Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
T |
9: 53,339,456 (GRCm39) |
E106D |
probably damaging |
Het |
A830018L16Rik |
A |
T |
1: 11,868,718 (GRCm39) |
N333Y |
probably damaging |
Het |
Abca4 |
T |
A |
3: 121,917,309 (GRCm39) |
M1007K |
possibly damaging |
Het |
Accsl |
T |
A |
2: 93,687,343 (GRCm39) |
I495F |
probably damaging |
Het |
Acsl3 |
T |
C |
1: 78,674,182 (GRCm39) |
S373P |
possibly damaging |
Het |
Adam7 |
A |
G |
14: 68,742,546 (GRCm39) |
I689T |
possibly damaging |
Het |
Akap11 |
G |
A |
14: 78,752,336 (GRCm39) |
T179I |
probably damaging |
Het |
Ankmy1 |
T |
C |
1: 92,816,187 (GRCm39) |
K309R |
possibly damaging |
Het |
Apaf1 |
A |
T |
10: 90,859,673 (GRCm39) |
I824N |
probably damaging |
Het |
Apc2 |
T |
A |
10: 80,148,488 (GRCm39) |
C1152S |
probably damaging |
Het |
Arhgap17 |
C |
A |
7: 122,899,727 (GRCm39) |
W409L |
probably damaging |
Het |
Arhgef15 |
T |
C |
11: 68,845,796 (GRCm39) |
I19V |
unknown |
Het |
Arnt |
C |
A |
3: 95,397,936 (GRCm39) |
P573H |
probably damaging |
Het |
Arvcf |
G |
A |
16: 18,223,882 (GRCm39) |
G932R |
probably damaging |
Het |
Atg4a-ps |
C |
T |
3: 103,553,044 (GRCm39) |
W99* |
probably null |
Het |
Atp13a5 |
T |
A |
16: 29,056,004 (GRCm39) |
D1052V |
probably benign |
Het |
Atp2b4 |
T |
C |
1: 133,642,797 (GRCm39) |
T1103A |
probably damaging |
Het |
B4galnt4 |
C |
A |
7: 140,647,335 (GRCm39) |
Q362K |
possibly damaging |
Het |
Cd320 |
T |
A |
17: 34,066,491 (GRCm39) |
N90K |
probably benign |
Het |
Cep170b |
A |
T |
12: 112,698,502 (GRCm39) |
I87F |
probably damaging |
Het |
Coq3 |
T |
G |
4: 21,900,486 (GRCm39) |
C238G |
probably benign |
Het |
Cpa5 |
A |
T |
6: 30,614,044 (GRCm39) |
Q62L |
probably benign |
Het |
Ctsg |
A |
T |
14: 56,339,110 (GRCm39) |
C49* |
probably null |
Het |
Cul9 |
T |
C |
17: 46,819,489 (GRCm39) |
T2000A |
probably damaging |
Het |
Dedd |
C |
T |
1: 171,167,790 (GRCm39) |
P155S |
probably benign |
Het |
Dnah1 |
A |
G |
14: 30,997,565 (GRCm39) |
S2598P |
probably damaging |
Het |
Dnah14 |
C |
T |
1: 181,433,459 (GRCm39) |
P379S |
possibly damaging |
Het |
Dync2h1 |
A |
T |
9: 7,165,703 (GRCm39) |
S519R |
probably benign |
Het |
Eea1 |
A |
G |
10: 95,874,660 (GRCm39) |
S1192G |
probably benign |
Het |
Eif5b |
T |
C |
1: 38,084,760 (GRCm39) |
I869T |
probably damaging |
Het |
Elavl4 |
C |
A |
4: 110,112,651 (GRCm39) |
|
probably benign |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Ets2 |
G |
A |
16: 95,520,037 (GRCm39) |
R421H |
probably damaging |
Het |
Exoc3l2 |
G |
A |
7: 19,203,635 (GRCm39) |
A76T |
possibly damaging |
Het |
Fam89b |
T |
C |
19: 5,778,757 (GRCm39) |
Y144C |
probably damaging |
Het |
Greb1 |
T |
C |
12: 16,749,580 (GRCm39) |
E1082G |
probably damaging |
Het |
Gtf3a |
A |
T |
5: 146,890,798 (GRCm39) |
|
probably null |
Het |
Hoxc12 |
C |
A |
15: 102,845,524 (GRCm39) |
F79L |
possibly damaging |
Het |
Hspb8 |
G |
T |
5: 116,547,491 (GRCm39) |
L164I |
probably damaging |
Het |
Ina |
C |
T |
19: 47,003,564 (GRCm39) |
A124V |
probably benign |
Het |
Inhbb |
T |
A |
1: 119,345,411 (GRCm39) |
I293F |
probably damaging |
Het |
Itpr3 |
A |
G |
17: 27,314,449 (GRCm39) |
Y633C |
possibly damaging |
Het |
Jag2 |
C |
T |
12: 112,872,949 (GRCm39) |
V1102I |
probably benign |
Het |
Kalrn |
A |
T |
16: 33,796,361 (GRCm39) |
F1138Y |
probably benign |
Het |
Large2 |
T |
A |
2: 92,200,853 (GRCm39) |
|
probably benign |
Het |
Lats2 |
A |
G |
14: 57,959,966 (GRCm39) |
S177P |
probably benign |
Het |
Lims2 |
G |
A |
18: 32,087,515 (GRCm39) |
R124H |
possibly damaging |
Het |
Lrp2 |
T |
A |
2: 69,313,787 (GRCm39) |
T2315S |
probably benign |
Het |
Lrrc4c |
A |
C |
2: 97,459,391 (GRCm39) |
T6P |
probably benign |
Het |
Man2b2 |
A |
T |
5: 36,978,378 (GRCm39) |
M302K |
probably damaging |
Het |
Mocos |
G |
A |
18: 24,834,542 (GRCm39) |
G860R |
possibly damaging |
Het |
Mylk3 |
T |
A |
8: 86,085,571 (GRCm39) |
D258V |
possibly damaging |
Het |
Nkx1-2 |
C |
T |
7: 132,201,240 (GRCm39) |
D6N |
probably damaging |
Het |
Nrp2 |
A |
G |
1: 62,758,176 (GRCm39) |
N54S |
possibly damaging |
Het |
Nt5el |
T |
C |
13: 105,256,473 (GRCm39) |
I514T |
possibly damaging |
Het |
Or2d2 |
A |
G |
7: 106,727,848 (GRCm39) |
F251L |
probably benign |
Het |
Pacsin1 |
A |
T |
17: 27,926,879 (GRCm39) |
T195S |
probably benign |
Het |
Pank4 |
T |
C |
4: 155,056,693 (GRCm39) |
|
probably null |
Het |
Pdgfra |
A |
T |
5: 75,327,180 (GRCm39) |
M126L |
probably benign |
Het |
Podxl |
T |
A |
6: 31,505,432 (GRCm39) |
T204S |
probably benign |
Het |
Pole |
G |
A |
5: 110,484,240 (GRCm39) |
D2175N |
probably damaging |
Het |
Pramel16 |
C |
T |
4: 143,677,267 (GRCm39) |
G104E |
probably benign |
Het |
Prkdc |
A |
G |
16: 15,587,749 (GRCm39) |
K2545E |
probably benign |
Het |
Prodh |
T |
C |
16: 17,897,849 (GRCm39) |
I183V |
probably benign |
Het |
Ptch1 |
T |
C |
13: 63,691,422 (GRCm39) |
D277G |
possibly damaging |
Het |
Rapgef5 |
G |
A |
12: 117,684,988 (GRCm39) |
V246M |
probably damaging |
Het |
Rubcnl |
A |
G |
14: 75,269,834 (GRCm39) |
N164S |
probably benign |
Het |
Samd4 |
A |
T |
14: 47,290,419 (GRCm39) |
L175F |
probably damaging |
Het |
Scart1 |
G |
A |
7: 139,808,642 (GRCm39) |
G851D |
probably damaging |
Het |
Scimp |
C |
A |
11: 70,688,893 (GRCm39) |
W41L |
possibly damaging |
Het |
Scn3a |
T |
A |
2: 65,291,843 (GRCm39) |
K1634N |
possibly damaging |
Het |
Spta1 |
A |
G |
1: 174,030,888 (GRCm39) |
R957G |
probably benign |
Het |
Sptlc3 |
T |
A |
2: 139,478,692 (GRCm39) |
N550K |
probably benign |
Het |
Srebf1 |
T |
C |
11: 60,094,361 (GRCm39) |
N609D |
probably null |
Het |
Styxl1 |
A |
T |
5: 135,776,664 (GRCm39) |
L164H |
probably benign |
Het |
Synpo2l |
A |
T |
14: 20,710,702 (GRCm39) |
D865E |
probably damaging |
Het |
Tnfsf15 |
T |
C |
4: 63,663,267 (GRCm39) |
M19V |
probably damaging |
Het |
Trappc8 |
G |
C |
18: 20,970,132 (GRCm39) |
R953G |
probably benign |
Het |
Trav13-1 |
A |
G |
14: 53,782,800 (GRCm39) |
N50S |
probably benign |
Het |
Trim12a |
T |
C |
7: 103,955,241 (GRCm39) |
K161E |
probably benign |
Het |
Vipr1 |
C |
A |
9: 121,493,640 (GRCm39) |
N230K |
probably damaging |
Het |
Xirp1 |
A |
T |
9: 119,847,557 (GRCm39) |
V3E |
probably damaging |
Het |
Zfp768 |
A |
G |
7: 126,943,892 (GRCm39) |
F82L |
probably benign |
Het |
|
Other mutations in Lrrk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Lrrk2
|
APN |
15 |
91,632,002 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL00542:Lrrk2
|
APN |
15 |
91,584,146 (GRCm39) |
missense |
probably benign |
|
IGL00770:Lrrk2
|
APN |
15 |
91,686,036 (GRCm39) |
splice site |
probably benign |
|
IGL00774:Lrrk2
|
APN |
15 |
91,686,036 (GRCm39) |
splice site |
probably benign |
|
IGL00791:Lrrk2
|
APN |
15 |
91,664,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00827:Lrrk2
|
APN |
15 |
91,639,993 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00843:Lrrk2
|
APN |
15 |
91,641,261 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01109:Lrrk2
|
APN |
15 |
91,623,035 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01293:Lrrk2
|
APN |
15 |
91,610,340 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01296:Lrrk2
|
APN |
15 |
91,567,345 (GRCm39) |
missense |
probably benign |
|
IGL01301:Lrrk2
|
APN |
15 |
91,651,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01360:Lrrk2
|
APN |
15 |
91,584,772 (GRCm39) |
splice site |
probably null |
|
IGL01465:Lrrk2
|
APN |
15 |
91,613,128 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01529:Lrrk2
|
APN |
15 |
91,696,516 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01557:Lrrk2
|
APN |
15 |
91,584,192 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01560:Lrrk2
|
APN |
15 |
91,659,191 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01991:Lrrk2
|
APN |
15 |
91,664,149 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02003:Lrrk2
|
APN |
15 |
91,615,694 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02325:Lrrk2
|
APN |
15 |
91,610,511 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02711:Lrrk2
|
APN |
15 |
91,570,025 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02869:Lrrk2
|
APN |
15 |
91,634,480 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03104:Lrrk2
|
APN |
15 |
91,631,958 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03179:Lrrk2
|
APN |
15 |
91,584,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03395:Lrrk2
|
APN |
15 |
91,681,617 (GRCm39) |
splice site |
probably null |
|
horned
|
UTSW |
15 |
91,657,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R1312_Lrrk2_980
|
UTSW |
15 |
91,584,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710_lrrk2_232
|
UTSW |
15 |
91,584,130 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5245_Lrrk2_127
|
UTSW |
15 |
91,680,292 (GRCm39) |
missense |
probably damaging |
1.00 |
spree
|
UTSW |
15 |
91,586,450 (GRCm39) |
missense |
probably benign |
0.00 |
Spur
|
UTSW |
15 |
91,659,198 (GRCm39) |
nonsense |
probably null |
|
3-1:Lrrk2
|
UTSW |
15 |
91,686,137 (GRCm39) |
missense |
probably benign |
0.01 |
ANU18:Lrrk2
|
UTSW |
15 |
91,651,542 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Lrrk2
|
UTSW |
15 |
91,557,561 (GRCm39) |
missense |
probably benign |
|
H8786:Lrrk2
|
UTSW |
15 |
91,557,561 (GRCm39) |
missense |
probably benign |
|
IGL02835:Lrrk2
|
UTSW |
15 |
91,698,863 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0014:Lrrk2
|
UTSW |
15 |
91,686,248 (GRCm39) |
splice site |
probably benign |
|
R0014:Lrrk2
|
UTSW |
15 |
91,686,248 (GRCm39) |
splice site |
probably benign |
|
R0078:Lrrk2
|
UTSW |
15 |
91,618,212 (GRCm39) |
missense |
probably benign |
0.01 |
R0100:Lrrk2
|
UTSW |
15 |
91,629,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R0282:Lrrk2
|
UTSW |
15 |
91,662,617 (GRCm39) |
splice site |
probably benign |
|
R0448:Lrrk2
|
UTSW |
15 |
91,593,508 (GRCm39) |
missense |
probably damaging |
0.99 |
R0449:Lrrk2
|
UTSW |
15 |
91,634,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R0610:Lrrk2
|
UTSW |
15 |
91,699,619 (GRCm39) |
missense |
probably benign |
|
R0617:Lrrk2
|
UTSW |
15 |
91,636,481 (GRCm39) |
missense |
probably benign |
0.00 |
R0632:Lrrk2
|
UTSW |
15 |
91,680,231 (GRCm39) |
missense |
probably damaging |
0.98 |
R0639:Lrrk2
|
UTSW |
15 |
91,657,199 (GRCm39) |
missense |
probably benign |
0.03 |
R0661:Lrrk2
|
UTSW |
15 |
91,671,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R0666:Lrrk2
|
UTSW |
15 |
91,641,273 (GRCm39) |
critical splice donor site |
probably null |
|
R0764:Lrrk2
|
UTSW |
15 |
91,659,249 (GRCm39) |
splice site |
probably null |
|
R0766:Lrrk2
|
UTSW |
15 |
91,584,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R0845:Lrrk2
|
UTSW |
15 |
91,640,165 (GRCm39) |
missense |
probably benign |
0.22 |
R0940:Lrrk2
|
UTSW |
15 |
91,613,284 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0970:Lrrk2
|
UTSW |
15 |
91,613,372 (GRCm39) |
missense |
probably benign |
0.22 |
R1080:Lrrk2
|
UTSW |
15 |
91,557,892 (GRCm39) |
missense |
probably benign |
0.01 |
R1114:Lrrk2
|
UTSW |
15 |
91,584,671 (GRCm39) |
nonsense |
probably null |
|
R1223:Lrrk2
|
UTSW |
15 |
91,557,838 (GRCm39) |
missense |
probably benign |
0.00 |
R1289:Lrrk2
|
UTSW |
15 |
91,696,563 (GRCm39) |
missense |
probably benign |
0.00 |
R1296:Lrrk2
|
UTSW |
15 |
91,613,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R1312:Lrrk2
|
UTSW |
15 |
91,584,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1637:Lrrk2
|
UTSW |
15 |
91,618,261 (GRCm39) |
missense |
probably benign |
|
R1773:Lrrk2
|
UTSW |
15 |
91,664,184 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1809:Lrrk2
|
UTSW |
15 |
91,584,095 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1839:Lrrk2
|
UTSW |
15 |
91,567,337 (GRCm39) |
missense |
probably benign |
0.00 |
R1946:Lrrk2
|
UTSW |
15 |
91,620,864 (GRCm39) |
splice site |
probably null |
|
R2160:Lrrk2
|
UTSW |
15 |
91,680,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R2232:Lrrk2
|
UTSW |
15 |
91,648,919 (GRCm39) |
missense |
probably benign |
0.05 |
R2419:Lrrk2
|
UTSW |
15 |
91,681,729 (GRCm39) |
splice site |
probably benign |
|
R2516:Lrrk2
|
UTSW |
15 |
91,640,130 (GRCm39) |
missense |
probably benign |
|
R3110:Lrrk2
|
UTSW |
15 |
91,698,898 (GRCm39) |
missense |
probably benign |
0.02 |
R3112:Lrrk2
|
UTSW |
15 |
91,698,898 (GRCm39) |
missense |
probably benign |
0.02 |
R3801:Lrrk2
|
UTSW |
15 |
91,621,314 (GRCm39) |
missense |
probably benign |
|
R3842:Lrrk2
|
UTSW |
15 |
91,640,119 (GRCm39) |
missense |
probably benign |
0.01 |
R3903:Lrrk2
|
UTSW |
15 |
91,631,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R3903:Lrrk2
|
UTSW |
15 |
91,631,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R3930:Lrrk2
|
UTSW |
15 |
91,651,664 (GRCm39) |
critical splice donor site |
probably null |
|
R3937:Lrrk2
|
UTSW |
15 |
91,662,707 (GRCm39) |
missense |
probably damaging |
0.98 |
R3938:Lrrk2
|
UTSW |
15 |
91,662,707 (GRCm39) |
missense |
probably damaging |
0.98 |
R3938:Lrrk2
|
UTSW |
15 |
91,596,983 (GRCm39) |
missense |
possibly damaging |
0.69 |
R3982:Lrrk2
|
UTSW |
15 |
91,593,487 (GRCm39) |
missense |
probably benign |
0.22 |
R4125:Lrrk2
|
UTSW |
15 |
91,699,686 (GRCm39) |
missense |
probably benign |
0.01 |
R4130:Lrrk2
|
UTSW |
15 |
91,639,997 (GRCm39) |
missense |
probably benign |
0.19 |
R4296:Lrrk2
|
UTSW |
15 |
91,584,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R4465:Lrrk2
|
UTSW |
15 |
91,632,023 (GRCm39) |
missense |
probably damaging |
0.96 |
R4478:Lrrk2
|
UTSW |
15 |
91,607,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R4517:Lrrk2
|
UTSW |
15 |
91,589,323 (GRCm39) |
missense |
probably benign |
|
R4539:Lrrk2
|
UTSW |
15 |
91,613,345 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4654:Lrrk2
|
UTSW |
15 |
91,649,884 (GRCm39) |
missense |
probably damaging |
0.96 |
R4710:Lrrk2
|
UTSW |
15 |
91,584,130 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4722:Lrrk2
|
UTSW |
15 |
91,573,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R4723:Lrrk2
|
UTSW |
15 |
91,648,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Lrrk2
|
UTSW |
15 |
91,649,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Lrrk2
|
UTSW |
15 |
91,573,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Lrrk2
|
UTSW |
15 |
91,649,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Lrrk2
|
UTSW |
15 |
91,573,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R4787:Lrrk2
|
UTSW |
15 |
91,597,031 (GRCm39) |
missense |
probably benign |
|
R4945:Lrrk2
|
UTSW |
15 |
91,689,123 (GRCm39) |
missense |
probably benign |
0.02 |
R4948:Lrrk2
|
UTSW |
15 |
91,687,592 (GRCm39) |
missense |
probably benign |
0.20 |
R5000:Lrrk2
|
UTSW |
15 |
91,634,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R5031:Lrrk2
|
UTSW |
15 |
91,584,822 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5067:Lrrk2
|
UTSW |
15 |
91,649,993 (GRCm39) |
missense |
probably benign |
0.01 |
R5245:Lrrk2
|
UTSW |
15 |
91,680,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R5341:Lrrk2
|
UTSW |
15 |
91,657,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R5460:Lrrk2
|
UTSW |
15 |
91,698,847 (GRCm39) |
splice site |
probably null |
|
R5551:Lrrk2
|
UTSW |
15 |
91,696,553 (GRCm39) |
missense |
probably benign |
|
R5574:Lrrk2
|
UTSW |
15 |
91,671,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R5577:Lrrk2
|
UTSW |
15 |
91,649,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R5685:Lrrk2
|
UTSW |
15 |
91,687,504 (GRCm39) |
nonsense |
probably null |
|
R5712:Lrrk2
|
UTSW |
15 |
91,586,425 (GRCm39) |
nonsense |
probably null |
|
R5728:Lrrk2
|
UTSW |
15 |
91,659,177 (GRCm39) |
missense |
probably benign |
0.36 |
R5782:Lrrk2
|
UTSW |
15 |
91,586,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R5788:Lrrk2
|
UTSW |
15 |
91,648,851 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5821:Lrrk2
|
UTSW |
15 |
91,593,593 (GRCm39) |
critical splice donor site |
probably null |
|
R5852:Lrrk2
|
UTSW |
15 |
91,640,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R5934:Lrrk2
|
UTSW |
15 |
91,618,249 (GRCm39) |
missense |
probably benign |
0.00 |
R5935:Lrrk2
|
UTSW |
15 |
91,630,034 (GRCm39) |
missense |
probably benign |
0.14 |
R5979:Lrrk2
|
UTSW |
15 |
91,657,148 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6101:Lrrk2
|
UTSW |
15 |
91,607,338 (GRCm39) |
missense |
probably benign |
0.10 |
R6114:Lrrk2
|
UTSW |
15 |
91,632,029 (GRCm39) |
missense |
probably benign |
0.33 |
R6259:Lrrk2
|
UTSW |
15 |
91,586,450 (GRCm39) |
missense |
probably benign |
0.00 |
R6417:Lrrk2
|
UTSW |
15 |
91,696,549 (GRCm39) |
missense |
probably benign |
0.03 |
R6420:Lrrk2
|
UTSW |
15 |
91,696,549 (GRCm39) |
missense |
probably benign |
0.03 |
R6737:Lrrk2
|
UTSW |
15 |
91,607,421 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7056:Lrrk2
|
UTSW |
15 |
91,659,198 (GRCm39) |
nonsense |
probably null |
|
R7072:Lrrk2
|
UTSW |
15 |
91,686,123 (GRCm39) |
missense |
probably benign |
0.03 |
R7109:Lrrk2
|
UTSW |
15 |
91,648,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R7128:Lrrk2
|
UTSW |
15 |
91,686,088 (GRCm39) |
missense |
probably benign |
|
R7144:Lrrk2
|
UTSW |
15 |
91,618,258 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7187:Lrrk2
|
UTSW |
15 |
91,641,204 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7270:Lrrk2
|
UTSW |
15 |
91,584,644 (GRCm39) |
missense |
probably benign |
0.01 |
R7356:Lrrk2
|
UTSW |
15 |
91,622,947 (GRCm39) |
missense |
probably benign |
0.07 |
R7360:Lrrk2
|
UTSW |
15 |
91,615,858 (GRCm39) |
critical splice donor site |
probably null |
|
R7373:Lrrk2
|
UTSW |
15 |
91,584,207 (GRCm39) |
critical splice donor site |
probably null |
|
R7465:Lrrk2
|
UTSW |
15 |
91,651,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R7477:Lrrk2
|
UTSW |
15 |
91,696,528 (GRCm39) |
missense |
probably damaging |
0.98 |
R7614:Lrrk2
|
UTSW |
15 |
91,657,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R7622:Lrrk2
|
UTSW |
15 |
91,696,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R7658:Lrrk2
|
UTSW |
15 |
91,584,561 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7679:Lrrk2
|
UTSW |
15 |
91,610,389 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7737:Lrrk2
|
UTSW |
15 |
91,699,649 (GRCm39) |
missense |
probably damaging |
0.98 |
R7739:Lrrk2
|
UTSW |
15 |
91,584,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R7740:Lrrk2
|
UTSW |
15 |
91,651,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7908:Lrrk2
|
UTSW |
15 |
91,610,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R8299:Lrrk2
|
UTSW |
15 |
91,557,443 (GRCm39) |
start gained |
probably benign |
|
R8389:Lrrk2
|
UTSW |
15 |
91,584,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R8462:Lrrk2
|
UTSW |
15 |
91,615,680 (GRCm39) |
missense |
probably benign |
|
R8698:Lrrk2
|
UTSW |
15 |
91,636,400 (GRCm39) |
missense |
probably benign |
0.38 |
R8947:Lrrk2
|
UTSW |
15 |
91,586,473 (GRCm39) |
nonsense |
probably null |
|
R9084:Lrrk2
|
UTSW |
15 |
91,634,469 (GRCm39) |
missense |
|
|
R9086:Lrrk2
|
UTSW |
15 |
91,640,051 (GRCm39) |
missense |
probably benign |
0.01 |
R9096:Lrrk2
|
UTSW |
15 |
91,557,459 (GRCm39) |
start gained |
probably benign |
|
R9097:Lrrk2
|
UTSW |
15 |
91,557,459 (GRCm39) |
start gained |
probably benign |
|
R9267:Lrrk2
|
UTSW |
15 |
91,584,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R9285:Lrrk2
|
UTSW |
15 |
91,662,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R9341:Lrrk2
|
UTSW |
15 |
91,584,618 (GRCm39) |
missense |
probably benign |
0.18 |
R9343:Lrrk2
|
UTSW |
15 |
91,584,618 (GRCm39) |
missense |
probably benign |
0.18 |
R9371:Lrrk2
|
UTSW |
15 |
91,607,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R9424:Lrrk2
|
UTSW |
15 |
91,636,388 (GRCm39) |
nonsense |
probably null |
|
R9489:Lrrk2
|
UTSW |
15 |
91,621,420 (GRCm39) |
missense |
probably benign |
0.37 |
R9502:Lrrk2
|
UTSW |
15 |
91,607,365 (GRCm39) |
missense |
probably damaging |
0.98 |
R9563:Lrrk2
|
UTSW |
15 |
91,634,043 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9576:Lrrk2
|
UTSW |
15 |
91,636,388 (GRCm39) |
nonsense |
probably null |
|
R9605:Lrrk2
|
UTSW |
15 |
91,621,420 (GRCm39) |
missense |
probably benign |
0.37 |
R9635:Lrrk2
|
UTSW |
15 |
91,696,527 (GRCm39) |
missense |
probably benign |
0.21 |
R9641:Lrrk2
|
UTSW |
15 |
91,671,251 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9660:Lrrk2
|
UTSW |
15 |
91,618,228 (GRCm39) |
missense |
probably benign |
0.00 |
R9673:Lrrk2
|
UTSW |
15 |
91,649,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R9708:Lrrk2
|
UTSW |
15 |
91,634,482 (GRCm39) |
nonsense |
probably null |
|
R9728:Lrrk2
|
UTSW |
15 |
91,618,228 (GRCm39) |
missense |
probably benign |
0.00 |
R9757:Lrrk2
|
UTSW |
15 |
91,695,229 (GRCm39) |
missense |
probably benign |
0.03 |
RF001:Lrrk2
|
UTSW |
15 |
91,620,836 (GRCm39) |
missense |
probably benign |
0.11 |
X0028:Lrrk2
|
UTSW |
15 |
91,623,054 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Lrrk2
|
UTSW |
15 |
91,610,443 (GRCm39) |
missense |
probably benign |
0.12 |
|