Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accsl |
A |
T |
2: 93,696,589 (GRCm39) |
|
probably benign |
Het |
Adam30 |
G |
A |
3: 98,070,222 (GRCm39) |
S685N |
probably benign |
Het |
Adamts12 |
T |
C |
15: 11,071,843 (GRCm39) |
V129A |
probably benign |
Het |
Agxt2 |
T |
C |
15: 10,373,837 (GRCm39) |
F81S |
probably damaging |
Het |
Ahnak2 |
A |
T |
12: 112,749,409 (GRCm39) |
I186N |
probably damaging |
Het |
Amz1 |
A |
T |
5: 140,737,691 (GRCm39) |
|
probably null |
Het |
Anapc5 |
G |
A |
5: 122,926,481 (GRCm39) |
A619V |
possibly damaging |
Het |
Aoc1l3 |
C |
A |
6: 48,967,173 (GRCm39) |
P707H |
probably damaging |
Het |
Bbox1 |
T |
C |
2: 110,095,956 (GRCm39) |
D336G |
probably damaging |
Het |
Bivm |
A |
G |
1: 44,165,942 (GRCm39) |
T131A |
probably benign |
Het |
Bpi |
A |
T |
2: 158,109,660 (GRCm39) |
I203F |
probably benign |
Het |
Cd151 |
A |
C |
7: 141,050,569 (GRCm39) |
T241P |
probably damaging |
Het |
Cdh20 |
G |
A |
1: 109,988,862 (GRCm39) |
V255I |
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,148,171 (GRCm39) |
|
probably benign |
Het |
Cul9 |
C |
G |
17: 46,833,101 (GRCm39) |
A1326P |
probably damaging |
Het |
Dclre1b |
A |
C |
3: 103,711,192 (GRCm39) |
S240A |
probably benign |
Het |
Ddc |
A |
C |
11: 11,796,634 (GRCm39) |
|
probably null |
Het |
Dkk1 |
T |
C |
19: 30,524,650 (GRCm39) |
R252G |
probably damaging |
Het |
Dmrtc2 |
T |
A |
7: 24,573,738 (GRCm39) |
M191K |
possibly damaging |
Het |
Eml6 |
A |
G |
11: 29,699,824 (GRCm39) |
S1771P |
possibly damaging |
Het |
Emx1 |
T |
C |
6: 85,165,353 (GRCm39) |
|
probably benign |
Het |
Fah |
T |
C |
7: 84,250,344 (GRCm39) |
M1V |
probably null |
Het |
Fmo6 |
A |
T |
1: 162,753,710 (GRCm39) |
M144K |
probably damaging |
Het |
Frem1 |
A |
G |
4: 82,868,589 (GRCm39) |
V1445A |
probably benign |
Het |
Fsd2 |
T |
C |
7: 81,209,518 (GRCm39) |
D108G |
probably benign |
Het |
Gfm2 |
A |
G |
13: 97,301,708 (GRCm39) |
|
probably null |
Het |
Ghrhr |
T |
A |
6: 55,365,254 (GRCm39) |
L416* |
probably null |
Het |
Glipr1l2 |
C |
A |
10: 111,919,371 (GRCm39) |
L31I |
possibly damaging |
Het |
Gm19965 |
T |
A |
1: 116,748,550 (GRCm39) |
|
probably benign |
Het |
Gpr149 |
A |
G |
3: 62,511,888 (GRCm39) |
L37P |
probably damaging |
Het |
Hoxa9 |
A |
G |
6: 52,202,693 (GRCm39) |
I131T |
probably damaging |
Het |
Htra4 |
T |
C |
8: 25,520,635 (GRCm39) |
D342G |
possibly damaging |
Het |
Idh1 |
G |
T |
1: 65,200,319 (GRCm39) |
N348K |
probably benign |
Het |
Impdh2 |
T |
C |
9: 108,439,028 (GRCm39) |
F99S |
probably benign |
Het |
Kank4 |
T |
C |
4: 98,653,806 (GRCm39) |
Y874C |
probably damaging |
Het |
Kazn |
A |
T |
4: 141,886,349 (GRCm39) |
|
probably benign |
Het |
Kcnq3 |
T |
A |
15: 65,871,891 (GRCm39) |
T593S |
probably benign |
Het |
Magi3 |
A |
G |
3: 103,968,946 (GRCm39) |
|
probably null |
Het |
Map3k19 |
A |
G |
1: 127,751,617 (GRCm39) |
V578A |
probably benign |
Het |
Meox2 |
T |
C |
12: 37,159,151 (GRCm39) |
C108R |
possibly damaging |
Het |
Nlrp9c |
C |
A |
7: 26,079,860 (GRCm39) |
C722F |
probably damaging |
Het |
Or2a5 |
T |
C |
6: 42,874,285 (GRCm39) |
V300A |
probably benign |
Het |
Pde10a |
C |
T |
17: 9,139,378 (GRCm39) |
|
probably benign |
Het |
Ppfia4 |
A |
G |
1: 134,260,021 (GRCm39) |
|
probably benign |
Het |
Psg18 |
T |
C |
7: 18,088,742 (GRCm39) |
M1V |
probably null |
Het |
Qtrt1 |
A |
G |
9: 21,323,782 (GRCm39) |
T136A |
probably benign |
Het |
Retsat |
T |
C |
6: 72,580,634 (GRCm39) |
|
probably benign |
Het |
Rxfp2 |
T |
C |
5: 149,975,021 (GRCm39) |
V210A |
probably benign |
Het |
Sfswap |
G |
A |
5: 129,584,207 (GRCm39) |
|
probably null |
Het |
Slc16a7 |
A |
T |
10: 125,067,241 (GRCm39) |
L133I |
possibly damaging |
Het |
Slc30a3 |
A |
T |
5: 31,244,154 (GRCm39) |
M376K |
probably damaging |
Het |
Spmip4 |
T |
A |
6: 50,566,121 (GRCm39) |
K118M |
probably damaging |
Het |
Srbd1 |
C |
T |
17: 86,405,940 (GRCm39) |
C620Y |
probably null |
Het |
Trip10 |
T |
A |
17: 57,560,363 (GRCm39) |
L100Q |
probably damaging |
Het |
Tyrp1 |
C |
T |
4: 80,763,105 (GRCm39) |
Q331* |
probably null |
Het |
Vangl2 |
G |
T |
1: 171,832,353 (GRCm39) |
T501N |
probably damaging |
Het |
Vdr |
A |
T |
15: 97,767,214 (GRCm39) |
Y185N |
probably benign |
Het |
Vmn1r123 |
C |
T |
7: 20,896,257 (GRCm39) |
P50S |
probably damaging |
Het |
Vmn1r158 |
T |
A |
7: 22,489,870 (GRCm39) |
H113L |
probably benign |
Het |
Vmn2r12 |
A |
T |
5: 109,240,720 (GRCm39) |
I131N |
probably benign |
Het |
Vmn2r72 |
T |
A |
7: 85,401,152 (GRCm39) |
E89V |
probably damaging |
Het |
Xrcc6 |
A |
G |
15: 81,915,364 (GRCm39) |
D94G |
probably damaging |
Het |
Zbtb32 |
T |
A |
7: 30,290,692 (GRCm39) |
E201V |
possibly damaging |
Het |
Zfp185 |
A |
T |
X: 72,042,929 (GRCm39) |
E138D |
possibly damaging |
Het |
Zmynd11 |
T |
A |
13: 9,739,585 (GRCm39) |
H437L |
probably damaging |
Het |
|
Other mutations in Lamc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00950:Lamc1
|
APN |
1 |
153,116,241 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01397:Lamc1
|
APN |
1 |
153,126,880 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01661:Lamc1
|
APN |
1 |
153,097,319 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01894:Lamc1
|
APN |
1 |
153,122,828 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02000:Lamc1
|
APN |
1 |
153,116,179 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02649:Lamc1
|
APN |
1 |
153,122,788 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02749:Lamc1
|
APN |
1 |
153,125,599 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02819:Lamc1
|
APN |
1 |
153,126,407 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02831:Lamc1
|
APN |
1 |
153,122,801 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03069:Lamc1
|
APN |
1 |
153,115,127 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03143:Lamc1
|
APN |
1 |
153,208,020 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03166:Lamc1
|
APN |
1 |
153,208,047 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03285:Lamc1
|
APN |
1 |
153,103,431 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL03294:Lamc1
|
APN |
1 |
153,138,392 (GRCm39) |
missense |
probably damaging |
1.00 |
pride
|
UTSW |
1 |
153,123,030 (GRCm39) |
missense |
probably benign |
0.01 |
Stratum
|
UTSW |
1 |
153,126,870 (GRCm39) |
nonsense |
probably null |
|
tier
|
UTSW |
1 |
153,126,268 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4280001:Lamc1
|
UTSW |
1 |
153,119,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R0003:Lamc1
|
UTSW |
1 |
153,138,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R0003:Lamc1
|
UTSW |
1 |
153,138,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R0027:Lamc1
|
UTSW |
1 |
153,138,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Lamc1
|
UTSW |
1 |
153,117,614 (GRCm39) |
unclassified |
probably benign |
|
R0078:Lamc1
|
UTSW |
1 |
153,104,936 (GRCm39) |
missense |
probably damaging |
0.96 |
R0157:Lamc1
|
UTSW |
1 |
153,138,353 (GRCm39) |
missense |
probably benign |
0.00 |
R0282:Lamc1
|
UTSW |
1 |
153,131,058 (GRCm39) |
missense |
probably benign |
|
R0374:Lamc1
|
UTSW |
1 |
153,126,811 (GRCm39) |
splice site |
probably benign |
|
R0494:Lamc1
|
UTSW |
1 |
153,122,682 (GRCm39) |
critical splice donor site |
probably null |
|
R0502:Lamc1
|
UTSW |
1 |
153,122,678 (GRCm39) |
splice site |
probably benign |
|
R0755:Lamc1
|
UTSW |
1 |
153,123,196 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0791:Lamc1
|
UTSW |
1 |
153,110,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0791:Lamc1
|
UTSW |
1 |
153,110,326 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0791:Lamc1
|
UTSW |
1 |
153,110,358 (GRCm39) |
missense |
probably benign |
0.01 |
R0792:Lamc1
|
UTSW |
1 |
153,110,326 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0792:Lamc1
|
UTSW |
1 |
153,110,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0792:Lamc1
|
UTSW |
1 |
153,110,358 (GRCm39) |
missense |
probably benign |
0.01 |
R0892:Lamc1
|
UTSW |
1 |
153,208,000 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0941:Lamc1
|
UTSW |
1 |
153,208,020 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0961:Lamc1
|
UTSW |
1 |
153,097,446 (GRCm39) |
missense |
probably benign |
0.03 |
R0961:Lamc1
|
UTSW |
1 |
153,097,392 (GRCm39) |
frame shift |
probably null |
|
R0963:Lamc1
|
UTSW |
1 |
153,119,132 (GRCm39) |
missense |
probably benign |
|
R1127:Lamc1
|
UTSW |
1 |
153,126,205 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1175:Lamc1
|
UTSW |
1 |
153,122,977 (GRCm39) |
splice site |
probably benign |
|
R1449:Lamc1
|
UTSW |
1 |
153,126,241 (GRCm39) |
missense |
probably benign |
|
R1481:Lamc1
|
UTSW |
1 |
153,097,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Lamc1
|
UTSW |
1 |
153,118,489 (GRCm39) |
missense |
probably benign |
0.34 |
R1583:Lamc1
|
UTSW |
1 |
153,119,224 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1643:Lamc1
|
UTSW |
1 |
153,133,818 (GRCm39) |
splice site |
probably benign |
|
R1652:Lamc1
|
UTSW |
1 |
153,125,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Lamc1
|
UTSW |
1 |
153,122,995 (GRCm39) |
missense |
probably benign |
0.04 |
R1854:Lamc1
|
UTSW |
1 |
153,125,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R2018:Lamc1
|
UTSW |
1 |
153,118,378 (GRCm39) |
missense |
probably benign |
0.07 |
R2170:Lamc1
|
UTSW |
1 |
153,124,888 (GRCm39) |
missense |
probably benign |
0.07 |
R2410:Lamc1
|
UTSW |
1 |
153,123,141 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3438:Lamc1
|
UTSW |
1 |
153,102,161 (GRCm39) |
missense |
probably benign |
0.04 |
R3615:Lamc1
|
UTSW |
1 |
153,126,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R3616:Lamc1
|
UTSW |
1 |
153,126,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R3699:Lamc1
|
UTSW |
1 |
153,130,951 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3811:Lamc1
|
UTSW |
1 |
153,138,454 (GRCm39) |
splice site |
probably null |
|
R4285:Lamc1
|
UTSW |
1 |
153,110,298 (GRCm39) |
missense |
probably damaging |
0.99 |
R4431:Lamc1
|
UTSW |
1 |
153,097,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R4579:Lamc1
|
UTSW |
1 |
153,123,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R4625:Lamc1
|
UTSW |
1 |
153,118,442 (GRCm39) |
missense |
probably benign |
0.04 |
R4649:Lamc1
|
UTSW |
1 |
153,104,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R4650:Lamc1
|
UTSW |
1 |
153,104,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R4651:Lamc1
|
UTSW |
1 |
153,104,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R4652:Lamc1
|
UTSW |
1 |
153,104,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R4653:Lamc1
|
UTSW |
1 |
153,104,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R4784:Lamc1
|
UTSW |
1 |
153,107,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Lamc1
|
UTSW |
1 |
153,107,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4853:Lamc1
|
UTSW |
1 |
153,104,846 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5216:Lamc1
|
UTSW |
1 |
153,103,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5217:Lamc1
|
UTSW |
1 |
153,103,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5218:Lamc1
|
UTSW |
1 |
153,103,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5219:Lamc1
|
UTSW |
1 |
153,103,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5468:Lamc1
|
UTSW |
1 |
153,109,310 (GRCm39) |
missense |
probably damaging |
0.99 |
R5597:Lamc1
|
UTSW |
1 |
153,127,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R5754:Lamc1
|
UTSW |
1 |
153,123,030 (GRCm39) |
missense |
probably benign |
0.01 |
R6233:Lamc1
|
UTSW |
1 |
153,099,412 (GRCm39) |
missense |
probably benign |
|
R6431:Lamc1
|
UTSW |
1 |
153,097,417 (GRCm39) |
missense |
probably benign |
0.21 |
R6636:Lamc1
|
UTSW |
1 |
153,117,721 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6888:Lamc1
|
UTSW |
1 |
153,138,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R7161:Lamc1
|
UTSW |
1 |
153,102,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R7240:Lamc1
|
UTSW |
1 |
153,110,396 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7388:Lamc1
|
UTSW |
1 |
153,124,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R7474:Lamc1
|
UTSW |
1 |
153,208,011 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7570:Lamc1
|
UTSW |
1 |
153,119,021 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7583:Lamc1
|
UTSW |
1 |
153,118,978 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7597:Lamc1
|
UTSW |
1 |
153,116,200 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7635:Lamc1
|
UTSW |
1 |
153,124,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R7976:Lamc1
|
UTSW |
1 |
153,123,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Lamc1
|
UTSW |
1 |
153,097,358 (GRCm39) |
missense |
probably benign |
0.04 |
R8207:Lamc1
|
UTSW |
1 |
153,126,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R8219:Lamc1
|
UTSW |
1 |
153,123,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R8227:Lamc1
|
UTSW |
1 |
153,099,500 (GRCm39) |
missense |
probably benign |
0.04 |
R8315:Lamc1
|
UTSW |
1 |
153,119,167 (GRCm39) |
missense |
probably benign |
0.00 |
R8417:Lamc1
|
UTSW |
1 |
153,106,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R8685:Lamc1
|
UTSW |
1 |
153,109,288 (GRCm39) |
missense |
probably benign |
0.31 |
R8827:Lamc1
|
UTSW |
1 |
153,097,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R8995:Lamc1
|
UTSW |
1 |
153,207,993 (GRCm39) |
missense |
probably benign |
0.00 |
R9061:Lamc1
|
UTSW |
1 |
153,126,870 (GRCm39) |
nonsense |
probably null |
|
R9141:Lamc1
|
UTSW |
1 |
153,123,196 (GRCm39) |
missense |
probably benign |
0.01 |
R9187:Lamc1
|
UTSW |
1 |
153,097,434 (GRCm39) |
nonsense |
probably null |
|
R9206:Lamc1
|
UTSW |
1 |
153,126,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R9222:Lamc1
|
UTSW |
1 |
153,119,087 (GRCm39) |
missense |
probably damaging |
0.96 |
R9297:Lamc1
|
UTSW |
1 |
153,127,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Lamc1
|
UTSW |
1 |
153,127,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Lamc1
|
UTSW |
1 |
153,115,009 (GRCm39) |
missense |
probably benign |
|
|