Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730061H03Rik |
C |
T |
14: 55,797,574 (GRCm39) |
|
probably benign |
Het |
Acsf2 |
A |
C |
11: 94,460,155 (GRCm39) |
M399R |
possibly damaging |
Het |
Adra2c |
C |
A |
5: 35,438,268 (GRCm39) |
R347S |
probably benign |
Het |
Akap9 |
A |
G |
5: 4,011,466 (GRCm39) |
K723R |
possibly damaging |
Het |
Anxa9 |
A |
C |
3: 95,215,324 (GRCm39) |
|
probably benign |
Het |
Aqr |
T |
C |
2: 113,943,832 (GRCm39) |
H1102R |
probably damaging |
Het |
Armh3 |
A |
T |
19: 45,808,726 (GRCm39) |
F655Y |
probably damaging |
Het |
Arrdc2 |
A |
G |
8: 71,290,162 (GRCm39) |
V173A |
probably benign |
Het |
Aspm |
T |
C |
1: 139,405,748 (GRCm39) |
V1545A |
probably benign |
Het |
Bbs5 |
C |
T |
2: 69,477,578 (GRCm39) |
|
probably benign |
Het |
Bnip2 |
A |
G |
9: 69,910,716 (GRCm39) |
T255A |
possibly damaging |
Het |
Cacna1b |
T |
C |
2: 24,538,535 (GRCm39) |
T1531A |
probably damaging |
Het |
Cast |
T |
C |
13: 74,955,942 (GRCm39) |
K9R |
probably benign |
Het |
Cfap46 |
A |
T |
7: 139,187,104 (GRCm39) |
|
probably null |
Het |
Cfap57 |
G |
T |
4: 118,450,251 (GRCm39) |
L624M |
probably damaging |
Het |
Cyp2c39 |
A |
T |
19: 39,552,323 (GRCm39) |
M339L |
probably benign |
Het |
Dcst1 |
T |
A |
3: 89,265,110 (GRCm39) |
T247S |
probably benign |
Het |
Dnajc18 |
T |
A |
18: 35,816,372 (GRCm39) |
I189F |
possibly damaging |
Het |
Eef2kmt |
T |
C |
16: 5,066,876 (GRCm39) |
T126A |
probably benign |
Het |
Epha2 |
A |
G |
4: 141,049,016 (GRCm39) |
E624G |
probably damaging |
Het |
Erbb3 |
G |
A |
10: 128,408,317 (GRCm39) |
H866Y |
probably benign |
Het |
F13a1 |
C |
T |
13: 37,100,837 (GRCm39) |
|
probably null |
Het |
Fgd3 |
T |
A |
13: 49,432,078 (GRCm39) |
N392I |
probably damaging |
Het |
Fgf7 |
A |
T |
2: 125,930,160 (GRCm39) |
M98L |
probably benign |
Het |
G2e3 |
T |
A |
12: 51,415,922 (GRCm39) |
S553T |
probably benign |
Het |
Glipr1 |
C |
A |
10: 111,829,411 (GRCm39) |
E117* |
probably null |
Het |
Gm11060 |
A |
T |
2: 104,924,128 (GRCm39) |
|
probably benign |
Het |
Gm4787 |
A |
G |
12: 81,424,403 (GRCm39) |
I585T |
probably damaging |
Het |
Gm6055 |
A |
T |
14: 48,316,915 (GRCm39) |
|
noncoding transcript |
Het |
Gpbar1 |
TACCAC |
TAC |
1: 74,318,704 (GRCm39) |
|
probably benign |
Het |
Gpt2 |
T |
A |
8: 86,246,068 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
A |
T |
5: 134,386,685 (GRCm39) |
Y345* |
probably null |
Het |
Hmcn1 |
T |
A |
1: 150,695,200 (GRCm39) |
T235S |
probably benign |
Het |
Igkv5-48 |
A |
G |
6: 69,703,738 (GRCm39) |
Y56H |
possibly damaging |
Het |
Il17re |
C |
T |
6: 113,446,530 (GRCm39) |
T427I |
probably benign |
Het |
Itpr3 |
A |
T |
17: 27,302,582 (GRCm39) |
D80V |
probably damaging |
Het |
Kif21a |
G |
T |
15: 90,833,213 (GRCm39) |
H1317N |
probably benign |
Het |
Kif28 |
T |
C |
1: 179,526,209 (GRCm39) |
K144E |
probably damaging |
Het |
Kif4-ps |
A |
C |
12: 101,113,330 (GRCm39) |
|
noncoding transcript |
Het |
Klk1b11 |
C |
T |
7: 43,427,160 (GRCm39) |
T148I |
probably damaging |
Het |
Klkb1 |
T |
A |
8: 45,739,995 (GRCm39) |
H99L |
probably damaging |
Het |
Kpna6 |
A |
C |
4: 129,550,198 (GRCm39) |
|
probably null |
Het |
Lama3 |
G |
T |
18: 12,685,883 (GRCm39) |
K1132N |
probably damaging |
Het |
Lcp1 |
T |
A |
14: 75,445,911 (GRCm39) |
L264* |
probably null |
Het |
Map2 |
T |
C |
1: 66,452,664 (GRCm39) |
V360A |
probably benign |
Het |
Med13 |
A |
T |
11: 86,189,673 (GRCm39) |
S1079T |
probably damaging |
Het |
Mettl13 |
A |
G |
1: 162,364,789 (GRCm39) |
M162T |
probably damaging |
Het |
Mppe1 |
T |
G |
18: 67,361,133 (GRCm39) |
E208A |
probably benign |
Het |
Msantd2 |
A |
C |
9: 37,400,675 (GRCm39) |
K19T |
possibly damaging |
Het |
Mylk3 |
A |
G |
8: 86,091,412 (GRCm39) |
V131A |
probably damaging |
Het |
Myocd |
A |
T |
11: 65,074,299 (GRCm39) |
S609T |
possibly damaging |
Het |
Ncbp3 |
G |
A |
11: 72,944,355 (GRCm39) |
|
probably null |
Het |
Neb |
T |
A |
2: 52,136,871 (GRCm39) |
L3203F |
probably damaging |
Het |
Notch2 |
C |
A |
3: 98,046,949 (GRCm39) |
T1756K |
probably benign |
Het |
Nphp4 |
A |
T |
4: 152,622,250 (GRCm39) |
R544W |
probably damaging |
Het |
Or3a1c |
A |
T |
11: 74,046,745 (GRCm39) |
Y255F |
probably benign |
Het |
Or4p18 |
T |
G |
2: 88,232,756 (GRCm39) |
H174P |
probably damaging |
Het |
Or5c1 |
A |
T |
2: 37,222,578 (GRCm39) |
D273V |
probably damaging |
Het |
Parp4 |
T |
A |
14: 56,827,355 (GRCm39) |
V163E |
possibly damaging |
Het |
Pcdhgb1 |
C |
A |
18: 37,815,425 (GRCm39) |
Q639K |
probably benign |
Het |
Pcsk7 |
T |
A |
9: 45,830,160 (GRCm39) |
M418K |
probably damaging |
Het |
Pglyrp4 |
T |
C |
3: 90,640,314 (GRCm39) |
I188T |
probably benign |
Het |
Pgs1 |
A |
G |
11: 117,896,345 (GRCm39) |
R339G |
probably benign |
Het |
Pik3r3 |
A |
G |
4: 116,143,388 (GRCm39) |
I294V |
probably benign |
Het |
Pik3r6 |
A |
G |
11: 68,430,771 (GRCm39) |
D520G |
probably damaging |
Het |
Pkdrej |
A |
G |
15: 85,704,610 (GRCm39) |
V442A |
probably benign |
Het |
Ppfibp1 |
T |
A |
6: 146,931,917 (GRCm39) |
|
probably benign |
Het |
Ppp3ca |
C |
A |
3: 136,640,810 (GRCm39) |
Q454K |
possibly damaging |
Het |
Ppp5c |
A |
T |
7: 16,743,861 (GRCm39) |
M191K |
probably damaging |
Het |
Prl4a1 |
A |
T |
13: 28,207,308 (GRCm39) |
Y194F |
possibly damaging |
Het |
Ptpn21 |
G |
T |
12: 98,646,362 (GRCm39) |
T1032K |
probably damaging |
Het |
Ptprh |
A |
T |
7: 4,554,006 (GRCm39) |
|
probably null |
Het |
Ptprm |
T |
A |
17: 66,985,062 (GRCm39) |
R1447S |
probably benign |
Het |
Pxk |
T |
A |
14: 8,140,734 (GRCm38) |
D236E |
probably damaging |
Het |
Qars1 |
T |
C |
9: 108,386,130 (GRCm39) |
F107S |
probably damaging |
Het |
Rbbp6 |
A |
G |
7: 122,599,031 (GRCm39) |
|
probably benign |
Het |
Rptor |
A |
T |
11: 119,712,466 (GRCm39) |
|
probably benign |
Het |
Rtn4 |
T |
A |
11: 29,690,994 (GRCm39) |
M1095K |
probably damaging |
Het |
Serpinb3b |
T |
A |
1: 107,082,445 (GRCm39) |
H273L |
probably benign |
Het |
Sgce |
G |
A |
6: 4,689,630 (GRCm39) |
T401M |
probably benign |
Het |
Slc12a6 |
C |
T |
2: 112,188,870 (GRCm39) |
R1083W |
probably damaging |
Het |
Slc45a4 |
A |
T |
15: 73,456,299 (GRCm39) |
M635K |
probably damaging |
Het |
Slc6a1 |
T |
A |
6: 114,284,662 (GRCm39) |
V240D |
probably damaging |
Het |
Snx9 |
G |
A |
17: 5,952,794 (GRCm39) |
|
probably null |
Het |
Spred3 |
A |
G |
7: 28,867,249 (GRCm39) |
V49A |
probably damaging |
Het |
Tars1 |
A |
G |
15: 11,390,477 (GRCm39) |
F334S |
probably damaging |
Het |
Tdpoz1 |
A |
G |
3: 93,578,454 (GRCm39) |
V110A |
probably benign |
Het |
Tfrc |
T |
G |
16: 32,437,097 (GRCm39) |
V252G |
probably damaging |
Het |
Tm6sf2 |
T |
C |
8: 70,528,128 (GRCm39) |
|
probably benign |
Het |
Txlnb |
T |
C |
10: 17,714,717 (GRCm39) |
V383A |
probably damaging |
Het |
Utp20 |
C |
A |
10: 88,652,811 (GRCm39) |
V368L |
probably benign |
Het |
Vmn2r12 |
A |
T |
5: 109,239,372 (GRCm39) |
V397E |
probably damaging |
Het |
Zdhhc12 |
G |
A |
2: 29,981,538 (GRCm39) |
R175W |
probably damaging |
Het |
Zfyve9 |
A |
G |
4: 108,538,097 (GRCm39) |
|
probably null |
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 |
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 |
|
|