P22S |
probably damaging |
Het |
Scn1a |
T |
G |
2: 66,151,379 (GRCm39) |
T797P |
probably damaging |
Het |
Sgsm2 |
A |
G |
11: 74,756,323 (GRCm39) |
V342A |
probably damaging |
Het |
Slc22a7 |
T |
G |
17: 46,749,113 (GRCm39) |
H68P |
possibly damaging |
Het |
Slc4a2 |
G |
A |
5: 24,640,575 (GRCm39) |
A652T |
probably benign |
Het |
Slc5a1 |
T |
A |
5: 33,290,733 (GRCm39) |
L106M |
probably benign |
Het |
Slco1c1 |
C |
T |
6: 141,477,258 (GRCm39) |
P19S |
probably damaging |
Het |
Snx1 |
A |
G |
9: 66,005,738 (GRCm39) |
F127S |
probably damaging |
Het |
Snx31 |
A |
T |
15: 36,534,576 (GRCm39) |
I199N |
probably damaging |
Het |
Snx33 |
T |
C |
9: 56,832,741 (GRCm39) |
I443V |
possibly damaging |
Het |
Sptbn1 |
A |
G |
11: 30,089,016 (GRCm39) |
F749L |
probably damaging |
Het |
Stoml3 |
T |
A |
3: 53,405,559 (GRCm39) |
Y53* |
probably null |
Het |
Stxbp2 |
A |
G |
8: 3,692,019 (GRCm39) |
T554A |
probably benign |
Het |
Tal1 |
T |
C |
4: 114,925,573 (GRCm39) |
I214T |
probably damaging |
Het |
Tas2r140 |
T |
A |
6: 40,468,344 (GRCm39) |
I58N |
probably damaging |
Het |
Thap1 |
A |
G |
8: 26,648,501 (GRCm39) |
Y8C |
probably damaging |
Het |
Thsd7a |
A |
T |
6: 12,555,368 (GRCm39) |
L172Q |
probably damaging |
Het |
Ube3c |
T |
A |
5: 29,842,740 (GRCm39) |
D735E |
probably damaging |
Het |
Unc80 |
G |
A |
1: 66,544,082 (GRCm39) |
D402N |
probably damaging |
Het |
Upf1 |
G |
T |
8: 70,786,779 (GRCm39) |
R902S |
probably benign |
Het |
Urb1 |
A |
G |
16: 90,570,982 (GRCm39) |
Y1276H |
probably damaging |
Het |
Urb1 |
A |
T |
16: 90,576,026 (GRCm39) |
F843L |
probably benign |
Het |
Vmn1r198 |
C |
T |
13: 22,539,402 (GRCm39) |
T296I |
probably benign |
Het |
Vmn1r33 |
A |
T |
6: 66,588,892 (GRCm39) |
S221T |
probably damaging |
Het |
Vmn2r103 |
A |
G |
17: 19,993,830 (GRCm39) |
D69G |
probably benign |
Het |
Vmn2r14 |
T |
G |
5: 109,364,226 (GRCm39) |
L563F |
possibly damaging |
Het |
Vmn2r60 |
G |
A |
7: 41,844,869 (GRCm39) |
G744D |
probably damaging |
Het |
Vstm4 |
T |
C |
14: 32,614,601 (GRCm39) |
V181A |
probably damaging |
Het |
Wdr72 |
G |
A |
9: 74,052,376 (GRCm39) |
V136I |
probably benign |
Het |
Zfp236 |
T |
A |
18: 82,638,457 (GRCm39) |
N1388Y |
probably damaging |
Het |
Zfp53 |
T |
A |
17: 21,728,839 (GRCm39) |
F291I |
probably damaging |
Het |
Zfp944 |
A |
T |
17: 22,558,889 (GRCm39) |
H119Q |
possibly 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 |
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 |
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 |
|