Other mutations in this stock |
Total: 118 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
T |
5: 109,884,144 (GRCm39) |
H571Q |
probably damaging |
Het |
Abcf2 |
T |
A |
5: 24,773,774 (GRCm39) |
M372L |
probably benign |
Het |
Acaca |
A |
C |
11: 84,206,795 (GRCm39) |
T1552P |
probably damaging |
Het |
Acaca |
A |
G |
11: 84,229,219 (GRCm39) |
D1682G |
probably damaging |
Het |
Acvr1b |
T |
C |
15: 101,091,906 (GRCm39) |
V62A |
probably benign |
Het |
Aimp1 |
C |
T |
3: 132,379,825 (GRCm39) |
V97M |
probably benign |
Het |
Aldh1l1 |
C |
T |
6: 90,554,813 (GRCm39) |
T557I |
possibly damaging |
Het |
Alpk1 |
T |
C |
3: 127,471,447 (GRCm39) |
T1012A |
probably damaging |
Het |
Amot |
G |
A |
X: 144,233,585 (GRCm39) |
|
probably benign |
Het |
Arap1 |
T |
A |
7: 101,037,829 (GRCm39) |
H477Q |
probably benign |
Het |
Arhgap18 |
T |
A |
10: 26,736,732 (GRCm39) |
|
probably benign |
Het |
Arhgef10l |
C |
T |
4: 140,242,684 (GRCm39) |
V862M |
probably damaging |
Het |
Arl4d |
A |
G |
11: 101,557,554 (GRCm39) |
I27V |
probably benign |
Het |
Asb18 |
G |
A |
1: 89,942,277 (GRCm39) |
P8L |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,977,616 (GRCm39) |
H2682R |
probably damaging |
Het |
Aspm |
T |
A |
1: 139,385,079 (GRCm39) |
V241E |
probably benign |
Het |
Atf7ip |
G |
T |
6: 136,586,217 (GRCm39) |
|
probably benign |
Het |
AY358078 |
T |
G |
14: 52,042,051 (GRCm39) |
M142R |
unknown |
Het |
C3 |
T |
A |
17: 57,526,592 (GRCm39) |
K796N |
possibly damaging |
Het |
Ceacam16 |
T |
C |
7: 19,590,041 (GRCm39) |
T301A |
probably damaging |
Het |
Ceacam5 |
T |
G |
7: 17,481,320 (GRCm39) |
Y356D |
probably benign |
Het |
Cep192 |
C |
T |
18: 67,984,838 (GRCm39) |
A1616V |
possibly damaging |
Het |
Cfap91 |
T |
A |
16: 38,141,781 (GRCm39) |
N384Y |
possibly damaging |
Het |
Cherp |
A |
T |
8: 73,216,994 (GRCm39) |
H645Q |
probably benign |
Het |
CK137956 |
T |
C |
4: 127,845,242 (GRCm39) |
D167G |
probably benign |
Het |
Clcn1 |
T |
A |
6: 42,275,860 (GRCm39) |
|
probably null |
Het |
Cntn1 |
C |
T |
15: 92,189,552 (GRCm39) |
T625I |
possibly damaging |
Het |
Cpn2 |
T |
A |
16: 30,078,142 (GRCm39) |
N520Y |
probably damaging |
Het |
Crocc |
G |
A |
4: 140,746,620 (GRCm39) |
R1762W |
probably damaging |
Het |
Cts3 |
C |
A |
13: 61,715,967 (GRCm39) |
V100F |
probably benign |
Het |
Ddx56 |
A |
T |
11: 6,216,934 (GRCm39) |
V87D |
probably damaging |
Het |
Dnah9 |
C |
T |
11: 66,010,420 (GRCm39) |
|
probably null |
Het |
Dock1 |
T |
A |
7: 134,700,456 (GRCm39) |
|
probably null |
Het |
Dst |
T |
A |
1: 34,191,552 (GRCm39) |
Y291* |
probably null |
Het |
Eif4g3 |
T |
C |
4: 137,898,442 (GRCm39) |
I1071T |
probably damaging |
Het |
Fblim1 |
T |
C |
4: 141,322,549 (GRCm39) |
Q78R |
probably damaging |
Het |
Fcamr |
C |
T |
1: 130,739,284 (GRCm39) |
P195S |
probably benign |
Het |
Fcho1 |
G |
A |
8: 72,161,666 (GRCm39) |
Q835* |
probably null |
Het |
Frem3 |
A |
G |
8: 81,339,741 (GRCm39) |
N678S |
probably benign |
Het |
Frk |
G |
A |
10: 34,483,878 (GRCm39) |
R413H |
probably benign |
Het |
Gm10619 |
C |
A |
7: 73,459,758 (GRCm39) |
|
noncoding transcript |
Het |
Gm12185 |
G |
A |
11: 48,806,583 (GRCm39) |
R203* |
probably null |
Het |
Gm12886 |
A |
G |
4: 121,280,174 (GRCm39) |
V34A |
probably benign |
Het |
Gna12 |
A |
T |
5: 140,746,707 (GRCm39) |
I246N |
probably damaging |
Het |
Gpm6a |
T |
C |
8: 55,507,867 (GRCm39) |
M201T |
probably benign |
Het |
Gpsm2 |
T |
G |
3: 108,608,225 (GRCm39) |
D220A |
probably benign |
Het |
Grip2 |
C |
G |
6: 91,760,623 (GRCm39) |
V325L |
probably benign |
Het |
Grk5 |
C |
A |
19: 61,065,200 (GRCm39) |
A288D |
probably damaging |
Het |
Herpud2 |
G |
A |
9: 25,021,953 (GRCm39) |
A231V |
possibly damaging |
Het |
Hmcn1 |
T |
C |
1: 150,624,834 (GRCm39) |
S1024G |
probably benign |
Het |
Hp1bp3 |
A |
G |
4: 137,957,820 (GRCm39) |
D295G |
probably damaging |
Het |
Igsf21 |
T |
C |
4: 139,761,703 (GRCm39) |
H325R |
probably damaging |
Het |
Ing2 |
T |
A |
8: 48,122,364 (GRCm39) |
L61F |
probably damaging |
Het |
Jak3 |
T |
C |
8: 72,138,590 (GRCm39) |
|
probably benign |
Het |
Kcnn3 |
T |
A |
3: 89,516,712 (GRCm39) |
C374S |
probably benign |
Het |
Klk1b22 |
A |
G |
7: 43,765,775 (GRCm39) |
|
probably benign |
Het |
Larp1 |
T |
C |
11: 57,940,764 (GRCm39) |
M630T |
possibly damaging |
Het |
Lhx5 |
T |
A |
5: 120,572,725 (GRCm39) |
C115S |
probably damaging |
Het |
Lmcd1 |
C |
A |
6: 112,305,712 (GRCm39) |
T271K |
probably benign |
Het |
Lpar1 |
G |
A |
4: 58,486,798 (GRCm39) |
R158* |
probably null |
Het |
Lyst |
T |
A |
13: 13,821,668 (GRCm39) |
C1347* |
probably null |
Het |
Map3k8 |
G |
A |
18: 4,332,389 (GRCm39) |
Q441* |
probably null |
Het |
Mboat1 |
T |
C |
13: 30,403,633 (GRCm39) |
V144A |
probably damaging |
Het |
Mcur1 |
C |
T |
13: 43,713,491 (GRCm39) |
G38S |
unknown |
Het |
Med13 |
T |
A |
11: 86,220,177 (GRCm39) |
M276L |
probably benign |
Het |
Mefv |
A |
G |
16: 3,526,528 (GRCm39) |
S699P |
possibly damaging |
Het |
Mfsd4a |
C |
A |
1: 131,987,077 (GRCm39) |
A62S |
probably damaging |
Het |
Mmp27 |
A |
G |
9: 7,571,459 (GRCm39) |
M1V |
probably null |
Het |
Myo1c |
C |
T |
11: 75,548,415 (GRCm39) |
T58I |
probably damaging |
Het |
Myom3 |
A |
T |
4: 135,538,066 (GRCm39) |
D1316V |
probably benign |
Het |
Naa25 |
T |
A |
5: 121,555,478 (GRCm39) |
C235S |
possibly damaging |
Het |
Naa25 |
C |
A |
5: 121,558,656 (GRCm39) |
R333S |
probably damaging |
Het |
Nav3 |
G |
A |
10: 109,539,233 (GRCm39) |
T2056I |
probably benign |
Het |
Nol4 |
A |
G |
18: 22,902,878 (GRCm39) |
Y378H |
probably damaging |
Het |
Npat |
G |
A |
9: 53,463,589 (GRCm39) |
R124Q |
probably damaging |
Het |
Npr3 |
T |
A |
15: 11,848,665 (GRCm39) |
E434V |
probably benign |
Het |
Nptx2 |
A |
G |
5: 144,485,130 (GRCm39) |
T208A |
probably benign |
Het |
Obscn |
C |
T |
11: 58,968,606 (GRCm39) |
V2798M |
probably damaging |
Het |
Odad4 |
C |
A |
11: 100,460,679 (GRCm39) |
|
probably null |
Het |
Or10j7 |
A |
T |
1: 173,011,976 (GRCm39) |
H8Q |
probably benign |
Het |
Or52r1 |
A |
G |
7: 102,537,250 (GRCm39) |
Y37H |
probably benign |
Het |
Or5b122 |
C |
T |
19: 13,562,779 (GRCm39) |
T37I |
probably benign |
Het |
Padi1 |
G |
A |
4: 140,541,967 (GRCm39) |
P652S |
probably damaging |
Het |
Pcdh1 |
G |
T |
18: 38,331,938 (GRCm39) |
P355Q |
probably damaging |
Het |
Pck2 |
G |
A |
14: 55,781,422 (GRCm39) |
R189H |
possibly damaging |
Het |
Pcsk5 |
T |
A |
19: 17,432,114 (GRCm39) |
K1500N |
possibly damaging |
Het |
Phc3 |
A |
T |
3: 31,002,865 (GRCm39) |
S218T |
probably damaging |
Het |
Piezo2 |
T |
A |
18: 63,239,355 (GRCm39) |
M510L |
possibly damaging |
Het |
Polr1g |
T |
C |
7: 19,091,904 (GRCm39) |
T68A |
possibly damaging |
Het |
Ppp1r3a |
A |
T |
6: 14,754,717 (GRCm39) |
Y177N |
probably damaging |
Het |
Psme2b |
A |
T |
11: 48,836,361 (GRCm39) |
D195E |
probably damaging |
Het |
Ptprr |
T |
C |
10: 116,088,827 (GRCm39) |
V463A |
probably damaging |
Het |
Pwwp2b |
G |
A |
7: 138,836,281 (GRCm39) |
R574Q |
probably damaging |
Het |
Rap1gds1 |
T |
A |
3: 138,756,314 (GRCm39) |
T14S |
possibly damaging |
Het |
Rbm11 |
A |
T |
16: 75,397,685 (GRCm39) |
K205M |
probably damaging |
Het |
Rfx1 |
T |
A |
8: 84,793,050 (GRCm39) |
|
probably benign |
Het |
Rnasel |
C |
A |
1: 153,630,169 (GRCm39) |
H228Q |
probably damaging |
Het |
Sap130 |
T |
A |
18: 31,831,640 (GRCm39) |
I710K |
probably benign |
Het |
Slc27a4 |
C |
A |
2: 29,695,733 (GRCm39) |
D89E |
probably benign |
Het |
Spata31d1b |
T |
C |
13: 59,863,779 (GRCm39) |
V309A |
probably benign |
Het |
Syt7 |
T |
G |
19: 10,421,354 (GRCm39) |
Y420D |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,515,859 (GRCm39) |
|
probably null |
Het |
Tbc1d10b |
A |
G |
7: 126,802,930 (GRCm39) |
S333P |
possibly damaging |
Het |
Tenm2 |
G |
A |
11: 35,914,209 (GRCm39) |
P2442S |
probably damaging |
Het |
Tenm3 |
C |
T |
8: 49,127,579 (GRCm39) |
C33Y |
probably damaging |
Het |
Timmdc1 |
A |
G |
16: 38,319,419 (GRCm39) |
L245P |
possibly damaging |
Het |
Tlr5 |
T |
C |
1: 182,800,012 (GRCm39) |
F5L |
probably benign |
Het |
Ttll4 |
T |
A |
1: 74,726,999 (GRCm39) |
F784L |
possibly damaging |
Het |
Tulp4 |
A |
G |
17: 6,189,387 (GRCm39) |
T70A |
possibly damaging |
Het |
Txndc17 |
T |
A |
11: 72,099,571 (GRCm39) |
N81K |
probably benign |
Het |
Ubr3 |
C |
T |
2: 69,830,895 (GRCm39) |
|
probably benign |
Het |
Uri1 |
A |
C |
7: 37,681,116 (GRCm39) |
V96G |
probably damaging |
Het |
Uspl1 |
T |
A |
5: 149,150,246 (GRCm39) |
I482N |
probably damaging |
Het |
Vmn1r229 |
A |
G |
17: 21,034,974 (GRCm39) |
N73S |
possibly damaging |
Het |
Vwa7 |
G |
T |
17: 35,243,388 (GRCm39) |
G689* |
probably null |
Het |
Zfp114 |
T |
A |
7: 23,877,164 (GRCm39) |
|
probably null |
Het |
Zfp618 |
A |
G |
4: 63,051,474 (GRCm39) |
S659G |
probably damaging |
Het |
Zfp872 |
A |
G |
9: 22,111,349 (GRCm39) |
K275R |
probably damaging |
Het |
|
Other mutations in Zzef1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Zzef1
|
APN |
11 |
72,765,952 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00898:Zzef1
|
APN |
11 |
72,765,999 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00970:Zzef1
|
APN |
11 |
72,806,071 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01062:Zzef1
|
APN |
11 |
72,765,795 (GRCm39) |
missense |
probably benign |
|
IGL01832:Zzef1
|
APN |
11 |
72,765,892 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02005:Zzef1
|
APN |
11 |
72,779,125 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02026:Zzef1
|
APN |
11 |
72,772,164 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02110:Zzef1
|
APN |
11 |
72,803,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02305:Zzef1
|
APN |
11 |
72,757,423 (GRCm39) |
splice site |
probably benign |
|
IGL02308:Zzef1
|
APN |
11 |
72,777,573 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02315:Zzef1
|
APN |
11 |
72,766,083 (GRCm39) |
nonsense |
probably null |
|
IGL02332:Zzef1
|
APN |
11 |
72,807,335 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02389:Zzef1
|
APN |
11 |
72,782,043 (GRCm39) |
missense |
probably benign |
|
IGL02389:Zzef1
|
APN |
11 |
72,790,364 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02451:Zzef1
|
APN |
11 |
72,792,214 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02541:Zzef1
|
APN |
11 |
72,763,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02950:Zzef1
|
APN |
11 |
72,808,525 (GRCm39) |
splice site |
probably benign |
|
IGL02953:Zzef1
|
APN |
11 |
72,746,224 (GRCm39) |
missense |
probably benign |
|
IGL03053:Zzef1
|
APN |
11 |
72,722,365 (GRCm39) |
splice site |
probably benign |
|
IGL03085:Zzef1
|
APN |
11 |
72,746,350 (GRCm39) |
splice site |
probably benign |
|
IGL03152:Zzef1
|
APN |
11 |
72,814,008 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03329:Zzef1
|
APN |
11 |
72,808,099 (GRCm39) |
splice site |
probably benign |
|
IGL03376:Zzef1
|
APN |
11 |
72,767,377 (GRCm39) |
splice site |
probably benign |
|
IGL03394:Zzef1
|
APN |
11 |
72,777,601 (GRCm39) |
splice site |
probably null |
|
Dreidel
|
UTSW |
11 |
72,799,295 (GRCm39) |
nonsense |
probably null |
|
Hanukkah
|
UTSW |
11 |
72,784,158 (GRCm39) |
missense |
probably benign |
0.00 |
Mezuzah
|
UTSW |
11 |
72,739,559 (GRCm39) |
nonsense |
probably null |
|
BB005:Zzef1
|
UTSW |
11 |
72,712,722 (GRCm39) |
missense |
probably damaging |
0.99 |
BB015:Zzef1
|
UTSW |
11 |
72,712,722 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4508001:Zzef1
|
UTSW |
11 |
72,786,002 (GRCm39) |
missense |
probably benign |
|
PIT4581001:Zzef1
|
UTSW |
11 |
72,790,498 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4810001:Zzef1
|
UTSW |
11 |
72,741,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Zzef1
|
UTSW |
11 |
72,708,791 (GRCm39) |
missense |
probably benign |
0.01 |
R0119:Zzef1
|
UTSW |
11 |
72,712,677 (GRCm39) |
missense |
probably benign |
|
R0136:Zzef1
|
UTSW |
11 |
72,712,677 (GRCm39) |
missense |
probably benign |
|
R0140:Zzef1
|
UTSW |
11 |
72,790,377 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0212:Zzef1
|
UTSW |
11 |
72,764,736 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0217:Zzef1
|
UTSW |
11 |
72,779,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R0220:Zzef1
|
UTSW |
11 |
72,756,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R0304:Zzef1
|
UTSW |
11 |
72,771,450 (GRCm39) |
missense |
probably benign |
0.10 |
R0400:Zzef1
|
UTSW |
11 |
72,786,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R0422:Zzef1
|
UTSW |
11 |
72,756,917 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0471:Zzef1
|
UTSW |
11 |
72,813,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R0557:Zzef1
|
UTSW |
11 |
72,808,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R0581:Zzef1
|
UTSW |
11 |
72,742,726 (GRCm39) |
missense |
probably benign |
0.00 |
R0599:Zzef1
|
UTSW |
11 |
72,804,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R0603:Zzef1
|
UTSW |
11 |
72,708,895 (GRCm39) |
missense |
probably benign |
0.00 |
R0657:Zzef1
|
UTSW |
11 |
72,712,677 (GRCm39) |
missense |
probably benign |
|
R0987:Zzef1
|
UTSW |
11 |
72,792,159 (GRCm39) |
small deletion |
probably benign |
|
R1246:Zzef1
|
UTSW |
11 |
72,765,735 (GRCm39) |
missense |
probably benign |
0.00 |
R1327:Zzef1
|
UTSW |
11 |
72,784,240 (GRCm39) |
critical splice donor site |
probably null |
|
R1438:Zzef1
|
UTSW |
11 |
72,803,771 (GRCm39) |
missense |
probably damaging |
0.96 |
R1466:Zzef1
|
UTSW |
11 |
72,815,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Zzef1
|
UTSW |
11 |
72,815,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R1485:Zzef1
|
UTSW |
11 |
72,791,635 (GRCm39) |
splice site |
probably null |
|
R1556:Zzef1
|
UTSW |
11 |
72,806,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Zzef1
|
UTSW |
11 |
72,739,559 (GRCm39) |
nonsense |
probably null |
|
R1584:Zzef1
|
UTSW |
11 |
72,815,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R1643:Zzef1
|
UTSW |
11 |
72,717,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R1646:Zzef1
|
UTSW |
11 |
72,754,862 (GRCm39) |
critical splice donor site |
probably null |
|
R1764:Zzef1
|
UTSW |
11 |
72,784,158 (GRCm39) |
missense |
probably benign |
0.00 |
R1777:Zzef1
|
UTSW |
11 |
72,801,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1900:Zzef1
|
UTSW |
11 |
72,739,540 (GRCm39) |
missense |
probably damaging |
0.99 |
R2096:Zzef1
|
UTSW |
11 |
72,763,465 (GRCm39) |
missense |
probably benign |
0.02 |
R2134:Zzef1
|
UTSW |
11 |
72,771,450 (GRCm39) |
missense |
probably benign |
0.02 |
R2157:Zzef1
|
UTSW |
11 |
72,739,460 (GRCm39) |
splice site |
probably benign |
|
R2183:Zzef1
|
UTSW |
11 |
72,777,544 (GRCm39) |
nonsense |
probably null |
|
R2192:Zzef1
|
UTSW |
11 |
72,800,982 (GRCm39) |
splice site |
probably null |
|
R2230:Zzef1
|
UTSW |
11 |
72,775,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R2259:Zzef1
|
UTSW |
11 |
72,791,459 (GRCm39) |
nonsense |
probably null |
|
R2384:Zzef1
|
UTSW |
11 |
72,749,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R2426:Zzef1
|
UTSW |
11 |
72,806,091 (GRCm39) |
missense |
probably benign |
0.01 |
R2915:Zzef1
|
UTSW |
11 |
72,801,152 (GRCm39) |
splice site |
probably null |
|
R3700:Zzef1
|
UTSW |
11 |
72,777,598 (GRCm39) |
missense |
probably null |
1.00 |
R3875:Zzef1
|
UTSW |
11 |
72,779,866 (GRCm39) |
missense |
probably benign |
0.22 |
R3902:Zzef1
|
UTSW |
11 |
72,799,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R3927:Zzef1
|
UTSW |
11 |
72,749,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R4086:Zzef1
|
UTSW |
11 |
72,765,879 (GRCm39) |
missense |
probably benign |
0.02 |
R4301:Zzef1
|
UTSW |
11 |
72,779,861 (GRCm39) |
missense |
probably damaging |
0.96 |
R4359:Zzef1
|
UTSW |
11 |
72,714,334 (GRCm39) |
missense |
probably damaging |
0.98 |
R4382:Zzef1
|
UTSW |
11 |
72,765,938 (GRCm39) |
missense |
probably benign |
0.00 |
R4453:Zzef1
|
UTSW |
11 |
72,763,465 (GRCm39) |
missense |
probably benign |
0.02 |
R4466:Zzef1
|
UTSW |
11 |
72,815,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R4471:Zzef1
|
UTSW |
11 |
72,804,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Zzef1
|
UTSW |
11 |
72,778,996 (GRCm39) |
missense |
probably benign |
0.32 |
R4511:Zzef1
|
UTSW |
11 |
72,778,996 (GRCm39) |
missense |
probably benign |
0.32 |
R4714:Zzef1
|
UTSW |
11 |
72,728,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Zzef1
|
UTSW |
11 |
72,750,449 (GRCm39) |
missense |
probably benign |
0.12 |
R4906:Zzef1
|
UTSW |
11 |
72,792,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R5075:Zzef1
|
UTSW |
11 |
72,749,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R5357:Zzef1
|
UTSW |
11 |
72,734,159 (GRCm39) |
nonsense |
probably null |
|
R5579:Zzef1
|
UTSW |
11 |
72,791,463 (GRCm39) |
missense |
probably damaging |
0.98 |
R5598:Zzef1
|
UTSW |
11 |
72,807,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R5725:Zzef1
|
UTSW |
11 |
72,746,308 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5765:Zzef1
|
UTSW |
11 |
72,712,763 (GRCm39) |
nonsense |
probably null |
|
R5928:Zzef1
|
UTSW |
11 |
72,803,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R6003:Zzef1
|
UTSW |
11 |
72,714,891 (GRCm39) |
splice site |
probably null |
|
R6047:Zzef1
|
UTSW |
11 |
72,756,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R6224:Zzef1
|
UTSW |
11 |
72,746,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R6225:Zzef1
|
UTSW |
11 |
72,760,631 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6287:Zzef1
|
UTSW |
11 |
72,813,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R6361:Zzef1
|
UTSW |
11 |
72,775,175 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6451:Zzef1
|
UTSW |
11 |
72,813,982 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6467:Zzef1
|
UTSW |
11 |
72,802,090 (GRCm39) |
critical splice donor site |
probably null |
|
R6484:Zzef1
|
UTSW |
11 |
72,786,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6493:Zzef1
|
UTSW |
11 |
72,804,129 (GRCm39) |
missense |
probably benign |
0.06 |
R6520:Zzef1
|
UTSW |
11 |
72,716,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R6527:Zzef1
|
UTSW |
11 |
72,765,816 (GRCm39) |
missense |
probably benign |
0.00 |
R6540:Zzef1
|
UTSW |
11 |
72,804,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R6608:Zzef1
|
UTSW |
11 |
72,803,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R6795:Zzef1
|
UTSW |
11 |
72,741,485 (GRCm39) |
missense |
probably benign |
0.00 |
R6927:Zzef1
|
UTSW |
11 |
72,803,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R6987:Zzef1
|
UTSW |
11 |
72,746,340 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7048:Zzef1
|
UTSW |
11 |
72,757,525 (GRCm39) |
nonsense |
probably null |
|
R7076:Zzef1
|
UTSW |
11 |
72,790,385 (GRCm39) |
missense |
probably benign |
0.00 |
R7099:Zzef1
|
UTSW |
11 |
72,763,475 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7132:Zzef1
|
UTSW |
11 |
72,808,697 (GRCm39) |
critical splice donor site |
probably null |
|
R7175:Zzef1
|
UTSW |
11 |
72,742,727 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7284:Zzef1
|
UTSW |
11 |
72,777,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R7300:Zzef1
|
UTSW |
11 |
72,765,830 (GRCm39) |
missense |
probably benign |
0.02 |
R7486:Zzef1
|
UTSW |
11 |
72,755,612 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7503:Zzef1
|
UTSW |
11 |
72,716,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Zzef1
|
UTSW |
11 |
72,784,104 (GRCm39) |
missense |
probably benign |
|
R7874:Zzef1
|
UTSW |
11 |
72,750,479 (GRCm39) |
missense |
probably benign |
0.01 |
R7898:Zzef1
|
UTSW |
11 |
72,687,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7928:Zzef1
|
UTSW |
11 |
72,712,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R8021:Zzef1
|
UTSW |
11 |
72,714,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R8145:Zzef1
|
UTSW |
11 |
72,799,295 (GRCm39) |
nonsense |
probably null |
|
R8255:Zzef1
|
UTSW |
11 |
72,765,955 (GRCm39) |
missense |
probably benign |
0.00 |
R8303:Zzef1
|
UTSW |
11 |
72,808,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Zzef1
|
UTSW |
11 |
72,777,572 (GRCm39) |
missense |
probably damaging |
0.97 |
R8492:Zzef1
|
UTSW |
11 |
72,763,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R8498:Zzef1
|
UTSW |
11 |
72,744,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R8547:Zzef1
|
UTSW |
11 |
72,735,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R8874:Zzef1
|
UTSW |
11 |
72,754,815 (GRCm39) |
missense |
probably benign |
0.00 |
R8885:Zzef1
|
UTSW |
11 |
72,687,402 (GRCm39) |
missense |
probably benign |
0.00 |
R8972:Zzef1
|
UTSW |
11 |
72,791,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R8979:Zzef1
|
UTSW |
11 |
72,766,003 (GRCm39) |
missense |
probably benign |
0.00 |
R9053:Zzef1
|
UTSW |
11 |
72,813,302 (GRCm39) |
missense |
probably benign |
|
R9108:Zzef1
|
UTSW |
11 |
72,790,604 (GRCm39) |
missense |
probably benign |
0.11 |
R9121:Zzef1
|
UTSW |
11 |
72,756,946 (GRCm39) |
nonsense |
probably null |
|
R9253:Zzef1
|
UTSW |
11 |
72,739,463 (GRCm39) |
splice site |
probably benign |
|
R9370:Zzef1
|
UTSW |
11 |
72,744,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R9408:Zzef1
|
UTSW |
11 |
72,755,653 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9467:Zzef1
|
UTSW |
11 |
72,807,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9468:Zzef1
|
UTSW |
11 |
72,814,009 (GRCm39) |
critical splice donor site |
probably null |
|
R9563:Zzef1
|
UTSW |
11 |
72,765,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R9647:Zzef1
|
UTSW |
11 |
72,760,651 (GRCm39) |
missense |
probably benign |
0.01 |
R9667:Zzef1
|
UTSW |
11 |
72,758,786 (GRCm39) |
missense |
probably benign |
|
R9742:Zzef1
|
UTSW |
11 |
72,749,179 (GRCm39) |
missense |
probably benign |
|
X0028:Zzef1
|
UTSW |
11 |
72,797,805 (GRCm39) |
missense |
probably benign |
0.29 |
Z1176:Zzef1
|
UTSW |
11 |
72,687,354 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zzef1
|
UTSW |
11 |
72,791,457 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Zzef1
|
UTSW |
11 |
72,717,004 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zzef1
|
UTSW |
11 |
72,687,138 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Zzef1
|
UTSW |
11 |
72,806,146 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1187:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1188:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1189:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1190:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1191:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
Z1192:Zzef1
|
UTSW |
11 |
72,780,008 (GRCm39) |
missense |
probably benign |
|
|