Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700067K01Rik |
T |
C |
8: 84,729,637 (GRCm39) |
|
probably benign |
Het |
A530064D06Rik |
G |
A |
17: 48,473,824 (GRCm39) |
T31I |
probably benign |
Het |
Abca17 |
A |
G |
17: 24,500,223 (GRCm39) |
F1323L |
probably benign |
Het |
Abcf3 |
T |
A |
16: 20,369,237 (GRCm39) |
N206K |
probably damaging |
Het |
Adam10 |
A |
G |
9: 70,673,223 (GRCm39) |
|
probably benign |
Het |
Adamtsl3 |
A |
T |
7: 82,172,390 (GRCm39) |
Q451L |
probably damaging |
Het |
Adgrl3 |
T |
A |
5: 81,708,752 (GRCm39) |
I413N |
probably benign |
Het |
Asb18 |
G |
T |
1: 89,920,893 (GRCm39) |
A128E |
probably damaging |
Het |
Atf7ip2 |
T |
C |
16: 10,059,743 (GRCm39) |
S428P |
possibly damaging |
Het |
Atp8b5 |
G |
T |
4: 43,291,672 (GRCm39) |
C15F |
possibly damaging |
Het |
Bahcc1 |
A |
G |
11: 120,178,146 (GRCm39) |
E2235G |
probably damaging |
Het |
Blnk |
G |
T |
19: 40,926,111 (GRCm39) |
S330* |
probably null |
Het |
Bpnt1 |
T |
G |
1: 185,088,808 (GRCm39) |
N319K |
probably benign |
Het |
Brip1 |
G |
A |
11: 86,043,493 (GRCm39) |
T357I |
possibly damaging |
Het |
Cadm1 |
T |
A |
9: 47,725,104 (GRCm39) |
D288E |
probably benign |
Het |
Calcoco2 |
A |
G |
11: 95,998,354 (GRCm39) |
V23A |
probably damaging |
Het |
Cand2 |
G |
A |
6: 115,780,766 (GRCm39) |
E1217K |
probably damaging |
Het |
Ccdc154 |
G |
T |
17: 25,386,259 (GRCm39) |
|
probably benign |
Het |
Cdk12 |
T |
C |
11: 98,120,935 (GRCm39) |
|
probably benign |
Het |
Clec4a3 |
A |
G |
6: 122,930,993 (GRCm39) |
|
probably null |
Het |
Cpne2 |
T |
A |
8: 95,274,970 (GRCm39) |
|
probably benign |
Het |
Cyfip1 |
T |
C |
7: 55,573,710 (GRCm39) |
|
probably null |
Het |
Cyp26c1 |
A |
G |
19: 37,675,009 (GRCm39) |
H110R |
probably damaging |
Het |
Cyp2j13 |
A |
G |
4: 95,959,932 (GRCm39) |
Y75H |
probably damaging |
Het |
Defb43 |
T |
A |
14: 63,249,287 (GRCm39) |
V10D |
probably damaging |
Het |
Dhx36 |
G |
A |
3: 62,401,162 (GRCm39) |
S368L |
possibly damaging |
Het |
Dock6 |
G |
A |
9: 21,715,923 (GRCm39) |
|
probably benign |
Het |
Elp2 |
T |
C |
18: 24,745,499 (GRCm39) |
|
probably benign |
Het |
Emilin3 |
A |
G |
2: 160,750,249 (GRCm39) |
L453P |
probably damaging |
Het |
Eml6 |
A |
T |
11: 29,755,065 (GRCm39) |
D903E |
probably benign |
Het |
Ep300 |
T |
C |
15: 81,500,335 (GRCm39) |
|
probably benign |
Het |
Ep400 |
G |
A |
5: 110,836,062 (GRCm39) |
T1899M |
unknown |
Het |
Fancg |
A |
G |
4: 43,002,998 (GRCm39) |
S620P |
probably benign |
Het |
Fbxo42 |
G |
A |
4: 140,922,550 (GRCm39) |
V239M |
probably damaging |
Het |
Fermt2 |
T |
C |
14: 45,706,776 (GRCm39) |
D340G |
probably benign |
Het |
Filip1 |
A |
T |
9: 79,726,672 (GRCm39) |
V649E |
probably damaging |
Het |
Fut8 |
G |
A |
12: 77,521,791 (GRCm39) |
E477K |
probably damaging |
Het |
Gbp3 |
G |
A |
3: 142,271,151 (GRCm39) |
G185D |
probably benign |
Het |
Gclc |
G |
T |
9: 77,694,080 (GRCm39) |
D345Y |
probably damaging |
Het |
Gfus |
A |
G |
15: 75,800,807 (GRCm39) |
V27A |
possibly damaging |
Het |
Gkn2 |
A |
G |
6: 87,352,800 (GRCm39) |
D43G |
possibly damaging |
Het |
Gnptab |
A |
G |
10: 88,279,166 (GRCm39) |
|
probably benign |
Het |
Greb1l |
C |
T |
18: 10,474,303 (GRCm39) |
T206I |
probably damaging |
Het |
Grk4 |
A |
G |
5: 34,905,611 (GRCm39) |
N452S |
probably benign |
Het |
Hcn2 |
G |
C |
10: 79,570,066 (GRCm39) |
|
probably null |
Het |
Hpn |
T |
C |
7: 30,808,585 (GRCm39) |
K76E |
possibly damaging |
Het |
Hspg2 |
A |
G |
4: 137,280,591 (GRCm39) |
D3268G |
probably damaging |
Het |
Immt |
A |
T |
6: 71,848,541 (GRCm39) |
Q467L |
possibly damaging |
Het |
Kalrn |
T |
C |
16: 33,936,778 (GRCm39) |
S1636G |
probably benign |
Het |
Kcnh8 |
T |
A |
17: 53,285,141 (GRCm39) |
L1037* |
probably null |
Het |
Klhl33 |
T |
C |
14: 51,129,851 (GRCm39) |
T548A |
probably damaging |
Het |
Klri2 |
T |
C |
6: 129,717,171 (GRCm39) |
I71V |
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,609,363 (GRCm39) |
C254S |
probably damaging |
Het |
Med12l |
A |
G |
3: 59,172,350 (GRCm39) |
Q1702R |
probably damaging |
Het |
Mga |
A |
T |
2: 119,750,391 (GRCm39) |
|
probably null |
Het |
Mis18a |
A |
T |
16: 90,517,561 (GRCm39) |
I172K |
possibly damaging |
Het |
Mrgpre |
T |
C |
7: 143,335,254 (GRCm39) |
D83G |
probably benign |
Het |
Mroh2a |
C |
A |
1: 88,170,142 (GRCm39) |
A685D |
possibly damaging |
Het |
Mrpl39 |
T |
C |
16: 84,531,282 (GRCm39) |
|
probably benign |
Het |
Mrrf |
C |
T |
2: 36,043,710 (GRCm39) |
A149V |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,432,024 (GRCm39) |
M2338K |
possibly damaging |
Het |
Myo18b |
T |
C |
5: 112,840,632 (GRCm39) |
Q2387R |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,964,780 (GRCm39) |
I943T |
probably damaging |
Het |
Ncapd3 |
T |
A |
9: 26,998,773 (GRCm39) |
N1254K |
probably benign |
Het |
Ncoa1 |
A |
T |
12: 4,299,758 (GRCm39) |
|
probably null |
Het |
Ncor2 |
C |
T |
5: 125,126,451 (GRCm39) |
A136T |
probably benign |
Het |
Opa1 |
T |
C |
16: 29,421,025 (GRCm39) |
|
probably benign |
Het |
Or13a25 |
A |
G |
7: 140,247,590 (GRCm39) |
D123G |
probably damaging |
Het |
Or5p59 |
C |
A |
7: 107,703,363 (GRCm39) |
Y282* |
probably null |
Het |
Or8b39 |
T |
A |
9: 37,996,423 (GRCm39) |
M97K |
possibly damaging |
Het |
Or9e1 |
T |
A |
11: 58,732,681 (GRCm39) |
I247N |
possibly damaging |
Het |
Pcdhb4 |
T |
C |
18: 37,440,795 (GRCm39) |
M35T |
probably benign |
Het |
Per3 |
T |
C |
4: 151,113,288 (GRCm39) |
I347V |
probably benign |
Het |
Pex13 |
G |
A |
11: 23,615,831 (GRCm39) |
P5L |
possibly damaging |
Het |
Phkb |
T |
A |
8: 86,602,322 (GRCm39) |
W38R |
probably damaging |
Het |
Plekhf1 |
A |
T |
7: 37,920,826 (GRCm39) |
D247E |
probably benign |
Het |
Plxnb2 |
A |
G |
15: 89,042,184 (GRCm39) |
S1607P |
probably benign |
Het |
Plxnc1 |
T |
A |
10: 94,635,194 (GRCm39) |
H1344L |
possibly damaging |
Het |
Potefam1 |
A |
C |
2: 111,034,482 (GRCm39) |
V350G |
possibly damaging |
Het |
Ptk7 |
T |
G |
17: 46,901,238 (GRCm39) |
N196H |
possibly damaging |
Het |
Rab27a |
G |
T |
9: 72,982,715 (GRCm39) |
D7Y |
probably damaging |
Het |
Rars2 |
T |
A |
4: 34,630,505 (GRCm39) |
C82* |
probably null |
Het |
Rccd1 |
A |
T |
7: 79,969,965 (GRCm39) |
|
probably benign |
Het |
Riiad1 |
T |
C |
3: 94,379,546 (GRCm39) |
I56V |
possibly damaging |
Het |
Rnase4 |
A |
G |
14: 51,342,507 (GRCm39) |
E77G |
probably damaging |
Het |
Rnf126 |
A |
T |
10: 79,597,441 (GRCm39) |
I157N |
possibly damaging |
Het |
Rnf207 |
T |
C |
4: 152,391,925 (GRCm39) |
R623G |
probably benign |
Het |
Rpusd1 |
T |
G |
17: 25,947,498 (GRCm39) |
F62V |
possibly damaging |
Het |
Rxfp1 |
T |
C |
3: 79,570,600 (GRCm39) |
|
probably null |
Het |
Scfd1 |
A |
T |
12: 51,459,411 (GRCm39) |
Q324L |
probably benign |
Het |
Skint3 |
G |
T |
4: 112,112,974 (GRCm39) |
E195* |
probably null |
Het |
Slc7a10 |
A |
T |
7: 34,896,758 (GRCm39) |
T165S |
probably benign |
Het |
Smagp |
A |
G |
15: 100,519,733 (GRCm39) |
I97T |
probably damaging |
Het |
Sostdc1 |
A |
G |
12: 36,367,340 (GRCm39) |
H172R |
probably damaging |
Het |
Spast |
A |
G |
17: 74,646,446 (GRCm39) |
|
probably benign |
Het |
Sspo |
G |
T |
6: 48,467,325 (GRCm39) |
|
probably benign |
Het |
Ston2 |
C |
T |
12: 91,707,240 (GRCm39) |
|
probably null |
Het |
Tas2r103 |
T |
G |
6: 133,013,313 (GRCm39) |
E251A |
probably benign |
Het |
Tbc1d2b |
A |
T |
9: 90,104,558 (GRCm39) |
|
probably benign |
Het |
Telo2 |
G |
A |
17: 25,332,139 (GRCm39) |
P143L |
probably benign |
Het |
Tgfbi |
A |
T |
13: 56,786,539 (GRCm39) |
Y674F |
probably null |
Het |
Tha1 |
T |
A |
11: 117,763,983 (GRCm39) |
|
probably benign |
Het |
Timp4 |
T |
A |
6: 115,226,814 (GRCm39) |
S110C |
probably damaging |
Het |
Tlr6 |
T |
C |
5: 65,111,935 (GRCm39) |
K324R |
probably benign |
Het |
Tnip3 |
A |
G |
6: 65,574,347 (GRCm39) |
E137G |
probably damaging |
Het |
Top6bl |
A |
G |
19: 4,676,216 (GRCm39) |
S639P |
probably damaging |
Het |
Trak1 |
T |
C |
9: 121,278,021 (GRCm39) |
|
probably null |
Het |
Trim47 |
A |
G |
11: 115,999,178 (GRCm39) |
S233P |
probably benign |
Het |
Tspoap1 |
A |
T |
11: 87,653,635 (GRCm39) |
E155V |
probably damaging |
Het |
Uggt1 |
A |
T |
1: 36,194,209 (GRCm39) |
L1343Q |
probably damaging |
Het |
Utp14b |
T |
C |
1: 78,642,452 (GRCm39) |
S117P |
probably benign |
Het |
Vmn1r124 |
A |
T |
7: 20,994,436 (GRCm39) |
V36D |
probably damaging |
Het |
Wdr27 |
T |
C |
17: 15,148,658 (GRCm39) |
T112A |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,065,367 (GRCm39) |
T1630A |
probably benign |
Het |
Zfp352 |
A |
G |
4: 90,112,156 (GRCm39) |
T99A |
probably benign |
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 |
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 |
R5589:Lama3
|
UTSW |
18 |
12,605,277 (GRCm39) |
missense |
possibly damaging |
0.46 |
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 |
|
|