Other mutations in this stock |
Total: 109 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
C |
9: 53,336,971 (GRCm39) |
T92P |
probably damaging |
Het |
Abca13 |
T |
C |
11: 9,243,810 (GRCm39) |
V1891A |
probably benign |
Het |
Abcc1 |
T |
A |
16: 14,228,791 (GRCm39) |
I346N |
probably damaging |
Het |
Afdn |
G |
T |
17: 14,105,770 (GRCm39) |
|
probably null |
Het |
Ahrr |
G |
A |
13: 74,431,143 (GRCm39) |
|
probably benign |
Het |
Akap13 |
A |
G |
7: 75,264,678 (GRCm39) |
D507G |
probably damaging |
Het |
Akap8 |
A |
T |
17: 32,535,234 (GRCm39) |
M260K |
possibly damaging |
Het |
Akr1b8 |
T |
C |
6: 34,342,194 (GRCm39) |
V265A |
probably benign |
Het |
Alpk3 |
C |
G |
7: 80,728,358 (GRCm39) |
P496R |
possibly damaging |
Het |
Ankrd13b |
A |
G |
11: 77,363,571 (GRCm39) |
V249A |
possibly damaging |
Het |
Arid4a |
T |
C |
12: 71,122,604 (GRCm39) |
V995A |
probably benign |
Het |
Ascc3 |
G |
T |
10: 50,625,022 (GRCm39) |
V1637L |
probably benign |
Het |
Atad2 |
G |
A |
15: 57,977,653 (GRCm39) |
A499V |
probably damaging |
Het |
Barhl2 |
G |
T |
5: 106,605,253 (GRCm39) |
A152E |
possibly damaging |
Het |
Bbs12 |
T |
A |
3: 37,375,194 (GRCm39) |
D547E |
probably damaging |
Het |
Btaf1 |
A |
G |
19: 36,981,934 (GRCm39) |
M1655V |
probably damaging |
Het |
Ccdc50 |
T |
A |
16: 27,225,408 (GRCm39) |
H40Q |
probably damaging |
Het |
Ccr9 |
A |
T |
9: 123,603,617 (GRCm39) |
|
probably benign |
Het |
Cdh15 |
A |
G |
8: 123,592,175 (GRCm39) |
D654G |
probably damaging |
Het |
Cebpz |
T |
C |
17: 79,233,553 (GRCm39) |
D758G |
probably damaging |
Het |
Cgn |
C |
T |
3: 94,672,960 (GRCm39) |
R906K |
possibly damaging |
Het |
Chil3 |
T |
A |
3: 106,067,839 (GRCm39) |
M109L |
possibly damaging |
Het |
Cntnap4 |
A |
T |
8: 113,569,148 (GRCm39) |
|
probably null |
Het |
Cyp4f18 |
C |
T |
8: 72,754,856 (GRCm39) |
|
probably benign |
Het |
Daam2 |
A |
G |
17: 49,770,952 (GRCm39) |
|
probably null |
Het |
Ddost |
T |
A |
4: 138,037,922 (GRCm39) |
H220Q |
probably benign |
Het |
Dennd2a |
C |
T |
6: 39,441,135 (GRCm39) |
|
probably benign |
Het |
Depdc1b |
G |
A |
13: 108,510,375 (GRCm39) |
V296I |
possibly damaging |
Het |
Dnaaf4 |
A |
T |
9: 72,879,618 (GRCm39) |
D386V |
probably damaging |
Het |
Dnah5 |
A |
T |
15: 28,299,256 (GRCm39) |
R1539S |
probably benign |
Het |
Dusp22 |
T |
C |
13: 30,889,641 (GRCm39) |
I74T |
probably damaging |
Het |
Epc1 |
A |
G |
18: 6,440,202 (GRCm39) |
|
probably benign |
Het |
Epha7 |
A |
G |
4: 28,961,301 (GRCm39) |
I845V |
probably benign |
Het |
Fanci |
C |
T |
7: 79,057,165 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
T |
A |
2: 125,205,564 (GRCm39) |
E1104V |
probably damaging |
Het |
Fbxo8 |
T |
A |
8: 57,043,132 (GRCm39) |
F205L |
probably damaging |
Het |
Fcgbpl1 |
G |
T |
7: 27,841,699 (GRCm39) |
V545L |
probably benign |
Het |
Fetub |
T |
C |
16: 22,748,506 (GRCm39) |
|
probably benign |
Het |
Frs3 |
T |
C |
17: 48,014,747 (GRCm39) |
V480A |
probably benign |
Het |
Gne |
C |
A |
4: 44,060,157 (GRCm39) |
E79* |
probably null |
Het |
Hrc |
T |
A |
7: 44,985,921 (GRCm39) |
H357Q |
probably benign |
Het |
Idh1 |
T |
C |
1: 65,201,079 (GRCm39) |
M291V |
probably damaging |
Het |
Il22b |
T |
A |
10: 118,129,090 (GRCm39) |
H133L |
probably benign |
Het |
Ino80b |
T |
C |
6: 83,101,072 (GRCm39) |
E165G |
probably damaging |
Het |
Inppl1 |
A |
T |
7: 101,477,706 (GRCm39) |
|
probably benign |
Het |
Ints15 |
G |
T |
5: 143,293,643 (GRCm39) |
T278K |
probably benign |
Het |
Ip6k2 |
T |
C |
9: 108,676,432 (GRCm39) |
|
probably benign |
Het |
Itga11 |
A |
T |
9: 62,667,628 (GRCm39) |
I654F |
probably damaging |
Het |
Jag2 |
G |
T |
12: 112,876,997 (GRCm39) |
|
probably benign |
Het |
Katna1 |
G |
T |
10: 7,619,513 (GRCm39) |
|
probably benign |
Het |
Kcnh4 |
G |
T |
11: 100,636,995 (GRCm39) |
S707Y |
probably benign |
Het |
Kcnn2 |
T |
G |
18: 45,693,585 (GRCm39) |
L387R |
probably damaging |
Het |
Khnyn |
A |
G |
14: 56,125,425 (GRCm39) |
T503A |
probably damaging |
Het |
Lama5 |
G |
T |
2: 179,823,359 (GRCm39) |
|
probably benign |
Het |
Lmbr1l |
A |
T |
15: 98,806,654 (GRCm39) |
|
probably benign |
Het |
Mast4 |
A |
T |
13: 102,890,669 (GRCm39) |
S870T |
possibly damaging |
Het |
Med1 |
A |
G |
11: 98,058,400 (GRCm39) |
Y266H |
probably benign |
Het |
Med13 |
A |
T |
11: 86,236,829 (GRCm39) |
N109K |
probably benign |
Het |
Mgam |
T |
C |
6: 40,737,969 (GRCm39) |
|
probably benign |
Het |
Mmp8 |
A |
G |
9: 7,561,455 (GRCm39) |
Q153R |
probably benign |
Het |
Mpeg1 |
C |
A |
19: 12,439,055 (GRCm39) |
T171N |
probably benign |
Het |
Mtus2 |
T |
C |
5: 148,043,829 (GRCm39) |
S806P |
probably benign |
Het |
Naip2 |
T |
A |
13: 100,285,350 (GRCm39) |
E1226V |
probably damaging |
Het |
Nav3 |
T |
C |
10: 109,602,989 (GRCm39) |
I1187V |
possibly damaging |
Het |
Nbeal1 |
T |
C |
1: 60,344,529 (GRCm39) |
|
probably benign |
Het |
Nbeal2 |
C |
A |
9: 110,467,231 (GRCm39) |
V653L |
probably damaging |
Het |
Ndufa9 |
G |
T |
6: 126,804,495 (GRCm39) |
|
probably benign |
Het |
Nlrp5 |
G |
T |
7: 23,129,582 (GRCm39) |
C883F |
probably damaging |
Het |
Nr0b2 |
C |
A |
4: 133,283,303 (GRCm39) |
|
probably null |
Het |
Or1m1 |
T |
A |
9: 18,666,629 (GRCm39) |
M101L |
possibly damaging |
Het |
Or6c209 |
T |
A |
10: 129,483,600 (GRCm39) |
V201E |
probably damaging |
Het |
Or6c69c |
G |
A |
10: 129,910,692 (GRCm39) |
V138I |
probably benign |
Het |
Or8b101 |
T |
A |
9: 38,020,782 (GRCm39) |
S267T |
possibly damaging |
Het |
Pkhd1 |
A |
T |
1: 20,620,046 (GRCm39) |
|
probably null |
Het |
Pkhd1l1 |
A |
G |
15: 44,386,134 (GRCm39) |
|
probably benign |
Het |
Ppm1l |
A |
G |
3: 69,456,794 (GRCm39) |
K237R |
probably benign |
Het |
Ppp1r18 |
T |
C |
17: 36,184,603 (GRCm39) |
|
probably benign |
Het |
Ptpn3 |
A |
T |
4: 57,204,958 (GRCm39) |
D734E |
probably benign |
Het |
Pxdn |
T |
C |
12: 30,065,528 (GRCm39) |
C1283R |
probably damaging |
Het |
Rbm12 |
A |
G |
2: 155,937,644 (GRCm39) |
|
probably benign |
Het |
Rttn |
A |
T |
18: 89,027,584 (GRCm39) |
|
probably benign |
Het |
Sgsm1 |
G |
T |
5: 113,411,571 (GRCm39) |
H431Q |
probably benign |
Het |
Siah3 |
A |
G |
14: 75,763,367 (GRCm39) |
N206S |
possibly damaging |
Het |
Slc22a15 |
G |
T |
3: 101,767,827 (GRCm39) |
D521E |
probably benign |
Het |
Sprr2k |
A |
T |
3: 92,340,770 (GRCm39) |
|
probably benign |
Het |
Stab2 |
G |
A |
10: 86,803,477 (GRCm39) |
|
probably benign |
Het |
Sval3 |
T |
A |
6: 41,945,120 (GRCm39) |
L16Q |
probably damaging |
Het |
Sycp2 |
C |
G |
2: 178,023,648 (GRCm39) |
S456T |
probably benign |
Het |
Tk1 |
T |
C |
11: 117,707,921 (GRCm39) |
|
probably benign |
Het |
Tlk2 |
C |
A |
11: 105,145,799 (GRCm39) |
A335E |
probably benign |
Het |
Tmtc1 |
T |
C |
6: 148,151,079 (GRCm39) |
K659E |
probably benign |
Het |
Tnk2 |
C |
T |
16: 32,499,408 (GRCm39) |
P907L |
probably benign |
Het |
Trim14 |
C |
A |
4: 46,522,043 (GRCm39) |
K211N |
probably damaging |
Het |
Trim15 |
A |
C |
17: 37,177,878 (GRCm39) |
L39R |
probably damaging |
Het |
Tspan15 |
T |
A |
10: 62,023,872 (GRCm39) |
T269S |
probably benign |
Het |
Ttc7 |
T |
A |
17: 87,669,292 (GRCm39) |
D646E |
probably benign |
Het |
Ttll6 |
A |
T |
11: 96,038,382 (GRCm39) |
Q410L |
probably benign |
Het |
Unc79 |
A |
G |
12: 103,027,666 (GRCm39) |
Q419R |
probably damaging |
Het |
Vcam1 |
A |
T |
3: 115,908,065 (GRCm39) |
Y666N |
possibly damaging |
Het |
Vmn1r10 |
A |
T |
6: 57,090,486 (GRCm39) |
Y26F |
probably damaging |
Het |
Vmn1r80 |
A |
G |
7: 11,927,775 (GRCm39) |
N295S |
probably benign |
Het |
Vmn2r114 |
A |
T |
17: 23,509,917 (GRCm39) |
H854Q |
probably benign |
Het |
Vmn2r2 |
A |
T |
3: 64,042,039 (GRCm39) |
D225E |
probably damaging |
Het |
Vmn2r4 |
A |
T |
3: 64,296,855 (GRCm39) |
Y643* |
probably null |
Het |
Vmn2r52 |
T |
A |
7: 9,893,393 (GRCm39) |
Y582F |
probably damaging |
Het |
Vmn2r60 |
G |
T |
7: 41,844,564 (GRCm39) |
L642F |
possibly damaging |
Het |
Zbtb20 |
T |
C |
16: 43,430,109 (GRCm39) |
S207P |
probably damaging |
Het |
Zic2 |
CCCACCACCACCATCACCACCACCACC |
CCCACCATCACCACCACCACC |
14: 122,713,776 (GRCm39) |
|
probably benign |
Het |
Zkscan7 |
G |
T |
9: 122,717,958 (GRCm39) |
E118* |
probably null |
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 |
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 |
|
R1595:Naip6
|
UTSW |
13 |
100,435,602 (GRCm39) |
missense |
probably damaging |
0.96 |
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 |
|