Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810010H24Rik |
T |
C |
11: 106,919,324 (GRCm39) |
V223A |
probably damaging |
Het |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Ahctf1 |
A |
T |
1: 179,611,675 (GRCm39) |
I565N |
possibly damaging |
Het |
Ank1 |
C |
T |
8: 23,572,300 (GRCm39) |
T70I |
probably damaging |
Het |
Atg16l1 |
C |
A |
1: 87,701,902 (GRCm39) |
S248* |
probably null |
Het |
Atp13a5 |
A |
T |
16: 29,169,566 (GRCm39) |
L42Q |
probably damaging |
Het |
Atxn1 |
T |
C |
13: 45,710,545 (GRCm39) |
N796D |
probably damaging |
Het |
C3 |
T |
A |
17: 57,530,236 (GRCm39) |
Y455F |
probably benign |
Het |
Card11 |
A |
T |
5: 140,862,275 (GRCm39) |
D1007E |
possibly damaging |
Het |
Cbr2 |
T |
C |
11: 120,621,697 (GRCm39) |
D60G |
possibly damaging |
Het |
Cgn |
T |
A |
3: 94,683,455 (GRCm39) |
E400V |
probably null |
Het |
Chil3 |
T |
A |
3: 106,057,477 (GRCm39) |
Y229F |
possibly damaging |
Het |
Clcn2 |
G |
A |
16: 20,525,965 (GRCm39) |
P785S |
probably damaging |
Het |
Clk1 |
T |
C |
1: 58,453,642 (GRCm39) |
I315V |
probably benign |
Het |
Cops6 |
A |
G |
5: 138,160,459 (GRCm39) |
D102G |
probably benign |
Het |
Dennd5a |
A |
G |
7: 109,513,983 (GRCm39) |
I743T |
possibly damaging |
Het |
Dnaaf5 |
T |
A |
5: 139,149,012 (GRCm39) |
L437Q |
probably damaging |
Het |
Dnah12 |
T |
A |
14: 26,431,326 (GRCm39) |
D381E |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Draxin |
C |
A |
4: 148,192,436 (GRCm39) |
R292L |
probably damaging |
Het |
Dst |
T |
C |
1: 34,289,728 (GRCm39) |
V5776A |
probably damaging |
Het |
Eddm13 |
G |
A |
7: 6,269,332 (GRCm39) |
|
probably benign |
Het |
Ercc4 |
G |
A |
16: 12,941,445 (GRCm39) |
|
probably benign |
Het |
Eya1 |
T |
A |
1: 14,254,582 (GRCm39) |
N417Y |
probably damaging |
Het |
Fam149b |
T |
A |
14: 20,413,439 (GRCm39) |
H219Q |
possibly damaging |
Het |
Fam227b |
G |
A |
2: 125,958,043 (GRCm39) |
P241S |
probably damaging |
Het |
Fat1 |
A |
T |
8: 45,484,300 (GRCm39) |
|
probably null |
Het |
Fbxl18 |
A |
G |
5: 142,872,435 (GRCm39) |
S267P |
probably damaging |
Het |
Fer1l4 |
T |
C |
2: 155,873,135 (GRCm39) |
Y1315C |
probably damaging |
Het |
Fgd2 |
T |
C |
17: 29,593,954 (GRCm39) |
|
probably null |
Het |
Gm7251 |
T |
A |
13: 49,958,656 (GRCm39) |
|
noncoding transcript |
Het |
Golt1a |
T |
C |
1: 133,248,006 (GRCm39) |
V78A |
probably damaging |
Het |
Gsn |
T |
A |
2: 35,188,933 (GRCm39) |
Y440N |
probably damaging |
Het |
Gtf2ird2 |
G |
T |
5: 134,245,824 (GRCm39) |
S694I |
possibly damaging |
Het |
H2-Ob |
T |
A |
17: 34,460,253 (GRCm39) |
|
probably null |
Het |
Hsp90b1 |
T |
C |
10: 86,532,617 (GRCm39) |
D353G |
probably benign |
Het |
Ilk |
A |
G |
7: 105,391,456 (GRCm39) |
D374G |
probably damaging |
Het |
Invs |
G |
A |
4: 48,421,807 (GRCm39) |
R813Q |
probably damaging |
Het |
Itga7 |
G |
A |
10: 128,785,316 (GRCm39) |
V836M |
possibly damaging |
Het |
Itln1 |
T |
A |
1: 171,360,958 (GRCm39) |
K45* |
probably null |
Het |
Ivd |
A |
G |
2: 118,710,946 (GRCm39) |
Y385C |
probably damaging |
Het |
Ivns1abp |
T |
A |
1: 151,238,953 (GRCm39) |
M589K |
possibly damaging |
Het |
Jakmip3 |
C |
T |
7: 138,621,951 (GRCm39) |
R284W |
probably damaging |
Het |
Kank3 |
T |
C |
17: 34,041,044 (GRCm39) |
L512P |
probably damaging |
Het |
Kcnn2 |
T |
A |
18: 45,818,352 (GRCm39) |
I483N |
possibly damaging |
Het |
Klk1b4 |
A |
G |
7: 43,860,492 (GRCm39) |
N170S |
probably benign |
Het |
Klk1b9 |
A |
C |
7: 43,445,419 (GRCm39) |
D203A |
probably damaging |
Het |
Lbr |
A |
T |
1: 181,647,453 (GRCm39) |
Y199* |
probably null |
Het |
Lcn6 |
T |
A |
2: 25,567,082 (GRCm39) |
|
probably null |
Het |
Lrriq1 |
T |
C |
10: 103,025,784 (GRCm39) |
D946G |
probably damaging |
Het |
Maml3 |
A |
T |
3: 51,598,196 (GRCm39) |
N183K |
possibly damaging |
Het |
Mprip |
T |
C |
11: 59,650,721 (GRCm39) |
V1475A |
possibly damaging |
Het |
Myh4 |
C |
A |
11: 67,147,189 (GRCm39) |
S1611R |
probably benign |
Het |
Nagpa |
A |
T |
16: 5,013,743 (GRCm39) |
M365K |
probably benign |
Het |
Nckap5l |
G |
T |
15: 99,324,457 (GRCm39) |
P682Q |
probably benign |
Het |
Nudt12 |
T |
C |
17: 59,303,499 (GRCm39) |
|
probably benign |
Het |
Nup153 |
T |
C |
13: 46,840,879 (GRCm39) |
T910A |
possibly damaging |
Het |
Or1e31 |
T |
A |
11: 73,690,473 (GRCm39) |
T37S |
possibly damaging |
Het |
Or5ae2 |
T |
C |
7: 84,505,646 (GRCm39) |
V23A |
probably damaging |
Het |
Or7c74 |
A |
G |
2: 37,160,937 (GRCm39) |
|
noncoding transcript |
Het |
Or8k53 |
A |
T |
2: 86,177,647 (GRCm39) |
F154L |
probably benign |
Het |
Pate14 |
T |
C |
9: 36,549,120 (GRCm39) |
N47D |
probably benign |
Het |
Pbx2 |
T |
A |
17: 34,813,673 (GRCm39) |
C224* |
probably null |
Het |
Pcdha6 |
A |
G |
18: 37,100,960 (GRCm39) |
D51G |
probably damaging |
Het |
Pnpla1 |
C |
T |
17: 29,104,558 (GRCm39) |
T538I |
possibly damaging |
Het |
Pnpla2 |
T |
C |
7: 141,039,204 (GRCm39) |
|
probably null |
Het |
Psme2b |
C |
T |
11: 48,836,654 (GRCm39) |
E98K |
probably benign |
Het |
Ranbp2 |
T |
A |
10: 58,297,717 (GRCm39) |
S375T |
probably benign |
Het |
Rimbp2 |
T |
C |
5: 128,880,985 (GRCm39) |
Y134C |
probably damaging |
Het |
Ryr1 |
G |
A |
7: 28,802,234 (GRCm39) |
|
probably null |
Het |
Sh3tc1 |
G |
T |
5: 35,857,633 (GRCm39) |
A1185D |
probably damaging |
Het |
Sin3b |
G |
A |
8: 73,471,184 (GRCm39) |
S377N |
probably benign |
Het |
Slc28a2 |
T |
C |
2: 122,288,371 (GRCm39) |
M554T |
possibly damaging |
Het |
Snhg11 |
T |
C |
2: 158,218,872 (GRCm39) |
|
probably benign |
Het |
Spink5 |
A |
T |
18: 44,139,479 (GRCm39) |
N614I |
probably damaging |
Het |
Tert |
T |
C |
13: 73,794,428 (GRCm39) |
|
probably null |
Het |
Thap4 |
T |
C |
1: 93,677,598 (GRCm39) |
Y396C |
probably damaging |
Het |
Tle2 |
T |
C |
10: 81,420,531 (GRCm39) |
L348P |
probably damaging |
Het |
Tmem104 |
T |
C |
11: 115,134,312 (GRCm39) |
S283P |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,953,949 (GRCm39) |
E602G |
possibly damaging |
Het |
Tpm4 |
A |
G |
8: 72,900,938 (GRCm39) |
K190R |
probably benign |
Het |
Ttf2 |
T |
C |
3: 100,870,485 (GRCm39) |
E196G |
probably benign |
Het |
Ugt3a1 |
T |
C |
15: 9,365,373 (GRCm39) |
W329R |
probably damaging |
Het |
Unc13a |
G |
A |
8: 72,094,121 (GRCm39) |
Q1327* |
probably null |
Het |
Vmn1r194 |
C |
T |
13: 22,429,058 (GRCm39) |
T225I |
probably benign |
Het |
Vmn1r215 |
T |
C |
13: 23,260,721 (GRCm39) |
S254P |
probably damaging |
Het |
Vmn2r109 |
T |
C |
17: 20,775,451 (GRCm39) |
E92G |
probably damaging |
Het |
Ythdc2 |
A |
G |
18: 44,987,809 (GRCm39) |
M625V |
probably benign |
Het |
Zfp106 |
A |
G |
2: 120,341,015 (GRCm39) |
W1832R |
probably damaging |
Het |
Zfp189 |
G |
A |
4: 49,530,438 (GRCm39) |
G514S |
probably damaging |
Het |
Zfp768 |
T |
C |
7: 126,942,875 (GRCm39) |
R418G |
probably damaging |
Het |
Zmynd11 |
C |
T |
13: 9,739,479 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ltbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Ltbp1
|
APN |
17 |
75,532,333 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00156:Ltbp1
|
APN |
17 |
75,692,155 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00161:Ltbp1
|
APN |
17 |
75,617,147 (GRCm39) |
splice site |
probably benign |
|
IGL00771:Ltbp1
|
APN |
17 |
75,669,511 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00822:Ltbp1
|
APN |
17 |
75,458,316 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01760:Ltbp1
|
APN |
17 |
75,534,145 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01796:Ltbp1
|
APN |
17 |
75,534,240 (GRCm39) |
splice site |
probably benign |
|
IGL01826:Ltbp1
|
APN |
17 |
75,599,835 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02372:Ltbp1
|
APN |
17 |
75,559,401 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02792:Ltbp1
|
APN |
17 |
75,589,989 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02862:Ltbp1
|
APN |
17 |
75,697,466 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03095:Ltbp1
|
APN |
17 |
75,589,413 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03345:Ltbp1
|
APN |
17 |
75,373,154 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03404:Ltbp1
|
APN |
17 |
75,532,301 (GRCm39) |
missense |
probably damaging |
0.97 |
Hiphop
|
UTSW |
17 |
75,666,452 (GRCm39) |
missense |
probably damaging |
0.99 |
Pygea
|
UTSW |
17 |
75,634,223 (GRCm39) |
nonsense |
probably null |
|
Twist
|
UTSW |
17 |
75,617,217 (GRCm39) |
missense |
probably damaging |
0.99 |
R0010:Ltbp1
|
UTSW |
17 |
75,670,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Ltbp1
|
UTSW |
17 |
75,670,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Ltbp1
|
UTSW |
17 |
75,671,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Ltbp1
|
UTSW |
17 |
75,671,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R0033:Ltbp1
|
UTSW |
17 |
75,583,504 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0033:Ltbp1
|
UTSW |
17 |
75,583,504 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0034:Ltbp1
|
UTSW |
17 |
75,354,563 (GRCm39) |
intron |
probably benign |
|
R0068:Ltbp1
|
UTSW |
17 |
75,666,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Ltbp1
|
UTSW |
17 |
75,666,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R0467:Ltbp1
|
UTSW |
17 |
75,589,424 (GRCm39) |
critical splice donor site |
probably null |
|
R0554:Ltbp1
|
UTSW |
17 |
75,532,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R0584:Ltbp1
|
UTSW |
17 |
75,670,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R0863:Ltbp1
|
UTSW |
17 |
75,559,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R0991:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1084:Ltbp1
|
UTSW |
17 |
75,666,420 (GRCm39) |
nonsense |
probably null |
|
R1114:Ltbp1
|
UTSW |
17 |
75,667,770 (GRCm39) |
missense |
probably benign |
|
R1177:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1179:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1195:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1195:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1195:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1245:Ltbp1
|
UTSW |
17 |
75,634,189 (GRCm39) |
splice site |
probably benign |
|
R1246:Ltbp1
|
UTSW |
17 |
75,692,156 (GRCm39) |
nonsense |
probably null |
|
R1258:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1259:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1260:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1262:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1265:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1267:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1269:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1272:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1411:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1579:Ltbp1
|
UTSW |
17 |
75,559,362 (GRCm39) |
missense |
probably benign |
0.00 |
R1694:Ltbp1
|
UTSW |
17 |
75,532,280 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1705:Ltbp1
|
UTSW |
17 |
75,692,196 (GRCm39) |
splice site |
probably null |
|
R1716:Ltbp1
|
UTSW |
17 |
75,622,019 (GRCm39) |
missense |
probably benign |
0.08 |
R1815:Ltbp1
|
UTSW |
17 |
75,559,375 (GRCm39) |
missense |
probably benign |
0.00 |
R1932:Ltbp1
|
UTSW |
17 |
75,620,029 (GRCm39) |
missense |
probably benign |
0.01 |
R1951:Ltbp1
|
UTSW |
17 |
75,458,372 (GRCm39) |
missense |
probably benign |
0.00 |
R2044:Ltbp1
|
UTSW |
17 |
75,583,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R2118:Ltbp1
|
UTSW |
17 |
75,617,154 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2120:Ltbp1
|
UTSW |
17 |
75,617,154 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2121:Ltbp1
|
UTSW |
17 |
75,617,154 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2122:Ltbp1
|
UTSW |
17 |
75,617,154 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2171:Ltbp1
|
UTSW |
17 |
75,598,312 (GRCm39) |
missense |
probably damaging |
0.99 |
R2237:Ltbp1
|
UTSW |
17 |
75,617,158 (GRCm39) |
missense |
probably benign |
0.31 |
R2655:Ltbp1
|
UTSW |
17 |
75,312,978 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2941:Ltbp1
|
UTSW |
17 |
75,486,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R3177:Ltbp1
|
UTSW |
17 |
75,666,273 (GRCm39) |
splice site |
probably null |
|
R3177:Ltbp1
|
UTSW |
17 |
75,583,475 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3277:Ltbp1
|
UTSW |
17 |
75,666,273 (GRCm39) |
splice site |
probably null |
|
R3277:Ltbp1
|
UTSW |
17 |
75,583,475 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3797:Ltbp1
|
UTSW |
17 |
75,669,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R3861:Ltbp1
|
UTSW |
17 |
75,666,333 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3897:Ltbp1
|
UTSW |
17 |
75,581,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R4002:Ltbp1
|
UTSW |
17 |
75,617,154 (GRCm39) |
missense |
probably benign |
0.09 |
R4057:Ltbp1
|
UTSW |
17 |
75,617,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R4261:Ltbp1
|
UTSW |
17 |
75,598,362 (GRCm39) |
nonsense |
probably null |
|
R4375:Ltbp1
|
UTSW |
17 |
75,619,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R4458:Ltbp1
|
UTSW |
17 |
75,583,502 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4519:Ltbp1
|
UTSW |
17 |
75,671,492 (GRCm39) |
missense |
probably benign |
0.14 |
R4529:Ltbp1
|
UTSW |
17 |
75,458,355 (GRCm39) |
missense |
probably benign |
0.21 |
R4614:Ltbp1
|
UTSW |
17 |
75,596,989 (GRCm39) |
intron |
probably benign |
|
R4724:Ltbp1
|
UTSW |
17 |
75,620,003 (GRCm39) |
missense |
probably damaging |
0.99 |
R4756:Ltbp1
|
UTSW |
17 |
75,532,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R4907:Ltbp1
|
UTSW |
17 |
75,312,899 (GRCm39) |
missense |
probably benign |
|
R4910:Ltbp1
|
UTSW |
17 |
75,634,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4976:Ltbp1
|
UTSW |
17 |
75,628,090 (GRCm39) |
critical splice donor site |
probably null |
|
R5047:Ltbp1
|
UTSW |
17 |
75,599,881 (GRCm39) |
splice site |
probably benign |
|
R5259:Ltbp1
|
UTSW |
17 |
75,670,357 (GRCm39) |
missense |
probably benign |
0.03 |
R5438:Ltbp1
|
UTSW |
17 |
75,598,321 (GRCm39) |
missense |
probably damaging |
0.98 |
R5583:Ltbp1
|
UTSW |
17 |
75,598,325 (GRCm39) |
missense |
probably benign |
0.00 |
R5757:Ltbp1
|
UTSW |
17 |
75,580,944 (GRCm39) |
splice site |
probably null |
|
R5950:Ltbp1
|
UTSW |
17 |
75,580,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Ltbp1
|
UTSW |
17 |
75,597,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R6267:Ltbp1
|
UTSW |
17 |
75,312,984 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6383:Ltbp1
|
UTSW |
17 |
75,666,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R6400:Ltbp1
|
UTSW |
17 |
75,458,397 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6861:Ltbp1
|
UTSW |
17 |
75,534,187 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6880:Ltbp1
|
UTSW |
17 |
75,628,044 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7168:Ltbp1
|
UTSW |
17 |
75,598,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R7198:Ltbp1
|
UTSW |
17 |
75,533,962 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7260:Ltbp1
|
UTSW |
17 |
75,373,139 (GRCm39) |
missense |
probably benign |
0.01 |
R7262:Ltbp1
|
UTSW |
17 |
75,671,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R7340:Ltbp1
|
UTSW |
17 |
75,634,223 (GRCm39) |
nonsense |
probably null |
|
R7443:Ltbp1
|
UTSW |
17 |
75,671,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R7510:Ltbp1
|
UTSW |
17 |
75,659,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R7676:Ltbp1
|
UTSW |
17 |
75,598,292 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7717:Ltbp1
|
UTSW |
17 |
75,597,073 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7720:Ltbp1
|
UTSW |
17 |
75,692,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R7799:Ltbp1
|
UTSW |
17 |
75,559,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R7944:Ltbp1
|
UTSW |
17 |
75,697,546 (GRCm39) |
makesense |
probably null |
|
R7945:Ltbp1
|
UTSW |
17 |
75,697,546 (GRCm39) |
makesense |
probably null |
|
R7976:Ltbp1
|
UTSW |
17 |
75,670,358 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8256:Ltbp1
|
UTSW |
17 |
75,622,236 (GRCm39) |
intron |
probably benign |
|
R8295:Ltbp1
|
UTSW |
17 |
75,486,184 (GRCm39) |
missense |
probably benign |
0.10 |
R8423:Ltbp1
|
UTSW |
17 |
75,599,852 (GRCm39) |
missense |
probably benign |
|
R8462:Ltbp1
|
UTSW |
17 |
75,620,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R8677:Ltbp1
|
UTSW |
17 |
75,655,753 (GRCm39) |
missense |
probably benign |
0.00 |
R8742:Ltbp1
|
UTSW |
17 |
75,617,217 (GRCm39) |
missense |
probably damaging |
0.99 |
R8766:Ltbp1
|
UTSW |
17 |
75,603,250 (GRCm39) |
nonsense |
probably null |
|
R8873:Ltbp1
|
UTSW |
17 |
75,486,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Ltbp1
|
UTSW |
17 |
75,486,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R9100:Ltbp1
|
UTSW |
17 |
75,622,103 (GRCm39) |
missense |
probably damaging |
0.96 |
R9100:Ltbp1
|
UTSW |
17 |
75,622,102 (GRCm39) |
missense |
probably benign |
0.10 |
R9141:Ltbp1
|
UTSW |
17 |
75,598,309 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9204:Ltbp1
|
UTSW |
17 |
75,670,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R9292:Ltbp1
|
UTSW |
17 |
75,583,436 (GRCm39) |
missense |
probably damaging |
0.99 |
R9381:Ltbp1
|
UTSW |
17 |
75,696,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R9423:Ltbp1
|
UTSW |
17 |
75,597,112 (GRCm39) |
missense |
probably benign |
|
R9426:Ltbp1
|
UTSW |
17 |
75,598,309 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9448:Ltbp1
|
UTSW |
17 |
75,666,455 (GRCm39) |
nonsense |
probably null |
|
R9519:Ltbp1
|
UTSW |
17 |
75,692,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R9523:Ltbp1
|
UTSW |
17 |
75,697,498 (GRCm39) |
missense |
probably benign |
0.29 |
R9625:Ltbp1
|
UTSW |
17 |
75,486,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R9671:Ltbp1
|
UTSW |
17 |
75,603,217 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0001:Ltbp1
|
UTSW |
17 |
75,534,173 (GRCm39) |
missense |
probably benign |
0.26 |
|