Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl10 |
A |
G |
2: 154,394,315 (GRCm39) |
E89G |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,419,016 (GRCm39) |
V5993E |
probably damaging |
Het |
Amdhd1 |
T |
C |
10: 93,372,936 (GRCm39) |
|
probably null |
Het |
Amph |
T |
C |
13: 19,334,011 (GRCm39) |
*691Q |
probably null |
Het |
Ankrd55 |
A |
G |
13: 112,492,644 (GRCm39) |
K272E |
probably benign |
Het |
Arhgef10l |
C |
T |
4: 140,244,126 (GRCm39) |
V838I |
possibly damaging |
Het |
Arl2 |
C |
A |
19: 6,184,774 (GRCm39) |
V160F |
probably benign |
Het |
Catsperb |
T |
C |
12: 101,412,297 (GRCm39) |
V128A |
possibly damaging |
Het |
Cdk11b |
T |
A |
4: 155,710,050 (GRCm39) |
L17H |
probably damaging |
Het |
Cpsf1 |
A |
T |
15: 76,480,314 (GRCm39) |
N1391K |
possibly damaging |
Het |
Cpxm2 |
C |
T |
7: 131,656,544 (GRCm39) |
A573T |
probably benign |
Het |
Cspg4b |
T |
A |
13: 113,455,501 (GRCm39) |
F516I |
|
Het |
Daxx |
T |
C |
17: 34,130,416 (GRCm39) |
S144P |
probably damaging |
Het |
Dpp3 |
T |
C |
19: 4,968,069 (GRCm39) |
D303G |
probably damaging |
Het |
Fam181a |
T |
A |
12: 103,282,132 (GRCm39) |
N12K |
probably damaging |
Het |
Flg2 |
A |
T |
3: 93,111,018 (GRCm39) |
R1015S |
unknown |
Het |
Fstl5 |
A |
G |
3: 76,443,600 (GRCm39) |
H315R |
probably benign |
Het |
Fut4 |
A |
G |
9: 14,662,689 (GRCm39) |
S202P |
probably damaging |
Het |
Gm5114 |
T |
C |
7: 39,057,708 (GRCm39) |
D637G |
possibly damaging |
Het |
Gstcd |
G |
T |
3: 132,790,704 (GRCm39) |
T21K |
probably benign |
Het |
Heca |
C |
T |
10: 17,791,121 (GRCm39) |
V312M |
probably benign |
Het |
Herpud1 |
A |
G |
8: 95,117,475 (GRCm39) |
R144G |
probably damaging |
Het |
Hycc2 |
T |
A |
1: 58,573,653 (GRCm39) |
T384S |
possibly damaging |
Het |
Ino80 |
A |
G |
2: 119,204,994 (GRCm39) |
S1511P |
possibly damaging |
Het |
Irf2bp2 |
T |
C |
8: 127,318,472 (GRCm39) |
T365A |
probably benign |
Het |
Klk1 |
G |
A |
7: 43,878,848 (GRCm39) |
G214E |
probably damaging |
Het |
Lama3 |
A |
T |
18: 12,715,701 (GRCm39) |
N1719I |
possibly damaging |
Het |
Lmna |
A |
G |
3: 88,392,297 (GRCm39) |
I365T |
probably damaging |
Het |
Lrp8 |
C |
A |
4: 107,659,647 (GRCm39) |
A13E |
possibly damaging |
Het |
Ly75 |
A |
G |
2: 60,136,778 (GRCm39) |
L1483P |
probably benign |
Het |
Maco1 |
T |
C |
4: 134,533,971 (GRCm39) |
D550G |
probably damaging |
Het |
Mid1 |
A |
G |
X: 168,768,073 (GRCm39) |
D407G |
probably benign |
Het |
Mpl |
G |
T |
4: 118,314,607 (GRCm39) |
A21E |
|
Het |
Mus81 |
C |
T |
19: 5,534,239 (GRCm39) |
G360S |
probably damaging |
Het |
Nmt2 |
T |
A |
2: 3,313,950 (GRCm39) |
S250T |
probably benign |
Het |
Nr1d1 |
C |
A |
11: 98,662,160 (GRCm39) |
R158L |
probably damaging |
Het |
Pcgf6 |
G |
A |
19: 47,039,153 (GRCm39) |
P36S |
unknown |
Het |
Peak1 |
A |
G |
9: 56,166,677 (GRCm39) |
V417A |
probably damaging |
Het |
Phf20l1 |
A |
G |
15: 66,476,689 (GRCm39) |
N262S |
probably benign |
Het |
Plaat5 |
T |
A |
19: 7,616,923 (GRCm39) |
F313I |
unknown |
Het |
Ppp2r5d |
A |
G |
17: 46,996,608 (GRCm39) |
V355A |
probably benign |
Het |
Rasa3 |
T |
C |
8: 13,636,897 (GRCm39) |
T395A |
probably benign |
Het |
Rims1 |
T |
A |
1: 22,416,697 (GRCm39) |
I432F |
probably benign |
Het |
Rnf123 |
C |
T |
9: 107,933,838 (GRCm39) |
C1080Y |
probably damaging |
Het |
Serpina3g |
T |
C |
12: 104,204,570 (GRCm39) |
|
probably benign |
Het |
Shank2 |
T |
A |
7: 143,964,901 (GRCm39) |
D836E |
possibly damaging |
Het |
Slc24a5 |
A |
C |
2: 124,922,591 (GRCm39) |
S118R |
probably damaging |
Het |
Smg1 |
G |
T |
7: 117,783,743 (GRCm39) |
H1048N |
unknown |
Het |
Specc1l |
T |
G |
10: 75,081,329 (GRCm39) |
S242A |
probably benign |
Het |
Tagap1 |
A |
T |
17: 7,224,111 (GRCm39) |
L195Q |
possibly damaging |
Het |
Trpc3 |
C |
A |
3: 36,704,216 (GRCm39) |
E580D |
probably benign |
Het |
Ttn |
A |
T |
2: 76,541,166 (GRCm39) |
V33940E |
probably benign |
Het |
Upp2 |
G |
T |
2: 58,681,817 (GRCm39) |
R318L |
probably benign |
Het |
Vezt |
T |
A |
10: 93,832,795 (GRCm39) |
E205D |
probably benign |
Het |
Vmn1r177 |
A |
G |
7: 23,565,535 (GRCm39) |
F114L |
probably benign |
Het |
Vmn2r53 |
C |
A |
7: 12,315,513 (GRCm39) |
E769* |
probably null |
Het |
Vnn3 |
T |
C |
10: 23,741,840 (GRCm39) |
Y382H |
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 |
|
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 |
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 |
|
|