Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam6a |
T |
G |
12: 113,544,400 (GRCm38) |
V131G |
possibly damaging |
Het |
Agr3 |
G |
T |
12: 35,948,350 (GRCm38) |
M149I |
probably benign |
Het |
Alox12b |
T |
A |
11: 69,164,010 (GRCm38) |
C280S |
possibly damaging |
Het |
Amhr2 |
C |
A |
15: 102,445,519 (GRCm38) |
Q16K |
probably benign |
Het |
Ank1 |
A |
G |
8: 23,119,365 (GRCm38) |
T1387A |
probably benign |
Het |
B3gnt9 |
A |
C |
8: 105,253,571 (GRCm38) |
F395C |
probably damaging |
Het |
BC048562 |
A |
G |
9: 108,445,706 (GRCm38) |
D80G |
probably damaging |
Het |
Ccdc65 |
T |
A |
15: 98,722,938 (GRCm38) |
M438K |
possibly damaging |
Het |
Ccz1 |
T |
C |
5: 144,001,433 (GRCm38) |
R240G |
probably damaging |
Het |
Cish |
A |
T |
9: 107,300,394 (GRCm38) |
S90C |
probably benign |
Het |
Col5a2 |
A |
T |
1: 45,391,838 (GRCm38) |
S881T |
possibly damaging |
Het |
Col6a6 |
G |
A |
9: 105,780,727 (GRCm38) |
T762I |
possibly damaging |
Het |
Cpa1 |
A |
G |
6: 30,640,061 (GRCm38) |
K49E |
probably benign |
Het |
Cpb1 |
T |
C |
3: 20,266,533 (GRCm38) |
|
probably null |
Het |
Csmd3 |
A |
G |
15: 48,287,546 (GRCm38) |
S483P |
probably damaging |
Het |
Cul9 |
G |
A |
17: 46,520,118 (GRCm38) |
T1643I |
possibly damaging |
Het |
Dock2 |
T |
C |
11: 34,708,811 (GRCm38) |
K314E |
possibly damaging |
Het |
Fam186b |
T |
G |
15: 99,278,690 (GRCm38) |
K773T |
probably damaging |
Het |
Fancl |
T |
A |
11: 26,468,672 (GRCm38) |
V259E |
probably benign |
Het |
Fat4 |
T |
G |
3: 38,892,007 (GRCm38) |
I1683S |
probably damaging |
Het |
Fcamr |
T |
A |
1: 130,804,619 (GRCm38) |
H114Q |
probably damaging |
Het |
Fndc11 |
T |
C |
2: 181,222,253 (GRCm38) |
F284L |
probably damaging |
Het |
Galns |
A |
G |
8: 122,584,910 (GRCm38) |
|
probably null |
Het |
Gch1 |
A |
G |
14: 47,189,180 (GRCm38) |
S30P |
probably benign |
Het |
Gcnt3 |
A |
G |
9: 70,035,064 (GRCm38) |
I74T |
probably benign |
Het |
Gfral |
A |
T |
9: 76,197,101 (GRCm38) |
C210S |
probably damaging |
Het |
Gm12666 |
G |
T |
4: 92,191,678 (GRCm38) |
Y24* |
probably null |
Het |
Gm26566 |
G |
A |
4: 88,722,010 (GRCm38) |
A13T |
unknown |
Het |
Gm9936 |
A |
T |
5: 114,857,105 (GRCm38) |
D150E |
unknown |
Het |
Gsn |
C |
A |
2: 35,283,991 (GRCm38) |
D75E |
probably benign |
Het |
Ighd2-7 |
T |
C |
12: 113,456,724 (GRCm38) |
T5A |
possibly damaging |
Het |
Ikbkap |
G |
T |
4: 56,786,711 (GRCm38) |
P411T |
probably damaging |
Het |
Itsn1 |
G |
T |
16: 91,852,894 (GRCm38) |
R152L |
probably benign |
Het |
Klhl3 |
A |
T |
13: 58,009,312 (GRCm38) |
L620Q |
probably damaging |
Het |
Lpl |
G |
A |
8: 68,887,583 (GRCm38) |
V77M |
probably benign |
Het |
Lrfn3 |
A |
T |
7: 30,359,491 (GRCm38) |
H436Q |
probably benign |
Het |
Lrp1b |
A |
G |
2: 40,679,215 (GRCm38) |
C3965R |
|
Het |
Lrrc2 |
G |
A |
9: 110,970,160 (GRCm38) |
|
probably null |
Het |
Manea |
C |
A |
4: 26,340,468 (GRCm38) |
D165Y |
probably damaging |
Het |
Myom1 |
A |
T |
17: 71,087,481 (GRCm38) |
Q992L |
probably damaging |
Het |
Nyap1 |
C |
T |
5: 137,735,132 (GRCm38) |
W546* |
probably null |
Het |
Olfml3 |
T |
G |
3: 103,736,966 (GRCm38) |
Y129S |
possibly damaging |
Het |
Olfr1346 |
A |
G |
7: 6,474,335 (GRCm38) |
E75G |
probably damaging |
Het |
Olfr187 |
C |
A |
16: 59,035,850 (GRCm38) |
V296F |
probably damaging |
Het |
Olfr826 |
T |
A |
10: 130,179,945 (GRCm38) |
I312F |
probably benign |
Het |
Olfr984 |
A |
T |
9: 40,100,568 (GRCm38) |
D307E |
probably benign |
Het |
P2rx6 |
A |
C |
16: 17,567,436 (GRCm38) |
|
probably null |
Het |
Plxnb2 |
A |
T |
15: 89,160,957 (GRCm38) |
Y1095* |
probably null |
Het |
Pmepa1 |
G |
A |
2: 173,228,001 (GRCm38) |
R216C |
probably damaging |
Het |
Prodh |
A |
G |
16: 18,084,755 (GRCm38) |
|
probably benign |
Het |
Ptch1 |
A |
G |
13: 63,542,173 (GRCm38) |
Y389H |
probably damaging |
Het |
Ptgs2 |
G |
T |
1: 150,101,091 (GRCm38) |
|
probably null |
Het |
Rbm14 |
A |
G |
19: 4,811,436 (GRCm38) |
Y25H |
probably damaging |
Het |
Rfc2 |
T |
C |
5: 134,593,258 (GRCm38) |
L197P |
probably damaging |
Het |
Rnf19b |
G |
T |
4: 129,073,604 (GRCm38) |
W313L |
probably damaging |
Het |
Sh3rf1 |
G |
T |
8: 61,372,551 (GRCm38) |
A527S |
probably benign |
Het |
Slc12a1 |
A |
G |
2: 125,190,298 (GRCm38) |
Y623C |
probably damaging |
Het |
Slc25a54 |
T |
A |
3: 109,098,616 (GRCm38) |
W147R |
probably damaging |
Het |
Slc4a1 |
A |
G |
11: 102,356,854 (GRCm38) |
L401P |
probably damaging |
Het |
Slc4a7 |
A |
G |
14: 14,796,073 (GRCm38) |
|
probably null |
Het |
Stab2 |
A |
G |
10: 86,863,556 (GRCm38) |
Y1933H |
probably damaging |
Het |
Supt5 |
A |
T |
7: 28,315,263 (GRCm38) |
V1037E |
probably damaging |
Het |
Sv2b |
A |
T |
7: 75,125,680 (GRCm38) |
H466Q |
probably benign |
Het |
Tmco5 |
G |
A |
2: 116,880,249 (GRCm38) |
E17K |
probably damaging |
Het |
Tmem69 |
G |
A |
4: 116,554,775 (GRCm38) |
S12F |
probably damaging |
Het |
Trp53 |
C |
A |
11: 69,587,566 (GRCm38) |
Y100* |
probably null |
Het |
Trpm7 |
A |
T |
2: 126,822,590 (GRCm38) |
H956Q |
probably benign |
Het |
Tsnaxip1 |
G |
A |
8: 105,842,503 (GRCm38) |
R495H |
probably benign |
Het |
Vmn1r237 |
A |
T |
17: 21,314,515 (GRCm38) |
I167F |
probably benign |
Het |
Vmn1r70 |
A |
G |
7: 10,634,365 (GRCm38) |
D260G |
probably benign |
Het |
Zbtb38 |
G |
A |
9: 96,688,891 (GRCm38) |
H47Y |
probably damaging |
Het |
Zfp184 |
G |
T |
13: 21,958,727 (GRCm38) |
C201F |
probably benign |
Het |
Zfp384 |
T |
A |
6: 125,024,833 (GRCm38) |
I147N |
possibly 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 |
R9098:Naip5
|
UTSW |
13 |
100,229,619 (GRCm38) |
missense |
possibly damaging |
0.67 |
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 |
100,219,830 (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 |
|