Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
G |
A |
5: 36,014,507 (GRCm39) |
D189N |
probably benign |
Het |
Adamts9 |
A |
T |
6: 92,775,114 (GRCm39) |
V1052D |
probably damaging |
Het |
Apob |
T |
C |
12: 8,057,847 (GRCm39) |
Y2077H |
probably damaging |
Het |
Apol7e |
A |
T |
15: 77,602,276 (GRCm39) |
K291N |
probably benign |
Het |
Arsk |
A |
T |
13: 76,242,027 (GRCm39) |
I82N |
probably damaging |
Het |
Art1 |
A |
G |
7: 101,756,286 (GRCm39) |
Q159R |
probably benign |
Het |
Atp2a2 |
A |
G |
5: 122,598,159 (GRCm39) |
V733A |
probably damaging |
Het |
Btn2a2 |
A |
T |
13: 23,666,130 (GRCm39) |
|
probably null |
Het |
Catsper1 |
C |
T |
19: 5,386,165 (GRCm39) |
P133S |
probably benign |
Het |
Celsr3 |
A |
G |
9: 108,726,266 (GRCm39) |
D3165G |
probably benign |
Het |
Cldn19 |
T |
A |
4: 119,114,116 (GRCm39) |
V86E |
probably damaging |
Het |
Ctnna1 |
T |
A |
18: 35,382,802 (GRCm39) |
D649E |
probably benign |
Het |
Cttnbp2 |
A |
G |
6: 18,405,217 (GRCm39) |
I1094T |
probably damaging |
Het |
Ddx24 |
T |
C |
12: 103,391,806 (GRCm39) |
|
probably benign |
Het |
Ern2 |
T |
A |
7: 121,769,389 (GRCm39) |
H879L |
probably damaging |
Het |
Etv4 |
T |
A |
11: 101,662,751 (GRCm39) |
H277L |
probably damaging |
Het |
Faap100 |
G |
T |
11: 120,267,837 (GRCm39) |
A312D |
probably damaging |
Het |
Glipr1l1 |
G |
A |
10: 111,914,308 (GRCm39) |
C223Y |
possibly damaging |
Het |
Gna14 |
T |
C |
19: 16,414,097 (GRCm39) |
S14P |
possibly damaging |
Het |
Hapln1 |
A |
G |
13: 89,749,634 (GRCm39) |
T60A |
probably damaging |
Het |
Hars2 |
T |
A |
18: 36,921,719 (GRCm39) |
Y273* |
probably null |
Het |
Ighv5-6 |
A |
T |
12: 113,589,242 (GRCm39) |
Y79* |
probably null |
Het |
Iqgap2 |
T |
A |
13: 95,768,682 (GRCm39) |
N1406I |
probably damaging |
Het |
Kalrn |
T |
C |
16: 33,860,304 (GRCm39) |
T215A |
possibly damaging |
Het |
Krtap13-1 |
T |
A |
16: 88,526,047 (GRCm39) |
S90R |
probably benign |
Het |
Mettl8 |
T |
C |
2: 70,795,913 (GRCm39) |
I372V |
probably benign |
Het |
Mfn1 |
A |
T |
3: 32,615,659 (GRCm39) |
T341S |
possibly damaging |
Het |
Mocos |
T |
A |
18: 24,797,142 (GRCm39) |
|
probably null |
Het |
Muc5b |
T |
C |
7: 141,415,036 (GRCm39) |
S2661P |
possibly damaging |
Het |
Myo15a |
C |
T |
11: 60,370,578 (GRCm39) |
P1113S |
probably benign |
Het |
Myo5a |
A |
T |
9: 75,111,127 (GRCm39) |
I1540F |
possibly damaging |
Het |
Myoc |
T |
C |
1: 162,476,156 (GRCm39) |
Y287H |
probably damaging |
Het |
Napepld |
A |
G |
5: 21,880,901 (GRCm39) |
F165L |
probably benign |
Het |
Ndufb10 |
T |
C |
17: 24,941,656 (GRCm39) |
E102G |
probably damaging |
Het |
Nrros |
T |
A |
16: 31,963,223 (GRCm39) |
I265F |
probably damaging |
Het |
Nrxn1 |
A |
T |
17: 90,897,460 (GRCm39) |
F891I |
possibly damaging |
Het |
Nsfl1c |
T |
C |
2: 151,346,085 (GRCm39) |
Y169H |
probably damaging |
Het |
Oas2 |
G |
A |
5: 120,876,516 (GRCm39) |
Q476* |
probably null |
Het |
Or51f5 |
A |
T |
7: 102,423,847 (GRCm39) |
I39F |
possibly damaging |
Het |
Pip4p1 |
T |
C |
14: 51,165,373 (GRCm39) |
H278R |
probably benign |
Het |
Piwil2 |
C |
T |
14: 70,660,416 (GRCm39) |
V70M |
probably damaging |
Het |
Prss23 |
A |
C |
7: 89,159,400 (GRCm39) |
V223G |
probably damaging |
Het |
Rarres2 |
A |
T |
6: 48,547,194 (GRCm39) |
L122Q |
probably benign |
Het |
Robo1 |
T |
C |
16: 72,780,598 (GRCm39) |
V776A |
probably benign |
Het |
Robo3 |
G |
A |
9: 37,330,507 (GRCm39) |
Q1008* |
probably null |
Het |
Robo4 |
G |
A |
9: 37,319,658 (GRCm39) |
C636Y |
probably damaging |
Het |
Sacm1l |
A |
G |
9: 123,395,464 (GRCm39) |
M196V |
probably benign |
Het |
Septin7 |
T |
A |
9: 25,199,589 (GRCm39) |
Y163N |
probably damaging |
Het |
Skint6 |
G |
A |
4: 112,870,176 (GRCm39) |
T594I |
possibly damaging |
Het |
Slc23a1 |
T |
C |
18: 35,759,545 (GRCm39) |
H13R |
probably benign |
Het |
Slc25a39 |
A |
C |
11: 102,295,719 (GRCm39) |
Y109* |
probably null |
Het |
Slc8a3 |
G |
A |
12: 81,246,405 (GRCm39) |
R883C |
probably damaging |
Het |
Spag17 |
A |
T |
3: 99,987,435 (GRCm39) |
Y1575F |
probably benign |
Het |
Spdye4c |
T |
A |
2: 128,438,705 (GRCm39) |
I321N |
probably damaging |
Het |
Stk32b |
G |
A |
5: 37,614,576 (GRCm39) |
P311S |
probably damaging |
Het |
Svs3a |
T |
A |
2: 164,132,040 (GRCm39) |
S203T |
probably benign |
Het |
Taf3 |
A |
T |
2: 9,922,989 (GRCm39) |
I45N |
probably damaging |
Het |
Taf7 |
T |
C |
18: 37,776,555 (GRCm39) |
N4S |
probably benign |
Het |
Tial1 |
T |
A |
7: 128,046,421 (GRCm39) |
D87V |
probably damaging |
Het |
Tmem120a |
T |
A |
5: 135,770,904 (GRCm39) |
E78V |
probably benign |
Het |
Tmem19 |
A |
G |
10: 115,183,165 (GRCm39) |
F137L |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trim30d |
T |
C |
7: 104,137,136 (GRCm39) |
K23E |
possibly damaging |
Het |
Ubxn7 |
C |
A |
16: 32,151,117 (GRCm39) |
H4Q |
unknown |
Het |
Usp40 |
C |
T |
1: 87,908,731 (GRCm39) |
R590H |
probably benign |
Het |
Vmn1r90 |
A |
G |
7: 14,296,011 (GRCm39) |
M22T |
possibly damaging |
Het |
Vmn2r1 |
G |
A |
3: 64,012,538 (GRCm39) |
V800M |
possibly damaging |
Het |
Vps11 |
A |
T |
9: 44,267,673 (GRCm39) |
I313N |
probably damaging |
Het |
Zhx1 |
A |
G |
15: 57,918,207 (GRCm39) |
V13A |
probably damaging |
Het |
Zic4 |
G |
A |
9: 91,260,805 (GRCm39) |
R20H |
probably benign |
Het |
Zp3r |
C |
T |
1: 130,510,616 (GRCm39) |
V369M |
probably damaging |
Het |
|
Other mutations in Pcnx2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00898:Pcnx2
|
APN |
8 |
126,614,324 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00900:Pcnx2
|
APN |
8 |
126,589,975 (GRCm39) |
splice site |
probably benign |
|
IGL01134:Pcnx2
|
APN |
8 |
126,589,889 (GRCm39) |
missense |
probably benign |
|
IGL01370:Pcnx2
|
APN |
8 |
126,528,222 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01452:Pcnx2
|
APN |
8 |
126,564,771 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01477:Pcnx2
|
APN |
8 |
126,512,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01610:Pcnx2
|
APN |
8 |
126,566,372 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01640:Pcnx2
|
APN |
8 |
126,528,297 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01645:Pcnx2
|
APN |
8 |
126,614,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01876:Pcnx2
|
APN |
8 |
126,592,770 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01933:Pcnx2
|
APN |
8 |
126,488,393 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02208:Pcnx2
|
APN |
8 |
126,478,894 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02573:Pcnx2
|
APN |
8 |
126,582,012 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02810:Pcnx2
|
APN |
8 |
126,613,942 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02859:Pcnx2
|
APN |
8 |
126,589,912 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02879:Pcnx2
|
APN |
8 |
126,498,796 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03202:Pcnx2
|
APN |
8 |
126,498,783 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03259:Pcnx2
|
APN |
8 |
126,480,388 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03395:Pcnx2
|
APN |
8 |
126,614,262 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03410:Pcnx2
|
APN |
8 |
126,613,779 (GRCm39) |
missense |
probably damaging |
1.00 |
gallen
|
UTSW |
8 |
126,617,859 (GRCm39) |
missense |
probably damaging |
1.00 |
hotzone
|
UTSW |
8 |
126,617,880 (GRCm39) |
missense |
probably benign |
0.00 |
R0107:Pcnx2
|
UTSW |
8 |
126,480,325 (GRCm39) |
missense |
probably benign |
0.29 |
R0477:Pcnx2
|
UTSW |
8 |
126,488,306 (GRCm39) |
missense |
probably damaging |
0.99 |
R0610:Pcnx2
|
UTSW |
8 |
126,566,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Pcnx2
|
UTSW |
8 |
126,487,459 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0894:Pcnx2
|
UTSW |
8 |
126,613,665 (GRCm39) |
splice site |
probably benign |
|
R1083:Pcnx2
|
UTSW |
8 |
126,498,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R1199:Pcnx2
|
UTSW |
8 |
126,614,053 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1296:Pcnx2
|
UTSW |
8 |
126,500,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Pcnx2
|
UTSW |
8 |
126,479,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R1467:Pcnx2
|
UTSW |
8 |
126,480,289 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1467:Pcnx2
|
UTSW |
8 |
126,480,289 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1524:Pcnx2
|
UTSW |
8 |
126,617,880 (GRCm39) |
missense |
probably benign |
0.00 |
R1537:Pcnx2
|
UTSW |
8 |
126,604,188 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1574:Pcnx2
|
UTSW |
8 |
126,500,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Pcnx2
|
UTSW |
8 |
126,500,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R1593:Pcnx2
|
UTSW |
8 |
126,486,012 (GRCm39) |
missense |
probably benign |
0.11 |
R1598:Pcnx2
|
UTSW |
8 |
126,498,825 (GRCm39) |
missense |
probably benign |
0.03 |
R1603:Pcnx2
|
UTSW |
8 |
126,566,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R1697:Pcnx2
|
UTSW |
8 |
126,577,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R1759:Pcnx2
|
UTSW |
8 |
126,500,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R1855:Pcnx2
|
UTSW |
8 |
126,534,735 (GRCm39) |
splice site |
probably benign |
|
R1863:Pcnx2
|
UTSW |
8 |
126,545,525 (GRCm39) |
missense |
probably damaging |
0.98 |
R1930:Pcnx2
|
UTSW |
8 |
126,614,453 (GRCm39) |
missense |
probably benign |
0.10 |
R1967:Pcnx2
|
UTSW |
8 |
126,542,422 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1974:Pcnx2
|
UTSW |
8 |
126,614,110 (GRCm39) |
missense |
probably benign |
0.00 |
R1998:Pcnx2
|
UTSW |
8 |
126,613,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R2034:Pcnx2
|
UTSW |
8 |
126,545,406 (GRCm39) |
critical splice donor site |
probably null |
|
R2072:Pcnx2
|
UTSW |
8 |
126,488,481 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2096:Pcnx2
|
UTSW |
8 |
126,485,987 (GRCm39) |
missense |
probably benign |
0.27 |
R2216:Pcnx2
|
UTSW |
8 |
126,614,816 (GRCm39) |
missense |
probably benign |
0.00 |
R2290:Pcnx2
|
UTSW |
8 |
126,604,334 (GRCm39) |
splice site |
probably benign |
|
R2373:Pcnx2
|
UTSW |
8 |
126,480,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R2484:Pcnx2
|
UTSW |
8 |
126,617,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R2849:Pcnx2
|
UTSW |
8 |
126,487,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R2891:Pcnx2
|
UTSW |
8 |
126,617,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R2892:Pcnx2
|
UTSW |
8 |
126,617,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R2970:Pcnx2
|
UTSW |
8 |
126,528,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R3013:Pcnx2
|
UTSW |
8 |
126,614,509 (GRCm39) |
missense |
probably benign |
0.05 |
R3608:Pcnx2
|
UTSW |
8 |
126,614,840 (GRCm39) |
missense |
probably benign |
|
R3876:Pcnx2
|
UTSW |
8 |
126,614,897 (GRCm39) |
missense |
probably benign |
|
R4349:Pcnx2
|
UTSW |
8 |
126,489,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R4352:Pcnx2
|
UTSW |
8 |
126,489,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R4353:Pcnx2
|
UTSW |
8 |
126,489,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R4361:Pcnx2
|
UTSW |
8 |
126,495,037 (GRCm39) |
nonsense |
probably null |
|
R4735:Pcnx2
|
UTSW |
8 |
126,554,780 (GRCm39) |
critical splice donor site |
probably null |
|
R4749:Pcnx2
|
UTSW |
8 |
126,614,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R4812:Pcnx2
|
UTSW |
8 |
126,592,678 (GRCm39) |
missense |
probably benign |
0.00 |
R4819:Pcnx2
|
UTSW |
8 |
126,581,969 (GRCm39) |
missense |
probably benign |
0.04 |
R4829:Pcnx2
|
UTSW |
8 |
126,587,797 (GRCm39) |
splice site |
probably null |
|
R4832:Pcnx2
|
UTSW |
8 |
126,478,927 (GRCm39) |
missense |
probably damaging |
0.99 |
R4876:Pcnx2
|
UTSW |
8 |
126,498,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Pcnx2
|
UTSW |
8 |
126,577,869 (GRCm39) |
missense |
probably benign |
0.00 |
R5057:Pcnx2
|
UTSW |
8 |
126,581,930 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5078:Pcnx2
|
UTSW |
8 |
126,478,895 (GRCm39) |
missense |
probably benign |
|
R5114:Pcnx2
|
UTSW |
8 |
126,564,749 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5195:Pcnx2
|
UTSW |
8 |
126,528,288 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5239:Pcnx2
|
UTSW |
8 |
126,587,821 (GRCm39) |
splice site |
probably null |
|
R5348:Pcnx2
|
UTSW |
8 |
126,545,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R5398:Pcnx2
|
UTSW |
8 |
126,614,687 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5448:Pcnx2
|
UTSW |
8 |
126,614,888 (GRCm39) |
missense |
probably benign |
0.14 |
R5534:Pcnx2
|
UTSW |
8 |
126,564,754 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5624:Pcnx2
|
UTSW |
8 |
126,488,262 (GRCm39) |
critical splice donor site |
probably null |
|
R5630:Pcnx2
|
UTSW |
8 |
126,587,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R5782:Pcnx2
|
UTSW |
8 |
126,480,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R5877:Pcnx2
|
UTSW |
8 |
126,480,467 (GRCm39) |
missense |
probably damaging |
0.99 |
R5879:Pcnx2
|
UTSW |
8 |
126,500,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R6114:Pcnx2
|
UTSW |
8 |
126,500,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R6152:Pcnx2
|
UTSW |
8 |
126,480,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R6154:Pcnx2
|
UTSW |
8 |
126,489,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R6283:Pcnx2
|
UTSW |
8 |
126,604,325 (GRCm39) |
missense |
probably damaging |
0.99 |
R6500:Pcnx2
|
UTSW |
8 |
126,480,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R6629:Pcnx2
|
UTSW |
8 |
126,617,851 (GRCm39) |
missense |
probably benign |
0.00 |
R6708:Pcnx2
|
UTSW |
8 |
126,587,692 (GRCm39) |
critical splice donor site |
probably null |
|
R6736:Pcnx2
|
UTSW |
8 |
126,479,056 (GRCm39) |
splice site |
probably null |
|
R6748:Pcnx2
|
UTSW |
8 |
126,577,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Pcnx2
|
UTSW |
8 |
126,498,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R6849:Pcnx2
|
UTSW |
8 |
126,587,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6947:Pcnx2
|
UTSW |
8 |
126,577,021 (GRCm39) |
critical splice donor site |
probably null |
|
R7034:Pcnx2
|
UTSW |
8 |
126,512,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R7100:Pcnx2
|
UTSW |
8 |
126,485,853 (GRCm39) |
missense |
probably benign |
0.16 |
R7124:Pcnx2
|
UTSW |
8 |
126,480,356 (GRCm39) |
missense |
probably damaging |
0.99 |
R7130:Pcnx2
|
UTSW |
8 |
126,480,323 (GRCm39) |
nonsense |
probably null |
|
R7133:Pcnx2
|
UTSW |
8 |
126,528,243 (GRCm39) |
missense |
probably benign |
0.01 |
R7271:Pcnx2
|
UTSW |
8 |
126,613,690 (GRCm39) |
missense |
probably benign |
|
R7326:Pcnx2
|
UTSW |
8 |
126,613,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R7373:Pcnx2
|
UTSW |
8 |
126,534,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R7397:Pcnx2
|
UTSW |
8 |
126,617,624 (GRCm39) |
splice site |
probably null |
|
R7662:Pcnx2
|
UTSW |
8 |
126,545,510 (GRCm39) |
nonsense |
probably null |
|
R7693:Pcnx2
|
UTSW |
8 |
126,613,864 (GRCm39) |
missense |
probably benign |
0.09 |
R7726:Pcnx2
|
UTSW |
8 |
126,577,069 (GRCm39) |
missense |
probably benign |
0.00 |
R7745:Pcnx2
|
UTSW |
8 |
126,577,846 (GRCm39) |
missense |
probably benign |
0.04 |
R7792:Pcnx2
|
UTSW |
8 |
126,618,757 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7797:Pcnx2
|
UTSW |
8 |
126,512,087 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7921:Pcnx2
|
UTSW |
8 |
126,564,602 (GRCm39) |
missense |
probably benign |
|
R7984:Pcnx2
|
UTSW |
8 |
126,485,865 (GRCm39) |
missense |
probably benign |
|
R8098:Pcnx2
|
UTSW |
8 |
126,495,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R8277:Pcnx2
|
UTSW |
8 |
126,592,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R8312:Pcnx2
|
UTSW |
8 |
126,489,589 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8354:Pcnx2
|
UTSW |
8 |
126,488,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R8378:Pcnx2
|
UTSW |
8 |
126,487,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R8713:Pcnx2
|
UTSW |
8 |
126,545,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8714:Pcnx2
|
UTSW |
8 |
126,500,546 (GRCm39) |
missense |
probably benign |
|
R8753:Pcnx2
|
UTSW |
8 |
126,613,999 (GRCm39) |
missense |
probably benign |
0.15 |
R8790:Pcnx2
|
UTSW |
8 |
126,604,306 (GRCm39) |
missense |
probably benign |
|
R8925:Pcnx2
|
UTSW |
8 |
126,614,659 (GRCm39) |
missense |
probably benign |
0.01 |
R8927:Pcnx2
|
UTSW |
8 |
126,614,659 (GRCm39) |
missense |
probably benign |
0.01 |
R8965:Pcnx2
|
UTSW |
8 |
126,485,853 (GRCm39) |
missense |
probably benign |
0.16 |
R9006:Pcnx2
|
UTSW |
8 |
126,613,996 (GRCm39) |
missense |
probably benign |
0.00 |
R9082:Pcnx2
|
UTSW |
8 |
126,613,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R9202:Pcnx2
|
UTSW |
8 |
126,616,416 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9315:Pcnx2
|
UTSW |
8 |
126,614,119 (GRCm39) |
missense |
probably benign |
0.00 |
R9434:Pcnx2
|
UTSW |
8 |
126,542,512 (GRCm39) |
missense |
probably benign |
0.00 |
R9660:Pcnx2
|
UTSW |
8 |
126,487,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R9686:Pcnx2
|
UTSW |
8 |
126,592,766 (GRCm39) |
missense |
probably benign |
|
R9766:Pcnx2
|
UTSW |
8 |
126,488,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R9778:Pcnx2
|
UTSW |
8 |
126,512,176 (GRCm39) |
missense |
probably benign |
0.00 |
R9792:Pcnx2
|
UTSW |
8 |
126,534,820 (GRCm39) |
missense |
probably damaging |
0.99 |
RF018:Pcnx2
|
UTSW |
8 |
126,604,258 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Pcnx2
|
UTSW |
8 |
126,592,757 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Pcnx2
|
UTSW |
8 |
126,553,667 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Pcnx2
|
UTSW |
8 |
126,564,753 (GRCm39) |
missense |
probably benign |
0.30 |
Z1176:Pcnx2
|
UTSW |
8 |
126,488,393 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Pcnx2
|
UTSW |
8 |
126,614,699 (GRCm39) |
nonsense |
probably null |
|
|