Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
A |
G |
1: 183,765,369 (GRCm39) |
V230A |
possibly damaging |
Het |
2010315B03Rik |
T |
C |
9: 124,056,631 (GRCm39) |
T123A |
possibly damaging |
Het |
Abca4 |
T |
C |
3: 121,899,019 (GRCm39) |
V667A |
probably damaging |
Het |
Abcb5 |
A |
G |
12: 118,929,040 (GRCm39) |
S4P |
possibly damaging |
Het |
Adam25 |
G |
T |
8: 41,207,163 (GRCm39) |
C143F |
probably damaging |
Het |
Ahnak |
C |
A |
19: 8,994,270 (GRCm39) |
H5185N |
probably benign |
Het |
Apobec4 |
A |
G |
1: 152,632,001 (GRCm39) |
T10A |
probably benign |
Het |
Ascc1 |
A |
G |
10: 59,885,624 (GRCm39) |
Y225C |
probably damaging |
Het |
Aspscr1 |
A |
T |
11: 120,579,771 (GRCm39) |
K39N |
possibly damaging |
Het |
Atf7ip |
C |
T |
6: 136,538,192 (GRCm39) |
P483L |
probably damaging |
Het |
Atp11a |
C |
G |
8: 12,863,118 (GRCm39) |
P99R |
probably damaging |
Het |
B4galnt1 |
G |
T |
10: 127,003,394 (GRCm39) |
V172F |
possibly damaging |
Het |
Bag6 |
C |
A |
17: 35,361,319 (GRCm39) |
P476H |
probably damaging |
Het |
Bltp1 |
C |
T |
3: 37,096,038 (GRCm39) |
T1108I |
probably benign |
Het |
C2cd3 |
A |
G |
7: 100,044,395 (GRCm39) |
K326E |
possibly damaging |
Het |
Casp1 |
A |
G |
9: 5,306,204 (GRCm39) |
D363G |
probably damaging |
Het |
Ccdc33 |
G |
T |
9: 58,024,840 (GRCm39) |
Q129K |
probably benign |
Het |
Ccdc88a |
T |
C |
11: 29,372,586 (GRCm39) |
I107T |
probably benign |
Het |
Cela2a |
T |
C |
4: 141,548,722 (GRCm39) |
N138S |
probably benign |
Het |
Cfap61 |
A |
C |
2: 145,877,122 (GRCm39) |
R460S |
probably damaging |
Het |
Clstn2 |
T |
C |
9: 97,345,612 (GRCm39) |
N579D |
possibly damaging |
Het |
Col13a1 |
C |
A |
10: 61,685,944 (GRCm39) |
G683W |
unknown |
Het |
Col4a2 |
G |
A |
8: 11,363,504 (GRCm39) |
R14Q |
possibly damaging |
Het |
Cpa6 |
A |
G |
1: 10,551,283 (GRCm39) |
S164P |
probably benign |
Het |
Cpq |
A |
G |
15: 33,497,484 (GRCm39) |
N408S |
probably benign |
Het |
Ctnnal1 |
T |
C |
4: 56,812,579 (GRCm39) |
T690A |
probably benign |
Het |
Cx3cl1 |
A |
T |
8: 95,506,835 (GRCm39) |
N280I |
probably benign |
Het |
Cyp2b19 |
C |
T |
7: 26,456,717 (GRCm39) |
R36C |
probably benign |
Het |
Ddx51 |
T |
C |
5: 110,803,174 (GRCm39) |
V269A |
probably damaging |
Het |
Dipk2a |
T |
C |
9: 94,402,688 (GRCm39) |
N325D |
possibly damaging |
Het |
Dlst |
G |
T |
12: 85,165,616 (GRCm39) |
|
probably null |
Het |
Dmkn |
G |
C |
7: 30,463,406 (GRCm39) |
A20P |
probably damaging |
Het |
Dnhd1 |
T |
C |
7: 105,304,948 (GRCm39) |
I330T |
probably damaging |
Het |
Dock3 |
G |
A |
9: 106,902,535 (GRCm39) |
H292Y |
probably damaging |
Het |
Ell |
A |
G |
8: 71,031,584 (GRCm39) |
D94G |
possibly damaging |
Het |
Enam |
T |
A |
5: 88,651,650 (GRCm39) |
L1053* |
probably null |
Het |
Fam3d |
T |
C |
14: 8,349,347 (GRCm38) |
E201G |
probably benign |
Het |
Frmd5 |
G |
T |
2: 121,393,344 (GRCm39) |
|
probably benign |
Het |
Gas2l1 |
G |
A |
11: 5,010,867 (GRCm39) |
S654L |
possibly damaging |
Het |
Gltpd2 |
G |
T |
11: 70,410,966 (GRCm39) |
E86* |
probably null |
Het |
Glyat |
T |
C |
19: 12,628,661 (GRCm39) |
L152P |
possibly damaging |
Het |
Gm17330 |
T |
C |
12: 24,018,783 (GRCm39) |
T22A |
probably damaging |
Het |
Gm9931 |
T |
A |
1: 147,157,591 (GRCm39) |
|
noncoding transcript |
Het |
Gpatch1 |
A |
T |
7: 34,998,730 (GRCm39) |
|
probably null |
Het |
Gpr4 |
T |
C |
7: 18,956,819 (GRCm39) |
L247P |
probably damaging |
Het |
Gtpbp3 |
G |
A |
8: 71,943,758 (GRCm39) |
E214K |
probably benign |
Het |
Hdac7 |
G |
T |
15: 97,709,468 (GRCm39) |
Q21K |
probably damaging |
Het |
Hivep3 |
A |
G |
4: 119,729,247 (GRCm39) |
|
probably benign |
Het |
Hk2 |
C |
T |
6: 82,716,631 (GRCm39) |
M300I |
possibly damaging |
Het |
Ighv1-61 |
T |
C |
12: 115,322,899 (GRCm39) |
Y71C |
probably damaging |
Het |
Il36b |
T |
C |
2: 24,044,630 (GRCm39) |
V10A |
probably benign |
Het |
Inpp5f |
G |
T |
7: 128,265,711 (GRCm39) |
S152I |
probably damaging |
Het |
Jag1 |
C |
A |
2: 136,938,229 (GRCm39) |
W257L |
probably damaging |
Het |
Jak2 |
T |
A |
19: 29,272,315 (GRCm39) |
N612K |
possibly damaging |
Het |
Kalrn |
T |
C |
16: 34,024,327 (GRCm39) |
D610G |
probably damaging |
Het |
Kbtbd6 |
A |
G |
14: 79,690,046 (GRCm39) |
D247G |
probably benign |
Het |
Kif15 |
A |
G |
9: 122,789,058 (GRCm39) |
|
probably null |
Het |
Kndc1 |
A |
G |
7: 139,510,036 (GRCm39) |
T1293A |
possibly damaging |
Het |
Lpar5 |
T |
C |
6: 125,059,170 (GRCm39) |
I297T |
possibly damaging |
Het |
Lpin2 |
T |
A |
17: 71,539,138 (GRCm39) |
|
probably benign |
Het |
Lypd10 |
T |
A |
7: 24,412,934 (GRCm39) |
L114Q |
probably damaging |
Het |
Mfsd4a |
A |
T |
1: 131,981,309 (GRCm39) |
L230Q |
probably damaging |
Het |
Mmp8 |
T |
C |
9: 7,565,550 (GRCm39) |
V313A |
probably benign |
Het |
Mrpl19 |
A |
T |
6: 81,941,266 (GRCm39) |
D98E |
probably damaging |
Het |
Mybl1 |
A |
G |
1: 9,760,340 (GRCm39) |
I86T |
probably damaging |
Het |
Nadk |
C |
A |
4: 155,669,684 (GRCm39) |
P157T |
probably benign |
Het |
Necab1 |
T |
C |
4: 15,052,628 (GRCm39) |
T117A |
probably damaging |
Het |
Nol11 |
A |
G |
11: 107,075,544 (GRCm39) |
|
probably benign |
Het |
Nucb2 |
G |
A |
7: 116,139,262 (GRCm39) |
|
probably null |
Het |
Nup58 |
G |
T |
14: 60,488,664 (GRCm39) |
P19T |
unknown |
Het |
Odf2 |
T |
A |
2: 29,794,046 (GRCm39) |
L301Q |
probably damaging |
Het |
Oog4 |
T |
C |
4: 143,165,445 (GRCm39) |
Y234C |
probably benign |
Het |
Or11j4 |
A |
G |
14: 50,630,257 (GRCm39) |
I15V |
probably benign |
Het |
Or1ab2 |
T |
A |
8: 72,864,044 (GRCm39) |
F211L |
probably damaging |
Het |
Papln |
T |
C |
12: 83,823,982 (GRCm39) |
|
probably null |
Het |
Paqr6 |
C |
T |
3: 88,273,236 (GRCm39) |
A76V |
probably benign |
Het |
Pclo |
A |
G |
5: 14,726,494 (GRCm39) |
|
probably benign |
Het |
Pdzd8 |
T |
C |
19: 59,333,743 (GRCm39) |
T93A |
possibly damaging |
Het |
Pkdrej |
A |
T |
15: 85,705,368 (GRCm39) |
Y189* |
probably null |
Het |
Pknox2 |
A |
T |
9: 36,834,934 (GRCm39) |
N178K |
possibly damaging |
Het |
Pla2g15 |
T |
A |
8: 106,889,691 (GRCm39) |
M321K |
probably benign |
Het |
Plxnd1 |
A |
C |
6: 115,935,581 (GRCm39) |
L1735R |
probably damaging |
Het |
Polm |
T |
A |
11: 5,787,663 (GRCm39) |
D30V |
possibly damaging |
Het |
Rap1gap2 |
T |
A |
11: 74,328,265 (GRCm39) |
I100F |
probably damaging |
Het |
Rasgef1c |
T |
A |
11: 49,869,294 (GRCm39) |
W414R |
probably benign |
Het |
Rassf1 |
A |
G |
9: 107,435,066 (GRCm39) |
D187G |
probably benign |
Het |
Rhag |
T |
C |
17: 41,147,329 (GRCm39) |
I397T |
probably benign |
Het |
Rnft2 |
A |
G |
5: 118,366,928 (GRCm39) |
F269S |
probably damaging |
Het |
Rnmt |
T |
C |
18: 68,447,196 (GRCm39) |
F360S |
probably damaging |
Het |
Ror2 |
C |
T |
13: 53,271,333 (GRCm39) |
A329T |
probably benign |
Het |
Slc4a1 |
T |
A |
11: 102,247,084 (GRCm39) |
N501I |
possibly damaging |
Het |
Slc4a7 |
T |
A |
14: 14,733,856 (GRCm38) |
S89T |
probably damaging |
Het |
Sptbn1 |
G |
A |
11: 30,050,660 (GRCm39) |
H2310Y |
probably benign |
Het |
Tbc1d9b |
C |
A |
11: 50,031,289 (GRCm39) |
N103K |
probably benign |
Het |
Tbxas1 |
T |
C |
6: 39,060,791 (GRCm39) |
|
probably null |
Het |
Tmem100 |
C |
T |
11: 89,926,389 (GRCm39) |
T72I |
probably damaging |
Het |
Ttc38 |
A |
G |
15: 85,737,164 (GRCm39) |
T350A |
probably benign |
Het |
Ubr4 |
C |
T |
4: 139,177,840 (GRCm39) |
T3241M |
probably damaging |
Het |
Unc13d |
A |
T |
11: 115,964,214 (GRCm39) |
M350K |
possibly damaging |
Het |
Vit |
T |
C |
17: 78,932,543 (GRCm39) |
I550T |
probably damaging |
Het |
Vmn1r31 |
C |
A |
6: 58,448,953 (GRCm39) |
*304L |
probably null |
Het |
Zbtb12 |
T |
A |
17: 35,115,377 (GRCm39) |
H387Q |
possibly damaging |
Het |
|
Other mutations in Fcgbp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00309:Fcgbp
|
APN |
7 |
27,784,555 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00331:Fcgbp
|
APN |
7 |
27,800,966 (GRCm39) |
splice site |
probably benign |
|
IGL00335:Fcgbp
|
APN |
7 |
27,785,560 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL00470:Fcgbp
|
APN |
7 |
27,774,511 (GRCm39) |
nonsense |
probably null |
|
IGL00491:Fcgbp
|
APN |
7 |
27,792,827 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00498:Fcgbp
|
APN |
7 |
27,791,222 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01296:Fcgbp
|
APN |
7 |
27,789,072 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01582:Fcgbp
|
APN |
7 |
27,793,067 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01929:Fcgbp
|
APN |
7 |
27,803,388 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02024:Fcgbp
|
APN |
7 |
27,805,799 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02027:Fcgbp
|
APN |
7 |
27,774,629 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02140:Fcgbp
|
APN |
7 |
27,791,379 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02162:Fcgbp
|
APN |
7 |
27,774,660 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02345:Fcgbp
|
APN |
7 |
27,771,068 (GRCm39) |
splice site |
probably benign |
|
IGL02377:Fcgbp
|
APN |
7 |
27,806,395 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02389:Fcgbp
|
APN |
7 |
27,774,596 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02423:Fcgbp
|
APN |
7 |
27,789,378 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02523:Fcgbp
|
APN |
7 |
27,804,157 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02561:Fcgbp
|
APN |
7 |
27,800,599 (GRCm39) |
intron |
probably benign |
|
IGL02631:Fcgbp
|
APN |
7 |
27,784,723 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02716:Fcgbp
|
APN |
7 |
27,800,859 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02836:Fcgbp
|
APN |
7 |
27,816,783 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02957:Fcgbp
|
APN |
7 |
27,791,272 (GRCm39) |
nonsense |
probably null |
|
IGL02971:Fcgbp
|
APN |
7 |
27,800,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03284:Fcgbp
|
APN |
7 |
27,784,857 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03379:Fcgbp
|
APN |
7 |
27,789,342 (GRCm39) |
missense |
possibly damaging |
0.76 |
bilge
|
UTSW |
7 |
27,816,762 (GRCm39) |
missense |
probably benign |
0.00 |
R6548_fcgbp_365
|
UTSW |
7 |
27,791,343 (GRCm39) |
missense |
probably benign |
0.00 |
swill
|
UTSW |
7 |
27,789,159 (GRCm39) |
missense |
probably damaging |
1.00 |
G1citation:Fcgbp
|
UTSW |
7 |
27,806,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02796:Fcgbp
|
UTSW |
7 |
27,800,576 (GRCm39) |
intron |
probably benign |
|
PIT4486001:Fcgbp
|
UTSW |
7 |
27,774,698 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0277:Fcgbp
|
UTSW |
7 |
27,784,918 (GRCm39) |
critical splice donor site |
probably null |
|
R0387:Fcgbp
|
UTSW |
7 |
27,790,879 (GRCm39) |
splice site |
probably benign |
|
R0586:Fcgbp
|
UTSW |
7 |
27,789,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R0981:Fcgbp
|
UTSW |
7 |
27,784,535 (GRCm39) |
nonsense |
probably null |
|
R0987:Fcgbp
|
UTSW |
7 |
27,793,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R1240:Fcgbp
|
UTSW |
7 |
27,819,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R1394:Fcgbp
|
UTSW |
7 |
27,792,804 (GRCm39) |
missense |
probably damaging |
0.98 |
R1395:Fcgbp
|
UTSW |
7 |
27,792,804 (GRCm39) |
missense |
probably damaging |
0.98 |
R1438:Fcgbp
|
UTSW |
7 |
27,803,158 (GRCm39) |
nonsense |
probably null |
|
R1474:Fcgbp
|
UTSW |
7 |
27,791,273 (GRCm39) |
missense |
probably benign |
0.00 |
R1521:Fcgbp
|
UTSW |
7 |
27,774,585 (GRCm39) |
missense |
probably benign |
0.00 |
R1740:Fcgbp
|
UTSW |
7 |
27,800,674 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1750:Fcgbp
|
UTSW |
7 |
27,792,868 (GRCm39) |
nonsense |
probably null |
|
R1772:Fcgbp
|
UTSW |
7 |
27,804,600 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1804:Fcgbp
|
UTSW |
7 |
27,785,564 (GRCm39) |
missense |
probably benign |
|
R1808:Fcgbp
|
UTSW |
7 |
27,784,515 (GRCm39) |
missense |
probably benign |
0.04 |
R1819:Fcgbp
|
UTSW |
7 |
27,784,708 (GRCm39) |
missense |
probably benign |
0.00 |
R1934:Fcgbp
|
UTSW |
7 |
27,806,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Fcgbp
|
UTSW |
7 |
27,793,617 (GRCm39) |
missense |
probably benign |
0.11 |
R2051:Fcgbp
|
UTSW |
7 |
27,819,785 (GRCm39) |
missense |
probably damaging |
0.97 |
R2072:Fcgbp
|
UTSW |
7 |
27,819,814 (GRCm39) |
missense |
probably damaging |
0.98 |
R2074:Fcgbp
|
UTSW |
7 |
27,819,814 (GRCm39) |
missense |
probably damaging |
0.98 |
R2124:Fcgbp
|
UTSW |
7 |
27,791,444 (GRCm39) |
missense |
probably benign |
0.03 |
R2155:Fcgbp
|
UTSW |
7 |
27,806,628 (GRCm39) |
missense |
probably benign |
0.00 |
R3015:Fcgbp
|
UTSW |
7 |
27,774,838 (GRCm39) |
splice site |
probably benign |
|
R3037:Fcgbp
|
UTSW |
7 |
27,802,127 (GRCm39) |
missense |
possibly damaging |
0.62 |
R3151:Fcgbp
|
UTSW |
7 |
27,816,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R3176:Fcgbp
|
UTSW |
7 |
27,791,086 (GRCm39) |
missense |
probably damaging |
0.99 |
R3177:Fcgbp
|
UTSW |
7 |
27,791,086 (GRCm39) |
missense |
probably damaging |
0.99 |
R3276:Fcgbp
|
UTSW |
7 |
27,791,086 (GRCm39) |
missense |
probably damaging |
0.99 |
R3277:Fcgbp
|
UTSW |
7 |
27,791,086 (GRCm39) |
missense |
probably damaging |
0.99 |
R3623:Fcgbp
|
UTSW |
7 |
27,800,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R3730:Fcgbp
|
UTSW |
7 |
27,784,882 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3935:Fcgbp
|
UTSW |
7 |
27,774,824 (GRCm39) |
missense |
probably benign |
0.00 |
R3936:Fcgbp
|
UTSW |
7 |
27,774,824 (GRCm39) |
missense |
probably benign |
0.00 |
R4041:Fcgbp
|
UTSW |
7 |
27,813,404 (GRCm39) |
missense |
probably benign |
0.01 |
R4056:Fcgbp
|
UTSW |
7 |
27,803,541 (GRCm39) |
missense |
probably benign |
0.09 |
R4057:Fcgbp
|
UTSW |
7 |
27,803,541 (GRCm39) |
missense |
probably benign |
0.09 |
R4708:Fcgbp
|
UTSW |
7 |
27,794,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4710:Fcgbp
|
UTSW |
7 |
27,794,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4779:Fcgbp
|
UTSW |
7 |
27,794,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Fcgbp
|
UTSW |
7 |
27,813,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R4863:Fcgbp
|
UTSW |
7 |
27,785,769 (GRCm39) |
missense |
probably benign |
0.33 |
R4926:Fcgbp
|
UTSW |
7 |
27,785,660 (GRCm39) |
missense |
probably damaging |
0.99 |
R4947:Fcgbp
|
UTSW |
7 |
27,789,237 (GRCm39) |
missense |
probably benign |
0.00 |
R4979:Fcgbp
|
UTSW |
7 |
27,816,995 (GRCm39) |
missense |
probably benign |
0.06 |
R5002:Fcgbp
|
UTSW |
7 |
27,785,528 (GRCm39) |
splice site |
probably null |
|
R5219:Fcgbp
|
UTSW |
7 |
27,803,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R5241:Fcgbp
|
UTSW |
7 |
27,784,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R5301:Fcgbp
|
UTSW |
7 |
27,793,099 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5306:Fcgbp
|
UTSW |
7 |
27,791,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R5335:Fcgbp
|
UTSW |
7 |
27,789,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Fcgbp
|
UTSW |
7 |
27,804,480 (GRCm39) |
missense |
probably benign |
0.05 |
R5418:Fcgbp
|
UTSW |
7 |
27,784,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R5527:Fcgbp
|
UTSW |
7 |
27,793,060 (GRCm39) |
missense |
probably benign |
|
R5583:Fcgbp
|
UTSW |
7 |
27,791,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R5698:Fcgbp
|
UTSW |
7 |
27,791,447 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5780:Fcgbp
|
UTSW |
7 |
27,784,643 (GRCm39) |
missense |
probably benign |
0.02 |
R5813:Fcgbp
|
UTSW |
7 |
27,800,919 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5910:Fcgbp
|
UTSW |
7 |
27,784,928 (GRCm39) |
splice site |
probably benign |
|
R5936:Fcgbp
|
UTSW |
7 |
27,786,117 (GRCm39) |
missense |
probably damaging |
0.98 |
R5992:Fcgbp
|
UTSW |
7 |
27,819,959 (GRCm39) |
missense |
probably benign |
0.05 |
R6091:Fcgbp
|
UTSW |
7 |
27,804,390 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6372:Fcgbp
|
UTSW |
7 |
27,806,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R6488:Fcgbp
|
UTSW |
7 |
27,792,963 (GRCm39) |
missense |
probably damaging |
0.96 |
R6548:Fcgbp
|
UTSW |
7 |
27,791,343 (GRCm39) |
missense |
probably benign |
0.00 |
R6553:Fcgbp
|
UTSW |
7 |
27,813,404 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6585:Fcgbp
|
UTSW |
7 |
27,813,404 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6695:Fcgbp
|
UTSW |
7 |
27,785,695 (GRCm39) |
nonsense |
probably null |
|
R6711:Fcgbp
|
UTSW |
7 |
27,789,098 (GRCm39) |
missense |
probably damaging |
0.99 |
R6803:Fcgbp
|
UTSW |
7 |
27,802,637 (GRCm39) |
missense |
probably benign |
0.00 |
R6822:Fcgbp
|
UTSW |
7 |
27,806,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R6907:Fcgbp
|
UTSW |
7 |
27,784,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R6912:Fcgbp
|
UTSW |
7 |
27,789,129 (GRCm39) |
missense |
probably benign |
0.15 |
R6924:Fcgbp
|
UTSW |
7 |
27,793,248 (GRCm39) |
missense |
probably benign |
|
R6943:Fcgbp
|
UTSW |
7 |
27,791,477 (GRCm39) |
missense |
probably benign |
0.22 |
R7060:Fcgbp
|
UTSW |
7 |
27,791,358 (GRCm39) |
missense |
probably benign |
0.20 |
R7103:Fcgbp
|
UTSW |
7 |
27,784,387 (GRCm39) |
missense |
probably benign |
0.00 |
R7208:Fcgbp
|
UTSW |
7 |
27,803,446 (GRCm39) |
missense |
probably benign |
0.01 |
R7291:Fcgbp
|
UTSW |
7 |
27,800,817 (GRCm39) |
missense |
probably benign |
0.00 |
R7301:Fcgbp
|
UTSW |
7 |
27,792,861 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7404:Fcgbp
|
UTSW |
7 |
27,800,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R7426:Fcgbp
|
UTSW |
7 |
27,785,949 (GRCm39) |
missense |
probably benign |
0.00 |
R7459:Fcgbp
|
UTSW |
7 |
27,806,710 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7475:Fcgbp
|
UTSW |
7 |
27,802,401 (GRCm39) |
missense |
probably damaging |
0.99 |
R7505:Fcgbp
|
UTSW |
7 |
27,789,099 (GRCm39) |
missense |
probably damaging |
0.97 |
R7517:Fcgbp
|
UTSW |
7 |
27,784,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R7519:Fcgbp
|
UTSW |
7 |
27,785,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R7524:Fcgbp
|
UTSW |
7 |
27,802,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R7649:Fcgbp
|
UTSW |
7 |
27,790,928 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7782:Fcgbp
|
UTSW |
7 |
27,784,460 (GRCm39) |
nonsense |
probably null |
|
R7820:Fcgbp
|
UTSW |
7 |
27,819,784 (GRCm39) |
missense |
probably benign |
0.01 |
R7831:Fcgbp
|
UTSW |
7 |
27,806,404 (GRCm39) |
missense |
probably damaging |
0.98 |
R7835:Fcgbp
|
UTSW |
7 |
27,816,632 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7947:Fcgbp
|
UTSW |
7 |
27,803,595 (GRCm39) |
critical splice donor site |
probably null |
|
R8086:Fcgbp
|
UTSW |
7 |
27,813,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R8137:Fcgbp
|
UTSW |
7 |
27,804,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R8154:Fcgbp
|
UTSW |
7 |
27,784,507 (GRCm39) |
missense |
probably benign |
0.00 |
R8169:Fcgbp
|
UTSW |
7 |
27,784,919 (GRCm39) |
critical splice donor site |
probably null |
|
R8176:Fcgbp
|
UTSW |
7 |
27,791,174 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8193:Fcgbp
|
UTSW |
7 |
27,804,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R8313:Fcgbp
|
UTSW |
7 |
27,785,769 (GRCm39) |
missense |
probably benign |
0.00 |
R8350:Fcgbp
|
UTSW |
7 |
27,793,614 (GRCm39) |
missense |
probably benign |
0.02 |
R8382:Fcgbp
|
UTSW |
7 |
27,816,762 (GRCm39) |
missense |
probably benign |
0.00 |
R8393:Fcgbp
|
UTSW |
7 |
27,806,815 (GRCm39) |
missense |
probably benign |
0.18 |
R8438:Fcgbp
|
UTSW |
7 |
27,789,231 (GRCm39) |
missense |
probably benign |
0.25 |
R8489:Fcgbp
|
UTSW |
7 |
27,804,435 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8495:Fcgbp
|
UTSW |
7 |
27,785,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R8707:Fcgbp
|
UTSW |
7 |
27,819,920 (GRCm39) |
missense |
probably benign |
0.01 |
R8736:Fcgbp
|
UTSW |
7 |
27,805,621 (GRCm39) |
missense |
probably benign |
0.05 |
R8816:Fcgbp
|
UTSW |
7 |
27,784,412 (GRCm39) |
missense |
probably benign |
0.09 |
R8905:Fcgbp
|
UTSW |
7 |
27,785,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R9031:Fcgbp
|
UTSW |
7 |
27,790,908 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9063:Fcgbp
|
UTSW |
7 |
27,791,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R9180:Fcgbp
|
UTSW |
7 |
27,803,198 (GRCm39) |
nonsense |
probably null |
|
R9262:Fcgbp
|
UTSW |
7 |
27,819,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R9439:Fcgbp
|
UTSW |
7 |
27,803,436 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9526:Fcgbp
|
UTSW |
7 |
27,790,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R9603:Fcgbp
|
UTSW |
7 |
27,802,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R9635:Fcgbp
|
UTSW |
7 |
27,800,832 (GRCm39) |
missense |
probably benign |
0.40 |
R9703:Fcgbp
|
UTSW |
7 |
27,806,400 (GRCm39) |
missense |
probably damaging |
0.98 |
R9711:Fcgbp
|
UTSW |
7 |
27,793,000 (GRCm39) |
missense |
probably benign |
0.00 |
R9733:Fcgbp
|
UTSW |
7 |
27,803,012 (GRCm39) |
missense |
probably damaging |
1.00 |
RF002:Fcgbp
|
UTSW |
7 |
27,789,180 (GRCm39) |
missense |
probably benign |
|
X0028:Fcgbp
|
UTSW |
7 |
27,803,445 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1186:Fcgbp
|
UTSW |
7 |
27,791,072 (GRCm39) |
missense |
probably benign |
|
Z1186:Fcgbp
|
UTSW |
7 |
27,789,180 (GRCm39) |
missense |
probably benign |
|
Z1186:Fcgbp
|
UTSW |
7 |
27,785,616 (GRCm39) |
missense |
probably benign |
|
Z1186:Fcgbp
|
UTSW |
7 |
27,803,309 (GRCm39) |
missense |
probably benign |
0.09 |
Z1186:Fcgbp
|
UTSW |
7 |
27,792,770 (GRCm39) |
missense |
probably benign |
|
|