Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930533L02Rik |
T |
C |
7: 124,917,767 (GRCm39) |
M53T |
unknown |
Het |
Abcb11 |
T |
A |
2: 69,089,820 (GRCm39) |
|
probably benign |
Het |
Acap2 |
C |
G |
16: 30,929,763 (GRCm39) |
A432P |
probably damaging |
Het |
Adamtsl1 |
A |
G |
4: 86,146,249 (GRCm39) |
R302G |
probably damaging |
Het |
Aoc1l1 |
A |
G |
6: 48,954,536 (GRCm39) |
E558G |
probably damaging |
Het |
Ap2b1 |
T |
G |
11: 83,241,944 (GRCm39) |
S608A |
possibly damaging |
Het |
Atp13a3 |
T |
A |
16: 30,171,116 (GRCm39) |
T310S |
possibly damaging |
Het |
Atp6v1b1 |
T |
C |
6: 83,734,834 (GRCm39) |
V382A |
probably benign |
Het |
Atp6v1g1 |
T |
A |
4: 63,468,304 (GRCm39) |
F102L |
probably benign |
Het |
B430306N03Rik |
T |
A |
17: 48,623,810 (GRCm39) |
V37D |
probably damaging |
Het |
Cacna1d |
T |
C |
14: 29,769,314 (GRCm39) |
Y1872C |
possibly damaging |
Het |
Carf |
T |
A |
1: 60,148,570 (GRCm39) |
Y54N |
probably damaging |
Het |
Cct5 |
T |
C |
15: 31,594,349 (GRCm39) |
E256G |
probably damaging |
Het |
Cd5 |
A |
G |
19: 10,700,620 (GRCm39) |
S295P |
probably benign |
Het |
Cenpb |
T |
C |
2: 131,020,517 (GRCm39) |
|
probably benign |
Het |
Cntnap3 |
A |
G |
13: 64,942,076 (GRCm39) |
M218T |
possibly damaging |
Het |
Colec11 |
C |
T |
12: 28,644,786 (GRCm39) |
R236H |
probably damaging |
Het |
Crem |
T |
A |
18: 3,288,098 (GRCm39) |
|
probably benign |
Het |
Csnk2a1 |
A |
G |
2: 152,096,201 (GRCm39) |
N58S |
probably benign |
Het |
Cyp2a4 |
T |
G |
7: 26,011,733 (GRCm39) |
M318R |
probably damaging |
Het |
Dhrs1 |
T |
A |
14: 55,981,116 (GRCm39) |
Q98L |
probably null |
Het |
Dnah11 |
G |
T |
12: 118,077,606 (GRCm39) |
Q1296K |
possibly damaging |
Het |
Edc4 |
T |
A |
8: 106,614,634 (GRCm39) |
D105E |
probably damaging |
Het |
Eid2b |
C |
T |
7: 27,977,198 (GRCm39) |
|
probably benign |
Het |
Exoc1 |
A |
T |
5: 76,680,693 (GRCm39) |
K28* |
probably null |
Het |
Fam114a1 |
A |
G |
5: 65,137,402 (GRCm39) |
D115G |
probably benign |
Het |
Fam151a |
A |
T |
4: 106,592,760 (GRCm39) |
|
probably null |
Het |
Gc |
T |
C |
5: 89,586,201 (GRCm39) |
Y313C |
probably damaging |
Het |
Gdpd1 |
A |
G |
11: 86,926,094 (GRCm39) |
Y284H |
probably benign |
Het |
Gm21957 |
T |
A |
7: 124,818,878 (GRCm39) |
|
noncoding transcript |
Het |
Golm1 |
G |
A |
13: 59,792,999 (GRCm39) |
Q169* |
probably null |
Het |
Greb1l |
T |
C |
18: 10,523,281 (GRCm39) |
V813A |
probably damaging |
Het |
Itih1 |
C |
T |
14: 30,659,800 (GRCm39) |
A279T |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lama1 |
T |
C |
17: 68,124,618 (GRCm39) |
C2893R |
probably damaging |
Het |
Loxhd1 |
A |
G |
18: 77,472,642 (GRCm39) |
D1053G |
probably damaging |
Het |
Map3k20 |
A |
G |
2: 72,228,729 (GRCm39) |
K316R |
probably benign |
Het |
Mapre3 |
A |
C |
5: 31,020,546 (GRCm39) |
|
probably null |
Het |
Mgam |
T |
A |
6: 40,737,962 (GRCm39) |
|
probably null |
Het |
Mical2 |
A |
C |
7: 111,917,810 (GRCm39) |
H389P |
probably benign |
Het |
Mtmr2 |
A |
G |
9: 13,711,248 (GRCm39) |
D347G |
probably damaging |
Het |
Nbeal2 |
G |
A |
9: 110,463,139 (GRCm39) |
L1309F |
probably benign |
Het |
Nid2 |
G |
A |
14: 19,828,111 (GRCm39) |
G516S |
probably benign |
Het |
Nodal |
A |
T |
10: 61,259,077 (GRCm39) |
E171D |
possibly damaging |
Het |
Notch2 |
T |
C |
3: 98,009,683 (GRCm39) |
S537P |
probably damaging |
Het |
Obox6 |
A |
G |
7: 15,567,532 (GRCm39) |
L305S |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,969,082 (GRCm39) |
D2715G |
probably damaging |
Het |
Or4k1 |
T |
A |
14: 50,377,580 (GRCm39) |
N172I |
probably damaging |
Het |
Or5g26 |
A |
C |
2: 85,494,090 (GRCm39) |
S229R |
probably benign |
Het |
Pcca |
T |
C |
14: 122,923,527 (GRCm39) |
S404P |
probably damaging |
Het |
Pcdh10 |
T |
C |
3: 45,334,906 (GRCm39) |
S407P |
probably damaging |
Het |
Plekha5 |
C |
A |
6: 140,516,044 (GRCm39) |
|
probably null |
Het |
Ptdss1 |
A |
G |
13: 67,101,619 (GRCm39) |
N72S |
probably benign |
Het |
Ptprs |
T |
C |
17: 56,761,984 (GRCm39) |
I43V |
probably null |
Het |
Pygm |
G |
A |
19: 6,441,511 (GRCm39) |
|
probably null |
Het |
Rab7 |
C |
T |
6: 87,989,300 (GRCm39) |
V57I |
probably benign |
Het |
Rasl10a |
A |
G |
11: 5,009,431 (GRCm39) |
|
probably null |
Het |
Rergl |
T |
C |
6: 139,471,832 (GRCm39) |
T106A |
probably benign |
Het |
Rnf17 |
T |
G |
14: 56,720,837 (GRCm39) |
V1023G |
probably damaging |
Het |
Rnf25 |
T |
A |
1: 74,633,126 (GRCm39) |
R409W |
probably damaging |
Het |
Rps6ka1 |
T |
C |
4: 133,600,280 (GRCm39) |
M1V |
probably null |
Het |
Rps6ka5 |
T |
C |
12: 100,585,874 (GRCm39) |
T140A |
possibly damaging |
Het |
Sbno2 |
T |
A |
10: 79,893,690 (GRCm39) |
I1204F |
possibly damaging |
Het |
Serpina16 |
A |
T |
12: 103,641,521 (GRCm39) |
I68N |
probably damaging |
Het |
Slc35a5 |
A |
G |
16: 44,964,628 (GRCm39) |
S202P |
probably damaging |
Het |
Slc35g3 |
G |
C |
11: 69,651,772 (GRCm39) |
S93W |
probably damaging |
Het |
Slc49a3 |
C |
T |
5: 108,593,487 (GRCm39) |
R117H |
probably damaging |
Het |
Smc1b |
A |
G |
15: 85,006,052 (GRCm39) |
|
probably benign |
Het |
Spag1 |
T |
C |
15: 36,227,287 (GRCm39) |
L648P |
probably damaging |
Het |
Tagap1 |
T |
C |
17: 7,224,102 (GRCm39) |
D198G |
probably benign |
Het |
Tedc2 |
T |
C |
17: 24,436,874 (GRCm39) |
E287G |
probably damaging |
Het |
Tjp1 |
C |
A |
7: 64,962,669 (GRCm39) |
R1089S |
probably damaging |
Het |
Tnrc6a |
CTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTT |
CTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTT |
7: 122,761,669 (GRCm39) |
|
probably benign |
Het |
Ttc38 |
T |
A |
15: 85,722,928 (GRCm39) |
D125E |
probably benign |
Het |
Uggt1 |
C |
T |
1: 36,231,495 (GRCm39) |
R490Q |
probably null |
Het |
Uroc1 |
T |
G |
6: 90,321,096 (GRCm39) |
L224R |
probably damaging |
Het |
Vmn1r228 |
A |
T |
17: 20,997,455 (GRCm39) |
I21N |
possibly damaging |
Het |
Vmn2r102 |
T |
G |
17: 19,896,949 (GRCm39) |
L99V |
probably damaging |
Het |
Vps13c |
C |
T |
9: 67,857,571 (GRCm39) |
S2601F |
probably benign |
Het |
Zfp462 |
T |
C |
4: 55,010,830 (GRCm39) |
L932P |
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 |
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 |
|
|