Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim3 |
C |
T |
18: 61,955,099 (GRCm39) |
A297T |
probably damaging |
Het |
Adprhl1 |
T |
A |
8: 13,275,118 (GRCm39) |
S547C |
probably damaging |
Het |
Ankrd63 |
G |
C |
2: 118,533,793 (GRCm39) |
R43G |
unknown |
Het |
Asah2 |
T |
C |
19: 32,035,254 (GRCm39) |
T24A |
probably benign |
Het |
Asb17 |
G |
A |
3: 153,550,447 (GRCm39) |
|
probably null |
Het |
Atp8b5 |
C |
T |
4: 43,342,640 (GRCm39) |
T437I |
probably benign |
Het |
Bbs2 |
T |
C |
8: 94,808,992 (GRCm39) |
D311G |
probably damaging |
Het |
Birc6 |
C |
T |
17: 74,946,789 (GRCm39) |
T2851I |
possibly damaging |
Het |
Bnip5 |
G |
A |
17: 29,124,298 (GRCm39) |
R335W |
probably damaging |
Het |
Cchcr1 |
T |
C |
17: 35,835,693 (GRCm39) |
W266R |
probably benign |
Het |
Col14a1 |
C |
A |
15: 55,252,024 (GRCm39) |
S560* |
probably null |
Het |
Crocc |
G |
A |
4: 140,753,497 (GRCm39) |
T1317M |
possibly damaging |
Het |
Cxxc1 |
T |
A |
18: 74,352,278 (GRCm39) |
V334E |
possibly damaging |
Het |
Cyp3a25 |
T |
A |
5: 145,923,635 (GRCm39) |
D336V |
probably damaging |
Het |
Dapk1 |
A |
G |
13: 60,867,455 (GRCm39) |
T221A |
probably benign |
Het |
Dnah11 |
G |
T |
12: 118,068,543 (GRCm39) |
T1605K |
probably benign |
Het |
Dnah7c |
T |
C |
1: 46,705,223 (GRCm39) |
V2412A |
possibly damaging |
Het |
Ect2l |
T |
A |
10: 18,035,529 (GRCm39) |
D524V |
probably damaging |
Het |
Ehbp1l1 |
T |
C |
19: 5,770,872 (GRCm39) |
E223G |
possibly damaging |
Het |
Ephb2 |
A |
T |
4: 136,498,524 (GRCm39) |
M185K |
probably damaging |
Het |
Fcer1a |
T |
C |
1: 173,049,083 (GRCm39) |
K243E |
probably damaging |
Het |
Fgfr1 |
T |
C |
8: 26,045,566 (GRCm39) |
V45A |
probably benign |
Het |
Filip1 |
T |
A |
9: 79,727,380 (GRCm39) |
E413V |
possibly damaging |
Het |
Frs3 |
T |
C |
17: 48,013,651 (GRCm39) |
|
probably null |
Het |
Fstl4 |
A |
G |
11: 53,024,898 (GRCm39) |
T257A |
probably benign |
Het |
Golga5 |
A |
T |
12: 102,450,778 (GRCm39) |
K477M |
probably damaging |
Het |
Gpr171 |
A |
T |
3: 59,005,622 (GRCm39) |
I51K |
probably damaging |
Het |
H1f0 |
T |
A |
15: 78,913,080 (GRCm39) |
Y53* |
probably null |
Het |
Hephl1 |
A |
G |
9: 14,981,047 (GRCm39) |
V795A |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,596,510 (GRCm39) |
D1775E |
probably benign |
Het |
Hs3st2 |
A |
G |
7: 121,100,168 (GRCm39) |
D338G |
possibly damaging |
Het |
Hsd3b6 |
T |
A |
3: 98,713,534 (GRCm39) |
Y255F |
probably benign |
Het |
Hspa9 |
T |
C |
18: 35,076,329 (GRCm39) |
N328D |
possibly damaging |
Het |
Hvcn1 |
T |
A |
5: 122,375,748 (GRCm39) |
I100N |
probably damaging |
Het |
Ifi207 |
C |
T |
1: 173,556,494 (GRCm39) |
S748N |
possibly damaging |
Het |
Katnip |
A |
T |
7: 125,464,434 (GRCm39) |
N1267I |
probably damaging |
Het |
Kcnma1 |
G |
T |
14: 24,052,902 (GRCm39) |
T180K |
unknown |
Het |
Kctd16 |
A |
G |
18: 40,391,826 (GRCm39) |
D138G |
probably damaging |
Het |
Kifc3 |
A |
G |
8: 95,830,092 (GRCm39) |
Y605H |
probably benign |
Het |
Kmt2d |
T |
A |
15: 98,743,376 (GRCm39) |
Q3928L |
unknown |
Het |
Lamb2 |
C |
T |
9: 108,364,782 (GRCm39) |
R1179C |
probably damaging |
Het |
Layn |
T |
A |
9: 50,968,670 (GRCm39) |
I358F |
possibly damaging |
Het |
Lrig1 |
G |
A |
6: 94,603,452 (GRCm39) |
T232M |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,418,577 (GRCm39) |
T38A |
|
Het |
Map3k14 |
A |
G |
11: 103,129,918 (GRCm39) |
V333A |
probably benign |
Het |
Med13 |
T |
C |
11: 86,177,272 (GRCm39) |
D1608G |
possibly damaging |
Het |
Mrps31 |
T |
G |
8: 22,911,429 (GRCm39) |
S224A |
probably benign |
Het |
Msh6 |
G |
T |
17: 88,282,548 (GRCm39) |
|
|
Het |
Ncapd3 |
A |
G |
9: 26,978,315 (GRCm39) |
D838G |
probably benign |
Het |
Nlrp1a |
C |
A |
11: 70,987,919 (GRCm39) |
E1184* |
probably null |
Het |
Npat |
T |
A |
9: 53,466,233 (GRCm39) |
|
probably null |
Het |
Nup210 |
A |
T |
6: 91,050,227 (GRCm39) |
I414N |
probably benign |
Het |
Or1e19 |
A |
T |
11: 73,316,419 (GRCm39) |
L130H |
probably damaging |
Het |
Or52n2 |
A |
T |
7: 104,542,181 (GRCm39) |
V218E |
possibly damaging |
Het |
Or5b122 |
T |
A |
19: 13,562,752 (GRCm39) |
I28N |
possibly damaging |
Het |
Or5h19 |
T |
C |
16: 58,856,603 (GRCm39) |
T166A |
possibly damaging |
Het |
Or6z5 |
T |
C |
7: 6,477,163 (GRCm39) |
L18P |
probably damaging |
Het |
Or8b12c |
A |
T |
9: 37,715,257 (GRCm39) |
T17S |
possibly damaging |
Het |
Or8h7 |
A |
C |
2: 86,721,217 (GRCm39) |
L101V |
probably benign |
Het |
Otud7b |
G |
C |
3: 96,043,936 (GRCm39) |
|
probably null |
Het |
Phf11d |
A |
C |
14: 59,596,942 (GRCm39) |
W86G |
probably benign |
Het |
Pik3c2b |
T |
A |
1: 133,018,444 (GRCm39) |
S964T |
probably damaging |
Het |
Pira1 |
T |
C |
7: 3,742,344 (GRCm39) |
Y61C |
probably damaging |
Het |
Plod3 |
G |
A |
5: 137,023,901 (GRCm39) |
V687I |
probably benign |
Het |
Poglut1 |
T |
G |
16: 38,358,284 (GRCm39) |
Y208S |
possibly damaging |
Het |
Pou1f1 |
T |
A |
16: 65,330,749 (GRCm39) |
L253H |
probably damaging |
Het |
Pou2f1 |
C |
T |
1: 165,738,955 (GRCm39) |
A166T |
unknown |
Het |
Rhbdl3 |
C |
T |
11: 80,237,659 (GRCm39) |
S297L |
probably damaging |
Het |
Rxra |
A |
T |
2: 27,631,866 (GRCm39) |
N179I |
probably damaging |
Het |
Ryr2 |
C |
T |
13: 11,750,506 (GRCm39) |
E1922K |
probably damaging |
Het |
Scube1 |
T |
C |
15: 83,499,211 (GRCm39) |
Y668C |
probably damaging |
Het |
Sec16b |
A |
G |
1: 157,358,927 (GRCm39) |
Y120C |
probably damaging |
Het |
Sec61b |
G |
T |
4: 47,483,047 (GRCm39) |
K92N |
probably damaging |
Het |
Skic3 |
T |
A |
13: 76,296,866 (GRCm39) |
Y1074* |
probably null |
Het |
Slc13a3 |
T |
C |
2: 165,275,984 (GRCm39) |
N254S |
possibly damaging |
Het |
Slc17a7 |
T |
A |
7: 44,822,354 (GRCm39) |
Y397N |
probably benign |
Het |
Slc25a3 |
A |
G |
10: 90,952,902 (GRCm39) |
V333A |
possibly damaging |
Het |
Slc7a8 |
A |
T |
14: 54,964,283 (GRCm39) |
V390E |
probably damaging |
Het |
Sorbs2 |
G |
A |
8: 46,212,233 (GRCm39) |
|
probably null |
Het |
Srgap1 |
T |
C |
10: 121,621,650 (GRCm39) |
N948D |
probably benign |
Het |
Tacc2 |
A |
T |
7: 130,225,066 (GRCm39) |
T584S |
probably benign |
Het |
Tec |
A |
T |
5: 72,920,961 (GRCm39) |
D471E |
probably damaging |
Het |
Tecpr2 |
C |
T |
12: 110,898,038 (GRCm39) |
A430V |
probably benign |
Het |
Tmcc2 |
A |
T |
1: 132,288,759 (GRCm39) |
D309E |
probably damaging |
Het |
Tmem82 |
G |
A |
4: 141,344,742 (GRCm39) |
A67V |
possibly damaging |
Het |
Ttc23l |
T |
C |
15: 10,551,663 (GRCm39) |
Q21R |
probably damaging |
Het |
Ubl3 |
A |
G |
5: 148,448,764 (GRCm39) |
F26L |
probably damaging |
Het |
Upf2 |
A |
G |
2: 6,045,014 (GRCm39) |
E1088G |
unknown |
Het |
Usp9y |
T |
A |
Y: 1,341,780 (GRCm39) |
I1362F |
probably benign |
Het |
Wnk4 |
T |
A |
11: 101,159,318 (GRCm39) |
|
probably null |
Het |
Wrn |
C |
G |
8: 33,738,994 (GRCm39) |
W1278S |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,251,153 (GRCm39) |
V1248D |
probably damaging |
Het |
Zfp12 |
T |
A |
5: 143,226,099 (GRCm39) |
V56D |
probably 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 |
R4705:Fcgbp
|
UTSW |
7 |
27,806,721 (GRCm39) |
missense |
probably benign |
0.44 |
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 |
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 |
|
|