Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700020N01Rik |
A |
G |
10: 21,469,337 (GRCm39) |
D17G |
probably damaging |
Het |
Abi3bp |
A |
G |
16: 56,353,316 (GRCm39) |
T82A |
possibly damaging |
Het |
Adgre4 |
A |
C |
17: 56,099,035 (GRCm39) |
E180D |
probably benign |
Het |
Aoc3 |
A |
G |
11: 101,227,273 (GRCm39) |
D382G |
possibly damaging |
Het |
Apob |
C |
A |
12: 8,060,742 (GRCm39) |
R3075S |
probably benign |
Het |
Aqr |
A |
G |
2: 113,971,458 (GRCm39) |
F459S |
probably damaging |
Het |
Bcr |
T |
C |
10: 74,967,475 (GRCm39) |
W570R |
probably damaging |
Het |
Bloc1s5 |
C |
T |
13: 38,787,895 (GRCm39) |
R163K |
probably benign |
Het |
Bod1 |
A |
T |
11: 31,619,267 (GRCm39) |
N101K |
possibly damaging |
Het |
Bysl |
A |
T |
17: 47,913,396 (GRCm39) |
S296T |
probably benign |
Het |
Chl1 |
G |
A |
6: 103,685,503 (GRCm39) |
|
probably null |
Het |
Clstn1 |
G |
A |
4: 149,731,312 (GRCm39) |
A885T |
probably benign |
Het |
Cyp3a25 |
G |
T |
5: 145,935,356 (GRCm39) |
P87T |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,623,626 (GRCm39) |
V3633A |
probably damaging |
Het |
Dynlt5 |
T |
C |
4: 102,859,735 (GRCm39) |
Y96H |
probably damaging |
Het |
Elp4 |
C |
A |
2: 105,622,622 (GRCm39) |
C241F |
possibly damaging |
Het |
Fat4 |
T |
A |
3: 39,055,327 (GRCm39) |
F4182Y |
probably benign |
Het |
Gabbr2 |
G |
A |
4: 46,787,521 (GRCm39) |
H381Y |
possibly damaging |
Het |
Gm10577 |
G |
T |
4: 100,877,515 (GRCm39) |
|
probably benign |
Het |
Gm9955 |
G |
T |
18: 24,842,314 (GRCm39) |
|
probably benign |
Het |
Gstm5 |
T |
A |
3: 107,804,635 (GRCm39) |
I73N |
probably damaging |
Het |
Gypa |
T |
A |
8: 81,223,331 (GRCm39) |
|
probably benign |
Het |
Hectd2 |
T |
A |
19: 36,546,831 (GRCm39) |
V64D |
probably damaging |
Het |
Igkv10-95 |
T |
A |
6: 68,657,543 (GRCm39) |
Y20N |
probably benign |
Het |
Il15 |
T |
C |
8: 83,064,188 (GRCm39) |
|
probably benign |
Het |
Iqca1 |
C |
A |
1: 90,070,453 (GRCm39) |
G133V |
probably null |
Het |
Kiz |
C |
A |
2: 146,697,978 (GRCm39) |
|
probably benign |
Het |
Lcmt2 |
C |
A |
2: 120,969,721 (GRCm39) |
S234I |
probably benign |
Het |
Lilra5 |
A |
G |
7: 4,244,956 (GRCm39) |
|
probably benign |
Het |
Lin37 |
T |
C |
7: 30,255,299 (GRCm39) |
E187G |
probably damaging |
Het |
Lrrc37 |
T |
C |
11: 103,507,714 (GRCm39) |
|
probably benign |
Het |
Mcmdc2 |
T |
A |
1: 9,982,039 (GRCm39) |
|
probably null |
Het |
Mctp1 |
T |
C |
13: 76,973,918 (GRCm39) |
|
probably null |
Het |
Mdp1 |
C |
A |
14: 55,896,726 (GRCm39) |
G112* |
probably null |
Het |
Mmp15 |
T |
C |
8: 96,098,762 (GRCm39) |
Y530H |
possibly damaging |
Het |
Mtss2 |
T |
C |
8: 111,454,029 (GRCm39) |
|
probably null |
Het |
Muc5ac |
T |
C |
7: 141,361,446 (GRCm39) |
S1586P |
probably benign |
Het |
Nap1l5 |
A |
T |
6: 58,883,757 (GRCm39) |
C66S |
possibly damaging |
Het |
Ninl |
G |
T |
2: 150,781,775 (GRCm39) |
Q1237K |
possibly damaging |
Het |
Or5p70 |
A |
T |
7: 107,994,470 (GRCm39) |
T48S |
possibly damaging |
Het |
Or9m1b |
T |
C |
2: 87,836,762 (GRCm39) |
E111G |
probably damaging |
Het |
Orc6 |
T |
G |
8: 86,027,783 (GRCm39) |
S37R |
possibly damaging |
Het |
Papss1 |
A |
C |
3: 131,288,854 (GRCm39) |
N119H |
possibly damaging |
Het |
Phf13 |
A |
T |
4: 152,076,069 (GRCm39) |
F278I |
probably damaging |
Het |
Pole2 |
C |
A |
12: 69,258,187 (GRCm39) |
A239S |
probably damaging |
Het |
Ppt2 |
T |
C |
17: 34,845,546 (GRCm39) |
D75G |
probably damaging |
Het |
Psd2 |
A |
G |
18: 36,136,044 (GRCm39) |
D443G |
possibly damaging |
Het |
Psen1 |
C |
A |
12: 83,761,594 (GRCm39) |
S132* |
probably null |
Het |
Psme4 |
A |
G |
11: 30,828,415 (GRCm39) |
T1812A |
probably damaging |
Het |
Rasgrf1 |
T |
C |
9: 89,797,535 (GRCm39) |
|
probably benign |
Het |
Reep3 |
A |
G |
10: 66,857,518 (GRCm39) |
|
probably benign |
Het |
Rexo4 |
A |
T |
2: 26,848,586 (GRCm39) |
|
probably benign |
Het |
Rnf6 |
A |
C |
5: 146,148,468 (GRCm39) |
S183R |
probably damaging |
Het |
Scai |
A |
T |
2: 38,993,749 (GRCm39) |
M297K |
probably damaging |
Het |
Scn9a |
A |
T |
2: 66,313,843 (GRCm39) |
S1947R |
probably benign |
Het |
Sema6c |
T |
C |
3: 95,080,021 (GRCm39) |
C772R |
possibly damaging |
Het |
Skint7 |
T |
C |
4: 111,837,542 (GRCm39) |
S107P |
possibly damaging |
Het |
Slc24a3 |
A |
G |
2: 145,448,715 (GRCm39) |
N420D |
probably benign |
Het |
Smc1b |
T |
C |
15: 84,955,021 (GRCm39) |
D1077G |
possibly damaging |
Het |
Smg7 |
G |
A |
1: 152,742,399 (GRCm39) |
P82L |
probably damaging |
Het |
Sp3 |
A |
C |
2: 72,801,342 (GRCm39) |
F268V |
probably damaging |
Het |
Srms |
T |
C |
2: 180,854,426 (GRCm39) |
D47G |
probably benign |
Het |
Ss18 |
A |
C |
18: 14,784,238 (GRCm39) |
M150R |
probably damaging |
Het |
Taf5 |
G |
A |
19: 47,063,293 (GRCm39) |
R281Q |
probably benign |
Het |
Tars1 |
T |
C |
15: 11,385,259 (GRCm39) |
K644R |
probably benign |
Het |
Tinag |
C |
A |
9: 76,859,285 (GRCm39) |
W441L |
probably damaging |
Het |
Tmtc1 |
T |
C |
6: 148,312,738 (GRCm39) |
S244G |
probably benign |
Het |
Tpr |
T |
C |
1: 150,309,476 (GRCm39) |
V1670A |
possibly damaging |
Het |
Trpv3 |
A |
G |
11: 73,187,640 (GRCm39) |
|
probably benign |
Het |
Uhrf1 |
G |
T |
17: 56,617,742 (GRCm39) |
V155L |
probably damaging |
Het |
Ush2a |
G |
A |
1: 188,132,475 (GRCm39) |
C899Y |
probably damaging |
Het |
Vmn2r115 |
G |
A |
17: 23,578,249 (GRCm39) |
R574H |
probably benign |
Het |
Vmn2r63 |
T |
C |
7: 42,577,434 (GRCm39) |
D368G |
probably benign |
Het |
Vps13a |
A |
G |
19: 16,758,105 (GRCm39) |
V10A |
probably damaging |
Het |
Wbp11 |
A |
G |
6: 136,791,636 (GRCm39) |
|
probably benign |
Het |
Zcwpw1 |
A |
G |
5: 137,797,854 (GRCm39) |
D145G |
probably benign |
Het |
Zfp607a |
G |
A |
7: 27,577,901 (GRCm39) |
V324I |
probably damaging |
Het |
Zfp618 |
A |
G |
4: 63,052,011 (GRCm39) |
I931V |
probably benign |
Het |
Zfp821 |
T |
C |
8: 110,451,174 (GRCm39) |
V389A |
possibly damaging |
Het |
Zfp976 |
T |
A |
7: 42,263,141 (GRCm39) |
H232L |
probably damaging |
Het |
|
Other mutations in Ankrd28 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00769:Ankrd28
|
APN |
14 |
31,465,322 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01335:Ankrd28
|
APN |
14 |
31,423,981 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01564:Ankrd28
|
APN |
14 |
31,477,724 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01624:Ankrd28
|
APN |
14 |
31,432,814 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01987:Ankrd28
|
APN |
14 |
31,500,931 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02100:Ankrd28
|
APN |
14 |
31,449,582 (GRCm39) |
unclassified |
probably benign |
|
IGL02307:Ankrd28
|
APN |
14 |
31,455,665 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02656:Ankrd28
|
APN |
14 |
31,424,197 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03069:Ankrd28
|
APN |
14 |
31,477,743 (GRCm39) |
nonsense |
probably null |
|
G1citation:Ankrd28
|
UTSW |
14 |
31,458,797 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0038:Ankrd28
|
UTSW |
14 |
31,429,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R0038:Ankrd28
|
UTSW |
14 |
31,429,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R0124:Ankrd28
|
UTSW |
14 |
31,449,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R0347:Ankrd28
|
UTSW |
14 |
31,423,979 (GRCm39) |
makesense |
probably null |
|
R0452:Ankrd28
|
UTSW |
14 |
31,470,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R0751:Ankrd28
|
UTSW |
14 |
31,486,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R1349:Ankrd28
|
UTSW |
14 |
31,467,218 (GRCm39) |
missense |
probably benign |
0.05 |
R1372:Ankrd28
|
UTSW |
14 |
31,467,218 (GRCm39) |
missense |
probably benign |
0.05 |
R1695:Ankrd28
|
UTSW |
14 |
31,429,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Ankrd28
|
UTSW |
14 |
31,453,982 (GRCm39) |
splice site |
probably benign |
|
R1938:Ankrd28
|
UTSW |
14 |
31,427,233 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2001:Ankrd28
|
UTSW |
14 |
31,467,293 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2162:Ankrd28
|
UTSW |
14 |
31,430,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R2352:Ankrd28
|
UTSW |
14 |
31,432,904 (GRCm39) |
missense |
probably benign |
0.05 |
R2357:Ankrd28
|
UTSW |
14 |
31,486,251 (GRCm39) |
nonsense |
probably null |
|
R3545:Ankrd28
|
UTSW |
14 |
31,437,217 (GRCm39) |
missense |
probably benign |
0.13 |
R3548:Ankrd28
|
UTSW |
14 |
31,437,217 (GRCm39) |
missense |
probably benign |
0.13 |
R3710:Ankrd28
|
UTSW |
14 |
31,470,808 (GRCm39) |
splice site |
probably benign |
|
R4282:Ankrd28
|
UTSW |
14 |
31,467,182 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4501:Ankrd28
|
UTSW |
14 |
31,428,753 (GRCm39) |
missense |
probably damaging |
0.97 |
R4513:Ankrd28
|
UTSW |
14 |
31,465,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658:Ankrd28
|
UTSW |
14 |
31,432,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Ankrd28
|
UTSW |
14 |
31,477,698 (GRCm39) |
missense |
probably benign |
0.43 |
R4732:Ankrd28
|
UTSW |
14 |
31,477,698 (GRCm39) |
missense |
probably benign |
0.43 |
R4733:Ankrd28
|
UTSW |
14 |
31,477,698 (GRCm39) |
missense |
probably benign |
0.43 |
R4776:Ankrd28
|
UTSW |
14 |
31,454,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Ankrd28
|
UTSW |
14 |
31,458,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Ankrd28
|
UTSW |
14 |
31,458,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5279:Ankrd28
|
UTSW |
14 |
31,456,963 (GRCm39) |
missense |
probably damaging |
0.99 |
R5633:Ankrd28
|
UTSW |
14 |
31,457,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R5809:Ankrd28
|
UTSW |
14 |
31,465,311 (GRCm39) |
missense |
probably benign |
0.19 |
R5959:Ankrd28
|
UTSW |
14 |
31,451,879 (GRCm39) |
missense |
probably benign |
0.16 |
R6228:Ankrd28
|
UTSW |
14 |
31,429,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R6358:Ankrd28
|
UTSW |
14 |
31,432,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R6533:Ankrd28
|
UTSW |
14 |
31,454,041 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6598:Ankrd28
|
UTSW |
14 |
31,430,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R6822:Ankrd28
|
UTSW |
14 |
31,458,797 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7352:Ankrd28
|
UTSW |
14 |
31,429,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R7396:Ankrd28
|
UTSW |
14 |
31,424,159 (GRCm39) |
missense |
probably benign |
0.00 |
R7462:Ankrd28
|
UTSW |
14 |
31,500,886 (GRCm39) |
missense |
probably benign |
0.40 |
R7517:Ankrd28
|
UTSW |
14 |
31,437,331 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7629:Ankrd28
|
UTSW |
14 |
31,437,221 (GRCm39) |
missense |
probably benign |
0.00 |
R7783:Ankrd28
|
UTSW |
14 |
31,428,770 (GRCm39) |
missense |
probably damaging |
0.99 |
R7981:Ankrd28
|
UTSW |
14 |
31,424,114 (GRCm39) |
missense |
probably benign |
0.08 |
R8401:Ankrd28
|
UTSW |
14 |
31,467,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R8483:Ankrd28
|
UTSW |
14 |
31,457,048 (GRCm39) |
splice site |
probably null |
|
R8752:Ankrd28
|
UTSW |
14 |
31,477,699 (GRCm39) |
start gained |
probably benign |
|
R8946:Ankrd28
|
UTSW |
14 |
31,430,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Ankrd28
|
UTSW |
14 |
31,477,698 (GRCm39) |
missense |
probably benign |
0.06 |
R9064:Ankrd28
|
UTSW |
14 |
31,454,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R9181:Ankrd28
|
UTSW |
14 |
31,470,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R9231:Ankrd28
|
UTSW |
14 |
31,429,234 (GRCm39) |
missense |
possibly damaging |
0.91 |
RF010:Ankrd28
|
UTSW |
14 |
31,500,943 (GRCm39) |
missense |
probably damaging |
1.00 |
|