Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931417E11Rik |
T |
C |
6: 73,469,534 (GRCm38) |
T11A |
probably benign |
Het |
A830018L16Rik |
A |
T |
1: 11,562,987 (GRCm38) |
D168V |
probably damaging |
Het |
Abcb4 |
A |
T |
5: 8,958,441 (GRCm38) |
D1203V |
probably damaging |
Het |
Acat2 |
G |
A |
17: 12,960,092 (GRCm38) |
|
probably benign |
Het |
Adam3 |
C |
T |
8: 24,689,468 (GRCm38) |
C611Y |
probably damaging |
Het |
Adgrb1 |
A |
G |
15: 74,543,340 (GRCm38) |
D638G |
probably damaging |
Het |
Adra1b |
T |
C |
11: 43,776,391 (GRCm38) |
N340D |
probably damaging |
Het |
Ankrd31 |
A |
G |
13: 96,780,371 (GRCm38) |
H131R |
probably damaging |
Het |
Aoc2 |
T |
C |
11: 101,326,338 (GRCm38) |
S416P |
possibly damaging |
Het |
Armc8 |
G |
A |
9: 99,505,309 (GRCm38) |
R419* |
probably null |
Het |
Atp6v1h |
T |
G |
1: 5,093,415 (GRCm38) |
V90G |
probably damaging |
Het |
Avl9 |
T |
C |
6: 56,730,643 (GRCm38) |
V191A |
probably benign |
Het |
Bsn |
G |
A |
9: 108,112,974 (GRCm38) |
P1860S |
possibly damaging |
Het |
Btd |
A |
G |
14: 31,662,276 (GRCm38) |
K73R |
probably benign |
Het |
Cd22 |
T |
C |
7: 30,867,966 (GRCm38) |
K731R |
probably benign |
Het |
Chmp7 |
C |
A |
14: 69,719,462 (GRCm38) |
L332F |
probably damaging |
Het |
Cldn11 |
A |
G |
3: 31,163,127 (GRCm38) |
E148G |
probably damaging |
Het |
Cmtm1 |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
8: 104,309,702 (GRCm38) |
|
probably null |
Het |
Cnbd1 |
A |
T |
4: 18,886,061 (GRCm38) |
Y319* |
probably null |
Het |
Cnnm4 |
A |
G |
1: 36,472,089 (GRCm38) |
T133A |
probably benign |
Het |
Cpeb4 |
A |
T |
11: 31,872,679 (GRCm38) |
E131V |
probably benign |
Het |
Ctns |
A |
G |
11: 73,187,735 (GRCm38) |
|
probably null |
Het |
Dhx36 |
C |
A |
3: 62,506,720 (GRCm38) |
E74* |
probably null |
Het |
Dhx36 |
C |
A |
3: 62,506,721 (GRCm38) |
Q73H |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,419,961 (GRCm38) |
T3802A |
|
Het |
Fbxo31 |
G |
A |
8: 121,554,397 (GRCm38) |
R337C |
probably damaging |
Het |
Flnc |
C |
T |
6: 29,455,519 (GRCm38) |
Q2056* |
probably null |
Het |
Fmo9 |
T |
C |
1: 166,664,630 (GRCm38) |
D408G |
possibly damaging |
Het |
Gipr |
C |
T |
7: 19,163,570 (GRCm38) |
S117N |
unknown |
Het |
Gm13088 |
A |
T |
4: 143,654,527 (GRCm38) |
Y309N |
probably benign |
Het |
Gm14412 |
T |
A |
2: 177,314,563 (GRCm38) |
H513L |
probably damaging |
Het |
Gm21663 |
G |
C |
5: 25,942,169 (GRCm38) |
C46W |
probably benign |
Het |
Gm29776 |
T |
G |
14: 54,695,229 (GRCm38) |
S393R |
probably damaging |
Het |
Gucy1a2 |
A |
T |
9: 3,634,489 (GRCm38) |
I178L |
probably benign |
Het |
Htr1b |
A |
T |
9: 81,632,428 (GRCm38) |
L42Q |
|
Het |
Htr2b |
T |
C |
1: 86,099,759 (GRCm38) |
T342A |
probably damaging |
Het |
Jph2 |
C |
T |
2: 163,339,553 (GRCm38) |
V564M |
probably damaging |
Het |
Kcnmb1 |
A |
G |
11: 33,964,806 (GRCm38) |
T36A |
probably damaging |
Het |
Krit1 |
A |
C |
5: 3,813,135 (GRCm38) |
K310N |
probably benign |
Het |
Lama1 |
C |
T |
17: 67,804,513 (GRCm38) |
T2253M |
|
Het |
Lpar6 |
C |
T |
14: 73,238,793 (GRCm38) |
L65F |
probably damaging |
Het |
Megf6 |
G |
A |
4: 154,269,703 (GRCm38) |
G1355R |
probably damaging |
Het |
Mkl2 |
A |
G |
16: 13,403,189 (GRCm38) |
H743R |
probably benign |
Het |
Mmp3 |
T |
A |
9: 7,446,936 (GRCm38) |
Y39N |
probably damaging |
Het |
Ms4a18 |
C |
A |
19: 11,013,377 (GRCm38) |
V118F |
|
Het |
Mthfr |
G |
A |
4: 148,041,625 (GRCm38) |
S51N |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,643,679 (GRCm38) |
T3773S |
unknown |
Het |
Mus81 |
T |
A |
19: 5,484,004 (GRCm38) |
K400* |
probably null |
Het |
Naaladl2 |
A |
T |
3: 24,433,180 (GRCm38) |
D192E |
probably benign |
Het |
Nek11 |
T |
A |
9: 105,293,657 (GRCm38) |
H393L |
probably benign |
Het |
Nmt2 |
T |
A |
2: 3,305,278 (GRCm38) |
|
probably benign |
Het |
Nmur2 |
T |
C |
11: 56,029,582 (GRCm38) |
D279G |
possibly damaging |
Het |
Nol4l |
C |
A |
2: 153,470,710 (GRCm38) |
R226L |
probably damaging |
Het |
Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,595,266 (GRCm38) |
|
probably benign |
Het |
Olfr961 |
A |
G |
9: 39,647,083 (GRCm38) |
D119G |
probably damaging |
Het |
Olfr97 |
T |
C |
17: 37,232,070 (GRCm38) |
Y100C |
probably benign |
Het |
Olfr992 |
T |
C |
2: 85,399,651 (GRCm38) |
N294S |
probably damaging |
Het |
Palm |
A |
G |
10: 79,819,154 (GRCm38) |
T249A |
probably benign |
Het |
Rhobtb3 |
A |
G |
13: 75,939,583 (GRCm38) |
I95T |
probably damaging |
Het |
Rnpep |
A |
T |
1: 135,278,821 (GRCm38) |
F178L |
possibly damaging |
Het |
Rsl1d1 |
A |
G |
16: 11,201,363 (GRCm38) |
S105P |
probably damaging |
Het |
Rxra |
C |
T |
2: 27,748,744 (GRCm38) |
T253I |
possibly damaging |
Het |
Schip1 |
A |
G |
3: 68,064,985 (GRCm38) |
D15G |
|
Het |
Sis |
T |
A |
3: 72,937,245 (GRCm38) |
I719F |
possibly damaging |
Het |
Snx18 |
A |
G |
13: 113,617,774 (GRCm38) |
S208P |
probably benign |
Het |
Srcap |
T |
C |
7: 127,552,644 (GRCm38) |
V2125A |
probably damaging |
Het |
Stx7 |
C |
T |
10: 24,182,826 (GRCm38) |
Q199* |
probably null |
Het |
Syt6 |
T |
C |
3: 103,585,579 (GRCm38) |
I134T |
probably damaging |
Het |
Tlr12 |
A |
G |
4: 128,617,077 (GRCm38) |
M460T |
probably benign |
Het |
Tnni3k |
T |
C |
3: 154,941,677 (GRCm38) |
T398A |
possibly damaging |
Het |
Tspan4 |
T |
C |
7: 141,491,903 (GRCm38) |
S188P |
probably benign |
Het |
Ubap2l |
A |
G |
3: 90,002,449 (GRCm38) |
S1025P |
unknown |
Het |
Ubl7 |
A |
G |
9: 57,921,752 (GRCm38) |
D219G |
probably benign |
Het |
Vmn2r115 |
C |
A |
17: 23,345,829 (GRCm38) |
T230K |
probably benign |
Het |
Vmn2r95 |
T |
A |
17: 18,439,905 (GRCm38) |
M193K |
possibly damaging |
Het |
Zfp639 |
A |
G |
3: 32,519,736 (GRCm38) |
E170G |
probably damaging |
Het |
Zfy1 |
A |
G |
Y: 725,987 (GRCm38) |
S593P |
possibly damaging |
Het |
Zscan4-ps1 |
T |
A |
7: 11,065,568 (GRCm38) |
T465S |
probably damaging |
Het |
|
Other mutations in Naip5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00096:Naip5
|
APN |
13 |
100,246,175 (GRCm38) |
nonsense |
probably null |
|
IGL00493:Naip5
|
APN |
13 |
100,230,771 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL01294:Naip5
|
APN |
13 |
100,217,080 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01405:Naip5
|
APN |
13 |
100,221,945 (GRCm38) |
missense |
probably benign |
0.11 |
IGL01568:Naip5
|
APN |
13 |
100,217,101 (GRCm38) |
missense |
probably benign |
0.26 |
IGL01804:Naip5
|
APN |
13 |
100,221,584 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02012:Naip5
|
APN |
13 |
100,223,339 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02183:Naip5
|
APN |
13 |
100,221,642 (GRCm38) |
missense |
probably benign |
0.41 |
IGL02449:Naip5
|
APN |
13 |
100,222,175 (GRCm38) |
missense |
probably benign |
0.34 |
IGL02815:Naip5
|
APN |
13 |
100,222,731 (GRCm38) |
missense |
probably benign |
|
IGL02992:Naip5
|
APN |
13 |
100,223,028 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03027:Naip5
|
APN |
13 |
100,223,016 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03234:Naip5
|
APN |
13 |
100,212,627 (GRCm38) |
missense |
probably damaging |
1.00 |
inwood2
|
UTSW |
13 |
100,223,014 (GRCm38) |
nonsense |
probably null |
|
inwood3
|
UTSW |
13 |
100,221,903 (GRCm38) |
nonsense |
probably null |
|
Nuchal
|
UTSW |
13 |
100,214,663 (GRCm38) |
missense |
possibly damaging |
0.82 |
PIT4131001:Naip5
|
UTSW |
13 |
100,219,760 (GRCm38) |
missense |
probably benign |
0.00 |
PIT4131001:Naip5
|
UTSW |
13 |
100,219,739 (GRCm38) |
missense |
probably benign |
|
R0001:Naip5
|
UTSW |
13 |
100,223,114 (GRCm38) |
missense |
probably benign |
|
R0001:Naip5
|
UTSW |
13 |
100,214,650 (GRCm38) |
critical splice donor site |
probably null |
|
R0462:Naip5
|
UTSW |
13 |
100,221,732 (GRCm38) |
missense |
probably damaging |
1.00 |
R0636:Naip5
|
UTSW |
13 |
100,219,688 (GRCm38) |
missense |
probably benign |
|
R0674:Naip5
|
UTSW |
13 |
100,223,199 (GRCm38) |
missense |
probably benign |
0.04 |
R0764:Naip5
|
UTSW |
13 |
100,217,105 (GRCm38) |
missense |
probably benign |
0.03 |
R0837:Naip5
|
UTSW |
13 |
100,230,743 (GRCm38) |
missense |
probably benign |
|
R1179:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R1302:Naip5
|
UTSW |
13 |
100,221,591 (GRCm38) |
missense |
possibly damaging |
0.91 |
R1441:Naip5
|
UTSW |
13 |
100,219,717 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1513:Naip5
|
UTSW |
13 |
100,222,206 (GRCm38) |
missense |
probably benign |
|
R1638:Naip5
|
UTSW |
13 |
100,212,669 (GRCm38) |
missense |
probably damaging |
1.00 |
R1651:Naip5
|
UTSW |
13 |
100,221,911 (GRCm38) |
missense |
probably benign |
0.41 |
R1707:Naip5
|
UTSW |
13 |
100,242,855 (GRCm38) |
missense |
probably damaging |
1.00 |
R1835:Naip5
|
UTSW |
13 |
100,223,218 (GRCm38) |
nonsense |
probably null |
|
R1836:Naip5
|
UTSW |
13 |
100,219,687 (GRCm38) |
missense |
probably benign |
0.18 |
R1972:Naip5
|
UTSW |
13 |
100,212,770 (GRCm38) |
missense |
probably damaging |
0.98 |
R2080:Naip5
|
UTSW |
13 |
100,221,533 (GRCm38) |
missense |
probably damaging |
1.00 |
R2333:Naip5
|
UTSW |
13 |
100,223,171 (GRCm38) |
missense |
probably damaging |
1.00 |
R2348:Naip5
|
UTSW |
13 |
100,219,738 (GRCm38) |
missense |
probably benign |
0.01 |
R3055:Naip5
|
UTSW |
13 |
100,221,878 (GRCm38) |
missense |
probably benign |
0.23 |
R3401:Naip5
|
UTSW |
13 |
100,221,903 (GRCm38) |
nonsense |
probably null |
|
R3723:Naip5
|
UTSW |
13 |
100,223,014 (GRCm38) |
nonsense |
probably null |
|
R3775:Naip5
|
UTSW |
13 |
100,223,394 (GRCm38) |
missense |
probably benign |
0.00 |
R3775:Naip5
|
UTSW |
13 |
100,223,375 (GRCm38) |
missense |
probably benign |
0.00 |
R4019:Naip5
|
UTSW |
13 |
100,223,375 (GRCm38) |
missense |
probably benign |
0.00 |
R4019:Naip5
|
UTSW |
13 |
100,223,394 (GRCm38) |
missense |
probably benign |
0.00 |
R4020:Naip5
|
UTSW |
13 |
100,223,394 (GRCm38) |
missense |
probably benign |
0.00 |
R4020:Naip5
|
UTSW |
13 |
100,223,375 (GRCm38) |
missense |
probably benign |
0.00 |
R4074:Naip5
|
UTSW |
13 |
100,246,064 (GRCm38) |
missense |
probably damaging |
1.00 |
R4082:Naip5
|
UTSW |
13 |
100,245,830 (GRCm38) |
missense |
probably damaging |
1.00 |
R4105:Naip5
|
UTSW |
13 |
100,219,739 (GRCm38) |
missense |
probably benign |
|
R4227:Naip5
|
UTSW |
13 |
100,212,768 (GRCm38) |
missense |
probably damaging |
0.99 |
R4639:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R4640:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R4641:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R4644:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R4645:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R4700:Naip5
|
UTSW |
13 |
100,223,414 (GRCm38) |
missense |
possibly damaging |
0.62 |
R4727:Naip5
|
UTSW |
13 |
100,221,870 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4729:Naip5
|
UTSW |
13 |
100,222,131 (GRCm38) |
missense |
possibly damaging |
0.75 |
R4816:Naip5
|
UTSW |
13 |
100,219,681 (GRCm38) |
missense |
probably benign |
0.32 |
R4816:Naip5
|
UTSW |
13 |
100,219,687 (GRCm38) |
missense |
probably benign |
0.01 |
R4816:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R4869:Naip5
|
UTSW |
13 |
100,245,131 (GRCm38) |
missense |
probably damaging |
1.00 |
R5162:Naip5
|
UTSW |
13 |
100,223,406 (GRCm38) |
missense |
possibly damaging |
0.78 |
R5244:Naip5
|
UTSW |
13 |
100,245,662 (GRCm38) |
missense |
probably benign |
0.08 |
R5411:Naip5
|
UTSW |
13 |
100,245,746 (GRCm38) |
missense |
possibly damaging |
0.54 |
R5632:Naip5
|
UTSW |
13 |
100,230,662 (GRCm38) |
splice site |
probably null |
|
R5760:Naip5
|
UTSW |
13 |
100,242,838 (GRCm38) |
missense |
probably damaging |
1.00 |
R5916:Naip5
|
UTSW |
13 |
100,222,701 (GRCm38) |
missense |
probably benign |
0.02 |
R6302:Naip5
|
UTSW |
13 |
100,223,166 (GRCm38) |
missense |
possibly damaging |
0.76 |
R6304:Naip5
|
UTSW |
13 |
100,223,166 (GRCm38) |
missense |
possibly damaging |
0.76 |
R6411:Naip5
|
UTSW |
13 |
100,223,405 (GRCm38) |
missense |
probably benign |
0.01 |
R6474:Naip5
|
UTSW |
13 |
100,214,663 (GRCm38) |
missense |
possibly damaging |
0.82 |
R6499:Naip5
|
UTSW |
13 |
100,221,594 (GRCm38) |
missense |
probably benign |
|
R6544:Naip5
|
UTSW |
13 |
100,223,144 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6827:Naip5
|
UTSW |
13 |
100,245,929 (GRCm38) |
missense |
possibly damaging |
0.48 |
R6954:Naip5
|
UTSW |
13 |
100,223,414 (GRCm38) |
missense |
probably damaging |
0.99 |
R7052:Naip5
|
UTSW |
13 |
100,222,347 (GRCm38) |
missense |
probably benign |
0.01 |
R7138:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R7141:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R7375:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7375:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7401:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7401:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7447:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7447:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7466:Naip5
|
UTSW |
13 |
100,221,986 (GRCm38) |
nonsense |
probably null |
|
R7491:Naip5
|
UTSW |
13 |
100,217,071 (GRCm38) |
missense |
probably benign |
0.18 |
R7559:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7559:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7562:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7562:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7588:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7588:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7589:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7589:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7590:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7590:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7742:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R7886:Naip5
|
UTSW |
13 |
100,246,181 (GRCm38) |
missense |
probably benign |
0.28 |
R7996:Naip5
|
UTSW |
13 |
100,221,656 (GRCm38) |
missense |
probably damaging |
1.00 |
R8026:Naip5
|
UTSW |
13 |
100,245,898 (GRCm38) |
missense |
probably damaging |
1.00 |
R8046:Naip5
|
UTSW |
13 |
100,222,233 (GRCm38) |
missense |
probably benign |
|
R8319:Naip5
|
UTSW |
13 |
100,221,659 (GRCm38) |
missense |
probably benign |
0.12 |
R8471:Naip5
|
UTSW |
13 |
100,221,645 (GRCm38) |
missense |
probably damaging |
0.99 |
R8480:Naip5
|
UTSW |
13 |
100,222,235 (GRCm38) |
missense |
probably damaging |
1.00 |
R8496:Naip5
|
UTSW |
13 |
100,212,739 (GRCm38) |
missense |
probably benign |
0.00 |
R8500:Naip5
|
UTSW |
13 |
100,222,712 (GRCm38) |
missense |
probably damaging |
0.98 |
R8712:Naip5
|
UTSW |
13 |
100,223,096 (GRCm38) |
missense |
possibly damaging |
0.61 |
R8780:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R8781:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R8788:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R8817:Naip5
|
UTSW |
13 |
100,212,699 (GRCm38) |
missense |
probably benign |
0.01 |
R8833:Naip5
|
UTSW |
13 |
100,222,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R8835:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R8958:Naip5
|
UTSW |
13 |
100,217,609 (GRCm38) |
nonsense |
probably null |
|
R9031:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9032:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9074:Naip5
|
UTSW |
13 |
100,221,756 (GRCm38) |
missense |
possibly damaging |
0.92 |
R9204:Naip5
|
UTSW |
13 |
100,222,500 (GRCm38) |
missense |
probably damaging |
1.00 |
R9223:Naip5
|
UTSW |
13 |
100,227,676 (GRCm38) |
missense |
probably benign |
0.05 |
R9358:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9389:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9403:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9518:Naip5
|
UTSW |
13 |
100,221,859 (GRCm38) |
missense |
probably benign |
|
R9568:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
R9568:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9569:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
R9569:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9570:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
R9572:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
R9581:Naip5
|
UTSW |
13 |
100,214,686 (GRCm38) |
missense |
probably benign |
0.11 |
R9627:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9725:Naip5
|
UTSW |
13 |
100,222,276 (GRCm38) |
missense |
possibly damaging |
0.94 |
R9763:Naip5
|
UTSW |
13 |
100,230,761 (GRCm38) |
missense |
probably damaging |
0.99 |
R9764:Naip5
|
UTSW |
13 |
100,230,761 (GRCm38) |
missense |
probably damaging |
0.99 |
R9765:Naip5
|
UTSW |
13 |
100,230,761 (GRCm38) |
missense |
probably damaging |
0.99 |
|