Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
T |
5: 8,980,796 (GRCm39) |
N593Y |
probably damaging |
Het |
Adamts16 |
C |
T |
13: 70,940,005 (GRCm39) |
S406N |
possibly damaging |
Het |
Adgrg1 |
G |
A |
8: 95,733,928 (GRCm39) |
V350I |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,659,030 (GRCm39) |
D2051E |
probably damaging |
Het |
Adrb2 |
C |
A |
18: 62,312,484 (GRCm39) |
V114L |
probably damaging |
Het |
Ago3 |
A |
G |
4: 126,247,520 (GRCm39) |
V599A |
probably damaging |
Het |
AI837181 |
T |
C |
19: 5,476,257 (GRCm39) |
V140A |
probably damaging |
Het |
Ankrd16 |
T |
A |
2: 11,788,443 (GRCm39) |
|
probably null |
Het |
Arnt2 |
A |
G |
7: 83,992,959 (GRCm39) |
S194P |
probably benign |
Het |
Art2b |
T |
C |
7: 101,229,153 (GRCm39) |
N249D |
probably benign |
Het |
Atat1 |
A |
G |
17: 36,220,232 (GRCm39) |
L60P |
probably damaging |
Het |
Atp2b1 |
A |
T |
10: 98,858,793 (GRCm39) |
I1159F |
probably damaging |
Het |
Atrip |
T |
A |
9: 108,900,935 (GRCm39) |
I135F |
probably damaging |
Het |
Bbs4 |
T |
G |
9: 59,237,698 (GRCm39) |
|
probably null |
Het |
Bdp1 |
A |
T |
13: 100,210,889 (GRCm39) |
|
probably null |
Het |
Best2 |
A |
G |
8: 85,737,390 (GRCm39) |
|
probably null |
Het |
Cacna1c |
A |
G |
6: 118,583,227 (GRCm39) |
I1516T |
probably damaging |
Het |
Cadps2 |
T |
C |
6: 23,599,479 (GRCm39) |
I276V |
probably damaging |
Het |
Carmil3 |
T |
C |
14: 55,736,087 (GRCm39) |
S610P |
probably damaging |
Het |
Caskin1 |
A |
G |
17: 24,719,745 (GRCm39) |
I375V |
probably damaging |
Het |
Ccdc168 |
G |
A |
1: 44,101,009 (GRCm39) |
P30S |
probably damaging |
Het |
Ccdc92b |
A |
G |
11: 74,520,835 (GRCm39) |
I46V |
probably benign |
Het |
Clec11a |
G |
T |
7: 43,954,098 (GRCm39) |
T285K |
probably benign |
Het |
Clk3 |
G |
T |
9: 57,672,469 (GRCm39) |
T111K |
probably benign |
Het |
Col6a6 |
G |
A |
9: 105,586,583 (GRCm39) |
R1813C |
probably damaging |
Het |
Col7a1 |
G |
A |
9: 108,789,078 (GRCm39) |
V798I |
unknown |
Het |
Ctrb1 |
C |
A |
8: 112,416,151 (GRCm39) |
W45L |
probably damaging |
Het |
Cubn |
T |
A |
2: 13,283,349 (GRCm39) |
S3530C |
probably benign |
Het |
Dio1 |
A |
G |
4: 107,163,977 (GRCm39) |
|
probably null |
Het |
Dock5 |
A |
T |
14: 67,994,584 (GRCm39) |
Y1825* |
probably null |
Het |
Duox1 |
A |
T |
2: 122,177,001 (GRCm39) |
Q1476L |
probably damaging |
Het |
Dync2h1 |
A |
T |
9: 7,001,377 (GRCm39) |
H3877Q |
probably damaging |
Het |
Enkd1 |
A |
G |
8: 106,434,208 (GRCm39) |
S85P |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,794,758 (GRCm39) |
D139G |
probably benign |
Het |
Ern1 |
A |
G |
11: 106,312,776 (GRCm39) |
S202P |
probably damaging |
Het |
F11r |
T |
C |
1: 171,289,459 (GRCm39) |
Y261H |
probably damaging |
Het |
Glp2r |
A |
T |
11: 67,637,618 (GRCm39) |
S138T |
probably benign |
Het |
Gpt2 |
A |
G |
8: 86,244,625 (GRCm39) |
Y306C |
probably damaging |
Het |
Grid2 |
G |
C |
6: 63,886,045 (GRCm39) |
R147P |
probably damaging |
Het |
Gtdc1 |
A |
G |
2: 44,642,198 (GRCm39) |
F128L |
possibly damaging |
Het |
H2-T15 |
A |
G |
17: 36,368,897 (GRCm39) |
F61S |
probably damaging |
Het |
Hacd4 |
T |
C |
4: 88,341,303 (GRCm39) |
T154A |
possibly damaging |
Het |
Heatr6 |
G |
T |
11: 83,660,046 (GRCm39) |
L530F |
probably damaging |
Het |
Hoxd8 |
A |
T |
2: 74,537,056 (GRCm39) |
D256V |
probably damaging |
Het |
Ints6 |
T |
C |
14: 62,931,089 (GRCm39) |
N865D |
probably benign |
Het |
Itpkc |
G |
T |
7: 26,927,084 (GRCm39) |
P277T |
possibly damaging |
Het |
Klc4 |
T |
C |
17: 46,947,553 (GRCm39) |
N383S |
probably damaging |
Het |
Klra6 |
T |
C |
6: 129,995,908 (GRCm39) |
Y150C |
possibly damaging |
Het |
Krt32 |
T |
A |
11: 99,975,670 (GRCm39) |
|
probably null |
Het |
Krt33a |
T |
C |
11: 99,903,535 (GRCm39) |
N199S |
probably benign |
Het |
Krt39 |
A |
C |
11: 99,410,649 (GRCm39) |
D174E |
probably damaging |
Het |
Krt82 |
G |
A |
15: 101,456,970 (GRCm39) |
R137W |
probably damaging |
Het |
Lgmn |
A |
T |
12: 102,368,183 (GRCm39) |
S193T |
probably damaging |
Het |
Limch1 |
G |
A |
5: 67,156,442 (GRCm39) |
R300H |
probably damaging |
Het |
Lrpap1 |
T |
A |
5: 35,254,974 (GRCm39) |
I221F |
probably benign |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Macf1 |
T |
C |
4: 123,264,459 (GRCm39) |
D4883G |
probably damaging |
Het |
Man2b2 |
A |
G |
5: 36,973,524 (GRCm39) |
V485A |
probably benign |
Het |
Map3k19 |
T |
C |
1: 127,750,859 (GRCm39) |
T831A |
probably benign |
Het |
Mdfic2 |
A |
G |
6: 98,225,151 (GRCm39) |
I44T |
probably benign |
Het |
Megf6 |
C |
G |
4: 154,340,523 (GRCm39) |
D471E |
possibly damaging |
Het |
Mettl8 |
A |
T |
2: 70,803,623 (GRCm39) |
F268L |
probably damaging |
Het |
Miip |
T |
C |
4: 147,950,422 (GRCm39) |
E58G |
probably benign |
Het |
Mycbp2 |
T |
A |
14: 103,466,840 (GRCm39) |
S1308C |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,392,909 (GRCm39) |
F2194L |
probably damaging |
Het |
Ndel1 |
A |
T |
11: 68,720,746 (GRCm39) |
H313Q |
probably benign |
Het |
Neb |
A |
T |
2: 52,118,862 (GRCm39) |
H3931Q |
probably benign |
Het |
Nfkb2 |
T |
A |
19: 46,296,491 (GRCm39) |
V253E |
probably damaging |
Het |
Niban1 |
T |
C |
1: 151,571,979 (GRCm39) |
I308T |
probably damaging |
Het |
Nono |
T |
C |
X: 100,485,429 (GRCm39) |
|
probably null |
Het |
Npc1l1 |
T |
A |
11: 6,164,588 (GRCm39) |
I1154F |
possibly damaging |
Het |
Nr2e1 |
T |
C |
10: 42,448,774 (GRCm39) |
T155A |
probably benign |
Het |
Oosp2 |
C |
T |
19: 11,626,959 (GRCm39) |
|
probably null |
Het |
Or2b2 |
A |
T |
13: 21,887,287 (GRCm39) |
I39F |
possibly damaging |
Het |
Pdap1 |
G |
A |
5: 145,069,726 (GRCm39) |
T93I |
probably benign |
Het |
Pde6c |
T |
A |
19: 38,145,967 (GRCm39) |
D418E |
probably damaging |
Het |
Pdha1 |
T |
A |
X: 158,910,354 (GRCm39) |
D255V |
probably damaging |
Het |
Polr2h |
T |
A |
16: 20,537,796 (GRCm39) |
D64E |
probably benign |
Het |
Psmb3 |
T |
C |
11: 97,601,981 (GRCm39) |
F117S |
probably benign |
Het |
Ptprq |
A |
T |
10: 107,418,249 (GRCm39) |
M1709K |
probably benign |
Het |
Rbm15 |
C |
T |
3: 107,238,868 (GRCm39) |
R510H |
probably damaging |
Het |
Rgs7 |
A |
T |
1: 174,980,769 (GRCm39) |
M85K |
possibly damaging |
Het |
Rpl27-ps3 |
T |
A |
18: 6,332,669 (GRCm39) |
V13D |
probably damaging |
Het |
Rtp2 |
T |
A |
16: 23,746,316 (GRCm39) |
D105V |
possibly damaging |
Het |
Scd3 |
T |
C |
19: 44,224,219 (GRCm39) |
Y151H |
probably benign |
Het |
Slc30a6 |
T |
G |
17: 74,715,858 (GRCm39) |
V106G |
probably damaging |
Het |
Slco1a4 |
T |
C |
6: 141,785,276 (GRCm39) |
I105V |
probably benign |
Het |
Sun3 |
T |
C |
11: 8,988,296 (GRCm39) |
I9V |
probably benign |
Het |
Syne2 |
T |
C |
12: 76,121,318 (GRCm39) |
V5928A |
probably damaging |
Het |
Tbr1 |
T |
A |
2: 61,642,600 (GRCm39) |
S622T |
probably damaging |
Het |
Tgm3 |
A |
G |
2: 129,871,889 (GRCm39) |
N306D |
probably damaging |
Het |
Tmem132d |
A |
G |
5: 127,860,828 (GRCm39) |
*1098Q |
probably null |
Het |
Tmem140 |
T |
C |
6: 34,849,747 (GRCm39) |
Y88H |
probably damaging |
Het |
Trim60 |
A |
T |
8: 65,453,964 (GRCm39) |
V95E |
possibly damaging |
Het |
Vamp3 |
A |
G |
4: 151,140,617 (GRCm39) |
|
probably null |
Het |
Vmn1r235 |
A |
C |
17: 21,481,785 (GRCm39) |
T37P |
probably damaging |
Het |
Vmn2r81 |
T |
G |
10: 79,129,571 (GRCm39) |
L821V |
probably damaging |
Het |
Vmn2r97 |
A |
G |
17: 19,160,500 (GRCm39) |
D545G |
probably benign |
Het |
Vps13c |
A |
T |
9: 67,793,558 (GRCm39) |
D437V |
probably damaging |
Het |
Wtip |
A |
T |
7: 33,818,363 (GRCm39) |
M268K |
probably benign |
Het |
Zfhx2 |
G |
T |
14: 55,312,189 (GRCm39) |
F168L |
probably benign |
Het |
Zscan22 |
G |
A |
7: 12,637,767 (GRCm39) |
R53K |
probably damaging |
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 |
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 |
R7343:Nav3
|
UTSW |
10 |
109,739,619 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
|