Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
T |
A |
11: 23,468,066 (GRCm39) |
M76L |
probably benign |
Het |
Adrm1b |
T |
A |
3: 92,336,112 (GRCm39) |
|
probably benign |
Het |
Alg1 |
T |
A |
16: 5,053,086 (GRCm39) |
W116R |
probably benign |
Het |
Ano3 |
A |
T |
2: 110,715,340 (GRCm39) |
S33T |
probably damaging |
Het |
Atp2b2 |
T |
C |
6: 113,751,400 (GRCm39) |
E556G |
possibly damaging |
Het |
Brca2 |
T |
A |
5: 150,480,597 (GRCm39) |
I2761K |
possibly damaging |
Het |
Ccdc68 |
G |
A |
18: 70,079,577 (GRCm39) |
G141E |
probably benign |
Het |
Cckbr |
T |
C |
7: 105,083,732 (GRCm39) |
V220A |
probably damaging |
Het |
Ccnd3 |
G |
A |
17: 47,909,544 (GRCm39) |
R45Q |
probably damaging |
Het |
Cdh24 |
G |
T |
14: 54,874,832 (GRCm39) |
T391N |
probably damaging |
Het |
Cldn11 |
A |
G |
3: 31,204,395 (GRCm39) |
T33A |
probably damaging |
Het |
Clec2e |
T |
A |
6: 129,075,391 (GRCm39) |
Y50F |
probably benign |
Het |
Cntnap1 |
A |
G |
11: 101,075,944 (GRCm39) |
N943D |
probably benign |
Het |
Cspg4b |
A |
G |
13: 113,454,484 (GRCm39) |
R177G |
possibly damaging |
Het |
Dmgdh |
T |
C |
13: 93,813,665 (GRCm39) |
V70A |
probably damaging |
Het |
Gm14496 |
C |
A |
2: 181,637,674 (GRCm39) |
Y249* |
probably null |
Het |
Gmnc |
T |
A |
16: 26,781,714 (GRCm39) |
H105L |
probably damaging |
Het |
Gpt2 |
A |
G |
8: 86,219,740 (GRCm39) |
Y62C |
probably damaging |
Het |
Ift80 |
T |
C |
3: 68,838,233 (GRCm39) |
R413G |
probably damaging |
Het |
Kctd16 |
C |
A |
18: 40,392,061 (GRCm39) |
D216E |
probably damaging |
Het |
Kif26b |
T |
C |
1: 178,743,864 (GRCm39) |
V873A |
probably benign |
Het |
Klra4 |
G |
T |
6: 130,039,117 (GRCm39) |
Q92K |
probably benign |
Het |
L1td1 |
C |
A |
4: 98,626,341 (GRCm39) |
N845K |
possibly damaging |
Het |
Loxhd1 |
T |
C |
18: 77,429,751 (GRCm39) |
I230T |
possibly damaging |
Het |
Lsg1 |
T |
C |
16: 30,399,819 (GRCm39) |
N160S |
probably damaging |
Het |
Lyzl4 |
G |
A |
9: 121,413,469 (GRCm39) |
R24C |
probably damaging |
Het |
Mib1 |
A |
G |
18: 10,794,488 (GRCm39) |
N658S |
probably benign |
Het |
Mmp8 |
T |
C |
9: 7,566,275 (GRCm39) |
I377T |
probably damaging |
Het |
Mtmr14 |
T |
C |
6: 113,238,243 (GRCm39) |
|
probably null |
Het |
Myo1c |
A |
G |
11: 75,548,414 (GRCm39) |
T58A |
possibly damaging |
Het |
Myo9a |
C |
T |
9: 59,802,527 (GRCm39) |
Q2005* |
probably null |
Het |
Neu3 |
G |
T |
7: 99,472,636 (GRCm39) |
P34T |
probably benign |
Het |
Nlrp4b |
G |
A |
7: 10,449,512 (GRCm39) |
V205I |
probably benign |
Het |
Or4b1b |
C |
T |
2: 90,112,313 (GRCm39) |
G202D |
probably damaging |
Het |
Or4k38 |
T |
C |
2: 111,165,850 (GRCm39) |
N191S |
possibly damaging |
Het |
Or5h23 |
A |
T |
16: 58,906,334 (GRCm39) |
S171T |
probably benign |
Het |
Or5t15 |
A |
G |
2: 86,681,118 (GRCm39) |
I308T |
unknown |
Het |
Or6c66 |
T |
G |
10: 129,461,319 (GRCm39) |
T204P |
probably damaging |
Het |
Or9m1 |
T |
C |
2: 87,733,691 (GRCm39) |
T110A |
probably benign |
Het |
Pcsk6 |
T |
C |
7: 65,578,933 (GRCm39) |
|
probably null |
Het |
Pik3c2a |
A |
G |
7: 116,016,893 (GRCm39) |
V288A |
probably benign |
Het |
Plcd3 |
T |
C |
11: 102,968,629 (GRCm39) |
D354G |
probably benign |
Het |
Prkdc |
C |
A |
16: 15,524,655 (GRCm39) |
N1219K |
probably benign |
Het |
Prl3d1 |
T |
A |
13: 27,278,927 (GRCm39) |
Y41N |
probably damaging |
Het |
Qrich2 |
C |
T |
11: 116,332,234 (GRCm39) |
G2321R |
probably damaging |
Het |
Rrbp1 |
T |
C |
2: 143,831,886 (GRCm39) |
I94V |
probably benign |
Het |
Serinc1 |
C |
A |
10: 57,399,262 (GRCm39) |
V214L |
probably benign |
Het |
Serpina9 |
G |
T |
12: 103,967,728 (GRCm39) |
N222K |
probably benign |
Het |
Smchd1 |
A |
G |
17: 71,747,956 (GRCm39) |
Y429H |
probably damaging |
Het |
Smyd1 |
C |
T |
6: 71,239,164 (GRCm39) |
V9M |
probably damaging |
Het |
Sostdc1 |
C |
T |
12: 36,367,246 (GRCm39) |
Q141* |
probably null |
Het |
Spam1 |
C |
T |
6: 24,796,109 (GRCm39) |
T20I |
probably benign |
Het |
Tex47 |
T |
C |
5: 7,354,834 (GRCm39) |
V5A |
probably benign |
Het |
Thbs4 |
T |
C |
13: 92,912,582 (GRCm39) |
|
probably null |
Het |
Trim45 |
C |
T |
3: 100,837,257 (GRCm39) |
P531L |
probably damaging |
Het |
Tshb |
A |
T |
3: 102,685,478 (GRCm39) |
Y50* |
probably null |
Het |
Ttn |
T |
C |
2: 76,599,320 (GRCm39) |
I19230V |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Uba6 |
G |
A |
5: 86,270,288 (GRCm39) |
T832I |
probably damaging |
Het |
Unc13d |
A |
T |
11: 115,960,579 (GRCm39) |
V497D |
probably damaging |
Het |
Usp13 |
T |
C |
3: 32,892,007 (GRCm39) |
V62A |
probably damaging |
Het |
Vmn1r215 |
A |
C |
13: 23,260,189 (GRCm39) |
L76F |
probably damaging |
Het |
Vmn1r215 |
G |
T |
13: 23,260,190 (GRCm39) |
G77C |
probably damaging |
Het |
Vmn2r5 |
T |
C |
3: 64,411,497 (GRCm39) |
D357G |
probably damaging |
Het |
Zbtb40 |
T |
C |
4: 136,722,594 (GRCm39) |
D828G |
probably damaging |
Het |
Zfp74 |
A |
T |
7: 29,633,990 (GRCm39) |
C573S |
probably damaging |
Het |
|
Other mutations in Lama3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Lama3
|
APN |
18 |
12,713,349 (GRCm39) |
missense |
probably benign |
|
IGL00272:Lama3
|
APN |
18 |
12,624,605 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00335:Lama3
|
APN |
18 |
12,582,645 (GRCm39) |
splice site |
probably benign |
|
IGL00836:Lama3
|
APN |
18 |
12,605,285 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01017:Lama3
|
APN |
18 |
12,574,200 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01025:Lama3
|
APN |
18 |
12,614,094 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01394:Lama3
|
APN |
18 |
12,664,983 (GRCm39) |
missense |
probably null |
0.39 |
IGL01545:Lama3
|
APN |
18 |
12,574,188 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01685:Lama3
|
APN |
18 |
12,586,937 (GRCm39) |
splice site |
probably benign |
|
IGL01863:Lama3
|
APN |
18 |
12,552,993 (GRCm39) |
splice site |
probably benign |
|
IGL01869:Lama3
|
APN |
18 |
12,657,820 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01894:Lama3
|
APN |
18 |
12,705,121 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02027:Lama3
|
APN |
18 |
12,649,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02106:Lama3
|
APN |
18 |
12,601,371 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02307:Lama3
|
APN |
18 |
12,714,840 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02342:Lama3
|
APN |
18 |
12,624,533 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Lama3
|
APN |
18 |
12,689,807 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02401:Lama3
|
APN |
18 |
12,690,784 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02517:Lama3
|
APN |
18 |
12,670,915 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02644:Lama3
|
APN |
18 |
12,658,910 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02733:Lama3
|
APN |
18 |
12,711,184 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02932:Lama3
|
APN |
18 |
12,661,858 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03006:Lama3
|
APN |
18 |
12,601,425 (GRCm39) |
splice site |
probably benign |
|
IGL03038:Lama3
|
APN |
18 |
12,552,307 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03064:Lama3
|
APN |
18 |
12,572,406 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL03146:Lama3
|
APN |
18 |
12,660,681 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03233:Lama3
|
APN |
18 |
12,614,095 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03255:Lama3
|
APN |
18 |
12,672,760 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03369:Lama3
|
APN |
18 |
12,686,340 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03412:Lama3
|
APN |
18 |
12,552,239 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02980:Lama3
|
UTSW |
18 |
12,686,288 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03014:Lama3
|
UTSW |
18 |
12,673,024 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0007:Lama3
|
UTSW |
18 |
12,630,938 (GRCm39) |
splice site |
probably benign |
|
R0007:Lama3
|
UTSW |
18 |
12,630,938 (GRCm39) |
splice site |
probably benign |
|
R0050:Lama3
|
UTSW |
18 |
12,537,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R0050:Lama3
|
UTSW |
18 |
12,537,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Lama3
|
UTSW |
18 |
12,661,762 (GRCm39) |
splice site |
probably benign |
|
R0063:Lama3
|
UTSW |
18 |
12,661,762 (GRCm39) |
splice site |
probably benign |
|
R0106:Lama3
|
UTSW |
18 |
12,537,039 (GRCm39) |
missense |
probably damaging |
0.96 |
R0148:Lama3
|
UTSW |
18 |
12,581,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R0165:Lama3
|
UTSW |
18 |
12,657,867 (GRCm39) |
missense |
probably damaging |
0.99 |
R0240:Lama3
|
UTSW |
18 |
12,672,880 (GRCm39) |
splice site |
probably null |
|
R0240:Lama3
|
UTSW |
18 |
12,672,880 (GRCm39) |
splice site |
probably null |
|
R0316:Lama3
|
UTSW |
18 |
12,652,934 (GRCm39) |
missense |
probably benign |
0.09 |
R0325:Lama3
|
UTSW |
18 |
12,615,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R0365:Lama3
|
UTSW |
18 |
12,640,064 (GRCm39) |
missense |
probably damaging |
0.96 |
R0390:Lama3
|
UTSW |
18 |
12,540,620 (GRCm39) |
missense |
probably benign |
0.10 |
R0408:Lama3
|
UTSW |
18 |
12,589,894 (GRCm39) |
missense |
probably benign |
|
R0449:Lama3
|
UTSW |
18 |
12,633,569 (GRCm39) |
splice site |
probably null |
|
R0453:Lama3
|
UTSW |
18 |
12,598,535 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0480:Lama3
|
UTSW |
18 |
12,583,481 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0536:Lama3
|
UTSW |
18 |
12,658,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R0545:Lama3
|
UTSW |
18 |
12,694,758 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0567:Lama3
|
UTSW |
18 |
12,682,309 (GRCm39) |
missense |
probably benign |
|
R0605:Lama3
|
UTSW |
18 |
12,640,006 (GRCm39) |
missense |
probably benign |
0.02 |
R0617:Lama3
|
UTSW |
18 |
12,552,315 (GRCm39) |
critical splice donor site |
probably null |
|
R0629:Lama3
|
UTSW |
18 |
12,552,302 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0671:Lama3
|
UTSW |
18 |
12,610,647 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0730:Lama3
|
UTSW |
18 |
12,589,907 (GRCm39) |
splice site |
probably benign |
|
R1216:Lama3
|
UTSW |
18 |
12,554,191 (GRCm39) |
splice site |
probably benign |
|
R1356:Lama3
|
UTSW |
18 |
12,633,634 (GRCm39) |
unclassified |
probably benign |
|
R1386:Lama3
|
UTSW |
18 |
12,610,427 (GRCm39) |
missense |
probably benign |
0.04 |
R1424:Lama3
|
UTSW |
18 |
12,653,048 (GRCm39) |
missense |
probably benign |
0.13 |
R1426:Lama3
|
UTSW |
18 |
12,614,155 (GRCm39) |
critical splice donor site |
probably null |
|
R1437:Lama3
|
UTSW |
18 |
12,682,284 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1468:Lama3
|
UTSW |
18 |
12,574,164 (GRCm39) |
missense |
probably benign |
0.00 |
R1468:Lama3
|
UTSW |
18 |
12,574,164 (GRCm39) |
missense |
probably benign |
0.00 |
R1472:Lama3
|
UTSW |
18 |
12,615,102 (GRCm39) |
missense |
probably benign |
0.23 |
R1557:Lama3
|
UTSW |
18 |
12,646,788 (GRCm39) |
splice site |
probably benign |
|
R1571:Lama3
|
UTSW |
18 |
12,672,774 (GRCm39) |
missense |
probably damaging |
0.98 |
R1599:Lama3
|
UTSW |
18 |
12,583,457 (GRCm39) |
nonsense |
probably null |
|
R1631:Lama3
|
UTSW |
18 |
12,540,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Lama3
|
UTSW |
18 |
12,665,256 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1648:Lama3
|
UTSW |
18 |
12,665,256 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1719:Lama3
|
UTSW |
18 |
12,612,929 (GRCm39) |
critical splice donor site |
probably null |
|
R1757:Lama3
|
UTSW |
18 |
12,598,556 (GRCm39) |
missense |
probably benign |
0.10 |
R1766:Lama3
|
UTSW |
18 |
12,535,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R1853:Lama3
|
UTSW |
18 |
12,646,762 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1856:Lama3
|
UTSW |
18 |
12,670,838 (GRCm39) |
nonsense |
probably null |
|
R1909:Lama3
|
UTSW |
18 |
12,714,855 (GRCm39) |
missense |
probably benign |
0.19 |
R1913:Lama3
|
UTSW |
18 |
12,628,336 (GRCm39) |
missense |
probably benign |
0.15 |
R1975:Lama3
|
UTSW |
18 |
12,586,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Lama3
|
UTSW |
18 |
12,657,778 (GRCm39) |
splice site |
probably benign |
|
R2059:Lama3
|
UTSW |
18 |
12,661,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R2060:Lama3
|
UTSW |
18 |
12,661,783 (GRCm39) |
missense |
probably benign |
0.30 |
R2086:Lama3
|
UTSW |
18 |
12,657,887 (GRCm39) |
missense |
probably benign |
0.39 |
R2115:Lama3
|
UTSW |
18 |
12,535,906 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2291:Lama3
|
UTSW |
18 |
12,658,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R2860:Lama3
|
UTSW |
18 |
12,586,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R2861:Lama3
|
UTSW |
18 |
12,586,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R2862:Lama3
|
UTSW |
18 |
12,586,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R3410:Lama3
|
UTSW |
18 |
12,546,915 (GRCm39) |
critical splice donor site |
probably null |
|
R3614:Lama3
|
UTSW |
18 |
12,581,345 (GRCm39) |
missense |
probably benign |
0.03 |
R3696:Lama3
|
UTSW |
18 |
12,572,532 (GRCm39) |
splice site |
probably benign |
|
R3752:Lama3
|
UTSW |
18 |
12,640,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R3967:Lama3
|
UTSW |
18 |
12,713,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R3968:Lama3
|
UTSW |
18 |
12,713,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R3969:Lama3
|
UTSW |
18 |
12,713,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R3970:Lama3
|
UTSW |
18 |
12,713,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Lama3
|
UTSW |
18 |
12,637,365 (GRCm39) |
nonsense |
probably null |
|
R4118:Lama3
|
UTSW |
18 |
12,583,488 (GRCm39) |
missense |
probably benign |
0.01 |
R4222:Lama3
|
UTSW |
18 |
12,583,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R4223:Lama3
|
UTSW |
18 |
12,583,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R4224:Lama3
|
UTSW |
18 |
12,583,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R4225:Lama3
|
UTSW |
18 |
12,583,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R4367:Lama3
|
UTSW |
18 |
12,646,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R4404:Lama3
|
UTSW |
18 |
12,715,588 (GRCm39) |
missense |
probably benign |
0.01 |
R4424:Lama3
|
UTSW |
18 |
12,652,929 (GRCm39) |
nonsense |
probably null |
|
R4483:Lama3
|
UTSW |
18 |
12,682,310 (GRCm39) |
missense |
probably benign |
0.32 |
R4484:Lama3
|
UTSW |
18 |
12,614,145 (GRCm39) |
missense |
probably benign |
|
R4516:Lama3
|
UTSW |
18 |
12,628,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R4556:Lama3
|
UTSW |
18 |
12,612,816 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4616:Lama3
|
UTSW |
18 |
12,637,454 (GRCm39) |
critical splice donor site |
probably null |
|
R4702:Lama3
|
UTSW |
18 |
12,711,086 (GRCm39) |
nonsense |
probably null |
|
R4704:Lama3
|
UTSW |
18 |
12,686,280 (GRCm39) |
missense |
probably benign |
0.08 |
R4750:Lama3
|
UTSW |
18 |
12,637,416 (GRCm39) |
missense |
probably benign |
0.25 |
R4753:Lama3
|
UTSW |
18 |
12,615,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R4767:Lama3
|
UTSW |
18 |
12,633,620 (GRCm39) |
missense |
probably benign |
0.32 |
R4777:Lama3
|
UTSW |
18 |
12,546,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R4782:Lama3
|
UTSW |
18 |
12,544,627 (GRCm39) |
nonsense |
probably null |
|
R4784:Lama3
|
UTSW |
18 |
12,582,601 (GRCm39) |
missense |
probably benign |
0.20 |
R4816:Lama3
|
UTSW |
18 |
12,610,661 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4833:Lama3
|
UTSW |
18 |
12,574,188 (GRCm39) |
missense |
probably benign |
0.01 |
R4854:Lama3
|
UTSW |
18 |
12,544,599 (GRCm39) |
missense |
probably benign |
0.00 |
R4863:Lama3
|
UTSW |
18 |
12,631,735 (GRCm39) |
intron |
probably benign |
|
R4863:Lama3
|
UTSW |
18 |
12,672,850 (GRCm39) |
missense |
probably damaging |
0.99 |
R4953:Lama3
|
UTSW |
18 |
12,581,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Lama3
|
UTSW |
18 |
12,685,883 (GRCm39) |
missense |
probably damaging |
0.98 |
R4996:Lama3
|
UTSW |
18 |
12,651,800 (GRCm39) |
missense |
probably benign |
0.24 |
R5049:Lama3
|
UTSW |
18 |
12,715,668 (GRCm39) |
missense |
probably benign |
0.19 |
R5057:Lama3
|
UTSW |
18 |
12,665,005 (GRCm39) |
missense |
probably null |
0.82 |
R5090:Lama3
|
UTSW |
18 |
12,675,459 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5122:Lama3
|
UTSW |
18 |
12,672,823 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5215:Lama3
|
UTSW |
18 |
12,710,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R5245:Lama3
|
UTSW |
18 |
12,552,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R5259:Lama3
|
UTSW |
18 |
12,598,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Lama3
|
UTSW |
18 |
12,685,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R5377:Lama3
|
UTSW |
18 |
12,586,803 (GRCm39) |
missense |
probably damaging |
0.99 |
R5432:Lama3
|
UTSW |
18 |
12,705,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R5500:Lama3
|
UTSW |
18 |
12,589,821 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5534:Lama3
|
UTSW |
18 |
12,686,267 (GRCm39) |
missense |
probably benign |
0.00 |
R5604:Lama3
|
UTSW |
18 |
12,572,405 (GRCm39) |
missense |
probably benign |
|
R5617:Lama3
|
UTSW |
18 |
12,631,993 (GRCm39) |
intron |
probably benign |
|
R5709:Lama3
|
UTSW |
18 |
12,672,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R5965:Lama3
|
UTSW |
18 |
12,562,944 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6042:Lama3
|
UTSW |
18 |
12,707,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R6065:Lama3
|
UTSW |
18 |
12,602,985 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6085:Lama3
|
UTSW |
18 |
12,615,156 (GRCm39) |
missense |
probably benign |
0.01 |
R6212:Lama3
|
UTSW |
18 |
12,646,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R6268:Lama3
|
UTSW |
18 |
12,657,794 (GRCm39) |
missense |
probably damaging |
0.98 |
R6276:Lama3
|
UTSW |
18 |
12,640,006 (GRCm39) |
missense |
probably benign |
0.02 |
R6366:Lama3
|
UTSW |
18 |
12,615,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Lama3
|
UTSW |
18 |
12,612,813 (GRCm39) |
missense |
probably benign |
0.44 |
R6493:Lama3
|
UTSW |
18 |
12,615,205 (GRCm39) |
critical splice donor site |
probably null |
|
R6505:Lama3
|
UTSW |
18 |
12,628,405 (GRCm39) |
missense |
probably benign |
0.02 |
R6563:Lama3
|
UTSW |
18 |
12,670,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R6582:Lama3
|
UTSW |
18 |
12,710,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R6585:Lama3
|
UTSW |
18 |
12,552,314 (GRCm39) |
critical splice donor site |
probably null |
|
R6609:Lama3
|
UTSW |
18 |
12,646,735 (GRCm39) |
missense |
probably damaging |
0.99 |
R6656:Lama3
|
UTSW |
18 |
12,682,283 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6833:Lama3
|
UTSW |
18 |
12,624,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R6834:Lama3
|
UTSW |
18 |
12,624,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Lama3
|
UTSW |
18 |
12,661,475 (GRCm39) |
missense |
probably damaging |
0.97 |
R7026:Lama3
|
UTSW |
18 |
12,649,605 (GRCm39) |
missense |
probably damaging |
0.98 |
R7088:Lama3
|
UTSW |
18 |
12,715,602 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7100:Lama3
|
UTSW |
18 |
12,715,701 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7102:Lama3
|
UTSW |
18 |
12,685,870 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7103:Lama3
|
UTSW |
18 |
12,664,936 (GRCm39) |
missense |
probably benign |
0.00 |
R7121:Lama3
|
UTSW |
18 |
12,595,839 (GRCm39) |
missense |
probably benign |
0.06 |
R7133:Lama3
|
UTSW |
18 |
12,672,843 (GRCm39) |
missense |
probably benign |
0.05 |
R7150:Lama3
|
UTSW |
18 |
12,601,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R7158:Lama3
|
UTSW |
18 |
12,589,869 (GRCm39) |
missense |
probably benign |
0.20 |
R7170:Lama3
|
UTSW |
18 |
12,537,133 (GRCm39) |
missense |
probably benign |
0.26 |
R7216:Lama3
|
UTSW |
18 |
12,563,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R7223:Lama3
|
UTSW |
18 |
12,715,665 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7243:Lama3
|
UTSW |
18 |
12,552,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R7282:Lama3
|
UTSW |
18 |
12,572,449 (GRCm39) |
missense |
probably damaging |
0.99 |
R7337:Lama3
|
UTSW |
18 |
12,640,097 (GRCm39) |
splice site |
probably null |
|
R7442:Lama3
|
UTSW |
18 |
12,605,238 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7487:Lama3
|
UTSW |
18 |
12,552,294 (GRCm39) |
missense |
probably benign |
|
R7604:Lama3
|
UTSW |
18 |
12,633,550 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7609:Lama3
|
UTSW |
18 |
12,664,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7650:Lama3
|
UTSW |
18 |
12,670,895 (GRCm39) |
missense |
probably benign |
0.01 |
R7894:Lama3
|
UTSW |
18 |
12,595,864 (GRCm39) |
missense |
probably benign |
0.07 |
R7975:Lama3
|
UTSW |
18 |
12,670,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R8099:Lama3
|
UTSW |
18 |
12,667,120 (GRCm39) |
missense |
probably damaging |
0.97 |
R8168:Lama3
|
UTSW |
18 |
12,639,999 (GRCm39) |
missense |
probably null |
|
R8219:Lama3
|
UTSW |
18 |
12,572,417 (GRCm39) |
missense |
probably benign |
0.07 |
R8227:Lama3
|
UTSW |
18 |
12,540,608 (GRCm39) |
missense |
probably benign |
|
R8229:Lama3
|
UTSW |
18 |
12,540,608 (GRCm39) |
missense |
probably benign |
|
R8298:Lama3
|
UTSW |
18 |
12,658,910 (GRCm39) |
missense |
probably benign |
0.12 |
R8351:Lama3
|
UTSW |
18 |
12,673,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R8364:Lama3
|
UTSW |
18 |
12,661,404 (GRCm39) |
missense |
probably damaging |
0.99 |
R8463:Lama3
|
UTSW |
18 |
12,582,896 (GRCm39) |
missense |
probably damaging |
0.96 |
R8515:Lama3
|
UTSW |
18 |
12,544,688 (GRCm39) |
missense |
probably null |
0.01 |
R8784:Lama3
|
UTSW |
18 |
12,554,212 (GRCm39) |
missense |
probably benign |
|
R8799:Lama3
|
UTSW |
18 |
12,624,000 (GRCm39) |
missense |
probably damaging |
0.96 |
R8874:Lama3
|
UTSW |
18 |
12,582,643 (GRCm39) |
critical splice donor site |
probably null |
|
R8938:Lama3
|
UTSW |
18 |
12,689,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R8967:Lama3
|
UTSW |
18 |
12,665,096 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9039:Lama3
|
UTSW |
18 |
12,614,120 (GRCm39) |
nonsense |
probably null |
|
R9126:Lama3
|
UTSW |
18 |
12,583,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R9200:Lama3
|
UTSW |
18 |
12,605,297 (GRCm39) |
missense |
probably benign |
0.00 |
R9203:Lama3
|
UTSW |
18 |
12,595,869 (GRCm39) |
missense |
probably benign |
0.04 |
R9246:Lama3
|
UTSW |
18 |
12,710,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R9284:Lama3
|
UTSW |
18 |
12,583,541 (GRCm39) |
nonsense |
probably null |
|
R9553:Lama3
|
UTSW |
18 |
12,563,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R9716:Lama3
|
UTSW |
18 |
12,583,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R9734:Lama3
|
UTSW |
18 |
12,682,320 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0019:Lama3
|
UTSW |
18 |
12,715,631 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1177:Lama3
|
UTSW |
18 |
12,562,936 (GRCm39) |
critical splice acceptor site |
probably null |
|
|