Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam32 |
A |
T |
8: 25,353,520 (GRCm39) |
W690R |
probably damaging |
Het |
Adgrg6 |
A |
G |
10: 14,308,694 (GRCm39) |
I800T |
probably benign |
Het |
Afg3l2 |
G |
A |
18: 67,573,292 (GRCm39) |
T170M |
probably damaging |
Het |
Ap1b1 |
T |
A |
11: 4,981,641 (GRCm39) |
N516K |
probably damaging |
Het |
Armcx6 |
A |
T |
X: 133,650,199 (GRCm39) |
C211S |
probably damaging |
Het |
Atp7b |
G |
A |
8: 22,501,570 (GRCm39) |
T781I |
probably damaging |
Het |
Cd96 |
T |
C |
16: 45,871,850 (GRCm39) |
T432A |
possibly damaging |
Het |
Col13a1 |
T |
C |
10: 61,696,267 (GRCm39) |
|
probably benign |
Het |
Ddx4 |
G |
T |
13: 112,757,311 (GRCm39) |
|
probably benign |
Het |
Dnm1l |
A |
T |
16: 16,132,175 (GRCm39) |
S666T |
probably damaging |
Het |
Duoxa1 |
C |
T |
2: 122,135,155 (GRCm39) |
V197M |
probably benign |
Het |
Gm6430 |
A |
T |
1: 96,952,554 (GRCm39) |
|
noncoding transcript |
Het |
Gtf2a1l |
G |
A |
17: 89,002,083 (GRCm39) |
R313H |
possibly damaging |
Het |
Gucy2c |
A |
T |
6: 136,685,385 (GRCm39) |
V852E |
probably damaging |
Het |
Kcnk1 |
G |
T |
8: 126,722,538 (GRCm39) |
V114L |
probably benign |
Het |
Klra3 |
G |
T |
6: 130,310,302 (GRCm39) |
Q73K |
probably damaging |
Het |
Lax1 |
A |
T |
1: 133,616,643 (GRCm39) |
M1K |
probably null |
Het |
Lce1k |
T |
C |
3: 92,713,882 (GRCm39) |
S101G |
unknown |
Het |
Med12l |
T |
C |
3: 59,164,503 (GRCm39) |
L1365P |
probably damaging |
Het |
Mtx2 |
T |
C |
2: 74,697,253 (GRCm39) |
S83P |
probably damaging |
Het |
Nefh |
A |
G |
11: 4,890,216 (GRCm39) |
I801T |
probably benign |
Het |
Or8g24 |
A |
G |
9: 38,989,669 (GRCm39) |
V124A |
probably benign |
Het |
Oxct2b |
A |
G |
4: 123,010,823 (GRCm39) |
I248V |
probably benign |
Het |
Pcdhgb2 |
A |
T |
18: 37,823,908 (GRCm39) |
I300F |
probably damaging |
Het |
Ptprc |
G |
A |
1: 137,992,272 (GRCm39) |
A1285V |
possibly damaging |
Het |
Rassf3 |
A |
G |
10: 121,250,297 (GRCm39) |
L172P |
probably damaging |
Het |
Rbm26 |
T |
A |
14: 105,380,270 (GRCm39) |
T516S |
probably benign |
Het |
Rpusd1 |
T |
C |
17: 25,949,705 (GRCm39) |
S292P |
probably benign |
Het |
Scamp5 |
A |
G |
9: 57,351,146 (GRCm39) |
V172A |
probably damaging |
Het |
Snx25 |
T |
C |
8: 46,502,560 (GRCm39) |
|
probably null |
Het |
Tmprss11g |
A |
G |
5: 86,640,661 (GRCm39) |
|
probably benign |
Het |
Ttll3 |
G |
C |
6: 113,369,471 (GRCm39) |
|
probably benign |
Het |
Uggt2 |
C |
T |
14: 119,256,919 (GRCm39) |
S1105N |
probably benign |
Het |
Usp45 |
T |
A |
4: 21,834,338 (GRCm39) |
Y805* |
probably null |
Het |
Zfp639 |
T |
C |
3: 32,573,900 (GRCm39) |
L175P |
probably damaging |
Het |
Zfp995 |
T |
C |
17: 22,099,247 (GRCm39) |
D329G |
probably benign |
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 |
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 |
|
R4922:Naip2
|
UTSW |
13 |
100,291,468 (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 |
|