Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
G |
7: 120,074,689 (GRCm39) |
N577S |
probably benign |
Het |
Ang4 |
A |
G |
14: 52,001,529 (GRCm39) |
S140P |
probably damaging |
Het |
Ankdd1b |
T |
C |
13: 96,556,306 (GRCm39) |
|
probably null |
Het |
Anln |
G |
T |
9: 22,274,019 (GRCm39) |
A606D |
probably benign |
Het |
Ano5 |
T |
G |
7: 51,237,480 (GRCm39) |
V768G |
possibly damaging |
Het |
Ccdc180 |
A |
T |
4: 45,900,461 (GRCm39) |
Y275F |
possibly damaging |
Het |
Chpf |
T |
C |
1: 75,453,271 (GRCm39) |
Y334C |
probably damaging |
Het |
Chrdl2 |
T |
C |
7: 99,682,863 (GRCm39) |
L381S |
probably damaging |
Het |
Cibar2 |
T |
C |
8: 120,893,372 (GRCm39) |
D273G |
probably benign |
Het |
Cox20 |
A |
T |
1: 178,150,126 (GRCm39) |
Y100F |
probably benign |
Het |
Dbn1 |
T |
C |
13: 55,623,322 (GRCm39) |
D433G |
possibly damaging |
Het |
Dclre1a |
A |
T |
19: 56,519,684 (GRCm39) |
I983N |
probably damaging |
Het |
Dok6 |
A |
T |
18: 89,578,182 (GRCm39) |
H78Q |
probably benign |
Het |
Efcab3 |
G |
A |
11: 104,624,539 (GRCm39) |
D878N |
probably benign |
Het |
Fpr1 |
A |
T |
17: 18,097,634 (GRCm39) |
F118L |
probably benign |
Het |
Fscn3 |
A |
G |
6: 28,430,175 (GRCm39) |
Y115C |
probably damaging |
Het |
Gabra4 |
A |
C |
5: 71,798,256 (GRCm39) |
|
probably null |
Het |
Gm45861 |
T |
C |
8: 28,072,751 (GRCm39) |
V1290A |
unknown |
Het |
Hivep1 |
T |
C |
13: 42,308,828 (GRCm39) |
V356A |
probably benign |
Het |
Ikbip |
T |
C |
10: 90,937,617 (GRCm39) |
Y97H |
possibly damaging |
Het |
Il10 |
A |
G |
1: 130,947,805 (GRCm39) |
T53A |
probably benign |
Het |
Inpp5f |
T |
C |
7: 128,296,526 (GRCm39) |
V959A |
probably benign |
Het |
Insr |
T |
C |
8: 3,308,415 (GRCm39) |
E207G |
probably benign |
Het |
Kndc1 |
T |
A |
7: 139,503,731 (GRCm39) |
S1012T |
probably damaging |
Het |
Krtap5-1 |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
7: 141,850,333 (GRCm39) |
|
probably benign |
Het |
Ksr2 |
T |
C |
5: 117,693,329 (GRCm39) |
V259A |
probably benign |
Het |
Lox |
A |
T |
18: 52,658,194 (GRCm39) |
Y326* |
probably null |
Het |
Lpin2 |
C |
A |
17: 71,537,269 (GRCm39) |
T272N |
probably benign |
Het |
Lrp2 |
C |
T |
2: 69,295,128 (GRCm39) |
E3397K |
probably damaging |
Het |
Megf11 |
G |
A |
9: 64,602,709 (GRCm39) |
C850Y |
possibly damaging |
Het |
Morc1 |
T |
C |
16: 48,319,147 (GRCm39) |
F284L |
probably benign |
Het |
Moxd2 |
T |
A |
6: 40,862,378 (GRCm39) |
D147V |
possibly damaging |
Het |
Mrpl21 |
T |
C |
19: 3,337,752 (GRCm39) |
L153P |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,280,917 (GRCm39) |
T1432A |
probably benign |
Het |
Ncoa5 |
T |
C |
2: 164,854,816 (GRCm39) |
H102R |
possibly damaging |
Het |
Ndel1 |
A |
T |
11: 68,720,806 (GRCm39) |
C293* |
probably null |
Het |
Ninl |
A |
T |
2: 150,808,016 (GRCm39) |
M82K |
probably benign |
Het |
Nrcam |
G |
A |
12: 44,587,858 (GRCm39) |
|
probably null |
Het |
Nup210l |
A |
T |
3: 90,030,036 (GRCm39) |
I250L |
probably benign |
Het |
Obscn |
T |
C |
11: 58,968,776 (GRCm39) |
E2532G |
possibly damaging |
Het |
Or1e1 |
C |
A |
11: 73,244,585 (GRCm39) |
A2E |
probably benign |
Het |
Or5v1 |
G |
T |
17: 37,809,868 (GRCm39) |
G109C |
probably damaging |
Het |
Or8j3c |
A |
G |
2: 86,253,583 (GRCm39) |
F146L |
probably benign |
Het |
Osgin1 |
G |
A |
8: 120,171,773 (GRCm39) |
S189N |
possibly damaging |
Het |
Otud7b |
A |
G |
3: 96,062,690 (GRCm39) |
E643G |
probably damaging |
Het |
Phldb2 |
T |
A |
16: 45,571,727 (GRCm39) |
T1222S |
probably damaging |
Het |
Pwp1 |
C |
T |
10: 85,723,914 (GRCm39) |
R472W |
probably damaging |
Het |
Rad21 |
T |
C |
15: 51,836,538 (GRCm39) |
Y211C |
probably damaging |
Het |
Rexo1 |
A |
G |
10: 80,386,572 (GRCm39) |
V162A |
probably benign |
Het |
Rtl1 |
C |
T |
12: 109,560,589 (GRCm39) |
V417I |
probably benign |
Het |
Setbp1 |
G |
A |
18: 78,826,639 (GRCm39) |
P1325S |
probably benign |
Het |
Shld1 |
A |
G |
2: 132,592,510 (GRCm39) |
T186A |
probably damaging |
Het |
Shld2 |
A |
G |
14: 33,959,523 (GRCm39) |
Y820H |
probably damaging |
Het |
Skint7 |
G |
T |
4: 111,839,423 (GRCm39) |
C239F |
probably benign |
Het |
Slc25a1 |
A |
G |
16: 17,744,138 (GRCm39) |
L221P |
probably benign |
Het |
Snrnp70 |
T |
A |
7: 45,026,214 (GRCm39) |
D385V |
unknown |
Het |
Sp7 |
A |
C |
15: 102,267,533 (GRCm39) |
V109G |
probably benign |
Het |
Syne1 |
A |
T |
10: 5,082,078 (GRCm39) |
Y849N |
probably damaging |
Het |
Tas2r108 |
T |
C |
6: 40,470,790 (GRCm39) |
F89L |
possibly damaging |
Het |
Tcf3 |
C |
T |
10: 80,246,301 (GRCm39) |
A581T |
possibly damaging |
Het |
Tcta |
A |
G |
9: 108,182,986 (GRCm39) |
L53P |
probably damaging |
Het |
Traf3ip2 |
C |
G |
10: 39,502,451 (GRCm39) |
Q200E |
probably damaging |
Het |
Trgc1 |
A |
T |
13: 19,400,691 (GRCm39) |
Y140F |
|
Het |
Tyk2 |
A |
T |
9: 21,036,263 (GRCm39) |
C75S |
probably damaging |
Het |
Ugt3a1 |
G |
A |
15: 9,311,903 (GRCm39) |
G382R |
probably damaging |
Het |
Upp2 |
G |
T |
2: 58,664,127 (GRCm39) |
|
probably null |
Het |
Vmn1r212 |
A |
T |
13: 23,067,323 (GRCm39) |
F337I |
unknown |
Het |
Vmn1r58 |
T |
C |
7: 5,414,242 (GRCm39) |
|
probably benign |
Het |
Vps13d |
A |
T |
4: 144,830,246 (GRCm39) |
V2856D |
|
Het |
Wdr37 |
A |
C |
13: 8,886,911 (GRCm39) |
L292R |
probably damaging |
Het |
Yipf3 |
T |
C |
17: 46,561,790 (GRCm39) |
I199T |
probably benign |
Het |
Zdhhc23 |
A |
G |
16: 43,791,907 (GRCm39) |
S289P |
possibly damaging |
Het |
Zfp229 |
A |
T |
17: 21,965,131 (GRCm39) |
K454* |
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 |
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 |
|
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 |
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 |
|