Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adat1 |
T |
C |
8: 112,698,793 (GRCm39) |
I344V |
probably benign |
Het |
Bmper |
A |
T |
9: 23,310,868 (GRCm39) |
Q434L |
probably damaging |
Het |
Cabyr |
A |
G |
18: 12,883,969 (GRCm39) |
Y152C |
probably benign |
Het |
Cactin |
G |
A |
10: 81,159,278 (GRCm39) |
|
probably null |
Het |
Cadps2 |
T |
C |
6: 23,599,505 (GRCm39) |
D238G |
probably damaging |
Het |
Card10 |
T |
C |
15: 78,671,671 (GRCm39) |
T598A |
possibly damaging |
Het |
Ctr9 |
C |
T |
7: 110,629,449 (GRCm39) |
P25L |
probably damaging |
Het |
Entpd5 |
T |
C |
12: 84,424,127 (GRCm39) |
T409A |
probably benign |
Het |
Exd1 |
A |
G |
2: 119,363,957 (GRCm39) |
V137A |
probably damaging |
Het |
Ift88 |
A |
G |
14: 57,683,067 (GRCm39) |
N248S |
probably benign |
Het |
Kntc1 |
T |
A |
5: 123,939,888 (GRCm39) |
Y1561N |
probably damaging |
Het |
Mef2c |
A |
G |
13: 83,802,730 (GRCm39) |
D227G |
probably benign |
Het |
Myh2 |
C |
T |
11: 67,084,567 (GRCm39) |
T1702M |
probably damaging |
Het |
Myo1e |
T |
A |
9: 70,234,437 (GRCm39) |
N263K |
probably benign |
Het |
Nfe2l1 |
A |
G |
11: 96,710,636 (GRCm39) |
L373P |
probably damaging |
Het |
Nob1 |
C |
T |
8: 108,142,860 (GRCm39) |
V274M |
possibly damaging |
Het |
Ntng2 |
A |
G |
2: 29,118,218 (GRCm39) |
C77R |
probably damaging |
Het |
Nynrin |
T |
G |
14: 56,101,335 (GRCm39) |
S335A |
probably benign |
Het |
Or10ad1c |
T |
C |
15: 98,085,649 (GRCm39) |
N10D |
probably damaging |
Het |
Or5p55 |
T |
C |
7: 107,567,459 (GRCm39) |
L285P |
probably damaging |
Het |
Pcdh7 |
T |
A |
5: 57,876,471 (GRCm39) |
W9R |
possibly damaging |
Het |
Pcdha1 |
A |
G |
18: 37,064,124 (GRCm39) |
T263A |
probably benign |
Het |
Per3 |
C |
T |
4: 151,128,015 (GRCm39) |
|
probably null |
Het |
Pgbd5 |
A |
G |
8: 125,107,021 (GRCm39) |
F265L |
probably damaging |
Het |
Ppm1k |
T |
G |
6: 57,487,755 (GRCm39) |
E356A |
probably benign |
Het |
Ptgfr |
G |
T |
3: 151,540,938 (GRCm39) |
T190K |
possibly damaging |
Het |
Sec24a |
A |
G |
11: 51,603,103 (GRCm39) |
Y782H |
probably damaging |
Het |
Setd1b |
T |
C |
5: 123,301,295 (GRCm39) |
|
probably benign |
Het |
Sfpq |
GCCGCCGCAGCAGCCTCCGCCGCAGCAGCC |
GCCGCCGCAGCAGCC |
4: 126,915,419 (GRCm39) |
|
probably benign |
Het |
Slc19a2 |
C |
T |
1: 164,090,323 (GRCm39) |
T253I |
possibly damaging |
Het |
Tcf4 |
C |
T |
18: 69,785,484 (GRCm39) |
T207M |
probably damaging |
Het |
Thada |
T |
C |
17: 84,700,897 (GRCm39) |
N1203S |
probably damaging |
Het |
Tln2 |
A |
T |
9: 67,304,917 (GRCm39) |
S5T |
probably damaging |
Het |
Traf4 |
C |
T |
11: 78,051,268 (GRCm39) |
R296Q |
probably benign |
Het |
Ttbk2 |
A |
G |
2: 120,655,751 (GRCm39) |
S38P |
probably benign |
Het |
Vrk1 |
G |
T |
12: 106,041,291 (GRCm39) |
Q395H |
possibly damaging |
Het |
Vwa3a |
G |
T |
7: 120,391,804 (GRCm39) |
|
probably benign |
Het |
Wdsub1 |
C |
T |
2: 59,692,028 (GRCm39) |
V335I |
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 |
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 |
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 |
|
|