Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
T |
C |
4: 144,349,364 (GRCm39) |
V207A |
probably benign |
Het |
Abcc10 |
C |
A |
17: 46,614,834 (GRCm39) |
|
probably null |
Het |
Abcc9 |
A |
C |
6: 142,634,742 (GRCm39) |
V174G |
possibly damaging |
Het |
Abl1 |
C |
T |
2: 31,669,086 (GRCm39) |
A155V |
probably damaging |
Het |
Aco2 |
T |
A |
15: 81,787,787 (GRCm39) |
D212E |
probably damaging |
Het |
Adam26b |
A |
T |
8: 43,973,529 (GRCm39) |
M491K |
probably benign |
Het |
Anapc5 |
G |
A |
5: 122,929,988 (GRCm39) |
|
probably benign |
Het |
Atf7 |
A |
G |
15: 102,471,757 (GRCm39) |
I46T |
probably damaging |
Het |
Cacna1b |
A |
G |
2: 24,497,612 (GRCm39) |
S2100P |
probably damaging |
Het |
Capn5 |
T |
A |
7: 97,775,137 (GRCm39) |
D501V |
probably damaging |
Het |
Cc2d2a |
A |
G |
5: 43,866,433 (GRCm39) |
M748V |
probably damaging |
Het |
Cd300c2 |
T |
C |
11: 114,891,662 (GRCm39) |
T71A |
probably damaging |
Het |
Chmp2a |
T |
C |
7: 12,767,758 (GRCm39) |
M56V |
probably benign |
Het |
Cilp |
A |
C |
9: 65,187,515 (GRCm39) |
R1203S |
probably benign |
Het |
Clp1 |
T |
A |
2: 84,556,322 (GRCm39) |
K53* |
probably null |
Het |
Crhbp |
T |
A |
13: 95,578,737 (GRCm39) |
D128V |
probably damaging |
Het |
Crispld1 |
T |
A |
1: 17,820,495 (GRCm39) |
I292N |
probably benign |
Het |
Cyp2c68 |
A |
T |
19: 39,677,526 (GRCm39) |
I488N |
probably benign |
Het |
Cyp3a57 |
A |
T |
5: 145,307,456 (GRCm39) |
M149L |
probably benign |
Het |
Ddx24 |
T |
A |
12: 103,390,547 (GRCm39) |
Q59L |
possibly damaging |
Het |
Ddx27 |
A |
G |
2: 166,871,439 (GRCm39) |
H512R |
possibly damaging |
Het |
Dlgap4 |
T |
A |
2: 156,604,821 (GRCm39) |
*993K |
probably null |
Het |
Dmxl2 |
A |
T |
9: 54,330,643 (GRCm39) |
|
probably null |
Het |
Dus4l |
A |
T |
12: 31,696,712 (GRCm39) |
F88L |
probably damaging |
Het |
Ep400 |
A |
T |
5: 110,904,071 (GRCm39) |
V176E |
probably damaging |
Het |
Fat3 |
T |
A |
9: 16,288,219 (GRCm39) |
K435* |
probably null |
Het |
Fsip2 |
T |
C |
2: 82,816,908 (GRCm39) |
C4214R |
probably benign |
Het |
Garin5a |
T |
G |
7: 44,150,428 (GRCm39) |
S207A |
probably damaging |
Het |
Gfral |
T |
C |
9: 76,072,087 (GRCm39) |
*394W |
probably null |
Het |
Glis1 |
T |
C |
4: 107,476,832 (GRCm39) |
S518P |
probably damaging |
Het |
H2-T10 |
A |
G |
17: 36,430,079 (GRCm39) |
|
probably null |
Het |
Hsbp1l1 |
T |
C |
18: 80,278,679 (GRCm39) |
T35A |
possibly damaging |
Het |
Ighv5-12 |
A |
G |
12: 113,665,837 (GRCm39) |
F87S |
probably damaging |
Het |
Ints13 |
A |
C |
6: 146,477,855 (GRCm39) |
D31E |
probably damaging |
Het |
Kbtbd12 |
C |
T |
6: 88,595,609 (GRCm39) |
D74N |
probably damaging |
Het |
Klrb1c |
A |
G |
6: 128,765,877 (GRCm39) |
|
probably benign |
Het |
Kmt5b |
A |
T |
19: 3,836,538 (GRCm39) |
H25L |
probably benign |
Het |
Krt28 |
A |
T |
11: 99,262,210 (GRCm39) |
M260K |
probably damaging |
Het |
Krt79 |
A |
G |
15: 101,838,220 (GRCm39) |
S512P |
probably damaging |
Het |
Maneal |
T |
C |
4: 124,750,937 (GRCm39) |
E273G |
possibly damaging |
Het |
Map4k3 |
T |
A |
17: 80,971,427 (GRCm39) |
Y80F |
possibly damaging |
Het |
Mbd6 |
A |
G |
10: 127,119,297 (GRCm39) |
V946A |
possibly damaging |
Het |
Mfsd14b |
A |
T |
13: 65,219,936 (GRCm39) |
|
probably null |
Het |
Mrpl46 |
C |
G |
7: 78,430,242 (GRCm39) |
W176S |
probably damaging |
Het |
Muc19 |
A |
G |
15: 91,768,468 (GRCm39) |
|
noncoding transcript |
Het |
Mup3 |
T |
G |
4: 62,002,809 (GRCm39) |
E184A |
possibly damaging |
Het |
Myo9a |
A |
G |
9: 59,781,911 (GRCm39) |
H1699R |
probably benign |
Het |
Ndrg2 |
T |
A |
14: 52,144,420 (GRCm39) |
T269S |
probably damaging |
Het |
Nfatc1 |
A |
T |
18: 80,693,037 (GRCm39) |
V688D |
probably benign |
Het |
Ninj2 |
T |
C |
6: 120,175,670 (GRCm39) |
I101T |
probably benign |
Het |
Nlrp10 |
T |
A |
7: 108,523,468 (GRCm39) |
M671L |
probably benign |
Het |
Npsr1 |
T |
A |
9: 24,224,510 (GRCm39) |
L296I |
probably damaging |
Het |
Or10d5 |
A |
G |
9: 39,861,983 (GRCm39) |
L28P |
probably benign |
Het |
Or52r1b |
G |
T |
7: 102,691,517 (GRCm39) |
R272L |
possibly damaging |
Het |
Pacsin1 |
T |
A |
17: 27,927,022 (GRCm39) |
D242E |
probably damaging |
Het |
Pcdh1 |
T |
C |
18: 38,330,420 (GRCm39) |
Y861C |
probably damaging |
Het |
Pcdha12 |
T |
C |
18: 37,153,443 (GRCm39) |
L54P |
probably damaging |
Het |
Pcdhb18 |
T |
A |
18: 37,624,853 (GRCm39) |
S728T |
probably benign |
Het |
Phyhd1 |
T |
A |
2: 30,167,022 (GRCm39) |
H108Q |
probably damaging |
Het |
Plcb1 |
A |
T |
2: 135,212,513 (GRCm39) |
I1035F |
probably damaging |
Het |
Plcl1 |
T |
C |
1: 55,735,309 (GRCm39) |
S217P |
possibly damaging |
Het |
Plppr2 |
G |
A |
9: 21,852,425 (GRCm39) |
R103H |
probably damaging |
Het |
Plxnb2 |
G |
A |
15: 89,041,638 (GRCm39) |
T1722I |
probably damaging |
Het |
Pole3 |
T |
C |
4: 62,442,668 (GRCm39) |
N53S |
probably damaging |
Het |
Ptk6 |
A |
T |
2: 180,841,488 (GRCm39) |
N140K |
possibly damaging |
Het |
Rab12 |
C |
T |
17: 66,804,418 (GRCm39) |
R180H |
probably damaging |
Het |
Rab36 |
G |
T |
10: 74,888,311 (GRCm39) |
V252L |
probably benign |
Het |
Ranbp3 |
T |
C |
17: 57,008,543 (GRCm39) |
|
probably null |
Het |
Rapgef2 |
A |
G |
3: 79,011,308 (GRCm39) |
L259P |
probably damaging |
Het |
Rigi |
T |
A |
4: 40,222,140 (GRCm39) |
M380L |
probably benign |
Het |
Scaf4 |
GGCTGCTGCTGCTGCTGCTGCTGCTG |
GGCTGCTGCTGCTGCTGCTGCTG |
16: 90,026,745 (GRCm39) |
|
probably benign |
Het |
Scd2 |
T |
C |
19: 44,288,142 (GRCm39) |
F178S |
probably damaging |
Het |
Shmt2 |
A |
G |
10: 127,356,250 (GRCm39) |
S87P |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,194,823 (GRCm39) |
D834V |
probably damaging |
Het |
Sorcs2 |
A |
C |
5: 36,203,874 (GRCm39) |
Y540* |
probably null |
Het |
Srpk2 |
T |
A |
5: 23,730,697 (GRCm39) |
Q274L |
possibly damaging |
Het |
Stradb |
T |
A |
1: 59,031,901 (GRCm39) |
M271K |
possibly damaging |
Het |
Tfec |
T |
A |
6: 16,867,592 (GRCm39) |
Q16L |
possibly damaging |
Het |
Tfg |
T |
C |
16: 56,521,450 (GRCm39) |
T63A |
probably benign |
Het |
Ticrr |
G |
A |
7: 79,339,715 (GRCm39) |
|
probably null |
Het |
Ticrr |
T |
A |
7: 79,345,044 (GRCm39) |
C1636* |
probably null |
Het |
Tln2 |
A |
G |
9: 67,219,147 (GRCm39) |
I266T |
probably damaging |
Het |
Tmcc1 |
G |
C |
6: 115,999,071 (GRCm39) |
R323G |
possibly damaging |
Het |
Tnnt3 |
A |
G |
7: 142,065,777 (GRCm39) |
E138G |
probably damaging |
Het |
Tpm2 |
C |
A |
4: 43,522,692 (GRCm39) |
E75* |
probably null |
Het |
Ttn |
T |
G |
2: 76,580,922 (GRCm39) |
T23324P |
probably damaging |
Het |
Ubr4 |
T |
G |
4: 139,119,349 (GRCm39) |
L176R |
probably damaging |
Het |
Uhrf2 |
G |
T |
19: 30,016,488 (GRCm39) |
D46Y |
probably damaging |
Het |
Ulbp1 |
A |
C |
10: 7,423,281 (GRCm39) |
S21A |
unknown |
Het |
Usp17lb |
C |
T |
7: 104,490,415 (GRCm39) |
G170R |
probably damaging |
Het |
Utp15 |
T |
C |
13: 98,394,433 (GRCm39) |
N153S |
probably benign |
Het |
Vcan |
T |
A |
13: 89,836,790 (GRCm39) |
E2918V |
probably damaging |
Het |
Vmn1r174 |
T |
A |
7: 23,453,919 (GRCm39) |
I195K |
probably damaging |
Het |
Vmn1r76 |
C |
T |
7: 11,665,062 (GRCm39) |
V16I |
probably benign |
Het |
Xdh |
T |
C |
17: 74,250,880 (GRCm39) |
D24G |
possibly damaging |
Het |
Xylb |
T |
A |
9: 119,190,198 (GRCm39) |
H68Q |
probably benign |
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 |
|
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 |
|
|
R6995: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 |
|
|
|