Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aarsd1 |
T |
G |
11: 101,308,018 (GRCm39) |
T28P |
probably benign |
Het |
Abcc1 |
C |
A |
16: 14,283,033 (GRCm39) |
R1170S |
probably damaging |
Het |
Adam8 |
T |
C |
7: 139,566,304 (GRCm39) |
N568S |
probably benign |
Het |
Arhgap17 |
T |
C |
7: 122,926,467 (GRCm39) |
R65G |
probably damaging |
Het |
Arid4b |
A |
C |
13: 14,310,804 (GRCm39) |
I136L |
probably benign |
Het |
Ash1l |
G |
T |
3: 88,873,304 (GRCm39) |
G29V |
possibly damaging |
Het |
Atp6v0a2 |
A |
G |
5: 124,784,676 (GRCm39) |
T320A |
probably damaging |
Het |
B4gat1 |
G |
A |
19: 5,089,686 (GRCm39) |
V228M |
probably benign |
Het |
Calcr |
T |
A |
6: 3,691,536 (GRCm39) |
H450L |
probably benign |
Het |
Cand1 |
A |
T |
10: 119,047,692 (GRCm39) |
N599K |
possibly damaging |
Het |
Cblif |
A |
T |
19: 11,740,587 (GRCm39) |
H407L |
probably benign |
Het |
Cel |
A |
T |
2: 28,450,649 (GRCm39) |
Y125* |
probably null |
Het |
Cfi |
T |
A |
3: 129,668,781 (GRCm39) |
N602K |
probably damaging |
Het |
Clstn1 |
G |
A |
4: 149,713,887 (GRCm39) |
A190T |
probably damaging |
Het |
Cmklr1 |
C |
T |
5: 113,752,354 (GRCm39) |
V216M |
probably benign |
Het |
Cntnap5a |
A |
G |
1: 115,987,852 (GRCm39) |
T128A |
probably benign |
Het |
Creld2 |
A |
G |
15: 88,710,610 (GRCm39) |
T342A |
probably benign |
Het |
Ctbp2 |
T |
C |
7: 132,616,041 (GRCm39) |
E298G |
probably damaging |
Het |
Ctsh |
A |
T |
9: 89,957,040 (GRCm39) |
E307V |
probably benign |
Het |
Cxcl10 |
T |
A |
5: 92,496,029 (GRCm39) |
D36V |
probably benign |
Het |
Dgkb |
A |
G |
12: 38,150,432 (GRCm39) |
T73A |
probably benign |
Het |
Dnah3 |
T |
G |
7: 119,629,208 (GRCm39) |
E1449A |
probably damaging |
Het |
Dpp6 |
T |
C |
5: 27,919,552 (GRCm39) |
M683T |
probably benign |
Het |
Foxn4 |
C |
A |
5: 114,396,760 (GRCm39) |
W241L |
probably damaging |
Het |
Gosr1 |
T |
C |
11: 76,621,033 (GRCm39) |
I219V |
probably benign |
Het |
Gtf2f2 |
T |
C |
14: 76,144,317 (GRCm39) |
D179G |
probably damaging |
Het |
Ighg2b |
A |
G |
12: 113,270,050 (GRCm39) |
Y323H |
|
Het |
Itpr2 |
A |
T |
6: 146,228,685 (GRCm39) |
H1303Q |
probably damaging |
Het |
Kif1b |
A |
C |
4: 149,298,547 (GRCm39) |
Y1040D |
possibly damaging |
Het |
Lbr |
C |
T |
1: 181,653,186 (GRCm39) |
|
probably null |
Het |
Lrp2 |
A |
G |
2: 69,309,634 (GRCm39) |
V2755A |
possibly damaging |
Het |
Lrp6 |
G |
T |
6: 134,427,781 (GRCm39) |
P1604T |
probably damaging |
Het |
Lrrcc1 |
T |
A |
3: 14,619,431 (GRCm39) |
C606S |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,275,917 (GRCm39) |
E6217G |
probably damaging |
Het |
Ms4a6d |
G |
A |
19: 11,567,437 (GRCm39) |
Q155* |
probably null |
Het |
Myo9b |
T |
C |
8: 71,808,418 (GRCm39) |
V1687A |
probably damaging |
Het |
Neb |
A |
T |
2: 52,171,679 (GRCm39) |
S1605T |
probably damaging |
Het |
Nuak1 |
T |
C |
10: 84,210,831 (GRCm39) |
E419G |
probably damaging |
Het |
Or14a260 |
G |
A |
7: 85,985,295 (GRCm39) |
T103I |
probably benign |
Het |
Or8c18 |
A |
G |
9: 38,203,574 (GRCm39) |
Y111C |
probably damaging |
Het |
Paip2b |
T |
A |
6: 83,791,808 (GRCm39) |
S25C |
probably damaging |
Het |
Pgbd5 |
G |
A |
8: 125,160,709 (GRCm39) |
R53C |
probably benign |
Het |
Plin4 |
T |
C |
17: 56,411,608 (GRCm39) |
T808A |
probably benign |
Het |
Pramel11 |
A |
T |
4: 143,623,520 (GRCm39) |
I218K |
probably benign |
Het |
Prex2 |
A |
G |
1: 11,232,549 (GRCm39) |
D872G |
probably benign |
Het |
Ptf1a |
A |
G |
2: 19,451,977 (GRCm39) |
*325W |
probably null |
Het |
Ptprg |
T |
C |
14: 12,237,151 (GRCm38) |
V1390A |
possibly damaging |
Het |
Rhpn2 |
A |
G |
7: 35,033,771 (GRCm39) |
T2A |
probably damaging |
Het |
Rpl18a |
T |
C |
8: 71,348,042 (GRCm39) |
N214D |
unknown |
Het |
Scp2 |
T |
A |
4: 107,948,518 (GRCm39) |
Y197F |
probably benign |
Het |
Sftpb |
G |
A |
6: 72,286,858 (GRCm39) |
R254H |
probably benign |
Het |
Slc17a9 |
T |
C |
2: 180,378,555 (GRCm39) |
L246P |
probably damaging |
Het |
Slc38a9 |
G |
T |
13: 112,806,125 (GRCm39) |
|
probably benign |
Het |
Slc4a1ap |
C |
T |
5: 31,693,634 (GRCm39) |
L523F |
possibly damaging |
Het |
Spats2l |
C |
A |
1: 57,925,106 (GRCm39) |
T168K |
possibly damaging |
Het |
Sstr1 |
A |
G |
12: 58,260,456 (GRCm39) |
S360G |
possibly damaging |
Het |
Taf1b |
A |
T |
12: 24,608,343 (GRCm39) |
K581* |
probably null |
Het |
Tfip11 |
T |
A |
5: 112,475,838 (GRCm39) |
M1K |
probably null |
Het |
Tgoln1 |
G |
C |
6: 72,593,261 (GRCm39) |
T73R |
probably benign |
Het |
Ttc23l |
G |
A |
15: 10,551,583 (GRCm39) |
H48Y |
probably benign |
Het |
Uggt2 |
T |
A |
14: 119,232,384 (GRCm39) |
H1489L |
possibly damaging |
Het |
Unc13b |
T |
C |
4: 43,258,703 (GRCm39) |
L1346P |
probably damaging |
Het |
Vmac |
T |
C |
17: 57,022,644 (GRCm39) |
E122G |
probably benign |
Het |
Vmn2r125 |
T |
C |
4: 156,703,138 (GRCm39) |
V172A |
probably damaging |
Het |
Zfp54 |
A |
G |
17: 21,648,014 (GRCm39) |
|
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 |
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 |
|
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 |
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 |
|