Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
T |
C |
11: 58,316,593 (GRCm39) |
I191T |
probably damaging |
Het |
2310003L06Rik |
T |
C |
5: 88,120,671 (GRCm39) |
L476P |
possibly damaging |
Het |
Aasdh |
T |
C |
5: 77,035,924 (GRCm39) |
D387G |
probably damaging |
Het |
Ahsa2 |
T |
A |
11: 23,440,415 (GRCm39) |
T327S |
probably benign |
Het |
Ap3d1 |
A |
T |
10: 80,553,678 (GRCm39) |
V523E |
probably damaging |
Het |
Baz2b |
C |
A |
2: 59,747,769 (GRCm39) |
R1298L |
probably damaging |
Het |
Cacna2d3 |
T |
C |
14: 28,765,503 (GRCm39) |
T802A |
possibly damaging |
Het |
Cdh23 |
G |
T |
10: 60,173,043 (GRCm39) |
T1714K |
probably damaging |
Het |
Chrna3 |
A |
T |
9: 54,923,408 (GRCm39) |
D133E |
probably benign |
Het |
Cnot1 |
C |
T |
8: 96,486,726 (GRCm39) |
|
probably null |
Het |
Col16a1 |
A |
T |
4: 129,990,295 (GRCm39) |
N1396Y |
unknown |
Het |
Cox11 |
A |
G |
11: 90,529,245 (GRCm39) |
N77S |
probably benign |
Het |
Ctsf |
T |
G |
19: 4,906,567 (GRCm39) |
F165V |
probably damaging |
Het |
Cytip |
A |
G |
2: 58,037,920 (GRCm39) |
V148A |
probably damaging |
Het |
Diaph1 |
T |
C |
18: 38,023,862 (GRCm39) |
I659V |
unknown |
Het |
Dmxl2 |
A |
T |
9: 54,368,370 (GRCm39) |
M26K |
probably benign |
Het |
Erp44 |
T |
A |
4: 48,196,904 (GRCm39) |
I340F |
probably benign |
Het |
Fam186a |
A |
G |
15: 99,852,678 (GRCm39) |
M180T |
unknown |
Het |
Frem2 |
C |
T |
3: 53,429,589 (GRCm39) |
V2793I |
probably benign |
Het |
Gm19410 |
A |
G |
8: 36,266,539 (GRCm39) |
E1064G |
probably damaging |
Het |
Gria4 |
T |
C |
9: 4,503,588 (GRCm39) |
I343V |
probably benign |
Het |
Grsf1 |
T |
A |
5: 88,819,150 (GRCm39) |
N228Y |
probably damaging |
Het |
H3c13 |
C |
A |
3: 96,176,309 (GRCm39) |
Y100* |
probably null |
Het |
Ighv1-18 |
A |
T |
12: 114,646,381 (GRCm39) |
N74K |
probably benign |
Het |
Kcnh6 |
A |
T |
11: 105,914,703 (GRCm39) |
T703S |
probably benign |
Het |
Lrp1b |
T |
A |
2: 41,000,798 (GRCm39) |
D2256V |
|
Het |
Lrrc63 |
T |
C |
14: 75,360,447 (GRCm39) |
T352A |
possibly damaging |
Het |
Lztfl1 |
T |
C |
9: 123,531,194 (GRCm39) |
E258G |
probably damaging |
Het |
Mcph1 |
T |
C |
8: 18,721,122 (GRCm39) |
I650T |
possibly damaging |
Het |
Mep1a |
T |
C |
17: 43,788,997 (GRCm39) |
D606G |
possibly damaging |
Het |
Muc16 |
T |
C |
9: 18,516,578 (GRCm39) |
I313M |
|
Het |
Myh7b |
A |
G |
2: 155,462,356 (GRCm39) |
Y353C |
probably null |
Het |
Nfatc1 |
A |
G |
18: 80,725,504 (GRCm39) |
L420P |
probably damaging |
Het |
Olfml1 |
A |
G |
7: 107,170,392 (GRCm39) |
E93G |
probably damaging |
Het |
Or6b1 |
A |
T |
6: 42,814,938 (GRCm39) |
E41V |
probably damaging |
Het |
Or8c11 |
A |
G |
9: 38,289,357 (GRCm39) |
H54R |
probably benign |
Het |
Pax1 |
A |
T |
2: 147,208,034 (GRCm39) |
N214I |
probably damaging |
Het |
Pcdhb17 |
C |
A |
18: 37,619,801 (GRCm39) |
H530Q |
probably benign |
Het |
Pcdhgb7 |
A |
T |
18: 37,885,321 (GRCm39) |
M164L |
probably benign |
Het |
Pcolce |
T |
C |
5: 137,603,474 (GRCm39) |
N453S |
probably benign |
Het |
Prr36 |
T |
C |
8: 4,262,982 (GRCm39) |
T895A |
probably benign |
Het |
Rab5a |
T |
A |
17: 53,807,485 (GRCm39) |
F174I |
probably damaging |
Het |
Rapgef4 |
A |
G |
2: 72,010,315 (GRCm39) |
D291G |
probably benign |
Het |
Rbm25 |
A |
T |
12: 83,721,864 (GRCm39) |
K683N |
possibly damaging |
Het |
Rbpj |
T |
C |
5: 53,803,240 (GRCm39) |
I156T |
probably damaging |
Het |
Rgsl1 |
A |
G |
1: 153,669,610 (GRCm39) |
S259P |
possibly damaging |
Het |
Ring1 |
T |
C |
17: 34,242,109 (GRCm39) |
D100G |
probably damaging |
Het |
Ryr3 |
A |
T |
2: 112,690,110 (GRCm39) |
D1166E |
probably damaging |
Het |
Sacs |
A |
G |
14: 61,443,539 (GRCm39) |
K1862E |
possibly damaging |
Het |
Scamp5 |
A |
G |
9: 57,354,465 (GRCm39) |
I63T |
possibly damaging |
Het |
Septin14 |
C |
T |
5: 129,763,092 (GRCm39) |
A334T |
possibly damaging |
Het |
Sh3rf2 |
A |
T |
18: 42,289,201 (GRCm39) |
Q706L |
probably benign |
Het |
Skap2 |
A |
T |
6: 51,884,934 (GRCm39) |
H242Q |
probably benign |
Het |
Spmap2l |
T |
C |
5: 77,164,444 (GRCm39) |
I149T |
probably benign |
Het |
Tfpt |
A |
G |
7: 3,623,744 (GRCm39) |
|
probably null |
Het |
Thg1l |
T |
G |
11: 45,846,120 (GRCm39) |
D58A |
probably damaging |
Het |
Thyn1 |
A |
G |
9: 26,918,143 (GRCm39) |
E177G |
probably benign |
Het |
Tmem151b |
C |
T |
17: 45,856,724 (GRCm39) |
A239T |
probably damaging |
Het |
Ttc21a |
T |
C |
9: 119,788,095 (GRCm39) |
V840A |
probably benign |
Het |
Usp32 |
A |
T |
11: 84,968,153 (GRCm39) |
V170E |
probably damaging |
Het |
Vmn2r29 |
A |
G |
7: 7,234,864 (GRCm39) |
V674A |
probably benign |
Het |
Vwa8 |
A |
G |
14: 79,263,513 (GRCm39) |
N781S |
probably damaging |
Het |
Zbtb7c |
C |
A |
18: 76,270,433 (GRCm39) |
Q174K |
probably benign |
Het |
Zeb1 |
T |
C |
18: 5,766,917 (GRCm39) |
I476T |
probably benign |
Het |
Zfp91 |
A |
T |
19: 12,754,241 (GRCm39) |
D282E |
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 |
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 |
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 |
|