Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb6 |
C |
T |
1: 75,153,944 (GRCm39) |
|
probably null |
Het |
Abcc10 |
G |
T |
17: 46,633,164 (GRCm39) |
P556H |
probably damaging |
Het |
Abcc9 |
A |
T |
6: 142,578,821 (GRCm39) |
D914E |
probably benign |
Het |
Adgrf4 |
A |
G |
17: 42,978,764 (GRCm39) |
V193A |
probably benign |
Het |
Adm |
A |
T |
7: 110,228,298 (GRCm39) |
T160S |
probably damaging |
Het |
Ammecr1l |
T |
C |
18: 31,905,173 (GRCm39) |
|
probably null |
Het |
Angpt2 |
T |
C |
8: 18,748,129 (GRCm39) |
D377G |
probably damaging |
Het |
Ankfn1 |
A |
G |
11: 89,313,593 (GRCm39) |
|
probably null |
Het |
Arhgap30 |
T |
G |
1: 171,235,909 (GRCm39) |
M761R |
probably benign |
Het |
Asb4 |
T |
G |
6: 5,390,692 (GRCm39) |
N28K |
probably damaging |
Het |
Cd177 |
A |
T |
7: 24,444,389 (GRCm39) |
D696E |
probably benign |
Het |
Cd200 |
G |
A |
16: 45,215,214 (GRCm39) |
T123I |
probably benign |
Het |
Cfap70 |
A |
G |
14: 20,497,604 (GRCm39) |
V50A |
probably benign |
Het |
Chaf1b |
T |
C |
16: 93,701,987 (GRCm39) |
|
probably null |
Het |
Chgb |
A |
C |
2: 132,635,657 (GRCm39) |
D533A |
probably benign |
Het |
Col12a1 |
A |
G |
9: 79,509,536 (GRCm39) |
Y3041H |
probably damaging |
Het |
Crot |
T |
C |
5: 9,024,186 (GRCm39) |
N337D |
probably benign |
Het |
Csad |
G |
A |
15: 102,086,217 (GRCm39) |
A51V |
probably damaging |
Het |
Cstdc7 |
T |
C |
18: 42,306,454 (GRCm39) |
M7T |
probably benign |
Het |
Cyp2b9 |
A |
G |
7: 25,900,332 (GRCm39) |
Y380C |
possibly damaging |
Het |
Dpysl2 |
G |
T |
14: 67,052,952 (GRCm39) |
A299E |
probably damaging |
Het |
Efcc1 |
A |
G |
6: 87,708,440 (GRCm39) |
E189G |
probably damaging |
Het |
Egfr |
T |
C |
11: 16,856,847 (GRCm39) |
I940T |
probably damaging |
Het |
Etnk2 |
T |
G |
1: 133,300,917 (GRCm39) |
L228R |
possibly damaging |
Het |
Fitm2 |
A |
G |
2: 163,311,610 (GRCm39) |
I201T |
probably benign |
Het |
Foxo1 |
A |
T |
3: 52,253,375 (GRCm39) |
M513L |
probably benign |
Het |
Galnt16 |
A |
T |
12: 80,637,410 (GRCm39) |
K379I |
probably damaging |
Het |
Gm57858 |
C |
T |
3: 36,073,146 (GRCm39) |
A379T |
probably damaging |
Het |
Gtf2a1 |
T |
A |
12: 91,556,323 (GRCm39) |
N6Y |
probably damaging |
Het |
Kcnc1 |
G |
A |
7: 46,077,010 (GRCm39) |
V271M |
probably benign |
Het |
Klhdc8b |
T |
A |
9: 108,328,362 (GRCm39) |
D30V |
probably damaging |
Het |
Lrrc7 |
G |
A |
3: 157,882,914 (GRCm39) |
Q448* |
probably null |
Het |
Med29 |
T |
C |
7: 28,091,928 (GRCm39) |
D54G |
probably damaging |
Het |
Mfn2 |
T |
C |
4: 147,979,153 (GRCm39) |
T60A |
probably benign |
Het |
Mroh1 |
T |
C |
15: 76,317,730 (GRCm39) |
|
probably benign |
Het |
Mxd1 |
A |
T |
6: 86,628,453 (GRCm39) |
V149E |
possibly damaging |
Het |
Ndn |
C |
T |
7: 61,998,256 (GRCm39) |
P34L |
probably benign |
Het |
Nhsl1 |
G |
T |
10: 18,402,096 (GRCm39) |
K1107N |
probably damaging |
Het |
Nlrc3 |
T |
C |
16: 3,783,166 (GRCm39) |
E81G |
probably benign |
Het |
Or10al3 |
G |
T |
17: 38,012,004 (GRCm39) |
A148S |
probably benign |
Het |
Or9e1 |
G |
T |
11: 58,732,478 (GRCm39) |
M179I |
probably benign |
Het |
Osbpl5 |
C |
T |
7: 143,256,955 (GRCm39) |
V392M |
possibly damaging |
Het |
Pcdhb22 |
T |
A |
18: 37,653,506 (GRCm39) |
V401E |
probably damaging |
Het |
Pcm1 |
T |
A |
8: 41,762,672 (GRCm39) |
H1444Q |
probably damaging |
Het |
Pdlim2 |
A |
G |
14: 70,402,193 (GRCm39) |
Y308H |
probably damaging |
Het |
Phf14 |
T |
G |
6: 11,988,752 (GRCm39) |
L664R |
possibly damaging |
Het |
Phkb |
T |
C |
8: 86,753,182 (GRCm39) |
|
probably benign |
Het |
Ptchd3 |
T |
A |
11: 121,721,420 (GRCm39) |
F98I |
probably damaging |
Het |
Ptprt |
C |
T |
2: 161,652,469 (GRCm39) |
|
probably null |
Het |
Rbp3 |
A |
T |
14: 33,678,155 (GRCm39) |
H701L |
possibly damaging |
Het |
Rgl1 |
T |
C |
1: 152,550,774 (GRCm39) |
|
probably benign |
Het |
Satb1 |
A |
T |
17: 52,089,729 (GRCm39) |
S373T |
possibly damaging |
Het |
Scn3a |
T |
A |
2: 65,329,323 (GRCm39) |
Y769F |
probably damaging |
Het |
Senp7 |
A |
G |
16: 56,005,131 (GRCm39) |
I922V |
probably damaging |
Het |
Serpina3g |
A |
G |
12: 104,205,531 (GRCm39) |
E90G |
probably benign |
Het |
Sh3rf2 |
C |
T |
18: 42,244,353 (GRCm39) |
T273I |
probably damaging |
Het |
Slc15a3 |
A |
G |
19: 10,831,675 (GRCm39) |
T350A |
probably benign |
Het |
Socs5 |
T |
C |
17: 87,441,623 (GRCm39) |
C188R |
probably damaging |
Het |
Tacr1 |
A |
G |
6: 82,380,723 (GRCm39) |
T45A |
probably benign |
Het |
Th |
A |
G |
7: 142,450,745 (GRCm39) |
V117A |
probably benign |
Het |
Thpo |
C |
A |
16: 20,547,206 (GRCm39) |
D81Y |
probably damaging |
Het |
Tmem229b-ps |
A |
G |
10: 53,351,385 (GRCm39) |
|
noncoding transcript |
Het |
Trpc4 |
A |
G |
3: 54,223,236 (GRCm39) |
E724G |
probably benign |
Het |
Ttn |
T |
C |
2: 76,576,977 (GRCm39) |
T24639A |
probably damaging |
Het |
Ulk4 |
A |
G |
9: 120,873,904 (GRCm39) |
S1176P |
probably damaging |
Het |
Urgcp |
T |
C |
11: 5,667,447 (GRCm39) |
D297G |
probably damaging |
Het |
Vmn1r168 |
G |
A |
7: 23,240,620 (GRCm39) |
G159D |
probably damaging |
Het |
Vmn1r67 |
A |
T |
7: 10,181,597 (GRCm39) |
N226I |
probably benign |
Het |
Vmn2r27 |
T |
C |
6: 124,208,574 (GRCm39) |
E57G |
probably benign |
Het |
Zdhhc14 |
G |
T |
17: 5,543,831 (GRCm39) |
R37L |
probably benign |
Het |
Zfp512b |
G |
A |
2: 181,230,229 (GRCm39) |
T499I |
probably damaging |
Het |
Zmym2 |
A |
T |
14: 57,158,187 (GRCm39) |
K575N |
probably benign |
Het |
|
Other mutations in Naip6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00677:Naip6
|
APN |
13 |
100,452,525 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01123:Naip6
|
APN |
13 |
100,440,946 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01151:Naip6
|
APN |
13 |
100,435,601 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01382:Naip6
|
APN |
13 |
100,436,364 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01415:Naip6
|
APN |
13 |
100,439,798 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01654:Naip6
|
APN |
13 |
100,435,853 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01662:Naip6
|
APN |
13 |
100,436,862 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01726:Naip6
|
APN |
13 |
100,439,760 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01810:Naip6
|
APN |
13 |
100,424,603 (GRCm39) |
splice site |
probably benign |
|
IGL01867:Naip6
|
APN |
13 |
100,436,820 (GRCm39) |
missense |
probably benign |
0.40 |
IGL01926:Naip6
|
APN |
13 |
100,436,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01964:Naip6
|
APN |
13 |
100,435,238 (GRCm39) |
splice site |
probably benign |
|
IGL02145:Naip6
|
APN |
13 |
100,433,486 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02160:Naip6
|
APN |
13 |
100,435,933 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02214:Naip6
|
APN |
13 |
100,452,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02342:Naip6
|
APN |
13 |
100,439,748 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02568:Naip6
|
APN |
13 |
100,452,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02573:Naip6
|
APN |
13 |
100,435,979 (GRCm39) |
nonsense |
probably null |
|
IGL02680:Naip6
|
APN |
13 |
100,420,256 (GRCm39) |
missense |
probably benign |
|
IGL02829:Naip6
|
APN |
13 |
100,437,273 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02833:Naip6
|
APN |
13 |
100,436,121 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Naip6
|
APN |
13 |
100,437,168 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02860:Naip6
|
APN |
13 |
100,436,984 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02886:Naip6
|
APN |
13 |
100,436,984 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03155:Naip6
|
APN |
13 |
100,452,932 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0032:Naip6
|
UTSW |
13 |
100,439,745 (GRCm39) |
missense |
probably benign |
0.00 |
R0310:Naip6
|
UTSW |
13 |
100,444,721 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0437:Naip6
|
UTSW |
13 |
100,433,432 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0472:Naip6
|
UTSW |
13 |
100,438,768 (GRCm39) |
missense |
probably benign |
0.02 |
R0560:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R0638:Naip6
|
UTSW |
13 |
100,437,036 (GRCm39) |
missense |
probably benign |
0.00 |
R0792:Naip6
|
UTSW |
13 |
100,420,274 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0963:Naip6
|
UTSW |
13 |
100,452,983 (GRCm39) |
missense |
probably benign |
0.11 |
R1102:Naip6
|
UTSW |
13 |
100,440,923 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1278:Naip6
|
UTSW |
13 |
100,436,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Naip6
|
UTSW |
13 |
100,436,748 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1462:Naip6
|
UTSW |
13 |
100,436,748 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1544:Naip6
|
UTSW |
13 |
100,452,983 (GRCm39) |
missense |
probably benign |
|
R1749:Naip6
|
UTSW |
13 |
100,444,763 (GRCm39) |
missense |
probably benign |
0.03 |
R1838:Naip6
|
UTSW |
13 |
100,452,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R1863:Naip6
|
UTSW |
13 |
100,437,067 (GRCm39) |
missense |
probably benign |
0.03 |
R1914:Naip6
|
UTSW |
13 |
100,435,936 (GRCm39) |
missense |
probably benign |
0.13 |
R2001:Naip6
|
UTSW |
13 |
100,437,237 (GRCm39) |
missense |
probably benign |
0.44 |
R2082:Naip6
|
UTSW |
13 |
100,440,852 (GRCm39) |
splice site |
probably null |
|
R2143:Naip6
|
UTSW |
13 |
100,436,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Naip6
|
UTSW |
13 |
100,435,495 (GRCm39) |
missense |
probably benign |
|
R2266:Naip6
|
UTSW |
13 |
100,420,067 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2284:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2285:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2286:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2351:Naip6
|
UTSW |
13 |
100,420,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R2363:Naip6
|
UTSW |
13 |
100,452,928 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2445:Naip6
|
UTSW |
13 |
100,437,176 (GRCm39) |
missense |
probably damaging |
0.99 |
R2971:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2975:Naip6
|
UTSW |
13 |
100,424,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R3081:Naip6
|
UTSW |
13 |
100,436,961 (GRCm39) |
missense |
probably benign |
|
R3082:Naip6
|
UTSW |
13 |
100,452,925 (GRCm39) |
missense |
probably benign |
0.00 |
R3122:Naip6
|
UTSW |
13 |
100,453,031 (GRCm39) |
missense |
probably benign |
0.00 |
R3417:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R3943:Naip6
|
UTSW |
13 |
100,431,247 (GRCm39) |
missense |
probably benign |
0.01 |
R3944:Naip6
|
UTSW |
13 |
100,431,247 (GRCm39) |
missense |
probably benign |
0.01 |
R4080:Naip6
|
UTSW |
13 |
100,435,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R4166:Naip6
|
UTSW |
13 |
100,452,657 (GRCm39) |
missense |
probably benign |
0.23 |
R4396:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4397:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4418:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4512:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4670:Naip6
|
UTSW |
13 |
100,431,239 (GRCm39) |
critical splice donor site |
probably null |
|
R4671:Naip6
|
UTSW |
13 |
100,431,239 (GRCm39) |
critical splice donor site |
probably null |
|
R4722:Naip6
|
UTSW |
13 |
100,443,580 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4811:Naip6
|
UTSW |
13 |
100,422,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R4900:Naip6
|
UTSW |
13 |
100,433,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R5162:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R5316:Naip6
|
UTSW |
13 |
100,420,290 (GRCm39) |
missense |
probably benign |
0.00 |
R5403:Naip6
|
UTSW |
13 |
100,436,585 (GRCm39) |
missense |
probably benign |
0.12 |
R5437:Naip6
|
UTSW |
13 |
100,439,812 (GRCm39) |
nonsense |
probably null |
|
R5507:Naip6
|
UTSW |
13 |
100,435,423 (GRCm39) |
missense |
probably benign |
0.01 |
R5631:Naip6
|
UTSW |
13 |
100,436,646 (GRCm39) |
missense |
probably benign |
0.02 |
R5657:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R5684:Naip6
|
UTSW |
13 |
100,436,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R5786:Naip6
|
UTSW |
13 |
100,436,724 (GRCm39) |
missense |
probably benign |
|
R5787:Naip6
|
UTSW |
13 |
100,436,724 (GRCm39) |
missense |
probably benign |
|
R5788:Naip6
|
UTSW |
13 |
100,436,724 (GRCm39) |
missense |
probably benign |
|
R5878:Naip6
|
UTSW |
13 |
100,436,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R5895:Naip6
|
UTSW |
13 |
100,452,500 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5898:Naip6
|
UTSW |
13 |
100,435,829 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6113:Naip6
|
UTSW |
13 |
100,435,794 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6141:Naip6
|
UTSW |
13 |
100,444,741 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6199:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R6321:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R6402:Naip6
|
UTSW |
13 |
100,437,226 (GRCm39) |
missense |
probably benign |
0.30 |
R6435:Naip6
|
UTSW |
13 |
100,431,249 (GRCm39) |
missense |
probably benign |
0.04 |
R6477:Naip6
|
UTSW |
13 |
100,452,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6601:Naip6
|
UTSW |
13 |
100,420,266 (GRCm39) |
missense |
probably benign |
|
R6638:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R6639:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R6804:Naip6
|
UTSW |
13 |
100,435,675 (GRCm39) |
missense |
probably benign |
|
R6922:Naip6
|
UTSW |
13 |
100,438,706 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6975:Naip6
|
UTSW |
13 |
100,452,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R7050:Naip6
|
UTSW |
13 |
100,452,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R7135:Naip6
|
UTSW |
13 |
100,436,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R7140:Naip6
|
UTSW |
13 |
100,436,708 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7182:Naip6
|
UTSW |
13 |
100,452,657 (GRCm39) |
missense |
probably benign |
0.23 |
R7196:Naip6
|
UTSW |
13 |
100,436,666 (GRCm39) |
missense |
probably benign |
0.10 |
R7234:Naip6
|
UTSW |
13 |
100,452,011 (GRCm39) |
nonsense |
probably null |
|
R7259:Naip6
|
UTSW |
13 |
100,440,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Naip6
|
UTSW |
13 |
100,435,896 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7332:Naip6
|
UTSW |
13 |
100,437,209 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7339:Naip6
|
UTSW |
13 |
100,452,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7353:Naip6
|
UTSW |
13 |
100,436,259 (GRCm39) |
missense |
probably benign |
0.00 |
R7485:Naip6
|
UTSW |
13 |
100,420,359 (GRCm39) |
missense |
probably benign |
0.07 |
R7597:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R7835:Naip6
|
UTSW |
13 |
100,452,512 (GRCm39) |
missense |
probably benign |
0.19 |
R7840:Naip6
|
UTSW |
13 |
100,451,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R8082:Naip6
|
UTSW |
13 |
100,436,961 (GRCm39) |
missense |
probably benign |
|
R8082:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R8103:Naip6
|
UTSW |
13 |
100,437,851 (GRCm39) |
missense |
probably benign |
0.00 |
R8164:Naip6
|
UTSW |
13 |
100,452,797 (GRCm39) |
missense |
probably benign |
0.00 |
R8206:Naip6
|
UTSW |
13 |
100,431,344 (GRCm39) |
nonsense |
probably null |
|
R8258:Naip6
|
UTSW |
13 |
100,452,920 (GRCm39) |
missense |
probably benign |
0.02 |
R8259:Naip6
|
UTSW |
13 |
100,452,920 (GRCm39) |
missense |
probably benign |
0.02 |
R8348:Naip6
|
UTSW |
13 |
100,436,894 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8405:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8406:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8441:Naip6
|
UTSW |
13 |
100,422,265 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8448:Naip6
|
UTSW |
13 |
100,436,894 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8465:Naip6
|
UTSW |
13 |
100,433,423 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8501:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8502:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8687:Naip6
|
UTSW |
13 |
100,435,636 (GRCm39) |
missense |
probably benign |
0.10 |
R8806:Naip6
|
UTSW |
13 |
100,437,161 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9186:Naip6
|
UTSW |
13 |
100,436,390 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9340:Naip6
|
UTSW |
13 |
100,452,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Naip6
|
UTSW |
13 |
100,437,893 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9585:Naip6
|
UTSW |
13 |
100,436,577 (GRCm39) |
missense |
probably damaging |
0.96 |
R9597:Naip6
|
UTSW |
13 |
100,436,646 (GRCm39) |
missense |
probably benign |
0.02 |
R9601:Naip6
|
UTSW |
13 |
100,436,961 (GRCm39) |
missense |
probably benign |
|
X0066:Naip6
|
UTSW |
13 |
100,451,970 (GRCm39) |
nonsense |
probably null |
|
Z1177:Naip6
|
UTSW |
13 |
100,437,308 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Naip6
|
UTSW |
13 |
100,435,925 (GRCm39) |
missense |
probably benign |
0.20 |
Z1177:Naip6
|
UTSW |
13 |
100,452,638 (GRCm39) |
missense |
probably damaging |
1.00 |
|