Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
T |
13: 81,727,713 (GRCm39) |
W309* |
probably null |
Het |
Aox1 |
G |
A |
1: 58,124,620 (GRCm39) |
V954I |
probably benign |
Het |
Asnsd1 |
A |
C |
1: 53,387,187 (GRCm39) |
|
probably null |
Het |
Aste1 |
A |
G |
9: 105,274,056 (GRCm39) |
K38E |
probably damaging |
Het |
Catsperg1 |
A |
G |
7: 28,899,664 (GRCm39) |
V339A |
probably damaging |
Het |
Ccdc13 |
A |
G |
9: 121,627,975 (GRCm39) |
|
probably benign |
Het |
Cd79b |
C |
A |
11: 106,203,267 (GRCm39) |
|
probably null |
Het |
Cemip2 |
C |
A |
19: 21,789,751 (GRCm39) |
N650K |
probably benign |
Het |
Chd3 |
A |
G |
11: 69,247,380 (GRCm39) |
L981P |
probably damaging |
Het |
Chia1 |
T |
C |
3: 106,029,761 (GRCm39) |
F132L |
probably damaging |
Het |
Dhx9 |
G |
A |
1: 153,348,209 (GRCm39) |
P336S |
probably damaging |
Het |
Dido1 |
T |
C |
2: 180,303,945 (GRCm39) |
K1320E |
probably damaging |
Het |
Dmbt1 |
G |
T |
7: 130,668,463 (GRCm39) |
C573F |
possibly damaging |
Het |
Dmtn |
A |
G |
14: 70,850,776 (GRCm39) |
I205T |
probably benign |
Het |
Efnb3 |
C |
A |
11: 69,447,591 (GRCm39) |
V181L |
probably benign |
Het |
Flg2 |
G |
T |
3: 93,109,166 (GRCm39) |
C398F |
possibly damaging |
Het |
Gabbr1 |
A |
G |
17: 37,380,257 (GRCm39) |
D604G |
probably damaging |
Het |
Glis2 |
T |
A |
16: 4,428,197 (GRCm39) |
L83* |
probably null |
Het |
Gm10719 |
T |
A |
9: 3,019,040 (GRCm39) |
|
probably null |
Homo |
Hipk3 |
T |
C |
2: 104,264,086 (GRCm39) |
D804G |
probably damaging |
Het |
Kcnd1 |
G |
C |
X: 7,690,148 (GRCm39) |
A23P |
probably damaging |
Homo |
Kcnj13 |
A |
G |
1: 87,314,256 (GRCm39) |
V322A |
probably benign |
Het |
Nav3 |
A |
G |
10: 109,688,426 (GRCm39) |
L617P |
probably damaging |
Het |
Npc1 |
ACAGCAGCAGCAGCAGCAG |
ACAGCAGCAGCAGCAG |
18: 12,369,249 (GRCm39) |
|
probably benign |
Het |
Or8b3b |
A |
G |
9: 38,584,510 (GRCm39) |
S90P |
probably benign |
Het |
Osgin1 |
G |
A |
8: 120,172,183 (GRCm39) |
V326I |
probably benign |
Het |
Pcsk7 |
A |
C |
9: 45,821,674 (GRCm39) |
N156T |
possibly damaging |
Het |
Pde4d |
C |
T |
13: 110,085,967 (GRCm39) |
S515L |
probably damaging |
Het |
Peg10 |
GC |
GCCCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Ppp2r5a |
T |
A |
1: 191,094,447 (GRCm39) |
Q191L |
probably benign |
Het |
Prom2 |
A |
G |
2: 127,381,695 (GRCm39) |
|
probably null |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Sart3 |
C |
T |
5: 113,881,267 (GRCm39) |
A938T |
probably benign |
Het |
Sh3glb2 |
T |
C |
2: 30,235,805 (GRCm39) |
E313G |
possibly damaging |
Het |
Slc13a1 |
A |
T |
6: 24,090,795 (GRCm39) |
Y541* |
probably null |
Het |
Smtnl2 |
G |
A |
11: 72,292,225 (GRCm39) |
A274V |
probably damaging |
Het |
Spata31h1 |
T |
A |
10: 82,126,946 (GRCm39) |
K2021N |
probably benign |
Het |
Speer1d |
C |
T |
5: 11,307,197 (GRCm39) |
T25I |
probably damaging |
Het |
Tm6sf2 |
T |
C |
8: 70,525,724 (GRCm39) |
V27A |
possibly damaging |
Het |
Tmem116 |
C |
T |
5: 121,629,171 (GRCm39) |
T188M |
probably benign |
Het |
Trim21 |
A |
G |
7: 102,208,646 (GRCm39) |
S358P |
probably damaging |
Het |
Ttc21a |
A |
G |
9: 119,795,838 (GRCm39) |
Y1224C |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,710,552 (GRCm39) |
|
probably benign |
Het |
Vmn2r99 |
A |
G |
17: 19,602,820 (GRCm39) |
Q525R |
probably benign |
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 |
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 |
R8456: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 |
|