Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
A |
T |
15: 81,950,065 (GRCm39) |
M1321L |
probably benign |
Het |
Adra1a |
C |
T |
14: 66,965,183 (GRCm39) |
T391I |
probably benign |
Het |
Atf7ip |
C |
A |
6: 136,583,812 (GRCm39) |
A1281D |
probably damaging |
Het |
BC005624 |
T |
C |
2: 30,866,023 (GRCm39) |
N141S |
probably benign |
Het |
Catsperg2 |
A |
T |
7: 29,397,257 (GRCm39) |
L1082Q |
possibly damaging |
Het |
Cavin2 |
C |
T |
1: 51,328,998 (GRCm39) |
R152C |
probably damaging |
Het |
Ccdc33 |
C |
T |
9: 57,940,489 (GRCm39) |
|
probably benign |
Het |
Cfap43 |
T |
C |
19: 47,784,135 (GRCm39) |
D466G |
probably benign |
Het |
Cfap46 |
C |
A |
7: 139,230,858 (GRCm39) |
M923I |
probably damaging |
Het |
Chd1l |
T |
A |
3: 97,479,883 (GRCm39) |
K621N |
probably benign |
Het |
Cnksr1 |
A |
G |
4: 133,955,575 (GRCm39) |
|
probably benign |
Het |
Cym |
T |
C |
3: 107,127,080 (GRCm39) |
H25R |
probably benign |
Het |
Dagla |
T |
A |
19: 10,248,489 (GRCm39) |
D57V |
probably damaging |
Het |
Dnah3 |
TTCCTC |
TTC |
7: 119,550,244 (GRCm39) |
|
probably benign |
Het |
Dse |
T |
A |
10: 34,029,038 (GRCm39) |
D684V |
probably damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Fbxo10 |
A |
T |
4: 45,058,760 (GRCm39) |
S326T |
probably benign |
Het |
Galntl5 |
G |
T |
5: 25,391,091 (GRCm39) |
|
probably benign |
Het |
Grm5 |
A |
G |
7: 87,453,232 (GRCm39) |
R290G |
possibly damaging |
Het |
Gtpbp3 |
A |
G |
8: 71,945,199 (GRCm39) |
T425A |
probably benign |
Het |
Hepacam2 |
A |
G |
6: 3,476,073 (GRCm39) |
I284T |
probably damaging |
Het |
Irs3 |
T |
C |
5: 137,642,548 (GRCm39) |
T297A |
probably benign |
Het |
Kmt2d |
G |
A |
15: 98,749,990 (GRCm39) |
|
probably benign |
Het |
Map4k4 |
T |
A |
1: 40,039,036 (GRCm39) |
|
probably benign |
Het |
Mfsd6 |
T |
C |
1: 52,697,542 (GRCm39) |
S782G |
probably benign |
Het |
Mis18a |
G |
A |
16: 90,523,969 (GRCm39) |
|
silent |
Het |
Mtpn |
C |
T |
6: 35,489,225 (GRCm39) |
D100N |
probably benign |
Het |
Myom2 |
G |
A |
8: 15,181,182 (GRCm39) |
|
probably null |
Het |
Ntaq1 |
A |
G |
15: 58,017,056 (GRCm39) |
N157S |
probably benign |
Het |
Or13a1 |
A |
T |
6: 116,470,900 (GRCm39) |
E110V |
probably damaging |
Het |
Or5g25 |
A |
G |
2: 85,478,239 (GRCm39) |
V142A |
probably benign |
Het |
Pde3b |
C |
T |
7: 114,108,106 (GRCm39) |
T568I |
probably benign |
Het |
Pip4p1 |
T |
C |
14: 51,166,499 (GRCm39) |
T160A |
probably benign |
Het |
Pkhd1 |
G |
T |
1: 20,451,685 (GRCm39) |
D2203E |
probably benign |
Het |
Ppp1r36 |
A |
G |
12: 76,473,566 (GRCm39) |
K66E |
possibly damaging |
Het |
Rfc1 |
C |
A |
5: 65,451,130 (GRCm39) |
M319I |
probably benign |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Runx1t1 |
T |
C |
4: 13,881,068 (GRCm39) |
V456A |
probably damaging |
Het |
Rxfp2 |
A |
G |
5: 149,966,589 (GRCm39) |
K109R |
probably benign |
Het |
Sgo2a |
T |
G |
1: 58,055,556 (GRCm39) |
V580G |
probably damaging |
Het |
Skint9 |
T |
C |
4: 112,271,080 (GRCm39) |
Q110R |
probably benign |
Het |
Slc38a9 |
A |
G |
13: 112,868,035 (GRCm39) |
Y507C |
probably damaging |
Het |
Smarca4 |
T |
A |
9: 21,589,238 (GRCm39) |
|
probably benign |
Het |
Tmem88 |
C |
G |
11: 69,288,504 (GRCm39) |
Q138H |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Tns3 |
A |
C |
11: 8,384,580 (GRCm39) |
F1413V |
probably damaging |
Het |
Trpm8 |
T |
C |
1: 88,312,433 (GRCm39) |
*1105Q |
probably null |
Het |
Zfp853 |
C |
T |
5: 143,274,424 (GRCm39) |
V399M |
unknown |
Het |
Zim1 |
T |
C |
7: 6,681,115 (GRCm39) |
R183G |
probably benign |
Het |
Zmiz1 |
T |
C |
14: 25,657,354 (GRCm39) |
S871P |
probably damaging |
Het |
|
Other mutations in Ifi205 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Ifi205
|
APN |
1 |
173,854,899 (GRCm39) |
splice site |
probably benign |
|
IGL02419:Ifi205
|
APN |
1 |
173,845,180 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02476:Ifi205
|
APN |
1 |
173,842,627 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03128:Ifi205
|
APN |
1 |
173,842,652 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03154:Ifi205
|
APN |
1 |
173,845,232 (GRCm39) |
splice site |
probably benign |
|
R0211:Ifi205
|
UTSW |
1 |
173,855,994 (GRCm39) |
missense |
probably benign |
|
R1932:Ifi205
|
UTSW |
1 |
173,855,980 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2397:Ifi205
|
UTSW |
1 |
173,845,141 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3115:Ifi205
|
UTSW |
1 |
173,855,901 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4534:Ifi205
|
UTSW |
1 |
173,845,207 (GRCm39) |
missense |
probably benign |
0.16 |
R4544:Ifi205
|
UTSW |
1 |
173,854,139 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4715:Ifi205
|
UTSW |
1 |
173,855,887 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4977:Ifi205
|
UTSW |
1 |
173,842,574 (GRCm39) |
missense |
probably benign |
0.07 |
R6061:Ifi205
|
UTSW |
1 |
173,854,830 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6510:Ifi205
|
UTSW |
1 |
173,845,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R7032:Ifi205
|
UTSW |
1 |
173,855,916 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7196:Ifi205
|
UTSW |
1 |
173,854,109 (GRCm39) |
missense |
probably damaging |
0.96 |
R7244:Ifi205
|
UTSW |
1 |
173,845,210 (GRCm39) |
nonsense |
probably null |
|
R7419:Ifi205
|
UTSW |
1 |
173,855,874 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7431:Ifi205
|
UTSW |
1 |
173,855,943 (GRCm39) |
missense |
probably benign |
|
R7660:Ifi205
|
UTSW |
1 |
173,855,814 (GRCm39) |
missense |
probably benign |
0.27 |
R7787:Ifi205
|
UTSW |
1 |
173,842,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R7787:Ifi205
|
UTSW |
1 |
173,842,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R9069:Ifi205
|
UTSW |
1 |
173,855,841 (GRCm39) |
missense |
probably benign |
|
R9163:Ifi205
|
UTSW |
1 |
173,844,988 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9348:Ifi205
|
UTSW |
1 |
173,844,997 (GRCm39) |
missense |
probably benign |
0.24 |
R9376:Ifi205
|
UTSW |
1 |
173,854,221 (GRCm39) |
missense |
probably benign |
|
R9477:Ifi205
|
UTSW |
1 |
173,854,155 (GRCm39) |
missense |
probably benign |
|
|