Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn4 |
C |
T |
7: 28,610,995 (GRCm39) |
V248M |
possibly damaging |
Het |
AW209491 |
A |
T |
13: 14,812,328 (GRCm39) |
I394F |
probably benign |
Het |
Cacna1d |
A |
T |
14: 29,796,967 (GRCm39) |
|
probably benign |
Het |
Cacna1i |
A |
T |
15: 80,265,373 (GRCm39) |
I1542F |
probably damaging |
Het |
Cep97 |
A |
T |
16: 55,735,924 (GRCm39) |
N291K |
possibly damaging |
Het |
Clasp2 |
A |
T |
9: 113,689,209 (GRCm39) |
|
probably benign |
Het |
Dennd1c |
T |
C |
17: 57,382,465 (GRCm39) |
Q67R |
probably damaging |
Het |
Eva1c |
A |
T |
16: 90,663,305 (GRCm39) |
D13V |
possibly damaging |
Het |
Fam151b |
T |
C |
13: 92,610,504 (GRCm39) |
K95R |
probably benign |
Het |
Gm13941 |
T |
C |
2: 110,889,761 (GRCm39) |
|
noncoding transcript |
Het |
Gps2 |
C |
T |
11: 69,805,607 (GRCm39) |
Q42* |
probably null |
Het |
Hivep1 |
T |
A |
13: 42,312,132 (GRCm39) |
D1457E |
probably benign |
Het |
L3mbtl1 |
A |
G |
2: 162,790,748 (GRCm39) |
K225E |
probably damaging |
Het |
Limch1 |
A |
G |
5: 67,131,965 (GRCm39) |
S143G |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,369,041 (GRCm39) |
K342E |
possibly damaging |
Het |
Mc5r |
T |
G |
18: 68,472,637 (GRCm39) |
M332R |
probably damaging |
Het |
Mcf2l |
A |
G |
8: 13,063,060 (GRCm39) |
T882A |
probably benign |
Het |
Mtrex |
C |
T |
13: 113,023,396 (GRCm39) |
V727I |
probably benign |
Het |
Plekha5 |
C |
T |
6: 140,470,629 (GRCm39) |
T90I |
probably damaging |
Het |
Ptbp2 |
T |
C |
3: 119,514,290 (GRCm39) |
T478A |
probably benign |
Het |
Rasgrp1 |
C |
A |
2: 117,125,301 (GRCm39) |
R246S |
probably damaging |
Het |
Rflnb |
A |
T |
11: 75,912,987 (GRCm39) |
S134T |
possibly damaging |
Het |
Rnf214 |
A |
G |
9: 45,778,796 (GRCm39) |
|
probably null |
Het |
Satb1 |
T |
C |
17: 52,111,364 (GRCm39) |
T165A |
probably damaging |
Het |
Scamp1 |
T |
C |
13: 94,340,658 (GRCm39) |
Y237C |
probably damaging |
Het |
Skint10 |
A |
T |
4: 112,568,753 (GRCm39) |
F321L |
probably benign |
Het |
Slc8a1 |
A |
G |
17: 81,745,188 (GRCm39) |
V672A |
probably benign |
Het |
Spats2 |
C |
A |
15: 99,110,168 (GRCm39) |
P522T |
possibly damaging |
Het |
Stkld1 |
A |
T |
2: 26,839,352 (GRCm39) |
E339D |
probably benign |
Het |
Tbc1d9 |
A |
G |
8: 83,960,872 (GRCm39) |
T241A |
probably damaging |
Het |
Ticrr |
A |
T |
7: 79,327,158 (GRCm39) |
D622V |
probably damaging |
Het |
Trmt1l |
T |
C |
1: 151,324,131 (GRCm39) |
V326A |
probably benign |
Het |
Ube3c |
A |
G |
5: 29,803,936 (GRCm39) |
T180A |
possibly damaging |
Het |
Unc13a |
A |
C |
8: 72,087,302 (GRCm39) |
F1482V |
probably damaging |
Het |
Unc79 |
A |
G |
12: 103,025,777 (GRCm39) |
E388G |
probably damaging |
Het |
Ush2a |
A |
T |
1: 188,697,043 (GRCm39) |
D5167V |
probably damaging |
Het |
Vmn2r93 |
A |
T |
17: 18,546,672 (GRCm39) |
H848L |
probably benign |
Het |
Zcchc9 |
T |
C |
13: 91,945,368 (GRCm39) |
I72V |
probably benign |
Het |
Zfc3h1 |
G |
T |
10: 115,259,379 (GRCm39) |
L1650F |
possibly damaging |
Het |
Zzz3 |
A |
G |
3: 152,134,040 (GRCm39) |
D366G |
possibly damaging |
Het |
|
Other mutations in Myf6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01138:Myf6
|
APN |
10 |
107,330,259 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03131:Myf6
|
APN |
10 |
107,330,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R0067:Myf6
|
UTSW |
10 |
107,329,340 (GRCm39) |
splice site |
probably null |
|
R0562:Myf6
|
UTSW |
10 |
107,330,420 (GRCm39) |
missense |
probably benign |
0.45 |
R1635:Myf6
|
UTSW |
10 |
107,330,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R1700:Myf6
|
UTSW |
10 |
107,329,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R4361:Myf6
|
UTSW |
10 |
107,330,293 (GRCm39) |
small deletion |
probably benign |
|
R4686:Myf6
|
UTSW |
10 |
107,329,689 (GRCm39) |
missense |
probably benign |
|
R5601:Myf6
|
UTSW |
10 |
107,330,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R6229:Myf6
|
UTSW |
10 |
107,330,280 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6705:Myf6
|
UTSW |
10 |
107,329,690 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7024:Myf6
|
UTSW |
10 |
107,330,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R9041:Myf6
|
UTSW |
10 |
107,329,225 (GRCm39) |
missense |
probably benign |
|
R9180:Myf6
|
UTSW |
10 |
107,329,318 (GRCm39) |
missense |
probably benign |
0.38 |
R9487:Myf6
|
UTSW |
10 |
107,330,073 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Myf6
|
UTSW |
10 |
107,330,121 (GRCm39) |
missense |
probably benign |
0.08 |
|