Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
G |
T |
7: 45,679,680 (GRCm39) |
T9K |
probably benign |
Het |
Ankrd28 |
T |
C |
14: 31,429,177 (GRCm39) |
H925R |
probably damaging |
Het |
Antxrl |
A |
T |
14: 33,778,556 (GRCm39) |
T128S |
probably damaging |
Het |
Atosa |
A |
G |
9: 74,913,645 (GRCm39) |
M100V |
possibly damaging |
Het |
Atp8b5 |
T |
C |
4: 43,304,674 (GRCm39) |
Y62H |
probably damaging |
Het |
Bmpr2 |
G |
T |
1: 59,906,595 (GRCm39) |
V563L |
probably benign |
Het |
Btn1a1 |
A |
T |
13: 23,648,521 (GRCm39) |
L104Q |
probably damaging |
Het |
Caskin1 |
C |
G |
17: 24,726,154 (GRCm39) |
D1420E |
probably damaging |
Het |
Cdc14a |
A |
T |
3: 116,144,862 (GRCm39) |
I150N |
probably damaging |
Het |
Cdc26 |
C |
T |
4: 62,321,031 (GRCm39) |
R4Q |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,236,496 (GRCm39) |
D160G |
probably damaging |
Het |
Cxcr4 |
A |
C |
1: 128,519,920 (GRCm39) |
|
probably null |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dgat1 |
T |
C |
15: 76,387,493 (GRCm39) |
N317S |
possibly damaging |
Het |
Disp1 |
G |
A |
1: 182,880,589 (GRCm39) |
T228M |
possibly damaging |
Het |
Dixdc1 |
A |
C |
9: 50,614,656 (GRCm39) |
|
probably null |
Het |
Dnase1l2 |
C |
A |
17: 24,661,492 (GRCm39) |
|
probably benign |
Het |
Dsg2 |
T |
C |
18: 20,727,350 (GRCm39) |
|
probably null |
Het |
Duox2 |
A |
T |
2: 122,117,674 (GRCm39) |
F887I |
probably benign |
Het |
Duxf4 |
A |
G |
10: 58,071,344 (GRCm39) |
M290T |
probably benign |
Het |
Efcab6 |
T |
C |
15: 83,851,825 (GRCm39) |
D351G |
possibly damaging |
Het |
Epg5 |
G |
T |
18: 77,991,677 (GRCm39) |
V125F |
possibly damaging |
Het |
Ephb1 |
T |
C |
9: 101,800,783 (GRCm39) |
R953G |
probably damaging |
Het |
Etfdh |
G |
T |
3: 79,519,336 (GRCm39) |
Y272* |
probably null |
Het |
Fam117b |
A |
G |
1: 60,008,207 (GRCm39) |
E347G |
probably damaging |
Het |
Gfra3 |
A |
T |
18: 34,828,846 (GRCm39) |
C183S |
probably damaging |
Het |
Gmip |
A |
G |
8: 70,268,773 (GRCm39) |
D466G |
probably damaging |
Het |
Golga5 |
G |
A |
12: 102,450,740 (GRCm39) |
M464I |
probably benign |
Het |
Gpd1 |
A |
T |
15: 99,621,146 (GRCm39) |
Q320L |
possibly damaging |
Het |
H2-Oa |
G |
T |
17: 34,312,851 (GRCm39) |
D43Y |
probably damaging |
Het |
Hecw1 |
T |
A |
13: 14,520,623 (GRCm39) |
I205F |
probably damaging |
Het |
Ighv8-13 |
A |
G |
12: 115,728,973 (GRCm39) |
Y95H |
probably damaging |
Het |
Igkv6-20 |
T |
C |
6: 70,313,081 (GRCm39) |
M31V |
possibly damaging |
Het |
Itih1 |
T |
C |
14: 30,653,217 (GRCm39) |
D737G |
probably benign |
Het |
Kcnc4 |
G |
C |
3: 107,355,693 (GRCm39) |
H252D |
probably damaging |
Het |
Kcnj14 |
T |
A |
7: 45,468,921 (GRCm39) |
T195S |
probably damaging |
Het |
Limch1 |
A |
T |
5: 67,173,845 (GRCm39) |
D642V |
probably damaging |
Het |
Lrp2 |
T |
G |
2: 69,312,710 (GRCm39) |
D2526A |
possibly damaging |
Het |
Lrrc8a |
A |
G |
2: 30,146,565 (GRCm39) |
T460A |
possibly damaging |
Het |
Lrrn4cl |
A |
G |
19: 8,829,135 (GRCm39) |
T38A |
probably benign |
Het |
Lypd8 |
A |
T |
11: 58,277,629 (GRCm39) |
Q137L |
possibly damaging |
Het |
Mapkapk3 |
A |
G |
9: 107,137,262 (GRCm39) |
Y206H |
probably damaging |
Het |
Mrc1 |
G |
A |
2: 14,276,115 (GRCm39) |
G483D |
probably benign |
Het |
Mrpl35 |
C |
A |
6: 71,800,661 (GRCm39) |
|
probably benign |
Het |
Mycbp2 |
T |
A |
14: 103,497,665 (GRCm39) |
H936L |
probably benign |
Het |
Myh3 |
A |
T |
11: 66,978,312 (GRCm39) |
Y433F |
probably benign |
Het |
Napb |
C |
T |
2: 148,540,098 (GRCm39) |
|
probably null |
Het |
Nbeal1 |
C |
A |
1: 60,335,083 (GRCm39) |
Q2288K |
probably benign |
Het |
Ndst3 |
G |
A |
3: 123,465,301 (GRCm39) |
Q224* |
probably null |
Het |
Nkapd1 |
A |
G |
9: 50,518,971 (GRCm39) |
S214P |
possibly damaging |
Het |
Nkd2 |
A |
G |
13: 73,969,579 (GRCm39) |
S284P |
probably benign |
Het |
Or10a2 |
T |
C |
7: 106,673,343 (GRCm39) |
Y103H |
probably damaging |
Het |
Or5b12 |
A |
T |
19: 12,897,301 (GRCm39) |
V124E |
probably damaging |
Het |
Or6k2 |
G |
A |
1: 173,979,712 (GRCm39) |
S210N |
probably benign |
Het |
Or8h10 |
T |
C |
2: 86,809,035 (GRCm39) |
Y35C |
probably damaging |
Het |
Pcdhb8 |
A |
G |
18: 37,490,037 (GRCm39) |
T572A |
probably benign |
Het |
Pcdhb9 |
A |
G |
18: 37,535,115 (GRCm39) |
I370V |
probably benign |
Het |
Pcsk5 |
T |
G |
19: 17,558,631 (GRCm39) |
E592A |
possibly damaging |
Het |
Pigc |
T |
C |
1: 161,798,036 (GRCm39) |
V6A |
probably benign |
Het |
Pla2g6 |
T |
G |
15: 79,189,924 (GRCm39) |
I389L |
probably benign |
Het |
Pnliprp2 |
T |
C |
19: 58,751,874 (GRCm39) |
|
probably null |
Het |
Psmb11 |
T |
C |
14: 54,863,646 (GRCm39) |
V288A |
probably benign |
Het |
Rapgef5 |
A |
G |
12: 117,685,398 (GRCm39) |
|
probably null |
Het |
Rcn3 |
T |
C |
7: 44,732,720 (GRCm39) |
N316S |
probably damaging |
Het |
Rgs6 |
A |
G |
12: 83,112,738 (GRCm39) |
K183E |
probably damaging |
Het |
Rhoc |
A |
G |
3: 104,700,297 (GRCm39) |
|
probably null |
Het |
Serinc5 |
T |
C |
13: 92,844,616 (GRCm39) |
C453R |
probably damaging |
Het |
Slc14a1 |
A |
C |
18: 78,159,614 (GRCm39) |
M93R |
probably damaging |
Het |
Slc25a3 |
A |
T |
10: 90,958,090 (GRCm39) |
D83E |
probably damaging |
Het |
Slc36a3 |
T |
C |
11: 55,015,777 (GRCm39) |
Y459C |
probably benign |
Het |
Slc44a5 |
A |
T |
3: 153,944,800 (GRCm39) |
Y139F |
probably benign |
Het |
Spag17 |
A |
T |
3: 99,929,918 (GRCm39) |
Q539L |
probably benign |
Het |
Stap2 |
C |
T |
17: 56,306,976 (GRCm39) |
V234M |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,544,231 (GRCm39) |
Y4450C |
probably damaging |
Het |
Taf6l |
C |
T |
19: 8,756,030 (GRCm39) |
R206Q |
probably benign |
Het |
Tbc1d23 |
C |
T |
16: 57,003,266 (GRCm39) |
V501I |
probably damaging |
Het |
Thap2 |
T |
C |
10: 115,208,751 (GRCm39) |
H123R |
probably damaging |
Het |
Tlx3 |
C |
A |
11: 33,152,432 (GRCm39) |
W221L |
probably benign |
Het |
Tmem262 |
T |
A |
19: 6,130,567 (GRCm39) |
|
probably null |
Het |
Tpmt |
C |
A |
13: 47,180,735 (GRCm39) |
R201S |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,831,655 (GRCm39) |
S1507P |
probably damaging |
Het |
Ttc9c |
T |
C |
19: 8,795,847 (GRCm39) |
E64G |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,640,790 (GRCm39) |
S13653T |
probably damaging |
Het |
Ugt3a1 |
G |
T |
15: 9,310,726 (GRCm39) |
W336L |
possibly damaging |
Het |
Vmn1r215 |
C |
A |
13: 23,260,633 (GRCm39) |
N224K |
probably benign |
Het |
Vmn2r59 |
C |
T |
7: 41,691,835 (GRCm39) |
|
probably null |
Het |
Wdfy3 |
A |
G |
5: 102,046,295 (GRCm39) |
S1853P |
possibly damaging |
Het |
Wdr36 |
A |
T |
18: 32,975,059 (GRCm39) |
Y137F |
possibly damaging |
Het |
Zdhhc17 |
T |
C |
10: 110,792,216 (GRCm39) |
D324G |
probably benign |
Het |
Zfp217 |
T |
C |
2: 169,961,497 (GRCm39) |
T277A |
probably benign |
Het |
Zfp451 |
A |
G |
1: 33,842,219 (GRCm39) |
|
probably benign |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
Zfp871 |
T |
C |
17: 32,994,858 (GRCm39) |
S106G |
possibly damaging |
Het |
|
Other mutations in Ep400 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Ep400
|
APN |
5 |
110,835,707 (GRCm39) |
missense |
unknown |
|
IGL00585:Ep400
|
APN |
5 |
110,903,771 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL00586:Ep400
|
APN |
5 |
110,887,460 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00816:Ep400
|
APN |
5 |
110,883,356 (GRCm39) |
unclassified |
probably benign |
|
IGL01066:Ep400
|
APN |
5 |
110,816,065 (GRCm39) |
splice site |
probably benign |
|
IGL01302:Ep400
|
APN |
5 |
110,889,914 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01568:Ep400
|
APN |
5 |
110,867,361 (GRCm39) |
missense |
unknown |
|
IGL01833:Ep400
|
APN |
5 |
110,827,874 (GRCm39) |
missense |
unknown |
|
IGL02086:Ep400
|
APN |
5 |
110,824,809 (GRCm39) |
splice site |
probably benign |
|
IGL02266:Ep400
|
APN |
5 |
110,843,163 (GRCm39) |
unclassified |
probably benign |
|
IGL02288:Ep400
|
APN |
5 |
110,831,702 (GRCm39) |
splice site |
probably benign |
|
IGL02301:Ep400
|
APN |
5 |
110,822,826 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Ep400
|
APN |
5 |
110,868,691 (GRCm39) |
missense |
unknown |
|
IGL02382:Ep400
|
APN |
5 |
110,849,594 (GRCm39) |
missense |
unknown |
|
IGL02419:Ep400
|
APN |
5 |
110,845,242 (GRCm39) |
splice site |
probably null |
|
IGL02591:Ep400
|
APN |
5 |
110,881,638 (GRCm39) |
unclassified |
probably benign |
|
IGL02981:Ep400
|
APN |
5 |
110,839,476 (GRCm39) |
splice site |
probably benign |
|
IGL02981:Ep400
|
APN |
5 |
110,903,969 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03173:Ep400
|
APN |
5 |
110,856,737 (GRCm39) |
unclassified |
probably benign |
|
IGL03244:Ep400
|
APN |
5 |
110,875,429 (GRCm39) |
missense |
unknown |
|
IGL03333:Ep400
|
APN |
5 |
110,851,432 (GRCm39) |
missense |
unknown |
|
santol
|
UTSW |
5 |
110,849,537 (GRCm39) |
missense |
unknown |
|
PIT4243001:Ep400
|
UTSW |
5 |
110,883,446 (GRCm39) |
missense |
unknown |
|
PIT4260001:Ep400
|
UTSW |
5 |
110,841,037 (GRCm39) |
nonsense |
probably null |
|
R0017:Ep400
|
UTSW |
5 |
110,821,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R0179:Ep400
|
UTSW |
5 |
110,816,515 (GRCm39) |
missense |
probably damaging |
0.99 |
R0243:Ep400
|
UTSW |
5 |
110,872,273 (GRCm39) |
splice site |
probably benign |
|
R0366:Ep400
|
UTSW |
5 |
110,849,537 (GRCm39) |
missense |
unknown |
|
R0508:Ep400
|
UTSW |
5 |
110,887,374 (GRCm39) |
missense |
probably benign |
0.00 |
R0541:Ep400
|
UTSW |
5 |
110,852,882 (GRCm39) |
missense |
unknown |
|
R0558:Ep400
|
UTSW |
5 |
110,832,933 (GRCm39) |
splice site |
probably benign |
|
R0576:Ep400
|
UTSW |
5 |
110,858,959 (GRCm39) |
unclassified |
probably benign |
|
R0595:Ep400
|
UTSW |
5 |
110,851,408 (GRCm39) |
missense |
unknown |
|
R0671:Ep400
|
UTSW |
5 |
110,836,062 (GRCm39) |
missense |
unknown |
|
R0763:Ep400
|
UTSW |
5 |
110,813,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Ep400
|
UTSW |
5 |
110,883,388 (GRCm39) |
unclassified |
probably benign |
|
R1300:Ep400
|
UTSW |
5 |
110,821,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R1439:Ep400
|
UTSW |
5 |
110,833,344 (GRCm39) |
missense |
unknown |
|
R1520:Ep400
|
UTSW |
5 |
110,839,644 (GRCm39) |
intron |
probably benign |
|
R1529:Ep400
|
UTSW |
5 |
110,887,311 (GRCm39) |
missense |
probably benign |
0.00 |
R1535:Ep400
|
UTSW |
5 |
110,856,032 (GRCm39) |
unclassified |
probably benign |
|
R1560:Ep400
|
UTSW |
5 |
110,818,972 (GRCm39) |
splice site |
probably null |
|
R1587:Ep400
|
UTSW |
5 |
110,874,768 (GRCm39) |
missense |
probably benign |
0.23 |
R1596:Ep400
|
UTSW |
5 |
110,856,727 (GRCm39) |
unclassified |
probably benign |
|
R1653:Ep400
|
UTSW |
5 |
110,841,040 (GRCm39) |
nonsense |
probably null |
|
R1711:Ep400
|
UTSW |
5 |
110,841,174 (GRCm39) |
unclassified |
probably benign |
|
R1774:Ep400
|
UTSW |
5 |
110,833,357 (GRCm39) |
missense |
unknown |
|
R1836:Ep400
|
UTSW |
5 |
110,852,920 (GRCm39) |
missense |
unknown |
|
R1905:Ep400
|
UTSW |
5 |
110,818,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Ep400
|
UTSW |
5 |
110,851,441 (GRCm39) |
missense |
unknown |
|
R2064:Ep400
|
UTSW |
5 |
110,883,270 (GRCm39) |
unclassified |
probably benign |
|
R2122:Ep400
|
UTSW |
5 |
110,856,716 (GRCm39) |
unclassified |
probably benign |
|
R2144:Ep400
|
UTSW |
5 |
110,851,384 (GRCm39) |
missense |
unknown |
|
R2215:Ep400
|
UTSW |
5 |
110,841,421 (GRCm39) |
unclassified |
probably benign |
|
R2252:Ep400
|
UTSW |
5 |
110,866,957 (GRCm39) |
missense |
unknown |
|
R2253:Ep400
|
UTSW |
5 |
110,866,957 (GRCm39) |
missense |
unknown |
|
R2483:Ep400
|
UTSW |
5 |
110,867,102 (GRCm39) |
missense |
unknown |
|
R2504:Ep400
|
UTSW |
5 |
110,816,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:Ep400
|
UTSW |
5 |
110,856,781 (GRCm39) |
unclassified |
probably benign |
|
R2842:Ep400
|
UTSW |
5 |
110,846,681 (GRCm39) |
nonsense |
probably null |
|
R2920:Ep400
|
UTSW |
5 |
110,903,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R3082:Ep400
|
UTSW |
5 |
110,841,096 (GRCm39) |
unclassified |
probably benign |
|
R3151:Ep400
|
UTSW |
5 |
110,851,435 (GRCm39) |
missense |
unknown |
|
R3552:Ep400
|
UTSW |
5 |
110,877,153 (GRCm39) |
missense |
unknown |
|
R3623:Ep400
|
UTSW |
5 |
110,867,102 (GRCm39) |
missense |
unknown |
|
R3779:Ep400
|
UTSW |
5 |
110,839,515 (GRCm39) |
missense |
unknown |
|
R3923:Ep400
|
UTSW |
5 |
110,904,389 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4062:Ep400
|
UTSW |
5 |
110,889,847 (GRCm39) |
missense |
probably benign |
0.10 |
R4508:Ep400
|
UTSW |
5 |
110,851,481 (GRCm39) |
missense |
unknown |
|
R4584:Ep400
|
UTSW |
5 |
110,881,763 (GRCm39) |
unclassified |
probably benign |
|
R4585:Ep400
|
UTSW |
5 |
110,901,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4586:Ep400
|
UTSW |
5 |
110,901,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4807:Ep400
|
UTSW |
5 |
110,843,444 (GRCm39) |
splice site |
probably null |
|
R4921:Ep400
|
UTSW |
5 |
110,813,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R4976:Ep400
|
UTSW |
5 |
110,868,622 (GRCm39) |
missense |
unknown |
|
R4976:Ep400
|
UTSW |
5 |
110,846,678 (GRCm39) |
missense |
unknown |
|
R5075:Ep400
|
UTSW |
5 |
110,833,351 (GRCm39) |
missense |
unknown |
|
R5120:Ep400
|
UTSW |
5 |
110,904,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R5122:Ep400
|
UTSW |
5 |
110,816,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R5223:Ep400
|
UTSW |
5 |
110,816,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R5284:Ep400
|
UTSW |
5 |
110,815,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R5388:Ep400
|
UTSW |
5 |
110,849,594 (GRCm39) |
missense |
unknown |
|
R5401:Ep400
|
UTSW |
5 |
110,831,037 (GRCm39) |
missense |
unknown |
|
R5431:Ep400
|
UTSW |
5 |
110,824,420 (GRCm39) |
missense |
unknown |
|
R5461:Ep400
|
UTSW |
5 |
110,824,550 (GRCm39) |
nonsense |
probably null |
|
R5568:Ep400
|
UTSW |
5 |
110,904,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R5650:Ep400
|
UTSW |
5 |
110,843,818 (GRCm39) |
critical splice donor site |
probably null |
|
R5778:Ep400
|
UTSW |
5 |
110,867,450 (GRCm39) |
missense |
unknown |
|
R5806:Ep400
|
UTSW |
5 |
110,903,420 (GRCm39) |
nonsense |
probably null |
|
R5814:Ep400
|
UTSW |
5 |
110,843,444 (GRCm39) |
splice site |
probably null |
|
R5830:Ep400
|
UTSW |
5 |
110,831,862 (GRCm39) |
missense |
unknown |
|
R5882:Ep400
|
UTSW |
5 |
110,903,453 (GRCm39) |
missense |
probably benign |
0.00 |
R5931:Ep400
|
UTSW |
5 |
110,883,386 (GRCm39) |
unclassified |
probably benign |
|
R5945:Ep400
|
UTSW |
5 |
110,830,732 (GRCm39) |
missense |
unknown |
|
R5966:Ep400
|
UTSW |
5 |
110,824,766 (GRCm39) |
missense |
unknown |
|
R5973:Ep400
|
UTSW |
5 |
110,877,697 (GRCm39) |
missense |
unknown |
|
R5980:Ep400
|
UTSW |
5 |
110,881,595 (GRCm39) |
unclassified |
probably benign |
|
R6000:Ep400
|
UTSW |
5 |
110,831,067 (GRCm39) |
missense |
unknown |
|
R6006:Ep400
|
UTSW |
5 |
110,852,825 (GRCm39) |
missense |
unknown |
|
R6053:Ep400
|
UTSW |
5 |
110,903,661 (GRCm39) |
missense |
probably benign |
0.22 |
R6145:Ep400
|
UTSW |
5 |
110,904,569 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6154:Ep400
|
UTSW |
5 |
110,903,799 (GRCm39) |
missense |
probably damaging |
0.97 |
R6169:Ep400
|
UTSW |
5 |
110,889,863 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6295:Ep400
|
UTSW |
5 |
110,901,675 (GRCm39) |
missense |
probably benign |
0.00 |
R6486:Ep400
|
UTSW |
5 |
110,845,084 (GRCm39) |
unclassified |
probably benign |
|
R6504:Ep400
|
UTSW |
5 |
110,856,703 (GRCm39) |
unclassified |
probably benign |
|
R6607:Ep400
|
UTSW |
5 |
110,831,180 (GRCm39) |
missense |
unknown |
|
R6657:Ep400
|
UTSW |
5 |
110,841,411 (GRCm39) |
unclassified |
probably benign |
|
R6660:Ep400
|
UTSW |
5 |
110,867,313 (GRCm39) |
nonsense |
probably null |
|
R6741:Ep400
|
UTSW |
5 |
110,824,761 (GRCm39) |
missense |
unknown |
|
R6933:Ep400
|
UTSW |
5 |
110,813,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6937:Ep400
|
UTSW |
5 |
110,859,018 (GRCm39) |
unclassified |
probably benign |
|
R7069:Ep400
|
UTSW |
5 |
110,815,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R7103:Ep400
|
UTSW |
5 |
110,881,651 (GRCm39) |
missense |
unknown |
|
R7156:Ep400
|
UTSW |
5 |
110,833,229 (GRCm39) |
missense |
unknown |
|
R7272:Ep400
|
UTSW |
5 |
110,903,511 (GRCm39) |
nonsense |
probably null |
|
R7365:Ep400
|
UTSW |
5 |
110,867,480 (GRCm39) |
missense |
unknown |
|
R7581:Ep400
|
UTSW |
5 |
110,903,891 (GRCm39) |
missense |
unknown |
|
R7684:Ep400
|
UTSW |
5 |
110,845,218 (GRCm39) |
missense |
unknown |
|
R7699:Ep400
|
UTSW |
5 |
110,843,898 (GRCm39) |
missense |
unknown |
|
R7700:Ep400
|
UTSW |
5 |
110,843,898 (GRCm39) |
missense |
unknown |
|
R7856:Ep400
|
UTSW |
5 |
110,814,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R7954:Ep400
|
UTSW |
5 |
110,816,599 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8098:Ep400
|
UTSW |
5 |
110,841,117 (GRCm39) |
missense |
unknown |
|
R8108:Ep400
|
UTSW |
5 |
110,835,749 (GRCm39) |
missense |
unknown |
|
R8260:Ep400
|
UTSW |
5 |
110,903,478 (GRCm39) |
nonsense |
probably null |
|
R8293:Ep400
|
UTSW |
5 |
110,856,758 (GRCm39) |
missense |
unknown |
|
R8314:Ep400
|
UTSW |
5 |
110,903,619 (GRCm39) |
missense |
unknown |
|
R8351:Ep400
|
UTSW |
5 |
110,887,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R8424:Ep400
|
UTSW |
5 |
110,841,144 (GRCm39) |
missense |
unknown |
|
R8459:Ep400
|
UTSW |
5 |
110,856,757 (GRCm39) |
missense |
unknown |
|
R8529:Ep400
|
UTSW |
5 |
110,867,102 (GRCm39) |
missense |
unknown |
|
R8688:Ep400
|
UTSW |
5 |
110,868,685 (GRCm39) |
missense |
unknown |
|
R8744:Ep400
|
UTSW |
5 |
110,889,925 (GRCm39) |
missense |
unknown |
|
R8923:Ep400
|
UTSW |
5 |
110,831,864 (GRCm39) |
missense |
unknown |
|
R9005:Ep400
|
UTSW |
5 |
110,858,959 (GRCm39) |
missense |
unknown |
|
R9087:Ep400
|
UTSW |
5 |
110,815,430 (GRCm39) |
nonsense |
probably null |
|
R9146:Ep400
|
UTSW |
5 |
110,849,635 (GRCm39) |
nonsense |
probably null |
|
R9383:Ep400
|
UTSW |
5 |
110,833,351 (GRCm39) |
missense |
unknown |
|
R9479:Ep400
|
UTSW |
5 |
110,877,730 (GRCm39) |
missense |
unknown |
|
R9496:Ep400
|
UTSW |
5 |
110,855,853 (GRCm39) |
missense |
unknown |
|
R9582:Ep400
|
UTSW |
5 |
110,824,315 (GRCm39) |
critical splice donor site |
probably null |
|
R9607:Ep400
|
UTSW |
5 |
110,831,805 (GRCm39) |
missense |
unknown |
|
R9712:Ep400
|
UTSW |
5 |
110,904,509 (GRCm39) |
missense |
unknown |
|
R9746:Ep400
|
UTSW |
5 |
110,889,872 (GRCm39) |
missense |
unknown |
|
X0012:Ep400
|
UTSW |
5 |
110,821,062 (GRCm39) |
small deletion |
probably benign |
|
X0021:Ep400
|
UTSW |
5 |
110,830,730 (GRCm39) |
missense |
unknown |
|
Z1176:Ep400
|
UTSW |
5 |
110,904,501 (GRCm39) |
missense |
unknown |
|
Z1177:Ep400
|
UTSW |
5 |
110,881,609 (GRCm39) |
missense |
unknown |
|
Z1177:Ep400
|
UTSW |
5 |
110,831,230 (GRCm39) |
missense |
unknown |
|
Z1188:Ep400
|
UTSW |
5 |
110,903,549 (GRCm39) |
missense |
unknown |
|
|