Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
T |
3: 137,775,712 (GRCm39) |
T1634S |
probably damaging |
Het |
Adgrl1 |
T |
A |
8: 84,665,693 (GRCm39) |
M1460K |
probably damaging |
Het |
Adig |
T |
A |
2: 158,347,773 (GRCm39) |
L29Q |
unknown |
Het |
Adnp |
T |
G |
2: 168,025,887 (GRCm39) |
K469N |
probably damaging |
Het |
Akap3 |
A |
G |
6: 126,842,200 (GRCm39) |
D273G |
probably benign |
Het |
Albfm1 |
A |
T |
5: 90,727,519 (GRCm39) |
Y379F |
probably damaging |
Het |
Ankrd34b |
T |
C |
13: 92,575,139 (GRCm39) |
Y124H |
possibly damaging |
Het |
Ap2b1 |
T |
G |
11: 83,223,948 (GRCm39) |
F221C |
possibly damaging |
Het |
Atp2c2 |
A |
G |
8: 120,469,160 (GRCm39) |
I358V |
possibly damaging |
Het |
BC051665 |
G |
A |
13: 60,930,536 (GRCm39) |
T272I |
probably benign |
Het |
Cdan1 |
G |
T |
2: 120,560,783 (GRCm39) |
A262E |
probably benign |
Het |
Ces1d |
C |
T |
8: 93,904,763 (GRCm39) |
V326I |
probably benign |
Het |
Chd3 |
T |
C |
11: 69,254,873 (GRCm39) |
R156G |
probably benign |
Het |
Clip1 |
C |
T |
5: 123,751,328 (GRCm39) |
E818K |
|
Het |
Col6a4 |
C |
T |
9: 105,877,519 (GRCm39) |
V2153M |
probably damaging |
Het |
Crlf3 |
T |
C |
11: 79,947,351 (GRCm39) |
N296D |
possibly damaging |
Het |
Cstdc6 |
C |
T |
16: 36,142,193 (GRCm39) |
G61D |
probably benign |
Het |
D130052B06Rik |
A |
G |
11: 33,573,594 (GRCm39) |
I109V |
probably benign |
Het |
Dcaf5 |
G |
T |
12: 80,385,483 (GRCm39) |
T881K |
probably benign |
Het |
Dennd4a |
C |
A |
9: 64,769,238 (GRCm39) |
T408K |
probably damaging |
Het |
Dnaaf9 |
C |
A |
2: 130,648,708 (GRCm39) |
R258L |
unknown |
Het |
Dnah2 |
A |
G |
11: 69,349,972 (GRCm39) |
|
probably null |
Het |
Eif1ad8 |
A |
T |
12: 87,564,006 (GRCm39) |
K114* |
probably null |
Het |
Eif2ak2 |
C |
T |
17: 79,173,760 (GRCm39) |
V273I |
probably benign |
Het |
Elac1 |
C |
T |
18: 73,872,359 (GRCm39) |
G212D |
probably damaging |
Het |
Ercc6l2 |
A |
G |
13: 64,013,798 (GRCm39) |
D623G |
probably damaging |
Het |
Exo1 |
T |
C |
1: 175,716,413 (GRCm39) |
F177L |
probably damaging |
Het |
Fat4 |
A |
G |
3: 38,944,562 (GRCm39) |
T1152A |
probably benign |
Het |
Fbxl12 |
G |
T |
9: 20,529,709 (GRCm39) |
|
probably null |
Het |
Fbxo43 |
T |
C |
15: 36,151,971 (GRCm39) |
Y582C |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,812,484 (GRCm39) |
N2934K |
possibly damaging |
Het |
Gna12 |
A |
G |
5: 140,815,847 (GRCm39) |
S69P |
probably damaging |
Het |
Gpatch8 |
C |
A |
11: 102,369,354 (GRCm39) |
G1395C |
probably damaging |
Het |
Gpr137c |
A |
G |
14: 45,516,148 (GRCm39) |
Y294C |
probably damaging |
Het |
Greb1 |
A |
G |
12: 16,724,673 (GRCm39) |
S1834P |
probably damaging |
Het |
Grin2b |
T |
C |
6: 135,757,249 (GRCm39) |
D404G |
probably damaging |
Het |
Hectd2 |
A |
T |
19: 36,574,478 (GRCm39) |
N236I |
probably damaging |
Het |
Hhip |
C |
T |
8: 80,713,641 (GRCm39) |
V562I |
probably benign |
Het |
Hipk2 |
G |
T |
6: 38,692,992 (GRCm39) |
T867N |
probably benign |
Het |
Hmgcl |
T |
C |
4: 135,689,424 (GRCm39) |
V294A |
possibly damaging |
Het |
Hnrnpl |
T |
A |
7: 28,513,400 (GRCm39) |
F158I |
|
Het |
Hspa5 |
T |
C |
2: 34,662,383 (GRCm39) |
V17A |
unknown |
Het |
Hspg2 |
T |
C |
4: 137,235,704 (GRCm39) |
V168A |
probably damaging |
Het |
Idh1 |
A |
G |
1: 65,205,284 (GRCm39) |
F227S |
probably damaging |
Het |
Iigp1c |
A |
G |
18: 60,379,355 (GRCm39) |
S297G |
possibly damaging |
Het |
Immp2l |
T |
C |
12: 41,160,915 (GRCm39) |
V71A |
possibly damaging |
Het |
Iqce |
G |
A |
5: 140,675,713 (GRCm39) |
R193* |
probably null |
Het |
Kcnq5 |
T |
C |
1: 21,472,526 (GRCm39) |
D907G |
probably benign |
Het |
Krt17 |
T |
A |
11: 100,148,613 (GRCm39) |
T306S |
probably benign |
Het |
Lhx3 |
T |
C |
2: 26,093,009 (GRCm39) |
D149G |
probably damaging |
Het |
Lrrc73 |
G |
A |
17: 46,565,488 (GRCm39) |
R73H |
probably damaging |
Het |
Mgat5b |
T |
C |
11: 116,875,809 (GRCm39) |
S678P |
probably benign |
Het |
Mink1 |
T |
C |
11: 70,502,305 (GRCm39) |
|
probably null |
Het |
Mroh5 |
T |
G |
15: 73,663,278 (GRCm39) |
|
probably null |
Het |
Muc5ac |
T |
A |
7: 141,363,254 (GRCm39) |
H2188Q |
unknown |
Het |
Muc5ac |
G |
C |
7: 141,363,424 (GRCm39) |
|
probably benign |
Het |
Musk |
G |
A |
4: 58,344,312 (GRCm39) |
G305D |
probably benign |
Het |
Mx1 |
A |
G |
16: 97,249,496 (GRCm39) |
I347T |
unknown |
Het |
Mybbp1a |
G |
T |
11: 72,334,338 (GRCm39) |
V198F |
probably damaging |
Het |
Mycbp2 |
A |
G |
14: 103,393,733 (GRCm39) |
S2943P |
probably damaging |
Het |
Myo18a |
G |
A |
11: 77,733,059 (GRCm39) |
R1363K |
probably damaging |
Het |
Or13g1 |
T |
C |
7: 85,955,799 (GRCm39) |
H174R |
probably damaging |
Het |
Or14j6 |
T |
C |
17: 38,215,328 (GRCm39) |
L297S |
probably benign |
Het |
Or1e26 |
A |
T |
11: 73,480,561 (GRCm39) |
M1K |
probably null |
Het |
Or1j13 |
T |
A |
2: 36,369,726 (GRCm39) |
N139Y |
possibly damaging |
Het |
Or5k15 |
T |
A |
16: 58,710,252 (GRCm39) |
E110D |
probably damaging |
Het |
Pecr |
T |
C |
1: 72,298,592 (GRCm39) |
D276G |
probably damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Ppp1cb |
A |
T |
5: 32,648,376 (GRCm39) |
T320S |
probably benign |
Het |
Ppp1r9a |
G |
T |
6: 5,159,716 (GRCm39) |
K1084N |
probably damaging |
Het |
Prdm2 |
A |
G |
4: 142,862,391 (GRCm39) |
S300P |
probably benign |
Het |
Prkg1 |
C |
T |
19: 30,602,090 (GRCm39) |
V389I |
probably damaging |
Het |
Psg25 |
C |
T |
7: 18,266,127 (GRCm39) |
|
probably benign |
Het |
Ptpn6 |
A |
G |
6: 124,698,821 (GRCm39) |
S498P |
possibly damaging |
Het |
Pus3 |
A |
G |
9: 35,477,965 (GRCm39) |
H399R |
probably benign |
Het |
Pus7 |
T |
C |
5: 23,983,450 (GRCm39) |
T6A |
probably benign |
Het |
Rnf169 |
A |
G |
7: 99,574,954 (GRCm39) |
V547A |
probably benign |
Het |
Rsf1 |
GGCGGCGGC |
GGCGGCGGCCGCGGCGGC |
7: 97,229,128 (GRCm39) |
|
probably benign |
Het |
Ryr1 |
C |
T |
7: 28,794,807 (GRCm39) |
D1194N |
probably benign |
Het |
Scn5a |
T |
C |
9: 119,320,610 (GRCm39) |
M1490V |
possibly damaging |
Het |
Sec23b |
A |
G |
2: 144,432,258 (GRCm39) |
D756G |
possibly damaging |
Het |
Selenoo |
T |
A |
15: 88,973,427 (GRCm39) |
M39K |
probably benign |
Het |
Septin8 |
T |
G |
11: 53,427,519 (GRCm39) |
V246G |
possibly damaging |
Het |
Serpina3k |
T |
A |
12: 104,309,367 (GRCm39) |
N270K |
probably damaging |
Het |
Setd5 |
G |
A |
6: 113,098,091 (GRCm39) |
R710H |
probably damaging |
Het |
Sirt4 |
A |
T |
5: 115,621,049 (GRCm39) |
I41N |
possibly damaging |
Het |
Slc26a9 |
T |
A |
1: 131,686,556 (GRCm39) |
Y425* |
probably null |
Het |
Slc4a9 |
A |
G |
18: 36,662,773 (GRCm39) |
E176G |
probably benign |
Het |
Speer1m |
T |
C |
5: 11,970,712 (GRCm39) |
I127T |
|
Het |
Spidr |
A |
T |
16: 15,784,680 (GRCm39) |
W463R |
probably benign |
Het |
Tenm4 |
G |
A |
7: 96,202,703 (GRCm39) |
R106H |
probably benign |
Het |
Tmcc1 |
G |
A |
6: 116,111,198 (GRCm39) |
Q28* |
probably null |
Het |
Tmem52b |
A |
G |
6: 129,493,651 (GRCm39) |
E88G |
probably damaging |
Het |
Trpc7 |
A |
T |
13: 56,974,710 (GRCm39) |
I402K |
probably benign |
Het |
Tshz3 |
T |
C |
7: 36,469,522 (GRCm39) |
Y504H |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,542,549 (GRCm39) |
E33479G |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,711,672 (GRCm39) |
R8290C |
unknown |
Het |
Urb1 |
T |
C |
16: 90,549,003 (GRCm39) |
D2235G |
possibly damaging |
Het |
Usp10 |
T |
C |
8: 120,668,283 (GRCm39) |
F195L |
probably benign |
Het |
Vmn1r31 |
A |
T |
6: 58,449,858 (GRCm39) |
F2L |
|
Het |
Vmn2r109 |
C |
T |
17: 20,761,336 (GRCm39) |
V674M |
probably damaging |
Het |
Vmn2r12 |
G |
A |
5: 109,245,655 (GRCm39) |
P26S |
possibly damaging |
Het |
Vmn2r61 |
T |
A |
7: 41,916,629 (GRCm39) |
M414K |
possibly damaging |
Het |
Yipf3 |
T |
C |
17: 46,562,585 (GRCm39) |
V330A |
probably benign |
Het |
Zic4 |
A |
T |
9: 91,261,450 (GRCm39) |
H235L |
probably benign |
Het |
Zxdc |
T |
A |
6: 90,346,642 (GRCm39) |
W16R |
unknown |
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 |
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 |
|