Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
G |
13: 77,471,493 (GRCm39) |
E966G |
probably benign |
Het |
9330159F19Rik |
T |
C |
10: 29,097,795 (GRCm39) |
V64A |
probably damaging |
Het |
Abcb5 |
G |
T |
12: 118,831,696 (GRCm39) |
Q1219K |
possibly damaging |
Het |
Acox2 |
A |
T |
14: 8,248,059 (GRCm38) |
C408S |
possibly damaging |
Het |
Acsf3 |
T |
A |
8: 123,506,922 (GRCm39) |
Y72N |
probably damaging |
Het |
Acss2 |
T |
A |
2: 155,400,550 (GRCm39) |
Y530N |
probably damaging |
Het |
Adam28 |
T |
C |
14: 68,886,870 (GRCm39) |
E48G |
possibly damaging |
Het |
Adgrv1 |
A |
C |
13: 81,652,232 (GRCm39) |
M2957R |
probably benign |
Het |
Adi1 |
C |
A |
12: 28,729,562 (GRCm39) |
D138E |
probably benign |
Het |
Alk |
A |
C |
17: 72,198,032 (GRCm39) |
L1228R |
probably damaging |
Het |
Alms1 |
T |
A |
6: 85,655,485 (GRCm39) |
S3344T |
possibly damaging |
Het |
Aox1 |
G |
A |
1: 58,348,150 (GRCm39) |
A623T |
probably benign |
Het |
Arhgef2 |
C |
T |
3: 88,546,766 (GRCm39) |
T545I |
probably damaging |
Het |
Atp8a2 |
T |
A |
14: 60,243,815 (GRCm39) |
N630I |
possibly damaging |
Het |
Bcl9 |
G |
T |
3: 97,113,186 (GRCm39) |
Q1090K |
probably damaging |
Het |
Bdp1 |
A |
G |
13: 100,171,653 (GRCm39) |
S2152P |
probably benign |
Het |
Birc6 |
T |
A |
17: 74,921,385 (GRCm39) |
S2155T |
probably benign |
Het |
Camk2b |
T |
C |
11: 5,922,384 (GRCm39) |
E488G |
probably damaging |
Het |
Capn9 |
T |
A |
8: 125,332,304 (GRCm39) |
|
probably null |
Het |
Cd209f |
A |
G |
8: 4,154,491 (GRCm39) |
S119P |
probably damaging |
Het |
Cep78 |
T |
C |
19: 15,946,533 (GRCm39) |
E433G |
probably damaging |
Het |
Chid1 |
G |
T |
7: 141,106,409 (GRCm39) |
|
probably null |
Het |
Cldnd2 |
T |
C |
7: 43,092,349 (GRCm39) |
S129P |
possibly damaging |
Het |
Cobll1 |
A |
T |
2: 64,956,580 (GRCm39) |
F289Y |
probably damaging |
Het |
Creb1 |
C |
T |
1: 64,590,109 (GRCm39) |
Q32* |
probably null |
Het |
Creb3l4 |
G |
T |
3: 90,146,210 (GRCm39) |
S182Y |
probably benign |
Het |
Dgcr2 |
A |
T |
16: 17,667,584 (GRCm39) |
C292S |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 31,093,901 (GRCm39) |
V4665A |
possibly damaging |
Het |
Dnah9 |
A |
T |
11: 66,009,667 (GRCm39) |
M740K |
probably benign |
Het |
Dnmt1 |
G |
A |
9: 20,829,542 (GRCm39) |
T687I |
probably damaging |
Het |
Ece1 |
C |
T |
4: 137,685,312 (GRCm39) |
R601W |
probably damaging |
Het |
Echdc2 |
C |
A |
4: 108,022,732 (GRCm39) |
R3S |
probably damaging |
Het |
Epha6 |
A |
T |
16: 60,026,108 (GRCm39) |
W445R |
probably damaging |
Het |
Ercc5 |
T |
A |
1: 44,220,035 (GRCm39) |
S1102R |
probably benign |
Het |
Fam228a |
T |
G |
12: 4,765,620 (GRCm39) |
T264P |
probably damaging |
Het |
Fzd6 |
T |
A |
15: 38,897,315 (GRCm39) |
I488N |
probably damaging |
Het |
Gabrg3 |
T |
G |
7: 56,379,389 (GRCm39) |
N338H |
probably damaging |
Het |
Gde1 |
A |
G |
7: 118,294,357 (GRCm39) |
F39L |
possibly damaging |
Het |
Gjb3 |
G |
A |
4: 127,220,224 (GRCm39) |
R103W |
probably damaging |
Het |
Gm4781 |
T |
A |
10: 100,232,582 (GRCm39) |
|
noncoding transcript |
Het |
Gm4846 |
T |
A |
1: 166,311,492 (GRCm39) |
T456S |
probably benign |
Het |
Gpx5 |
A |
G |
13: 21,471,624 (GRCm39) |
I193T |
probably benign |
Het |
H3c2 |
T |
A |
13: 23,936,715 (GRCm39) |
V118D |
probably damaging |
Het |
Herc2 |
A |
T |
7: 55,804,853 (GRCm39) |
K2294* |
probably null |
Het |
Iqgap3 |
T |
A |
3: 88,015,675 (GRCm39) |
V19D |
probably damaging |
Het |
Itga5 |
T |
C |
15: 103,254,441 (GRCm39) |
I1006V |
probably damaging |
Het |
Lamb1 |
C |
T |
12: 31,351,093 (GRCm39) |
T781I |
probably benign |
Het |
Lias |
A |
G |
5: 65,549,686 (GRCm39) |
T57A |
probably benign |
Het |
Lin37 |
C |
A |
7: 30,256,368 (GRCm39) |
R108L |
probably damaging |
Het |
Lrrd1 |
A |
T |
5: 3,915,709 (GRCm39) |
T769S |
probably benign |
Het |
Mamstr |
T |
C |
7: 45,294,387 (GRCm39) |
W414R |
probably damaging |
Het |
Mtmr11 |
T |
G |
3: 96,072,103 (GRCm39) |
S233R |
probably damaging |
Het |
Myh1 |
A |
T |
11: 67,095,648 (GRCm39) |
I266F |
probably damaging |
Het |
Myt1 |
C |
A |
2: 181,439,068 (GRCm39) |
Q197K |
probably benign |
Het |
Naip5 |
G |
T |
13: 100,356,195 (GRCm39) |
T1140K |
probably benign |
Het |
Ncf2 |
G |
A |
1: 152,683,822 (GRCm39) |
V14M |
probably damaging |
Het |
Ndufb11b |
T |
C |
15: 81,865,068 (GRCm39) |
V103A |
probably damaging |
Het |
Nhsl1 |
G |
T |
10: 18,400,653 (GRCm39) |
R626S |
possibly damaging |
Het |
Nol12 |
T |
A |
15: 78,822,089 (GRCm39) |
V108E |
probably damaging |
Het |
Nr1i2 |
G |
T |
16: 38,069,644 (GRCm39) |
P420Q |
probably damaging |
Het |
Nup155 |
A |
G |
15: 8,184,464 (GRCm39) |
I1286M |
possibly damaging |
Het |
Ocrl |
T |
A |
X: 47,050,993 (GRCm39) |
I74N |
probably damaging |
Het |
Or4c10b |
A |
C |
2: 89,711,629 (GRCm39) |
H153P |
probably damaging |
Het |
Or51b17 |
A |
G |
7: 103,542,592 (GRCm39) |
S117P |
probably damaging |
Het |
Or5ak23 |
A |
G |
2: 85,244,749 (GRCm39) |
V158A |
probably benign |
Het |
Pard3b |
C |
T |
1: 62,676,763 (GRCm39) |
S999L |
probably benign |
Het |
Pax9 |
A |
G |
12: 56,746,839 (GRCm39) |
E225G |
probably benign |
Het |
Pdcd4 |
T |
G |
19: 53,914,650 (GRCm39) |
L335R |
probably damaging |
Het |
Pdgfra |
T |
A |
5: 75,343,675 (GRCm39) |
M732K |
possibly damaging |
Het |
Pkhd1 |
G |
T |
1: 20,187,293 (GRCm39) |
Q3672K |
probably benign |
Het |
Pold2 |
A |
G |
11: 5,823,454 (GRCm39) |
L325P |
possibly damaging |
Het |
Pom121l2 |
A |
T |
13: 22,167,954 (GRCm39) |
T742S |
probably benign |
Het |
Ppfia1 |
C |
T |
7: 144,073,368 (GRCm39) |
E208K |
probably benign |
Het |
Prex2 |
A |
T |
1: 11,207,004 (GRCm39) |
R521W |
probably damaging |
Het |
Prr23a4 |
C |
A |
9: 98,785,535 (GRCm39) |
R67S |
probably benign |
Het |
Rhpn2 |
T |
C |
7: 35,071,813 (GRCm39) |
L226P |
probably benign |
Het |
Rps12 |
C |
A |
10: 23,661,527 (GRCm39) |
D95Y |
probably damaging |
Het |
Sardh |
T |
A |
2: 27,105,194 (GRCm39) |
D643V |
possibly damaging |
Het |
Sars1 |
T |
C |
3: 108,343,260 (GRCm39) |
D77G |
probably benign |
Het |
Scin |
C |
A |
12: 40,174,697 (GRCm39) |
V129F |
probably damaging |
Het |
Semp2l1 |
T |
G |
1: 32,584,758 (GRCm39) |
D384A |
probably damaging |
Het |
Sftpa1 |
T |
A |
14: 40,854,803 (GRCm39) |
M66K |
possibly damaging |
Het |
Sgo1 |
T |
C |
17: 53,994,799 (GRCm39) |
K28E |
probably damaging |
Het |
Sim2 |
G |
T |
16: 93,924,436 (GRCm39) |
|
probably null |
Het |
Srp54b |
T |
A |
12: 55,296,945 (GRCm39) |
|
probably null |
Het |
Stard7 |
T |
C |
2: 127,137,480 (GRCm39) |
V310A |
probably benign |
Het |
Tasp1 |
T |
C |
2: 139,793,477 (GRCm39) |
D233G |
probably damaging |
Het |
Tdrd6 |
G |
T |
17: 43,936,480 (GRCm39) |
L1523M |
probably benign |
Het |
Tle3 |
A |
G |
9: 61,321,305 (GRCm39) |
D639G |
probably damaging |
Het |
Tmem128 |
A |
G |
5: 38,417,750 (GRCm39) |
D2G |
probably damaging |
Het |
Tmem163 |
A |
G |
1: 127,605,246 (GRCm39) |
S41P |
probably benign |
Het |
Ttn |
C |
T |
2: 76,559,505 (GRCm39) |
S29632N |
probably damaging |
Het |
Tuba4a |
A |
G |
1: 75,192,754 (GRCm39) |
S287P |
probably benign |
Het |
Ubn1 |
G |
C |
16: 4,895,255 (GRCm39) |
G767A |
probably benign |
Het |
Ugdh |
A |
T |
5: 65,577,634 (GRCm39) |
C288* |
probably null |
Het |
Upf2 |
T |
A |
2: 6,055,135 (GRCm39) |
|
probably null |
Het |
Vmn1r2 |
T |
C |
4: 3,172,836 (GRCm39) |
S252P |
probably damaging |
Het |
Vmn1r28 |
A |
C |
6: 58,242,237 (GRCm39) |
T27P |
probably damaging |
Het |
Vmn1r77 |
T |
C |
7: 11,775,338 (GRCm39) |
I38T |
probably benign |
Het |
Vmn2r51 |
C |
A |
7: 9,832,090 (GRCm39) |
E499* |
probably null |
Het |
Vmn2r51 |
G |
T |
7: 9,832,091 (GRCm39) |
Y498* |
probably null |
Het |
Vmn2r53 |
A |
T |
7: 12,334,812 (GRCm39) |
W283R |
probably damaging |
Het |
Vpreb1a |
T |
A |
16: 16,686,933 (GRCm39) |
T15S |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,910,378 (GRCm39) |
S3381P |
probably damaging |
Het |
Wnt2 |
A |
T |
6: 18,023,234 (GRCm39) |
D138E |
probably damaging |
Het |
Zdhhc22 |
A |
G |
12: 87,030,204 (GRCm39) |
V248A |
probably benign |
Het |
Zfp30 |
T |
A |
7: 29,492,805 (GRCm39) |
I434N |
probably damaging |
Het |
Zfp316 |
A |
G |
5: 143,239,178 (GRCm39) |
L947P |
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 |
|
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 |
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 |
|
|