Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Api5 |
T |
C |
2: 94,252,726 (GRCm39) |
Y348C |
probably benign |
Het |
Ark2n |
T |
C |
18: 77,740,855 (GRCm39) |
T285A |
probably benign |
Het |
Arl14 |
A |
G |
3: 69,130,405 (GRCm39) |
E184G |
probably benign |
Het |
Asap3 |
T |
C |
4: 135,965,541 (GRCm39) |
|
probably null |
Het |
Atp11b |
T |
A |
3: 35,893,311 (GRCm39) |
V36E |
probably damaging |
Het |
Atp13a4 |
C |
T |
16: 29,298,659 (GRCm39) |
S100N |
probably benign |
Het |
Cd27 |
T |
C |
6: 125,213,756 (GRCm39) |
T34A |
probably benign |
Het |
Clec10a |
T |
C |
11: 70,061,436 (GRCm39) |
S274P |
probably benign |
Het |
Cntnap2 |
C |
T |
6: 46,147,206 (GRCm39) |
T484I |
probably benign |
Het |
Cpsf1 |
CCCCTGCATGAGGCAGGTCCC |
CCCC |
15: 76,481,655 (GRCm39) |
|
probably null |
Het |
Cracd |
A |
T |
5: 77,013,947 (GRCm39) |
|
probably benign |
Het |
Def8 |
T |
C |
8: 124,183,449 (GRCm39) |
S304P |
probably benign |
Het |
Dgkd |
G |
A |
1: 87,867,962 (GRCm39) |
V299M |
probably damaging |
Het |
Ephb2 |
T |
C |
4: 136,384,861 (GRCm39) |
D850G |
probably damaging |
Het |
Gjd3 |
T |
C |
11: 102,691,130 (GRCm39) |
N291S |
possibly damaging |
Het |
Hc |
T |
C |
2: 34,922,138 (GRCm39) |
I563V |
probably benign |
Het |
Hells |
C |
T |
19: 38,919,909 (GRCm39) |
Q20* |
probably null |
Het |
Hid1 |
G |
C |
11: 115,245,462 (GRCm39) |
P448A |
possibly damaging |
Het |
Igkv8-24 |
C |
T |
6: 70,193,947 (GRCm39) |
R87H |
possibly damaging |
Het |
Irf6 |
A |
G |
1: 192,851,662 (GRCm39) |
S418G |
probably damaging |
Het |
Kcnv2 |
T |
A |
19: 27,301,420 (GRCm39) |
C424S |
possibly damaging |
Het |
Lmln |
T |
A |
16: 32,927,370 (GRCm39) |
|
probably null |
Het |
Myo1a |
A |
T |
10: 127,551,189 (GRCm39) |
I678F |
possibly damaging |
Het |
Papolg |
GGACTTGGGATACTTACGCTTTG |
GG |
11: 23,829,857 (GRCm39) |
|
probably benign |
Het |
Ppfibp1 |
T |
A |
6: 146,901,153 (GRCm39) |
|
probably null |
Het |
Sardh |
T |
C |
2: 27,108,867 (GRCm39) |
T623A |
possibly damaging |
Het |
Scml4 |
A |
G |
10: 42,823,107 (GRCm39) |
N251D |
probably damaging |
Het |
Skap1 |
T |
C |
11: 96,416,870 (GRCm39) |
Y52H |
probably damaging |
Het |
Srp68 |
G |
A |
11: 116,156,290 (GRCm39) |
R113W |
probably damaging |
Het |
Srsf12 |
T |
C |
4: 33,209,196 (GRCm39) |
|
probably benign |
Het |
Stat5b |
A |
G |
11: 100,688,526 (GRCm39) |
M312T |
probably benign |
Het |
Tma7 |
T |
C |
9: 108,911,262 (GRCm39) |
|
probably benign |
Het |
Tmem120b |
T |
G |
5: 123,254,710 (GRCm39) |
F304V |
probably damaging |
Het |
Tns3 |
G |
A |
11: 8,499,057 (GRCm39) |
L9F |
probably damaging |
Het |
Tns3 |
G |
T |
11: 8,499,058 (GRCm39) |
D8E |
probably damaging |
Het |
Tsc2 |
C |
T |
17: 24,829,473 (GRCm39) |
A765T |
probably damaging |
Het |
Tut7 |
C |
T |
13: 59,955,975 (GRCm39) |
C45Y |
probably damaging |
Het |
Uba1y |
A |
G |
Y: 825,465 (GRCm39) |
I276V |
probably benign |
Homo |
Upb1 |
T |
G |
10: 75,248,723 (GRCm39) |
L81R |
probably damaging |
Het |
Uros |
C |
A |
7: 133,302,569 (GRCm39) |
C73F |
probably damaging |
Het |
Zfp820 |
T |
C |
17: 22,038,384 (GRCm39) |
I315V |
probably benign |
Het |
|
Other mutations in Nup98 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00662:Nup98
|
APN |
7 |
101,844,194 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00789:Nup98
|
APN |
7 |
101,803,178 (GRCm39) |
missense |
probably benign |
|
IGL00798:Nup98
|
APN |
7 |
101,796,411 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01562:Nup98
|
APN |
7 |
101,835,125 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01942:Nup98
|
APN |
7 |
101,843,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02109:Nup98
|
APN |
7 |
101,832,693 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02490:Nup98
|
APN |
7 |
101,801,573 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03184:Nup98
|
APN |
7 |
101,832,752 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4519001:Nup98
|
UTSW |
7 |
101,784,171 (GRCm39) |
missense |
probably benign |
0.00 |
R0040:Nup98
|
UTSW |
7 |
101,841,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Nup98
|
UTSW |
7 |
101,788,859 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0309:Nup98
|
UTSW |
7 |
101,801,635 (GRCm39) |
missense |
probably null |
|
R0471:Nup98
|
UTSW |
7 |
101,788,004 (GRCm39) |
missense |
probably benign |
0.13 |
R0538:Nup98
|
UTSW |
7 |
101,835,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Nup98
|
UTSW |
7 |
101,801,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R0881:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R0900:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1120:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1159:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Nup98
|
UTSW |
7 |
101,788,008 (GRCm39) |
missense |
probably benign |
0.00 |
R1469:Nup98
|
UTSW |
7 |
101,788,008 (GRCm39) |
missense |
probably benign |
0.00 |
R1470:Nup98
|
UTSW |
7 |
101,796,513 (GRCm39) |
missense |
probably damaging |
0.98 |
R1470:Nup98
|
UTSW |
7 |
101,796,513 (GRCm39) |
missense |
probably damaging |
0.98 |
R1545:Nup98
|
UTSW |
7 |
101,784,087 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1775:Nup98
|
UTSW |
7 |
101,784,144 (GRCm39) |
missense |
probably benign |
0.03 |
R1889:Nup98
|
UTSW |
7 |
101,809,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Nup98
|
UTSW |
7 |
101,829,631 (GRCm39) |
missense |
probably damaging |
0.96 |
R3423:Nup98
|
UTSW |
7 |
101,834,084 (GRCm39) |
missense |
probably benign |
0.03 |
R4361:Nup98
|
UTSW |
7 |
101,794,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Nup98
|
UTSW |
7 |
101,834,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Nup98
|
UTSW |
7 |
101,802,403 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4910:Nup98
|
UTSW |
7 |
101,845,007 (GRCm39) |
missense |
unknown |
|
R4924:Nup98
|
UTSW |
7 |
101,784,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Nup98
|
UTSW |
7 |
101,794,862 (GRCm39) |
missense |
probably benign |
0.00 |
R5069:Nup98
|
UTSW |
7 |
101,794,862 (GRCm39) |
missense |
probably benign |
0.00 |
R5233:Nup98
|
UTSW |
7 |
101,845,029 (GRCm39) |
missense |
unknown |
|
R5779:Nup98
|
UTSW |
7 |
101,801,568 (GRCm39) |
missense |
probably benign |
|
R5922:Nup98
|
UTSW |
7 |
101,803,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Nup98
|
UTSW |
7 |
101,829,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R6039:Nup98
|
UTSW |
7 |
101,784,002 (GRCm39) |
missense |
probably benign |
|
R6039:Nup98
|
UTSW |
7 |
101,784,002 (GRCm39) |
missense |
probably benign |
|
R6343:Nup98
|
UTSW |
7 |
101,843,957 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6364:Nup98
|
UTSW |
7 |
101,825,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R6462:Nup98
|
UTSW |
7 |
101,844,223 (GRCm39) |
missense |
probably benign |
0.03 |
R6900:Nup98
|
UTSW |
7 |
101,835,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Nup98
|
UTSW |
7 |
101,844,248 (GRCm39) |
missense |
unknown |
|
R7218:Nup98
|
UTSW |
7 |
101,841,107 (GRCm39) |
splice site |
probably null |
|
R7235:Nup98
|
UTSW |
7 |
101,774,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7307:Nup98
|
UTSW |
7 |
101,784,002 (GRCm39) |
missense |
probably benign |
|
R7402:Nup98
|
UTSW |
7 |
101,784,144 (GRCm39) |
missense |
probably benign |
0.00 |
R7427:Nup98
|
UTSW |
7 |
101,784,208 (GRCm39) |
splice site |
probably null |
|
R7428:Nup98
|
UTSW |
7 |
101,784,208 (GRCm39) |
splice site |
probably null |
|
R7584:Nup98
|
UTSW |
7 |
101,825,596 (GRCm39) |
missense |
probably benign |
0.02 |
R7646:Nup98
|
UTSW |
7 |
101,803,242 (GRCm39) |
missense |
probably benign |
0.01 |
R7648:Nup98
|
UTSW |
7 |
101,773,404 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7742:Nup98
|
UTSW |
7 |
101,802,464 (GRCm39) |
splice site |
probably null |
|
R7827:Nup98
|
UTSW |
7 |
101,773,569 (GRCm39) |
missense |
probably benign |
0.10 |
R7884:Nup98
|
UTSW |
7 |
101,825,556 (GRCm39) |
missense |
probably benign |
0.12 |
R7943:Nup98
|
UTSW |
7 |
101,844,029 (GRCm39) |
missense |
probably benign |
0.10 |
R8034:Nup98
|
UTSW |
7 |
101,794,930 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8952:Nup98
|
UTSW |
7 |
101,835,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R9060:Nup98
|
UTSW |
7 |
101,783,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R9099:Nup98
|
UTSW |
7 |
101,844,173 (GRCm39) |
missense |
probably damaging |
0.98 |
R9146:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9148:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9223:Nup98
|
UTSW |
7 |
101,834,167 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9246:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9249:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9272:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9274:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9283:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9326:Nup98
|
UTSW |
7 |
101,788,037 (GRCm39) |
missense |
probably benign |
0.02 |
R9466:Nup98
|
UTSW |
7 |
101,818,611 (GRCm39) |
missense |
probably benign |
0.05 |
R9492:Nup98
|
UTSW |
7 |
101,778,252 (GRCm39) |
missense |
probably benign |
0.11 |
R9661:Nup98
|
UTSW |
7 |
101,782,019 (GRCm39) |
nonsense |
probably null |
|
T0970:Nup98
|
UTSW |
7 |
101,835,959 (GRCm39) |
unclassified |
probably benign |
|
X0054:Nup98
|
UTSW |
7 |
101,796,415 (GRCm39) |
missense |
probably damaging |
1.00 |
|