Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930474N05Rik |
A |
T |
14: 35,818,657 (GRCm39) |
K218N |
probably benign |
Het |
Acot11 |
T |
C |
4: 106,619,652 (GRCm39) |
E156G |
probably benign |
Het |
Arhgef28 |
A |
T |
13: 98,094,224 (GRCm39) |
N973K |
probably damaging |
Het |
B4galt3 |
T |
C |
1: 171,101,821 (GRCm39) |
|
probably benign |
Het |
Bmpr1a |
T |
C |
14: 34,165,769 (GRCm39) |
|
probably benign |
Het |
Camkmt |
A |
T |
17: 85,702,087 (GRCm39) |
I184F |
probably benign |
Het |
Ccdc33 |
T |
C |
9: 58,024,737 (GRCm39) |
Y163C |
probably damaging |
Het |
Ccdc9 |
A |
G |
7: 16,014,701 (GRCm39) |
|
probably benign |
Het |
Dars2 |
A |
T |
1: 160,888,318 (GRCm39) |
C201S |
possibly damaging |
Het |
Dnajc1 |
A |
T |
2: 18,312,767 (GRCm39) |
S194R |
possibly damaging |
Het |
Dock8 |
A |
G |
19: 25,148,941 (GRCm39) |
D1473G |
probably benign |
Het |
Dpm2 |
T |
A |
2: 32,462,961 (GRCm39) |
|
probably null |
Het |
Dsg4 |
T |
C |
18: 20,591,628 (GRCm39) |
S456P |
probably damaging |
Het |
Gys1 |
T |
C |
7: 45,089,425 (GRCm39) |
S195P |
probably damaging |
Het |
Heatr6 |
G |
T |
11: 83,670,290 (GRCm39) |
E948* |
probably null |
Het |
Itgal |
G |
A |
7: 126,910,445 (GRCm39) |
R518Q |
possibly damaging |
Het |
Klhdc8b |
G |
C |
9: 108,326,422 (GRCm39) |
R158G |
possibly damaging |
Het |
Klhl41 |
G |
A |
2: 69,500,554 (GRCm39) |
R5Q |
probably benign |
Het |
Lrrtm4 |
A |
T |
6: 79,999,103 (GRCm39) |
T172S |
probably benign |
Het |
Lypd1 |
A |
G |
1: 125,840,604 (GRCm39) |
|
probably benign |
Het |
Mei1 |
T |
C |
15: 81,975,562 (GRCm39) |
F121S |
possibly damaging |
Het |
Mtor |
C |
T |
4: 148,622,817 (GRCm39) |
R1966W |
probably damaging |
Het |
Nebl |
G |
T |
2: 17,409,026 (GRCm39) |
D392E |
possibly damaging |
Het |
Notch2 |
C |
A |
3: 98,024,057 (GRCm39) |
N840K |
possibly damaging |
Het |
Nubp1 |
T |
C |
16: 10,240,678 (GRCm39) |
|
probably benign |
Het |
Or5w16 |
A |
T |
2: 87,577,017 (GRCm39) |
Q159L |
probably benign |
Het |
Or7g19 |
T |
C |
9: 18,856,444 (GRCm39) |
S167P |
probably damaging |
Het |
Pcdh17 |
T |
A |
14: 84,684,897 (GRCm39) |
S455T |
probably damaging |
Het |
Picalm |
C |
A |
7: 89,779,876 (GRCm39) |
H32Q |
probably benign |
Het |
Pold1 |
T |
C |
7: 44,184,516 (GRCm39) |
E828G |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rala |
A |
T |
13: 18,063,233 (GRCm39) |
N119K |
probably benign |
Het |
Rasal2 |
A |
T |
1: 156,975,362 (GRCm39) |
V1149E |
possibly damaging |
Het |
Rd3 |
A |
G |
1: 191,715,501 (GRCm39) |
Y92C |
probably damaging |
Het |
Rps18-ps6 |
A |
T |
13: 97,897,071 (GRCm39) |
F9Y |
probably benign |
Het |
Sart1 |
A |
T |
19: 5,431,752 (GRCm39) |
D635E |
probably damaging |
Het |
Sec16b |
A |
G |
1: 157,365,116 (GRCm39) |
T335A |
possibly damaging |
Het |
Slc11a2 |
C |
T |
15: 100,303,679 (GRCm39) |
G185R |
probably damaging |
Het |
Slc2a12 |
G |
A |
10: 22,540,967 (GRCm39) |
R274H |
probably damaging |
Het |
Spag17 |
T |
C |
3: 100,032,618 (GRCm39) |
V2276A |
probably damaging |
Het |
Tcam1 |
G |
A |
11: 106,174,904 (GRCm39) |
E120K |
probably benign |
Het |
Tenm2 |
T |
C |
11: 36,054,557 (GRCm39) |
D601G |
probably damaging |
Het |
Tmem168 |
C |
A |
6: 13,603,360 (GRCm39) |
C2F |
probably damaging |
Het |
Tmem80 |
A |
G |
7: 140,913,609 (GRCm39) |
Y13C |
probably damaging |
Het |
Try4 |
T |
A |
6: 41,281,296 (GRCm39) |
N79K |
probably benign |
Het |
Vldlr |
C |
A |
19: 27,225,318 (GRCm39) |
N798K |
probably damaging |
Het |
Wdr41 |
A |
G |
13: 95,131,813 (GRCm39) |
|
probably benign |
Het |
Zfp30 |
A |
T |
7: 29,492,160 (GRCm39) |
E138V |
probably damaging |
Het |
Zfp366 |
A |
C |
13: 99,365,786 (GRCm39) |
T316P |
probably damaging |
Het |
Zfp563 |
A |
T |
17: 33,323,659 (GRCm39) |
S85C |
possibly damaging |
Het |
Znfx1 |
T |
C |
2: 166,883,621 (GRCm39) |
H162R |
probably damaging |
Het |
|
Other mutations in Myh7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Myh7
|
APN |
14 |
55,224,845 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01025:Myh7
|
APN |
14 |
55,216,994 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01092:Myh7
|
APN |
14 |
55,209,089 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01384:Myh7
|
APN |
14 |
55,208,916 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Myh7
|
APN |
14 |
55,226,336 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01671:Myh7
|
APN |
14 |
55,210,381 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01923:Myh7
|
APN |
14 |
55,222,916 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02183:Myh7
|
APN |
14 |
55,212,188 (GRCm39) |
missense |
probably benign |
|
IGL02379:Myh7
|
APN |
14 |
55,216,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02884:Myh7
|
APN |
14 |
55,230,276 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02898:Myh7
|
APN |
14 |
55,221,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Myh7
|
APN |
14 |
55,221,007 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03061:Myh7
|
APN |
14 |
55,228,661 (GRCm39) |
unclassified |
probably benign |
|
IGL03145:Myh7
|
APN |
14 |
55,220,802 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03250:Myh7
|
APN |
14 |
55,229,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03394:Myh7
|
APN |
14 |
55,212,818 (GRCm39) |
missense |
probably damaging |
1.00 |
BB008:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
BB018:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0019:Myh7
|
UTSW |
14 |
55,221,191 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0030:Myh7
|
UTSW |
14 |
55,229,427 (GRCm39) |
missense |
probably benign |
0.00 |
R0183:Myh7
|
UTSW |
14 |
55,216,333 (GRCm39) |
missense |
probably benign |
0.02 |
R0230:Myh7
|
UTSW |
14 |
55,211,390 (GRCm39) |
missense |
probably benign |
0.03 |
R0295:Myh7
|
UTSW |
14 |
55,222,278 (GRCm39) |
splice site |
probably benign |
|
R0423:Myh7
|
UTSW |
14 |
55,216,646 (GRCm39) |
missense |
probably benign |
0.06 |
R0541:Myh7
|
UTSW |
14 |
55,212,158 (GRCm39) |
missense |
probably benign |
|
R0581:Myh7
|
UTSW |
14 |
55,222,953 (GRCm39) |
missense |
probably benign |
0.02 |
R0786:Myh7
|
UTSW |
14 |
55,230,330 (GRCm39) |
start codon destroyed |
probably null |
|
R0866:Myh7
|
UTSW |
14 |
55,210,596 (GRCm39) |
missense |
probably benign |
|
R1068:Myh7
|
UTSW |
14 |
55,224,776 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1075:Myh7
|
UTSW |
14 |
55,224,860 (GRCm39) |
missense |
probably benign |
|
R1124:Myh7
|
UTSW |
14 |
55,211,327 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1140:Myh7
|
UTSW |
14 |
55,210,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1260:Myh7
|
UTSW |
14 |
55,225,908 (GRCm39) |
missense |
probably benign |
0.00 |
R1653:Myh7
|
UTSW |
14 |
55,228,246 (GRCm39) |
missense |
probably benign |
0.00 |
R1677:Myh7
|
UTSW |
14 |
55,224,973 (GRCm39) |
missense |
probably benign |
0.17 |
R1760:Myh7
|
UTSW |
14 |
55,210,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1838:Myh7
|
UTSW |
14 |
55,210,637 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1839:Myh7
|
UTSW |
14 |
55,210,637 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2483:Myh7
|
UTSW |
14 |
55,210,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R2566:Myh7
|
UTSW |
14 |
55,220,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R3623:Myh7
|
UTSW |
14 |
55,210,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R3916:Myh7
|
UTSW |
14 |
55,211,503 (GRCm39) |
missense |
probably damaging |
0.97 |
R4236:Myh7
|
UTSW |
14 |
55,228,575 (GRCm39) |
missense |
probably benign |
0.34 |
R4471:Myh7
|
UTSW |
14 |
55,229,311 (GRCm39) |
nonsense |
probably null |
|
R4700:Myh7
|
UTSW |
14 |
55,225,778 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4805:Myh7
|
UTSW |
14 |
55,222,590 (GRCm39) |
missense |
probably benign |
0.27 |
R4880:Myh7
|
UTSW |
14 |
55,216,045 (GRCm39) |
missense |
probably benign |
0.18 |
R4975:Myh7
|
UTSW |
14 |
55,209,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R4982:Myh7
|
UTSW |
14 |
55,210,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R5004:Myh7
|
UTSW |
14 |
55,209,140 (GRCm39) |
missense |
probably damaging |
0.99 |
R5107:Myh7
|
UTSW |
14 |
55,223,881 (GRCm39) |
intron |
probably benign |
|
R5124:Myh7
|
UTSW |
14 |
55,223,199 (GRCm39) |
nonsense |
probably null |
|
R5256:Myh7
|
UTSW |
14 |
55,216,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R5335:Myh7
|
UTSW |
14 |
55,224,020 (GRCm39) |
intron |
probably benign |
|
R5581:Myh7
|
UTSW |
14 |
55,216,411 (GRCm39) |
missense |
probably benign |
0.00 |
R5861:Myh7
|
UTSW |
14 |
55,226,347 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5957:Myh7
|
UTSW |
14 |
55,226,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Myh7
|
UTSW |
14 |
55,208,259 (GRCm39) |
missense |
probably benign |
0.01 |
R6184:Myh7
|
UTSW |
14 |
55,226,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R6232:Myh7
|
UTSW |
14 |
55,226,753 (GRCm39) |
missense |
probably benign |
0.00 |
R6268:Myh7
|
UTSW |
14 |
55,226,741 (GRCm39) |
missense |
probably benign |
0.00 |
R6274:Myh7
|
UTSW |
14 |
55,216,943 (GRCm39) |
missense |
probably damaging |
0.97 |
R6345:Myh7
|
UTSW |
14 |
55,221,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Myh7
|
UTSW |
14 |
55,226,351 (GRCm39) |
missense |
probably benign |
0.00 |
R6641:Myh7
|
UTSW |
14 |
55,219,737 (GRCm39) |
missense |
probably benign |
0.37 |
R6755:Myh7
|
UTSW |
14 |
55,229,770 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6952:Myh7
|
UTSW |
14 |
55,229,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7025:Myh7
|
UTSW |
14 |
55,212,101 (GRCm39) |
nonsense |
probably null |
|
R7201:Myh7
|
UTSW |
14 |
55,228,402 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7257:Myh7
|
UTSW |
14 |
55,209,947 (GRCm39) |
splice site |
probably null |
|
R7296:Myh7
|
UTSW |
14 |
55,227,482 (GRCm39) |
missense |
probably benign |
0.05 |
R7709:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7710:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7817:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7858:Myh7
|
UTSW |
14 |
55,227,500 (GRCm39) |
missense |
probably benign |
0.09 |
R7869:Myh7
|
UTSW |
14 |
55,226,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R7870:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7887:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7931:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7936:Myh7
|
UTSW |
14 |
55,216,920 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8056:Myh7
|
UTSW |
14 |
55,210,776 (GRCm39) |
nonsense |
probably null |
|
R8061:Myh7
|
UTSW |
14 |
55,228,398 (GRCm39) |
missense |
probably benign |
|
R8101:Myh7
|
UTSW |
14 |
55,210,776 (GRCm39) |
nonsense |
probably null |
|
R8202:Myh7
|
UTSW |
14 |
55,227,497 (GRCm39) |
missense |
probably benign |
|
R8504:Myh7
|
UTSW |
14 |
55,227,786 (GRCm39) |
missense |
probably damaging |
0.98 |
R8560:Myh7
|
UTSW |
14 |
55,213,405 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8843:Myh7
|
UTSW |
14 |
55,212,752 (GRCm39) |
missense |
probably damaging |
0.98 |
R8903:Myh7
|
UTSW |
14 |
55,230,228 (GRCm39) |
nonsense |
probably null |
|
R8926:Myh7
|
UTSW |
14 |
55,222,533 (GRCm39) |
missense |
probably benign |
0.33 |
R8936:Myh7
|
UTSW |
14 |
55,228,440 (GRCm39) |
missense |
probably benign |
0.00 |
R9182:Myh7
|
UTSW |
14 |
55,226,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R9260:Myh7
|
UTSW |
14 |
55,224,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R9264:Myh7
|
UTSW |
14 |
55,213,454 (GRCm39) |
missense |
probably benign |
0.01 |
R9288:Myh7
|
UTSW |
14 |
55,222,932 (GRCm39) |
missense |
probably benign |
0.35 |
R9362:Myh7
|
UTSW |
14 |
55,222,932 (GRCm39) |
missense |
probably benign |
0.00 |
R9497:Myh7
|
UTSW |
14 |
55,217,841 (GRCm39) |
missense |
probably benign |
0.12 |
R9561:Myh7
|
UTSW |
14 |
55,216,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R9663:Myh7
|
UTSW |
14 |
55,221,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R9789:Myh7
|
UTSW |
14 |
55,229,384 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1192:Myh7
|
UTSW |
14 |
55,220,748 (GRCm39) |
missense |
probably damaging |
0.99 |
|