Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
T |
A |
13: 81,652,097 (GRCm39) |
|
probably null |
Het |
Adh7 |
A |
C |
3: 137,929,716 (GRCm39) |
T131P |
possibly damaging |
Het |
Agxt |
G |
A |
1: 93,065,701 (GRCm39) |
G190D |
probably damaging |
Het |
AI182371 |
A |
G |
2: 34,978,815 (GRCm39) |
I193T |
probably damaging |
Het |
Akna |
T |
A |
4: 63,297,547 (GRCm39) |
T836S |
probably benign |
Het |
Alox12 |
T |
C |
11: 70,144,069 (GRCm39) |
|
probably null |
Het |
Anapc2 |
C |
A |
2: 25,163,075 (GRCm39) |
T104K |
probably benign |
Het |
Ank1 |
T |
C |
8: 23,583,935 (GRCm39) |
L346P |
probably damaging |
Het |
Ankfn1 |
A |
T |
11: 89,332,217 (GRCm39) |
I443N |
probably damaging |
Het |
Arhgef17 |
G |
A |
7: 100,539,680 (GRCm39) |
T1066I |
probably damaging |
Het |
Atg2a |
C |
A |
19: 6,296,801 (GRCm39) |
|
probably null |
Het |
Bpifb5 |
T |
A |
2: 154,065,776 (GRCm39) |
H24Q |
probably benign |
Het |
Brd9 |
A |
G |
13: 74,092,862 (GRCm39) |
E283G |
probably damaging |
Het |
Cadm2 |
C |
A |
16: 66,581,727 (GRCm39) |
V184F |
probably damaging |
Het |
Casr |
A |
G |
16: 36,315,499 (GRCm39) |
V857A |
probably benign |
Het |
Ccdc18 |
A |
T |
5: 108,339,843 (GRCm39) |
Q796L |
probably damaging |
Het |
Cep290 |
T |
C |
10: 100,332,690 (GRCm39) |
V263A |
probably benign |
Het |
Clec10a |
A |
T |
11: 70,060,645 (GRCm39) |
N167Y |
probably damaging |
Het |
Cog1 |
A |
G |
11: 113,543,058 (GRCm39) |
I189V |
possibly damaging |
Het |
Commd2 |
A |
G |
3: 57,554,269 (GRCm39) |
I144T |
probably benign |
Het |
Cse1l |
A |
G |
2: 166,768,292 (GRCm39) |
T197A |
probably benign |
Het |
Csmd3 |
A |
T |
15: 47,683,794 (GRCm39) |
S1783R |
probably benign |
Het |
Cxxc1 |
T |
C |
18: 74,352,278 (GRCm39) |
V334A |
possibly damaging |
Het |
Dennd2d |
A |
G |
3: 106,394,236 (GRCm39) |
I39V |
probably benign |
Het |
Dgkz |
G |
A |
2: 91,768,405 (GRCm39) |
P734S |
probably damaging |
Het |
Diaph3 |
T |
C |
14: 86,893,916 (GRCm39) |
D31G |
probably damaging |
Het |
Dlec1 |
T |
C |
9: 118,956,518 (GRCm39) |
S731P |
probably benign |
Het |
Dmac2l |
G |
A |
12: 69,787,845 (GRCm39) |
D94N |
probably benign |
Het |
Dnah11 |
T |
C |
12: 117,894,991 (GRCm39) |
R3619G |
probably benign |
Het |
Doc2b |
A |
G |
11: 75,662,783 (GRCm39) |
L405P |
probably damaging |
Het |
Dock3 |
A |
T |
9: 106,829,563 (GRCm39) |
I1117N |
probably damaging |
Het |
Dock3 |
G |
A |
9: 106,874,112 (GRCm39) |
A453V |
probably benign |
Het |
Ece2 |
T |
A |
16: 20,461,263 (GRCm39) |
I474N |
probably damaging |
Het |
Etv4 |
A |
T |
11: 101,662,513 (GRCm39) |
|
probably null |
Het |
Fam171b |
A |
T |
2: 83,710,442 (GRCm39) |
M705L |
probably benign |
Het |
Frem2 |
T |
C |
3: 53,561,631 (GRCm39) |
K959E |
probably benign |
Het |
Fyn |
T |
C |
10: 39,408,066 (GRCm39) |
M251T |
possibly damaging |
Het |
Galnt13 |
G |
A |
2: 54,747,869 (GRCm39) |
G250E |
probably damaging |
Het |
Ggh |
T |
C |
4: 20,054,204 (GRCm39) |
|
probably null |
Het |
Glcci1 |
A |
G |
6: 8,591,620 (GRCm39) |
E222G |
probably damaging |
Het |
Gm1968 |
G |
A |
16: 29,777,659 (GRCm39) |
|
noncoding transcript |
Het |
Gm3604 |
T |
A |
13: 62,519,414 (GRCm39) |
I52F |
possibly damaging |
Het |
Gm43302 |
T |
C |
5: 105,422,635 (GRCm39) |
I466V |
probably benign |
Het |
Gm9789 |
T |
C |
16: 88,955,034 (GRCm39) |
S48P |
unknown |
Het |
Gpat3 |
A |
T |
5: 101,031,254 (GRCm39) |
Y136F |
probably benign |
Het |
Gpr171 |
T |
C |
3: 59,005,142 (GRCm39) |
D211G |
possibly damaging |
Het |
Grep1 |
T |
A |
17: 23,936,118 (GRCm39) |
|
probably benign |
Het |
Hs3st1 |
T |
C |
5: 39,771,791 (GRCm39) |
K284R |
probably benign |
Het |
Htr2a |
C |
T |
14: 74,882,608 (GRCm39) |
A198V |
possibly damaging |
Het |
Ice1 |
C |
A |
13: 70,754,023 (GRCm39) |
D688Y |
probably damaging |
Het |
Jade1 |
T |
C |
3: 41,559,431 (GRCm39) |
M504T |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,420,250 (GRCm39) |
|
probably null |
Het |
Lsr |
A |
T |
7: 30,671,517 (GRCm39) |
I72N |
possibly damaging |
Het |
Magel2 |
G |
A |
7: 62,028,557 (GRCm39) |
R487H |
possibly damaging |
Het |
Mertk |
A |
G |
2: 128,624,446 (GRCm39) |
D619G |
probably benign |
Het |
Myo1b |
A |
T |
1: 51,838,722 (GRCm39) |
V245E |
probably damaging |
Het |
Myrip |
T |
A |
9: 120,253,689 (GRCm39) |
L254Q |
probably benign |
Het |
Ncoa7 |
T |
C |
10: 30,647,725 (GRCm39) |
Y17C |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,187,003 (GRCm39) |
E7G |
probably benign |
Het |
Ninl |
A |
G |
2: 150,817,867 (GRCm39) |
V99A |
probably damaging |
Het |
Noct |
G |
T |
3: 51,155,333 (GRCm39) |
E34* |
probably null |
Het |
Notch1 |
A |
T |
2: 26,362,125 (GRCm39) |
Y1043* |
probably null |
Het |
Or10v1 |
T |
C |
19: 11,873,855 (GRCm39) |
S157P |
possibly damaging |
Het |
Or13a21 |
T |
A |
7: 139,999,326 (GRCm39) |
Y120F |
probably benign |
Het |
Or2d3 |
A |
G |
7: 106,490,483 (GRCm39) |
Y278H |
probably damaging |
Het |
Or6c88 |
G |
A |
10: 129,406,640 (GRCm39) |
G39R |
probably damaging |
Het |
Pde7b |
C |
A |
10: 20,355,432 (GRCm39) |
R104L |
possibly damaging |
Het |
Pkn1 |
C |
A |
8: 84,396,966 (GRCm39) |
R890L |
possibly damaging |
Het |
Podn |
A |
T |
4: 107,878,764 (GRCm39) |
Y368N |
probably damaging |
Het |
Polr1b |
G |
A |
2: 128,960,019 (GRCm39) |
|
probably null |
Het |
Ppp1r3c |
A |
T |
19: 36,711,361 (GRCm39) |
F136L |
probably benign |
Het |
Ppp2ca |
T |
A |
11: 52,011,800 (GRCm39) |
F260Y |
probably damaging |
Het |
Prss39 |
A |
G |
1: 34,537,616 (GRCm39) |
S27G |
possibly damaging |
Het |
Ptch1 |
A |
G |
13: 63,689,101 (GRCm39) |
V340A |
probably benign |
Het |
Ranbp17 |
T |
C |
11: 33,247,394 (GRCm39) |
I246V |
probably damaging |
Het |
Rilpl1 |
T |
A |
5: 124,653,618 (GRCm39) |
D181V |
probably damaging |
Het |
Sdk1 |
T |
A |
5: 142,080,354 (GRCm39) |
V1282D |
probably damaging |
Het |
Sh3rf2 |
T |
C |
18: 42,282,887 (GRCm39) |
S514P |
probably damaging |
Het |
Slc35f2 |
A |
T |
9: 53,716,992 (GRCm39) |
I252F |
possibly damaging |
Het |
Slc7a1 |
A |
G |
5: 148,272,403 (GRCm39) |
Y425H |
possibly damaging |
Het |
Spaca4 |
G |
T |
7: 45,374,984 (GRCm39) |
|
probably benign |
Het |
Spata31d1b |
T |
C |
13: 59,863,733 (GRCm39) |
S294P |
possibly damaging |
Het |
Ssh1 |
T |
G |
5: 114,090,064 (GRCm39) |
T342P |
probably damaging |
Het |
Stk10 |
T |
A |
11: 32,483,440 (GRCm39) |
S13T |
possibly damaging |
Het |
Tbx1 |
G |
T |
16: 18,402,843 (GRCm39) |
D214E |
probably benign |
Het |
Tdp1 |
A |
G |
12: 99,878,571 (GRCm39) |
E453G |
probably damaging |
Het |
Tlr1 |
T |
C |
5: 65,084,319 (GRCm39) |
Y86C |
probably damaging |
Het |
Tmem241 |
A |
T |
18: 12,176,297 (GRCm39) |
C124S |
possibly damaging |
Het |
Trp63 |
A |
G |
16: 25,703,599 (GRCm39) |
M516V |
probably benign |
Het |
Ttc28 |
T |
C |
5: 111,248,677 (GRCm39) |
V210A |
possibly damaging |
Het |
Tut1 |
C |
T |
19: 8,942,850 (GRCm39) |
R646W |
probably benign |
Het |
Ubald1 |
C |
T |
16: 4,694,261 (GRCm39) |
E49K |
possibly damaging |
Het |
Usp28 |
T |
C |
9: 48,949,096 (GRCm39) |
Y897H |
probably benign |
Het |
Vmn2r27 |
A |
C |
6: 124,168,730 (GRCm39) |
F800C |
probably damaging |
Het |
Vmn2r83 |
T |
A |
10: 79,327,759 (GRCm39) |
M789K |
probably damaging |
Het |
Vwa8 |
A |
G |
14: 79,300,002 (GRCm39) |
D945G |
probably benign |
Het |
Wdhd1 |
T |
A |
14: 47,482,507 (GRCm39) |
K947N |
possibly damaging |
Het |
Wdr12 |
A |
T |
1: 60,123,007 (GRCm39) |
|
probably null |
Het |
Xrra1 |
A |
T |
7: 99,520,564 (GRCm39) |
E57V |
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 |
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 |
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 |
|