Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AI182371 |
T |
A |
2: 34,978,753 (GRCm39) |
K203* |
probably null |
Het |
Akr1c13 |
T |
C |
13: 4,242,436 (GRCm39) |
|
probably benign |
Het |
Amer3 |
A |
G |
1: 34,627,074 (GRCm39) |
S438G |
probably damaging |
Het |
Aqp9 |
T |
A |
9: 71,070,543 (GRCm39) |
|
probably null |
Het |
Art4 |
G |
T |
6: 136,831,848 (GRCm39) |
H98N |
probably damaging |
Het |
Bdh1 |
T |
C |
16: 31,266,422 (GRCm39) |
S70P |
probably benign |
Het |
Ccdc61 |
A |
C |
7: 18,625,030 (GRCm39) |
Y503D |
probably damaging |
Het |
Cd180 |
A |
T |
13: 102,841,503 (GRCm39) |
N183I |
probably damaging |
Het |
Cd200r2 |
C |
T |
16: 44,729,537 (GRCm39) |
A64V |
probably damaging |
Het |
Ceacam9 |
A |
C |
7: 16,457,780 (GRCm39) |
K98Q |
probably benign |
Het |
Cep44 |
AACGC |
A |
8: 56,994,018 (GRCm39) |
|
probably null |
Het |
Cfap77 |
G |
T |
2: 28,845,625 (GRCm39) |
D247E |
probably benign |
Het |
Cftr |
T |
C |
6: 18,227,972 (GRCm39) |
M388T |
probably benign |
Het |
Chrnb1 |
G |
A |
11: 69,675,476 (GRCm39) |
H493Y |
probably damaging |
Het |
Ckap2 |
A |
C |
8: 22,667,402 (GRCm39) |
M153R |
probably benign |
Het |
Cnot6l |
A |
G |
5: 96,278,987 (GRCm39) |
V77A |
probably benign |
Het |
Col12a1 |
C |
T |
9: 79,562,689 (GRCm39) |
E1798K |
possibly damaging |
Het |
Cth |
T |
A |
3: 157,630,522 (GRCm39) |
D49V |
probably benign |
Het |
Ctnnb1 |
T |
C |
9: 120,784,482 (GRCm39) |
S425P |
probably damaging |
Het |
Ctnnd1 |
T |
C |
2: 84,441,129 (GRCm39) |
N690S |
probably benign |
Het |
Dennd2b |
A |
G |
7: 109,124,553 (GRCm39) |
L1096P |
probably damaging |
Het |
Dennd4c |
A |
G |
4: 86,692,568 (GRCm39) |
D26G |
probably damaging |
Het |
Dlg5 |
G |
A |
14: 24,295,280 (GRCm39) |
P80L |
probably damaging |
Het |
Dnai3 |
T |
C |
3: 145,761,373 (GRCm39) |
D661G |
probably benign |
Het |
Eef2k |
A |
G |
7: 120,502,707 (GRCm39) |
|
probably null |
Het |
Ephb2 |
C |
T |
4: 136,386,376 (GRCm39) |
R791H |
probably damaging |
Het |
Erh |
T |
C |
12: 80,687,757 (GRCm39) |
Y22C |
probably benign |
Het |
F5 |
C |
T |
1: 164,020,897 (GRCm39) |
T1124I |
possibly damaging |
Het |
Fam220a |
T |
A |
5: 143,549,226 (GRCm39) |
C213S |
possibly damaging |
Het |
Fat2 |
G |
T |
11: 55,201,258 (GRCm39) |
N605K |
probably damaging |
Het |
Ganab |
C |
A |
19: 8,891,933 (GRCm39) |
S780* |
probably null |
Het |
Gbgt1 |
C |
T |
2: 28,392,219 (GRCm39) |
P67S |
probably damaging |
Het |
Gm17190 |
G |
T |
13: 96,219,287 (GRCm39) |
G208* |
probably null |
Het |
Grhl2 |
A |
G |
15: 37,291,860 (GRCm39) |
Y316C |
probably damaging |
Het |
H2-T10 |
T |
C |
17: 36,431,741 (GRCm39) |
T38A |
probably benign |
Het |
Ins1 |
A |
G |
19: 52,252,858 (GRCm39) |
|
probably benign |
Het |
Ippk |
T |
C |
13: 49,585,943 (GRCm39) |
|
probably null |
Het |
Klc4 |
T |
A |
17: 46,950,836 (GRCm39) |
I258F |
probably benign |
Het |
Manba |
C |
A |
3: 135,248,154 (GRCm39) |
L348I |
probably benign |
Het |
Mgam |
A |
G |
6: 40,721,723 (GRCm39) |
N347S |
probably benign |
Het |
Myo18b |
T |
C |
5: 112,871,758 (GRCm39) |
T2108A |
probably benign |
Het |
Nsa2 |
C |
T |
13: 97,267,728 (GRCm39) |
A242T |
probably benign |
Het |
Nsd2 |
G |
A |
5: 34,039,491 (GRCm39) |
W834* |
probably null |
Het |
Or10q3 |
T |
A |
19: 11,847,680 (GRCm39) |
D300V |
possibly damaging |
Het |
Or5p50 |
A |
T |
7: 107,422,129 (GRCm39) |
C182* |
probably null |
Het |
Or5w1 |
T |
C |
2: 87,486,740 (GRCm39) |
N175S |
possibly damaging |
Het |
Or8s16 |
T |
C |
15: 98,211,261 (GRCm39) |
M57V |
probably damaging |
Het |
Pam |
A |
T |
1: 97,769,972 (GRCm39) |
D599E |
probably damaging |
Het |
Phf20l1 |
A |
G |
15: 66,508,733 (GRCm39) |
K864R |
probably damaging |
Het |
Pip4p2 |
T |
A |
4: 14,912,477 (GRCm39) |
Y195* |
probably null |
Het |
Plcl2 |
A |
G |
17: 50,915,496 (GRCm39) |
D835G |
probably damaging |
Het |
Ppm1m |
C |
A |
9: 106,073,356 (GRCm39) |
A329S |
probably damaging |
Het |
Prep |
T |
C |
10: 45,026,534 (GRCm39) |
V486A |
probably benign |
Het |
Prkcb |
A |
T |
7: 122,116,067 (GRCm39) |
N182I |
probably damaging |
Het |
Prkcz |
A |
G |
4: 155,356,059 (GRCm39) |
F355S |
probably damaging |
Het |
Psg20 |
C |
T |
7: 18,418,392 (GRCm39) |
S125N |
probably benign |
Het |
Psmd12 |
A |
G |
11: 107,382,883 (GRCm39) |
D234G |
probably benign |
Het |
Pvrig-ps |
A |
T |
5: 138,340,270 (GRCm39) |
M14L |
probably benign |
Het |
Rabgap1l |
C |
T |
1: 160,054,054 (GRCm39) |
|
probably null |
Het |
Rfc1 |
A |
T |
5: 65,432,769 (GRCm39) |
C764S |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,757,302 (GRCm39) |
D351G |
probably benign |
Het |
Scart1 |
T |
C |
7: 139,800,619 (GRCm39) |
|
probably null |
Het |
Serpinb9g |
T |
C |
13: 33,679,150 (GRCm39) |
F340S |
probably benign |
Het |
Sirpb1c |
C |
A |
3: 15,886,430 (GRCm39) |
L315F |
probably damaging |
Het |
Slc24a1 |
C |
G |
9: 64,835,686 (GRCm39) |
E814Q |
unknown |
Het |
Slc26a11 |
A |
T |
11: 119,265,328 (GRCm39) |
Q355L |
probably damaging |
Het |
Sp100 |
C |
T |
1: 85,634,960 (GRCm39) |
L483F |
possibly damaging |
Het |
Ston1 |
T |
A |
17: 88,943,329 (GRCm39) |
M245K |
probably benign |
Het |
Swap70 |
T |
A |
7: 109,873,979 (GRCm39) |
D442E |
probably benign |
Het |
Syne2 |
T |
A |
12: 76,092,960 (GRCm39) |
V450D |
possibly damaging |
Het |
Tbck |
T |
A |
3: 132,458,324 (GRCm39) |
N651K |
probably damaging |
Het |
Timd4 |
A |
T |
11: 46,708,585 (GRCm39) |
T204S |
probably benign |
Het |
Tmem102 |
A |
G |
11: 69,695,711 (GRCm39) |
L87P |
probably damaging |
Het |
Tmprss11e |
T |
A |
5: 86,857,339 (GRCm39) |
T325S |
probably benign |
Het |
Trpm1 |
G |
A |
7: 63,890,330 (GRCm39) |
V978M |
probably damaging |
Het |
Wdr12 |
A |
T |
1: 60,133,670 (GRCm39) |
D19E |
probably benign |
Het |
Wdr35 |
G |
A |
12: 9,055,773 (GRCm39) |
V482I |
probably benign |
Het |
Zer1 |
T |
C |
2: 29,991,496 (GRCm39) |
|
probably null |
Het |
Zfp503 |
T |
C |
14: 22,036,079 (GRCm39) |
D279G |
probably benign |
Het |
Zfp870 |
A |
T |
17: 33,102,736 (GRCm39) |
C198S |
possibly damaging |
Het |
Zftraf1 |
C |
T |
15: 76,532,386 (GRCm39) |
D241N |
probably benign |
Het |
Zfyve26 |
C |
T |
12: 79,334,581 (GRCm39) |
E146K |
probably benign |
Het |
Zkscan6 |
T |
C |
11: 65,719,357 (GRCm39) |
V459A |
probably damaging |
Het |
|
Other mutations in Naip5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00096:Naip5
|
APN |
13 |
100,382,683 (GRCm39) |
nonsense |
probably null |
|
IGL00493:Naip5
|
APN |
13 |
100,367,279 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01294:Naip5
|
APN |
13 |
100,353,588 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01405:Naip5
|
APN |
13 |
100,358,453 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01568:Naip5
|
APN |
13 |
100,353,609 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01804:Naip5
|
APN |
13 |
100,358,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02012:Naip5
|
APN |
13 |
100,359,847 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02183:Naip5
|
APN |
13 |
100,358,150 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02449:Naip5
|
APN |
13 |
100,358,683 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02815:Naip5
|
APN |
13 |
100,359,239 (GRCm39) |
missense |
probably benign |
|
IGL02992:Naip5
|
APN |
13 |
100,359,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Naip5
|
APN |
13 |
100,359,524 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03234:Naip5
|
APN |
13 |
100,349,135 (GRCm39) |
missense |
probably damaging |
1.00 |
inwood2
|
UTSW |
13 |
100,359,522 (GRCm39) |
nonsense |
probably null |
|
inwood3
|
UTSW |
13 |
100,358,411 (GRCm39) |
nonsense |
probably null |
|
Nuchal
|
UTSW |
13 |
100,351,171 (GRCm39) |
missense |
possibly damaging |
0.82 |
PIT4131001:Naip5
|
UTSW |
13 |
100,356,268 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4131001:Naip5
|
UTSW |
13 |
100,356,247 (GRCm39) |
missense |
probably benign |
|
R0001:Naip5
|
UTSW |
13 |
100,359,622 (GRCm39) |
missense |
probably benign |
|
R0001:Naip5
|
UTSW |
13 |
100,351,158 (GRCm39) |
critical splice donor site |
probably null |
|
R0462:Naip5
|
UTSW |
13 |
100,358,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R0636:Naip5
|
UTSW |
13 |
100,356,196 (GRCm39) |
missense |
probably benign |
|
R0674:Naip5
|
UTSW |
13 |
100,359,707 (GRCm39) |
missense |
probably benign |
0.04 |
R0764:Naip5
|
UTSW |
13 |
100,353,613 (GRCm39) |
missense |
probably benign |
0.03 |
R0837:Naip5
|
UTSW |
13 |
100,367,251 (GRCm39) |
missense |
probably benign |
|
R1179:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R1302:Naip5
|
UTSW |
13 |
100,358,099 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1441:Naip5
|
UTSW |
13 |
100,356,225 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1513:Naip5
|
UTSW |
13 |
100,358,714 (GRCm39) |
missense |
probably benign |
|
R1638:Naip5
|
UTSW |
13 |
100,349,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R1651:Naip5
|
UTSW |
13 |
100,358,419 (GRCm39) |
missense |
probably benign |
0.41 |
R1707:Naip5
|
UTSW |
13 |
100,379,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Naip5
|
UTSW |
13 |
100,359,726 (GRCm39) |
nonsense |
probably null |
|
R1836:Naip5
|
UTSW |
13 |
100,356,195 (GRCm39) |
missense |
probably benign |
0.18 |
R1972:Naip5
|
UTSW |
13 |
100,349,278 (GRCm39) |
missense |
probably damaging |
0.98 |
R2080:Naip5
|
UTSW |
13 |
100,358,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R2333:Naip5
|
UTSW |
13 |
100,359,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R2348:Naip5
|
UTSW |
13 |
100,356,246 (GRCm39) |
missense |
probably benign |
0.01 |
R3055:Naip5
|
UTSW |
13 |
100,358,386 (GRCm39) |
missense |
probably benign |
0.23 |
R3401:Naip5
|
UTSW |
13 |
100,358,411 (GRCm39) |
nonsense |
probably null |
|
R3723:Naip5
|
UTSW |
13 |
100,359,522 (GRCm39) |
nonsense |
probably null |
|
R3775:Naip5
|
UTSW |
13 |
100,359,902 (GRCm39) |
missense |
probably benign |
0.00 |
R3775:Naip5
|
UTSW |
13 |
100,359,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4019:Naip5
|
UTSW |
13 |
100,359,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4019:Naip5
|
UTSW |
13 |
100,359,902 (GRCm39) |
missense |
probably benign |
0.00 |
R4020:Naip5
|
UTSW |
13 |
100,359,902 (GRCm39) |
missense |
probably benign |
0.00 |
R4020:Naip5
|
UTSW |
13 |
100,359,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4074:Naip5
|
UTSW |
13 |
100,382,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R4082:Naip5
|
UTSW |
13 |
100,382,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R4105:Naip5
|
UTSW |
13 |
100,356,247 (GRCm39) |
missense |
probably benign |
|
R4227:Naip5
|
UTSW |
13 |
100,349,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R4639:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4640:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4641:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4644:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4645:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4700:Naip5
|
UTSW |
13 |
100,359,922 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4727:Naip5
|
UTSW |
13 |
100,358,378 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4729:Naip5
|
UTSW |
13 |
100,358,639 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4816:Naip5
|
UTSW |
13 |
100,356,189 (GRCm39) |
missense |
probably benign |
0.32 |
R4816:Naip5
|
UTSW |
13 |
100,356,195 (GRCm39) |
missense |
probably benign |
0.01 |
R4816:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R4869:Naip5
|
UTSW |
13 |
100,381,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5162:Naip5
|
UTSW |
13 |
100,359,914 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5244:Naip5
|
UTSW |
13 |
100,382,170 (GRCm39) |
missense |
probably benign |
0.08 |
R5411:Naip5
|
UTSW |
13 |
100,382,254 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5632:Naip5
|
UTSW |
13 |
100,367,170 (GRCm39) |
splice site |
probably null |
|
R5760:Naip5
|
UTSW |
13 |
100,379,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Naip5
|
UTSW |
13 |
100,359,209 (GRCm39) |
missense |
probably benign |
0.02 |
R6302:Naip5
|
UTSW |
13 |
100,359,674 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6304:Naip5
|
UTSW |
13 |
100,359,674 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6411:Naip5
|
UTSW |
13 |
100,359,913 (GRCm39) |
missense |
probably benign |
0.01 |
R6474:Naip5
|
UTSW |
13 |
100,351,171 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6499:Naip5
|
UTSW |
13 |
100,358,102 (GRCm39) |
missense |
probably benign |
|
R6544:Naip5
|
UTSW |
13 |
100,359,652 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6827:Naip5
|
UTSW |
13 |
100,382,437 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6954:Naip5
|
UTSW |
13 |
100,359,922 (GRCm39) |
missense |
probably damaging |
0.99 |
R7052:Naip5
|
UTSW |
13 |
100,358,855 (GRCm39) |
missense |
probably benign |
0.01 |
R7138:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R7141:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R7375:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7375:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7401:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7401:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7447:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7447:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7491:Naip5
|
UTSW |
13 |
100,353,579 (GRCm39) |
missense |
probably benign |
0.18 |
R7559:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7559:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7562:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7562:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7588:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7588:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7589:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7589:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7590:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7590:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7742:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R7886:Naip5
|
UTSW |
13 |
100,382,689 (GRCm39) |
missense |
probably benign |
0.28 |
R7996:Naip5
|
UTSW |
13 |
100,358,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R8026:Naip5
|
UTSW |
13 |
100,382,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R8046:Naip5
|
UTSW |
13 |
100,358,741 (GRCm39) |
missense |
probably benign |
|
R8319:Naip5
|
UTSW |
13 |
100,358,167 (GRCm39) |
missense |
probably benign |
0.12 |
R8471:Naip5
|
UTSW |
13 |
100,358,153 (GRCm39) |
missense |
probably damaging |
0.99 |
R8480:Naip5
|
UTSW |
13 |
100,358,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R8496:Naip5
|
UTSW |
13 |
100,349,247 (GRCm39) |
missense |
probably benign |
0.00 |
R8500:Naip5
|
UTSW |
13 |
100,359,220 (GRCm39) |
missense |
probably damaging |
0.98 |
R8712:Naip5
|
UTSW |
13 |
100,359,604 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8780:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8781:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8788:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8817:Naip5
|
UTSW |
13 |
100,349,207 (GRCm39) |
missense |
probably benign |
0.01 |
R8833:Naip5
|
UTSW |
13 |
100,359,442 (GRCm39) |
missense |
probably damaging |
0.97 |
R8835:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8958:Naip5
|
UTSW |
13 |
100,354,117 (GRCm39) |
nonsense |
probably null |
|
R9031:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9032:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9074:Naip5
|
UTSW |
13 |
100,358,264 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9098:Naip5
|
UTSW |
13 |
100,366,127 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9204:Naip5
|
UTSW |
13 |
100,359,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R9223:Naip5
|
UTSW |
13 |
100,364,184 (GRCm39) |
missense |
probably benign |
0.05 |
R9358:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9389:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9403:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9518:Naip5
|
UTSW |
13 |
100,358,367 (GRCm39) |
missense |
probably benign |
|
R9568:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9568:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9569:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9569:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9570:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9572:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9581:Naip5
|
UTSW |
13 |
100,351,194 (GRCm39) |
missense |
probably benign |
0.11 |
R9627:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9725:Naip5
|
UTSW |
13 |
100,358,784 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9763:Naip5
|
UTSW |
13 |
100,367,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R9764:Naip5
|
UTSW |
13 |
100,367,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R9765:Naip5
|
UTSW |
13 |
100,367,269 (GRCm39) |
missense |
probably damaging |
0.99 |
|