Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
T |
C |
11: 72,086,580 (GRCm39) |
K277R |
probably damaging |
Het |
Aatf |
T |
C |
11: 84,363,926 (GRCm39) |
Y267C |
probably benign |
Het |
Abi3bp |
A |
G |
16: 56,414,860 (GRCm39) |
T341A |
probably damaging |
Het |
Acer2 |
T |
C |
4: 86,792,823 (GRCm39) |
F33S |
probably damaging |
Het |
Actr1b |
A |
G |
1: 36,740,244 (GRCm39) |
V299A |
possibly damaging |
Het |
Ampd3 |
T |
A |
7: 110,390,387 (GRCm39) |
|
probably null |
Het |
Atm |
A |
C |
9: 53,355,300 (GRCm39) |
I2898R |
probably damaging |
Het |
Bpifb6 |
G |
C |
2: 153,748,812 (GRCm39) |
K269N |
possibly damaging |
Het |
Cacna1c |
T |
C |
6: 118,575,684 (GRCm39) |
E1927G |
possibly damaging |
Het |
Cacna1c |
T |
A |
6: 118,629,675 (GRCm39) |
T1249S |
probably benign |
Het |
Cars2 |
TCCCC |
TCCC |
8: 11,579,599 (GRCm39) |
|
probably null |
Het |
Cbll1 |
A |
G |
12: 31,537,507 (GRCm39) |
V415A |
probably benign |
Het |
Cd300lf |
C |
T |
11: 115,015,195 (GRCm39) |
V132I |
probably benign |
Het |
Chd2 |
T |
C |
7: 73,113,419 (GRCm39) |
E1187G |
probably damaging |
Het |
Cntrl |
T |
C |
2: 35,019,805 (GRCm39) |
L544P |
probably damaging |
Het |
Cryga |
A |
C |
1: 65,142,169 (GRCm39) |
S75A |
probably benign |
Het |
Dcbld1 |
T |
A |
10: 52,195,576 (GRCm39) |
Y261* |
probably null |
Het |
Ddx11 |
G |
A |
17: 66,457,724 (GRCm39) |
|
probably null |
Het |
Dgke |
C |
T |
11: 88,931,575 (GRCm39) |
V560I |
probably benign |
Het |
Dst |
A |
C |
1: 34,267,753 (GRCm39) |
D5065A |
probably damaging |
Het |
Dusp16 |
C |
A |
6: 134,697,456 (GRCm39) |
|
probably null |
Het |
Eif4enif1 |
T |
A |
11: 3,177,793 (GRCm39) |
V395E |
probably damaging |
Het |
Enox1 |
A |
G |
14: 77,815,204 (GRCm39) |
T121A |
probably damaging |
Het |
Enpp4 |
G |
T |
17: 44,413,371 (GRCm39) |
N54K |
probably benign |
Het |
Erc2 |
A |
T |
14: 27,802,112 (GRCm39) |
K764M |
probably damaging |
Het |
Ercc6 |
G |
T |
14: 32,248,360 (GRCm39) |
E304* |
probably null |
Het |
Fam117a |
T |
A |
11: 95,254,971 (GRCm39) |
C115S |
possibly damaging |
Het |
Fcrl5 |
G |
A |
3: 87,355,631 (GRCm39) |
G448E |
probably damaging |
Het |
Galntl5 |
T |
C |
5: 25,391,163 (GRCm39) |
S21P |
probably benign |
Het |
Garnl3 |
T |
C |
2: 32,994,892 (GRCm39) |
D39G |
probably benign |
Het |
Gm14295 |
C |
T |
2: 176,500,782 (GRCm39) |
Q91* |
probably null |
Het |
Grb10 |
T |
A |
11: 11,920,639 (GRCm39) |
|
probably benign |
Het |
Grip1 |
C |
T |
10: 119,911,369 (GRCm39) |
Q696* |
probably null |
Het |
Herc2 |
T |
A |
7: 55,802,914 (GRCm39) |
C2112* |
probably null |
Het |
Herc2 |
T |
G |
7: 55,854,466 (GRCm39) |
L3797R |
possibly damaging |
Het |
Ighm |
T |
C |
12: 113,385,187 (GRCm39) |
I258V |
unknown |
Het |
Jarid2 |
T |
A |
13: 45,056,539 (GRCm39) |
Y443N |
possibly damaging |
Het |
Kif13b |
A |
G |
14: 64,976,083 (GRCm39) |
Y466C |
probably damaging |
Het |
Krtap4-6 |
T |
A |
11: 99,556,245 (GRCm39) |
R161* |
probably null |
Het |
Lingo4 |
G |
A |
3: 94,310,697 (GRCm39) |
G545E |
probably benign |
Het |
Lmo2 |
T |
G |
2: 103,800,946 (GRCm39) |
V39G |
possibly damaging |
Het |
Loricrin |
C |
A |
3: 91,989,119 (GRCm39) |
G56* |
probably null |
Het |
Lrfn1 |
A |
G |
7: 28,159,169 (GRCm39) |
R363G |
probably benign |
Het |
Lrp1b |
T |
C |
2: 40,547,537 (GRCm39) |
D446G |
probably benign |
Het |
Magel2 |
G |
A |
7: 62,028,427 (GRCm39) |
V444M |
probably damaging |
Het |
Mkx |
A |
T |
18: 7,000,591 (GRCm39) |
|
probably null |
Het |
Ms4a7 |
A |
T |
19: 11,310,659 (GRCm39) |
I20N |
possibly damaging |
Het |
Myo5b |
A |
G |
18: 74,750,062 (GRCm39) |
Y173C |
probably damaging |
Het |
Nek1 |
C |
T |
8: 61,525,343 (GRCm39) |
Q594* |
probably null |
Het |
Nipbl |
T |
C |
15: 8,330,379 (GRCm39) |
M2349V |
possibly damaging |
Het |
Nmnat2 |
A |
T |
1: 152,952,717 (GRCm39) |
H102L |
probably damaging |
Het |
Nup155 |
T |
A |
15: 8,182,639 (GRCm39) |
C1201S |
probably damaging |
Het |
Or2y8 |
C |
A |
11: 52,035,423 (GRCm39) |
R311S |
probably benign |
Het |
Or4a76 |
G |
A |
2: 89,460,975 (GRCm39) |
T89I |
probably damaging |
Het |
Or52x1 |
G |
A |
7: 104,852,599 (GRCm39) |
T317I |
probably damaging |
Het |
Osbpl1a |
A |
G |
18: 12,952,560 (GRCm39) |
|
probably null |
Het |
Pcnt |
A |
G |
10: 76,221,632 (GRCm39) |
V1998A |
probably benign |
Het |
Pitpnc1 |
T |
C |
11: 107,117,092 (GRCm39) |
H193R |
probably damaging |
Het |
Pitpnm1 |
T |
C |
19: 4,160,522 (GRCm39) |
L781P |
probably damaging |
Het |
Prdm14 |
A |
T |
1: 13,189,160 (GRCm39) |
C395S |
probably damaging |
Het |
Prmt8 |
A |
G |
6: 127,688,767 (GRCm39) |
I201T |
probably damaging |
Het |
Pter |
T |
C |
2: 12,983,352 (GRCm39) |
V119A |
probably damaging |
Het |
Rab11fip4 |
T |
C |
11: 79,581,655 (GRCm39) |
|
probably null |
Het |
Rgs9 |
T |
C |
11: 109,159,813 (GRCm39) |
N173S |
probably benign |
Het |
Rorb |
C |
A |
19: 18,955,221 (GRCm39) |
V47L |
possibly damaging |
Het |
Rtn4r |
A |
G |
16: 17,969,046 (GRCm39) |
Y158C |
probably damaging |
Het |
Sdr16c5 |
C |
T |
4: 4,016,162 (GRCm39) |
G88E |
probably damaging |
Het |
Sfxn1 |
C |
T |
13: 54,247,899 (GRCm39) |
T208I |
probably benign |
Het |
Sgo2b |
C |
T |
8: 64,380,827 (GRCm39) |
M668I |
probably benign |
Het |
Slc52a3 |
G |
T |
2: 151,849,529 (GRCm39) |
|
probably null |
Het |
Smco1 |
A |
T |
16: 32,092,832 (GRCm39) |
M168L |
probably benign |
Het |
Spata31d1d |
G |
A |
13: 59,876,278 (GRCm39) |
T419I |
possibly damaging |
Het |
Spata31d1e |
T |
C |
13: 59,890,497 (GRCm39) |
D441G |
probably benign |
Het |
Spink5 |
T |
C |
18: 44,147,824 (GRCm39) |
S857P |
probably damaging |
Het |
Stk35 |
T |
A |
2: 129,652,808 (GRCm39) |
Y436* |
probably null |
Het |
Tmem225 |
T |
A |
9: 40,059,731 (GRCm39) |
I37N |
probably damaging |
Het |
Unkl |
T |
C |
17: 25,450,839 (GRCm39) |
*232R |
probably null |
Het |
Usp16 |
A |
G |
16: 87,280,079 (GRCm39) |
N813S |
probably benign |
Het |
Vmn1r128 |
A |
T |
7: 21,084,221 (GRCm39) |
*308C |
probably null |
Het |
Vmn2r45 |
A |
G |
7: 8,475,207 (GRCm39) |
V607A |
probably benign |
Het |
Vmn2r63 |
A |
T |
7: 42,578,059 (GRCm39) |
|
probably null |
Het |
Wnk4 |
A |
T |
11: 101,164,824 (GRCm39) |
N718Y |
probably damaging |
Het |
Zfp503 |
G |
C |
14: 22,035,868 (GRCm39) |
Y349* |
probably null |
Het |
Zfp990 |
T |
A |
4: 145,264,673 (GRCm39) |
F557Y |
possibly damaging |
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 |
|
R5011:Ltbp1
|
UTSW |
17 |
75,373,152 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
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 |
|