Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
A |
G |
10: 79,842,360 (GRCm39) |
E1098G |
probably benign |
Het |
Akap1 |
T |
A |
11: 88,725,557 (GRCm39) |
|
probably null |
Het |
Arhgap26 |
T |
C |
18: 39,244,901 (GRCm39) |
V182A |
possibly damaging |
Het |
Arhgef19 |
A |
G |
4: 140,977,926 (GRCm39) |
K545R |
probably benign |
Het |
Asph |
C |
T |
4: 9,537,722 (GRCm39) |
R352Q |
probably benign |
Het |
B3glct |
T |
A |
5: 149,650,254 (GRCm39) |
I119N |
probably damaging |
Het |
Bltp3b |
A |
G |
10: 89,647,954 (GRCm39) |
T1339A |
probably benign |
Het |
Camsap3 |
C |
T |
8: 3,650,679 (GRCm39) |
R236* |
probably null |
Het |
Ccser2 |
A |
T |
14: 36,612,331 (GRCm39) |
M792K |
probably benign |
Het |
Ceacam5 |
C |
T |
7: 17,479,624 (GRCm39) |
T247I |
possibly damaging |
Het |
Dnah9 |
A |
G |
11: 66,047,764 (GRCm39) |
S19P |
probably damaging |
Het |
Dtwd1 |
A |
G |
2: 126,000,451 (GRCm39) |
E129G |
probably damaging |
Het |
Ebf3 |
T |
A |
7: 136,800,916 (GRCm39) |
M490L |
probably benign |
Het |
Elp1 |
ACTTCTTCTTCTTCTTCTTCTTC |
ACTTCTTCTTCTTCTTCTTC |
4: 56,781,176 (GRCm39) |
|
probably benign |
Het |
Erbb4 |
A |
G |
1: 68,110,789 (GRCm39) |
L1008S |
probably damaging |
Het |
Ereg |
C |
T |
5: 91,237,993 (GRCm39) |
P160S |
possibly damaging |
Het |
Exoc6b |
ATTT |
ATTTT |
6: 84,821,077 (GRCm39) |
|
probably null |
Het |
Fmn1 |
A |
G |
2: 113,195,385 (GRCm39) |
T362A |
unknown |
Het |
Gm14326 |
A |
T |
2: 177,590,312 (GRCm39) |
D16E |
probably benign |
Het |
H1f8 |
A |
T |
6: 115,925,745 (GRCm39) |
M181L |
probably benign |
Het |
H3c1 |
A |
T |
13: 23,946,083 (GRCm39) |
F85Y |
probably damaging |
Het |
Herc6 |
A |
T |
6: 57,575,548 (GRCm39) |
T190S |
probably benign |
Het |
Lama1 |
T |
G |
17: 68,044,491 (GRCm39) |
I130S |
|
Het |
Letm2 |
T |
C |
8: 26,071,729 (GRCm39) |
D391G |
probably damaging |
Het |
Map3k9 |
T |
C |
12: 81,780,892 (GRCm39) |
I423V |
probably damaging |
Het |
Melk |
T |
A |
4: 44,312,191 (GRCm39) |
C168S |
possibly damaging |
Het |
Naa16 |
A |
T |
14: 79,596,915 (GRCm39) |
N356K |
probably benign |
Het |
Nup214 |
A |
G |
2: 31,929,372 (GRCm39) |
N1873S |
probably benign |
Het |
Or2y1f |
C |
T |
11: 49,184,385 (GRCm39) |
P79L |
probably damaging |
Het |
Or8b41 |
T |
A |
9: 38,054,981 (GRCm39) |
C178* |
probably null |
Het |
Pom121 |
A |
G |
5: 135,410,032 (GRCm39) |
F1042L |
unknown |
Het |
Pramel51 |
T |
A |
12: 88,143,986 (GRCm39) |
T284S |
probably benign |
Het |
Pxdn |
T |
C |
12: 30,061,889 (GRCm39) |
S1334P |
probably damaging |
Het |
Ranbp1 |
C |
T |
16: 18,063,170 (GRCm39) |
E69K |
probably damaging |
Het |
Rasl11a |
T |
C |
5: 146,782,045 (GRCm39) |
S7P |
probably damaging |
Het |
Rev1 |
G |
A |
1: 38,098,324 (GRCm39) |
R740* |
probably null |
Het |
Rnf157 |
C |
T |
11: 116,240,246 (GRCm39) |
V443M |
probably benign |
Het |
Sh2b1 |
TGGGGACCAGCTCAGCCACGGGGACCAGCTC |
TGGGGACCAGCTCAGCCACGGGGACCAGCTCAGCCACGGGGACCAGCTC |
7: 126,066,742 (GRCm39) |
|
probably benign |
Het |
Sh2b1 |
C |
CAGCCACGGGGCCTAGCTA |
7: 126,066,772 (GRCm39) |
|
probably null |
Het |
Siah2 |
T |
C |
3: 58,583,503 (GRCm39) |
N261S |
probably benign |
Het |
Sumf2 |
T |
G |
5: 129,889,003 (GRCm39) |
W264G |
possibly damaging |
Het |
Tal1 |
G |
T |
4: 114,920,625 (GRCm39) |
A100S |
probably benign |
Het |
Tmprss9 |
A |
G |
10: 80,730,251 (GRCm39) |
D717G |
possibly damaging |
Het |
Tox2 |
G |
T |
2: 163,046,550 (GRCm39) |
R9L |
unknown |
Het |
Traj46 |
A |
G |
14: 54,409,795 (GRCm39) |
E1G |
|
Het |
Unc80 |
A |
G |
1: 66,680,788 (GRCm39) |
D2128G |
possibly damaging |
Het |
Usp21 |
A |
T |
1: 171,112,290 (GRCm39) |
F308I |
probably damaging |
Het |
Vgf |
A |
T |
5: 137,061,265 (GRCm39) |
I476F |
probably damaging |
Het |
Vps35 |
G |
A |
8: 85,987,934 (GRCm39) |
T739I |
possibly damaging |
Het |
Wdr95 |
G |
T |
5: 149,502,572 (GRCm39) |
C279F |
probably damaging |
Het |
Zbtb32 |
T |
C |
7: 30,289,381 (GRCm39) |
S94G |
unknown |
Het |
Zdhhc13 |
T |
A |
7: 48,452,747 (GRCm39) |
I153N |
probably damaging |
Het |
|
Other mutations in Scn3a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00953:Scn3a
|
APN |
2 |
65,327,736 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01086:Scn3a
|
APN |
2 |
65,300,503 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01141:Scn3a
|
APN |
2 |
65,325,457 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01150:Scn3a
|
APN |
2 |
65,327,709 (GRCm39) |
splice site |
probably null |
|
IGL01564:Scn3a
|
APN |
2 |
65,291,790 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01594:Scn3a
|
APN |
2 |
65,291,775 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01751:Scn3a
|
APN |
2 |
65,291,596 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01803:Scn3a
|
APN |
2 |
65,352,127 (GRCm39) |
unclassified |
probably benign |
|
IGL01822:Scn3a
|
APN |
2 |
65,325,608 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02063:Scn3a
|
APN |
2 |
65,291,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02142:Scn3a
|
APN |
2 |
65,356,965 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02198:Scn3a
|
APN |
2 |
65,338,833 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02501:Scn3a
|
APN |
2 |
65,356,899 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02608:Scn3a
|
APN |
2 |
65,354,510 (GRCm39) |
nonsense |
probably null |
|
IGL02645:Scn3a
|
APN |
2 |
65,344,871 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02653:Scn3a
|
APN |
2 |
65,291,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03077:Scn3a
|
APN |
2 |
65,367,016 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03099:Scn3a
|
APN |
2 |
65,367,016 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03299:Scn3a
|
APN |
2 |
65,327,860 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03327:Scn3a
|
APN |
2 |
65,367,016 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03346:Scn3a
|
APN |
2 |
65,367,016 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03355:Scn3a
|
APN |
2 |
65,290,912 (GRCm39) |
missense |
possibly damaging |
0.91 |
curtsey
|
UTSW |
2 |
65,295,180 (GRCm39) |
missense |
probably damaging |
1.00 |
dip
|
UTSW |
2 |
65,354,523 (GRCm39) |
missense |
probably benign |
0.01 |
Regime
|
UTSW |
2 |
65,355,194 (GRCm39) |
missense |
possibly damaging |
0.93 |
Willpower
|
UTSW |
2 |
65,356,098 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0019:Scn3a
|
UTSW |
2 |
65,292,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R0316:Scn3a
|
UTSW |
2 |
65,291,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Scn3a
|
UTSW |
2 |
65,338,918 (GRCm39) |
missense |
probably damaging |
0.97 |
R0414:Scn3a
|
UTSW |
2 |
65,356,326 (GRCm39) |
splice site |
probably benign |
|
R0609:Scn3a
|
UTSW |
2 |
65,366,854 (GRCm39) |
missense |
probably damaging |
0.96 |
R0613:Scn3a
|
UTSW |
2 |
65,302,628 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0645:Scn3a
|
UTSW |
2 |
65,355,194 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0665:Scn3a
|
UTSW |
2 |
65,314,755 (GRCm39) |
missense |
probably null |
0.00 |
R0667:Scn3a
|
UTSW |
2 |
65,314,755 (GRCm39) |
missense |
probably null |
0.00 |
R0710:Scn3a
|
UTSW |
2 |
65,299,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R1202:Scn3a
|
UTSW |
2 |
65,336,491 (GRCm39) |
missense |
probably benign |
0.07 |
R1440:Scn3a
|
UTSW |
2 |
65,359,785 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1447:Scn3a
|
UTSW |
2 |
65,300,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R1564:Scn3a
|
UTSW |
2 |
65,344,979 (GRCm39) |
missense |
probably damaging |
0.98 |
R1595:Scn3a
|
UTSW |
2 |
65,329,323 (GRCm39) |
missense |
probably damaging |
0.99 |
R1775:Scn3a
|
UTSW |
2 |
65,302,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R1781:Scn3a
|
UTSW |
2 |
65,302,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Scn3a
|
UTSW |
2 |
65,314,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R1924:Scn3a
|
UTSW |
2 |
65,291,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Scn3a
|
UTSW |
2 |
65,291,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Scn3a
|
UTSW |
2 |
65,351,210 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2174:Scn3a
|
UTSW |
2 |
65,337,550 (GRCm39) |
missense |
probably damaging |
0.99 |
R2656:Scn3a
|
UTSW |
2 |
65,356,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R2680:Scn3a
|
UTSW |
2 |
65,366,880 (GRCm39) |
missense |
probably benign |
0.04 |
R3882:Scn3a
|
UTSW |
2 |
65,312,623 (GRCm39) |
missense |
probably benign |
0.03 |
R4019:Scn3a
|
UTSW |
2 |
65,356,295 (GRCm39) |
intron |
probably benign |
|
R4106:Scn3a
|
UTSW |
2 |
65,325,379 (GRCm39) |
missense |
probably benign |
0.07 |
R4108:Scn3a
|
UTSW |
2 |
65,325,379 (GRCm39) |
missense |
probably benign |
0.07 |
R4109:Scn3a
|
UTSW |
2 |
65,325,379 (GRCm39) |
missense |
probably benign |
0.07 |
R4225:Scn3a
|
UTSW |
2 |
65,366,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R4419:Scn3a
|
UTSW |
2 |
65,297,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R4552:Scn3a
|
UTSW |
2 |
65,354,523 (GRCm39) |
missense |
probably benign |
0.01 |
R4687:Scn3a
|
UTSW |
2 |
65,295,074 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4780:Scn3a
|
UTSW |
2 |
65,336,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Scn3a
|
UTSW |
2 |
65,291,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R4856:Scn3a
|
UTSW |
2 |
65,291,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R4886:Scn3a
|
UTSW |
2 |
65,291,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R4914:Scn3a
|
UTSW |
2 |
65,291,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Scn3a
|
UTSW |
2 |
65,291,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4918:Scn3a
|
UTSW |
2 |
65,291,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Scn3a
|
UTSW |
2 |
65,302,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R5101:Scn3a
|
UTSW |
2 |
65,291,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R5128:Scn3a
|
UTSW |
2 |
65,338,862 (GRCm39) |
missense |
probably benign |
0.08 |
R5132:Scn3a
|
UTSW |
2 |
65,298,548 (GRCm39) |
missense |
probably benign |
0.09 |
R5297:Scn3a
|
UTSW |
2 |
65,299,378 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5595:Scn3a
|
UTSW |
2 |
65,291,057 (GRCm39) |
missense |
probably benign |
|
R5699:Scn3a
|
UTSW |
2 |
65,337,608 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5730:Scn3a
|
UTSW |
2 |
65,325,604 (GRCm39) |
missense |
probably benign |
0.00 |
R5735:Scn3a
|
UTSW |
2 |
65,314,803 (GRCm39) |
missense |
probably benign |
0.09 |
R5735:Scn3a
|
UTSW |
2 |
65,312,622 (GRCm39) |
missense |
probably damaging |
0.98 |
R5855:Scn3a
|
UTSW |
2 |
65,295,074 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5888:Scn3a
|
UTSW |
2 |
65,327,742 (GRCm39) |
missense |
probably benign |
0.06 |
R5898:Scn3a
|
UTSW |
2 |
65,345,039 (GRCm39) |
missense |
probably damaging |
0.96 |
R5935:Scn3a
|
UTSW |
2 |
65,295,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R5970:Scn3a
|
UTSW |
2 |
65,325,125 (GRCm39) |
intron |
probably benign |
|
R6214:Scn3a
|
UTSW |
2 |
65,325,380 (GRCm39) |
missense |
probably benign |
0.29 |
R6215:Scn3a
|
UTSW |
2 |
65,325,380 (GRCm39) |
missense |
probably benign |
0.29 |
R6235:Scn3a
|
UTSW |
2 |
65,291,679 (GRCm39) |
missense |
probably damaging |
0.97 |
R6307:Scn3a
|
UTSW |
2 |
65,302,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R6355:Scn3a
|
UTSW |
2 |
65,291,643 (GRCm39) |
missense |
probably damaging |
0.99 |
R6376:Scn3a
|
UTSW |
2 |
65,291,843 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6517:Scn3a
|
UTSW |
2 |
65,327,907 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6775:Scn3a
|
UTSW |
2 |
65,352,159 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6893:Scn3a
|
UTSW |
2 |
65,356,098 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6986:Scn3a
|
UTSW |
2 |
65,338,962 (GRCm39) |
missense |
probably damaging |
0.97 |
R7065:Scn3a
|
UTSW |
2 |
65,295,199 (GRCm39) |
missense |
probably benign |
|
R7078:Scn3a
|
UTSW |
2 |
65,327,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7146:Scn3a
|
UTSW |
2 |
65,313,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R7240:Scn3a
|
UTSW |
2 |
65,299,386 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7294:Scn3a
|
UTSW |
2 |
65,302,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R7352:Scn3a
|
UTSW |
2 |
65,356,045 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7636:Scn3a
|
UTSW |
2 |
65,328,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R7708:Scn3a
|
UTSW |
2 |
65,313,512 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7733:Scn3a
|
UTSW |
2 |
65,338,994 (GRCm39) |
missense |
probably benign |
0.08 |
R7761:Scn3a
|
UTSW |
2 |
65,359,798 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7792:Scn3a
|
UTSW |
2 |
65,297,334 (GRCm39) |
nonsense |
probably null |
|
R7828:Scn3a
|
UTSW |
2 |
65,338,918 (GRCm39) |
missense |
probably damaging |
0.97 |
R7875:Scn3a
|
UTSW |
2 |
65,327,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:Scn3a
|
UTSW |
2 |
65,366,859 (GRCm39) |
missense |
probably damaging |
0.96 |
R7958:Scn3a
|
UTSW |
2 |
65,336,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R7965:Scn3a
|
UTSW |
2 |
65,336,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Scn3a
|
UTSW |
2 |
65,361,154 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8345:Scn3a
|
UTSW |
2 |
65,329,335 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8356:Scn3a
|
UTSW |
2 |
65,291,017 (GRCm39) |
missense |
probably benign |
0.08 |
R8527:Scn3a
|
UTSW |
2 |
65,327,863 (GRCm39) |
missense |
probably damaging |
0.99 |
R8688:Scn3a
|
UTSW |
2 |
65,356,047 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8731:Scn3a
|
UTSW |
2 |
65,298,507 (GRCm39) |
nonsense |
probably null |
|
R8901:Scn3a
|
UTSW |
2 |
65,352,252 (GRCm39) |
missense |
probably benign |
0.00 |
R8910:Scn3a
|
UTSW |
2 |
65,338,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R9011:Scn3a
|
UTSW |
2 |
65,352,170 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9364:Scn3a
|
UTSW |
2 |
65,291,596 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9460:Scn3a
|
UTSW |
2 |
65,300,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R9496:Scn3a
|
UTSW |
2 |
65,312,493 (GRCm39) |
critical splice donor site |
probably null |
|
R9542:Scn3a
|
UTSW |
2 |
65,366,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R9563:Scn3a
|
UTSW |
2 |
65,291,595 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Scn3a
|
UTSW |
2 |
65,355,191 (GRCm39) |
nonsense |
probably null |
|
X0062:Scn3a
|
UTSW |
2 |
65,297,345 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Scn3a
|
UTSW |
2 |
65,329,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|