Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
T |
C |
11: 110,103,165 (GRCm39) |
S809G |
probably benign |
Het |
Ap4b1 |
T |
A |
3: 103,725,161 (GRCm39) |
|
probably null |
Het |
Aqp12 |
A |
G |
1: 92,934,606 (GRCm39) |
Q161R |
possibly damaging |
Het |
Atp8a2 |
A |
G |
14: 60,028,689 (GRCm39) |
I926T |
probably benign |
Het |
Cacna2d1 |
A |
T |
5: 16,504,988 (GRCm39) |
N314I |
probably damaging |
Het |
Cd209d |
A |
G |
8: 3,927,113 (GRCm39) |
S81P |
probably damaging |
Het |
Cdcp1 |
T |
A |
9: 123,007,086 (GRCm39) |
K554* |
probably null |
Het |
Celsr1 |
A |
G |
15: 85,816,658 (GRCm39) |
Y1762H |
probably benign |
Het |
Cklf |
A |
G |
8: 104,983,983 (GRCm39) |
T49A |
possibly damaging |
Het |
Col12a1 |
T |
G |
9: 79,600,820 (GRCm39) |
I755L |
probably benign |
Het |
Cts3 |
G |
A |
13: 61,715,368 (GRCm39) |
Q140* |
probably null |
Het |
Ddx1 |
A |
T |
12: 13,294,967 (GRCm39) |
|
probably null |
Het |
Dnah3 |
C |
A |
7: 119,570,402 (GRCm39) |
E2262* |
probably null |
Het |
Dnah5 |
A |
G |
15: 28,290,294 (GRCm39) |
N1228S |
probably benign |
Het |
Dsg1a |
G |
A |
18: 20,464,561 (GRCm39) |
R352Q |
probably damaging |
Het |
Efcab5 |
A |
G |
11: 77,042,679 (GRCm39) |
F25L |
probably damaging |
Het |
Efhd1 |
T |
A |
1: 87,192,404 (GRCm39) |
V78D |
probably damaging |
Het |
Eif5a2 |
T |
C |
3: 28,847,967 (GRCm39) |
|
probably null |
Het |
Elp2 |
T |
A |
18: 24,744,983 (GRCm39) |
V101D |
possibly damaging |
Het |
Enpp2 |
A |
T |
15: 54,773,592 (GRCm39) |
|
probably null |
Het |
Fbxo21 |
G |
T |
5: 118,146,129 (GRCm39) |
R584L |
probably benign |
Het |
Fbxw22 |
G |
T |
9: 109,211,196 (GRCm39) |
F368L |
possibly damaging |
Het |
Gcn1 |
T |
C |
5: 115,720,356 (GRCm39) |
I409T |
probably benign |
Het |
Gm12887 |
T |
C |
4: 121,473,655 (GRCm39) |
Y65C |
probably damaging |
Het |
Gria4 |
G |
A |
9: 4,537,637 (GRCm39) |
Q224* |
probably null |
Het |
Hdac5 |
C |
T |
11: 102,089,631 (GRCm39) |
V860M |
probably damaging |
Het |
Ino80 |
G |
A |
2: 119,212,417 (GRCm39) |
R1302C |
probably damaging |
Het |
Kcns2 |
A |
T |
15: 34,838,966 (GRCm39) |
I110F |
probably damaging |
Het |
Lrig3 |
A |
G |
10: 125,846,036 (GRCm39) |
T822A |
probably damaging |
Het |
Mapk6 |
T |
C |
9: 75,302,851 (GRCm39) |
D214G |
probably damaging |
Het |
Mcm2 |
A |
T |
6: 88,869,060 (GRCm39) |
L264Q |
probably benign |
Het |
Mpnd |
A |
T |
17: 56,317,455 (GRCm39) |
Y64F |
probably damaging |
Het |
Muc1 |
T |
A |
3: 89,139,079 (GRCm39) |
M520K |
possibly damaging |
Het |
Muc4 |
T |
A |
16: 32,577,276 (GRCm39) |
S189T |
probably benign |
Het |
Myh13 |
T |
C |
11: 67,242,945 (GRCm39) |
S953P |
possibly damaging |
Het |
Ncf2 |
A |
T |
1: 152,706,230 (GRCm39) |
M281L |
probably benign |
Het |
Nipal2 |
A |
G |
15: 34,648,841 (GRCm39) |
I116T |
probably damaging |
Het |
Nptn |
T |
C |
9: 58,531,015 (GRCm39) |
L46P |
probably benign |
Het |
Or2b6 |
A |
T |
13: 21,823,214 (GRCm39) |
S160T |
probably damaging |
Het |
Or4k77 |
A |
G |
2: 111,199,552 (GRCm39) |
T192A |
probably benign |
Het |
Or51ag1 |
C |
A |
7: 103,155,896 (GRCm39) |
V86F |
probably damaging |
Het |
Or5ae1 |
T |
A |
7: 84,565,325 (GRCm39) |
F113I |
probably damaging |
Het |
Pgr |
A |
T |
9: 8,902,069 (GRCm39) |
Y534F |
possibly damaging |
Het |
Pip4k2a |
A |
T |
2: 18,877,093 (GRCm39) |
|
probably null |
Het |
Pkd1l2 |
C |
G |
8: 117,767,514 (GRCm39) |
V1259L |
probably benign |
Het |
Ppp1r12a |
A |
G |
10: 108,085,426 (GRCm39) |
E457G |
probably damaging |
Het |
Rasa4 |
T |
A |
5: 136,133,491 (GRCm39) |
V650D |
probably benign |
Het |
Rem2 |
C |
T |
14: 54,713,766 (GRCm39) |
|
probably benign |
Het |
Rps18-ps6 |
A |
T |
13: 97,896,868 (GRCm39) |
Y77N |
possibly damaging |
Het |
Sdc1 |
G |
A |
12: 8,840,409 (GRCm39) |
R62Q |
possibly damaging |
Het |
Sdk1 |
A |
G |
5: 141,934,261 (GRCm39) |
E366G |
possibly damaging |
Het |
Setd2 |
T |
A |
9: 110,433,248 (GRCm39) |
H2406Q |
probably damaging |
Het |
Slc30a5 |
A |
G |
13: 100,949,891 (GRCm39) |
V397A |
probably benign |
Het |
Slc36a2 |
A |
T |
11: 55,075,739 (GRCm39) |
L16H |
possibly damaging |
Het |
Slc44a1 |
T |
C |
4: 53,542,468 (GRCm39) |
V334A |
probably benign |
Het |
Sox8 |
A |
T |
17: 25,786,456 (GRCm39) |
Y416N |
possibly damaging |
Het |
Speg |
T |
C |
1: 75,387,807 (GRCm39) |
V1416A |
possibly damaging |
Het |
Stimate |
T |
C |
14: 30,586,391 (GRCm39) |
L72S |
possibly damaging |
Het |
Stk24 |
T |
A |
14: 121,574,983 (GRCm39) |
I42F |
probably damaging |
Het |
Tasor2 |
A |
G |
13: 3,634,498 (GRCm39) |
|
probably null |
Het |
Tcerg1 |
T |
A |
18: 42,685,646 (GRCm39) |
L661Q |
possibly damaging |
Het |
Tpp1 |
G |
A |
7: 105,396,880 (GRCm39) |
R417W |
probably damaging |
Het |
Trim12a |
T |
A |
7: 103,955,264 (GRCm39) |
D153V |
possibly damaging |
Het |
Trpm2 |
T |
C |
10: 77,778,778 (GRCm39) |
N396S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,637,427 (GRCm39) |
K5695R |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,640,631 (GRCm39) |
R11960C |
probably damaging |
Het |
Tulp3 |
A |
C |
6: 128,310,906 (GRCm39) |
|
probably null |
Het |
Uaca |
T |
A |
9: 60,779,438 (GRCm39) |
L1273H |
probably damaging |
Het |
Usp33 |
A |
G |
3: 152,073,919 (GRCm39) |
E255G |
probably damaging |
Het |
Vmn2r54 |
T |
G |
7: 12,350,138 (GRCm39) |
|
probably null |
Het |
Vwa8 |
C |
T |
14: 79,145,670 (GRCm39) |
R116C |
probably damaging |
Het |
Wnt5b |
A |
T |
6: 119,423,315 (GRCm39) |
F116L |
probably benign |
Het |
Zbtb12 |
CTTCAT |
CTTCATTCAT |
17: 35,115,284 (GRCm39) |
|
probably null |
Het |
Zbtb12 |
TCATC |
TCATCCATC |
17: 35,115,286 (GRCm39) |
|
probably null |
Het |
Zfp408 |
G |
A |
2: 91,476,353 (GRCm39) |
T367I |
probably damaging |
Het |
Zfp512b |
G |
A |
2: 181,230,286 (GRCm39) |
A480V |
possibly damaging |
Het |
Zfp560 |
T |
C |
9: 20,258,949 (GRCm39) |
T638A |
probably benign |
Het |
Zfp932 |
G |
T |
5: 110,156,854 (GRCm39) |
G151V |
probably damaging |
Het |
Zpbp |
T |
C |
11: 11,302,696 (GRCm39) |
K320E |
probably damaging |
Het |
Zranb2 |
C |
T |
3: 157,243,277 (GRCm39) |
P91L |
probably damaging |
Het |
|
Other mutations in F5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00840:F5
|
APN |
1 |
164,007,093 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00843:F5
|
APN |
1 |
164,039,360 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00904:F5
|
APN |
1 |
164,021,578 (GRCm39) |
missense |
probably benign |
|
IGL00913:F5
|
APN |
1 |
164,032,465 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01099:F5
|
APN |
1 |
164,021,903 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01134:F5
|
APN |
1 |
164,019,548 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01313:F5
|
APN |
1 |
164,021,181 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01635:F5
|
APN |
1 |
164,035,427 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01697:F5
|
APN |
1 |
164,021,621 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01768:F5
|
APN |
1 |
164,003,914 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01795:F5
|
APN |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01835:F5
|
APN |
1 |
164,021,937 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01843:F5
|
APN |
1 |
164,039,395 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01989:F5
|
APN |
1 |
164,003,876 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02036:F5
|
APN |
1 |
164,010,571 (GRCm39) |
splice site |
probably benign |
|
IGL02065:F5
|
APN |
1 |
164,017,695 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02077:F5
|
APN |
1 |
164,026,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02139:F5
|
APN |
1 |
164,020,243 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02210:F5
|
APN |
1 |
164,017,710 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02415:F5
|
APN |
1 |
164,019,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02440:F5
|
APN |
1 |
164,034,635 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02471:F5
|
APN |
1 |
164,001,860 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02535:F5
|
APN |
1 |
164,026,302 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02537:F5
|
APN |
1 |
164,020,686 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02628:F5
|
APN |
1 |
164,021,644 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02638:F5
|
APN |
1 |
164,012,177 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02824:F5
|
APN |
1 |
164,021,916 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02977:F5
|
APN |
1 |
164,021,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03028:F5
|
APN |
1 |
164,020,569 (GRCm39) |
nonsense |
probably null |
|
IGL03064:F5
|
APN |
1 |
164,023,163 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03127:F5
|
APN |
1 |
164,021,107 (GRCm39) |
missense |
probably benign |
0.45 |
IGL03131:F5
|
APN |
1 |
163,989,388 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03348:F5
|
APN |
1 |
164,021,721 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03387:F5
|
APN |
1 |
164,020,801 (GRCm39) |
missense |
probably damaging |
1.00 |
James_dean
|
UTSW |
1 |
164,032,389 (GRCm39) |
missense |
probably benign |
0.43 |
BB002:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
BB012:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
R0002:F5
|
UTSW |
1 |
164,029,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0095:F5
|
UTSW |
1 |
164,019,537 (GRCm39) |
nonsense |
probably null |
|
R0116:F5
|
UTSW |
1 |
164,012,483 (GRCm39) |
missense |
probably benign |
0.01 |
R0359:F5
|
UTSW |
1 |
164,007,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R0426:F5
|
UTSW |
1 |
164,010,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R0452:F5
|
UTSW |
1 |
164,012,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R0457:F5
|
UTSW |
1 |
164,021,769 (GRCm39) |
missense |
probably benign |
0.00 |
R0520:F5
|
UTSW |
1 |
164,037,156 (GRCm39) |
missense |
probably benign |
0.15 |
R0522:F5
|
UTSW |
1 |
164,039,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R0554:F5
|
UTSW |
1 |
164,007,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R0575:F5
|
UTSW |
1 |
164,003,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R0739:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1062:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1063:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1149:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1149:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1150:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1151:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1152:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1221:F5
|
UTSW |
1 |
163,989,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1284:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1286:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1358:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1360:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1362:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1383:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:F5
|
UTSW |
1 |
164,026,402 (GRCm39) |
missense |
probably benign |
0.02 |
R1465:F5
|
UTSW |
1 |
164,026,402 (GRCm39) |
missense |
probably benign |
0.02 |
R1545:F5
|
UTSW |
1 |
164,036,529 (GRCm39) |
nonsense |
probably null |
|
R1561:F5
|
UTSW |
1 |
164,014,472 (GRCm39) |
nonsense |
probably null |
|
R1623:F5
|
UTSW |
1 |
164,023,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:F5
|
UTSW |
1 |
164,035,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1689:F5
|
UTSW |
1 |
164,026,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1705:F5
|
UTSW |
1 |
164,045,059 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1732:F5
|
UTSW |
1 |
164,001,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:F5
|
UTSW |
1 |
164,020,104 (GRCm39) |
missense |
probably benign |
0.04 |
R1774:F5
|
UTSW |
1 |
164,020,104 (GRCm39) |
missense |
probably benign |
0.04 |
R1799:F5
|
UTSW |
1 |
164,021,100 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1800:F5
|
UTSW |
1 |
164,010,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R1842:F5
|
UTSW |
1 |
164,012,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R1915:F5
|
UTSW |
1 |
164,010,486 (GRCm39) |
missense |
probably damaging |
0.97 |
R1926:F5
|
UTSW |
1 |
164,007,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2025:F5
|
UTSW |
1 |
164,037,044 (GRCm39) |
missense |
probably benign |
0.05 |
R2198:F5
|
UTSW |
1 |
164,034,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:F5
|
UTSW |
1 |
164,019,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R2264:F5
|
UTSW |
1 |
164,021,971 (GRCm39) |
missense |
probably benign |
0.32 |
R2281:F5
|
UTSW |
1 |
164,023,289 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2407:F5
|
UTSW |
1 |
164,039,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R2445:F5
|
UTSW |
1 |
164,017,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R2860:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2861:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2862:F5
|
UTSW |
1 |
164,012,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R2899:F5
|
UTSW |
1 |
164,014,469 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2910:F5
|
UTSW |
1 |
164,032,389 (GRCm39) |
missense |
probably benign |
0.43 |
R2912:F5
|
UTSW |
1 |
164,021,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R2996:F5
|
UTSW |
1 |
164,010,486 (GRCm39) |
missense |
probably damaging |
0.97 |
R3745:F5
|
UTSW |
1 |
164,014,348 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3901:F5
|
UTSW |
1 |
164,003,798 (GRCm39) |
missense |
probably benign |
0.08 |
R3902:F5
|
UTSW |
1 |
164,003,798 (GRCm39) |
missense |
probably benign |
0.08 |
R4365:F5
|
UTSW |
1 |
164,012,519 (GRCm39) |
missense |
probably damaging |
0.98 |
R4448:F5
|
UTSW |
1 |
164,026,468 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4490:F5
|
UTSW |
1 |
164,044,964 (GRCm39) |
missense |
probably benign |
0.40 |
R4514:F5
|
UTSW |
1 |
163,979,566 (GRCm39) |
unclassified |
probably benign |
|
R4598:F5
|
UTSW |
1 |
164,032,366 (GRCm39) |
missense |
probably benign |
0.05 |
R4608:F5
|
UTSW |
1 |
164,036,598 (GRCm39) |
missense |
probably benign |
0.12 |
R4661:F5
|
UTSW |
1 |
164,012,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:F5
|
UTSW |
1 |
164,001,755 (GRCm39) |
missense |
probably benign |
0.00 |
R4689:F5
|
UTSW |
1 |
163,979,542 (GRCm39) |
unclassified |
probably benign |
|
R4716:F5
|
UTSW |
1 |
164,021,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R4732:F5
|
UTSW |
1 |
164,009,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:F5
|
UTSW |
1 |
164,009,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R4854:F5
|
UTSW |
1 |
164,019,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:F5
|
UTSW |
1 |
164,039,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:F5
|
UTSW |
1 |
164,021,755 (GRCm39) |
missense |
probably benign |
|
R5001:F5
|
UTSW |
1 |
164,023,139 (GRCm39) |
missense |
probably benign |
0.00 |
R5042:F5
|
UTSW |
1 |
164,047,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:F5
|
UTSW |
1 |
164,019,601 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5061:F5
|
UTSW |
1 |
164,021,749 (GRCm39) |
missense |
probably benign |
0.00 |
R5143:F5
|
UTSW |
1 |
164,039,397 (GRCm39) |
missense |
probably damaging |
0.98 |
R5622:F5
|
UTSW |
1 |
164,020,134 (GRCm39) |
missense |
probably benign |
0.09 |
R5626:F5
|
UTSW |
1 |
164,036,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R5658:F5
|
UTSW |
1 |
164,019,907 (GRCm39) |
missense |
probably damaging |
0.96 |
R5702:F5
|
UTSW |
1 |
164,022,116 (GRCm39) |
nonsense |
probably null |
|
R5795:F5
|
UTSW |
1 |
163,979,578 (GRCm39) |
missense |
probably benign |
0.09 |
R5884:F5
|
UTSW |
1 |
164,023,215 (GRCm39) |
missense |
probably benign |
0.01 |
R6036:F5
|
UTSW |
1 |
164,012,565 (GRCm39) |
missense |
probably damaging |
0.99 |
R6036:F5
|
UTSW |
1 |
164,012,565 (GRCm39) |
missense |
probably damaging |
0.99 |
R6151:F5
|
UTSW |
1 |
164,017,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:F5
|
UTSW |
1 |
164,009,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R6345:F5
|
UTSW |
1 |
164,019,520 (GRCm39) |
missense |
probably benign |
0.13 |
R6391:F5
|
UTSW |
1 |
164,021,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R6542:F5
|
UTSW |
1 |
164,022,037 (GRCm39) |
missense |
probably benign |
0.32 |
R6620:F5
|
UTSW |
1 |
164,014,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:F5
|
UTSW |
1 |
164,021,076 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6754:F5
|
UTSW |
1 |
164,021,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:F5
|
UTSW |
1 |
164,014,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R6802:F5
|
UTSW |
1 |
164,006,925 (GRCm39) |
missense |
probably damaging |
0.98 |
R6810:F5
|
UTSW |
1 |
164,014,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R6983:F5
|
UTSW |
1 |
164,021,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R7000:F5
|
UTSW |
1 |
164,007,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R7151:F5
|
UTSW |
1 |
164,029,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:F5
|
UTSW |
1 |
164,046,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R7230:F5
|
UTSW |
1 |
164,012,522 (GRCm39) |
missense |
probably benign |
|
R7324:F5
|
UTSW |
1 |
164,021,150 (GRCm39) |
small deletion |
probably benign |
|
R7350:F5
|
UTSW |
1 |
164,020,277 (GRCm39) |
missense |
probably benign |
0.08 |
R7466:F5
|
UTSW |
1 |
164,020,897 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7503:F5
|
UTSW |
1 |
164,019,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R7626:F5
|
UTSW |
1 |
164,014,481 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7742:F5
|
UTSW |
1 |
164,035,453 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7837:F5
|
UTSW |
1 |
164,014,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R7848:F5
|
UTSW |
1 |
163,989,446 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7925:F5
|
UTSW |
1 |
164,003,935 (GRCm39) |
critical splice donor site |
probably null |
|
R8053:F5
|
UTSW |
1 |
164,020,338 (GRCm39) |
missense |
probably benign |
0.26 |
R8094:F5
|
UTSW |
1 |
164,036,509 (GRCm39) |
missense |
probably benign |
0.06 |
R8175:F5
|
UTSW |
1 |
164,019,834 (GRCm39) |
nonsense |
probably null |
|
R8209:F5
|
UTSW |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
R8226:F5
|
UTSW |
1 |
164,021,959 (GRCm39) |
missense |
probably benign |
0.00 |
R8266:F5
|
UTSW |
1 |
164,012,693 (GRCm39) |
critical splice donor site |
probably null |
|
R8517:F5
|
UTSW |
1 |
164,003,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R8684:F5
|
UTSW |
1 |
164,045,111 (GRCm39) |
missense |
probably benign |
0.01 |
R8941:F5
|
UTSW |
1 |
164,026,440 (GRCm39) |
missense |
probably benign |
0.19 |
R9130:F5
|
UTSW |
1 |
164,001,830 (GRCm39) |
missense |
probably benign |
0.37 |
R9181:F5
|
UTSW |
1 |
164,019,895 (GRCm39) |
missense |
probably benign |
0.00 |
R9186:F5
|
UTSW |
1 |
164,021,470 (GRCm39) |
missense |
probably benign |
|
R9233:F5
|
UTSW |
1 |
164,047,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R9314:F5
|
UTSW |
1 |
164,029,146 (GRCm39) |
missense |
probably benign |
0.01 |
R9631:F5
|
UTSW |
1 |
164,014,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:F5
|
UTSW |
1 |
164,021,730 (GRCm39) |
missense |
probably benign |
0.15 |
X0024:F5
|
UTSW |
1 |
164,020,557 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:F5
|
UTSW |
1 |
163,981,954 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:F5
|
UTSW |
1 |
164,012,085 (GRCm39) |
missense |
probably damaging |
0.97 |
|