Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
T |
C |
11: 119,909,681 (GRCm39) |
D28G |
probably benign |
Het |
Abcg1 |
T |
A |
17: 31,311,369 (GRCm39) |
S125T |
probably damaging |
Het |
Actbl2 |
T |
C |
13: 111,392,717 (GRCm39) |
S351P |
possibly damaging |
Het |
Ankrd34b |
A |
G |
13: 92,575,569 (GRCm39) |
|
probably null |
Het |
BC051665 |
C |
T |
13: 60,930,468 (GRCm39) |
V295I |
probably benign |
Het |
C1qtnf2 |
A |
G |
11: 43,381,983 (GRCm39) |
N265S |
probably damaging |
Het |
Ccdc14 |
C |
T |
16: 34,542,220 (GRCm39) |
R573* |
probably null |
Het |
Cd55b |
A |
T |
1: 130,337,612 (GRCm39) |
Y247N |
probably damaging |
Het |
Celsr2 |
A |
T |
3: 108,320,907 (GRCm39) |
V635E |
probably benign |
Het |
Clec16a |
T |
C |
16: 10,377,551 (GRCm39) |
|
probably benign |
Het |
Clec4b1 |
A |
G |
6: 123,042,904 (GRCm39) |
Y41C |
probably damaging |
Het |
Cntn5 |
A |
T |
9: 10,172,126 (GRCm39) |
D19E |
probably benign |
Het |
Cop1 |
A |
G |
1: 159,060,375 (GRCm39) |
N53S |
probably damaging |
Het |
Cplane1 |
G |
A |
15: 8,248,700 (GRCm39) |
E1750K |
probably damaging |
Het |
Csad |
A |
T |
15: 102,097,102 (GRCm39) |
M1K |
probably null |
Het |
Cyb5rl |
A |
G |
4: 106,938,142 (GRCm39) |
I200V |
probably benign |
Het |
Cyp26a1 |
A |
G |
19: 37,686,790 (GRCm39) |
T81A |
probably damaging |
Het |
Cyp2d12 |
A |
T |
15: 82,443,237 (GRCm39) |
H433L |
probably benign |
Het |
D7Ertd443e |
T |
A |
7: 133,951,208 (GRCm39) |
|
probably null |
Het |
Dennd1b |
A |
G |
1: 139,097,908 (GRCm39) |
|
probably benign |
Het |
Dmap1 |
G |
T |
4: 117,532,495 (GRCm39) |
T357K |
probably damaging |
Het |
Dzip1 |
G |
T |
14: 119,118,456 (GRCm39) |
T759K |
probably benign |
Het |
Elmo2 |
A |
G |
2: 165,140,607 (GRCm39) |
V300A |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,810,364 (GRCm39) |
D864G |
possibly damaging |
Het |
Epha3 |
T |
A |
16: 63,423,988 (GRCm39) |
I534F |
probably damaging |
Het |
Epha4 |
A |
C |
1: 77,359,628 (GRCm39) |
Y742D |
probably damaging |
Het |
Ergic2 |
A |
G |
6: 148,106,272 (GRCm39) |
|
probably null |
Het |
Ero1a |
A |
T |
14: 45,536,545 (GRCm39) |
|
probably null |
Het |
Fam229a |
A |
G |
4: 129,385,279 (GRCm39) |
D70G |
probably damaging |
Het |
Fbn2 |
C |
T |
18: 58,226,431 (GRCm39) |
R781Q |
probably damaging |
Het |
Fbxo16 |
A |
T |
14: 65,508,163 (GRCm39) |
|
probably benign |
Het |
Fbxo39 |
T |
A |
11: 72,208,111 (GRCm39) |
S154R |
probably benign |
Het |
Fer |
T |
A |
17: 64,298,575 (GRCm39) |
|
probably null |
Het |
Filip1l |
A |
T |
16: 57,391,410 (GRCm39) |
D428V |
probably damaging |
Het |
Filip1l |
A |
G |
16: 57,391,025 (GRCm39) |
I538V |
possibly damaging |
Het |
Fsip2 |
T |
C |
2: 82,809,954 (GRCm39) |
I2091T |
possibly damaging |
Het |
Glyat |
A |
C |
19: 12,628,762 (GRCm39) |
T186P |
possibly damaging |
Het |
Gm10604 |
A |
G |
4: 11,980,083 (GRCm39) |
S74P |
unknown |
Het |
Gm4787 |
T |
G |
12: 81,425,911 (GRCm39) |
K82N |
possibly damaging |
Het |
Hectd4 |
T |
C |
5: 121,358,683 (GRCm39) |
I50T |
unknown |
Het |
Hectd4 |
T |
C |
5: 121,402,030 (GRCm39) |
S373P |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,562,618 (GRCm39) |
C2313* |
probably null |
Het |
Hrob |
T |
C |
11: 102,146,122 (GRCm39) |
Y133H |
possibly damaging |
Het |
Igfn1 |
A |
T |
1: 135,897,054 (GRCm39) |
S1171T |
probably benign |
Het |
Ints8 |
T |
C |
4: 11,241,642 (GRCm39) |
D267G |
probably benign |
Het |
Itln1 |
A |
G |
1: 171,356,727 (GRCm39) |
C251R |
probably damaging |
Het |
Jcad |
C |
T |
18: 4,674,026 (GRCm39) |
T596M |
probably damaging |
Het |
Kcnj16 |
C |
T |
11: 110,916,409 (GRCm39) |
T357M |
probably benign |
Het |
Kif13a |
G |
A |
13: 46,967,676 (GRCm39) |
T346M |
probably damaging |
Het |
Klhl24 |
G |
A |
16: 19,938,917 (GRCm39) |
A491T |
probably benign |
Het |
Kntc1 |
C |
T |
5: 123,916,410 (GRCm39) |
Q748* |
probably null |
Het |
Krt25 |
T |
A |
11: 99,208,122 (GRCm39) |
K369* |
probably null |
Het |
Krt75 |
C |
T |
15: 101,476,466 (GRCm39) |
R433Q |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,793,293 (GRCm39) |
F582L |
unknown |
Het |
Lysmd1 |
G |
A |
3: 95,045,708 (GRCm39) |
V182I |
probably benign |
Het |
Mab21l2 |
T |
A |
3: 86,454,862 (GRCm39) |
E46V |
probably damaging |
Het |
Magi2 |
A |
T |
5: 20,563,934 (GRCm39) |
K355N |
probably damaging |
Het |
Marchf10 |
T |
C |
11: 105,276,398 (GRCm39) |
D630G |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,875,147 (GRCm39) |
I1215N |
probably damaging |
Het |
Nckap1 |
G |
A |
2: 80,360,562 (GRCm39) |
T523I |
probably benign |
Het |
Nexmif |
T |
A |
X: 103,127,999 (GRCm39) |
D1306V |
probably damaging |
Het |
Nfkb1 |
A |
C |
3: 135,295,090 (GRCm39) |
I918R |
possibly damaging |
Het |
Nt5el |
A |
G |
13: 105,246,250 (GRCm39) |
I270M |
probably benign |
Het |
Nup50 |
A |
T |
15: 84,817,859 (GRCm39) |
T93S |
probably benign |
Het |
Nwd2 |
T |
C |
5: 63,961,717 (GRCm39) |
Y434H |
probably benign |
Het |
Or13a28 |
T |
C |
7: 140,218,397 (GRCm39) |
V261A |
probably benign |
Het |
Osbpl1a |
C |
A |
18: 13,038,088 (GRCm39) |
V288L |
probably benign |
Het |
Pan3 |
A |
G |
5: 147,463,846 (GRCm39) |
E562G |
possibly damaging |
Het |
Pappa |
T |
A |
4: 65,099,126 (GRCm39) |
Y548* |
probably null |
Het |
Phf3 |
A |
T |
1: 30,849,870 (GRCm39) |
L1181Q |
probably damaging |
Het |
Phip |
T |
C |
9: 82,797,392 (GRCm39) |
H537R |
possibly damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,348,824 (GRCm39) |
I240T |
probably damaging |
Het |
Pole |
G |
A |
5: 110,438,368 (GRCm39) |
|
probably null |
Het |
Polq |
T |
A |
16: 36,832,304 (GRCm39) |
S15T |
unknown |
Het |
Prrt2 |
T |
C |
7: 126,619,396 (GRCm39) |
E23G |
possibly damaging |
Het |
Prss37 |
A |
T |
6: 40,494,760 (GRCm39) |
|
probably null |
Het |
Prune2 |
T |
C |
19: 16,977,400 (GRCm39) |
L45P |
probably damaging |
Het |
Psd |
A |
T |
19: 46,313,352 (GRCm39) |
M6K |
possibly damaging |
Het |
Psmd1 |
A |
G |
1: 86,017,719 (GRCm39) |
E510G |
possibly damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Pxdn |
T |
A |
12: 30,053,405 (GRCm39) |
I1194N |
probably damaging |
Het |
Rbp3 |
C |
T |
14: 33,677,975 (GRCm39) |
T641M |
probably damaging |
Het |
Rgmb |
C |
A |
17: 16,027,909 (GRCm39) |
R270L |
probably benign |
Het |
Rpgrip1l |
A |
G |
8: 92,007,344 (GRCm39) |
|
probably null |
Het |
Rps2 |
G |
A |
17: 24,939,353 (GRCm39) |
|
probably benign |
Het |
Rsbn1l |
G |
T |
5: 21,107,364 (GRCm39) |
A550E |
probably damaging |
Het |
S1pr4 |
C |
T |
10: 81,335,138 (GRCm39) |
R112H |
probably benign |
Het |
Scfd2 |
T |
C |
5: 74,691,838 (GRCm39) |
N148S |
probably damaging |
Het |
Scin |
C |
T |
12: 40,131,705 (GRCm39) |
M276I |
probably benign |
Het |
Sec24d |
T |
C |
3: 123,147,255 (GRCm39) |
I708T |
possibly damaging |
Het |
Skint11 |
T |
A |
4: 114,086,009 (GRCm39) |
F41I |
possibly damaging |
Het |
Slc15a4 |
A |
T |
5: 127,694,303 (GRCm39) |
F44Y |
possibly damaging |
Het |
Slc6a18 |
A |
G |
13: 73,823,925 (GRCm39) |
Y72H |
probably benign |
Het |
Slc7a11 |
A |
T |
3: 50,332,195 (GRCm39) |
|
probably null |
Het |
Slc7a14 |
G |
T |
3: 31,291,650 (GRCm39) |
N209K |
possibly damaging |
Het |
Sstr2 |
T |
C |
11: 113,515,257 (GRCm39) |
C59R |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,884,997 (GRCm39) |
|
probably null |
Het |
Stag1 |
G |
T |
9: 100,748,263 (GRCm39) |
S475I |
probably damaging |
Het |
Stxbp5l |
A |
G |
16: 36,936,029 (GRCm39) |
Y1183H |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,135,628 (GRCm39) |
|
probably null |
Het |
Tm9sf2 |
A |
G |
14: 122,396,096 (GRCm39) |
T653A |
probably benign |
Het |
Tmeff1 |
T |
C |
4: 48,662,059 (GRCm39) |
S366P |
possibly damaging |
Het |
Tnnt2 |
G |
T |
1: 135,779,803 (GRCm39) |
W300L |
probably damaging |
Het |
Traj32 |
A |
G |
14: 54,423,560 (GRCm39) |
|
probably benign |
Het |
Trp53bp2 |
A |
T |
1: 182,269,204 (GRCm39) |
M223L |
probably benign |
Het |
Tsga10 |
G |
A |
1: 37,854,758 (GRCm39) |
T246M |
probably damaging |
Het |
Txn2 |
A |
T |
15: 77,810,870 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
A |
2: 69,768,542 (GRCm39) |
F450I |
probably damaging |
Het |
Usp47 |
T |
C |
7: 111,703,677 (GRCm39) |
|
probably null |
Het |
Vars2 |
C |
T |
17: 35,975,685 (GRCm39) |
R244Q |
probably damaging |
Het |
Xrra1 |
T |
A |
7: 99,546,803 (GRCm39) |
F251L |
probably damaging |
Het |
Zfp804a |
G |
A |
2: 82,087,863 (GRCm39) |
R564Q |
probably benign |
Het |
Zfp983 |
T |
C |
17: 21,877,883 (GRCm39) |
C29R |
probably 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 |
|
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 |
R6228:Ep400
|
UTSW |
5 |
110,818,808 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|