Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam11 |
G |
A |
11: 102,667,501 (GRCm39) |
R687Q |
possibly damaging |
Het |
AI987944 |
A |
G |
7: 41,024,232 (GRCm39) |
L249P |
probably damaging |
Het |
Ankrd28 |
T |
A |
14: 31,458,797 (GRCm39) |
|
probably null |
Het |
Bahcc1 |
T |
C |
11: 120,178,547 (GRCm39) |
S2369P |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,887,377 (GRCm39) |
S902P |
possibly damaging |
Het |
Birc6 |
A |
T |
17: 74,905,039 (GRCm39) |
K1277N |
probably damaging |
Het |
Brwd1 |
T |
C |
16: 95,842,474 (GRCm39) |
E821G |
probably benign |
Het |
Cct8l1 |
T |
C |
5: 25,722,937 (GRCm39) |
S551P |
possibly damaging |
Het |
Cmtm1 |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
8: 105,036,334 (GRCm39) |
|
probably null |
Het |
Cyp2c39 |
A |
T |
19: 39,525,261 (GRCm39) |
D188V |
probably damaging |
Het |
Dclk3 |
G |
T |
9: 111,268,405 (GRCm39) |
A25S |
probably benign |
Het |
Dpep2 |
A |
T |
8: 106,711,873 (GRCm39) |
M518K |
probably benign |
Het |
Dst |
T |
C |
1: 34,314,755 (GRCm39) |
V6462A |
probably damaging |
Het |
Entpd3 |
T |
C |
9: 120,391,104 (GRCm39) |
|
probably null |
Het |
Epm2aip1 |
T |
C |
9: 111,101,624 (GRCm39) |
V199A |
probably damaging |
Het |
Fam193b |
A |
G |
13: 55,689,504 (GRCm39) |
|
probably benign |
Het |
Fam50b |
G |
A |
13: 34,931,084 (GRCm39) |
E187K |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,479,441 (GRCm39) |
D2829G |
probably damaging |
Het |
Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,450 (GRCm39) |
|
probably benign |
Het |
Grik5 |
C |
T |
7: 24,745,780 (GRCm39) |
R431Q |
possibly damaging |
Het |
H2-Aa |
C |
T |
17: 34,506,651 (GRCm39) |
|
probably null |
Het |
Igsf9 |
T |
A |
1: 172,324,730 (GRCm39) |
S883T |
possibly damaging |
Het |
Kcnh7 |
T |
G |
2: 62,618,248 (GRCm39) |
I414L |
probably damaging |
Het |
Kcnma1 |
T |
C |
14: 24,053,812 (GRCm39) |
|
probably null |
Het |
Kcnmb1 |
T |
C |
11: 33,914,686 (GRCm39) |
|
probably benign |
Het |
Kmt2d |
A |
G |
15: 98,747,340 (GRCm39) |
|
probably benign |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Map3k13 |
G |
A |
16: 21,741,013 (GRCm39) |
S780N |
probably benign |
Het |
Nlgn1 |
T |
C |
3: 26,187,796 (GRCm39) |
T30A |
probably benign |
Het |
Nucb1 |
A |
G |
7: 45,148,289 (GRCm39) |
F175L |
probably damaging |
Het |
Pax6 |
T |
A |
2: 105,516,268 (GRCm39) |
V182E |
probably benign |
Het |
Ptger1 |
A |
G |
8: 84,395,279 (GRCm39) |
D252G |
probably benign |
Het |
Rexo4 |
T |
C |
2: 26,850,283 (GRCm39) |
D275G |
probably damaging |
Het |
Ripk4 |
T |
C |
16: 97,547,236 (GRCm39) |
D342G |
probably damaging |
Het |
Rpl10l |
A |
T |
12: 66,330,987 (GRCm39) |
C49S |
possibly damaging |
Het |
Sema7a |
T |
C |
9: 57,867,619 (GRCm39) |
F457S |
probably damaging |
Het |
Shank3 |
G |
A |
15: 89,415,830 (GRCm39) |
D155N |
probably damaging |
Het |
Smpd3 |
G |
A |
8: 106,992,596 (GRCm39) |
|
probably benign |
Het |
Smpd4 |
T |
C |
16: 17,458,097 (GRCm39) |
V465A |
probably damaging |
Het |
Sohlh2 |
T |
C |
3: 55,115,107 (GRCm39) |
V364A |
probably damaging |
Het |
Sos2 |
C |
T |
12: 69,697,423 (GRCm39) |
R99Q |
probably damaging |
Het |
Spry2 |
G |
A |
14: 106,130,791 (GRCm39) |
Q132* |
probably null |
Het |
Tbx19 |
G |
T |
1: 164,967,709 (GRCm39) |
P346Q |
probably damaging |
Het |
Tdrd6 |
A |
G |
17: 43,938,106 (GRCm39) |
Y981H |
probably damaging |
Het |
Tinag |
T |
C |
9: 76,938,984 (GRCm39) |
K165E |
probably benign |
Het |
Tubb4a |
A |
T |
17: 57,387,904 (GRCm39) |
I374N |
probably damaging |
Het |
Umodl1 |
C |
T |
17: 31,205,528 (GRCm39) |
Q708* |
probably null |
Het |
Vmn2r3 |
A |
T |
3: 64,194,876 (GRCm39) |
V14E |
probably benign |
Het |
Zfp82 |
G |
A |
7: 29,755,712 (GRCm39) |
L457F |
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 |
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 |
|
|