Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
A |
G |
7: 40,644,149 (GRCm39) |
Y606C |
probably benign |
Het |
Acad9 |
A |
G |
3: 36,139,630 (GRCm39) |
Y410C |
probably damaging |
Het |
Acot6 |
C |
T |
12: 84,156,149 (GRCm39) |
P366S |
probably damaging |
Het |
Adrm1b |
T |
C |
3: 92,336,315 (GRCm39) |
|
probably benign |
Het |
Anks1 |
G |
T |
17: 28,273,273 (GRCm39) |
G964V |
probably damaging |
Het |
Apol7a |
A |
T |
15: 77,274,176 (GRCm39) |
|
probably benign |
Het |
Arid3c |
G |
A |
4: 41,725,087 (GRCm39) |
A320V |
probably damaging |
Het |
Bnip3l |
A |
T |
14: 67,237,101 (GRCm39) |
N50K |
probably benign |
Het |
C1qtnf4 |
C |
A |
2: 90,720,297 (GRCm39) |
A190D |
probably benign |
Het |
Calhm5 |
A |
T |
10: 33,972,189 (GRCm39) |
M82K |
probably benign |
Het |
Cdcp3 |
G |
T |
7: 130,824,400 (GRCm39) |
W165L |
probably damaging |
Het |
Cdh1 |
G |
T |
8: 107,387,545 (GRCm39) |
V482L |
probably benign |
Het |
Cdrt4 |
A |
C |
11: 62,883,486 (GRCm39) |
I63L |
probably benign |
Het |
Cic |
A |
T |
7: 24,970,736 (GRCm39) |
T156S |
possibly damaging |
Het |
Ckm |
A |
G |
7: 19,154,156 (GRCm39) |
N301S |
probably benign |
Het |
Colgalt1 |
C |
T |
8: 72,076,165 (GRCm39) |
R539C |
probably damaging |
Het |
Cop1 |
A |
G |
1: 159,134,154 (GRCm39) |
D132G |
probably damaging |
Het |
Cpd |
G |
T |
11: 76,675,881 (GRCm39) |
N1257K |
probably benign |
Het |
Cyp2c67 |
T |
C |
19: 39,604,123 (GRCm39) |
H411R |
probably damaging |
Het |
Cyp2r1 |
A |
T |
7: 114,152,316 (GRCm39) |
F5I |
probably damaging |
Het |
Dclk3 |
T |
A |
9: 111,296,768 (GRCm39) |
L104Q |
possibly damaging |
Het |
Dnah7c |
A |
T |
1: 46,494,973 (GRCm39) |
Q67L |
probably benign |
Het |
Dnm1l |
C |
A |
16: 16,147,671 (GRCm39) |
E365* |
probably null |
Het |
Dst |
A |
T |
1: 34,205,315 (GRCm39) |
I502F |
probably damaging |
Het |
Espl1 |
T |
C |
15: 102,212,535 (GRCm39) |
V547A |
possibly damaging |
Het |
Foxa1 |
C |
T |
12: 57,589,264 (GRCm39) |
A319T |
probably benign |
Het |
Frem1 |
G |
T |
4: 82,904,838 (GRCm39) |
H859N |
probably damaging |
Het |
Frem3 |
T |
A |
8: 81,339,208 (GRCm39) |
D500E |
probably damaging |
Het |
Gpatch2l |
G |
A |
12: 86,290,958 (GRCm39) |
R47H |
probably damaging |
Het |
Grip1 |
A |
G |
10: 119,822,375 (GRCm39) |
D394G |
probably damaging |
Het |
Gsap |
C |
A |
5: 21,476,235 (GRCm39) |
T589K |
possibly damaging |
Het |
Gsg1l |
A |
G |
7: 125,522,658 (GRCm39) |
V190A |
probably damaging |
Het |
Kcnmb1 |
A |
T |
11: 33,920,131 (GRCm39) |
T115S |
probably benign |
Het |
Kirrel2 |
A |
C |
7: 30,154,604 (GRCm39) |
F169C |
probably damaging |
Het |
L3mbtl1 |
C |
T |
2: 162,803,368 (GRCm39) |
T397M |
probably damaging |
Het |
Lamc2 |
G |
A |
1: 153,012,508 (GRCm39) |
T722M |
probably benign |
Het |
Lrig1 |
T |
C |
6: 94,588,610 (GRCm39) |
D513G |
possibly damaging |
Het |
Lrrk1 |
T |
C |
7: 65,942,090 (GRCm39) |
D716G |
probably damaging |
Het |
Matn4 |
G |
A |
2: 164,231,584 (GRCm39) |
R582* |
probably null |
Het |
Mdn1 |
A |
T |
4: 32,733,374 (GRCm39) |
R3133W |
probably benign |
Het |
Mmp7 |
A |
G |
9: 7,695,489 (GRCm39) |
D122G |
probably damaging |
Het |
Naaladl1 |
A |
G |
19: 6,165,578 (GRCm39) |
D744G |
possibly damaging |
Het |
Nampt |
T |
G |
12: 32,898,742 (GRCm39) |
Y453D |
probably benign |
Het |
Nlrp12 |
A |
G |
7: 3,288,481 (GRCm39) |
V677A |
probably benign |
Het |
Ntng2 |
T |
C |
2: 29,087,080 (GRCm39) |
N414S |
probably damaging |
Het |
Or1e16 |
A |
G |
11: 73,286,410 (GRCm39) |
V146A |
probably benign |
Het |
Or4g17 |
A |
G |
2: 111,209,708 (GRCm39) |
D121G |
probably damaging |
Het |
Or5p52 |
A |
G |
7: 107,502,829 (GRCm39) |
R302G |
probably benign |
Het |
Or9m1b |
A |
C |
2: 87,836,529 (GRCm39) |
F189V |
probably benign |
Het |
Parp4 |
A |
C |
14: 56,851,196 (GRCm39) |
Q733P |
probably damaging |
Het |
Pdcl3 |
G |
A |
1: 39,034,417 (GRCm39) |
V56I |
probably benign |
Het |
Pepd |
A |
G |
7: 34,721,144 (GRCm39) |
Y256C |
probably damaging |
Het |
Plg |
G |
T |
17: 12,637,938 (GRCm39) |
R788L |
probably benign |
Het |
Plod1 |
A |
T |
4: 148,000,675 (GRCm39) |
|
probably benign |
Het |
Ptprc |
A |
G |
1: 138,016,482 (GRCm39) |
V513A |
probably damaging |
Het |
Pxdn |
T |
C |
12: 30,045,370 (GRCm39) |
I373T |
possibly damaging |
Het |
Qrfprl |
A |
T |
6: 65,418,285 (GRCm39) |
K151I |
probably damaging |
Het |
Rbbp8 |
G |
A |
18: 11,851,965 (GRCm39) |
G262E |
probably damaging |
Het |
Rfc2 |
T |
A |
5: 134,623,104 (GRCm39) |
Y240* |
probably null |
Het |
Rps15 |
A |
G |
10: 80,129,598 (GRCm39) |
E71G |
possibly damaging |
Het |
Rsrc1 |
C |
T |
3: 66,901,982 (GRCm39) |
P44L |
unknown |
Het |
Ryr1 |
A |
C |
7: 28,793,607 (GRCm39) |
M1287R |
probably damaging |
Het |
Scart2 |
G |
A |
7: 139,841,514 (GRCm39) |
D273N |
probably benign |
Het |
Serpina9 |
A |
G |
12: 103,967,495 (GRCm39) |
L300P |
probably damaging |
Het |
Sh3rf2 |
G |
A |
18: 42,234,606 (GRCm39) |
A130T |
probably damaging |
Het |
Slc12a8 |
G |
A |
16: 33,355,263 (GRCm39) |
W26* |
probably null |
Het |
Snx18 |
A |
T |
13: 113,731,265 (GRCm39) |
H576Q |
probably damaging |
Het |
Tagln3 |
G |
A |
16: 45,543,321 (GRCm39) |
T107I |
probably benign |
Het |
Thap1 |
C |
A |
8: 26,652,679 (GRCm39) |
T139K |
probably damaging |
Het |
Tle4 |
T |
A |
19: 14,541,817 (GRCm39) |
|
probably null |
Het |
Tmem87a |
A |
T |
2: 120,193,409 (GRCm39) |
M502K |
possibly damaging |
Het |
Tpcn2 |
A |
T |
7: 144,810,522 (GRCm39) |
V605E |
probably benign |
Het |
Trgj1 |
C |
A |
13: 19,394,529 (GRCm39) |
|
probably benign |
Het |
Tsc2 |
A |
T |
17: 24,847,028 (GRCm39) |
V179E |
probably damaging |
Het |
Ubap2l |
T |
C |
3: 89,916,548 (GRCm39) |
T909A |
probably damaging |
Het |
Ubl4b |
T |
G |
3: 107,462,140 (GRCm39) |
Q40P |
probably damaging |
Het |
Vmn1r229 |
A |
G |
17: 21,035,277 (GRCm39) |
D174G |
probably damaging |
Het |
Vmn2r50 |
A |
T |
7: 9,779,964 (GRCm39) |
Y472* |
probably null |
Het |
Vmn2r74 |
T |
A |
7: 85,601,943 (GRCm39) |
D565V |
probably benign |
Het |
Vmn2r74 |
T |
A |
7: 85,606,860 (GRCm39) |
|
probably null |
Het |
Vmn2r82 |
T |
A |
10: 79,232,377 (GRCm39) |
V792E |
probably damaging |
Het |
Zfp335 |
G |
A |
2: 164,735,210 (GRCm39) |
Q1179* |
probably null |
Het |
Zmynd12 |
A |
C |
4: 119,310,772 (GRCm39) |
K327Q |
probably benign |
Het |
Zwilch |
G |
A |
9: 64,072,731 (GRCm39) |
Q27* |
probably null |
Het |
|
Other mutations in Lama1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Lama1
|
APN |
17 |
68,122,923 (GRCm39) |
missense |
probably benign |
|
IGL00336:Lama1
|
APN |
17 |
68,120,943 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01066:Lama1
|
APN |
17 |
68,050,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01140:Lama1
|
APN |
17 |
68,109,928 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01291:Lama1
|
APN |
17 |
68,045,865 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01296:Lama1
|
APN |
17 |
68,052,046 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01317:Lama1
|
APN |
17 |
68,125,696 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01490:Lama1
|
APN |
17 |
68,057,579 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL01506:Lama1
|
APN |
17 |
68,092,065 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01508:Lama1
|
APN |
17 |
68,116,356 (GRCm39) |
splice site |
probably benign |
|
IGL01522:Lama1
|
APN |
17 |
68,059,769 (GRCm39) |
splice site |
probably benign |
|
IGL01530:Lama1
|
APN |
17 |
68,103,785 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01541:Lama1
|
APN |
17 |
68,092,065 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01677:Lama1
|
APN |
17 |
68,086,143 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01886:Lama1
|
APN |
17 |
68,114,792 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01994:Lama1
|
APN |
17 |
68,059,434 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02017:Lama1
|
APN |
17 |
68,071,720 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02021:Lama1
|
APN |
17 |
68,128,621 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02026:Lama1
|
APN |
17 |
68,116,287 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02044:Lama1
|
APN |
17 |
68,118,485 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02120:Lama1
|
APN |
17 |
68,023,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02425:Lama1
|
APN |
17 |
68,118,480 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02549:Lama1
|
APN |
17 |
68,097,830 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02642:Lama1
|
APN |
17 |
68,119,361 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02795:Lama1
|
APN |
17 |
68,045,889 (GRCm39) |
splice site |
probably null |
|
IGL02798:Lama1
|
APN |
17 |
68,102,186 (GRCm39) |
splice site |
probably benign |
|
IGL02863:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02870:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02876:Lama1
|
APN |
17 |
68,057,687 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02885:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02891:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02978:Lama1
|
APN |
17 |
68,093,076 (GRCm39) |
nonsense |
probably null |
|
IGL03064:Lama1
|
APN |
17 |
68,086,099 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03076:Lama1
|
APN |
17 |
68,023,794 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03110:Lama1
|
APN |
17 |
68,105,981 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03143:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03159:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03268:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
ANU05:Lama1
|
UTSW |
17 |
68,045,865 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4472001:Lama1
|
UTSW |
17 |
68,071,699 (GRCm39) |
missense |
|
|
R0047:Lama1
|
UTSW |
17 |
68,102,181 (GRCm39) |
splice site |
probably benign |
|
R0047:Lama1
|
UTSW |
17 |
68,102,181 (GRCm39) |
splice site |
probably benign |
|
R0050:Lama1
|
UTSW |
17 |
68,089,051 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0096:Lama1
|
UTSW |
17 |
68,112,408 (GRCm39) |
missense |
probably benign |
0.12 |
R0096:Lama1
|
UTSW |
17 |
68,112,408 (GRCm39) |
missense |
probably benign |
0.12 |
R0111:Lama1
|
UTSW |
17 |
68,044,493 (GRCm39) |
missense |
probably damaging |
0.98 |
R0116:Lama1
|
UTSW |
17 |
68,083,918 (GRCm39) |
missense |
probably benign |
0.10 |
R0121:Lama1
|
UTSW |
17 |
68,105,508 (GRCm39) |
splice site |
probably benign |
|
R0278:Lama1
|
UTSW |
17 |
68,117,178 (GRCm39) |
missense |
probably null |
0.98 |
R0281:Lama1
|
UTSW |
17 |
68,124,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Lama1
|
UTSW |
17 |
68,082,846 (GRCm39) |
missense |
possibly damaging |
0.45 |
R0419:Lama1
|
UTSW |
17 |
68,098,605 (GRCm39) |
critical splice donor site |
probably null |
|
R0512:Lama1
|
UTSW |
17 |
68,086,129 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0514:Lama1
|
UTSW |
17 |
68,071,693 (GRCm39) |
missense |
probably benign |
0.40 |
R0562:Lama1
|
UTSW |
17 |
68,122,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R0632:Lama1
|
UTSW |
17 |
68,059,363 (GRCm39) |
splice site |
probably benign |
|
R0645:Lama1
|
UTSW |
17 |
68,080,707 (GRCm39) |
missense |
probably benign |
0.01 |
R0712:Lama1
|
UTSW |
17 |
68,086,037 (GRCm39) |
splice site |
probably null |
|
R0763:Lama1
|
UTSW |
17 |
68,079,813 (GRCm39) |
missense |
probably damaging |
0.97 |
R0941:Lama1
|
UTSW |
17 |
68,082,860 (GRCm39) |
missense |
probably benign |
0.10 |
R1025:Lama1
|
UTSW |
17 |
68,059,893 (GRCm39) |
missense |
probably benign |
0.00 |
R1084:Lama1
|
UTSW |
17 |
68,111,464 (GRCm39) |
missense |
probably benign |
0.12 |
R1103:Lama1
|
UTSW |
17 |
68,097,942 (GRCm39) |
missense |
probably damaging |
0.98 |
R1420:Lama1
|
UTSW |
17 |
68,097,942 (GRCm39) |
missense |
probably damaging |
0.98 |
R1430:Lama1
|
UTSW |
17 |
68,089,150 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1569:Lama1
|
UTSW |
17 |
68,087,613 (GRCm39) |
splice site |
probably null |
|
R1575:Lama1
|
UTSW |
17 |
68,117,404 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1613:Lama1
|
UTSW |
17 |
68,114,918 (GRCm39) |
missense |
probably benign |
0.42 |
R1620:Lama1
|
UTSW |
17 |
68,074,028 (GRCm39) |
missense |
probably benign |
0.01 |
R1629:Lama1
|
UTSW |
17 |
68,112,423 (GRCm39) |
missense |
probably benign |
0.00 |
R1645:Lama1
|
UTSW |
17 |
68,044,677 (GRCm39) |
missense |
probably benign |
0.14 |
R1652:Lama1
|
UTSW |
17 |
68,114,841 (GRCm39) |
missense |
probably damaging |
0.97 |
R1674:Lama1
|
UTSW |
17 |
68,098,239 (GRCm39) |
missense |
probably benign |
|
R1678:Lama1
|
UTSW |
17 |
68,117,150 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1710:Lama1
|
UTSW |
17 |
68,060,786 (GRCm39) |
missense |
probably benign |
0.00 |
R1712:Lama1
|
UTSW |
17 |
68,024,181 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1737:Lama1
|
UTSW |
17 |
68,109,916 (GRCm39) |
missense |
probably benign |
0.36 |
R1757:Lama1
|
UTSW |
17 |
68,004,378 (GRCm39) |
missense |
unknown |
|
R1757:Lama1
|
UTSW |
17 |
68,070,831 (GRCm39) |
missense |
probably benign |
0.40 |
R1813:Lama1
|
UTSW |
17 |
68,098,218 (GRCm39) |
missense |
probably benign |
|
R1896:Lama1
|
UTSW |
17 |
68,098,218 (GRCm39) |
missense |
probably benign |
|
R1945:Lama1
|
UTSW |
17 |
68,052,848 (GRCm39) |
missense |
probably benign |
0.14 |
R2086:Lama1
|
UTSW |
17 |
68,124,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Lama1
|
UTSW |
17 |
68,080,860 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2178:Lama1
|
UTSW |
17 |
68,076,510 (GRCm39) |
missense |
probably benign |
0.07 |
R2183:Lama1
|
UTSW |
17 |
68,098,004 (GRCm39) |
missense |
probably damaging |
0.98 |
R2197:Lama1
|
UTSW |
17 |
68,059,936 (GRCm39) |
missense |
probably benign |
0.02 |
R2213:Lama1
|
UTSW |
17 |
68,084,029 (GRCm39) |
nonsense |
probably null |
|
R2260:Lama1
|
UTSW |
17 |
68,044,502 (GRCm39) |
missense |
probably damaging |
0.96 |
R2356:Lama1
|
UTSW |
17 |
68,117,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R2420:Lama1
|
UTSW |
17 |
68,057,548 (GRCm39) |
missense |
probably benign |
0.00 |
R2421:Lama1
|
UTSW |
17 |
68,057,548 (GRCm39) |
missense |
probably benign |
0.00 |
R2422:Lama1
|
UTSW |
17 |
68,057,548 (GRCm39) |
missense |
probably benign |
0.00 |
R2424:Lama1
|
UTSW |
17 |
68,105,660 (GRCm39) |
missense |
probably benign |
0.09 |
R2442:Lama1
|
UTSW |
17 |
68,075,312 (GRCm39) |
missense |
probably benign |
0.04 |
R3147:Lama1
|
UTSW |
17 |
68,044,653 (GRCm39) |
missense |
probably damaging |
0.98 |
R3414:Lama1
|
UTSW |
17 |
68,044,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Lama1
|
UTSW |
17 |
68,075,328 (GRCm39) |
missense |
probably benign |
0.40 |
R3820:Lama1
|
UTSW |
17 |
68,086,041 (GRCm39) |
splice site |
probably null |
|
R3821:Lama1
|
UTSW |
17 |
68,086,041 (GRCm39) |
splice site |
probably null |
|
R3822:Lama1
|
UTSW |
17 |
68,086,041 (GRCm39) |
splice site |
probably null |
|
R4012:Lama1
|
UTSW |
17 |
68,119,368 (GRCm39) |
nonsense |
probably null |
|
R4113:Lama1
|
UTSW |
17 |
68,071,698 (GRCm39) |
missense |
probably benign |
0.01 |
R4133:Lama1
|
UTSW |
17 |
68,119,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Lama1
|
UTSW |
17 |
68,057,650 (GRCm39) |
missense |
probably damaging |
0.98 |
R4259:Lama1
|
UTSW |
17 |
68,059,413 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4278:Lama1
|
UTSW |
17 |
68,098,512 (GRCm39) |
missense |
probably null |
0.00 |
R4321:Lama1
|
UTSW |
17 |
68,078,078 (GRCm39) |
missense |
probably benign |
0.03 |
R4374:Lama1
|
UTSW |
17 |
68,111,513 (GRCm39) |
missense |
probably benign |
0.00 |
R4386:Lama1
|
UTSW |
17 |
68,080,707 (GRCm39) |
missense |
probably benign |
0.01 |
R4463:Lama1
|
UTSW |
17 |
68,068,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R4629:Lama1
|
UTSW |
17 |
68,112,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4630:Lama1
|
UTSW |
17 |
68,101,295 (GRCm39) |
missense |
probably benign |
0.00 |
R4633:Lama1
|
UTSW |
17 |
68,105,579 (GRCm39) |
missense |
probably damaging |
0.96 |
R4668:Lama1
|
UTSW |
17 |
68,059,429 (GRCm39) |
missense |
probably benign |
0.27 |
R4684:Lama1
|
UTSW |
17 |
68,080,773 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4745:Lama1
|
UTSW |
17 |
68,045,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Lama1
|
UTSW |
17 |
68,080,854 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4797:Lama1
|
UTSW |
17 |
68,023,770 (GRCm39) |
missense |
probably benign |
0.04 |
R4803:Lama1
|
UTSW |
17 |
68,116,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R4925:Lama1
|
UTSW |
17 |
68,101,309 (GRCm39) |
missense |
probably benign |
0.02 |
R4939:Lama1
|
UTSW |
17 |
68,044,470 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4952:Lama1
|
UTSW |
17 |
68,074,561 (GRCm39) |
critical splice donor site |
probably null |
|
R4975:Lama1
|
UTSW |
17 |
68,045,829 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4977:Lama1
|
UTSW |
17 |
68,044,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R5039:Lama1
|
UTSW |
17 |
68,052,888 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5047:Lama1
|
UTSW |
17 |
68,050,276 (GRCm39) |
nonsense |
probably null |
|
R5195:Lama1
|
UTSW |
17 |
68,071,795 (GRCm39) |
missense |
probably benign |
0.13 |
R5230:Lama1
|
UTSW |
17 |
68,052,078 (GRCm39) |
nonsense |
probably null |
|
R5236:Lama1
|
UTSW |
17 |
68,111,487 (GRCm39) |
missense |
probably benign |
0.24 |
R5254:Lama1
|
UTSW |
17 |
68,063,711 (GRCm39) |
missense |
probably benign |
0.01 |
R5345:Lama1
|
UTSW |
17 |
68,124,558 (GRCm39) |
missense |
probably benign |
|
R5438:Lama1
|
UTSW |
17 |
68,107,769 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5521:Lama1
|
UTSW |
17 |
68,087,889 (GRCm39) |
nonsense |
probably null |
|
R5568:Lama1
|
UTSW |
17 |
68,075,293 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5645:Lama1
|
UTSW |
17 |
68,109,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R5665:Lama1
|
UTSW |
17 |
68,077,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5727:Lama1
|
UTSW |
17 |
68,122,219 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5757:Lama1
|
UTSW |
17 |
68,045,782 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5795:Lama1
|
UTSW |
17 |
68,103,722 (GRCm39) |
missense |
probably benign |
0.02 |
R5857:Lama1
|
UTSW |
17 |
68,114,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R5894:Lama1
|
UTSW |
17 |
68,086,042 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5974:Lama1
|
UTSW |
17 |
68,080,722 (GRCm39) |
missense |
probably benign |
0.31 |
R6032:Lama1
|
UTSW |
17 |
68,057,638 (GRCm39) |
missense |
probably benign |
0.01 |
R6032:Lama1
|
UTSW |
17 |
68,057,638 (GRCm39) |
missense |
probably benign |
0.01 |
R6120:Lama1
|
UTSW |
17 |
68,087,612 (GRCm39) |
critical splice donor site |
probably null |
|
R6219:Lama1
|
UTSW |
17 |
68,097,851 (GRCm39) |
missense |
probably benign |
0.08 |
R6224:Lama1
|
UTSW |
17 |
68,109,982 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6249:Lama1
|
UTSW |
17 |
68,105,599 (GRCm39) |
missense |
probably benign |
|
R6265:Lama1
|
UTSW |
17 |
68,057,650 (GRCm39) |
missense |
probably damaging |
0.98 |
R6276:Lama1
|
UTSW |
17 |
68,091,083 (GRCm39) |
splice site |
probably null |
|
R6284:Lama1
|
UTSW |
17 |
68,117,091 (GRCm39) |
missense |
probably damaging |
0.99 |
R6337:Lama1
|
UTSW |
17 |
68,093,014 (GRCm39) |
missense |
probably benign |
0.27 |
R6414:Lama1
|
UTSW |
17 |
68,053,905 (GRCm39) |
critical splice donor site |
probably null |
|
R6631:Lama1
|
UTSW |
17 |
68,081,477 (GRCm39) |
missense |
probably benign |
0.21 |
R6659:Lama1
|
UTSW |
17 |
68,125,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R6660:Lama1
|
UTSW |
17 |
68,111,495 (GRCm39) |
missense |
probably benign |
0.05 |
R6677:Lama1
|
UTSW |
17 |
68,102,228 (GRCm39) |
missense |
probably benign |
0.14 |
R6763:Lama1
|
UTSW |
17 |
68,053,868 (GRCm39) |
missense |
unknown |
|
R6787:Lama1
|
UTSW |
17 |
68,091,020 (GRCm39) |
missense |
unknown |
|
R6831:Lama1
|
UTSW |
17 |
68,063,749 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6855:Lama1
|
UTSW |
17 |
68,089,150 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6910:Lama1
|
UTSW |
17 |
68,098,459 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6934:Lama1
|
UTSW |
17 |
68,081,538 (GRCm39) |
missense |
probably benign |
0.04 |
R6945:Lama1
|
UTSW |
17 |
68,120,861 (GRCm39) |
missense |
|
|
R6984:Lama1
|
UTSW |
17 |
68,086,107 (GRCm39) |
missense |
|
|
R6989:Lama1
|
UTSW |
17 |
68,060,753 (GRCm39) |
missense |
|
|
R6994:Lama1
|
UTSW |
17 |
68,060,820 (GRCm39) |
missense |
|
|
R7035:Lama1
|
UTSW |
17 |
68,088,044 (GRCm39) |
missense |
|
|
R7133:Lama1
|
UTSW |
17 |
68,089,141 (GRCm39) |
missense |
|
|
R7172:Lama1
|
UTSW |
17 |
68,111,540 (GRCm39) |
missense |
|
|
R7197:Lama1
|
UTSW |
17 |
68,044,700 (GRCm39) |
nonsense |
probably null |
|
R7217:Lama1
|
UTSW |
17 |
68,071,668 (GRCm39) |
missense |
|
|
R7229:Lama1
|
UTSW |
17 |
68,059,441 (GRCm39) |
missense |
|
|
R7264:Lama1
|
UTSW |
17 |
68,050,292 (GRCm39) |
missense |
|
|
R7311:Lama1
|
UTSW |
17 |
68,074,380 (GRCm39) |
missense |
|
|
R7394:Lama1
|
UTSW |
17 |
68,024,256 (GRCm39) |
missense |
|
|
R7419:Lama1
|
UTSW |
17 |
68,024,169 (GRCm39) |
missense |
|
|
R7460:Lama1
|
UTSW |
17 |
68,074,013 (GRCm39) |
missense |
|
|
R7492:Lama1
|
UTSW |
17 |
68,124,646 (GRCm39) |
missense |
|
|
R7494:Lama1
|
UTSW |
17 |
68,118,441 (GRCm39) |
missense |
|
|
R7552:Lama1
|
UTSW |
17 |
68,044,662 (GRCm39) |
missense |
|
|
R7576:Lama1
|
UTSW |
17 |
68,089,036 (GRCm39) |
missense |
|
|
R7583:Lama1
|
UTSW |
17 |
68,068,616 (GRCm39) |
missense |
|
|
R7649:Lama1
|
UTSW |
17 |
68,044,549 (GRCm39) |
missense |
|
|
R7663:Lama1
|
UTSW |
17 |
68,087,875 (GRCm39) |
missense |
|
|
R7667:Lama1
|
UTSW |
17 |
68,087,592 (GRCm39) |
missense |
|
|
R7688:Lama1
|
UTSW |
17 |
68,068,623 (GRCm39) |
missense |
|
|
R7693:Lama1
|
UTSW |
17 |
68,124,026 (GRCm39) |
missense |
|
|
R7748:Lama1
|
UTSW |
17 |
68,057,585 (GRCm39) |
missense |
|
|
R7778:Lama1
|
UTSW |
17 |
68,111,468 (GRCm39) |
missense |
|
|
R7824:Lama1
|
UTSW |
17 |
68,111,468 (GRCm39) |
missense |
|
|
R7861:Lama1
|
UTSW |
17 |
68,116,216 (GRCm39) |
missense |
|
|
R7884:Lama1
|
UTSW |
17 |
68,076,430 (GRCm39) |
missense |
|
|
R8029:Lama1
|
UTSW |
17 |
68,124,589 (GRCm39) |
missense |
|
|
R8078:Lama1
|
UTSW |
17 |
68,098,289 (GRCm39) |
missense |
|
|
R8101:Lama1
|
UTSW |
17 |
68,052,917 (GRCm39) |
missense |
|
|
R8313:Lama1
|
UTSW |
17 |
68,057,515 (GRCm39) |
missense |
|
|
R8356:Lama1
|
UTSW |
17 |
68,044,491 (GRCm39) |
missense |
|
|
R8366:Lama1
|
UTSW |
17 |
68,125,699 (GRCm39) |
missense |
|
|
R8403:Lama1
|
UTSW |
17 |
68,052,918 (GRCm39) |
missense |
|
|
R8456:Lama1
|
UTSW |
17 |
68,044,491 (GRCm39) |
missense |
|
|
R8466:Lama1
|
UTSW |
17 |
68,120,948 (GRCm39) |
missense |
|
|
R8678:Lama1
|
UTSW |
17 |
68,124,098 (GRCm39) |
missense |
|
|
R8728:Lama1
|
UTSW |
17 |
68,125,663 (GRCm39) |
missense |
|
|
R8796:Lama1
|
UTSW |
17 |
68,117,146 (GRCm39) |
missense |
|
|
R8885:Lama1
|
UTSW |
17 |
68,080,779 (GRCm39) |
missense |
|
|
R8893:Lama1
|
UTSW |
17 |
68,112,367 (GRCm39) |
missense |
|
|
R8898:Lama1
|
UTSW |
17 |
68,128,610 (GRCm39) |
missense |
|
|
R8909:Lama1
|
UTSW |
17 |
68,079,736 (GRCm39) |
missense |
|
|
R9025:Lama1
|
UTSW |
17 |
68,119,491 (GRCm39) |
missense |
|
|
R9045:Lama1
|
UTSW |
17 |
68,060,838 (GRCm39) |
missense |
|
|
R9098:Lama1
|
UTSW |
17 |
68,111,508 (GRCm39) |
missense |
|
|
R9114:Lama1
|
UTSW |
17 |
68,128,669 (GRCm39) |
missense |
|
|
R9173:Lama1
|
UTSW |
17 |
68,076,597 (GRCm39) |
missense |
|
|
R9190:Lama1
|
UTSW |
17 |
68,111,514 (GRCm39) |
missense |
|
|
R9381:Lama1
|
UTSW |
17 |
68,044,479 (GRCm39) |
missense |
|
|
R9429:Lama1
|
UTSW |
17 |
68,118,449 (GRCm39) |
missense |
|
|
R9504:Lama1
|
UTSW |
17 |
68,128,661 (GRCm39) |
missense |
|
|
R9558:Lama1
|
UTSW |
17 |
68,124,004 (GRCm39) |
missense |
|
|
R9647:Lama1
|
UTSW |
17 |
68,024,170 (GRCm39) |
missense |
|
|
R9651:Lama1
|
UTSW |
17 |
68,101,215 (GRCm39) |
missense |
|
|
R9654:Lama1
|
UTSW |
17 |
68,101,266 (GRCm39) |
missense |
|
|
R9710:Lama1
|
UTSW |
17 |
68,129,404 (GRCm39) |
missense |
|
|
R9733:Lama1
|
UTSW |
17 |
68,116,940 (GRCm39) |
missense |
|
|
RF001:Lama1
|
UTSW |
17 |
68,059,897 (GRCm39) |
missense |
|
|
RF013:Lama1
|
UTSW |
17 |
68,088,057 (GRCm39) |
missense |
|
|
V8831:Lama1
|
UTSW |
17 |
68,059,878 (GRCm39) |
missense |
probably benign |
0.00 |
X0024:Lama1
|
UTSW |
17 |
68,045,883 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Lama1
|
UTSW |
17 |
68,101,305 (GRCm39) |
missense |
probably benign |
0.06 |
X0028:Lama1
|
UTSW |
17 |
68,074,417 (GRCm39) |
missense |
probably benign |
0.00 |
X0066:Lama1
|
UTSW |
17 |
68,118,561 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Lama1
|
UTSW |
17 |
68,117,166 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Lama1
|
UTSW |
17 |
68,078,077 (GRCm39) |
missense |
probably benign |
0.25 |
Z1088:Lama1
|
UTSW |
17 |
68,059,878 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Lama1
|
UTSW |
17 |
68,059,878 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Lama1
|
UTSW |
17 |
68,059,878 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Lama1
|
UTSW |
17 |
68,105,639 (GRCm39) |
missense |
|
|
|