Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Amigo2 |
T |
C |
15: 97,143,166 (GRCm39) |
T419A |
probably damaging |
Het |
Baiap2l1 |
A |
C |
5: 144,217,691 (GRCm39) |
I298M |
possibly damaging |
Het |
BC005624 |
G |
T |
2: 30,863,748 (GRCm39) |
A245D |
probably benign |
Het |
Cdh23 |
T |
A |
10: 60,150,390 (GRCm39) |
I2527F |
probably damaging |
Het |
Celsr1 |
T |
C |
15: 85,915,615 (GRCm39) |
H786R |
possibly damaging |
Het |
Cerkl |
A |
G |
2: 79,168,922 (GRCm39) |
V427A |
possibly damaging |
Het |
Cfap43 |
G |
T |
19: 47,885,765 (GRCm39) |
C283* |
probably null |
Het |
Chfr |
G |
A |
5: 110,302,803 (GRCm39) |
A455T |
probably benign |
Het |
Cldn13 |
T |
A |
5: 134,943,850 (GRCm39) |
I112F |
possibly damaging |
Het |
Cyb5rl |
T |
A |
4: 106,925,875 (GRCm39) |
V19E |
probably benign |
Het |
Dcp1a |
A |
G |
14: 30,244,883 (GRCm39) |
T570A |
possibly damaging |
Het |
Dlgap2 |
T |
A |
8: 14,828,295 (GRCm39) |
C568S |
probably benign |
Het |
Ecm2 |
T |
C |
13: 49,671,859 (GRCm39) |
L120P |
probably damaging |
Het |
Gpr156 |
T |
C |
16: 37,812,416 (GRCm39) |
S251P |
probably damaging |
Het |
Gpr182 |
T |
C |
10: 127,585,790 (GRCm39) |
N387S |
probably benign |
Het |
Grid1 |
T |
C |
14: 35,291,595 (GRCm39) |
V834A |
possibly damaging |
Het |
Igkv8-34 |
T |
C |
6: 70,021,337 (GRCm39) |
S42G |
probably benign |
Het |
Kctd17 |
CAGCTGGAGGAGC |
CAGC |
15: 78,321,113 (GRCm39) |
|
probably benign |
Het |
Lrrc19 |
T |
A |
4: 94,527,587 (GRCm39) |
D208V |
probably benign |
Het |
Lrrc9 |
C |
T |
12: 72,528,317 (GRCm39) |
T872I |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,279,245 (GRCm39) |
|
probably null |
Het |
Mrpl13 |
A |
G |
15: 55,420,679 (GRCm39) |
M1T |
probably null |
Het |
Ncapg |
C |
T |
5: 45,831,805 (GRCm39) |
T217I |
probably damaging |
Het |
Nim1k |
G |
A |
13: 120,174,022 (GRCm39) |
P291S |
probably damaging |
Het |
Or8c11 |
G |
A |
9: 38,289,912 (GRCm39) |
G239D |
probably damaging |
Het |
Or8k31-ps1 |
A |
T |
2: 86,356,415 (GRCm39) |
Y35* |
probably null |
Het |
Padi6 |
T |
C |
4: 140,464,687 (GRCm39) |
M181V |
probably damaging |
Het |
Pax7 |
T |
A |
4: 139,557,514 (GRCm39) |
I86F |
probably damaging |
Het |
Pbk |
T |
A |
14: 66,054,680 (GRCm39) |
Y271N |
probably benign |
Het |
Rabgap1 |
C |
T |
2: 37,385,710 (GRCm39) |
P492L |
probably benign |
Het |
Rhno1 |
G |
T |
6: 128,334,728 (GRCm39) |
D198E |
probably damaging |
Het |
Slc40a1 |
T |
C |
1: 45,950,439 (GRCm39) |
S338G |
probably damaging |
Het |
Slc45a3 |
A |
G |
1: 131,905,928 (GRCm39) |
Y317C |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,532,270 (GRCm39) |
S2842R |
probably benign |
Het |
Tle2 |
C |
T |
10: 81,413,518 (GRCm39) |
T119I |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,553,938 (GRCm39) |
V30922I |
possibly damaging |
Het |
Usp33 |
C |
T |
3: 152,080,297 (GRCm39) |
P476L |
probably damaging |
Het |
Wdr38 |
T |
C |
2: 38,889,361 (GRCm39) |
Y51H |
probably damaging |
Het |
|
Other mutations in Scn2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Scn2a
|
APN |
2 |
65,594,784 (GRCm39) |
missense |
probably benign |
|
IGL00159:Scn2a
|
APN |
2 |
65,573,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00418:Scn2a
|
APN |
2 |
65,594,866 (GRCm39) |
missense |
probably benign |
0.43 |
IGL00753:Scn2a
|
APN |
2 |
65,514,207 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL00770:Scn2a
|
APN |
2 |
65,566,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00774:Scn2a
|
APN |
2 |
65,566,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00847:Scn2a
|
APN |
2 |
65,501,078 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01155:Scn2a
|
APN |
2 |
65,548,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01329:Scn2a
|
APN |
2 |
65,547,852 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01537:Scn2a
|
APN |
2 |
65,546,219 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01672:Scn2a
|
APN |
2 |
65,582,278 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01958:Scn2a
|
APN |
2 |
65,532,173 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02028:Scn2a
|
APN |
2 |
65,594,002 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02142:Scn2a
|
APN |
2 |
65,546,182 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02160:Scn2a
|
APN |
2 |
65,560,460 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02183:Scn2a
|
APN |
2 |
65,501,947 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02341:Scn2a
|
APN |
2 |
65,518,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02504:Scn2a
|
APN |
2 |
65,514,228 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02530:Scn2a
|
APN |
2 |
65,560,522 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02621:Scn2a
|
APN |
2 |
65,579,223 (GRCm39) |
splice site |
probably benign |
|
IGL02652:Scn2a
|
APN |
2 |
65,532,382 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02966:Scn2a
|
APN |
2 |
65,532,188 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03188:Scn2a
|
APN |
2 |
65,501,997 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03329:Scn2a
|
APN |
2 |
65,594,973 (GRCm39) |
missense |
probably benign |
|
IGL03336:Scn2a
|
APN |
2 |
65,519,088 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Scn2a
|
APN |
2 |
65,594,557 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4280001:Scn2a
|
UTSW |
2 |
65,546,074 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4362001:Scn2a
|
UTSW |
2 |
65,514,182 (GRCm39) |
missense |
probably benign |
0.09 |
PIT4403001:Scn2a
|
UTSW |
2 |
65,542,252 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4520001:Scn2a
|
UTSW |
2 |
65,518,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R0021:Scn2a
|
UTSW |
2 |
65,500,859 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0141:Scn2a
|
UTSW |
2 |
65,542,160 (GRCm39) |
missense |
probably benign |
0.01 |
R0240:Scn2a
|
UTSW |
2 |
65,566,118 (GRCm39) |
missense |
probably benign |
0.32 |
R0240:Scn2a
|
UTSW |
2 |
65,566,118 (GRCm39) |
missense |
probably benign |
0.32 |
R0335:Scn2a
|
UTSW |
2 |
65,512,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R0508:Scn2a
|
UTSW |
2 |
65,548,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R0558:Scn2a
|
UTSW |
2 |
65,542,269 (GRCm39) |
missense |
probably benign |
0.26 |
R0600:Scn2a
|
UTSW |
2 |
65,532,177 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0667:Scn2a
|
UTSW |
2 |
65,582,340 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1178:Scn2a
|
UTSW |
2 |
65,517,123 (GRCm39) |
splice site |
probably benign |
|
R1244:Scn2a
|
UTSW |
2 |
65,593,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R1386:Scn2a
|
UTSW |
2 |
65,519,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Scn2a
|
UTSW |
2 |
65,532,335 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1440:Scn2a
|
UTSW |
2 |
65,594,938 (GRCm39) |
missense |
probably benign |
|
R1448:Scn2a
|
UTSW |
2 |
65,514,189 (GRCm39) |
missense |
probably benign |
0.17 |
R1460:Scn2a
|
UTSW |
2 |
65,532,187 (GRCm39) |
missense |
probably damaging |
0.96 |
R1553:Scn2a
|
UTSW |
2 |
65,544,180 (GRCm39) |
nonsense |
probably null |
|
R1642:Scn2a
|
UTSW |
2 |
65,514,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Scn2a
|
UTSW |
2 |
65,501,111 (GRCm39) |
splice site |
probably null |
|
R1981:Scn2a
|
UTSW |
2 |
65,520,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R2002:Scn2a
|
UTSW |
2 |
65,512,427 (GRCm39) |
missense |
probably null |
1.00 |
R2068:Scn2a
|
UTSW |
2 |
65,582,417 (GRCm39) |
missense |
probably benign |
0.14 |
R2125:Scn2a
|
UTSW |
2 |
65,582,423 (GRCm39) |
nonsense |
probably null |
|
R2126:Scn2a
|
UTSW |
2 |
65,582,423 (GRCm39) |
nonsense |
probably null |
|
R2876:Scn2a
|
UTSW |
2 |
65,546,241 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2878:Scn2a
|
UTSW |
2 |
65,518,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R3113:Scn2a
|
UTSW |
2 |
65,579,129 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3749:Scn2a
|
UTSW |
2 |
65,544,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R3750:Scn2a
|
UTSW |
2 |
65,544,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R3765:Scn2a
|
UTSW |
2 |
65,513,054 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3850:Scn2a
|
UTSW |
2 |
65,512,375 (GRCm39) |
missense |
probably benign |
0.14 |
R4585:Scn2a
|
UTSW |
2 |
65,573,395 (GRCm39) |
splice site |
probably null |
|
R4586:Scn2a
|
UTSW |
2 |
65,573,395 (GRCm39) |
splice site |
probably null |
|
R4588:Scn2a
|
UTSW |
2 |
65,544,111 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4622:Scn2a
|
UTSW |
2 |
65,582,371 (GRCm39) |
missense |
probably benign |
0.04 |
R5108:Scn2a
|
UTSW |
2 |
65,518,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R5161:Scn2a
|
UTSW |
2 |
65,594,935 (GRCm39) |
missense |
probably benign |
0.00 |
R5235:Scn2a
|
UTSW |
2 |
65,582,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R5464:Scn2a
|
UTSW |
2 |
65,532,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Scn2a
|
UTSW |
2 |
65,537,639 (GRCm39) |
nonsense |
probably null |
|
R5630:Scn2a
|
UTSW |
2 |
65,556,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R5715:Scn2a
|
UTSW |
2 |
65,547,928 (GRCm39) |
missense |
probably benign |
0.27 |
R5730:Scn2a
|
UTSW |
2 |
65,512,882 (GRCm39) |
nonsense |
probably null |
|
R5734:Scn2a
|
UTSW |
2 |
65,548,066 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5779:Scn2a
|
UTSW |
2 |
65,594,827 (GRCm39) |
missense |
probably benign |
0.00 |
R6133:Scn2a
|
UTSW |
2 |
65,573,448 (GRCm39) |
missense |
probably benign |
0.35 |
R6547:Scn2a
|
UTSW |
2 |
65,546,241 (GRCm39) |
missense |
probably benign |
0.29 |
R6549:Scn2a
|
UTSW |
2 |
65,595,018 (GRCm39) |
missense |
probably benign |
0.05 |
R6818:Scn2a
|
UTSW |
2 |
65,519,013 (GRCm39) |
nonsense |
probably null |
|
R6999:Scn2a
|
UTSW |
2 |
65,512,453 (GRCm39) |
missense |
probably benign |
|
R7069:Scn2a
|
UTSW |
2 |
65,594,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7073:Scn2a
|
UTSW |
2 |
65,558,787 (GRCm39) |
missense |
probably benign |
0.00 |
R7125:Scn2a
|
UTSW |
2 |
65,594,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R7178:Scn2a
|
UTSW |
2 |
65,579,197 (GRCm39) |
nonsense |
probably null |
|
R7179:Scn2a
|
UTSW |
2 |
65,532,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Scn2a
|
UTSW |
2 |
65,578,663 (GRCm39) |
missense |
probably benign |
0.01 |
R7227:Scn2a
|
UTSW |
2 |
65,582,367 (GRCm39) |
missense |
probably damaging |
0.98 |
R7269:Scn2a
|
UTSW |
2 |
65,594,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R7358:Scn2a
|
UTSW |
2 |
65,512,850 (GRCm39) |
nonsense |
probably null |
|
R7388:Scn2a
|
UTSW |
2 |
65,518,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R7491:Scn2a
|
UTSW |
2 |
65,532,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R7619:Scn2a
|
UTSW |
2 |
65,546,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R7695:Scn2a
|
UTSW |
2 |
65,542,251 (GRCm39) |
missense |
probably damaging |
0.99 |
R7735:Scn2a
|
UTSW |
2 |
65,594,013 (GRCm39) |
missense |
probably benign |
0.40 |
R7911:Scn2a
|
UTSW |
2 |
65,512,427 (GRCm39) |
missense |
probably null |
1.00 |
R8096:Scn2a
|
UTSW |
2 |
65,594,366 (GRCm39) |
missense |
probably damaging |
0.98 |
R8172:Scn2a
|
UTSW |
2 |
65,520,672 (GRCm39) |
missense |
probably benign |
0.01 |
R8220:Scn2a
|
UTSW |
2 |
65,520,620 (GRCm39) |
missense |
probably benign |
0.01 |
R8416:Scn2a
|
UTSW |
2 |
65,511,345 (GRCm39) |
missense |
probably benign |
0.00 |
R8850:Scn2a
|
UTSW |
2 |
65,518,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Scn2a
|
UTSW |
2 |
65,546,002 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8977:Scn2a
|
UTSW |
2 |
65,594,014 (GRCm39) |
missense |
probably damaging |
0.99 |
R8992:Scn2a
|
UTSW |
2 |
65,594,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R9190:Scn2a
|
UTSW |
2 |
65,511,346 (GRCm39) |
missense |
probably benign |
0.00 |
R9206:Scn2a
|
UTSW |
2 |
65,548,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R9355:Scn2a
|
UTSW |
2 |
65,594,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R9452:Scn2a
|
UTSW |
2 |
65,595,163 (GRCm39) |
missense |
probably benign |
|
R9529:Scn2a
|
UTSW |
2 |
65,594,932 (GRCm39) |
missense |
probably damaging |
0.99 |
R9567:Scn2a
|
UTSW |
2 |
65,518,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R9569:Scn2a
|
UTSW |
2 |
65,560,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R9657:Scn2a
|
UTSW |
2 |
65,566,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R9715:Scn2a
|
UTSW |
2 |
65,579,149 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9761:Scn2a
|
UTSW |
2 |
65,566,030 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Scn2a
|
UTSW |
2 |
65,582,212 (GRCm39) |
missense |
possibly damaging |
0.84 |
Z1177:Scn2a
|
UTSW |
2 |
65,548,079 (GRCm39) |
missense |
probably benign |
0.07 |
|