Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acbd5 |
A |
T |
2: 22,984,356 (GRCm39) |
D294V |
probably damaging |
Het |
Actn2 |
A |
T |
13: 12,355,320 (GRCm39) |
I21N |
probably benign |
Het |
Adamts2 |
C |
A |
11: 50,558,942 (GRCm39) |
P219H |
possibly damaging |
Het |
Atg16l2 |
A |
G |
7: 100,939,113 (GRCm39) |
F584L |
probably benign |
Het |
Ccdc81 |
C |
T |
7: 89,535,390 (GRCm39) |
R282Q |
probably benign |
Het |
Ccn4 |
G |
T |
15: 66,763,448 (GRCm39) |
V12L |
possibly damaging |
Het |
Cd200r3 |
G |
A |
16: 44,771,811 (GRCm39) |
C25Y |
possibly damaging |
Het |
Cdkl4 |
C |
T |
17: 80,863,731 (GRCm39) |
|
probably null |
Het |
Chrne |
T |
C |
11: 70,509,254 (GRCm39) |
E109G |
possibly damaging |
Het |
Clmp |
A |
G |
9: 40,693,856 (GRCm39) |
T358A |
probably benign |
Het |
Cmtr1 |
G |
T |
17: 29,906,021 (GRCm39) |
|
probably null |
Het |
Col25a1 |
A |
G |
3: 130,343,699 (GRCm39) |
E389G |
probably damaging |
Het |
Ctc1 |
C |
T |
11: 68,911,968 (GRCm39) |
T49M |
probably damaging |
Het |
Cyth3 |
T |
A |
5: 143,687,127 (GRCm39) |
M120K |
probably damaging |
Het |
D430041D05Rik |
T |
A |
2: 103,983,308 (GRCm39) |
E1996V |
probably damaging |
Het |
Dnah9 |
T |
C |
11: 65,928,463 (GRCm39) |
M2069V |
probably damaging |
Het |
Dsg1c |
T |
C |
18: 20,408,234 (GRCm39) |
Y428H |
probably damaging |
Het |
Exosc8 |
T |
A |
3: 54,641,752 (GRCm39) |
T7S |
probably damaging |
Het |
Fam178b |
A |
G |
1: 36,683,405 (GRCm39) |
I105T |
probably damaging |
Het |
Fam181a |
T |
A |
12: 103,282,591 (GRCm39) |
Y165* |
probably null |
Het |
Fbn2 |
G |
T |
18: 58,181,620 (GRCm39) |
N1880K |
possibly damaging |
Het |
Gbgt1 |
A |
T |
2: 28,394,988 (GRCm39) |
M209L |
probably benign |
Het |
Gkn2 |
C |
A |
6: 87,355,152 (GRCm39) |
Y120* |
probably null |
Het |
Gm14295 |
T |
A |
2: 176,499,157 (GRCm39) |
D1E |
probably damaging |
Het |
Gpr141 |
A |
T |
13: 19,936,082 (GRCm39) |
|
probably null |
Het |
Gramd2b |
C |
A |
18: 56,565,423 (GRCm39) |
P26Q |
probably benign |
Het |
Greb1 |
A |
G |
12: 16,724,771 (GRCm39) |
I1801T |
probably damaging |
Het |
Gstm3 |
T |
A |
3: 107,875,151 (GRCm39) |
I64F |
possibly damaging |
Het |
Gtse1 |
A |
G |
15: 85,751,779 (GRCm39) |
Y324C |
probably benign |
Het |
Hal |
C |
G |
10: 93,352,159 (GRCm39) |
T650R |
probably benign |
Het |
Hdac7 |
G |
A |
15: 97,706,285 (GRCm39) |
Q293* |
probably null |
Het |
Hdlbp |
A |
T |
1: 93,351,591 (GRCm39) |
N437K |
probably damaging |
Het |
Hif1an |
A |
G |
19: 44,557,862 (GRCm39) |
D248G |
probably damaging |
Het |
Hivep3 |
T |
C |
4: 119,952,901 (GRCm39) |
S406P |
possibly damaging |
Het |
Hmcn2 |
A |
T |
2: 31,348,051 (GRCm39) |
D4899V |
possibly damaging |
Het |
Ikzf3 |
C |
T |
11: 98,381,157 (GRCm39) |
|
probably null |
Het |
Inka2 |
G |
A |
3: 105,624,136 (GRCm39) |
G151D |
probably damaging |
Het |
Itgb4 |
C |
A |
11: 115,882,142 (GRCm39) |
Y819* |
probably null |
Het |
Itpripl1 |
T |
C |
2: 126,983,555 (GRCm39) |
D189G |
possibly damaging |
Het |
Kmt2e |
A |
G |
5: 23,687,500 (GRCm39) |
Y450C |
probably damaging |
Het |
Mc4r |
A |
G |
18: 66,993,068 (GRCm39) |
L15P |
probably benign |
Het |
Mical1 |
T |
G |
10: 41,357,389 (GRCm39) |
|
probably null |
Het |
Mical3 |
C |
T |
6: 121,001,768 (GRCm39) |
V575M |
probably damaging |
Het |
Mki67 |
A |
T |
7: 135,310,547 (GRCm39) |
|
probably null |
Het |
Mocs2 |
G |
A |
13: 114,961,158 (GRCm39) |
E52K |
probably benign |
Het |
Myo7b |
T |
C |
18: 32,133,104 (GRCm39) |
N415S |
probably damaging |
Het |
Notch1 |
G |
A |
2: 26,368,624 (GRCm39) |
T555I |
possibly damaging |
Het |
Notch3 |
T |
C |
17: 32,358,165 (GRCm39) |
D1686G |
probably benign |
Het |
Oit3 |
A |
G |
10: 59,264,061 (GRCm39) |
F358L |
probably damaging |
Het |
Or10x1 |
A |
C |
1: 174,196,515 (GRCm39) |
I11L |
probably benign |
Het |
Or6k4 |
A |
T |
1: 173,964,883 (GRCm39) |
D191V |
probably damaging |
Het |
Orai1 |
T |
A |
5: 123,167,265 (GRCm39) |
I146N |
probably damaging |
Het |
Pck1 |
A |
G |
2: 172,996,511 (GRCm39) |
I142V |
probably benign |
Het |
Pdap1 |
C |
T |
5: 145,069,739 (GRCm39) |
V89M |
possibly damaging |
Het |
Phf11a |
T |
C |
14: 59,525,000 (GRCm39) |
D68G |
possibly damaging |
Het |
Pilrb2 |
T |
C |
5: 137,869,510 (GRCm39) |
N30S |
probably damaging |
Het |
Pkd1 |
G |
A |
17: 24,797,243 (GRCm39) |
V2551I |
probably damaging |
Het |
Pnpla7 |
T |
C |
2: 24,942,611 (GRCm39) |
V132A |
probably damaging |
Het |
Prr35 |
G |
A |
17: 26,166,508 (GRCm39) |
P343L |
probably benign |
Het |
Rad18 |
C |
T |
6: 112,605,480 (GRCm39) |
S398N |
probably damaging |
Het |
Rdh16f1 |
C |
A |
10: 127,626,722 (GRCm39) |
N258K |
probably benign |
Het |
Riox2 |
A |
G |
16: 59,303,405 (GRCm39) |
H240R |
probably damaging |
Het |
Ruvbl1 |
C |
T |
6: 88,462,752 (GRCm39) |
A292V |
probably damaging |
Het |
Ryr1 |
C |
T |
7: 28,794,915 (GRCm39) |
G1151S |
probably damaging |
Het |
Serpinb9b |
T |
C |
13: 33,213,548 (GRCm39) |
I35T |
possibly damaging |
Het |
Slc1a1 |
T |
A |
19: 28,882,122 (GRCm39) |
M328K |
probably benign |
Het |
Slc7a13 |
A |
T |
4: 19,824,031 (GRCm39) |
T267S |
possibly damaging |
Het |
Speer3 |
G |
T |
5: 13,846,335 (GRCm39) |
M218I |
probably benign |
Het |
Sptan1 |
A |
G |
2: 29,876,432 (GRCm39) |
I271V |
probably damaging |
Het |
Swap70 |
A |
G |
7: 109,863,255 (GRCm39) |
T195A |
probably benign |
Het |
Tgs1 |
T |
A |
4: 3,585,964 (GRCm39) |
N280K |
probably benign |
Het |
Tonsl |
A |
G |
15: 76,522,709 (GRCm39) |
C181R |
probably damaging |
Het |
Trdn |
A |
G |
10: 33,134,098 (GRCm39) |
K333R |
possibly damaging |
Het |
Trpc4 |
T |
A |
3: 54,206,600 (GRCm39) |
M600K |
probably damaging |
Het |
Ubr3 |
C |
T |
2: 69,808,067 (GRCm39) |
Q1183* |
probably null |
Het |
Ubxn4 |
T |
A |
1: 128,200,588 (GRCm39) |
L360I |
possibly damaging |
Het |
Ugt2b1 |
T |
A |
5: 87,074,267 (GRCm39) |
T31S |
probably benign |
Het |
Uspl1 |
T |
C |
5: 149,152,009 (GRCm39) |
S1056P |
probably damaging |
Het |
Vmn2r60 |
A |
T |
7: 41,785,279 (GRCm39) |
K164* |
probably null |
Het |
Vwce |
T |
A |
19: 10,624,108 (GRCm39) |
L333* |
probably null |
Het |
Wdr95 |
T |
A |
5: 149,497,581 (GRCm39) |
L253Q |
probably damaging |
Het |
Zfp113 |
T |
C |
5: 138,143,930 (GRCm39) |
M107V |
probably benign |
Het |
Zfp142 |
T |
C |
1: 74,610,934 (GRCm39) |
T851A |
possibly 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 |
|
R1662:F5
|
UTSW |
1 |
164,035,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:F5
|
UTSW |
1 |
164,007,089 (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 |
|