Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arl14ep |
G |
T |
2: 106,799,663 (GRCm39) |
H59Q |
probably damaging |
Het |
Atp6v0a4 |
T |
A |
6: 38,055,749 (GRCm39) |
I321F |
possibly damaging |
Het |
Cdr2l |
A |
G |
11: 115,284,651 (GRCm39) |
D329G |
possibly damaging |
Het |
Cep55 |
A |
G |
19: 38,058,364 (GRCm39) |
E319G |
probably damaging |
Het |
Cfhr2 |
C |
T |
1: 139,741,265 (GRCm39) |
V237I |
probably benign |
Het |
Clasrp |
A |
G |
7: 19,318,703 (GRCm39) |
|
probably null |
Het |
Col12a1 |
C |
A |
9: 79,607,632 (GRCm39) |
E399* |
probably null |
Het |
Cyp19a1 |
T |
A |
9: 54,080,647 (GRCm39) |
I237F |
probably benign |
Het |
Dnajc6 |
T |
G |
4: 101,494,010 (GRCm39) |
N847K |
probably damaging |
Het |
E330013P04Rik |
C |
G |
19: 60,150,453 (GRCm39) |
|
noncoding transcript |
Het |
Entpd2 |
A |
G |
2: 25,289,429 (GRCm39) |
T304A |
probably benign |
Het |
Fam107b |
A |
T |
2: 3,773,907 (GRCm39) |
I35L |
probably benign |
Het |
Fgg |
A |
T |
3: 82,920,175 (GRCm39) |
Y318F |
probably benign |
Het |
Fitm1 |
A |
C |
14: 55,814,076 (GRCm39) |
T191P |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,924,583 (GRCm39) |
M3675V |
probably damaging |
Het |
Fry |
C |
T |
5: 150,401,454 (GRCm39) |
R731W |
probably damaging |
Het |
Galnt17 |
A |
T |
5: 131,335,237 (GRCm39) |
S68T |
probably benign |
Het |
Glp2r |
G |
T |
11: 67,648,419 (GRCm39) |
Y94* |
probably null |
Het |
Grm1 |
C |
T |
10: 10,812,257 (GRCm39) |
A256T |
probably damaging |
Het |
Hoxd13 |
A |
G |
2: 74,499,027 (GRCm39) |
Y125C |
probably benign |
Het |
Hspa14 |
A |
T |
2: 3,492,646 (GRCm39) |
I373K |
probably benign |
Het |
Ifnlr1 |
A |
G |
4: 135,432,593 (GRCm39) |
E343G |
probably benign |
Het |
Ighv5-9 |
A |
G |
12: 113,625,582 (GRCm39) |
S54P |
probably benign |
Het |
Insyn2b |
G |
A |
11: 34,352,231 (GRCm39) |
G91E |
probably damaging |
Het |
Irf2bpl |
A |
G |
12: 86,928,892 (GRCm39) |
S594P |
possibly damaging |
Het |
Kcnq2 |
A |
G |
2: 180,728,766 (GRCm39) |
S548P |
probably damaging |
Het |
Lrp2 |
G |
A |
2: 69,302,712 (GRCm39) |
R3006W |
probably damaging |
Het |
Lrrc4c |
A |
T |
2: 97,459,646 (GRCm39) |
I91F |
probably damaging |
Het |
Mdh1b |
T |
C |
1: 63,750,663 (GRCm39) |
D435G |
probably benign |
Het |
Mettl3 |
A |
T |
14: 52,537,184 (GRCm39) |
S182T |
probably damaging |
Het |
Mllt6 |
A |
G |
11: 97,569,233 (GRCm39) |
T862A |
probably benign |
Het |
Mmp27 |
G |
T |
9: 7,578,983 (GRCm39) |
R412I |
probably damaging |
Het |
Mstn |
A |
G |
1: 53,105,582 (GRCm39) |
N308S |
possibly damaging |
Het |
Ncapg |
A |
G |
5: 45,828,551 (GRCm39) |
T101A |
probably benign |
Het |
Ngf |
C |
T |
3: 102,427,790 (GRCm39) |
R180W |
probably damaging |
Het |
Notch1 |
G |
A |
2: 26,364,136 (GRCm39) |
Q862* |
probably null |
Het |
Nsrp1 |
T |
C |
11: 76,936,570 (GRCm39) |
D542G |
probably damaging |
Het |
Nup214 |
C |
A |
2: 31,873,171 (GRCm39) |
T255K |
probably benign |
Het |
Or5b21 |
T |
A |
19: 12,839,916 (GRCm39) |
M259K |
probably damaging |
Het |
Or8b43 |
T |
A |
9: 38,360,679 (GRCm39) |
D170E |
probably benign |
Het |
Papln |
C |
T |
12: 83,829,677 (GRCm39) |
P911S |
probably benign |
Het |
Pdxdc1 |
A |
G |
16: 13,693,933 (GRCm39) |
V163A |
probably benign |
Het |
Plekhj1 |
A |
T |
10: 80,633,609 (GRCm39) |
I76N |
probably damaging |
Het |
Pnp2 |
A |
G |
14: 51,201,025 (GRCm39) |
|
probably null |
Het |
Polr3gl |
T |
C |
3: 96,487,208 (GRCm39) |
E89G |
probably benign |
Het |
Polrmt |
A |
G |
10: 79,582,385 (GRCm39) |
M1T |
probably null |
Het |
Prss37 |
A |
G |
6: 40,491,917 (GRCm39) |
I221T |
possibly damaging |
Het |
Ptx4 |
C |
T |
17: 25,342,139 (GRCm39) |
Q205* |
probably null |
Het |
Qsox1 |
T |
C |
1: 155,655,414 (GRCm39) |
E583G |
probably benign |
Het |
Riok3 |
T |
A |
18: 12,288,300 (GRCm39) |
N492K |
probably benign |
Het |
Sec13 |
A |
G |
6: 113,712,153 (GRCm39) |
W61R |
probably damaging |
Het |
Slc20a2 |
T |
C |
8: 23,051,221 (GRCm39) |
V418A |
possibly damaging |
Het |
Smad9 |
G |
A |
3: 54,696,651 (GRCm39) |
V239I |
probably benign |
Het |
Stmn2 |
A |
G |
3: 8,610,792 (GRCm39) |
E92G |
probably damaging |
Het |
Taf1c |
A |
G |
8: 120,325,537 (GRCm39) |
V775A |
probably benign |
Het |
Thsd7a |
T |
A |
6: 12,330,991 (GRCm39) |
I1384L |
probably benign |
Het |
Tnxb |
A |
G |
17: 34,932,606 (GRCm39) |
Y2275C |
probably damaging |
Het |
Trmo |
G |
T |
4: 46,382,388 (GRCm39) |
T243N |
probably benign |
Het |
Tyrp1 |
C |
T |
4: 80,758,883 (GRCm39) |
A252V |
probably damaging |
Het |
Vasp |
T |
C |
7: 18,991,642 (GRCm39) |
*376W |
probably null |
Het |
Vmn1r231 |
T |
C |
17: 21,110,613 (GRCm39) |
I101V |
possibly damaging |
Het |
Zfp532 |
T |
C |
18: 65,756,837 (GRCm39) |
S257P |
probably benign |
Het |
Zfp563 |
G |
A |
17: 33,324,683 (GRCm39) |
C426Y |
probably damaging |
Het |
Zfp647 |
TGCACG |
TGCACGCACG |
15: 76,795,244 (GRCm39) |
|
probably null |
Het |
Zfp703 |
C |
A |
8: 27,469,801 (GRCm39) |
H488Q |
probably damaging |
Het |
Zfp964 |
A |
G |
8: 70,116,758 (GRCm39) |
N452D |
possibly damaging |
Het |
Zfyve28 |
A |
C |
5: 34,390,698 (GRCm39) |
Y188D |
probably damaging |
Het |
|
Other mutations in Etl4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00907:Etl4
|
APN |
2 |
20,771,289 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00944:Etl4
|
APN |
2 |
20,534,865 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01078:Etl4
|
APN |
2 |
20,811,342 (GRCm39) |
nonsense |
probably null |
|
IGL01099:Etl4
|
APN |
2 |
20,811,922 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01337:Etl4
|
APN |
2 |
20,790,198 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01348:Etl4
|
APN |
2 |
20,811,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01349:Etl4
|
APN |
2 |
20,718,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01407:Etl4
|
APN |
2 |
20,748,667 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01552:Etl4
|
APN |
2 |
20,783,000 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01662:Etl4
|
APN |
2 |
20,811,460 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01687:Etl4
|
APN |
2 |
20,534,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01793:Etl4
|
APN |
2 |
20,748,709 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01844:Etl4
|
APN |
2 |
20,811,493 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02025:Etl4
|
APN |
2 |
20,811,337 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02088:Etl4
|
APN |
2 |
20,811,359 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02134:Etl4
|
APN |
2 |
20,811,240 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02369:Etl4
|
APN |
2 |
20,535,000 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02480:Etl4
|
APN |
2 |
20,793,335 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02560:Etl4
|
APN |
2 |
20,748,529 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Etl4
|
APN |
2 |
20,812,840 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02893:Etl4
|
APN |
2 |
20,765,021 (GRCm39) |
splice site |
probably benign |
|
IGL02951:Etl4
|
APN |
2 |
20,806,348 (GRCm39) |
splice site |
probably benign |
|
IGL03119:Etl4
|
APN |
2 |
20,718,198 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Etl4
|
APN |
2 |
20,789,993 (GRCm39) |
nonsense |
probably null |
|
IGL03379:Etl4
|
APN |
2 |
20,666,827 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0038:Etl4
|
UTSW |
2 |
20,748,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R0038:Etl4
|
UTSW |
2 |
20,748,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R0095:Etl4
|
UTSW |
2 |
20,748,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0100:Etl4
|
UTSW |
2 |
20,344,716 (GRCm39) |
missense |
probably benign |
|
R0311:Etl4
|
UTSW |
2 |
20,811,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R0346:Etl4
|
UTSW |
2 |
20,764,463 (GRCm39) |
critical splice donor site |
probably null |
|
R0348:Etl4
|
UTSW |
2 |
20,782,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R0379:Etl4
|
UTSW |
2 |
20,812,165 (GRCm39) |
missense |
probably damaging |
0.98 |
R0571:Etl4
|
UTSW |
2 |
20,748,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R0697:Etl4
|
UTSW |
2 |
20,748,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0707:Etl4
|
UTSW |
2 |
20,810,382 (GRCm39) |
splice site |
probably benign |
|
R0980:Etl4
|
UTSW |
2 |
20,806,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R1120:Etl4
|
UTSW |
2 |
20,811,514 (GRCm39) |
missense |
probably benign |
0.00 |
R1254:Etl4
|
UTSW |
2 |
20,812,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R1346:Etl4
|
UTSW |
2 |
20,810,955 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1460:Etl4
|
UTSW |
2 |
20,793,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R1503:Etl4
|
UTSW |
2 |
20,748,685 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1547:Etl4
|
UTSW |
2 |
20,790,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R1627:Etl4
|
UTSW |
2 |
20,806,390 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1635:Etl4
|
UTSW |
2 |
20,811,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R1716:Etl4
|
UTSW |
2 |
20,748,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R1795:Etl4
|
UTSW |
2 |
20,812,837 (GRCm39) |
critical splice donor site |
probably null |
|
R1885:Etl4
|
UTSW |
2 |
20,748,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R2039:Etl4
|
UTSW |
2 |
20,790,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Etl4
|
UTSW |
2 |
20,748,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Etl4
|
UTSW |
2 |
20,790,153 (GRCm39) |
missense |
probably benign |
0.27 |
R2153:Etl4
|
UTSW |
2 |
20,803,545 (GRCm39) |
missense |
probably benign |
0.00 |
R2403:Etl4
|
UTSW |
2 |
20,812,117 (GRCm39) |
nonsense |
probably null |
|
R2883:Etl4
|
UTSW |
2 |
20,810,985 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2985:Etl4
|
UTSW |
2 |
20,786,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R3402:Etl4
|
UTSW |
2 |
20,786,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R3696:Etl4
|
UTSW |
2 |
20,806,473 (GRCm39) |
critical splice donor site |
probably null |
|
R3755:Etl4
|
UTSW |
2 |
20,748,348 (GRCm39) |
missense |
probably benign |
0.10 |
R3813:Etl4
|
UTSW |
2 |
20,793,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R3829:Etl4
|
UTSW |
2 |
20,790,232 (GRCm39) |
missense |
probably benign |
0.07 |
R3887:Etl4
|
UTSW |
2 |
20,534,772 (GRCm39) |
nonsense |
probably null |
|
R3888:Etl4
|
UTSW |
2 |
20,534,772 (GRCm39) |
nonsense |
probably null |
|
R3889:Etl4
|
UTSW |
2 |
20,534,772 (GRCm39) |
nonsense |
probably null |
|
R3958:Etl4
|
UTSW |
2 |
20,344,854 (GRCm39) |
missense |
probably benign |
|
R3959:Etl4
|
UTSW |
2 |
20,344,854 (GRCm39) |
missense |
probably benign |
|
R3960:Etl4
|
UTSW |
2 |
20,344,854 (GRCm39) |
missense |
probably benign |
|
R4058:Etl4
|
UTSW |
2 |
20,810,830 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4074:Etl4
|
UTSW |
2 |
20,814,030 (GRCm39) |
utr 3 prime |
probably benign |
|
R4077:Etl4
|
UTSW |
2 |
20,812,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R4078:Etl4
|
UTSW |
2 |
20,812,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R4127:Etl4
|
UTSW |
2 |
20,748,886 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4200:Etl4
|
UTSW |
2 |
20,786,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R4492:Etl4
|
UTSW |
2 |
20,811,676 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4514:Etl4
|
UTSW |
2 |
20,666,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Etl4
|
UTSW |
2 |
20,811,496 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4825:Etl4
|
UTSW |
2 |
20,811,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4888:Etl4
|
UTSW |
2 |
20,344,922 (GRCm39) |
critical splice donor site |
probably null |
|
R4943:Etl4
|
UTSW |
2 |
20,812,092 (GRCm39) |
missense |
probably benign |
0.05 |
R5121:Etl4
|
UTSW |
2 |
20,344,922 (GRCm39) |
critical splice donor site |
probably null |
|
R5191:Etl4
|
UTSW |
2 |
20,344,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R5198:Etl4
|
UTSW |
2 |
20,718,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5199:Etl4
|
UTSW |
2 |
20,748,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R5470:Etl4
|
UTSW |
2 |
20,534,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R5513:Etl4
|
UTSW |
2 |
20,748,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R5620:Etl4
|
UTSW |
2 |
20,535,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5635:Etl4
|
UTSW |
2 |
20,811,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R5641:Etl4
|
UTSW |
2 |
20,811,273 (GRCm39) |
frame shift |
probably null |
|
R5690:Etl4
|
UTSW |
2 |
20,810,647 (GRCm39) |
missense |
probably benign |
0.01 |
R5784:Etl4
|
UTSW |
2 |
20,811,016 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5794:Etl4
|
UTSW |
2 |
20,811,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R5908:Etl4
|
UTSW |
2 |
20,748,718 (GRCm39) |
missense |
probably damaging |
0.96 |
R5982:Etl4
|
UTSW |
2 |
20,785,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Etl4
|
UTSW |
2 |
20,718,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Etl4
|
UTSW |
2 |
20,806,362 (GRCm39) |
missense |
probably damaging |
0.98 |
R6238:Etl4
|
UTSW |
2 |
20,806,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R6248:Etl4
|
UTSW |
2 |
20,813,900 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6292:Etl4
|
UTSW |
2 |
20,748,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R6610:Etl4
|
UTSW |
2 |
20,718,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R6739:Etl4
|
UTSW |
2 |
20,718,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6846:Etl4
|
UTSW |
2 |
20,748,919 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6863:Etl4
|
UTSW |
2 |
20,811,120 (GRCm39) |
missense |
probably benign |
0.01 |
R6873:Etl4
|
UTSW |
2 |
20,802,803 (GRCm39) |
splice site |
probably null |
|
R7003:Etl4
|
UTSW |
2 |
20,810,695 (GRCm39) |
missense |
probably benign |
0.03 |
R7155:Etl4
|
UTSW |
2 |
20,811,742 (GRCm39) |
missense |
probably damaging |
0.96 |
R7207:Etl4
|
UTSW |
2 |
20,714,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R7230:Etl4
|
UTSW |
2 |
20,802,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R7305:Etl4
|
UTSW |
2 |
20,714,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R7389:Etl4
|
UTSW |
2 |
20,789,904 (GRCm39) |
nonsense |
probably null |
|
R7396:Etl4
|
UTSW |
2 |
20,803,449 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7441:Etl4
|
UTSW |
2 |
20,749,000 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7626:Etl4
|
UTSW |
2 |
20,718,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7776:Etl4
|
UTSW |
2 |
20,811,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R7779:Etl4
|
UTSW |
2 |
20,714,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R7798:Etl4
|
UTSW |
2 |
20,786,757 (GRCm39) |
critical splice donor site |
probably null |
|
R7851:Etl4
|
UTSW |
2 |
20,748,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R7861:Etl4
|
UTSW |
2 |
20,810,721 (GRCm39) |
missense |
probably benign |
|
R7901:Etl4
|
UTSW |
2 |
20,294,821 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8053:Etl4
|
UTSW |
2 |
20,666,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Etl4
|
UTSW |
2 |
20,811,451 (GRCm39) |
missense |
probably benign |
0.06 |
R8133:Etl4
|
UTSW |
2 |
20,811,082 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8203:Etl4
|
UTSW |
2 |
20,789,916 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8238:Etl4
|
UTSW |
2 |
20,811,342 (GRCm39) |
nonsense |
probably null |
|
R8263:Etl4
|
UTSW |
2 |
20,748,965 (GRCm39) |
missense |
probably benign |
0.00 |
R8299:Etl4
|
UTSW |
2 |
20,748,874 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8318:Etl4
|
UTSW |
2 |
20,793,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Etl4
|
UTSW |
2 |
20,785,857 (GRCm39) |
missense |
probably damaging |
0.96 |
R8443:Etl4
|
UTSW |
2 |
20,810,977 (GRCm39) |
missense |
probably benign |
0.04 |
R8525:Etl4
|
UTSW |
2 |
20,534,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R8679:Etl4
|
UTSW |
2 |
20,714,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R8918:Etl4
|
UTSW |
2 |
20,811,246 (GRCm39) |
missense |
probably benign |
0.00 |
R8918:Etl4
|
UTSW |
2 |
20,748,733 (GRCm39) |
missense |
probably benign |
|
R9062:Etl4
|
UTSW |
2 |
20,748,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R9095:Etl4
|
UTSW |
2 |
20,782,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R9200:Etl4
|
UTSW |
2 |
20,786,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R9416:Etl4
|
UTSW |
2 |
20,748,784 (GRCm39) |
missense |
probably benign |
0.17 |
R9437:Etl4
|
UTSW |
2 |
20,813,872 (GRCm39) |
missense |
probably benign |
0.20 |
R9451:Etl4
|
UTSW |
2 |
20,813,926 (GRCm39) |
missense |
probably benign |
0.03 |
R9489:Etl4
|
UTSW |
2 |
20,771,345 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9531:Etl4
|
UTSW |
2 |
20,294,818 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R9605:Etl4
|
UTSW |
2 |
20,771,345 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9623:Etl4
|
UTSW |
2 |
20,811,052 (GRCm39) |
missense |
|
|
R9631:Etl4
|
UTSW |
2 |
20,666,749 (GRCm39) |
missense |
probably benign |
0.28 |
R9632:Etl4
|
UTSW |
2 |
20,666,749 (GRCm39) |
missense |
probably benign |
0.28 |
R9646:Etl4
|
UTSW |
2 |
20,802,724 (GRCm39) |
missense |
probably benign |
0.00 |
R9732:Etl4
|
UTSW |
2 |
20,748,373 (GRCm39) |
missense |
probably damaging |
0.98 |
R9755:Etl4
|
UTSW |
2 |
20,790,048 (GRCm39) |
missense |
probably benign |
0.17 |
R9771:Etl4
|
UTSW |
2 |
20,811,537 (GRCm39) |
missense |
probably benign |
|
RF003:Etl4
|
UTSW |
2 |
20,524,729 (GRCm39) |
nonsense |
probably null |
|
X0018:Etl4
|
UTSW |
2 |
20,814,001 (GRCm39) |
missense |
probably damaging |
0.98 |
X0022:Etl4
|
UTSW |
2 |
20,714,375 (GRCm39) |
missense |
probably damaging |
1.00 |
|