Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb2 |
G |
T |
4: 129,901,645 (GRCm39) |
C423F |
probably damaging |
Het |
Akap11 |
A |
T |
14: 78,750,220 (GRCm39) |
Y722* |
probably null |
Het |
Albfm1 |
A |
G |
5: 90,727,570 (GRCm39) |
H396R |
possibly damaging |
Het |
Anxa3 |
A |
T |
5: 96,968,288 (GRCm39) |
I114F |
probably damaging |
Het |
Arfgef3 |
T |
A |
10: 18,467,934 (GRCm39) |
R1755S |
probably damaging |
Het |
Atf7ip |
A |
T |
6: 136,537,039 (GRCm39) |
T91S |
possibly damaging |
Het |
Bcl2 |
C |
A |
1: 106,640,376 (GRCm39) |
A79S |
probably benign |
Het |
Bltp1 |
T |
A |
3: 37,041,314 (GRCm39) |
I2564K |
probably damaging |
Het |
Bmerb1 |
A |
G |
16: 13,804,683 (GRCm39) |
H10R |
possibly damaging |
Het |
Bmp10 |
C |
T |
6: 87,410,557 (GRCm39) |
P117S |
probably benign |
Het |
Bmpr2 |
A |
G |
1: 59,906,583 (GRCm39) |
T559A |
probably benign |
Het |
Cd200r1 |
A |
T |
16: 44,610,039 (GRCm39) |
Y86F |
probably damaging |
Het |
Cemip |
T |
A |
7: 83,596,308 (GRCm39) |
|
probably benign |
Het |
Cfap251 |
T |
C |
5: 123,394,116 (GRCm39) |
V335A |
probably benign |
Het |
Cfap52 |
A |
G |
11: 67,822,548 (GRCm39) |
|
probably null |
Het |
Chml |
T |
C |
1: 175,514,712 (GRCm39) |
H60R |
possibly damaging |
Het |
Cic |
TCCCCC |
TCCCCCCCC |
7: 24,991,095 (GRCm39) |
|
probably benign |
Het |
Clec12a |
A |
G |
6: 129,336,441 (GRCm39) |
Y201C |
probably damaging |
Het |
Col15a1 |
T |
C |
4: 47,258,719 (GRCm39) |
V370A |
probably benign |
Het |
Cpsf3 |
T |
C |
12: 21,351,538 (GRCm39) |
I353T |
probably damaging |
Het |
Csf2rb |
T |
A |
15: 78,230,667 (GRCm39) |
V470E |
probably benign |
Het |
Cyp4a10 |
C |
A |
4: 115,378,291 (GRCm39) |
Q126K |
probably benign |
Het |
Dennd1b |
T |
C |
1: 139,013,652 (GRCm39) |
S249P |
probably damaging |
Het |
Dnase2a |
A |
G |
8: 85,635,625 (GRCm39) |
|
probably null |
Het |
Dpp10 |
T |
C |
1: 123,305,882 (GRCm39) |
N490S |
probably benign |
Het |
Drgx |
A |
T |
14: 32,330,363 (GRCm39) |
N160I |
probably damaging |
Het |
Enc1 |
C |
T |
13: 97,382,243 (GRCm39) |
A251V |
probably benign |
Het |
Fancd2 |
T |
C |
6: 113,562,434 (GRCm39) |
V1258A |
probably benign |
Het |
Fancm |
G |
A |
12: 65,153,666 (GRCm39) |
|
probably null |
Het |
Fbxo16 |
C |
T |
14: 65,536,657 (GRCm39) |
T177I |
probably benign |
Het |
Gm1965 |
T |
C |
6: 89,123,525 (GRCm39) |
|
noncoding transcript |
Het |
Hal |
A |
T |
10: 93,339,401 (GRCm39) |
M497L |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,497,378 (GRCm39) |
L3936S |
possibly damaging |
Het |
Hs3st4 |
G |
T |
7: 123,996,410 (GRCm39) |
G359W |
probably damaging |
Het |
Il6st |
C |
T |
13: 112,639,399 (GRCm39) |
P608L |
probably damaging |
Het |
Kctd18 |
A |
C |
1: 58,004,707 (GRCm39) |
|
probably benign |
Het |
Kntc1 |
T |
A |
5: 123,940,309 (GRCm39) |
S1636T |
probably damaging |
Het |
Lrrn1 |
A |
T |
6: 107,545,311 (GRCm39) |
S370C |
probably damaging |
Het |
Mtcl1 |
A |
C |
17: 66,655,474 (GRCm39) |
C968G |
probably benign |
Het |
Mylip |
G |
A |
13: 45,562,238 (GRCm39) |
A347T |
probably damaging |
Het |
Ncoa4-ps |
A |
G |
12: 119,226,252 (GRCm39) |
|
noncoding transcript |
Het |
Neu4 |
T |
A |
1: 93,950,200 (GRCm39) |
V53E |
probably damaging |
Het |
Nxpe3 |
T |
C |
16: 55,680,687 (GRCm39) |
I302V |
probably benign |
Het |
Or11i1 |
A |
T |
3: 106,729,576 (GRCm39) |
C100S |
probably damaging |
Het |
Or4c15b |
A |
T |
2: 89,112,811 (GRCm39) |
L243Q |
possibly damaging |
Het |
Otos |
T |
C |
1: 92,572,090 (GRCm39) |
T79A |
probably damaging |
Het |
Pde4a |
T |
C |
9: 21,122,009 (GRCm39) |
I578T |
probably damaging |
Het |
Pramel17 |
T |
A |
4: 101,692,729 (GRCm39) |
M424L |
probably benign |
Het |
Prex2 |
C |
T |
1: 11,240,164 (GRCm39) |
P927S |
probably damaging |
Het |
Prune2 |
A |
T |
19: 17,100,116 (GRCm39) |
K1873N |
probably benign |
Het |
Ptk7 |
C |
A |
17: 46,887,417 (GRCm39) |
|
probably null |
Het |
Reln |
T |
A |
5: 22,200,585 (GRCm39) |
|
probably null |
Het |
Rgl2 |
A |
G |
17: 34,151,749 (GRCm39) |
|
probably benign |
Het |
Rnf145 |
T |
A |
11: 44,448,063 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,724,849 (GRCm39) |
E2488G |
probably damaging |
Het |
Sgo2b |
A |
T |
8: 64,379,664 (GRCm39) |
M1056K |
possibly damaging |
Het |
Snapc4 |
A |
G |
2: 26,259,245 (GRCm39) |
V635A |
probably benign |
Het |
Snx19 |
T |
A |
9: 30,348,763 (GRCm39) |
Y101N |
probably benign |
Het |
Sorl1 |
C |
A |
9: 41,925,746 (GRCm39) |
|
probably null |
Het |
Sp110 |
C |
G |
1: 85,516,839 (GRCm39) |
E219D |
probably damaging |
Het |
Speer4a2 |
A |
T |
5: 26,289,791 (GRCm39) |
I212N |
probably damaging |
Het |
Tmem30b |
G |
A |
12: 73,592,488 (GRCm39) |
P209L |
probably damaging |
Het |
Trbv12-2 |
G |
T |
6: 41,096,081 (GRCm39) |
C52F |
probably damaging |
Het |
Tsc2 |
T |
A |
17: 24,819,343 (GRCm39) |
D1304V |
probably benign |
Het |
Ugt2b36 |
T |
C |
5: 87,214,183 (GRCm39) |
Y487C |
probably damaging |
Het |
Vmn1r10 |
T |
A |
6: 57,090,811 (GRCm39) |
N134K |
probably damaging |
Het |
Wdr27 |
C |
A |
17: 15,141,016 (GRCm39) |
|
probably null |
Het |
Wdr75 |
T |
C |
1: 45,855,638 (GRCm39) |
F430L |
probably damaging |
Het |
Zfp629 |
A |
G |
7: 127,211,299 (GRCm39) |
I170T |
probably damaging |
Het |
|
Other mutations in Naip2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00515:Naip2
|
APN |
13 |
100,291,395 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00676:Naip2
|
APN |
13 |
100,289,140 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00870:Naip2
|
APN |
13 |
100,288,568 (GRCm39) |
splice site |
probably benign |
|
IGL00908:Naip2
|
APN |
13 |
100,297,157 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00916:Naip2
|
APN |
13 |
100,297,939 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00949:Naip2
|
APN |
13 |
100,298,099 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01010:Naip2
|
APN |
13 |
100,291,446 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01642:Naip2
|
APN |
13 |
100,297,445 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01884:Naip2
|
APN |
13 |
100,325,329 (GRCm39) |
splice site |
probably benign |
|
IGL01917:Naip2
|
APN |
13 |
100,298,591 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02015:Naip2
|
APN |
13 |
100,298,115 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL02315:Naip2
|
APN |
13 |
100,297,744 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02328:Naip2
|
APN |
13 |
100,297,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02735:Naip2
|
APN |
13 |
100,296,722 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02738:Naip2
|
APN |
13 |
100,325,685 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02887:Naip2
|
APN |
13 |
100,298,020 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02894:Naip2
|
APN |
13 |
100,320,297 (GRCm39) |
missense |
probably benign |
|
IGL02894:Naip2
|
APN |
13 |
100,297,505 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02974:Naip2
|
APN |
13 |
100,298,186 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03024:Naip2
|
APN |
13 |
100,325,862 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL03056:Naip2
|
APN |
13 |
100,298,795 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03281:Naip2
|
APN |
13 |
100,298,128 (GRCm39) |
missense |
probably damaging |
0.99 |
R0131:Naip2
|
UTSW |
13 |
100,320,296 (GRCm39) |
missense |
probably benign |
0.01 |
R0131:Naip2
|
UTSW |
13 |
100,320,296 (GRCm39) |
missense |
probably benign |
0.01 |
R0132:Naip2
|
UTSW |
13 |
100,320,296 (GRCm39) |
missense |
probably benign |
0.01 |
R0310:Naip2
|
UTSW |
13 |
100,285,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R0367:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R0368:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R0422:Naip2
|
UTSW |
13 |
100,297,621 (GRCm39) |
missense |
probably benign |
0.10 |
R0441:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R0445:Naip2
|
UTSW |
13 |
100,298,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0446:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R0464:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R0466:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R0467:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R0486:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R0533:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R0853:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R0853:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R0855:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R0855:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R0904:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R0904:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R0906:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R0906:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R0908:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R0908:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R0959:Naip2
|
UTSW |
13 |
100,291,419 (GRCm39) |
missense |
probably benign |
0.03 |
R0959:Naip2
|
UTSW |
13 |
100,291,386 (GRCm39) |
missense |
probably benign |
0.01 |
R0962:Naip2
|
UTSW |
13 |
100,315,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R1024:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R1024:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R1186:Naip2
|
UTSW |
13 |
100,298,545 (GRCm39) |
frame shift |
probably null |
|
R1186:Naip2
|
UTSW |
13 |
100,298,489 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1217:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R1217:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R1340:Naip2
|
UTSW |
13 |
100,325,630 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1342:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R1342:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R1404:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R1423:Naip2
|
UTSW |
13 |
100,291,355 (GRCm39) |
intron |
probably benign |
|
R1423:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R1423:Naip2
|
UTSW |
13 |
100,291,386 (GRCm39) |
missense |
probably benign |
0.01 |
R1423:Naip2
|
UTSW |
13 |
100,291,380 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1426:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R1426:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R1472:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R1575:Naip2
|
UTSW |
13 |
100,291,537 (GRCm39) |
intron |
probably benign |
|
R1575:Naip2
|
UTSW |
13 |
100,291,529 (GRCm39) |
missense |
probably benign |
0.00 |
R1576:Naip2
|
UTSW |
13 |
100,291,529 (GRCm39) |
missense |
probably benign |
0.00 |
R1576:Naip2
|
UTSW |
13 |
100,291,537 (GRCm39) |
intron |
probably benign |
|
R1599:Naip2
|
UTSW |
13 |
100,298,489 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1640:Naip2
|
UTSW |
13 |
100,298,489 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1641:Naip2
|
UTSW |
13 |
100,298,489 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1642:Naip2
|
UTSW |
13 |
100,298,489 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1643:Naip2
|
UTSW |
13 |
100,298,489 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1644:Naip2
|
UTSW |
13 |
100,319,437 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1681:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R1681:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R1891:Naip2
|
UTSW |
13 |
100,291,395 (GRCm39) |
missense |
probably benign |
0.00 |
R1913:Naip2
|
UTSW |
13 |
100,288,665 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1937:Naip2
|
UTSW |
13 |
100,298,368 (GRCm39) |
missense |
probably benign |
0.00 |
R1937:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
|
R1993:Naip2
|
UTSW |
13 |
100,298,515 (GRCm39) |
missense |
probably benign |
0.03 |
R2001:Naip2
|
UTSW |
13 |
100,281,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R2055:Naip2
|
UTSW |
13 |
100,315,880 (GRCm39) |
missense |
probably benign |
0.07 |
R2198:Naip2
|
UTSW |
13 |
100,289,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R2906:Naip2
|
UTSW |
13 |
100,298,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R2931:Naip2
|
UTSW |
13 |
100,291,529 (GRCm39) |
missense |
probably benign |
0.00 |
R3014:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R3016:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R3037:Naip2
|
UTSW |
13 |
100,291,457 (GRCm39) |
missense |
probably benign |
0.08 |
R3414:Naip2
|
UTSW |
13 |
100,325,771 (GRCm39) |
nonsense |
probably null |
|
R3437:Naip2
|
UTSW |
13 |
100,291,419 (GRCm39) |
missense |
probably benign |
0.03 |
R3713:Naip2
|
UTSW |
13 |
100,298,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Naip2
|
UTSW |
13 |
100,289,142 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3847:Naip2
|
UTSW |
13 |
100,315,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Naip2
|
UTSW |
13 |
100,315,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R3848:Naip2
|
UTSW |
13 |
100,315,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R3848:Naip2
|
UTSW |
13 |
100,315,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R3849:Naip2
|
UTSW |
13 |
100,315,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R3849:Naip2
|
UTSW |
13 |
100,315,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R3850:Naip2
|
UTSW |
13 |
100,315,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R3850:Naip2
|
UTSW |
13 |
100,315,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R3891:Naip2
|
UTSW |
13 |
100,297,606 (GRCm39) |
missense |
probably damaging |
0.99 |
R4419:Naip2
|
UTSW |
13 |
100,297,133 (GRCm39) |
missense |
probably benign |
0.03 |
R4456:Naip2
|
UTSW |
13 |
100,291,419 (GRCm39) |
missense |
probably benign |
0.03 |
R4458:Naip2
|
UTSW |
13 |
100,291,419 (GRCm39) |
missense |
probably benign |
0.03 |
R4689:Naip2
|
UTSW |
13 |
100,285,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R4797:Naip2
|
UTSW |
13 |
100,298,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R4852:Naip2
|
UTSW |
13 |
100,298,044 (GRCm39) |
missense |
probably benign |
|
R5135:Naip2
|
UTSW |
13 |
100,315,948 (GRCm39) |
missense |
probably damaging |
0.98 |
R5185:Naip2
|
UTSW |
13 |
100,325,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R5265:Naip2
|
UTSW |
13 |
100,289,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R5451:Naip2
|
UTSW |
13 |
100,325,368 (GRCm39) |
missense |
probably benign |
0.12 |
R5521:Naip2
|
UTSW |
13 |
100,291,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R5737:Naip2
|
UTSW |
13 |
100,298,362 (GRCm39) |
missense |
probably benign |
0.38 |
R6244:Naip2
|
UTSW |
13 |
100,288,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R6478:Naip2
|
UTSW |
13 |
100,298,549 (GRCm39) |
missense |
probably benign |
|
R6480:Naip2
|
UTSW |
13 |
100,298,549 (GRCm39) |
missense |
probably benign |
|
R6481:Naip2
|
UTSW |
13 |
100,298,549 (GRCm39) |
missense |
probably benign |
|
R6490:Naip2
|
UTSW |
13 |
100,297,193 (GRCm39) |
missense |
probably benign |
|
R6653:Naip2
|
UTSW |
13 |
100,288,644 (GRCm39) |
missense |
probably benign |
0.00 |
R6653:Naip2
|
UTSW |
13 |
100,298,352 (GRCm39) |
missense |
probably benign |
|
R6768:Naip2
|
UTSW |
13 |
100,314,832 (GRCm39) |
nonsense |
probably null |
|
R6791:Naip2
|
UTSW |
13 |
100,291,468 (GRCm39) |
missense |
probably benign |
|
R6793:Naip2
|
UTSW |
13 |
100,291,468 (GRCm39) |
missense |
probably benign |
|
R6890:Naip2
|
UTSW |
13 |
100,298,549 (GRCm39) |
missense |
probably benign |
|
R7036:Naip2
|
UTSW |
13 |
100,291,529 (GRCm39) |
missense |
probably benign |
0.00 |
R7213:Naip2
|
UTSW |
13 |
100,323,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R7342:Naip2
|
UTSW |
13 |
100,325,864 (GRCm39) |
missense |
probably benign |
0.09 |
R7445:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R7572:Naip2
|
UTSW |
13 |
100,291,468 (GRCm39) |
missense |
probably benign |
|
R7699:Naip2
|
UTSW |
13 |
100,296,877 (GRCm39) |
missense |
probably benign |
0.00 |
R7840:Naip2
|
UTSW |
13 |
100,280,917 (GRCm39) |
missense |
probably benign |
0.14 |
R7874:Naip2
|
UTSW |
13 |
100,291,468 (GRCm39) |
missense |
probably benign |
|
R7874:Naip2
|
UTSW |
13 |
100,291,459 (GRCm39) |
missense |
probably benign |
0.00 |
R8038:Naip2
|
UTSW |
13 |
100,298,570 (GRCm39) |
missense |
probably benign |
0.00 |
R8065:Naip2
|
UTSW |
13 |
100,325,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R8094:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R8166:Naip2
|
UTSW |
13 |
100,298,515 (GRCm39) |
missense |
probably benign |
0.03 |
R8378:Naip2
|
UTSW |
13 |
100,298,290 (GRCm39) |
missense |
probably benign |
0.01 |
R8669:Naip2
|
UTSW |
13 |
100,325,477 (GRCm39) |
missense |
probably benign |
0.05 |
R8691:Naip2
|
UTSW |
13 |
100,297,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Naip2
|
UTSW |
13 |
100,280,914 (GRCm39) |
missense |
probably benign |
|
R8720:Naip2
|
UTSW |
13 |
100,298,630 (GRCm39) |
missense |
probably benign |
0.04 |
R8888:Naip2
|
UTSW |
13 |
100,325,644 (GRCm39) |
missense |
probably benign |
0.01 |
R8895:Naip2
|
UTSW |
13 |
100,325,644 (GRCm39) |
missense |
probably benign |
0.01 |
R9031:Naip2
|
UTSW |
13 |
100,314,776 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9072:Naip2
|
UTSW |
13 |
100,291,468 (GRCm39) |
missense |
probably benign |
|
R9072:Naip2
|
UTSW |
13 |
100,291,459 (GRCm39) |
missense |
probably benign |
0.00 |
R9074:Naip2
|
UTSW |
13 |
100,291,468 (GRCm39) |
missense |
probably benign |
|
R9074:Naip2
|
UTSW |
13 |
100,291,459 (GRCm39) |
missense |
probably benign |
0.00 |
R9077:Naip2
|
UTSW |
13 |
100,291,468 (GRCm39) |
missense |
probably benign |
|
R9077:Naip2
|
UTSW |
13 |
100,291,459 (GRCm39) |
missense |
probably benign |
0.00 |
R9176:Naip2
|
UTSW |
13 |
100,298,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R9219:Naip2
|
UTSW |
13 |
100,297,213 (GRCm39) |
missense |
probably benign |
0.06 |
R9358:Naip2
|
UTSW |
13 |
100,298,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R9371:Naip2
|
UTSW |
13 |
100,298,354 (GRCm39) |
nonsense |
probably null |
|
R9414:Naip2
|
UTSW |
13 |
100,298,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R9415:Naip2
|
UTSW |
13 |
100,298,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R9416:Naip2
|
UTSW |
13 |
100,298,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R9708:Naip2
|
UTSW |
13 |
100,298,087 (GRCm39) |
missense |
probably damaging |
0.99 |
V5622:Naip2
|
UTSW |
13 |
100,291,537 (GRCm39) |
intron |
probably benign |
|
V5622:Naip2
|
UTSW |
13 |
100,291,529 (GRCm39) |
missense |
probably benign |
0.00 |
V5622:Naip2
|
UTSW |
13 |
100,291,529 (GRCm39) |
missense |
probably benign |
0.00 |
X0063:Naip2
|
UTSW |
13 |
100,298,266 (GRCm39) |
missense |
probably damaging |
1.00 |
Y5405:Naip2
|
UTSW |
13 |
100,291,468 (GRCm39) |
missense |
probably benign |
|
Z1088:Naip2
|
UTSW |
13 |
100,298,417 (GRCm39) |
missense |
probably benign |
|
Z1176:Naip2
|
UTSW |
13 |
100,298,417 (GRCm39) |
missense |
probably benign |
|
Z1176:Naip2
|
UTSW |
13 |
100,298,101 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Naip2
|
UTSW |
13 |
100,298,417 (GRCm39) |
missense |
probably benign |
|
Z1177:Naip2
|
UTSW |
13 |
100,289,137 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1177:Naip2
|
UTSW |
13 |
100,299,373 (GRCm39) |
missense |
probably benign |
0.01 |
|