Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J04Rik |
T |
C |
12: 11,272,141 (GRCm39) |
|
noncoding transcript |
Het |
A930003A15Rik |
C |
T |
16: 19,702,487 (GRCm39) |
|
noncoding transcript |
Het |
Abca13 |
A |
G |
11: 9,259,130 (GRCm39) |
Y2952C |
probably damaging |
Het |
Actrt2 |
T |
C |
4: 154,751,747 (GRCm39) |
T130A |
probably benign |
Het |
Adamts7 |
T |
A |
9: 90,068,515 (GRCm39) |
D475E |
probably benign |
Het |
Adgrf5 |
A |
G |
17: 43,761,874 (GRCm39) |
S1190G |
probably benign |
Het |
Adgrg6 |
A |
T |
10: 14,317,243 (GRCm39) |
C526S |
probably damaging |
Het |
Aldoc |
T |
C |
11: 78,215,947 (GRCm39) |
V151A |
probably damaging |
Het |
Arsj |
A |
T |
3: 126,158,445 (GRCm39) |
E8V |
probably benign |
Het |
Asph |
T |
C |
4: 9,622,005 (GRCm39) |
K167E |
possibly damaging |
Het |
Auts2 |
G |
A |
5: 131,469,221 (GRCm39) |
P475S |
probably benign |
Het |
C1d |
A |
G |
11: 17,212,742 (GRCm39) |
D29G |
possibly damaging |
Het |
Calb1 |
T |
A |
4: 15,895,721 (GRCm39) |
|
probably benign |
Het |
Ceacam15 |
A |
T |
7: 16,407,391 (GRCm39) |
F42Y |
probably damaging |
Het |
Cpm |
A |
G |
10: 117,506,202 (GRCm39) |
N188D |
possibly damaging |
Het |
Cts6 |
A |
T |
13: 61,349,974 (GRCm39) |
Y36N |
possibly damaging |
Het |
Cux1 |
T |
C |
5: 136,337,154 (GRCm39) |
K657R |
probably damaging |
Het |
Cyp2a22 |
G |
T |
7: 26,632,916 (GRCm39) |
P429T |
probably damaging |
Het |
Dipk2a |
T |
C |
9: 94,402,451 (GRCm39) |
N404D |
possibly damaging |
Het |
Dock3 |
T |
C |
9: 106,939,244 (GRCm39) |
E168G |
possibly damaging |
Het |
Dot1l |
A |
G |
10: 80,617,984 (GRCm39) |
N324S |
probably benign |
Het |
Dusp13b |
A |
C |
14: 21,793,546 (GRCm39) |
|
probably benign |
Het |
Eif4g1 |
T |
A |
16: 20,500,095 (GRCm39) |
|
probably benign |
Het |
Fan1 |
G |
T |
7: 64,023,301 (GRCm39) |
Y121* |
probably null |
Het |
Foxn4 |
T |
C |
5: 114,398,991 (GRCm39) |
E80G |
possibly damaging |
Het |
Gal3st2c |
C |
A |
1: 93,937,178 (GRCm39) |
H374Q |
possibly damaging |
Het |
Gm973 |
A |
T |
1: 59,595,435 (GRCm39) |
I409F |
probably damaging |
Het |
Gpr18 |
T |
A |
14: 122,149,579 (GRCm39) |
T149S |
probably damaging |
Het |
Gsr |
A |
G |
8: 34,170,333 (GRCm39) |
E206G |
probably damaging |
Het |
Hal |
A |
G |
10: 93,343,301 (GRCm39) |
H515R |
probably damaging |
Het |
Heatr5b |
A |
G |
17: 79,102,548 (GRCm39) |
S1277P |
possibly damaging |
Het |
Hmcn2 |
A |
G |
2: 31,286,722 (GRCm39) |
E2125G |
probably damaging |
Het |
Ikzf4 |
A |
G |
10: 128,476,988 (GRCm39) |
C108R |
probably damaging |
Het |
Kcnh2 |
A |
G |
5: 24,553,440 (GRCm39) |
V59A |
probably benign |
Het |
Khdrbs1 |
A |
G |
4: 129,614,635 (GRCm39) |
V306A |
probably benign |
Het |
Kif11 |
A |
T |
19: 37,398,195 (GRCm39) |
I674L |
probably benign |
Het |
Lrp1b |
A |
T |
2: 41,136,033 (GRCm39) |
C1646S |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,266,141 (GRCm39) |
|
probably null |
Het |
Mib1 |
C |
A |
18: 10,808,086 (GRCm39) |
N944K |
probably benign |
Het |
Mical3 |
C |
A |
6: 120,938,586 (GRCm39) |
E262* |
probably null |
Het |
Mms22l |
C |
T |
4: 24,502,792 (GRCm39) |
Q55* |
probably null |
Het |
Mplkipl1 |
C |
T |
19: 61,164,364 (GRCm39) |
G24R |
unknown |
Het |
Mrps11 |
T |
C |
7: 78,441,689 (GRCm39) |
|
probably null |
Het |
Myh8 |
A |
G |
11: 67,177,084 (GRCm39) |
E412G |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,778,355 (GRCm39) |
D1370E |
probably benign |
Het |
Ncapd2 |
A |
G |
6: 125,150,572 (GRCm39) |
V843A |
probably benign |
Het |
Nell1 |
A |
G |
7: 49,770,310 (GRCm39) |
E123G |
possibly damaging |
Het |
Nkd1 |
A |
G |
8: 89,316,383 (GRCm39) |
D213G |
probably benign |
Het |
Nlrp1b |
T |
C |
11: 71,052,669 (GRCm39) |
T920A |
probably benign |
Het |
Or5k8 |
A |
T |
16: 58,644,469 (GRCm39) |
I201N |
possibly damaging |
Het |
Or6c208 |
G |
A |
10: 129,223,915 (GRCm39) |
V138M |
probably benign |
Het |
Or8k40 |
T |
A |
2: 86,584,906 (GRCm39) |
M59L |
possibly damaging |
Het |
Pde8b |
C |
T |
13: 95,178,447 (GRCm39) |
A566T |
possibly damaging |
Het |
Pds5b |
T |
A |
5: 150,724,066 (GRCm39) |
S1214R |
probably benign |
Het |
Pld1 |
T |
C |
3: 28,083,393 (GRCm39) |
I171T |
probably benign |
Het |
Plekha5 |
T |
A |
6: 140,496,912 (GRCm39) |
V154E |
probably damaging |
Het |
Plxna2 |
A |
T |
1: 194,494,458 (GRCm39) |
I1892L |
probably benign |
Het |
Ppp1r16b |
A |
G |
2: 158,603,383 (GRCm39) |
Y436C |
possibly damaging |
Het |
Proc |
T |
A |
18: 32,260,526 (GRCm39) |
T200S |
probably benign |
Het |
Psap |
T |
G |
10: 60,136,630 (GRCm39) |
C536W |
probably damaging |
Het |
Ptger2 |
G |
A |
14: 45,226,471 (GRCm39) |
R17H |
possibly damaging |
Het |
Rab42 |
A |
G |
4: 132,030,504 (GRCm39) |
F49L |
possibly damaging |
Het |
Racgap1 |
C |
A |
15: 99,524,087 (GRCm39) |
S440I |
probably benign |
Het |
Rdh10 |
G |
A |
1: 16,201,287 (GRCm39) |
|
probably benign |
Het |
Rnft2 |
T |
A |
5: 118,370,471 (GRCm39) |
S244C |
probably damaging |
Het |
Sftpc |
T |
C |
14: 70,759,718 (GRCm39) |
|
probably null |
Het |
Shcbp1 |
A |
C |
8: 4,789,178 (GRCm39) |
V547G |
probably damaging |
Het |
Slc6a13 |
T |
C |
6: 121,302,104 (GRCm39) |
S229P |
probably damaging |
Het |
Soat2 |
A |
T |
15: 102,066,144 (GRCm39) |
|
probably benign |
Het |
Swap70 |
A |
G |
7: 109,867,079 (GRCm39) |
K294E |
probably benign |
Het |
Tcim |
C |
A |
8: 24,928,725 (GRCm39) |
R63L |
probably damaging |
Het |
Tek |
G |
A |
4: 94,751,898 (GRCm39) |
V1013I |
probably damaging |
Het |
Tg |
T |
A |
15: 66,607,120 (GRCm39) |
M219K |
probably benign |
Het |
Tie1 |
A |
G |
4: 118,343,808 (GRCm39) |
S45P |
possibly damaging |
Het |
Tmem59 |
A |
T |
4: 107,047,915 (GRCm39) |
|
probably benign |
Het |
Togaram1 |
A |
T |
12: 65,029,224 (GRCm39) |
E882D |
possibly damaging |
Het |
Tram1l1 |
T |
A |
3: 124,115,509 (GRCm39) |
M223K |
possibly damaging |
Het |
Tssk5 |
C |
T |
15: 76,256,668 (GRCm39) |
R280Q |
probably benign |
Het |
Uspl1 |
T |
A |
5: 149,151,405 (GRCm39) |
D669E |
probably damaging |
Het |
Vav1 |
C |
A |
17: 57,606,839 (GRCm39) |
|
probably null |
Het |
Vcl |
A |
T |
14: 21,065,007 (GRCm39) |
E634V |
probably benign |
Het |
Zfp672 |
A |
T |
11: 58,207,281 (GRCm39) |
C347S |
probably benign |
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 |
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 |
R9645: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 |
|