Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
G |
T |
16: 90,853,085 (GRCm39) |
T17K |
probably benign |
Het |
Agbl1 |
T |
C |
7: 76,416,120 (GRCm39) |
S714P |
probably damaging |
Het |
Araf |
A |
G |
X: 20,719,835 (GRCm39) |
|
probably benign |
Het |
Armc3 |
G |
A |
2: 19,290,948 (GRCm39) |
|
probably null |
Het |
Armc8 |
A |
T |
9: 99,365,227 (GRCm39) |
D638E |
probably benign |
Het |
Bpifb5 |
C |
T |
2: 154,067,068 (GRCm39) |
T107I |
possibly damaging |
Het |
Ces1e |
A |
C |
8: 93,938,977 (GRCm39) |
|
probably null |
Het |
Col4a3 |
C |
A |
1: 82,647,492 (GRCm39) |
|
probably benign |
Het |
Col4a5 |
A |
G |
X: 140,382,669 (GRCm39) |
|
probably benign |
Het |
Crocc |
T |
C |
4: 140,765,231 (GRCm39) |
H477R |
probably benign |
Het |
Dgkd |
C |
A |
1: 87,842,863 (GRCm39) |
N130K |
probably benign |
Het |
Dock1 |
C |
T |
7: 134,379,174 (GRCm39) |
Q634* |
probably null |
Het |
Dzip3 |
C |
T |
16: 48,801,351 (GRCm39) |
V58I |
probably benign |
Het |
Fndc3a |
A |
G |
14: 72,793,807 (GRCm39) |
|
probably benign |
Het |
Glp2r |
C |
T |
11: 67,612,817 (GRCm39) |
R379H |
probably damaging |
Het |
Kctd12b |
T |
A |
X: 152,472,330 (GRCm39) |
M120L |
probably benign |
Het |
Krt33b |
A |
G |
11: 99,916,189 (GRCm39) |
V258A |
probably benign |
Het |
Lpin1 |
T |
A |
12: 16,591,770 (GRCm39) |
N819I |
probably damaging |
Het |
Lurap1l |
T |
C |
4: 80,871,866 (GRCm39) |
S120P |
probably damaging |
Het |
Lysmd4 |
T |
C |
7: 66,875,672 (GRCm39) |
S112P |
probably damaging |
Het |
Myo1e |
A |
G |
9: 70,274,971 (GRCm39) |
K708R |
probably benign |
Het |
Nr3c1 |
T |
A |
18: 39,554,610 (GRCm39) |
|
probably benign |
Het |
Nup62cl |
G |
T |
X: 138,922,780 (GRCm39) |
N239K |
probably benign |
Het |
Nwd1 |
A |
T |
8: 73,434,210 (GRCm39) |
E1269V |
probably damaging |
Het |
Or52e7 |
C |
T |
7: 104,685,152 (GRCm39) |
T249M |
probably damaging |
Het |
Pcdh9 |
A |
C |
14: 93,564,204 (GRCm39) |
L1084R |
probably damaging |
Het |
Plxnd1 |
A |
G |
6: 115,955,218 (GRCm39) |
M543T |
probably benign |
Het |
Prss53 |
T |
A |
7: 127,487,964 (GRCm39) |
T173S |
possibly damaging |
Het |
Reep2 |
C |
A |
18: 34,973,807 (GRCm39) |
|
probably benign |
Het |
Rp1 |
T |
C |
1: 4,419,003 (GRCm39) |
D703G |
probably benign |
Het |
Sbf2 |
T |
G |
7: 110,159,502 (GRCm39) |
D36A |
probably damaging |
Het |
Sh3kbp1 |
C |
T |
X: 158,586,724 (GRCm39) |
R99W |
probably damaging |
Het |
Sis |
T |
A |
3: 72,863,523 (GRCm39) |
R238S |
probably benign |
Het |
Slc35e2 |
T |
A |
4: 155,703,019 (GRCm39) |
V344D |
probably damaging |
Het |
Specc1 |
G |
A |
11: 62,019,194 (GRCm39) |
V678I |
probably benign |
Het |
Supt6 |
T |
C |
11: 78,123,623 (GRCm39) |
D49G |
possibly damaging |
Het |
Tecpr1 |
G |
A |
5: 144,146,821 (GRCm39) |
A515V |
probably benign |
Het |
Tlr4 |
G |
A |
4: 66,752,298 (GRCm39) |
|
probably null |
Het |
Tmco5b |
A |
G |
2: 113,118,619 (GRCm39) |
E114G |
probably damaging |
Het |
Tspear |
A |
T |
10: 77,688,690 (GRCm39) |
|
probably benign |
Het |
Txlnb |
T |
A |
10: 17,719,116 (GRCm39) |
V649E |
probably benign |
Het |
Utp20 |
A |
G |
10: 88,651,818 (GRCm39) |
|
probably benign |
Het |
Virma |
G |
A |
4: 11,546,031 (GRCm39) |
R1673Q |
probably damaging |
Het |
Vmn2r70 |
T |
A |
7: 85,214,211 (GRCm39) |
T314S |
probably benign |
Het |
|
Other mutations in Zfp938 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00659:Zfp938
|
APN |
10 |
82,063,355 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL00743:Zfp938
|
APN |
10 |
82,062,317 (GRCm39) |
missense |
probably benign |
|
IGL01764:Zfp938
|
APN |
10 |
82,063,624 (GRCm39) |
splice site |
probably benign |
|
IGL01814:Zfp938
|
APN |
10 |
82,062,052 (GRCm39) |
missense |
probably benign |
|
IGL02865:Zfp938
|
APN |
10 |
82,062,026 (GRCm39) |
missense |
probably benign |
0.33 |
R0372:Zfp938
|
UTSW |
10 |
82,063,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R0666:Zfp938
|
UTSW |
10 |
82,061,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R0964:Zfp938
|
UTSW |
10 |
82,061,253 (GRCm39) |
missense |
probably benign |
0.00 |
R1453:Zfp938
|
UTSW |
10 |
82,063,632 (GRCm39) |
critical splice donor site |
probably null |
|
R1672:Zfp938
|
UTSW |
10 |
82,060,982 (GRCm39) |
missense |
probably benign |
|
R1929:Zfp938
|
UTSW |
10 |
82,061,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Zfp938
|
UTSW |
10 |
82,061,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Zfp938
|
UTSW |
10 |
82,061,876 (GRCm39) |
missense |
probably benign |
|
R2271:Zfp938
|
UTSW |
10 |
82,061,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R2900:Zfp938
|
UTSW |
10 |
82,061,340 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4502:Zfp938
|
UTSW |
10 |
82,062,105 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4503:Zfp938
|
UTSW |
10 |
82,062,105 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4886:Zfp938
|
UTSW |
10 |
82,061,957 (GRCm39) |
missense |
probably benign |
0.33 |
R4934:Zfp938
|
UTSW |
10 |
82,062,012 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5174:Zfp938
|
UTSW |
10 |
82,061,838 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5410:Zfp938
|
UTSW |
10 |
82,061,092 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6284:Zfp938
|
UTSW |
10 |
82,063,400 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6491:Zfp938
|
UTSW |
10 |
82,063,363 (GRCm39) |
makesense |
probably null |
|
R6575:Zfp938
|
UTSW |
10 |
82,061,160 (GRCm39) |
nonsense |
probably null |
|
R6649:Zfp938
|
UTSW |
10 |
82,061,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R7992:Zfp938
|
UTSW |
10 |
82,061,777 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8211:Zfp938
|
UTSW |
10 |
82,062,419 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8313:Zfp938
|
UTSW |
10 |
82,061,422 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8963:Zfp938
|
UTSW |
10 |
82,061,287 (GRCm39) |
missense |
possibly damaging |
0.61 |
X0066:Zfp938
|
UTSW |
10 |
82,061,931 (GRCm39) |
missense |
probably benign |
0.33 |
|