Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110032F04Rik |
T |
C |
3: 68,777,597 (GRCm39) |
V186A |
possibly damaging |
Het |
1700088E04Rik |
A |
T |
15: 79,019,409 (GRCm39) |
M198K |
probably damaging |
Het |
4933402J07Rik |
A |
G |
8: 88,294,601 (GRCm39) |
K84R |
probably null |
Het |
Aamdc |
T |
C |
7: 97,199,773 (GRCm39) |
|
probably null |
Het |
Abcc9 |
A |
G |
6: 142,617,282 (GRCm39) |
V594A |
probably damaging |
Het |
Adamts13 |
G |
A |
2: 26,879,414 (GRCm39) |
D656N |
probably benign |
Het |
Adcy10 |
G |
T |
1: 165,334,213 (GRCm39) |
C122F |
probably damaging |
Het |
Adi1 |
A |
G |
12: 28,725,252 (GRCm39) |
M1V |
probably null |
Het |
Ahnak |
G |
A |
19: 8,989,824 (GRCm39) |
|
probably benign |
Het |
Akt1 |
G |
T |
12: 112,623,521 (GRCm39) |
P313Q |
probably damaging |
Het |
Ano3 |
A |
T |
2: 110,498,067 (GRCm39) |
M758K |
probably damaging |
Het |
Baz2a |
T |
A |
10: 127,958,999 (GRCm39) |
N1168K |
probably benign |
Het |
Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
Bcap29 |
A |
G |
12: 31,674,202 (GRCm39) |
I131T |
probably benign |
Het |
Brd10 |
G |
T |
19: 29,694,616 (GRCm39) |
L1626I |
possibly damaging |
Het |
Btnl6 |
T |
C |
17: 34,732,966 (GRCm39) |
D299G |
possibly damaging |
Het |
Ccdc66 |
A |
G |
14: 27,222,524 (GRCm39) |
I73T |
probably benign |
Het |
Cdh2 |
A |
G |
18: 16,760,754 (GRCm39) |
S538P |
probably benign |
Het |
Cfap54 |
T |
A |
10: 92,803,390 (GRCm39) |
M1551L |
probably benign |
Het |
Chd2 |
G |
A |
7: 73,151,873 (GRCm39) |
A243V |
probably damaging |
Het |
Cntnap1 |
T |
A |
11: 101,073,845 (GRCm39) |
N665K |
probably damaging |
Het |
Colgalt2 |
C |
T |
1: 152,360,749 (GRCm39) |
T262I |
possibly damaging |
Het |
Cyp24a1 |
T |
C |
2: 170,338,098 (GRCm39) |
I149V |
probably benign |
Het |
Cyp2a5 |
T |
A |
7: 26,534,970 (GRCm39) |
|
probably null |
Het |
Dab2 |
A |
G |
15: 6,366,080 (GRCm39) |
|
probably null |
Het |
Dnah17 |
T |
A |
11: 117,917,606 (GRCm39) |
I4158F |
probably damaging |
Het |
Dnm2 |
G |
A |
9: 21,385,975 (GRCm39) |
|
probably null |
Het |
Dpp7 |
A |
T |
2: 25,242,398 (GRCm39) |
|
probably benign |
Het |
Epha6 |
T |
A |
16: 59,780,776 (GRCm39) |
I642F |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,369,397 (GRCm39) |
S415G |
probably benign |
Het |
Fancd2 |
A |
G |
6: 113,530,683 (GRCm39) |
T439A |
probably benign |
Het |
Fat1 |
G |
A |
8: 45,466,102 (GRCm39) |
V1431M |
possibly damaging |
Het |
Fhod3 |
G |
A |
18: 25,223,305 (GRCm39) |
A884T |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,820,515 (GRCm39) |
D5416G |
possibly damaging |
Het |
Gabarap |
C |
T |
11: 69,882,678 (GRCm39) |
|
probably benign |
Het |
Garre1 |
T |
C |
7: 33,938,333 (GRCm39) |
|
probably benign |
Het |
Gm11544 |
C |
T |
11: 94,736,532 (GRCm39) |
|
noncoding transcript |
Het |
Gnat2 |
A |
C |
3: 108,007,964 (GRCm39) |
K304Q |
probably benign |
Het |
Gpr141b |
T |
A |
13: 19,913,840 (GRCm39) |
|
noncoding transcript |
Het |
Gramd4 |
C |
T |
15: 86,019,057 (GRCm39) |
A575V |
probably benign |
Het |
Gtpbp10 |
G |
A |
5: 5,589,295 (GRCm39) |
A274V |
possibly damaging |
Het |
Gzmb |
A |
G |
14: 56,497,679 (GRCm39) |
I187T |
probably damaging |
Het |
H2-M10.2 |
G |
A |
17: 36,595,219 (GRCm39) |
T315I |
probably damaging |
Het |
Haus5 |
A |
T |
7: 30,356,452 (GRCm39) |
F524I |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,403,253 (GRCm39) |
S4391G |
probably benign |
Het |
Herc2 |
T |
A |
7: 55,748,165 (GRCm39) |
L511* |
probably null |
Het |
Htt |
T |
A |
5: 34,982,184 (GRCm39) |
C923S |
probably benign |
Het |
Idua |
T |
C |
5: 108,817,247 (GRCm39) |
S7P |
probably benign |
Het |
Ighv16-1 |
A |
T |
12: 114,032,466 (GRCm39) |
L112Q |
probably damaging |
Het |
Igkv1-110 |
A |
G |
6: 68,248,185 (GRCm39) |
K98R |
probably benign |
Het |
Kif15 |
G |
A |
9: 122,831,191 (GRCm39) |
|
probably null |
Het |
Leng9 |
C |
A |
7: 4,152,029 (GRCm39) |
G216W |
probably damaging |
Het |
Lrpprc |
A |
G |
17: 85,014,584 (GRCm39) |
L1306S |
probably benign |
Het |
Lztfl1 |
C |
A |
9: 123,544,454 (GRCm39) |
E20D |
possibly damaging |
Het |
Maob |
T |
C |
X: 16,582,662 (GRCm39) |
T400A |
probably benign |
Het |
Map3k4 |
C |
T |
17: 12,490,667 (GRCm39) |
E255K |
probably damaging |
Het |
Megf9 |
G |
A |
4: 70,452,665 (GRCm39) |
T132M |
probably damaging |
Het |
Mob4 |
T |
C |
1: 55,184,411 (GRCm39) |
|
probably benign |
Het |
Mttp |
G |
A |
3: 137,821,811 (GRCm39) |
A252V |
probably benign |
Het |
Mxi1 |
A |
G |
19: 53,358,745 (GRCm39) |
D226G |
probably damaging |
Het |
Myh14 |
A |
G |
7: 44,274,566 (GRCm39) |
S1249P |
probably benign |
Het |
Mylk |
G |
A |
16: 34,742,737 (GRCm39) |
G1083D |
probably benign |
Het |
Mylk4 |
T |
G |
13: 32,905,960 (GRCm39) |
I408L |
probably benign |
Het |
Nbas |
A |
G |
12: 13,533,740 (GRCm39) |
S1792G |
probably benign |
Het |
Nelfb |
A |
G |
2: 25,099,981 (GRCm39) |
V212A |
probably damaging |
Het |
Nisch |
T |
C |
14: 30,899,587 (GRCm39) |
|
probably benign |
Het |
Nqo1 |
C |
G |
8: 108,115,477 (GRCm39) |
D267H |
probably benign |
Het |
Or8u10 |
C |
A |
2: 85,915,190 (GRCm39) |
L310F |
probably benign |
Het |
Pcid2 |
T |
A |
8: 13,135,425 (GRCm39) |
I195F |
probably damaging |
Het |
Pgd |
A |
T |
4: 149,241,048 (GRCm39) |
|
probably benign |
Het |
Prim2 |
T |
C |
1: 33,503,145 (GRCm39) |
M430V |
probably benign |
Het |
Prkaa1 |
A |
G |
15: 5,190,101 (GRCm39) |
T40A |
probably damaging |
Het |
Ptges |
T |
C |
2: 30,793,232 (GRCm39) |
|
probably benign |
Het |
Ptprn |
T |
C |
1: 75,234,909 (GRCm39) |
E226G |
probably benign |
Het |
Rab14 |
A |
G |
2: 35,079,978 (GRCm39) |
F55S |
probably damaging |
Het |
Ralgps2 |
A |
T |
1: 156,684,637 (GRCm39) |
|
probably benign |
Het |
Rgs11 |
C |
T |
17: 26,426,542 (GRCm39) |
H258Y |
probably benign |
Het |
Rhpn2 |
T |
C |
7: 35,075,774 (GRCm39) |
|
probably null |
Het |
Rprd2 |
A |
T |
3: 95,681,483 (GRCm39) |
V452E |
probably damaging |
Het |
Scube3 |
C |
A |
17: 28,384,989 (GRCm39) |
H646Q |
probably damaging |
Het |
Selp |
A |
T |
1: 163,953,909 (GRCm39) |
I70F |
probably damaging |
Het |
Septin2 |
A |
G |
1: 93,426,849 (GRCm39) |
I153V |
probably damaging |
Het |
Sh3rf3 |
G |
A |
10: 58,649,905 (GRCm39) |
S170N |
probably benign |
Het |
Skint4 |
A |
T |
4: 112,000,963 (GRCm39) |
I353F |
possibly damaging |
Het |
Slc16a12 |
A |
G |
19: 34,657,780 (GRCm39) |
I41T |
possibly damaging |
Het |
Snai2 |
T |
C |
16: 14,524,881 (GRCm39) |
F129S |
probably damaging |
Het |
Top3b |
C |
T |
16: 16,708,526 (GRCm39) |
R629* |
probably null |
Het |
Trim17 |
T |
A |
11: 58,862,270 (GRCm39) |
V434E |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,615,327 (GRCm39) |
P15051L |
probably damaging |
Het |
Uggt2 |
A |
T |
14: 119,239,259 (GRCm39) |
I1391N |
probably damaging |
Het |
Usp8 |
A |
T |
2: 126,596,958 (GRCm39) |
M923L |
probably damaging |
Het |
Vmn1r176 |
T |
C |
7: 23,534,463 (GRCm39) |
H230R |
possibly damaging |
Het |
Vmn1r217 |
C |
A |
13: 23,298,159 (GRCm39) |
D248Y |
probably damaging |
Het |
Vmn2r14 |
A |
T |
5: 109,363,976 (GRCm39) |
C647S |
probably damaging |
Het |
Vwa5b1 |
A |
G |
4: 138,332,851 (GRCm39) |
I237T |
probably damaging |
Het |
Zan |
T |
A |
5: 137,391,423 (GRCm39) |
D4687V |
unknown |
Het |
Zfp273 |
T |
C |
13: 67,973,484 (GRCm39) |
V204A |
probably benign |
Het |
Zfp956 |
T |
G |
6: 47,928,987 (GRCm39) |
|
probably benign |
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 |
|
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 |
|
R5629:Pcnx2
|
UTSW |
8 |
126,624,780 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|