Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm1 |
A |
T |
7: 119,257,538 (GRCm39) |
T435S |
probably damaging |
Het |
Agtpbp1 |
G |
A |
13: 59,648,014 (GRCm39) |
T602I |
probably benign |
Het |
Ahnak2 |
T |
A |
12: 112,749,154 (GRCm39) |
D231V |
probably damaging |
Het |
Ampd3 |
G |
A |
7: 110,392,876 (GRCm39) |
D215N |
probably benign |
Het |
Ate1 |
A |
G |
7: 130,105,523 (GRCm39) |
S332P |
probably damaging |
Het |
Ces1f |
T |
C |
8: 93,998,513 (GRCm39) |
E161G |
probably benign |
Het |
Ces2g |
A |
G |
8: 105,692,628 (GRCm39) |
|
probably benign |
Het |
Cntnap4 |
T |
G |
8: 113,529,796 (GRCm39) |
L668R |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Csf1 |
A |
G |
3: 107,655,960 (GRCm39) |
V245A |
probably benign |
Het |
Ctss |
A |
G |
3: 95,457,448 (GRCm39) |
Y302C |
probably damaging |
Het |
Dbt |
C |
T |
3: 116,328,432 (GRCm39) |
H158Y |
probably benign |
Het |
Dennd6b |
T |
C |
15: 89,070,386 (GRCm39) |
I428V |
probably benign |
Het |
Dnah9 |
G |
A |
11: 65,860,781 (GRCm39) |
|
probably benign |
Het |
Dock3 |
G |
T |
9: 106,790,467 (GRCm39) |
Q1419K |
possibly damaging |
Het |
Enpp6 |
A |
G |
8: 47,519,035 (GRCm39) |
K268E |
probably damaging |
Het |
Eps15l1 |
T |
G |
8: 73,135,341 (GRCm39) |
|
probably benign |
Het |
Gm10800 |
C |
A |
2: 98,496,925 (GRCm39) |
M209I |
probably benign |
Het |
Herc3 |
C |
T |
6: 58,851,293 (GRCm39) |
P514L |
probably damaging |
Het |
Mark2 |
T |
C |
19: 7,263,287 (GRCm39) |
D160G |
probably damaging |
Het |
Mbd4 |
A |
G |
6: 115,821,529 (GRCm39) |
|
probably null |
Het |
Mink1 |
T |
C |
11: 70,503,868 (GRCm39) |
W1263R |
probably damaging |
Het |
Nlrp14 |
A |
T |
7: 106,780,465 (GRCm39) |
|
probably benign |
Het |
Osbp |
T |
C |
19: 11,961,322 (GRCm39) |
Y454H |
probably damaging |
Het |
Pak5 |
T |
C |
2: 135,942,704 (GRCm39) |
K479E |
possibly damaging |
Het |
Pard3 |
C |
A |
8: 127,888,058 (GRCm39) |
D73E |
probably damaging |
Het |
Pmp22 |
A |
T |
11: 63,049,076 (GRCm39) |
|
probably null |
Het |
Slc36a2 |
A |
G |
11: 55,053,621 (GRCm39) |
L339P |
probably damaging |
Het |
Smg1 |
G |
A |
7: 117,811,666 (GRCm39) |
T104I |
possibly damaging |
Het |
Stx18 |
T |
A |
5: 38,249,908 (GRCm39) |
Y74N |
probably damaging |
Het |
Stxbp5 |
A |
T |
10: 9,638,492 (GRCm39) |
H1102Q |
probably damaging |
Het |
Tom1l2 |
T |
C |
11: 60,120,960 (GRCm39) |
K450E |
probably damaging |
Het |
Tpo |
T |
C |
12: 30,150,389 (GRCm39) |
Q497R |
probably benign |
Het |
Tsc2 |
A |
G |
17: 24,849,978 (GRCm39) |
|
probably benign |
Het |
Tut7 |
A |
T |
13: 59,953,142 (GRCm39) |
D99E |
probably benign |
Het |
Vit |
G |
A |
17: 78,907,264 (GRCm39) |
G229R |
probably benign |
Het |
Vwf |
T |
A |
6: 125,659,775 (GRCm39) |
I2658N |
probably benign |
Het |
Wdr36 |
T |
A |
18: 32,992,360 (GRCm39) |
D632E |
probably damaging |
Het |
Zfp654 |
A |
G |
16: 64,605,181 (GRCm39) |
V466A |
probably benign |
Het |
Zfp941 |
T |
C |
7: 140,393,185 (GRCm39) |
D58G |
probably benign |
Het |
|
Other mutations in Scn4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Scn4a
|
APN |
11 |
106,210,745 (GRCm39) |
missense |
probably benign |
|
IGL00846:Scn4a
|
APN |
11 |
106,218,944 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01063:Scn4a
|
APN |
11 |
106,221,190 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01450:Scn4a
|
APN |
11 |
106,215,487 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01922:Scn4a
|
APN |
11 |
106,229,978 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02589:Scn4a
|
APN |
11 |
106,218,958 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03171:Scn4a
|
APN |
11 |
106,236,418 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03338:Scn4a
|
APN |
11 |
106,211,671 (GRCm39) |
missense |
probably damaging |
1.00 |
BB004:Scn4a
|
UTSW |
11 |
106,233,209 (GRCm39) |
missense |
probably damaging |
1.00 |
BB014:Scn4a
|
UTSW |
11 |
106,233,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Scn4a
|
UTSW |
11 |
106,239,231 (GRCm39) |
splice site |
probably benign |
|
R0013:Scn4a
|
UTSW |
11 |
106,239,231 (GRCm39) |
splice site |
probably benign |
|
R0025:Scn4a
|
UTSW |
11 |
106,215,386 (GRCm39) |
missense |
probably benign |
0.39 |
R0050:Scn4a
|
UTSW |
11 |
106,211,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R0113:Scn4a
|
UTSW |
11 |
106,236,262 (GRCm39) |
missense |
probably benign |
0.00 |
R0193:Scn4a
|
UTSW |
11 |
106,211,364 (GRCm39) |
nonsense |
probably null |
|
R0410:Scn4a
|
UTSW |
11 |
106,214,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R0512:Scn4a
|
UTSW |
11 |
106,236,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R0532:Scn4a
|
UTSW |
11 |
106,221,226 (GRCm39) |
missense |
probably benign |
0.45 |
R1112:Scn4a
|
UTSW |
11 |
106,211,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R1279:Scn4a
|
UTSW |
11 |
106,226,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R1564:Scn4a
|
UTSW |
11 |
106,236,367 (GRCm39) |
missense |
probably benign |
|
R1712:Scn4a
|
UTSW |
11 |
106,236,373 (GRCm39) |
missense |
probably benign |
0.20 |
R1712:Scn4a
|
UTSW |
11 |
106,230,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Scn4a
|
UTSW |
11 |
106,211,646 (GRCm39) |
missense |
probably benign |
0.31 |
R1900:Scn4a
|
UTSW |
11 |
106,218,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R2057:Scn4a
|
UTSW |
11 |
106,226,550 (GRCm39) |
missense |
probably damaging |
0.97 |
R2209:Scn4a
|
UTSW |
11 |
106,230,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R3416:Scn4a
|
UTSW |
11 |
106,221,239 (GRCm39) |
missense |
probably benign |
0.00 |
R3788:Scn4a
|
UTSW |
11 |
106,235,100 (GRCm39) |
missense |
probably damaging |
0.96 |
R3853:Scn4a
|
UTSW |
11 |
106,210,932 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3861:Scn4a
|
UTSW |
11 |
106,216,950 (GRCm39) |
splice site |
probably benign |
|
R3912:Scn4a
|
UTSW |
11 |
106,211,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R3983:Scn4a
|
UTSW |
11 |
106,238,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R4036:Scn4a
|
UTSW |
11 |
106,212,883 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4358:Scn4a
|
UTSW |
11 |
106,239,683 (GRCm39) |
splice site |
probably null |
|
R4556:Scn4a
|
UTSW |
11 |
106,211,272 (GRCm39) |
missense |
probably benign |
0.32 |
R4677:Scn4a
|
UTSW |
11 |
106,214,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R4863:Scn4a
|
UTSW |
11 |
106,210,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R4924:Scn4a
|
UTSW |
11 |
106,210,914 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5081:Scn4a
|
UTSW |
11 |
106,239,553 (GRCm39) |
missense |
probably damaging |
0.99 |
R5298:Scn4a
|
UTSW |
11 |
106,230,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5407:Scn4a
|
UTSW |
11 |
106,211,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R5634:Scn4a
|
UTSW |
11 |
106,220,830 (GRCm39) |
missense |
probably benign |
|
R6381:Scn4a
|
UTSW |
11 |
106,211,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R6468:Scn4a
|
UTSW |
11 |
106,236,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R6489:Scn4a
|
UTSW |
11 |
106,240,006 (GRCm39) |
missense |
probably benign |
0.26 |
R6549:Scn4a
|
UTSW |
11 |
106,234,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R6606:Scn4a
|
UTSW |
11 |
106,218,899 (GRCm39) |
missense |
probably benign |
0.39 |
R7037:Scn4a
|
UTSW |
11 |
106,211,726 (GRCm39) |
missense |
probably damaging |
0.98 |
R7064:Scn4a
|
UTSW |
11 |
106,212,983 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7182:Scn4a
|
UTSW |
11 |
106,221,134 (GRCm39) |
missense |
probably benign |
0.21 |
R7194:Scn4a
|
UTSW |
11 |
106,215,062 (GRCm39) |
missense |
probably benign |
0.32 |
R7531:Scn4a
|
UTSW |
11 |
106,239,523 (GRCm39) |
splice site |
probably null |
|
R7552:Scn4a
|
UTSW |
11 |
106,239,995 (GRCm39) |
missense |
probably benign |
0.22 |
R7570:Scn4a
|
UTSW |
11 |
106,211,299 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7635:Scn4a
|
UTSW |
11 |
106,215,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R7823:Scn4a
|
UTSW |
11 |
106,233,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7832:Scn4a
|
UTSW |
11 |
106,212,841 (GRCm39) |
missense |
probably benign |
0.01 |
R7927:Scn4a
|
UTSW |
11 |
106,233,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Scn4a
|
UTSW |
11 |
106,221,157 (GRCm39) |
missense |
probably benign |
0.02 |
R8131:Scn4a
|
UTSW |
11 |
106,232,367 (GRCm39) |
missense |
probably benign |
|
R9093:Scn4a
|
UTSW |
11 |
106,210,638 (GRCm39) |
missense |
probably benign |
|
R9099:Scn4a
|
UTSW |
11 |
106,211,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R9137:Scn4a
|
UTSW |
11 |
106,214,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R9163:Scn4a
|
UTSW |
11 |
106,217,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R9255:Scn4a
|
UTSW |
11 |
106,215,054 (GRCm39) |
missense |
probably damaging |
0.99 |
R9627:Scn4a
|
UTSW |
11 |
106,212,839 (GRCm39) |
missense |
probably benign |
|
R9780:Scn4a
|
UTSW |
11 |
106,226,235 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Scn4a
|
UTSW |
11 |
106,220,887 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Scn4a
|
UTSW |
11 |
106,213,004 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Scn4a
|
UTSW |
11 |
106,232,356 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Scn4a
|
UTSW |
11 |
106,232,355 (GRCm39) |
missense |
probably benign |
0.26 |
Z1176:Scn4a
|
UTSW |
11 |
106,212,734 (GRCm39) |
missense |
probably null |
0.29 |
Z1177:Scn4a
|
UTSW |
11 |
106,232,368 (GRCm39) |
missense |
probably benign |
|
Z1177:Scn4a
|
UTSW |
11 |
106,221,034 (GRCm39) |
missense |
not run |
|
|