Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430033K04Rik |
T |
C |
5: 138,644,793 (GRCm39) |
V226A |
probably benign |
Het |
Acan |
G |
T |
7: 78,749,653 (GRCm39) |
V1475F |
probably benign |
Het |
Acin1 |
T |
A |
14: 54,901,913 (GRCm39) |
R626S |
probably benign |
Het |
Aff3 |
T |
C |
1: 38,249,121 (GRCm39) |
K662R |
probably damaging |
Het |
Ankrd11 |
C |
T |
8: 123,617,682 (GRCm39) |
A2057T |
probably benign |
Het |
Ano9 |
T |
G |
7: 140,687,388 (GRCm39) |
N309T |
probably benign |
Het |
Ap3d1 |
G |
A |
10: 80,545,062 (GRCm39) |
S1092L |
probably benign |
Het |
B4galt7 |
C |
T |
13: 55,756,556 (GRCm39) |
H257Y |
probably damaging |
Het |
BC051665 |
G |
T |
13: 60,932,545 (GRCm39) |
Q47K |
possibly damaging |
Het |
Brip1 |
A |
G |
11: 85,952,512 (GRCm39) |
F1090L |
probably benign |
Het |
Cabin1 |
A |
G |
10: 75,494,543 (GRCm39) |
V1612A |
probably benign |
Het |
Ccar1 |
A |
T |
10: 62,602,369 (GRCm39) |
D434E |
probably benign |
Het |
Ccdc15 |
T |
C |
9: 37,227,083 (GRCm39) |
D297G |
probably benign |
Het |
Celsr3 |
C |
A |
9: 108,704,691 (GRCm39) |
Y391* |
probably null |
Het |
Cfap52 |
A |
G |
11: 67,837,179 (GRCm39) |
I194T |
possibly damaging |
Het |
Ctif |
T |
C |
18: 75,757,352 (GRCm39) |
E67G |
probably benign |
Het |
Cxcr6 |
T |
C |
9: 123,639,151 (GRCm39) |
F58L |
possibly damaging |
Het |
Cyp2c69 |
T |
C |
19: 39,869,593 (GRCm39) |
E142G |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,115,750 (GRCm39) |
R1549S |
possibly damaging |
Het |
Duxf3 |
A |
T |
10: 58,066,803 (GRCm39) |
H75Q |
probably benign |
Het |
Ehbp1 |
A |
T |
11: 22,051,052 (GRCm39) |
I500N |
probably damaging |
Het |
F13a1 |
A |
T |
13: 37,082,154 (GRCm39) |
S517T |
probably benign |
Het |
Fbln7 |
C |
T |
2: 128,719,316 (GRCm39) |
R38C |
probably damaging |
Het |
Fn1 |
T |
C |
1: 71,667,629 (GRCm39) |
N788S |
probably benign |
Het |
Foxc1 |
A |
T |
13: 31,991,882 (GRCm39) |
E231V |
probably damaging |
Het |
Gal3st2b |
T |
C |
1: 93,866,328 (GRCm39) |
S10P |
probably damaging |
Het |
Gm6899 |
G |
A |
11: 26,543,592 (GRCm39) |
C53Y |
unknown |
Het |
Hps3 |
T |
C |
3: 20,084,831 (GRCm39) |
E119G |
probably benign |
Het |
Impg2 |
A |
G |
16: 56,038,767 (GRCm39) |
E135G |
probably damaging |
Het |
Kalrn |
G |
A |
16: 34,032,583 (GRCm39) |
T1155M |
probably benign |
Het |
Kcna6 |
G |
A |
6: 126,716,022 (GRCm39) |
A289V |
probably benign |
Het |
Kcnh5 |
T |
C |
12: 75,134,191 (GRCm39) |
M453V |
probably benign |
Het |
Krt222 |
A |
G |
11: 99,131,320 (GRCm39) |
V75A |
possibly damaging |
Het |
Lmtk3 |
A |
T |
7: 45,450,431 (GRCm39) |
T1432S |
unknown |
Het |
Ltbp3 |
C |
G |
19: 5,802,099 (GRCm39) |
N758K |
probably damaging |
Het |
Map6d1 |
T |
A |
16: 20,055,377 (GRCm39) |
H153L |
possibly damaging |
Het |
Mefv |
A |
G |
16: 3,528,782 (GRCm39) |
L583P |
probably damaging |
Het |
Mrps28 |
T |
C |
3: 8,867,389 (GRCm39) |
T160A |
probably damaging |
Het |
Mtcl2 |
T |
C |
2: 156,869,390 (GRCm39) |
K1082E |
probably damaging |
Het |
Muc6 |
T |
C |
7: 141,217,783 (GRCm39) |
T2297A |
possibly damaging |
Het |
Mx1 |
G |
T |
16: 97,253,409 (GRCm39) |
D338E |
probably benign |
Het |
Myom1 |
G |
A |
17: 71,399,204 (GRCm39) |
R1120H |
probably benign |
Het |
Nif3l1 |
T |
C |
1: 58,487,074 (GRCm39) |
F87L |
probably benign |
Het |
Or1e35 |
T |
A |
11: 73,797,713 (GRCm39) |
M202L |
probably benign |
Het |
Or4p22 |
T |
C |
2: 88,317,373 (GRCm39) |
V99A |
possibly damaging |
Het |
Pex10 |
T |
A |
4: 155,153,264 (GRCm39) |
L111Q |
probably damaging |
Het |
Phf1 |
T |
C |
17: 27,154,130 (GRCm39) |
|
probably null |
Het |
Pigp |
A |
T |
16: 94,166,278 (GRCm39) |
Y143* |
probably null |
Het |
Pou2af2 |
A |
G |
9: 51,229,579 (GRCm39) |
|
probably null |
Het |
Prrc2a |
A |
G |
17: 35,381,176 (GRCm39) |
|
probably null |
Het |
Psd |
GCC |
GC |
19: 46,301,841 (GRCm39) |
|
probably null |
Het |
Pum3 |
A |
G |
19: 27,403,412 (GRCm39) |
S30P |
probably benign |
Het |
Rab12 |
A |
G |
17: 66,826,421 (GRCm39) |
S97P |
probably damaging |
Het |
Rigi |
T |
C |
4: 40,220,437 (GRCm39) |
E482G |
possibly damaging |
Het |
Ros1 |
A |
G |
10: 51,948,148 (GRCm39) |
|
probably null |
Het |
Scp2 |
A |
T |
4: 107,948,519 (GRCm39) |
Y197N |
probably benign |
Het |
Serpinb10 |
T |
C |
1: 107,474,488 (GRCm39) |
F217L |
possibly damaging |
Het |
Shank3 |
T |
G |
15: 89,409,453 (GRCm39) |
M604R |
possibly damaging |
Het |
Slc22a29 |
A |
G |
19: 8,184,488 (GRCm39) |
S238P |
probably benign |
Het |
Smarcc1 |
A |
G |
9: 109,986,410 (GRCm39) |
D237G |
probably damaging |
Het |
Stag3 |
T |
C |
5: 138,299,701 (GRCm39) |
S871P |
possibly damaging |
Het |
Tmem132d |
A |
G |
5: 128,346,075 (GRCm39) |
F149S |
probably damaging |
Het |
Tmem25 |
C |
T |
9: 44,706,515 (GRCm39) |
E333K |
|
Het |
Togaram1 |
T |
A |
12: 65,066,082 (GRCm39) |
Y1695* |
probably null |
Het |
Tox3 |
G |
A |
8: 90,984,574 (GRCm39) |
P202S |
probably damaging |
Het |
Trim34b |
T |
A |
7: 103,980,474 (GRCm39) |
N187K |
probably benign |
Het |
Vcan |
A |
G |
13: 89,841,081 (GRCm39) |
S1488P |
probably benign |
Het |
Vps26a |
A |
C |
10: 62,305,791 (GRCm39) |
V124G |
probably benign |
Het |
Vps50 |
T |
G |
6: 3,516,706 (GRCm39) |
S63A |
possibly damaging |
Het |
Wbp4 |
T |
A |
14: 79,707,553 (GRCm39) |
E186V |
possibly damaging |
Het |
Zfp52 |
A |
G |
17: 21,781,937 (GRCm39) |
D595G |
possibly damaging |
Het |
Zfr2 |
C |
A |
10: 81,084,252 (GRCm39) |
S1* |
probably null |
Het |
|
Other mutations in Ltbp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00471:Ltbp2
|
APN |
12 |
84,837,838 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00938:Ltbp2
|
APN |
12 |
84,878,573 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01397:Ltbp2
|
APN |
12 |
84,837,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01570:Ltbp2
|
APN |
12 |
84,840,807 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01631:Ltbp2
|
APN |
12 |
84,855,920 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01662:Ltbp2
|
APN |
12 |
84,856,020 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01728:Ltbp2
|
APN |
12 |
84,837,783 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01839:Ltbp2
|
APN |
12 |
84,840,432 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL01946:Ltbp2
|
APN |
12 |
84,877,522 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01977:Ltbp2
|
APN |
12 |
84,876,973 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02220:Ltbp2
|
APN |
12 |
84,876,083 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02340:Ltbp2
|
APN |
12 |
84,839,729 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02430:Ltbp2
|
APN |
12 |
84,846,175 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02492:Ltbp2
|
APN |
12 |
84,856,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02517:Ltbp2
|
APN |
12 |
84,832,091 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02794:Ltbp2
|
APN |
12 |
84,838,709 (GRCm39) |
missense |
probably damaging |
1.00 |
deft
|
UTSW |
12 |
84,900,686 (GRCm39) |
missense |
probably damaging |
0.98 |
masterful
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
practiced
|
UTSW |
12 |
84,856,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R0045:Ltbp2
|
UTSW |
12 |
84,860,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R0045:Ltbp2
|
UTSW |
12 |
84,856,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R0091:Ltbp2
|
UTSW |
12 |
84,840,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Ltbp2
|
UTSW |
12 |
84,846,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0166:Ltbp2
|
UTSW |
12 |
84,833,132 (GRCm39) |
missense |
probably benign |
0.28 |
R0265:Ltbp2
|
UTSW |
12 |
84,832,743 (GRCm39) |
splice site |
probably null |
|
R0394:Ltbp2
|
UTSW |
12 |
84,853,198 (GRCm39) |
splice site |
probably benign |
|
R0535:Ltbp2
|
UTSW |
12 |
84,837,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R0535:Ltbp2
|
UTSW |
12 |
84,831,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Ltbp2
|
UTSW |
12 |
84,860,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Ltbp2
|
UTSW |
12 |
84,860,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Ltbp2
|
UTSW |
12 |
84,838,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Ltbp2
|
UTSW |
12 |
84,877,555 (GRCm39) |
nonsense |
probably null |
|
R1880:Ltbp2
|
UTSW |
12 |
84,876,045 (GRCm39) |
missense |
probably benign |
0.45 |
R1894:Ltbp2
|
UTSW |
12 |
84,834,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R1900:Ltbp2
|
UTSW |
12 |
84,877,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Ltbp2
|
UTSW |
12 |
84,876,879 (GRCm39) |
missense |
probably benign |
0.01 |
R1912:Ltbp2
|
UTSW |
12 |
84,832,637 (GRCm39) |
missense |
probably damaging |
0.98 |
R1993:Ltbp2
|
UTSW |
12 |
84,855,220 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1995:Ltbp2
|
UTSW |
12 |
84,855,220 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2069:Ltbp2
|
UTSW |
12 |
84,840,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R2126:Ltbp2
|
UTSW |
12 |
84,832,483 (GRCm39) |
splice site |
probably null |
|
R2139:Ltbp2
|
UTSW |
12 |
84,862,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R2341:Ltbp2
|
UTSW |
12 |
84,855,937 (GRCm39) |
missense |
probably benign |
0.08 |
R2511:Ltbp2
|
UTSW |
12 |
84,851,183 (GRCm39) |
splice site |
probably null |
|
R3737:Ltbp2
|
UTSW |
12 |
84,851,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R3738:Ltbp2
|
UTSW |
12 |
84,851,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R3739:Ltbp2
|
UTSW |
12 |
84,851,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R3889:Ltbp2
|
UTSW |
12 |
84,831,681 (GRCm39) |
unclassified |
probably benign |
|
R4034:Ltbp2
|
UTSW |
12 |
84,851,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4542:Ltbp2
|
UTSW |
12 |
84,878,593 (GRCm39) |
nonsense |
probably null |
|
R4621:Ltbp2
|
UTSW |
12 |
84,856,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Ltbp2
|
UTSW |
12 |
84,856,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Ltbp2
|
UTSW |
12 |
84,840,414 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5080:Ltbp2
|
UTSW |
12 |
84,850,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R5116:Ltbp2
|
UTSW |
12 |
84,856,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R5351:Ltbp2
|
UTSW |
12 |
84,837,132 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5445:Ltbp2
|
UTSW |
12 |
84,856,428 (GRCm39) |
missense |
probably null |
1.00 |
R5608:Ltbp2
|
UTSW |
12 |
84,834,238 (GRCm39) |
splice site |
probably null |
|
R5784:Ltbp2
|
UTSW |
12 |
84,915,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5838:Ltbp2
|
UTSW |
12 |
84,835,875 (GRCm39) |
missense |
probably benign |
0.16 |
R5859:Ltbp2
|
UTSW |
12 |
84,840,837 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6004:Ltbp2
|
UTSW |
12 |
84,922,923 (GRCm39) |
missense |
probably benign |
0.00 |
R6028:Ltbp2
|
UTSW |
12 |
84,831,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6347:Ltbp2
|
UTSW |
12 |
84,900,686 (GRCm39) |
missense |
probably damaging |
0.98 |
R6615:Ltbp2
|
UTSW |
12 |
84,860,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6636:Ltbp2
|
UTSW |
12 |
84,922,612 (GRCm39) |
missense |
probably benign |
0.00 |
R6637:Ltbp2
|
UTSW |
12 |
84,922,612 (GRCm39) |
missense |
probably benign |
0.00 |
R6755:Ltbp2
|
UTSW |
12 |
84,841,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6759:Ltbp2
|
UTSW |
12 |
84,834,184 (GRCm39) |
missense |
probably damaging |
0.99 |
R6806:Ltbp2
|
UTSW |
12 |
84,856,012 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6968:Ltbp2
|
UTSW |
12 |
84,835,857 (GRCm39) |
critical splice donor site |
probably null |
|
R7084:Ltbp2
|
UTSW |
12 |
84,915,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Ltbp2
|
UTSW |
12 |
84,834,166 (GRCm39) |
nonsense |
probably null |
|
R7374:Ltbp2
|
UTSW |
12 |
84,876,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R7501:Ltbp2
|
UTSW |
12 |
84,877,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R7523:Ltbp2
|
UTSW |
12 |
84,837,808 (GRCm39) |
missense |
probably benign |
0.00 |
R7754:Ltbp2
|
UTSW |
12 |
84,860,012 (GRCm39) |
critical splice donor site |
probably null |
|
R7827:Ltbp2
|
UTSW |
12 |
84,836,655 (GRCm39) |
missense |
probably benign |
0.19 |
R8042:Ltbp2
|
UTSW |
12 |
84,838,673 (GRCm39) |
missense |
probably damaging |
0.99 |
R8110:Ltbp2
|
UTSW |
12 |
84,850,676 (GRCm39) |
nonsense |
probably null |
|
R8411:Ltbp2
|
UTSW |
12 |
84,833,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8688:Ltbp2
|
UTSW |
12 |
84,850,578 (GRCm39) |
missense |
probably benign |
0.20 |
R8711:Ltbp2
|
UTSW |
12 |
84,900,515 (GRCm39) |
missense |
probably benign |
0.00 |
R8712:Ltbp2
|
UTSW |
12 |
84,853,124 (GRCm39) |
missense |
probably benign |
0.08 |
R8893:Ltbp2
|
UTSW |
12 |
84,875,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R8978:Ltbp2
|
UTSW |
12 |
84,834,164 (GRCm39) |
missense |
probably benign |
0.00 |
R9016:Ltbp2
|
UTSW |
12 |
84,856,467 (GRCm39) |
missense |
probably benign |
0.02 |
R9123:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9129:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9132:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9144:Ltbp2
|
UTSW |
12 |
84,856,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R9150:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9152:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9156:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9157:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9158:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9159:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9160:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9199:Ltbp2
|
UTSW |
12 |
84,832,750 (GRCm39) |
missense |
probably benign |
0.09 |
R9212:Ltbp2
|
UTSW |
12 |
84,839,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9276:Ltbp2
|
UTSW |
12 |
84,876,885 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9276:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9278:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9279:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9280:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9281:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9312:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9313:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9331:Ltbp2
|
UTSW |
12 |
84,922,965 (GRCm39) |
missense |
probably benign |
|
R9355:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9375:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9377:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9378:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9450:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9457:Ltbp2
|
UTSW |
12 |
84,835,927 (GRCm39) |
missense |
probably benign |
0.19 |
R9486:Ltbp2
|
UTSW |
12 |
84,878,648 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9505:Ltbp2
|
UTSW |
12 |
84,900,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R9512:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9581:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9582:Ltbp2
|
UTSW |
12 |
84,837,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9747:Ltbp2
|
UTSW |
12 |
84,915,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R9792:Ltbp2
|
UTSW |
12 |
84,876,128 (GRCm39) |
missense |
probably damaging |
0.99 |
R9795:Ltbp2
|
UTSW |
12 |
84,876,128 (GRCm39) |
missense |
probably damaging |
0.99 |
X0017:Ltbp2
|
UTSW |
12 |
84,875,302 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Ltbp2
|
UTSW |
12 |
84,876,973 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ltbp2
|
UTSW |
12 |
84,922,627 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Ltbp2
|
UTSW |
12 |
84,876,090 (GRCm39) |
missense |
possibly damaging |
0.87 |
|