Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
A |
T |
7: 40,642,480 (GRCm39) |
T141S |
probably benign |
Het |
4930578I06Rik |
G |
A |
14: 64,223,714 (GRCm39) |
R21* |
probably null |
Het |
Abca15 |
A |
G |
7: 119,965,009 (GRCm39) |
E757G |
possibly damaging |
Het |
Abca5 |
T |
C |
11: 110,192,353 (GRCm39) |
T720A |
probably benign |
Het |
Actr5 |
T |
A |
2: 158,474,376 (GRCm39) |
|
probably null |
Het |
Adgrl3 |
T |
C |
5: 81,841,563 (GRCm39) |
|
probably benign |
Het |
Adra1a |
A |
G |
14: 66,875,241 (GRCm39) |
D72G |
probably damaging |
Het |
Ahcyl |
T |
C |
16: 45,974,264 (GRCm39) |
E371G |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,985,242 (GRCm39) |
L2175F |
probably benign |
Het |
AK157302 |
A |
G |
13: 21,679,833 (GRCm39) |
T120A |
possibly damaging |
Het |
Apol7a |
G |
A |
15: 77,273,454 (GRCm39) |
A336V |
probably benign |
Het |
Asic1 |
C |
A |
15: 99,596,780 (GRCm39) |
H525Q |
probably benign |
Het |
Atxn7l2 |
T |
C |
3: 108,112,090 (GRCm39) |
D335G |
possibly damaging |
Het |
Bpgm |
G |
T |
6: 34,481,284 (GRCm39) |
R227L |
possibly damaging |
Het |
Calm4 |
T |
A |
13: 3,888,320 (GRCm39) |
V142E |
possibly damaging |
Het |
Catsperg1 |
A |
T |
7: 28,890,044 (GRCm39) |
L721Q |
probably damaging |
Het |
Cdh26 |
A |
G |
2: 178,091,691 (GRCm39) |
I83M |
probably damaging |
Het |
Cep295 |
A |
C |
9: 15,234,050 (GRCm39) |
S2249A |
possibly damaging |
Het |
Cfhr4 |
G |
A |
1: 139,629,584 (GRCm39) |
T799I |
probably benign |
Het |
Cln3 |
A |
G |
7: 126,179,361 (GRCm39) |
F139L |
probably damaging |
Het |
Cmpk2 |
T |
A |
12: 26,528,055 (GRCm39) |
L424Q |
possibly damaging |
Het |
Col12a1 |
A |
T |
9: 79,615,130 (GRCm39) |
V53E |
probably benign |
Het |
Csmd1 |
G |
A |
8: 15,968,208 (GRCm39) |
R3140C |
possibly damaging |
Het |
Dagla |
A |
G |
19: 10,248,922 (GRCm39) |
W11R |
probably damaging |
Het |
Dbx2 |
C |
T |
15: 95,522,778 (GRCm39) |
V310M |
probably benign |
Het |
Disp2 |
T |
A |
2: 118,622,717 (GRCm39) |
C1150S |
probably benign |
Het |
Dock3 |
T |
C |
9: 106,900,987 (GRCm39) |
D326G |
probably damaging |
Het |
Dph1 |
G |
T |
11: 75,076,783 (GRCm39) |
|
probably benign |
Het |
Dyrk1b |
C |
A |
7: 27,886,059 (GRCm39) |
T594K |
probably damaging |
Het |
Evx2 |
C |
A |
2: 74,486,331 (GRCm39) |
A353S |
probably benign |
Het |
Garin1b |
T |
A |
6: 29,326,576 (GRCm39) |
V231E |
probably benign |
Het |
Greb1 |
A |
C |
12: 16,746,443 (GRCm39) |
S1276A |
probably benign |
Het |
Hhipl1 |
T |
A |
12: 108,285,661 (GRCm39) |
C490* |
probably null |
Het |
Hmmr |
G |
T |
11: 40,606,729 (GRCm39) |
T231K |
probably damaging |
Het |
Hspa4l |
A |
C |
3: 40,733,832 (GRCm39) |
E526D |
probably benign |
Het |
Ibsp |
A |
G |
5: 104,458,000 (GRCm39) |
E179G |
probably benign |
Het |
Ift140 |
C |
T |
17: 25,254,777 (GRCm39) |
A150V |
probably benign |
Het |
Igf2bp2 |
A |
G |
16: 21,889,059 (GRCm39) |
S416P |
probably benign |
Het |
Ighe |
T |
C |
12: 113,235,363 (GRCm39) |
K294E |
unknown |
Het |
Ino80 |
G |
A |
2: 119,213,441 (GRCm39) |
R1249C |
probably damaging |
Het |
Iqca1 |
C |
A |
1: 90,070,453 (GRCm39) |
G133V |
probably null |
Het |
Kng2 |
T |
A |
16: 22,819,344 (GRCm39) |
N231Y |
possibly damaging |
Het |
Lca5 |
A |
T |
9: 83,281,792 (GRCm39) |
C331S |
probably benign |
Het |
Lrrc1 |
A |
G |
9: 77,379,488 (GRCm39) |
I101T |
possibly damaging |
Het |
Lrrk2 |
A |
T |
15: 91,699,619 (GRCm39) |
I2489L |
probably benign |
Het |
Lyz3 |
A |
G |
10: 117,073,635 (GRCm39) |
F66S |
probably benign |
Het |
Mapk9 |
A |
C |
11: 49,754,400 (GRCm39) |
N51T |
probably benign |
Het |
Marf1 |
C |
T |
16: 13,960,398 (GRCm39) |
A549T |
probably damaging |
Het |
Nek2 |
T |
A |
1: 191,554,627 (GRCm39) |
V113D |
probably damaging |
Het |
Nr4a3 |
C |
A |
4: 48,051,903 (GRCm39) |
A248E |
probably benign |
Het |
Nrp1 |
T |
C |
8: 129,229,099 (GRCm39) |
I859T |
probably damaging |
Het |
Olfm5 |
A |
T |
7: 103,803,652 (GRCm39) |
Y195* |
probably null |
Het |
Or13j1 |
T |
A |
4: 43,706,400 (GRCm39) |
H56L |
possibly damaging |
Het |
Or1n2 |
T |
A |
2: 36,797,671 (GRCm39) |
W238R |
probably damaging |
Het |
Or8g35 |
A |
G |
9: 39,381,119 (GRCm39) |
L301P |
probably damaging |
Het |
Oxtr |
C |
T |
6: 112,454,138 (GRCm39) |
R42Q |
probably benign |
Het |
Pdpk1 |
T |
C |
17: 24,317,145 (GRCm39) |
|
probably null |
Het |
Ryr2 |
T |
A |
13: 11,637,838 (GRCm39) |
H3731L |
probably damaging |
Het |
Sdr16c5 |
T |
G |
4: 4,016,116 (GRCm39) |
E103D |
possibly damaging |
Het |
Setdb2 |
A |
C |
14: 59,654,919 (GRCm39) |
S324A |
possibly damaging |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Slc17a8 |
A |
T |
10: 89,412,488 (GRCm39) |
I499K |
probably damaging |
Het |
Slc2a9 |
T |
A |
5: 38,537,285 (GRCm39) |
I389F |
probably damaging |
Het |
Slc30a1 |
T |
C |
1: 191,641,536 (GRCm39) |
V394A |
probably damaging |
Het |
Slc41a2 |
A |
G |
10: 83,119,592 (GRCm39) |
I390T |
possibly damaging |
Het |
Slco1a1 |
A |
G |
6: 141,864,187 (GRCm39) |
|
probably null |
Het |
Slit2 |
A |
G |
5: 48,433,016 (GRCm39) |
K1053E |
possibly damaging |
Het |
Smarca2 |
T |
A |
19: 26,668,791 (GRCm39) |
L930Q |
probably damaging |
Het |
Snx6 |
T |
C |
12: 54,798,574 (GRCm39) |
H387R |
probably damaging |
Het |
Sox5 |
A |
T |
6: 143,779,165 (GRCm39) |
M622K |
possibly damaging |
Het |
Ston1 |
C |
A |
17: 88,942,709 (GRCm39) |
N38K |
possibly damaging |
Het |
Strbp |
C |
T |
2: 37,474,089 (GRCm39) |
V658I |
probably damaging |
Het |
Strn3 |
T |
C |
12: 51,657,231 (GRCm39) |
|
probably null |
Het |
Suco |
T |
G |
1: 161,687,072 (GRCm39) |
D96A |
probably benign |
Het |
Suco |
A |
G |
1: 161,691,601 (GRCm39) |
|
probably benign |
Het |
Sytl2 |
A |
T |
7: 90,030,061 (GRCm39) |
|
probably benign |
Het |
Tmem41b |
T |
A |
7: 109,580,290 (GRCm39) |
M25L |
probably benign |
Het |
Tmem41b |
T |
A |
7: 109,580,292 (GRCm39) |
D91V |
probably damaging |
Het |
Tmem50b |
C |
T |
16: 91,380,174 (GRCm39) |
A68T |
probably damaging |
Het |
Tmprss11e |
G |
A |
5: 86,855,206 (GRCm39) |
Q400* |
probably null |
Het |
Tnfsf13b |
G |
A |
8: 10,081,661 (GRCm39) |
|
probably null |
Het |
Trappc8 |
A |
G |
18: 20,970,245 (GRCm39) |
V916A |
probably damaging |
Het |
Trdn |
G |
T |
10: 33,350,449 (GRCm39) |
V673F |
probably damaging |
Het |
Trim28 |
G |
T |
7: 12,759,711 (GRCm39) |
|
probably benign |
Het |
Txnrd2 |
T |
C |
16: 18,291,632 (GRCm39) |
V427A |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,204,587 (GRCm39) |
|
probably benign |
Het |
Vmn1r36 |
A |
G |
6: 66,693,404 (GRCm39) |
L51P |
probably damaging |
Het |
Vmn1r63 |
T |
A |
7: 5,806,063 (GRCm39) |
M190L |
possibly damaging |
Het |
Vmn2r116 |
T |
A |
17: 23,606,286 (GRCm39) |
N399K |
probably damaging |
Het |
Vmn2r117 |
T |
C |
17: 23,694,488 (GRCm39) |
N453S |
probably benign |
Het |
Wbp1l |
T |
A |
19: 46,643,109 (GRCm39) |
I370N |
probably damaging |
Het |
Zfp445 |
T |
C |
9: 122,682,046 (GRCm39) |
K632E |
probably benign |
Het |
Zfp850 |
C |
T |
7: 27,688,819 (GRCm39) |
R463H |
probably damaging |
Het |
Zyg11a |
A |
G |
4: 108,062,054 (GRCm39) |
L249P |
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 |
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 |
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 |
|
|