Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb10 |
A |
G |
8: 124,709,195 (GRCm39) |
S120P |
probably benign |
Het |
Actr3b |
T |
A |
5: 26,036,743 (GRCm39) |
Y185* |
probably null |
Het |
Atg101 |
T |
A |
15: 101,188,382 (GRCm39) |
H162Q |
possibly damaging |
Het |
Btf3 |
T |
A |
13: 98,449,659 (GRCm39) |
Q109L |
possibly damaging |
Het |
Camk2d |
G |
A |
3: 126,574,091 (GRCm39) |
G166D |
probably damaging |
Het |
Capn7 |
T |
G |
14: 31,071,844 (GRCm39) |
|
probably null |
Het |
Cd209f |
A |
G |
8: 4,155,537 (GRCm39) |
V17A |
probably benign |
Het |
Cenpf |
A |
G |
1: 189,385,656 (GRCm39) |
V2208A |
possibly damaging |
Het |
Cnga1 |
C |
T |
5: 72,776,404 (GRCm39) |
V20I |
possibly damaging |
Het |
Comp |
T |
C |
8: 70,828,713 (GRCm39) |
C182R |
probably damaging |
Het |
Ctsl |
A |
G |
13: 64,516,840 (GRCm39) |
|
probably null |
Het |
Cyp3a44 |
G |
T |
5: 145,725,215 (GRCm39) |
Q329K |
probably damaging |
Het |
Dcpp1 |
A |
T |
17: 24,099,971 (GRCm39) |
|
probably null |
Het |
Dhx38 |
A |
G |
8: 110,280,891 (GRCm39) |
V831A |
probably damaging |
Het |
Dkk2 |
T |
C |
3: 131,791,858 (GRCm39) |
M22T |
probably benign |
Het |
Dnah2 |
C |
T |
11: 69,346,742 (GRCm39) |
E2615K |
probably damaging |
Het |
Dpy19l3 |
A |
G |
7: 35,426,713 (GRCm39) |
|
probably null |
Het |
Gm12888 |
T |
G |
4: 121,176,655 (GRCm39) |
I49L |
probably benign |
Het |
Insyn2b |
C |
A |
11: 34,352,936 (GRCm39) |
S326Y |
probably benign |
Het |
Kif15 |
T |
A |
9: 122,815,252 (GRCm39) |
M194K |
probably damaging |
Het |
Mael |
G |
T |
1: 166,053,244 (GRCm39) |
Q254K |
probably benign |
Het |
Nek9 |
T |
C |
12: 85,361,322 (GRCm39) |
D461G |
probably benign |
Het |
Nlrp12 |
T |
C |
7: 3,281,825 (GRCm39) |
N819S |
probably benign |
Het |
Ntng1 |
T |
A |
3: 109,739,871 (GRCm39) |
N390Y |
probably damaging |
Het |
Or5g25 |
A |
G |
2: 85,478,434 (GRCm39) |
I77T |
probably benign |
Het |
P2ry14 |
C |
T |
3: 59,022,738 (GRCm39) |
V250I |
probably damaging |
Het |
Phf2 |
T |
A |
13: 48,985,589 (GRCm39) |
K64* |
probably null |
Het |
Phip |
T |
C |
9: 82,797,392 (GRCm39) |
H537R |
possibly damaging |
Het |
Ppa2 |
A |
G |
3: 133,032,445 (GRCm39) |
T97A |
probably damaging |
Het |
Psd |
G |
A |
19: 46,313,088 (GRCm39) |
|
probably null |
Het |
Psg23 |
T |
A |
7: 18,348,668 (GRCm39) |
E46D |
probably damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Rab11b |
A |
G |
17: 33,967,976 (GRCm39) |
Y74H |
probably damaging |
Het |
Rfc3 |
A |
T |
5: 151,568,383 (GRCm39) |
S194R |
probably benign |
Het |
Sema4d |
A |
T |
13: 51,864,037 (GRCm39) |
I414N |
probably damaging |
Het |
Serpinb1a |
A |
T |
13: 33,031,437 (GRCm39) |
D120E |
probably damaging |
Het |
Snai2 |
T |
A |
16: 14,524,861 (GRCm39) |
H122Q |
possibly damaging |
Het |
Spats2l |
T |
C |
1: 57,985,458 (GRCm39) |
S504P |
probably benign |
Het |
Sprr2j-ps |
T |
C |
3: 92,326,412 (GRCm39) |
S96P |
unknown |
Het |
Sspo |
G |
T |
6: 48,438,608 (GRCm39) |
V1559L |
probably benign |
Het |
Tas2r118 |
T |
G |
6: 23,969,912 (GRCm39) |
I50L |
possibly damaging |
Het |
Tdrd3 |
C |
T |
14: 87,743,788 (GRCm39) |
Q573* |
probably null |
Het |
Thoc2l |
T |
C |
5: 104,667,835 (GRCm39) |
S786P |
possibly damaging |
Het |
Tlnrd1 |
G |
A |
7: 83,532,062 (GRCm39) |
T123I |
probably benign |
Het |
Tmem214 |
T |
A |
5: 31,033,714 (GRCm39) |
L555H |
probably damaging |
Het |
Tmprss12 |
T |
A |
15: 100,183,117 (GRCm39) |
M153K |
probably benign |
Het |
Tmprss9 |
G |
A |
10: 80,725,268 (GRCm39) |
G410S |
probably damaging |
Het |
Trpm6 |
T |
A |
19: 18,803,116 (GRCm39) |
M853K |
probably damaging |
Het |
Vmn1r35 |
A |
G |
6: 66,655,929 (GRCm39) |
I247T |
possibly damaging |
Het |
Zcchc7 |
C |
A |
4: 44,931,059 (GRCm39) |
P404T |
probably damaging |
Het |
Zzef1 |
T |
C |
11: 72,763,465 (GRCm39) |
F1371L |
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 |
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 |
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 |
|
|