Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
A |
3: 121,899,113 (GRCm39) |
C698* |
probably null |
Het |
Acacb |
G |
A |
5: 114,345,387 (GRCm39) |
V947M |
probably benign |
Het |
Acadsb |
T |
G |
7: 131,042,968 (GRCm39) |
L343R |
probably damaging |
Het |
Adgrf2 |
C |
T |
17: 43,021,874 (GRCm39) |
E317K |
probably damaging |
Het |
Agap2 |
A |
G |
10: 126,923,154 (GRCm39) |
T663A |
unknown |
Het |
Akap8 |
A |
T |
17: 32,535,515 (GRCm39) |
F166L |
possibly damaging |
Het |
Ankrd17 |
A |
T |
5: 90,390,836 (GRCm39) |
M2278K |
probably benign |
Het |
Avl9 |
T |
C |
6: 56,705,242 (GRCm39) |
S148P |
probably damaging |
Het |
Brf1 |
T |
C |
12: 112,933,835 (GRCm39) |
E266G |
probably damaging |
Het |
Cabin1 |
T |
C |
10: 75,581,187 (GRCm39) |
K380E |
probably damaging |
Het |
Catsper2 |
T |
C |
2: 121,227,544 (GRCm39) |
D542G |
possibly damaging |
Het |
Cbln4 |
C |
A |
2: 171,884,095 (GRCm39) |
D42Y |
probably damaging |
Het |
Ccn6 |
T |
A |
10: 39,034,473 (GRCm39) |
Q43L |
possibly damaging |
Het |
Cd5 |
C |
T |
19: 10,697,668 (GRCm39) |
R437Q |
probably damaging |
Het |
Ceacam18 |
G |
C |
7: 43,288,706 (GRCm39) |
E152D |
possibly damaging |
Het |
Chd8 |
A |
G |
14: 52,451,955 (GRCm39) |
S1347P |
possibly damaging |
Het |
Chodl |
T |
G |
16: 78,738,335 (GRCm39) |
I101R |
probably damaging |
Het |
Clk4 |
T |
G |
11: 51,168,759 (GRCm39) |
F377L |
probably damaging |
Het |
Cntnap3 |
C |
T |
13: 64,929,539 (GRCm39) |
|
probably null |
Het |
Dab2 |
A |
G |
15: 6,458,780 (GRCm39) |
S231G |
probably benign |
Het |
Disp2 |
T |
A |
2: 118,617,361 (GRCm39) |
H118Q |
probably benign |
Het |
Dnah10 |
T |
C |
5: 124,900,009 (GRCm39) |
F3869S |
probably damaging |
Het |
Edil3 |
C |
T |
13: 89,279,847 (GRCm39) |
T175I |
probably damaging |
Het |
Eif1ad18 |
T |
G |
12: 88,050,648 (GRCm39) |
I61R |
probably damaging |
Het |
Fap |
A |
G |
2: 62,372,522 (GRCm39) |
S319P |
probably benign |
Het |
Frmpd2 |
T |
A |
14: 33,293,761 (GRCm39) |
V1309E |
probably benign |
Het |
Galntl5 |
T |
A |
5: 25,394,842 (GRCm39) |
S70T |
probably benign |
Het |
Gm5622 |
G |
T |
14: 51,893,339 (GRCm39) |
E89* |
probably null |
Het |
Gna15 |
G |
A |
10: 81,343,881 (GRCm39) |
T260M |
probably damaging |
Het |
Gucy2c |
A |
G |
6: 136,705,342 (GRCm39) |
I531T |
probably damaging |
Het |
Heatr5b |
A |
G |
17: 79,135,417 (GRCm39) |
V238A |
probably damaging |
Het |
Htr2a |
A |
G |
14: 74,943,182 (GRCm39) |
Y254C |
probably damaging |
Het |
Inpp5b |
A |
G |
4: 124,679,065 (GRCm39) |
R491G |
probably damaging |
Het |
Kcnt2 |
C |
T |
1: 140,523,778 (GRCm39) |
L1093F |
possibly damaging |
Het |
Kcp |
C |
A |
6: 29,491,861 (GRCm39) |
E922* |
probably null |
Het |
Lrp2 |
G |
A |
2: 69,296,089 (GRCm39) |
A3340V |
possibly damaging |
Het |
Lrrn1 |
T |
G |
6: 107,545,336 (GRCm39) |
V378G |
probably damaging |
Het |
Net1 |
G |
A |
13: 3,938,510 (GRCm39) |
R126C |
probably damaging |
Het |
Nipsnap3a |
T |
C |
4: 52,993,978 (GRCm39) |
C20R |
probably benign |
Het |
Nxpe2 |
C |
T |
9: 48,232,006 (GRCm39) |
C317Y |
probably damaging |
Het |
Or10v9 |
T |
A |
19: 11,832,652 (GRCm39) |
I222F |
probably damaging |
Het |
Or52h1 |
T |
C |
7: 103,829,504 (GRCm39) |
Y37C |
probably damaging |
Het |
Or8b8 |
T |
C |
9: 37,809,360 (GRCm39) |
I220T |
probably damaging |
Het |
Or8g54 |
T |
G |
9: 39,707,086 (GRCm39) |
Y138* |
probably null |
Het |
Orm1 |
T |
A |
4: 63,262,949 (GRCm39) |
W39R |
probably damaging |
Het |
Pds5b |
A |
T |
5: 150,724,142 (GRCm39) |
K1240* |
probably null |
Het |
Pdss1 |
T |
A |
2: 22,802,681 (GRCm39) |
H173Q |
probably damaging |
Het |
Pebp1 |
A |
G |
5: 117,423,882 (GRCm39) |
W84R |
probably damaging |
Het |
Pla2g4e |
C |
T |
2: 120,001,759 (GRCm39) |
C630Y |
probably damaging |
Het |
Plaat3 |
T |
A |
19: 7,556,550 (GRCm39) |
V117E |
probably damaging |
Het |
Plekho2 |
G |
T |
9: 65,463,635 (GRCm39) |
Q405K |
probably benign |
Het |
Plppr2 |
T |
A |
9: 21,855,708 (GRCm39) |
V227E |
probably damaging |
Het |
Pphln1-ps1 |
T |
A |
16: 13,495,589 (GRCm39) |
D229E |
probably benign |
Het |
Rapgef4 |
T |
C |
2: 72,028,707 (GRCm39) |
S393P |
probably damaging |
Het |
Rapgefl1 |
A |
G |
11: 98,737,900 (GRCm39) |
|
probably null |
Het |
Ripk3 |
C |
A |
14: 56,025,803 (GRCm39) |
R19L |
probably benign |
Het |
Rnase10 |
G |
T |
14: 51,247,167 (GRCm39) |
V182F |
probably damaging |
Het |
Rsf1 |
T |
A |
7: 97,319,002 (GRCm39) |
S917R |
|
Het |
Sephs2 |
T |
C |
7: 126,872,187 (GRCm39) |
N302S |
possibly damaging |
Het |
Slc13a2 |
C |
T |
11: 78,289,950 (GRCm39) |
V455M |
possibly damaging |
Het |
Slc30a2 |
A |
T |
4: 134,071,429 (GRCm39) |
D54V |
probably benign |
Het |
Slco6c1 |
T |
C |
1: 97,047,706 (GRCm39) |
E199G |
possibly damaging |
Het |
Snx27 |
A |
T |
3: 94,436,247 (GRCm39) |
M256K |
probably benign |
Het |
Spag4 |
T |
A |
2: 155,908,519 (GRCm39) |
S150T |
probably benign |
Het |
Spon1 |
T |
A |
7: 113,635,945 (GRCm39) |
C720S |
probably damaging |
Het |
Tbc1d22a |
T |
C |
15: 86,123,356 (GRCm39) |
S166P |
probably benign |
Het |
Tbc1d9 |
T |
C |
8: 83,937,113 (GRCm39) |
I65T |
probably damaging |
Het |
Tmem176a |
T |
A |
6: 48,820,953 (GRCm39) |
V141D |
probably damaging |
Het |
Tmem268 |
G |
A |
4: 63,480,687 (GRCm39) |
|
probably benign |
Het |
Tonsl |
A |
G |
15: 76,518,976 (GRCm39) |
V519A |
probably benign |
Het |
Ttn |
G |
A |
2: 76,612,376 (GRCm39) |
P17204S |
possibly damaging |
Het |
Wrap53 |
T |
A |
11: 69,454,694 (GRCm39) |
D225V |
probably benign |
Het |
Zfhx4 |
G |
A |
3: 5,477,107 (GRCm39) |
A3241T |
possibly damaging |
Het |
Zfp1002 |
T |
C |
2: 150,097,372 (GRCm39) |
H47R |
probably damaging |
Het |
Znfx1 |
T |
C |
2: 166,898,697 (GRCm39) |
R76G |
probably benign |
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 |
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 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7447:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7466:Naip5
|
UTSW |
13 |
100,358,494 (GRCm39) |
nonsense |
probably null |
|
R7491:Naip5
|
UTSW |
13 |
100,353,579 (GRCm39) |
missense |
probably benign |
0.18 |
R7559:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7559:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|