Other mutations in this stock |
Total: 118 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adat1 |
A |
G |
8: 112,713,867 (GRCm39) |
L104P |
possibly damaging |
Het |
Adgrf5 |
T |
C |
17: 43,741,443 (GRCm39) |
V360A |
probably benign |
Het |
Ahnak |
G |
A |
19: 8,982,092 (GRCm39) |
M1125I |
probably benign |
Het |
Akap12 |
T |
C |
10: 4,304,804 (GRCm39) |
V538A |
probably benign |
Het |
Arhgef10l |
T |
C |
4: 140,242,749 (GRCm39) |
D1088G |
possibly damaging |
Het |
Atp7b |
A |
T |
8: 22,517,689 (GRCm39) |
L268Q |
probably damaging |
Het |
Atxn2 |
A |
C |
5: 121,917,654 (GRCm39) |
N516T |
probably damaging |
Het |
Cacna1h |
T |
C |
17: 25,616,328 (GRCm39) |
M184V |
possibly damaging |
Het |
Cacnb2 |
G |
T |
2: 14,619,163 (GRCm39) |
R66L |
probably benign |
Het |
Casp8ap2 |
A |
G |
4: 32,631,867 (GRCm39) |
E96G |
probably damaging |
Het |
Ccdc78 |
G |
T |
17: 26,007,755 (GRCm39) |
R264L |
probably damaging |
Het |
Cdh4 |
G |
A |
2: 179,439,351 (GRCm39) |
R166H |
probably damaging |
Het |
Cog7 |
C |
T |
7: 121,529,797 (GRCm39) |
D615N |
possibly damaging |
Het |
Crtc2 |
T |
C |
3: 90,164,690 (GRCm39) |
V115A |
probably benign |
Het |
Crybg1 |
A |
G |
10: 43,874,412 (GRCm39) |
S899P |
probably damaging |
Het |
Ctdnep1 |
T |
A |
11: 69,879,461 (GRCm39) |
V128E |
probably damaging |
Het |
Ctnna3 |
A |
G |
10: 64,795,621 (GRCm39) |
K780E |
probably benign |
Het |
Cul7 |
T |
A |
17: 46,974,116 (GRCm39) |
L1467H |
probably damaging |
Het |
Dazap2 |
T |
A |
15: 100,515,946 (GRCm39) |
Y91* |
probably null |
Het |
Dcdc5 |
T |
C |
2: 106,182,014 (GRCm39) |
|
noncoding transcript |
Het |
Dppa1 |
T |
A |
11: 46,501,300 (GRCm39) |
R74S |
possibly damaging |
Het |
Elovl1 |
A |
T |
4: 118,289,197 (GRCm39) |
T241S |
probably benign |
Het |
Eya1 |
G |
T |
1: 14,344,774 (GRCm39) |
Q86K |
probably damaging |
Het |
Fam110d |
T |
C |
4: 133,978,661 (GRCm39) |
*272W |
probably null |
Het |
Fancm |
A |
T |
12: 65,168,478 (GRCm39) |
M1614L |
probably benign |
Het |
Fpr3 |
T |
A |
17: 18,191,277 (GRCm39) |
W183R |
probably damaging |
Het |
Galnt13 |
G |
A |
2: 54,744,657 (GRCm39) |
V119I |
probably benign |
Het |
Garin4 |
T |
A |
1: 190,896,219 (GRCm39) |
R141S |
probably benign |
Het |
Gcfc2 |
T |
C |
6: 81,900,793 (GRCm39) |
S36P |
probably benign |
Het |
Gdap2 |
T |
A |
3: 100,101,931 (GRCm39) |
D412E |
possibly damaging |
Het |
Gm12258 |
T |
C |
11: 58,750,381 (GRCm39) |
C41R |
probably damaging |
Het |
Hipk1 |
T |
G |
3: 103,685,098 (GRCm39) |
E172D |
probably benign |
Het |
Hmgcs1 |
T |
G |
13: 120,165,127 (GRCm39) |
L326R |
probably benign |
Het |
Hs6st1 |
C |
A |
1: 36,107,967 (GRCm39) |
R77S |
probably damaging |
Het |
Ifit3 |
A |
T |
19: 34,564,573 (GRCm39) |
N40Y |
probably damaging |
Het |
Il1a |
T |
A |
2: 129,146,661 (GRCm39) |
Q144L |
possibly damaging |
Het |
Itga7 |
A |
G |
10: 128,793,680 (GRCm39) |
E1128G |
possibly damaging |
Het |
Itih2 |
T |
C |
2: 10,111,558 (GRCm39) |
D460G |
probably damaging |
Het |
Ivns1abp |
G |
A |
1: 151,227,309 (GRCm39) |
C39Y |
probably damaging |
Het |
Kif22 |
G |
T |
7: 126,627,011 (GRCm39) |
A646E |
probably damaging |
Het |
Klhl29 |
T |
C |
12: 5,141,307 (GRCm39) |
Y559C |
probably damaging |
Het |
Klhl7 |
T |
A |
5: 24,354,108 (GRCm39) |
|
probably null |
Het |
Klhl9 |
A |
G |
4: 88,640,230 (GRCm39) |
S4P |
probably benign |
Het |
Klk10 |
A |
G |
7: 43,432,304 (GRCm39) |
Q79R |
probably benign |
Het |
Klk6 |
T |
C |
7: 43,478,699 (GRCm39) |
|
probably null |
Het |
Kpna2rt |
T |
A |
17: 90,217,734 (GRCm39) |
N4I |
possibly damaging |
Het |
Lamc2 |
C |
T |
1: 153,042,009 (GRCm39) |
E42K |
probably benign |
Het |
Lingo3 |
T |
C |
10: 80,671,555 (GRCm39) |
D125G |
probably benign |
Het |
Map1b |
T |
C |
13: 99,569,247 (GRCm39) |
N1158S |
unknown |
Het |
Masp1 |
T |
A |
16: 23,313,387 (GRCm39) |
N183Y |
probably damaging |
Het |
Mdga2 |
A |
G |
12: 66,615,700 (GRCm39) |
Y636H |
probably benign |
Het |
Mical2 |
T |
A |
7: 111,980,817 (GRCm39) |
S264T |
probably damaging |
Het |
Mif |
A |
G |
10: 75,695,375 (GRCm39) |
V95A |
possibly damaging |
Het |
Mmp17 |
G |
A |
5: 129,672,152 (GRCm39) |
|
probably null |
Het |
Mmp23 |
T |
C |
4: 155,735,174 (GRCm39) |
R390G |
possibly damaging |
Het |
Ncoa6 |
A |
C |
2: 155,257,142 (GRCm39) |
S800R |
possibly damaging |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Nr2e3 |
A |
T |
9: 59,856,488 (GRCm39) |
S67R |
probably damaging |
Het |
Odf2l |
T |
C |
3: 144,854,797 (GRCm39) |
S545P |
possibly damaging |
Het |
Or10d3 |
A |
T |
9: 39,462,080 (GRCm39) |
V29E |
possibly damaging |
Het |
Or4a47 |
G |
A |
2: 89,665,516 (GRCm39) |
R258* |
probably null |
Het |
Or52s1b |
T |
A |
7: 102,822,658 (GRCm39) |
Y62F |
probably benign |
Het |
Or5k1b |
C |
T |
16: 58,581,216 (GRCm39) |
E108K |
probably damaging |
Het |
Or7e176 |
A |
C |
9: 20,171,728 (GRCm39) |
Q197H |
possibly damaging |
Het |
Or7g27 |
C |
T |
9: 19,249,948 (GRCm39) |
S64F |
probably benign |
Het |
Or8b51 |
T |
G |
9: 38,569,014 (GRCm39) |
I225L |
probably damaging |
Het |
Otog |
A |
T |
7: 45,908,688 (GRCm39) |
H562L |
possibly damaging |
Het |
Pcdh15 |
T |
C |
10: 74,430,023 (GRCm39) |
V1250A |
probably damaging |
Het |
Pde1c |
A |
G |
6: 56,150,592 (GRCm39) |
V309A |
possibly damaging |
Het |
Pfkfb4 |
A |
C |
9: 108,836,373 (GRCm39) |
T134P |
probably damaging |
Het |
Phc3 |
G |
T |
3: 30,990,724 (GRCm39) |
Q498K |
possibly damaging |
Het |
Phlpp1 |
T |
C |
1: 106,320,049 (GRCm39) |
V1348A |
probably damaging |
Het |
Pik3ap1 |
T |
C |
19: 41,309,997 (GRCm39) |
D441G |
probably damaging |
Het |
Pkd1l2 |
T |
C |
8: 117,792,239 (GRCm39) |
|
probably null |
Het |
Pla2g4a |
T |
C |
1: 149,733,437 (GRCm39) |
|
probably null |
Het |
Pola2 |
A |
T |
19: 5,998,434 (GRCm39) |
I376N |
probably damaging |
Het |
Pold2 |
T |
A |
11: 5,826,833 (GRCm39) |
N34Y |
probably damaging |
Het |
Ppp2r5c |
T |
C |
12: 110,521,320 (GRCm39) |
L281P |
probably damaging |
Het |
Prss46 |
A |
G |
9: 110,678,703 (GRCm39) |
I29V |
probably benign |
Het |
Ranbp6 |
A |
T |
19: 29,788,846 (GRCm39) |
V502E |
probably benign |
Het |
Rdh14 |
T |
C |
12: 10,444,613 (GRCm39) |
F155L |
probably damaging |
Het |
Rnaseh2a |
A |
T |
8: 85,692,487 (GRCm39) |
|
probably null |
Het |
Rpp30 |
A |
G |
19: 36,071,785 (GRCm39) |
T118A |
possibly damaging |
Het |
Rragd |
T |
C |
4: 32,996,005 (GRCm39) |
F117L |
probably damaging |
Het |
Rxylt1 |
A |
G |
10: 121,926,384 (GRCm39) |
W243R |
probably damaging |
Het |
S100a2 |
T |
A |
3: 90,498,599 (GRCm39) |
|
probably null |
Het |
Septin12 |
T |
C |
16: 4,814,340 (GRCm39) |
K43R |
probably damaging |
Het |
Sh3tc2 |
A |
G |
18: 62,141,559 (GRCm39) |
E1080G |
probably damaging |
Het |
Slc26a9 |
A |
G |
1: 131,678,415 (GRCm39) |
K27R |
probably damaging |
Het |
Spata17 |
T |
A |
1: 186,926,191 (GRCm39) |
K46N |
probably damaging |
Het |
St14 |
A |
C |
9: 31,019,511 (GRCm39) |
D103E |
probably benign |
Het |
St6galnac2 |
T |
A |
11: 116,575,173 (GRCm39) |
Q222L |
possibly damaging |
Het |
Tdrd9 |
T |
C |
12: 112,002,844 (GRCm39) |
V831A |
probably damaging |
Het |
Tert |
A |
G |
13: 73,790,175 (GRCm39) |
E843G |
probably damaging |
Het |
Tex21 |
A |
G |
12: 76,251,044 (GRCm39) |
V464A |
probably benign |
Het |
Tmem232 |
T |
A |
17: 65,791,496 (GRCm39) |
H124L |
probably damaging |
Het |
Tnfrsf19 |
T |
G |
14: 61,242,555 (GRCm39) |
S110R |
probably damaging |
Het |
Tnnt3 |
A |
T |
7: 142,069,562 (GRCm39) |
K272* |
probably null |
Het |
Tnxb |
T |
C |
17: 34,930,477 (GRCm39) |
L2054P |
probably damaging |
Het |
Trcg1 |
A |
C |
9: 57,149,748 (GRCm39) |
D440A |
probably benign |
Het |
Trpm3 |
A |
G |
19: 22,878,585 (GRCm39) |
E504G |
probably damaging |
Het |
Trpm5 |
C |
T |
7: 142,636,626 (GRCm39) |
R437H |
probably benign |
Het |
Ttn |
T |
C |
2: 76,571,511 (GRCm39) |
R18134G |
probably damaging |
Het |
Uchl5 |
A |
C |
1: 143,674,160 (GRCm39) |
M64L |
possibly damaging |
Het |
Urb1 |
G |
A |
16: 90,550,751 (GRCm39) |
R2034W |
probably damaging |
Het |
Usp44 |
T |
A |
10: 93,683,048 (GRCm39) |
C452* |
probably null |
Het |
Uvssa |
G |
A |
5: 33,571,278 (GRCm39) |
A641T |
probably damaging |
Het |
Vmn1r204 |
T |
A |
13: 22,741,248 (GRCm39) |
I293N |
probably benign |
Het |
Vmn2r84 |
A |
T |
10: 130,225,137 (GRCm39) |
C458S |
probably benign |
Het |
Vmn2r85 |
T |
G |
10: 130,261,788 (GRCm39) |
H183P |
probably damaging |
Het |
Vps13d |
G |
T |
4: 144,832,431 (GRCm39) |
T2825K |
probably benign |
Het |
Zc3hc1 |
T |
A |
6: 30,376,024 (GRCm39) |
I179F |
probably benign |
Het |
Zfp112 |
A |
G |
7: 23,825,210 (GRCm39) |
N393D |
probably damaging |
Het |
Zfp558 |
A |
G |
9: 18,367,859 (GRCm39) |
S310P |
possibly damaging |
Het |
Zfp560 |
A |
C |
9: 20,260,071 (GRCm39) |
|
probably null |
Het |
Zfp668 |
C |
T |
7: 127,466,252 (GRCm39) |
E311K |
probably benign |
Het |
Zfp763 |
T |
A |
17: 33,252,276 (GRCm39) |
M1L |
probably benign |
Het |
Zfp947 |
A |
T |
17: 22,364,813 (GRCm39) |
M287K |
probably benign |
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 |
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 |
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 |
|
|