Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl4 |
G |
A |
3: 95,588,194 (GRCm39) |
R598C |
probably damaging |
Het |
Adra2a |
T |
C |
19: 54,034,818 (GRCm39) |
L58P |
probably damaging |
Het |
Ajm1 |
C |
CTCTA |
2: 25,469,733 (GRCm39) |
|
probably null |
Het |
Alox5ap |
A |
G |
5: 149,201,927 (GRCm39) |
D2G |
probably damaging |
Het |
Arid1b |
G |
A |
17: 5,377,961 (GRCm39) |
V1238M |
possibly damaging |
Het |
Bank1 |
A |
G |
3: 135,960,764 (GRCm39) |
V31A |
probably benign |
Het |
Bptf |
G |
A |
11: 106,953,391 (GRCm39) |
T2117M |
probably damaging |
Het |
Cadps |
G |
A |
14: 12,522,401 (GRCm38) |
R588* |
probably null |
Het |
Cavin4 |
A |
G |
4: 48,672,214 (GRCm39) |
I220V |
probably benign |
Het |
Cep192 |
G |
A |
18: 67,974,699 (GRCm39) |
M1267I |
probably benign |
Het |
Cers5 |
G |
A |
15: 99,670,244 (GRCm39) |
|
probably benign |
Het |
Cfap65 |
A |
T |
1: 74,964,274 (GRCm39) |
I558N |
probably damaging |
Het |
Cfh |
A |
T |
1: 140,028,621 (GRCm39) |
S1025T |
probably benign |
Het |
Cftr |
A |
G |
6: 18,268,107 (GRCm39) |
I689V |
probably benign |
Het |
Cgrrf1 |
T |
C |
14: 47,069,785 (GRCm39) |
I18T |
probably damaging |
Het |
CK137956 |
A |
G |
4: 127,864,519 (GRCm39) |
S37P |
probably damaging |
Het |
Clca4a |
T |
C |
3: 144,676,416 (GRCm39) |
D88G |
probably benign |
Het |
Col11a1 |
G |
A |
3: 113,961,141 (GRCm39) |
G1166D |
probably damaging |
Het |
Col24a1 |
G |
A |
3: 145,166,589 (GRCm39) |
G1075S |
probably damaging |
Het |
Crispld2 |
C |
T |
8: 120,752,852 (GRCm39) |
T299M |
probably damaging |
Het |
Cyb561a3 |
T |
A |
19: 10,562,701 (GRCm39) |
Y114N |
probably damaging |
Het |
Cyp3a57 |
T |
A |
5: 145,307,773 (GRCm39) |
W147R |
possibly damaging |
Het |
Dnah2 |
C |
A |
11: 69,346,789 (GRCm39) |
R2599L |
possibly damaging |
Het |
Dock1 |
T |
A |
7: 134,373,207 (GRCm39) |
S525T |
probably benign |
Het |
Drc7 |
T |
G |
8: 95,789,025 (GRCm39) |
|
probably null |
Het |
Efhd2 |
G |
T |
4: 141,587,192 (GRCm39) |
|
probably null |
Het |
Epb41l1 |
A |
T |
2: 156,367,142 (GRCm39) |
E658D |
probably benign |
Het |
Evi5 |
C |
T |
5: 107,896,184 (GRCm39) |
S753N |
probably benign |
Het |
Exoc3 |
A |
T |
13: 74,337,319 (GRCm39) |
D427E |
probably benign |
Het |
Fbxw9 |
A |
G |
8: 85,792,740 (GRCm39) |
D363G |
probably damaging |
Het |
Fcer2a |
T |
C |
8: 3,732,910 (GRCm39) |
Y277C |
probably damaging |
Het |
Fstl5 |
A |
T |
3: 76,229,523 (GRCm39) |
Y108F |
probably damaging |
Het |
Gcn1 |
A |
G |
5: 115,749,108 (GRCm39) |
D1880G |
probably benign |
Het |
Gm4924 |
T |
A |
10: 82,214,948 (GRCm39) |
Y915* |
probably null |
Het |
Gpr139 |
T |
A |
7: 118,743,875 (GRCm39) |
I237F |
probably benign |
Het |
Hao2 |
A |
G |
3: 98,784,498 (GRCm39) |
L289S |
probably damaging |
Het |
Hexim1 |
A |
G |
11: 103,007,793 (GRCm39) |
S16G |
probably benign |
Het |
Hmgcs1 |
T |
A |
13: 120,161,535 (GRCm39) |
M109K |
probably damaging |
Het |
Hs3st4 |
T |
A |
7: 123,996,052 (GRCm39) |
N239K |
possibly damaging |
Het |
Hsd3b5 |
T |
A |
3: 98,529,328 (GRCm39) |
N101Y |
probably damaging |
Het |
Idh2 |
G |
A |
7: 79,747,966 (GRCm39) |
P245S |
probably damaging |
Het |
Irx3 |
A |
G |
8: 92,525,530 (GRCm39) |
|
probably benign |
Het |
Lilra5 |
A |
T |
7: 4,244,931 (GRCm39) |
D234V |
probably benign |
Het |
Lrfn5 |
G |
A |
12: 61,886,476 (GRCm39) |
S88N |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,343,721 (GRCm39) |
S879R |
possibly damaging |
Het |
Lsm11 |
A |
G |
11: 45,824,781 (GRCm39) |
S249P |
probably benign |
Het |
Ltbp1 |
C |
T |
17: 75,534,187 (GRCm39) |
A543V |
possibly damaging |
Het |
Mbd1 |
GTCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC |
GTCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC |
18: 74,406,645 (GRCm39) |
|
|
Het |
Mier2 |
C |
T |
10: 79,376,990 (GRCm39) |
|
probably benign |
Het |
Mup6 |
G |
C |
4: 60,004,093 (GRCm39) |
G70A |
probably benign |
Het |
Neb |
A |
G |
2: 52,085,732 (GRCm39) |
L5258P |
probably damaging |
Het |
Nlrc5 |
G |
A |
8: 95,247,857 (GRCm39) |
|
probably benign |
Het |
Nr6a1 |
A |
T |
2: 38,630,597 (GRCm39) |
F207I |
possibly damaging |
Het |
Or2y1 |
A |
T |
11: 49,385,632 (GRCm39) |
T91S |
probably benign |
Het |
Or5k17 |
A |
T |
16: 58,746,867 (GRCm39) |
D22E |
probably benign |
Het |
Or8b43 |
T |
C |
9: 38,360,731 (GRCm39) |
C188R |
probably damaging |
Het |
Osbp2 |
A |
G |
11: 3,665,191 (GRCm39) |
V51A |
possibly damaging |
Het |
Papln |
G |
T |
12: 83,821,723 (GRCm39) |
C317F |
probably damaging |
Het |
Pdcd7 |
T |
C |
9: 65,265,904 (GRCm39) |
S454P |
probably damaging |
Het |
Pde4a |
C |
T |
9: 21,116,597 (GRCm39) |
T473I |
probably damaging |
Het |
Peg10 |
CC |
CCCCATCAGGC |
6: 4,756,350 (GRCm39) |
|
probably benign |
Het |
Peg10 |
C |
CCCATCAGGA |
6: 4,756,351 (GRCm39) |
|
probably benign |
Het |
Peg3 |
G |
T |
7: 6,714,385 (GRCm39) |
S279* |
probably null |
Het |
Rbl1 |
A |
G |
2: 156,994,887 (GRCm39) |
Y929H |
probably damaging |
Het |
Rsf1 |
G |
GACGGCGGCA |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Sall3 |
C |
A |
18: 81,017,590 (GRCm39) |
E113* |
probably null |
Het |
Scn5a |
A |
C |
9: 119,359,089 (GRCm39) |
F653V |
probably damaging |
Het |
Selenok |
T |
A |
14: 29,692,005 (GRCm39) |
N14K |
possibly damaging |
Het |
Slc22a20 |
T |
C |
19: 6,021,838 (GRCm39) |
T426A |
probably benign |
Het |
Slc4a2 |
T |
A |
5: 24,640,007 (GRCm39) |
S563T |
probably damaging |
Het |
Sspo |
T |
A |
6: 48,464,889 (GRCm39) |
S3798T |
probably benign |
Het |
Stag3 |
G |
T |
5: 138,302,969 (GRCm39) |
R63L |
possibly damaging |
Het |
Stard9 |
A |
T |
2: 120,535,667 (GRCm39) |
M3975L |
probably benign |
Het |
Syne2 |
C |
A |
12: 75,956,040 (GRCm39) |
T582K |
probably damaging |
Het |
Synj1 |
G |
A |
16: 90,760,768 (GRCm39) |
Q748* |
probably null |
Het |
Tas2r109 |
T |
C |
6: 132,957,048 (GRCm39) |
D294G |
probably benign |
Het |
Tbl1xr1 |
C |
T |
3: 22,245,603 (GRCm39) |
T203M |
possibly damaging |
Het |
Tbl1xr1 |
T |
A |
3: 22,245,703 (GRCm39) |
|
probably null |
Het |
Tcf7l2 |
A |
G |
19: 55,730,955 (GRCm39) |
D19G |
probably damaging |
Het |
Tecta |
A |
G |
9: 42,248,633 (GRCm39) |
V1923A |
possibly damaging |
Het |
Ttf2 |
T |
C |
3: 100,876,941 (GRCm39) |
E8G |
possibly damaging |
Het |
Vps13b |
T |
A |
15: 35,576,541 (GRCm39) |
V983E |
probably damaging |
Het |
Vps35l |
A |
G |
7: 118,342,898 (GRCm39) |
H32R |
probably damaging |
Het |
Vwa2 |
T |
C |
19: 56,890,025 (GRCm39) |
V210A |
probably benign |
Het |
Xkr6 |
T |
A |
14: 64,057,093 (GRCm39) |
Y335N |
probably benign |
Het |
Zfp97 |
A |
G |
17: 17,365,437 (GRCm39) |
H312R |
probably damaging |
Het |
|
Other mutations in Tg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Tg
|
APN |
15 |
66,719,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00230:Tg
|
APN |
15 |
66,699,139 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00324:Tg
|
APN |
15 |
66,565,273 (GRCm39) |
missense |
probably benign |
|
IGL00428:Tg
|
APN |
15 |
66,645,273 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00703:Tg
|
APN |
15 |
66,568,338 (GRCm39) |
missense |
probably benign |
0.34 |
IGL00808:Tg
|
APN |
15 |
66,555,662 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00833:Tg
|
APN |
15 |
66,560,650 (GRCm39) |
missense |
probably benign |
0.34 |
IGL00899:Tg
|
APN |
15 |
66,545,922 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00921:Tg
|
APN |
15 |
66,636,302 (GRCm39) |
missense |
probably benign |
0.28 |
IGL00975:Tg
|
APN |
15 |
66,553,731 (GRCm39) |
missense |
probably benign |
|
IGL01288:Tg
|
APN |
15 |
66,608,125 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01397:Tg
|
APN |
15 |
66,567,941 (GRCm39) |
splice site |
probably benign |
|
IGL01634:Tg
|
APN |
15 |
66,601,415 (GRCm39) |
missense |
probably benign |
0.34 |
IGL01646:Tg
|
APN |
15 |
66,549,936 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01704:Tg
|
APN |
15 |
66,543,200 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01958:Tg
|
APN |
15 |
66,631,335 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02093:Tg
|
APN |
15 |
66,564,223 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02113:Tg
|
APN |
15 |
66,577,179 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02138:Tg
|
APN |
15 |
66,589,082 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02156:Tg
|
APN |
15 |
66,577,197 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02169:Tg
|
APN |
15 |
66,629,792 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02342:Tg
|
APN |
15 |
66,636,140 (GRCm39) |
missense |
probably benign |
|
IGL02434:Tg
|
APN |
15 |
66,636,191 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02506:Tg
|
APN |
15 |
66,613,443 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02513:Tg
|
APN |
15 |
66,577,123 (GRCm39) |
missense |
probably benign |
|
IGL02549:Tg
|
APN |
15 |
66,711,210 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02669:Tg
|
APN |
15 |
66,620,575 (GRCm39) |
splice site |
probably benign |
|
IGL02756:Tg
|
APN |
15 |
66,606,435 (GRCm39) |
missense |
probably benign |
|
IGL02800:Tg
|
APN |
15 |
66,629,735 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02828:Tg
|
APN |
15 |
66,554,243 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02927:Tg
|
APN |
15 |
66,549,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03061:Tg
|
APN |
15 |
66,543,254 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03105:Tg
|
APN |
15 |
66,586,955 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03160:Tg
|
APN |
15 |
66,711,152 (GRCm39) |
nonsense |
probably null |
|
IGL03242:Tg
|
APN |
15 |
66,555,647 (GRCm39) |
missense |
probably damaging |
0.99 |
Also_ran
|
UTSW |
15 |
66,550,688 (GRCm39) |
missense |
probably damaging |
1.00 |
bedraggled
|
UTSW |
15 |
66,612,563 (GRCm39) |
missense |
probably damaging |
1.00 |
foster
|
UTSW |
15 |
66,565,109 (GRCm39) |
nonsense |
probably null |
|
hognose
|
UTSW |
15 |
66,589,057 (GRCm39) |
missense |
probably damaging |
0.99 |
ito
|
UTSW |
15 |
66,638,011 (GRCm39) |
nonsense |
probably null |
|
ito2
|
UTSW |
15 |
66,543,245 (GRCm39) |
missense |
probably damaging |
1.00 |
ito3
|
UTSW |
15 |
66,645,323 (GRCm39) |
missense |
probably damaging |
1.00 |
ito4
|
UTSW |
15 |
66,568,369 (GRCm39) |
missense |
possibly damaging |
0.47 |
Papua
|
UTSW |
15 |
66,545,899 (GRCm39) |
missense |
probably damaging |
1.00 |
Pipistrella
|
UTSW |
15 |
66,567,984 (GRCm39) |
missense |
probably damaging |
1.00 |
pluribus
|
UTSW |
15 |
66,587,012 (GRCm39) |
missense |
probably damaging |
0.98 |
samarai
|
UTSW |
15 |
66,629,855 (GRCm39) |
critical splice donor site |
probably null |
|
sariba
|
UTSW |
15 |
66,566,719 (GRCm39) |
missense |
probably benign |
0.01 |
ticker
|
UTSW |
15 |
66,699,231 (GRCm39) |
nonsense |
probably null |
|
Vampire
|
UTSW |
15 |
66,554,676 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03134:Tg
|
UTSW |
15 |
66,612,567 (GRCm39) |
missense |
probably damaging |
1.00 |
P0019:Tg
|
UTSW |
15 |
66,560,712 (GRCm39) |
missense |
probably benign |
0.01 |
R0121:Tg
|
UTSW |
15 |
66,612,630 (GRCm39) |
missense |
probably benign |
0.04 |
R0135:Tg
|
UTSW |
15 |
66,566,719 (GRCm39) |
missense |
probably benign |
0.01 |
R0227:Tg
|
UTSW |
15 |
66,570,295 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0448:Tg
|
UTSW |
15 |
66,636,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R0453:Tg
|
UTSW |
15 |
66,700,382 (GRCm39) |
missense |
probably benign |
0.09 |
R0504:Tg
|
UTSW |
15 |
66,554,253 (GRCm39) |
missense |
probably damaging |
0.97 |
R0543:Tg
|
UTSW |
15 |
66,601,446 (GRCm39) |
missense |
probably benign |
0.13 |
R0638:Tg
|
UTSW |
15 |
66,589,057 (GRCm39) |
missense |
probably damaging |
0.99 |
R0639:Tg
|
UTSW |
15 |
66,613,333 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0646:Tg
|
UTSW |
15 |
66,601,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R0666:Tg
|
UTSW |
15 |
66,609,370 (GRCm39) |
missense |
probably benign |
|
R0673:Tg
|
UTSW |
15 |
66,613,333 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0689:Tg
|
UTSW |
15 |
66,711,253 (GRCm39) |
splice site |
probably benign |
|
R0704:Tg
|
UTSW |
15 |
66,629,729 (GRCm39) |
missense |
probably benign |
0.02 |
R0730:Tg
|
UTSW |
15 |
66,550,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R0830:Tg
|
UTSW |
15 |
66,596,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R0959:Tg
|
UTSW |
15 |
66,579,859 (GRCm39) |
missense |
probably damaging |
0.98 |
R1027:Tg
|
UTSW |
15 |
66,544,258 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1061:Tg
|
UTSW |
15 |
66,570,408 (GRCm39) |
missense |
probably benign |
0.09 |
R1086:Tg
|
UTSW |
15 |
66,555,911 (GRCm39) |
missense |
probably benign |
|
R1103:Tg
|
UTSW |
15 |
66,591,504 (GRCm39) |
missense |
probably benign |
0.45 |
R1240:Tg
|
UTSW |
15 |
66,700,397 (GRCm39) |
missense |
probably benign |
0.16 |
R1281:Tg
|
UTSW |
15 |
66,568,338 (GRCm39) |
missense |
probably benign |
0.34 |
R1470:Tg
|
UTSW |
15 |
66,721,312 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1470:Tg
|
UTSW |
15 |
66,721,312 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1531:Tg
|
UTSW |
15 |
66,722,351 (GRCm39) |
missense |
probably benign |
0.02 |
R1544:Tg
|
UTSW |
15 |
66,577,081 (GRCm39) |
missense |
probably benign |
0.04 |
R1550:Tg
|
UTSW |
15 |
66,565,279 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1575:Tg
|
UTSW |
15 |
66,601,534 (GRCm39) |
critical splice donor site |
probably null |
|
R1638:Tg
|
UTSW |
15 |
66,568,015 (GRCm39) |
nonsense |
probably null |
|
R1655:Tg
|
UTSW |
15 |
66,700,417 (GRCm39) |
critical splice donor site |
probably null |
|
R1671:Tg
|
UTSW |
15 |
66,564,236 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1789:Tg
|
UTSW |
15 |
66,609,397 (GRCm39) |
missense |
probably benign |
0.00 |
R1883:Tg
|
UTSW |
15 |
66,543,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R1984:Tg
|
UTSW |
15 |
66,554,691 (GRCm39) |
missense |
probably benign |
|
R2063:Tg
|
UTSW |
15 |
66,700,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R2092:Tg
|
UTSW |
15 |
66,721,456 (GRCm39) |
missense |
probably null |
0.26 |
R2109:Tg
|
UTSW |
15 |
66,601,443 (GRCm39) |
missense |
probably benign |
0.02 |
R2128:Tg
|
UTSW |
15 |
66,566,743 (GRCm39) |
missense |
probably benign |
0.10 |
R2129:Tg
|
UTSW |
15 |
66,566,743 (GRCm39) |
missense |
probably benign |
0.10 |
R2207:Tg
|
UTSW |
15 |
66,553,788 (GRCm39) |
missense |
probably benign |
0.15 |
R2219:Tg
|
UTSW |
15 |
66,553,782 (GRCm39) |
missense |
probably benign |
0.03 |
R2228:Tg
|
UTSW |
15 |
66,545,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R2229:Tg
|
UTSW |
15 |
66,545,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R2259:Tg
|
UTSW |
15 |
66,555,747 (GRCm39) |
missense |
probably benign |
|
R2994:Tg
|
UTSW |
15 |
66,553,802 (GRCm39) |
missense |
probably benign |
|
R3904:Tg
|
UTSW |
15 |
66,638,011 (GRCm39) |
nonsense |
probably null |
|
R3946:Tg
|
UTSW |
15 |
66,545,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R3965:Tg
|
UTSW |
15 |
66,556,039 (GRCm39) |
missense |
probably benign |
|
R4245:Tg
|
UTSW |
15 |
66,568,318 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4451:Tg
|
UTSW |
15 |
66,637,996 (GRCm39) |
missense |
probably benign |
0.01 |
R4487:Tg
|
UTSW |
15 |
66,543,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R4489:Tg
|
UTSW |
15 |
66,579,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Tg
|
UTSW |
15 |
66,607,120 (GRCm39) |
missense |
probably benign |
0.23 |
R4659:Tg
|
UTSW |
15 |
66,545,769 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4728:Tg
|
UTSW |
15 |
66,554,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R4760:Tg
|
UTSW |
15 |
66,565,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R4797:Tg
|
UTSW |
15 |
66,629,855 (GRCm39) |
critical splice donor site |
probably null |
|
R4944:Tg
|
UTSW |
15 |
66,636,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R4998:Tg
|
UTSW |
15 |
66,545,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R5009:Tg
|
UTSW |
15 |
66,568,435 (GRCm39) |
missense |
probably benign |
0.01 |
R5025:Tg
|
UTSW |
15 |
66,579,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5035:Tg
|
UTSW |
15 |
66,553,662 (GRCm39) |
splice site |
probably null |
|
R5049:Tg
|
UTSW |
15 |
66,699,231 (GRCm39) |
nonsense |
probably null |
|
R5073:Tg
|
UTSW |
15 |
66,607,101 (GRCm39) |
missense |
probably benign |
0.05 |
R5169:Tg
|
UTSW |
15 |
66,550,629 (GRCm39) |
nonsense |
probably null |
|
R5185:Tg
|
UTSW |
15 |
66,645,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R5227:Tg
|
UTSW |
15 |
66,631,416 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5300:Tg
|
UTSW |
15 |
66,550,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R5334:Tg
|
UTSW |
15 |
66,549,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Tg
|
UTSW |
15 |
66,549,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R5402:Tg
|
UTSW |
15 |
66,611,017 (GRCm39) |
missense |
probably damaging |
0.98 |
R5441:Tg
|
UTSW |
15 |
66,568,369 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5509:Tg
|
UTSW |
15 |
66,699,142 (GRCm39) |
missense |
probably benign |
0.45 |
R5580:Tg
|
UTSW |
15 |
66,557,149 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5582:Tg
|
UTSW |
15 |
66,565,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R5624:Tg
|
UTSW |
15 |
66,709,906 (GRCm39) |
missense |
probably benign |
0.11 |
R5686:Tg
|
UTSW |
15 |
66,560,738 (GRCm39) |
missense |
probably benign |
0.28 |
R6042:Tg
|
UTSW |
15 |
66,555,842 (GRCm39) |
missense |
probably benign |
0.01 |
R6122:Tg
|
UTSW |
15 |
66,700,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R6146:Tg
|
UTSW |
15 |
66,545,216 (GRCm39) |
splice site |
probably null |
|
R6159:Tg
|
UTSW |
15 |
66,607,096 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6223:Tg
|
UTSW |
15 |
66,579,771 (GRCm39) |
missense |
probably benign |
0.15 |
R6480:Tg
|
UTSW |
15 |
66,543,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R6505:Tg
|
UTSW |
15 |
66,631,407 (GRCm39) |
missense |
probably damaging |
0.99 |
R6531:Tg
|
UTSW |
15 |
66,711,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R6614:Tg
|
UTSW |
15 |
66,607,108 (GRCm39) |
missense |
probably damaging |
0.99 |
R6698:Tg
|
UTSW |
15 |
66,711,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Tg
|
UTSW |
15 |
66,550,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R6837:Tg
|
UTSW |
15 |
66,567,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6888:Tg
|
UTSW |
15 |
66,568,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R6933:Tg
|
UTSW |
15 |
66,636,158 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6983:Tg
|
UTSW |
15 |
66,565,207 (GRCm39) |
missense |
probably benign |
0.01 |
R7078:Tg
|
UTSW |
15 |
66,545,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7244:Tg
|
UTSW |
15 |
66,612,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Tg
|
UTSW |
15 |
66,566,633 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7334:Tg
|
UTSW |
15 |
66,597,121 (GRCm39) |
missense |
probably benign |
0.01 |
R7418:Tg
|
UTSW |
15 |
66,568,432 (GRCm39) |
missense |
probably damaging |
0.99 |
R7485:Tg
|
UTSW |
15 |
66,568,437 (GRCm39) |
missense |
probably benign |
0.04 |
R7524:Tg
|
UTSW |
15 |
66,568,010 (GRCm39) |
missense |
probably benign |
0.01 |
R7529:Tg
|
UTSW |
15 |
66,566,617 (GRCm39) |
missense |
probably damaging |
0.99 |
R7540:Tg
|
UTSW |
15 |
66,561,776 (GRCm39) |
missense |
probably benign |
0.16 |
R7583:Tg
|
UTSW |
15 |
66,636,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R7594:Tg
|
UTSW |
15 |
66,601,432 (GRCm39) |
missense |
probably benign |
0.20 |
R7667:Tg
|
UTSW |
15 |
66,587,012 (GRCm39) |
missense |
probably damaging |
0.98 |
R7722:Tg
|
UTSW |
15 |
66,636,158 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7790:Tg
|
UTSW |
15 |
66,721,453 (GRCm39) |
missense |
probably damaging |
0.99 |
R7838:Tg
|
UTSW |
15 |
66,565,112 (GRCm39) |
missense |
probably benign |
0.00 |
R7890:Tg
|
UTSW |
15 |
66,555,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R7904:Tg
|
UTSW |
15 |
66,577,128 (GRCm39) |
missense |
probably benign |
0.08 |
R7919:Tg
|
UTSW |
15 |
66,555,923 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7921:Tg
|
UTSW |
15 |
66,555,642 (GRCm39) |
missense |
probably benign |
0.08 |
R8037:Tg
|
UTSW |
15 |
66,560,724 (GRCm39) |
missense |
probably benign |
0.00 |
R8038:Tg
|
UTSW |
15 |
66,560,724 (GRCm39) |
missense |
probably benign |
0.00 |
R8214:Tg
|
UTSW |
15 |
66,645,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R8304:Tg
|
UTSW |
15 |
66,565,109 (GRCm39) |
nonsense |
probably null |
|
R8688:Tg
|
UTSW |
15 |
66,566,802 (GRCm39) |
critical splice donor site |
probably benign |
|
R8709:Tg
|
UTSW |
15 |
66,553,786 (GRCm39) |
missense |
probably benign |
0.08 |
R8714:Tg
|
UTSW |
15 |
66,555,891 (GRCm39) |
missense |
probably damaging |
0.97 |
R8901:Tg
|
UTSW |
15 |
66,557,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R8917:Tg
|
UTSW |
15 |
66,645,332 (GRCm39) |
critical splice donor site |
probably null |
|
R9023:Tg
|
UTSW |
15 |
66,555,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Tg
|
UTSW |
15 |
66,570,310 (GRCm39) |
missense |
probably benign |
0.01 |
R9310:Tg
|
UTSW |
15 |
66,699,118 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9361:Tg
|
UTSW |
15 |
66,557,246 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9389:Tg
|
UTSW |
15 |
66,561,173 (GRCm39) |
missense |
probably benign |
0.04 |
R9501:Tg
|
UTSW |
15 |
66,718,923 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9510:Tg
|
UTSW |
15 |
66,545,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R9594:Tg
|
UTSW |
15 |
66,607,109 (GRCm39) |
nonsense |
probably null |
|
R9629:Tg
|
UTSW |
15 |
66,555,587 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9701:Tg
|
UTSW |
15 |
66,637,991 (GRCm39) |
missense |
probably benign |
0.03 |
R9743:Tg
|
UTSW |
15 |
66,561,839 (GRCm39) |
missense |
probably benign |
0.18 |
R9748:Tg
|
UTSW |
15 |
66,719,008 (GRCm39) |
missense |
possibly damaging |
0.91 |
T0975:Tg
|
UTSW |
15 |
66,560,712 (GRCm39) |
missense |
probably benign |
0.01 |
X0005:Tg
|
UTSW |
15 |
66,560,712 (GRCm39) |
missense |
probably benign |
0.01 |
X0065:Tg
|
UTSW |
15 |
66,554,303 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Tg
|
UTSW |
15 |
66,620,592 (GRCm39) |
missense |
probably benign |
0.10 |
Z1177:Tg
|
UTSW |
15 |
66,721,396 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Tg
|
UTSW |
15 |
66,557,159 (GRCm39) |
missense |
possibly damaging |
0.49 |
|