Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr1 |
A |
G |
1: 173,159,712 (GRCm39) |
V269A |
probably benign |
Het |
Acsl1 |
G |
A |
8: 46,984,109 (GRCm39) |
G543R |
probably damaging |
Het |
Adam18 |
T |
C |
8: 25,141,838 (GRCm39) |
N244D |
probably benign |
Het |
Adgra3 |
C |
T |
5: 50,147,607 (GRCm39) |
V478M |
probably benign |
Het |
Arhgap39 |
C |
T |
15: 76,619,086 (GRCm39) |
D833N |
probably damaging |
Het |
Arhgef10 |
A |
T |
8: 15,041,070 (GRCm39) |
E723V |
probably damaging |
Het |
Arid3a |
C |
A |
10: 79,787,128 (GRCm39) |
N519K |
possibly damaging |
Het |
Atrn |
T |
A |
2: 130,841,085 (GRCm39) |
Y1162* |
probably null |
Het |
Cacng5 |
T |
A |
11: 107,768,777 (GRCm39) |
N172Y |
probably benign |
Het |
Cct8 |
C |
T |
16: 87,284,594 (GRCm39) |
V198M |
probably damaging |
Het |
Cep192 |
G |
A |
18: 67,991,089 (GRCm39) |
S1857N |
probably damaging |
Het |
Cherp |
A |
T |
8: 73,216,991 (GRCm39) |
D657E |
possibly damaging |
Het |
Clca3a2 |
T |
G |
3: 144,796,610 (GRCm39) |
D199A |
probably damaging |
Het |
Cops7b |
A |
G |
1: 86,532,798 (GRCm39) |
T219A |
probably benign |
Het |
Crb1 |
C |
T |
1: 139,126,352 (GRCm39) |
M1392I |
probably damaging |
Het |
Csf3r |
A |
C |
4: 125,937,616 (GRCm39) |
E833D |
probably damaging |
Het |
Cutc |
A |
G |
19: 43,756,655 (GRCm39) |
E247G |
probably damaging |
Het |
Cyp2c38 |
A |
G |
19: 39,451,449 (GRCm39) |
L17P |
probably damaging |
Het |
D5Ertd615e |
T |
A |
5: 45,320,796 (GRCm39) |
|
noncoding transcript |
Het |
Ddx60 |
G |
T |
8: 62,422,691 (GRCm39) |
G643W |
probably damaging |
Het |
Depdc1a |
C |
T |
3: 159,226,497 (GRCm39) |
T268I |
probably damaging |
Het |
Dgke |
T |
C |
11: 88,943,296 (GRCm39) |
E231G |
probably benign |
Het |
Dhrs7b |
T |
A |
11: 60,746,513 (GRCm39) |
|
probably benign |
Het |
Dll3 |
A |
G |
7: 28,000,974 (GRCm39) |
V27A |
probably damaging |
Het |
Dnmt3c |
T |
A |
2: 153,556,861 (GRCm39) |
|
probably null |
Het |
Duox1 |
T |
C |
2: 122,176,861 (GRCm39) |
F1461L |
probably damaging |
Het |
Enpep |
A |
G |
3: 129,106,323 (GRCm39) |
V301A |
possibly damaging |
Het |
Eny2 |
T |
A |
15: 44,299,000 (GRCm39) |
|
probably null |
Het |
Esr1 |
A |
G |
10: 4,947,911 (GRCm39) |
D488G |
probably damaging |
Het |
Ets1 |
A |
G |
9: 32,641,476 (GRCm39) |
K110E |
probably damaging |
Het |
Eya2 |
T |
A |
2: 165,557,876 (GRCm39) |
Y157* |
probably null |
Het |
F830045P16Rik |
T |
G |
2: 129,314,608 (GRCm39) |
D223A |
possibly damaging |
Het |
Fbh1 |
A |
G |
2: 11,763,230 (GRCm39) |
Y475H |
probably damaging |
Het |
Fbxo39 |
T |
C |
11: 72,208,419 (GRCm39) |
I257T |
probably damaging |
Het |
Fkbp10 |
T |
C |
11: 100,306,740 (GRCm39) |
V23A |
probably damaging |
Het |
Foxp3 |
A |
G |
X: 7,453,583 (GRCm39) |
I128V |
possibly damaging |
Het |
Fzd7 |
T |
C |
1: 59,522,867 (GRCm39) |
F250S |
probably damaging |
Het |
Gaa |
A |
G |
11: 119,172,062 (GRCm39) |
T722A |
possibly damaging |
Het |
Gemin5 |
A |
G |
11: 58,030,377 (GRCm39) |
V816A |
probably benign |
Het |
Glb1l3 |
T |
A |
9: 26,740,389 (GRCm39) |
T314S |
probably benign |
Het |
H2-Ab1 |
A |
G |
17: 34,483,942 (GRCm39) |
E101G |
possibly damaging |
Het |
Hydin |
A |
C |
8: 111,325,720 (GRCm39) |
T4710P |
probably damaging |
Het |
Ica1 |
C |
T |
6: 8,754,627 (GRCm39) |
V48M |
probably damaging |
Het |
Ica1 |
T |
C |
6: 8,754,683 (GRCm39) |
Y29C |
probably damaging |
Het |
Ints7 |
T |
A |
1: 191,346,666 (GRCm39) |
|
probably null |
Het |
Iqub |
T |
C |
6: 24,505,809 (GRCm39) |
E33G |
probably benign |
Het |
Itgb1bp2 |
T |
A |
X: 100,492,806 (GRCm39) |
C10S |
probably damaging |
Het |
Katnip |
T |
C |
7: 125,442,518 (GRCm39) |
L809S |
probably benign |
Het |
Kcnd1 |
T |
A |
X: 7,697,461 (GRCm39) |
I391N |
possibly damaging |
Het |
Kdm8 |
T |
C |
7: 125,051,812 (GRCm39) |
L135P |
probably damaging |
Het |
Ksr1 |
T |
C |
11: 78,916,109 (GRCm39) |
D574G |
probably damaging |
Het |
Lama5 |
C |
T |
2: 179,826,250 (GRCm39) |
R2331H |
probably benign |
Het |
Larp1 |
C |
A |
11: 57,933,646 (GRCm39) |
N357K |
possibly damaging |
Het |
Lgi3 |
C |
T |
14: 70,771,992 (GRCm39) |
|
probably benign |
Het |
Lmbrd1 |
T |
A |
1: 24,785,878 (GRCm39) |
|
probably benign |
Het |
Methig1 |
A |
T |
15: 100,272,825 (GRCm39) |
K53* |
probably null |
Het |
Mfap3 |
T |
A |
11: 57,420,469 (GRCm39) |
I150N |
probably damaging |
Het |
Mug1 |
A |
T |
6: 121,817,186 (GRCm39) |
Q85L |
probably benign |
Het |
Npl |
A |
G |
1: 153,391,155 (GRCm39) |
V200A |
probably damaging |
Het |
Nuf2 |
A |
T |
1: 169,326,503 (GRCm39) |
|
probably benign |
Het |
Obscn |
A |
G |
11: 59,003,533 (GRCm39) |
V1255A |
probably damaging |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or5h18 |
C |
T |
16: 58,847,491 (GRCm39) |
V260M |
possibly damaging |
Het |
Or8b51 |
T |
C |
9: 38,569,478 (GRCm39) |
D70G |
probably damaging |
Het |
P2rx1 |
T |
C |
11: 72,903,787 (GRCm39) |
V283A |
probably damaging |
Het |
Pex2 |
C |
A |
3: 5,626,355 (GRCm39) |
L151F |
probably damaging |
Het |
Pias1 |
A |
G |
9: 62,800,400 (GRCm39) |
|
probably benign |
Het |
Pmfbp1 |
A |
T |
8: 110,257,105 (GRCm39) |
|
probably benign |
Het |
Pogz |
A |
G |
3: 94,783,947 (GRCm39) |
K545E |
possibly damaging |
Het |
Ppp3cb |
T |
C |
14: 20,553,309 (GRCm39) |
|
probably null |
Het |
Prl |
G |
A |
13: 27,248,911 (GRCm39) |
D189N |
probably damaging |
Het |
Prpf6 |
A |
G |
2: 181,292,920 (GRCm39) |
N794S |
probably benign |
Het |
Prr36 |
G |
A |
8: 4,263,930 (GRCm39) |
Q579* |
probably null |
Het |
Rabepk |
A |
T |
2: 34,675,592 (GRCm39) |
H179Q |
probably damaging |
Het |
Rest |
T |
C |
5: 77,430,598 (GRCm39) |
S1006P |
probably damaging |
Het |
Rimklb |
A |
C |
6: 122,441,175 (GRCm39) |
|
probably benign |
Het |
Rnpepl1 |
T |
C |
1: 92,846,587 (GRCm39) |
|
probably benign |
Het |
Ro60 |
A |
T |
1: 143,633,489 (GRCm39) |
D536E |
possibly damaging |
Het |
Sacs |
T |
A |
14: 61,428,928 (GRCm39) |
L329Q |
probably damaging |
Het |
Safb |
C |
T |
17: 56,913,025 (GRCm39) |
R914C |
probably damaging |
Het |
Setd5 |
A |
T |
6: 113,091,994 (GRCm39) |
I272F |
probably damaging |
Het |
Sgk1 |
G |
T |
10: 21,872,209 (GRCm39) |
A262S |
probably benign |
Het |
Skint2 |
G |
A |
4: 112,481,238 (GRCm39) |
V34I |
possibly damaging |
Het |
Skint5 |
G |
C |
4: 113,512,869 (GRCm39) |
Q888E |
unknown |
Het |
Slc4a3 |
T |
C |
1: 75,528,472 (GRCm39) |
|
probably benign |
Het |
Sox10 |
T |
C |
15: 79,047,519 (GRCm39) |
E133G |
probably damaging |
Het |
Spryd3 |
G |
A |
15: 102,038,835 (GRCm39) |
R129* |
probably null |
Het |
Stag1 |
T |
A |
9: 100,810,144 (GRCm39) |
N782K |
probably benign |
Het |
Stam |
T |
C |
2: 14,122,306 (GRCm39) |
L132P |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,528,077 (GRCm39) |
S1445T |
probably damaging |
Het |
Syt5 |
C |
T |
7: 4,546,108 (GRCm39) |
R94Q |
probably benign |
Het |
Tbc1d23 |
A |
T |
16: 56,992,177 (GRCm39) |
H594Q |
probably damaging |
Het |
Tecta |
T |
A |
9: 42,249,235 (GRCm39) |
I1871F |
probably damaging |
Het |
Tek |
A |
G |
4: 94,692,549 (GRCm39) |
D219G |
probably benign |
Het |
Thrb |
T |
C |
14: 18,033,643 (GRCm38) |
F469L |
probably damaging |
Het |
Tyr |
T |
C |
7: 87,142,429 (GRCm39) |
S44G |
possibly damaging |
Het |
Usp20 |
T |
A |
2: 30,907,487 (GRCm39) |
V673E |
probably benign |
Het |
Usp28 |
T |
C |
9: 48,948,513 (GRCm39) |
S873P |
probably damaging |
Het |
Usp43 |
C |
T |
11: 67,788,100 (GRCm39) |
V306M |
possibly damaging |
Het |
Wdr17 |
G |
T |
8: 55,104,456 (GRCm39) |
|
probably null |
Het |
Wsb2 |
T |
G |
5: 117,514,744 (GRCm39) |
|
probably benign |
Het |
Xkrx |
A |
T |
X: 133,051,715 (GRCm39) |
L312Q |
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 |
|
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 |
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 |
|