Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503B20Rik |
A |
T |
3: 146,650,660 (GRCm38) |
Y164* |
probably null |
Het |
4932438A13Rik |
A |
G |
3: 36,949,843 (GRCm38) |
|
probably null |
Het |
9130019O22Rik |
T |
C |
7: 127,386,535 (GRCm38) |
T95A |
unknown |
Het |
Abce1 |
G |
A |
8: 79,699,374 (GRCm38) |
T258M |
probably benign |
Het |
Actl7b |
G |
C |
4: 56,740,693 (GRCm38) |
P222A |
probably benign |
Het |
Adam2 |
T |
C |
14: 66,056,541 (GRCm38) |
N279S |
probably benign |
Het |
Adamts13 |
A |
G |
2: 27,005,206 (GRCm38) |
D1103G |
probably benign |
Het |
Aff1 |
G |
A |
5: 103,847,809 (GRCm38) |
S1089N |
probably benign |
Het |
Ahcyl2 |
T |
C |
6: 29,768,556 (GRCm38) |
S7P |
unknown |
Het |
Anks1b |
A |
G |
10: 90,260,846 (GRCm38) |
|
probably null |
Het |
Azin1 |
A |
C |
15: 38,491,634 (GRCm38) |
D359E |
probably damaging |
Het |
Bahd1 |
A |
G |
2: 118,916,310 (GRCm38) |
T137A |
probably benign |
Het |
C1qbp |
A |
G |
11: 70,978,772 (GRCm38) |
S162P |
probably damaging |
Het |
C1rb |
A |
G |
6: 124,580,484 (GRCm38) |
M527V |
not run |
Het |
Ccdc88c |
A |
T |
12: 100,930,547 (GRCm38) |
D1381E |
probably damaging |
Het |
Ccdc90b |
A |
G |
7: 92,578,530 (GRCm38) |
Y234C |
probably damaging |
Het |
Cyp11b2 |
A |
T |
15: 74,853,750 (GRCm38) |
|
probably null |
Het |
Dchs1 |
A |
G |
7: 105,765,982 (GRCm38) |
V665A |
probably damaging |
Het |
Dhx8 |
T |
C |
11: 101,764,797 (GRCm38) |
S1119P |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,092,168 (GRCm38) |
D2512G |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 30,813,095 (GRCm38) |
Y4130H |
probably damaging |
Het |
E4f1 |
G |
T |
17: 24,455,233 (GRCm38) |
A19D |
unknown |
Het |
Eftud2 |
T |
C |
11: 102,848,012 (GRCm38) |
D517G |
possibly damaging |
Het |
Epha6 |
T |
A |
16: 60,205,772 (GRCm38) |
I436F |
possibly damaging |
Het |
Epha7 |
C |
T |
4: 28,871,937 (GRCm38) |
S422L |
probably benign |
Het |
Ezh1 |
A |
G |
11: 101,217,029 (GRCm38) |
M74T |
probably benign |
Het |
Fam71d |
C |
A |
12: 78,715,014 (GRCm38) |
Q151K |
probably damaging |
Het |
Galnt14 |
T |
A |
17: 73,504,921 (GRCm38) |
K435M |
possibly damaging |
Het |
Gde1 |
A |
T |
7: 118,705,536 (GRCm38) |
Y39N |
possibly damaging |
Het |
Gldn |
G |
A |
9: 54,338,593 (GRCm38) |
R476Q |
probably benign |
Het |
Gm32742 |
G |
T |
9: 51,156,762 (GRCm38) |
R307S |
probably benign |
Het |
Gnao1 |
T |
G |
8: 93,944,344 (GRCm38) |
N150K |
|
Het |
Gpr135 |
A |
T |
12: 72,069,867 (GRCm38) |
D375E |
possibly damaging |
Het |
Gria4 |
A |
G |
9: 4,464,315 (GRCm38) |
M549T |
probably damaging |
Het |
Grik3 |
C |
A |
4: 125,623,635 (GRCm38) |
D90E |
probably damaging |
Het |
Hivep3 |
CGG |
CG |
4: 120,097,911 (GRCm38) |
1141 |
probably null |
Het |
Hspd1 |
T |
C |
1: 55,080,337 (GRCm38) |
E327G |
probably benign |
Het |
Kif6 |
T |
C |
17: 49,671,101 (GRCm38) |
I107T |
probably damaging |
Het |
Kmt2e |
C |
T |
5: 23,501,765 (GRCm38) |
T1442M |
not run |
Het |
Lpcat3 |
A |
G |
6: 124,702,530 (GRCm38) |
N331S |
probably benign |
Het |
Lrrc63 |
C |
A |
14: 75,084,969 (GRCm38) |
W565L |
possibly damaging |
Het |
Maats1 |
C |
A |
16: 38,298,236 (GRCm38) |
E734* |
probably null |
Het |
Malrd1 |
A |
G |
2: 15,925,192 (GRCm38) |
N1503S |
unknown |
Het |
Mcm7 |
C |
T |
5: 138,169,724 (GRCm38) |
V38I |
probably benign |
Het |
Mphosph9 |
C |
T |
5: 124,316,117 (GRCm38) |
V106I |
probably benign |
Het |
Mroh8 |
G |
T |
2: 157,269,564 (GRCm38) |
L157I |
possibly damaging |
Het |
Mta2 |
T |
A |
19: 8,945,836 (GRCm38) |
S91T |
probably damaging |
Het |
Muc5ac |
A |
T |
7: 141,809,709 (GRCm38) |
Q2252H |
unknown |
Het |
Ndufs7 |
G |
T |
10: 80,253,697 (GRCm38) |
V59L |
probably benign |
Het |
Nrxn2 |
T |
C |
19: 6,531,961 (GRCm38) |
L1642P |
probably damaging |
Het |
Olfr1053 |
G |
A |
2: 86,314,900 (GRCm38) |
P129S |
probably damaging |
Het |
Pbxip1 |
A |
T |
3: 89,445,595 (GRCm38) |
I183L |
probably benign |
Het |
Peak1 |
A |
T |
9: 56,241,207 (GRCm38) |
L1085* |
probably null |
Het |
Phf20l1 |
A |
G |
15: 66,604,084 (GRCm38) |
T189A |
probably benign |
Het |
Poteg |
T |
A |
8: 27,458,655 (GRCm38) |
|
probably null |
Het |
Proc |
G |
A |
18: 32,134,778 (GRCm38) |
|
probably null |
Het |
Prr36 |
G |
A |
8: 4,214,836 (GRCm38) |
R277C |
unknown |
Het |
Ptpn3 |
T |
C |
4: 57,240,845 (GRCm38) |
N257D |
probably damaging |
Het |
Rnf5 |
C |
A |
17: 34,601,664 (GRCm38) |
V150L |
probably benign |
Het |
Sbf2 |
T |
A |
7: 110,378,067 (GRCm38) |
Q666L |
possibly damaging |
Het |
Sdk2 |
C |
T |
11: 113,829,969 (GRCm38) |
R1378H |
possibly damaging |
Het |
Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,819,695 (GRCm38) |
|
probably benign |
Het |
Sipa1l2 |
A |
T |
8: 125,419,272 (GRCm38) |
V1681E |
probably benign |
Het |
Slc15a5 |
A |
T |
6: 138,079,786 (GRCm38) |
L44Q |
probably damaging |
Het |
Slc29a1 |
C |
A |
17: 45,592,324 (GRCm38) |
|
probably null |
Het |
Slc5a8 |
G |
T |
10: 88,904,960 (GRCm38) |
V246F |
possibly damaging |
Het |
Spint2 |
T |
C |
7: 29,258,519 (GRCm38) |
E154G |
probably damaging |
Het |
Sycp1 |
A |
T |
3: 102,913,433 (GRCm38) |
S413T |
probably damaging |
Het |
Tpsg1 |
G |
T |
17: 25,373,210 (GRCm38) |
G86V |
probably damaging |
Het |
Trio |
A |
T |
15: 27,736,445 (GRCm38) |
|
probably null |
Het |
Unc13b |
A |
G |
4: 43,170,102 (GRCm38) |
Y310C |
unknown |
Het |
Unc13b |
A |
G |
4: 43,256,776 (GRCm38) |
T1155A |
possibly damaging |
Het |
Vmn2r79 |
A |
G |
7: 87,003,384 (GRCm38) |
|
probably null |
Het |
Xpo7 |
T |
A |
14: 70,671,670 (GRCm38) |
S803C |
probably damaging |
Het |
|
Other mutations in Lama3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Lama3
|
APN |
18 |
12,580,292 (GRCm38) |
missense |
probably benign |
|
IGL00272:Lama3
|
APN |
18 |
12,491,548 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00335:Lama3
|
APN |
18 |
12,449,588 (GRCm38) |
splice site |
probably benign |
|
IGL00836:Lama3
|
APN |
18 |
12,472,228 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01017:Lama3
|
APN |
18 |
12,441,143 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01025:Lama3
|
APN |
18 |
12,481,037 (GRCm38) |
missense |
probably benign |
0.09 |
IGL01394:Lama3
|
APN |
18 |
12,531,926 (GRCm38) |
missense |
probably null |
0.39 |
IGL01545:Lama3
|
APN |
18 |
12,441,131 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01685:Lama3
|
APN |
18 |
12,453,880 (GRCm38) |
splice site |
probably benign |
|
IGL01863:Lama3
|
APN |
18 |
12,419,936 (GRCm38) |
splice site |
probably benign |
|
IGL01869:Lama3
|
APN |
18 |
12,524,763 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL01894:Lama3
|
APN |
18 |
12,572,064 (GRCm38) |
missense |
probably benign |
0.09 |
IGL02027:Lama3
|
APN |
18 |
12,516,513 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02106:Lama3
|
APN |
18 |
12,468,314 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02307:Lama3
|
APN |
18 |
12,581,783 (GRCm38) |
missense |
probably benign |
0.09 |
IGL02342:Lama3
|
APN |
18 |
12,491,476 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02377:Lama3
|
APN |
18 |
12,556,750 (GRCm38) |
missense |
possibly damaging |
0.49 |
IGL02401:Lama3
|
APN |
18 |
12,557,727 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02517:Lama3
|
APN |
18 |
12,537,858 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02644:Lama3
|
APN |
18 |
12,525,853 (GRCm38) |
missense |
probably benign |
0.12 |
IGL02733:Lama3
|
APN |
18 |
12,578,127 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02932:Lama3
|
APN |
18 |
12,528,801 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03006:Lama3
|
APN |
18 |
12,468,368 (GRCm38) |
splice site |
probably benign |
|
IGL03038:Lama3
|
APN |
18 |
12,419,250 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03064:Lama3
|
APN |
18 |
12,439,349 (GRCm38) |
missense |
possibly damaging |
0.72 |
IGL03146:Lama3
|
APN |
18 |
12,527,624 (GRCm38) |
missense |
possibly damaging |
0.66 |
IGL03233:Lama3
|
APN |
18 |
12,481,038 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03255:Lama3
|
APN |
18 |
12,539,703 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03369:Lama3
|
APN |
18 |
12,553,283 (GRCm38) |
missense |
probably benign |
0.05 |
IGL03412:Lama3
|
APN |
18 |
12,419,182 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02980:Lama3
|
UTSW |
18 |
12,553,231 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03014:Lama3
|
UTSW |
18 |
12,539,967 (GRCm38) |
missense |
possibly damaging |
0.95 |
R0007:Lama3
|
UTSW |
18 |
12,497,881 (GRCm38) |
splice site |
probably benign |
|
R0007:Lama3
|
UTSW |
18 |
12,497,881 (GRCm38) |
splice site |
probably benign |
|
R0050:Lama3
|
UTSW |
18 |
12,404,103 (GRCm38) |
missense |
probably damaging |
1.00 |
R0050:Lama3
|
UTSW |
18 |
12,404,103 (GRCm38) |
missense |
probably damaging |
1.00 |
R0063:Lama3
|
UTSW |
18 |
12,528,705 (GRCm38) |
splice site |
probably benign |
|
R0063:Lama3
|
UTSW |
18 |
12,528,705 (GRCm38) |
splice site |
probably benign |
|
R0106:Lama3
|
UTSW |
18 |
12,403,982 (GRCm38) |
missense |
probably damaging |
0.96 |
R0148:Lama3
|
UTSW |
18 |
12,448,272 (GRCm38) |
missense |
probably damaging |
1.00 |
R0165:Lama3
|
UTSW |
18 |
12,524,810 (GRCm38) |
missense |
probably damaging |
0.99 |
R0240:Lama3
|
UTSW |
18 |
12,539,823 (GRCm38) |
splice site |
probably null |
|
R0240:Lama3
|
UTSW |
18 |
12,539,823 (GRCm38) |
splice site |
probably null |
|
R0316:Lama3
|
UTSW |
18 |
12,519,877 (GRCm38) |
missense |
probably benign |
0.09 |
R0325:Lama3
|
UTSW |
18 |
12,482,126 (GRCm38) |
missense |
probably damaging |
1.00 |
R0365:Lama3
|
UTSW |
18 |
12,507,007 (GRCm38) |
missense |
probably damaging |
0.96 |
R0390:Lama3
|
UTSW |
18 |
12,407,563 (GRCm38) |
missense |
probably benign |
0.10 |
R0408:Lama3
|
UTSW |
18 |
12,456,837 (GRCm38) |
missense |
probably benign |
|
R0449:Lama3
|
UTSW |
18 |
12,500,512 (GRCm38) |
splice site |
probably null |
|
R0453:Lama3
|
UTSW |
18 |
12,465,478 (GRCm38) |
missense |
possibly damaging |
0.63 |
R0480:Lama3
|
UTSW |
18 |
12,450,424 (GRCm38) |
missense |
possibly damaging |
0.81 |
R0536:Lama3
|
UTSW |
18 |
12,525,894 (GRCm38) |
missense |
probably damaging |
1.00 |
R0545:Lama3
|
UTSW |
18 |
12,561,701 (GRCm38) |
missense |
possibly damaging |
0.90 |
R0567:Lama3
|
UTSW |
18 |
12,549,252 (GRCm38) |
missense |
probably benign |
|
R0605:Lama3
|
UTSW |
18 |
12,506,949 (GRCm38) |
missense |
probably benign |
0.02 |
R0617:Lama3
|
UTSW |
18 |
12,419,258 (GRCm38) |
critical splice donor site |
probably null |
|
R0629:Lama3
|
UTSW |
18 |
12,419,245 (GRCm38) |
missense |
possibly damaging |
0.79 |
R0671:Lama3
|
UTSW |
18 |
12,477,590 (GRCm38) |
missense |
possibly damaging |
0.80 |
R0730:Lama3
|
UTSW |
18 |
12,456,850 (GRCm38) |
splice site |
probably benign |
|
R1216:Lama3
|
UTSW |
18 |
12,421,134 (GRCm38) |
splice site |
probably benign |
|
R1356:Lama3
|
UTSW |
18 |
12,500,577 (GRCm38) |
unclassified |
probably benign |
|
R1386:Lama3
|
UTSW |
18 |
12,477,370 (GRCm38) |
missense |
probably benign |
0.04 |
R1424:Lama3
|
UTSW |
18 |
12,519,991 (GRCm38) |
missense |
probably benign |
0.13 |
R1426:Lama3
|
UTSW |
18 |
12,481,098 (GRCm38) |
critical splice donor site |
probably null |
|
R1437:Lama3
|
UTSW |
18 |
12,549,227 (GRCm38) |
missense |
possibly damaging |
0.46 |
R1468:Lama3
|
UTSW |
18 |
12,441,107 (GRCm38) |
missense |
probably benign |
0.00 |
R1468:Lama3
|
UTSW |
18 |
12,441,107 (GRCm38) |
missense |
probably benign |
0.00 |
R1472:Lama3
|
UTSW |
18 |
12,482,045 (GRCm38) |
missense |
probably benign |
0.23 |
R1557:Lama3
|
UTSW |
18 |
12,513,731 (GRCm38) |
splice site |
probably benign |
|
R1571:Lama3
|
UTSW |
18 |
12,539,717 (GRCm38) |
missense |
probably damaging |
0.98 |
R1599:Lama3
|
UTSW |
18 |
12,450,400 (GRCm38) |
nonsense |
probably null |
|
R1631:Lama3
|
UTSW |
18 |
12,407,494 (GRCm38) |
missense |
probably damaging |
1.00 |
R1647:Lama3
|
UTSW |
18 |
12,532,199 (GRCm38) |
missense |
possibly damaging |
0.90 |
R1648:Lama3
|
UTSW |
18 |
12,532,199 (GRCm38) |
missense |
possibly damaging |
0.90 |
R1719:Lama3
|
UTSW |
18 |
12,479,872 (GRCm38) |
critical splice donor site |
probably null |
|
R1757:Lama3
|
UTSW |
18 |
12,465,499 (GRCm38) |
missense |
probably benign |
0.10 |
R1766:Lama3
|
UTSW |
18 |
12,402,062 (GRCm38) |
missense |
probably damaging |
1.00 |
R1853:Lama3
|
UTSW |
18 |
12,513,705 (GRCm38) |
missense |
possibly damaging |
0.75 |
R1856:Lama3
|
UTSW |
18 |
12,537,781 (GRCm38) |
nonsense |
probably null |
|
R1909:Lama3
|
UTSW |
18 |
12,581,798 (GRCm38) |
missense |
probably benign |
0.19 |
R1913:Lama3
|
UTSW |
18 |
12,495,279 (GRCm38) |
missense |
probably benign |
0.15 |
R1975:Lama3
|
UTSW |
18 |
12,453,863 (GRCm38) |
missense |
probably damaging |
1.00 |
R2014:Lama3
|
UTSW |
18 |
12,524,721 (GRCm38) |
splice site |
probably benign |
|
R2059:Lama3
|
UTSW |
18 |
12,528,333 (GRCm38) |
missense |
probably damaging |
0.98 |
R2060:Lama3
|
UTSW |
18 |
12,528,726 (GRCm38) |
missense |
probably benign |
0.30 |
R2086:Lama3
|
UTSW |
18 |
12,524,830 (GRCm38) |
missense |
probably benign |
0.39 |
R2115:Lama3
|
UTSW |
18 |
12,402,849 (GRCm38) |
missense |
possibly damaging |
0.94 |
R2291:Lama3
|
UTSW |
18 |
12,525,079 (GRCm38) |
missense |
probably damaging |
0.98 |
R2860:Lama3
|
UTSW |
18 |
12,453,750 (GRCm38) |
missense |
probably damaging |
1.00 |
R2861:Lama3
|
UTSW |
18 |
12,453,750 (GRCm38) |
missense |
probably damaging |
1.00 |
R2862:Lama3
|
UTSW |
18 |
12,453,750 (GRCm38) |
missense |
probably damaging |
1.00 |
R3410:Lama3
|
UTSW |
18 |
12,413,858 (GRCm38) |
critical splice donor site |
probably null |
|
R3614:Lama3
|
UTSW |
18 |
12,448,288 (GRCm38) |
missense |
probably benign |
0.03 |
R3696:Lama3
|
UTSW |
18 |
12,439,475 (GRCm38) |
splice site |
probably benign |
|
R3752:Lama3
|
UTSW |
18 |
12,507,029 (GRCm38) |
missense |
probably damaging |
1.00 |
R3967:Lama3
|
UTSW |
18 |
12,580,341 (GRCm38) |
missense |
probably damaging |
1.00 |
R3968:Lama3
|
UTSW |
18 |
12,580,341 (GRCm38) |
missense |
probably damaging |
1.00 |
R3969:Lama3
|
UTSW |
18 |
12,580,341 (GRCm38) |
missense |
probably damaging |
1.00 |
R3970:Lama3
|
UTSW |
18 |
12,580,341 (GRCm38) |
missense |
probably damaging |
1.00 |
R4088:Lama3
|
UTSW |
18 |
12,504,308 (GRCm38) |
nonsense |
probably null |
|
R4118:Lama3
|
UTSW |
18 |
12,450,431 (GRCm38) |
missense |
probably benign |
0.01 |
R4222:Lama3
|
UTSW |
18 |
12,450,403 (GRCm38) |
missense |
probably damaging |
1.00 |
R4223:Lama3
|
UTSW |
18 |
12,450,403 (GRCm38) |
missense |
probably damaging |
1.00 |
R4224:Lama3
|
UTSW |
18 |
12,450,403 (GRCm38) |
missense |
probably damaging |
1.00 |
R4225:Lama3
|
UTSW |
18 |
12,450,403 (GRCm38) |
missense |
probably damaging |
1.00 |
R4367:Lama3
|
UTSW |
18 |
12,513,690 (GRCm38) |
missense |
probably damaging |
1.00 |
R4404:Lama3
|
UTSW |
18 |
12,582,531 (GRCm38) |
missense |
probably benign |
0.01 |
R4424:Lama3
|
UTSW |
18 |
12,519,872 (GRCm38) |
nonsense |
probably null |
|
R4483:Lama3
|
UTSW |
18 |
12,549,253 (GRCm38) |
missense |
probably benign |
0.32 |
R4484:Lama3
|
UTSW |
18 |
12,481,088 (GRCm38) |
missense |
probably benign |
|
R4516:Lama3
|
UTSW |
18 |
12,495,358 (GRCm38) |
missense |
probably damaging |
1.00 |
R4556:Lama3
|
UTSW |
18 |
12,479,759 (GRCm38) |
missense |
possibly damaging |
0.63 |
R4616:Lama3
|
UTSW |
18 |
12,504,397 (GRCm38) |
critical splice donor site |
probably null |
|
R4702:Lama3
|
UTSW |
18 |
12,578,029 (GRCm38) |
nonsense |
probably null |
|
R4704:Lama3
|
UTSW |
18 |
12,553,223 (GRCm38) |
missense |
probably benign |
0.08 |
R4750:Lama3
|
UTSW |
18 |
12,504,359 (GRCm38) |
missense |
probably benign |
0.25 |
R4753:Lama3
|
UTSW |
18 |
12,482,084 (GRCm38) |
missense |
probably damaging |
1.00 |
R4767:Lama3
|
UTSW |
18 |
12,500,563 (GRCm38) |
missense |
probably benign |
0.32 |
R4777:Lama3
|
UTSW |
18 |
12,413,771 (GRCm38) |
missense |
probably damaging |
1.00 |
R4782:Lama3
|
UTSW |
18 |
12,411,570 (GRCm38) |
nonsense |
probably null |
|
R4784:Lama3
|
UTSW |
18 |
12,449,544 (GRCm38) |
missense |
probably benign |
0.20 |
R4816:Lama3
|
UTSW |
18 |
12,477,604 (GRCm38) |
missense |
possibly damaging |
0.93 |
R4833:Lama3
|
UTSW |
18 |
12,441,131 (GRCm38) |
missense |
probably benign |
0.01 |
R4854:Lama3
|
UTSW |
18 |
12,411,542 (GRCm38) |
missense |
probably benign |
0.00 |
R4863:Lama3
|
UTSW |
18 |
12,498,678 (GRCm38) |
intron |
probably benign |
|
R4863:Lama3
|
UTSW |
18 |
12,539,793 (GRCm38) |
missense |
probably damaging |
0.99 |
R4953:Lama3
|
UTSW |
18 |
12,448,305 (GRCm38) |
missense |
probably damaging |
1.00 |
R4974:Lama3
|
UTSW |
18 |
12,552,826 (GRCm38) |
missense |
probably damaging |
0.98 |
R4996:Lama3
|
UTSW |
18 |
12,518,743 (GRCm38) |
missense |
probably benign |
0.24 |
R5049:Lama3
|
UTSW |
18 |
12,582,611 (GRCm38) |
missense |
probably benign |
0.19 |
R5057:Lama3
|
UTSW |
18 |
12,531,948 (GRCm38) |
missense |
probably null |
0.82 |
R5090:Lama3
|
UTSW |
18 |
12,542,402 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5122:Lama3
|
UTSW |
18 |
12,539,766 (GRCm38) |
missense |
possibly damaging |
0.53 |
R5215:Lama3
|
UTSW |
18 |
12,577,900 (GRCm38) |
missense |
probably damaging |
1.00 |
R5245:Lama3
|
UTSW |
18 |
12,419,893 (GRCm38) |
missense |
probably damaging |
1.00 |
R5259:Lama3
|
UTSW |
18 |
12,465,508 (GRCm38) |
missense |
probably damaging |
1.00 |
R5320:Lama3
|
UTSW |
18 |
12,552,855 (GRCm38) |
missense |
probably damaging |
0.99 |
R5377:Lama3
|
UTSW |
18 |
12,453,746 (GRCm38) |
missense |
probably damaging |
0.99 |
R5432:Lama3
|
UTSW |
18 |
12,572,066 (GRCm38) |
missense |
probably damaging |
1.00 |
R5500:Lama3
|
UTSW |
18 |
12,456,764 (GRCm38) |
missense |
possibly damaging |
0.93 |
R5534:Lama3
|
UTSW |
18 |
12,553,210 (GRCm38) |
missense |
probably benign |
0.00 |
R5589:Lama3
|
UTSW |
18 |
12,472,220 (GRCm38) |
missense |
possibly damaging |
0.46 |
R5604:Lama3
|
UTSW |
18 |
12,439,348 (GRCm38) |
missense |
probably benign |
|
R5617:Lama3
|
UTSW |
18 |
12,498,936 (GRCm38) |
intron |
probably benign |
|
R5709:Lama3
|
UTSW |
18 |
12,539,799 (GRCm38) |
missense |
probably damaging |
1.00 |
R5965:Lama3
|
UTSW |
18 |
12,429,887 (GRCm38) |
missense |
possibly damaging |
0.67 |
R6042:Lama3
|
UTSW |
18 |
12,574,254 (GRCm38) |
missense |
probably damaging |
1.00 |
R6065:Lama3
|
UTSW |
18 |
12,469,928 (GRCm38) |
missense |
possibly damaging |
0.53 |
R6085:Lama3
|
UTSW |
18 |
12,482,099 (GRCm38) |
missense |
probably benign |
0.01 |
R6212:Lama3
|
UTSW |
18 |
12,513,645 (GRCm38) |
missense |
probably damaging |
1.00 |
R6268:Lama3
|
UTSW |
18 |
12,524,737 (GRCm38) |
missense |
probably damaging |
0.98 |
R6276:Lama3
|
UTSW |
18 |
12,506,949 (GRCm38) |
missense |
probably benign |
0.02 |
R6366:Lama3
|
UTSW |
18 |
12,482,137 (GRCm38) |
missense |
probably damaging |
1.00 |
R6393:Lama3
|
UTSW |
18 |
12,479,756 (GRCm38) |
missense |
probably benign |
0.44 |
R6493:Lama3
|
UTSW |
18 |
12,482,148 (GRCm38) |
critical splice donor site |
probably null |
|
R6505:Lama3
|
UTSW |
18 |
12,495,348 (GRCm38) |
missense |
probably benign |
0.02 |
R6563:Lama3
|
UTSW |
18 |
12,537,766 (GRCm38) |
missense |
probably damaging |
1.00 |
R6582:Lama3
|
UTSW |
18 |
12,577,840 (GRCm38) |
missense |
probably damaging |
1.00 |
R6585:Lama3
|
UTSW |
18 |
12,419,257 (GRCm38) |
critical splice donor site |
probably null |
|
R6609:Lama3
|
UTSW |
18 |
12,513,678 (GRCm38) |
missense |
probably damaging |
0.99 |
R6656:Lama3
|
UTSW |
18 |
12,549,226 (GRCm38) |
missense |
possibly damaging |
0.66 |
R6833:Lama3
|
UTSW |
18 |
12,491,548 (GRCm38) |
missense |
probably damaging |
1.00 |
R6834:Lama3
|
UTSW |
18 |
12,491,548 (GRCm38) |
missense |
probably damaging |
1.00 |
R7019:Lama3
|
UTSW |
18 |
12,528,418 (GRCm38) |
missense |
probably damaging |
0.97 |
R7026:Lama3
|
UTSW |
18 |
12,516,548 (GRCm38) |
missense |
probably damaging |
0.98 |
R7088:Lama3
|
UTSW |
18 |
12,582,545 (GRCm38) |
missense |
possibly damaging |
0.90 |
R7100:Lama3
|
UTSW |
18 |
12,582,644 (GRCm38) |
missense |
possibly damaging |
0.80 |
R7102:Lama3
|
UTSW |
18 |
12,552,813 (GRCm38) |
missense |
possibly damaging |
0.66 |
R7103:Lama3
|
UTSW |
18 |
12,531,879 (GRCm38) |
missense |
probably benign |
0.00 |
R7121:Lama3
|
UTSW |
18 |
12,462,782 (GRCm38) |
missense |
probably benign |
0.06 |
R7133:Lama3
|
UTSW |
18 |
12,539,786 (GRCm38) |
missense |
probably benign |
0.05 |
R7150:Lama3
|
UTSW |
18 |
12,468,289 (GRCm38) |
missense |
probably damaging |
1.00 |
R7158:Lama3
|
UTSW |
18 |
12,456,812 (GRCm38) |
missense |
probably benign |
0.20 |
R7170:Lama3
|
UTSW |
18 |
12,404,076 (GRCm38) |
missense |
probably benign |
0.26 |
R7216:Lama3
|
UTSW |
18 |
12,430,000 (GRCm38) |
missense |
probably damaging |
1.00 |
R7223:Lama3
|
UTSW |
18 |
12,582,608 (GRCm38) |
missense |
possibly damaging |
0.53 |
R7243:Lama3
|
UTSW |
18 |
12,419,845 (GRCm38) |
missense |
probably damaging |
1.00 |
R7282:Lama3
|
UTSW |
18 |
12,439,392 (GRCm38) |
missense |
probably damaging |
0.99 |
R7337:Lama3
|
UTSW |
18 |
12,507,040 (GRCm38) |
splice site |
probably null |
|
R7442:Lama3
|
UTSW |
18 |
12,472,181 (GRCm38) |
critical splice acceptor site |
probably null |
|
R7487:Lama3
|
UTSW |
18 |
12,419,237 (GRCm38) |
missense |
probably benign |
|
R7609:Lama3
|
UTSW |
18 |
12,531,834 (GRCm38) |
critical splice acceptor site |
probably null |
|
R7650:Lama3
|
UTSW |
18 |
12,537,838 (GRCm38) |
missense |
probably benign |
0.01 |
R7894:Lama3
|
UTSW |
18 |
12,462,807 (GRCm38) |
missense |
probably benign |
0.07 |
R7975:Lama3
|
UTSW |
18 |
12,537,739 (GRCm38) |
missense |
probably damaging |
1.00 |
R8099:Lama3
|
UTSW |
18 |
12,534,063 (GRCm38) |
missense |
probably damaging |
0.97 |
R8168:Lama3
|
UTSW |
18 |
12,506,942 (GRCm38) |
missense |
probably null |
|
R8219:Lama3
|
UTSW |
18 |
12,439,360 (GRCm38) |
missense |
probably benign |
0.07 |
R8227:Lama3
|
UTSW |
18 |
12,407,551 (GRCm38) |
missense |
probably benign |
|
R8229:Lama3
|
UTSW |
18 |
12,407,551 (GRCm38) |
missense |
probably benign |
|
R8298:Lama3
|
UTSW |
18 |
12,525,853 (GRCm38) |
missense |
probably benign |
0.12 |
R8351:Lama3
|
UTSW |
18 |
12,540,613 (GRCm38) |
missense |
probably damaging |
1.00 |
R8364:Lama3
|
UTSW |
18 |
12,528,347 (GRCm38) |
missense |
probably damaging |
0.99 |
R8463:Lama3
|
UTSW |
18 |
12,449,839 (GRCm38) |
missense |
probably damaging |
0.96 |
R8515:Lama3
|
UTSW |
18 |
12,411,631 (GRCm38) |
missense |
probably null |
0.01 |
R8784:Lama3
|
UTSW |
18 |
12,421,155 (GRCm38) |
missense |
probably benign |
|
R8799:Lama3
|
UTSW |
18 |
12,490,943 (GRCm38) |
missense |
probably damaging |
0.96 |
R8874:Lama3
|
UTSW |
18 |
12,449,586 (GRCm38) |
critical splice donor site |
probably null |
|
R8938:Lama3
|
UTSW |
18 |
12,556,705 (GRCm38) |
missense |
probably damaging |
1.00 |
R8967:Lama3
|
UTSW |
18 |
12,532,039 (GRCm38) |
missense |
possibly damaging |
0.46 |
R9039:Lama3
|
UTSW |
18 |
12,481,063 (GRCm38) |
nonsense |
probably null |
|
R9126:Lama3
|
UTSW |
18 |
12,450,470 (GRCm38) |
missense |
probably damaging |
1.00 |
R9200:Lama3
|
UTSW |
18 |
12,472,240 (GRCm38) |
missense |
probably benign |
0.00 |
R9203:Lama3
|
UTSW |
18 |
12,462,812 (GRCm38) |
missense |
probably benign |
0.04 |
R9246:Lama3
|
UTSW |
18 |
12,577,902 (GRCm38) |
missense |
probably damaging |
0.99 |
R9284:Lama3
|
UTSW |
18 |
12,450,484 (GRCm38) |
nonsense |
probably null |
|
R9553:Lama3
|
UTSW |
18 |
12,429,962 (GRCm38) |
missense |
probably damaging |
1.00 |
R9716:Lama3
|
UTSW |
18 |
12,450,403 (GRCm38) |
missense |
probably damaging |
1.00 |
R9734:Lama3
|
UTSW |
18 |
12,549,263 (GRCm38) |
missense |
possibly damaging |
0.94 |
X0019:Lama3
|
UTSW |
18 |
12,582,574 (GRCm38) |
missense |
possibly damaging |
0.94 |
Z1177:Lama3
|
UTSW |
18 |
12,429,879 (GRCm38) |
critical splice acceptor site |
probably null |
|
|