Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
A |
C |
6: 83,139,353 (GRCm39) |
N426T |
probably benign |
Het |
6430548M08Rik |
A |
G |
8: 120,872,327 (GRCm39) |
D85G |
probably benign |
Het |
Abcb11 |
C |
T |
2: 69,130,211 (GRCm39) |
D282N |
probably damaging |
Het |
Abcg3 |
A |
T |
5: 105,116,100 (GRCm39) |
F245I |
probably benign |
Het |
Abhd17a |
G |
T |
10: 80,419,991 (GRCm39) |
F231L |
possibly damaging |
Het |
Adgra1 |
A |
T |
7: 139,456,058 (GRCm39) |
D562V |
probably damaging |
Het |
Akap7 |
C |
A |
10: 25,165,567 (GRCm39) |
|
probably benign |
Het |
Akap9 |
A |
G |
5: 4,096,364 (GRCm39) |
D2413G |
probably damaging |
Het |
Akr1c18 |
A |
T |
13: 4,187,236 (GRCm39) |
C193S |
probably damaging |
Het |
Aloxe3 |
A |
T |
11: 69,023,569 (GRCm39) |
M231L |
probably benign |
Het |
Apoh |
A |
G |
11: 108,286,674 (GRCm39) |
T33A |
probably benign |
Het |
Atp13a5 |
T |
C |
16: 29,140,567 (GRCm39) |
N330D |
probably benign |
Het |
C1ql3 |
T |
G |
2: 13,015,589 (GRCm39) |
M24L |
probably benign |
Het |
Cacna1d |
T |
C |
14: 29,845,014 (GRCm39) |
N712S |
probably benign |
Het |
Cbs |
T |
C |
17: 31,838,113 (GRCm39) |
M379V |
possibly damaging |
Het |
Ccdc167 |
T |
C |
17: 29,924,517 (GRCm39) |
D28G |
probably damaging |
Het |
Ccp110 |
A |
T |
7: 118,323,798 (GRCm39) |
Q679L |
probably benign |
Het |
Ccz1 |
A |
T |
5: 143,935,000 (GRCm39) |
L310H |
probably damaging |
Het |
Cerkl |
A |
T |
2: 79,259,104 (GRCm39) |
D44E |
probably damaging |
Het |
Cfap221 |
T |
A |
1: 119,922,828 (GRCm39) |
E38V |
possibly damaging |
Het |
Chia1 |
T |
A |
3: 106,039,331 (GRCm39) |
*474R |
probably null |
Het |
Clint1 |
C |
T |
11: 45,774,590 (GRCm39) |
T32M |
probably damaging |
Het |
Clk3 |
A |
T |
9: 57,668,239 (GRCm39) |
F227L |
probably damaging |
Het |
Col5a3 |
C |
T |
9: 20,705,242 (GRCm39) |
|
probably null |
Het |
Cul2 |
T |
C |
18: 3,426,873 (GRCm39) |
I501T |
probably benign |
Het |
Dag1 |
G |
A |
9: 108,086,292 (GRCm39) |
A283V |
possibly damaging |
Het |
Ddr2 |
A |
T |
1: 169,809,647 (GRCm39) |
W777R |
probably damaging |
Het |
Deaf1 |
A |
T |
7: 140,902,871 (GRCm39) |
V151D |
probably damaging |
Het |
Dido1 |
A |
T |
2: 180,316,914 (GRCm39) |
V631E |
possibly damaging |
Het |
Dpp4 |
G |
A |
2: 62,189,245 (GRCm39) |
Q429* |
probably null |
Het |
Dscaml1 |
A |
G |
9: 45,664,214 (GRCm39) |
R2030G |
probably benign |
Het |
Dsel |
C |
T |
1: 111,789,303 (GRCm39) |
G411S |
probably damaging |
Het |
E2f8 |
T |
A |
7: 48,517,713 (GRCm39) |
M697L |
probably damaging |
Het |
Eef2kmt |
C |
A |
16: 5,065,299 (GRCm39) |
G303W |
probably damaging |
Het |
Eif2ak1 |
A |
G |
5: 143,814,489 (GRCm39) |
Y182C |
probably damaging |
Het |
Epha6 |
G |
T |
16: 59,780,793 (GRCm39) |
A636E |
probably damaging |
Het |
Fancd2 |
G |
A |
6: 113,513,900 (GRCm39) |
V95I |
probably benign |
Het |
Fbln5 |
A |
T |
12: 101,727,075 (GRCm39) |
C292S |
probably damaging |
Het |
Fgfr4 |
A |
G |
13: 55,306,968 (GRCm39) |
Y219C |
probably damaging |
Het |
Frem1 |
T |
G |
4: 82,912,359 (GRCm39) |
K670T |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,809,711 (GRCm39) |
H2010L |
probably benign |
Het |
Gas2l2 |
A |
T |
11: 83,312,816 (GRCm39) |
L832* |
probably null |
Het |
Gbe1 |
A |
G |
16: 70,157,903 (GRCm39) |
T101A |
probably benign |
Het |
Gm5114 |
T |
A |
7: 39,058,180 (GRCm39) |
I480F |
probably damaging |
Het |
Gm7145 |
A |
T |
1: 117,913,842 (GRCm39) |
R241S |
probably damaging |
Het |
Gnal |
G |
A |
18: 67,268,596 (GRCm39) |
V161I |
probably benign |
Het |
Gtpbp1 |
T |
C |
15: 79,575,243 (GRCm39) |
C46R |
probably benign |
Het |
Gucy2c |
A |
T |
6: 136,679,746 (GRCm39) |
L971Q |
probably damaging |
Het |
Hsp90b1 |
T |
C |
10: 86,528,047 (GRCm39) |
E740G |
probably damaging |
Het |
Lingo2 |
G |
A |
4: 35,709,450 (GRCm39) |
L177F |
possibly damaging |
Het |
Mfsd6l |
A |
G |
11: 68,447,874 (GRCm39) |
T242A |
possibly damaging |
Het |
Mmadhc |
C |
T |
2: 50,181,457 (GRCm39) |
R71K |
probably damaging |
Het |
Mrm3 |
G |
T |
11: 76,140,726 (GRCm39) |
V245L |
probably damaging |
Het |
Noc3l |
A |
T |
19: 38,783,468 (GRCm39) |
V636D |
probably damaging |
Het |
Nwd1 |
A |
T |
8: 73,438,410 (GRCm39) |
Q1486L |
probably damaging |
Het |
Or10aa1 |
A |
T |
1: 173,870,419 (GRCm39) |
K301M |
probably damaging |
Het |
Or2y10 |
A |
G |
11: 49,455,329 (GRCm39) |
T194A |
possibly damaging |
Het |
Or3a10 |
G |
T |
11: 73,935,726 (GRCm39) |
R125S |
possibly damaging |
Het |
Or4c11c |
T |
G |
2: 88,662,190 (GRCm39) |
I243R |
probably damaging |
Het |
Or6c5b |
C |
G |
10: 129,245,852 (GRCm39) |
L206V |
possibly damaging |
Het |
Pax9 |
T |
A |
12: 56,742,647 (GRCm39) |
M1K |
probably null |
Het |
Pcdha1 |
T |
C |
18: 37,063,702 (GRCm39) |
V122A |
probably damaging |
Het |
Pgpep1l |
A |
T |
7: 67,887,469 (GRCm39) |
S44T |
probably damaging |
Het |
Pla2g3 |
C |
T |
11: 3,443,022 (GRCm39) |
L452F |
possibly damaging |
Het |
Plbd2 |
G |
A |
5: 120,631,214 (GRCm39) |
R188W |
probably damaging |
Het |
Ppp1r42 |
G |
A |
1: 10,039,082 (GRCm39) |
P346L |
probably benign |
Het |
Prdm8 |
T |
A |
5: 98,332,375 (GRCm39) |
V92D |
probably damaging |
Het |
Ripor2 |
C |
A |
13: 24,885,427 (GRCm39) |
S554* |
probably null |
Het |
Rps19 |
T |
C |
7: 24,584,571 (GRCm39) |
V4A |
probably damaging |
Het |
Rrm2b |
T |
A |
15: 37,944,817 (GRCm39) |
I159F |
probably benign |
Het |
Rusc1 |
C |
A |
3: 88,999,057 (GRCm39) |
G242W |
probably damaging |
Het |
Sarm1 |
A |
G |
11: 78,388,083 (GRCm39) |
S68P |
possibly damaging |
Het |
Sctr |
G |
A |
1: 119,949,955 (GRCm39) |
R48Q |
probably benign |
Het |
Slc22a4 |
A |
G |
11: 53,877,364 (GRCm39) |
F509S |
possibly damaging |
Het |
Slc39a12 |
G |
A |
2: 14,456,811 (GRCm39) |
A600T |
probably damaging |
Het |
Spta1 |
A |
T |
1: 174,050,915 (GRCm39) |
H1798L |
probably damaging |
Het |
Sulf2 |
T |
G |
2: 165,919,536 (GRCm39) |
D804A |
possibly damaging |
Het |
Suz12 |
A |
T |
11: 79,910,529 (GRCm39) |
E316D |
probably benign |
Het |
Tbrg4 |
A |
G |
11: 6,570,065 (GRCm39) |
S270P |
probably benign |
Het |
Tecta |
T |
C |
9: 42,248,628 (GRCm39) |
T1925A |
probably damaging |
Het |
Thrap3 |
A |
T |
4: 126,072,223 (GRCm39) |
F390I |
probably damaging |
Het |
Tpr |
C |
A |
1: 150,269,245 (GRCm39) |
A70E |
unknown |
Het |
Trpv4 |
G |
C |
5: 114,774,520 (GRCm39) |
P188R |
probably benign |
Het |
Txlna |
A |
C |
4: 129,525,953 (GRCm39) |
L298R |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,140,749 (GRCm39) |
S1223P |
probably benign |
Het |
Ucp1 |
A |
T |
8: 84,021,881 (GRCm39) |
T238S |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,147,943 (GRCm39) |
S957G |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,438,868 (GRCm39) |
N3496D |
|
Het |
Vmn2r50 |
T |
C |
7: 9,784,277 (GRCm39) |
|
probably null |
Het |
Wdr54 |
A |
G |
6: 83,131,921 (GRCm39) |
V130A |
probably benign |
Het |
Zfp692 |
A |
T |
11: 58,202,331 (GRCm39) |
E362V |
probably damaging |
Het |
Zfp811 |
A |
G |
17: 33,016,487 (GRCm39) |
Y518H |
probably damaging |
Het |
Zfp994 |
A |
C |
17: 22,419,049 (GRCm39) |
C633W |
probably benign |
Het |
|
Other mutations in Nav3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00095:Nav3
|
APN |
10 |
109,677,594 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00425:Nav3
|
APN |
10 |
109,539,368 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00465:Nav3
|
APN |
10 |
109,688,607 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00531:Nav3
|
APN |
10 |
109,539,171 (GRCm39) |
missense |
probably null |
0.99 |
IGL00575:Nav3
|
APN |
10 |
109,600,626 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00770:Nav3
|
APN |
10 |
109,652,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00774:Nav3
|
APN |
10 |
109,652,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00858:Nav3
|
APN |
10 |
109,578,493 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00935:Nav3
|
APN |
10 |
109,541,527 (GRCm39) |
missense |
probably benign |
|
IGL01638:Nav3
|
APN |
10 |
109,688,724 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01662:Nav3
|
APN |
10 |
109,605,119 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01670:Nav3
|
APN |
10 |
109,550,102 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01885:Nav3
|
APN |
10 |
109,578,521 (GRCm39) |
nonsense |
probably null |
|
IGL01979:Nav3
|
APN |
10 |
109,540,790 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02121:Nav3
|
APN |
10 |
109,594,897 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02210:Nav3
|
APN |
10 |
109,602,851 (GRCm39) |
missense |
probably benign |
|
IGL02523:Nav3
|
APN |
10 |
109,605,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02573:Nav3
|
APN |
10 |
109,702,835 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02633:Nav3
|
APN |
10 |
109,527,997 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02810:Nav3
|
APN |
10 |
109,652,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02964:Nav3
|
APN |
10 |
109,572,814 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03015:Nav3
|
APN |
10 |
109,554,158 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03288:Nav3
|
APN |
10 |
109,594,878 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03310:Nav3
|
APN |
10 |
109,660,433 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4377001:Nav3
|
UTSW |
10 |
109,552,466 (GRCm39) |
missense |
probably damaging |
0.99 |
R0010:Nav3
|
UTSW |
10 |
109,659,087 (GRCm39) |
splice site |
probably benign |
|
R0043:Nav3
|
UTSW |
10 |
109,603,379 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0053:Nav3
|
UTSW |
10 |
109,602,778 (GRCm39) |
splice site |
probably benign |
|
R0053:Nav3
|
UTSW |
10 |
109,602,778 (GRCm39) |
splice site |
probably benign |
|
R0077:Nav3
|
UTSW |
10 |
109,552,503 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0219:Nav3
|
UTSW |
10 |
109,702,791 (GRCm39) |
critical splice donor site |
probably null |
|
R0310:Nav3
|
UTSW |
10 |
109,602,989 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0380:Nav3
|
UTSW |
10 |
109,594,740 (GRCm39) |
splice site |
probably benign |
|
R0403:Nav3
|
UTSW |
10 |
109,602,964 (GRCm39) |
missense |
probably damaging |
0.98 |
R0480:Nav3
|
UTSW |
10 |
109,689,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Nav3
|
UTSW |
10 |
109,659,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R0637:Nav3
|
UTSW |
10 |
109,606,058 (GRCm39) |
missense |
probably benign |
0.25 |
R0847:Nav3
|
UTSW |
10 |
109,739,718 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0988:Nav3
|
UTSW |
10 |
109,552,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R1272:Nav3
|
UTSW |
10 |
109,572,860 (GRCm39) |
missense |
probably damaging |
0.98 |
R1295:Nav3
|
UTSW |
10 |
109,527,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R1405:Nav3
|
UTSW |
10 |
109,606,194 (GRCm39) |
splice site |
probably benign |
|
R1406:Nav3
|
UTSW |
10 |
109,719,495 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1406:Nav3
|
UTSW |
10 |
109,719,495 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1420:Nav3
|
UTSW |
10 |
109,659,115 (GRCm39) |
missense |
probably benign |
0.02 |
R1449:Nav3
|
UTSW |
10 |
109,689,372 (GRCm39) |
missense |
probably benign |
0.13 |
R1458:Nav3
|
UTSW |
10 |
109,555,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Nav3
|
UTSW |
10 |
109,596,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Nav3
|
UTSW |
10 |
109,596,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Nav3
|
UTSW |
10 |
109,563,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R1537:Nav3
|
UTSW |
10 |
109,702,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R1539:Nav3
|
UTSW |
10 |
109,603,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R1581:Nav3
|
UTSW |
10 |
109,659,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R1586:Nav3
|
UTSW |
10 |
109,689,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Nav3
|
UTSW |
10 |
109,688,984 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1725:Nav3
|
UTSW |
10 |
109,659,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1742:Nav3
|
UTSW |
10 |
109,605,074 (GRCm39) |
missense |
probably benign |
|
R1793:Nav3
|
UTSW |
10 |
109,539,233 (GRCm39) |
missense |
probably benign |
0.00 |
R1830:Nav3
|
UTSW |
10 |
109,659,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R1834:Nav3
|
UTSW |
10 |
109,555,883 (GRCm39) |
missense |
probably damaging |
0.99 |
R1881:Nav3
|
UTSW |
10 |
109,688,420 (GRCm39) |
missense |
probably damaging |
0.96 |
R1922:Nav3
|
UTSW |
10 |
109,541,467 (GRCm39) |
missense |
probably benign |
0.43 |
R1944:Nav3
|
UTSW |
10 |
109,552,391 (GRCm39) |
missense |
probably damaging |
0.99 |
R1981:Nav3
|
UTSW |
10 |
109,554,951 (GRCm39) |
splice site |
probably benign |
|
R1985:Nav3
|
UTSW |
10 |
109,606,045 (GRCm39) |
splice site |
probably benign |
|
R1996:Nav3
|
UTSW |
10 |
109,689,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R2051:Nav3
|
UTSW |
10 |
109,660,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R2062:Nav3
|
UTSW |
10 |
109,555,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R2139:Nav3
|
UTSW |
10 |
109,688,996 (GRCm39) |
missense |
probably benign |
0.22 |
R2248:Nav3
|
UTSW |
10 |
109,532,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R2420:Nav3
|
UTSW |
10 |
109,699,674 (GRCm39) |
missense |
probably damaging |
0.98 |
R2444:Nav3
|
UTSW |
10 |
109,600,776 (GRCm39) |
missense |
probably benign |
0.09 |
R3026:Nav3
|
UTSW |
10 |
109,660,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R3052:Nav3
|
UTSW |
10 |
109,739,613 (GRCm39) |
missense |
probably damaging |
0.99 |
R3441:Nav3
|
UTSW |
10 |
109,540,789 (GRCm39) |
missense |
probably benign |
0.01 |
R3845:Nav3
|
UTSW |
10 |
109,689,237 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3929:Nav3
|
UTSW |
10 |
109,520,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R3932:Nav3
|
UTSW |
10 |
109,529,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R4056:Nav3
|
UTSW |
10 |
109,716,394 (GRCm39) |
critical splice donor site |
probably null |
|
R4057:Nav3
|
UTSW |
10 |
109,716,394 (GRCm39) |
critical splice donor site |
probably null |
|
R4120:Nav3
|
UTSW |
10 |
109,739,605 (GRCm39) |
critical splice donor site |
probably null |
|
R4244:Nav3
|
UTSW |
10 |
109,605,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R4361:Nav3
|
UTSW |
10 |
109,688,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R4512:Nav3
|
UTSW |
10 |
109,529,943 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4514:Nav3
|
UTSW |
10 |
109,529,943 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4700:Nav3
|
UTSW |
10 |
109,600,796 (GRCm39) |
missense |
probably benign |
0.10 |
R4815:Nav3
|
UTSW |
10 |
109,659,413 (GRCm39) |
missense |
probably benign |
|
R4981:Nav3
|
UTSW |
10 |
109,716,553 (GRCm39) |
missense |
probably benign |
|
R5042:Nav3
|
UTSW |
10 |
109,605,129 (GRCm39) |
missense |
probably benign |
0.27 |
R5251:Nav3
|
UTSW |
10 |
109,689,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R5252:Nav3
|
UTSW |
10 |
109,550,152 (GRCm39) |
small deletion |
probably benign |
|
R5273:Nav3
|
UTSW |
10 |
109,528,899 (GRCm39) |
critical splice donor site |
probably null |
|
R5288:Nav3
|
UTSW |
10 |
109,688,966 (GRCm39) |
missense |
probably benign |
0.10 |
R5407:Nav3
|
UTSW |
10 |
109,702,796 (GRCm39) |
missense |
probably benign |
0.28 |
R5533:Nav3
|
UTSW |
10 |
109,719,539 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5561:Nav3
|
UTSW |
10 |
109,552,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R5577:Nav3
|
UTSW |
10 |
109,605,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R5656:Nav3
|
UTSW |
10 |
109,600,494 (GRCm39) |
missense |
probably damaging |
0.96 |
R5872:Nav3
|
UTSW |
10 |
109,600,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R6023:Nav3
|
UTSW |
10 |
109,659,376 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6061:Nav3
|
UTSW |
10 |
109,702,845 (GRCm39) |
nonsense |
probably null |
|
R6189:Nav3
|
UTSW |
10 |
109,555,880 (GRCm39) |
missense |
probably damaging |
0.98 |
R6214:Nav3
|
UTSW |
10 |
109,688,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6215:Nav3
|
UTSW |
10 |
109,688,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6264:Nav3
|
UTSW |
10 |
109,524,694 (GRCm39) |
missense |
probably damaging |
0.97 |
R6500:Nav3
|
UTSW |
10 |
109,600,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Nav3
|
UTSW |
10 |
109,555,891 (GRCm39) |
missense |
probably damaging |
0.99 |
R6868:Nav3
|
UTSW |
10 |
109,529,027 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7079:Nav3
|
UTSW |
10 |
109,603,153 (GRCm39) |
missense |
probably benign |
0.16 |
R7099:Nav3
|
UTSW |
10 |
109,539,195 (GRCm39) |
missense |
probably benign |
0.11 |
R7139:Nav3
|
UTSW |
10 |
109,689,338 (GRCm39) |
missense |
probably benign |
0.44 |
R7238:Nav3
|
UTSW |
10 |
109,689,185 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7338:Nav3
|
UTSW |
10 |
109,605,073 (GRCm39) |
missense |
probably benign |
0.04 |
R7383:Nav3
|
UTSW |
10 |
109,552,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R7391:Nav3
|
UTSW |
10 |
109,539,317 (GRCm39) |
missense |
probably benign |
0.07 |
R7399:Nav3
|
UTSW |
10 |
109,688,795 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7457:Nav3
|
UTSW |
10 |
109,532,189 (GRCm39) |
nonsense |
probably null |
|
R7462:Nav3
|
UTSW |
10 |
109,659,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R7542:Nav3
|
UTSW |
10 |
109,659,394 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7659:Nav3
|
UTSW |
10 |
109,602,851 (GRCm39) |
missense |
probably benign |
0.09 |
R7749:Nav3
|
UTSW |
10 |
109,539,213 (GRCm39) |
missense |
probably damaging |
0.99 |
R7794:Nav3
|
UTSW |
10 |
109,524,717 (GRCm39) |
missense |
probably benign |
0.08 |
R7876:Nav3
|
UTSW |
10 |
109,689,359 (GRCm39) |
missense |
probably benign |
0.26 |
R8048:Nav3
|
UTSW |
10 |
109,600,779 (GRCm39) |
missense |
probably benign |
0.13 |
R8104:Nav3
|
UTSW |
10 |
109,594,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R8125:Nav3
|
UTSW |
10 |
109,688,520 (GRCm39) |
missense |
probably damaging |
0.99 |
R8275:Nav3
|
UTSW |
10 |
109,527,984 (GRCm39) |
missense |
noncoding transcript |
|
R8325:Nav3
|
UTSW |
10 |
109,541,464 (GRCm39) |
missense |
probably benign |
0.24 |
R8336:Nav3
|
UTSW |
10 |
109,603,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R8523:Nav3
|
UTSW |
10 |
109,659,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R8529:Nav3
|
UTSW |
10 |
109,689,192 (GRCm39) |
missense |
probably benign |
0.09 |
R8745:Nav3
|
UTSW |
10 |
109,659,311 (GRCm39) |
missense |
probably benign |
0.08 |
R8752:Nav3
|
UTSW |
10 |
109,596,165 (GRCm39) |
intron |
probably benign |
|
R8794:Nav3
|
UTSW |
10 |
109,605,032 (GRCm39) |
nonsense |
probably null |
|
R8816:Nav3
|
UTSW |
10 |
109,699,721 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9029:Nav3
|
UTSW |
10 |
109,699,613 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9117:Nav3
|
UTSW |
10 |
109,520,100 (GRCm39) |
missense |
probably benign |
0.41 |
R9126:Nav3
|
UTSW |
10 |
109,541,524 (GRCm39) |
missense |
probably benign |
|
R9258:Nav3
|
UTSW |
10 |
109,550,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R9347:Nav3
|
UTSW |
10 |
109,738,955 (GRCm39) |
missense |
probably damaging |
0.98 |
R9353:Nav3
|
UTSW |
10 |
109,554,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R9366:Nav3
|
UTSW |
10 |
109,659,364 (GRCm39) |
missense |
probably damaging |
0.99 |
R9384:Nav3
|
UTSW |
10 |
109,554,158 (GRCm39) |
missense |
probably damaging |
0.98 |
R9428:Nav3
|
UTSW |
10 |
109,605,176 (GRCm39) |
missense |
probably benign |
|
R9454:Nav3
|
UTSW |
10 |
109,835,864 (GRCm39) |
missense |
probably benign |
0.01 |
R9516:Nav3
|
UTSW |
10 |
109,520,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R9521:Nav3
|
UTSW |
10 |
109,835,845 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9622:Nav3
|
UTSW |
10 |
109,603,103 (GRCm39) |
missense |
probably benign |
|
R9689:Nav3
|
UTSW |
10 |
109,605,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R9796:Nav3
|
UTSW |
10 |
109,527,969 (GRCm39) |
missense |
probably damaging |
0.99 |
X0012:Nav3
|
UTSW |
10 |
109,527,958 (GRCm39) |
missense |
probably damaging |
1.00 |
|