Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre1 |
A |
G |
17: 57,717,947 (GRCm39) |
I320V |
probably benign |
Het |
Akap6 |
T |
C |
12: 52,842,787 (GRCm39) |
V45A |
probably benign |
Het |
Ankrd28 |
A |
T |
14: 31,465,242 (GRCm39) |
S312T |
probably damaging |
Het |
Cenpn |
A |
G |
8: 117,660,135 (GRCm39) |
Y68C |
probably damaging |
Het |
Cntn3 |
A |
T |
6: 102,145,943 (GRCm39) |
I966N |
probably benign |
Het |
D630003M21Rik |
T |
C |
2: 158,046,722 (GRCm39) |
T752A |
probably benign |
Het |
Dmxl2 |
A |
C |
9: 54,327,168 (GRCm39) |
S952R |
probably null |
Het |
Dop1a |
G |
A |
9: 86,402,612 (GRCm39) |
E1271K |
probably benign |
Het |
Fgfr3 |
A |
G |
5: 33,880,460 (GRCm39) |
|
probably benign |
Het |
Gm10110 |
A |
G |
14: 90,135,151 (GRCm39) |
|
noncoding transcript |
Het |
Got1l1 |
C |
T |
8: 27,688,513 (GRCm39) |
M279I |
probably benign |
Het |
Guf1 |
T |
C |
5: 69,719,005 (GRCm39) |
V230A |
probably benign |
Het |
Hsd17b14 |
C |
T |
7: 45,212,339 (GRCm39) |
L124F |
probably benign |
Het |
Id3 |
G |
T |
4: 135,871,669 (GRCm39) |
|
probably benign |
Het |
Itga8 |
T |
C |
2: 12,187,547 (GRCm39) |
S711G |
probably benign |
Het |
Lgr4 |
T |
C |
2: 109,842,361 (GRCm39) |
M782T |
possibly damaging |
Het |
Lsm12 |
T |
C |
11: 102,057,909 (GRCm39) |
|
probably null |
Het |
Map1b |
T |
A |
13: 99,580,741 (GRCm39) |
D117V |
probably damaging |
Het |
Map3k11 |
A |
G |
19: 5,752,238 (GRCm39) |
T807A |
probably damaging |
Het |
Mapk14 |
T |
C |
17: 28,943,798 (GRCm39) |
F129S |
probably damaging |
Het |
Mapkbp1 |
T |
A |
2: 119,854,174 (GRCm39) |
I1257N |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,880,456 (GRCm39) |
Y459H |
probably damaging |
Het |
Mkln1 |
T |
C |
6: 31,410,093 (GRCm39) |
|
probably benign |
Het |
Msh5 |
A |
T |
17: 35,249,664 (GRCm39) |
I627N |
possibly damaging |
Het |
Nfkbiz |
T |
C |
16: 55,637,204 (GRCm39) |
H488R |
probably benign |
Het |
Nrg1 |
G |
T |
8: 32,967,105 (GRCm39) |
|
probably benign |
Het |
Or1j19 |
A |
G |
2: 36,676,782 (GRCm39) |
M82V |
probably benign |
Het |
Or51q1 |
T |
C |
7: 103,628,648 (GRCm39) |
V89A |
probably benign |
Het |
Or51t4 |
T |
C |
7: 102,597,945 (GRCm39) |
L81P |
probably damaging |
Het |
Or5b120 |
A |
T |
19: 13,479,986 (GRCm39) |
Y93F |
probably benign |
Het |
Plec |
C |
T |
15: 76,070,418 (GRCm39) |
V931M |
probably damaging |
Het |
Plekhg4 |
T |
A |
8: 106,107,034 (GRCm39) |
C910S |
probably damaging |
Het |
Ppp1r18 |
A |
G |
17: 36,179,196 (GRCm39) |
E357G |
probably damaging |
Het |
Pramel23 |
T |
C |
4: 143,424,718 (GRCm39) |
M242V |
probably benign |
Het |
Rbm11 |
T |
C |
16: 75,393,475 (GRCm39) |
F57S |
probably damaging |
Het |
Sbp |
G |
A |
17: 24,164,286 (GRCm39) |
G183D |
probably benign |
Het |
Skint5 |
A |
G |
4: 113,599,382 (GRCm39) |
V719A |
unknown |
Het |
Slc16a7 |
T |
G |
10: 125,069,308 (GRCm39) |
|
probably null |
Het |
Slc29a1 |
A |
C |
17: 45,899,992 (GRCm39) |
Y232* |
probably null |
Het |
Slc7a8 |
C |
G |
14: 54,973,247 (GRCm39) |
G240A |
possibly damaging |
Het |
Spanxn4 |
A |
T |
12: 62,734,886 (GRCm39) |
|
noncoding transcript |
Het |
Spata31d1d |
T |
C |
13: 59,876,368 (GRCm39) |
Q389R |
probably benign |
Het |
Srgap1 |
A |
G |
10: 121,706,231 (GRCm39) |
|
probably null |
Het |
St6gal2 |
A |
T |
17: 55,790,018 (GRCm39) |
N351Y |
probably benign |
Het |
Tle2 |
A |
G |
10: 81,423,394 (GRCm39) |
D491G |
probably damaging |
Het |
Tmem33 |
T |
C |
5: 67,443,468 (GRCm39) |
V215A |
probably benign |
Het |
Trav6-3 |
A |
G |
14: 53,667,548 (GRCm39) |
T7A |
probably benign |
Het |
Ube2q2 |
C |
A |
9: 55,057,084 (GRCm39) |
P56T |
probably benign |
Het |
Unc79 |
T |
C |
12: 102,988,019 (GRCm39) |
V208A |
probably damaging |
Het |
Xkr7 |
T |
C |
2: 152,896,553 (GRCm39) |
I469T |
probably benign |
Het |
|
Other mutations in Cfap96 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01335:Cfap96
|
APN |
8 |
46,426,642 (GRCm39) |
unclassified |
probably benign |
|
D4043:Cfap96
|
UTSW |
8 |
46,409,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Cfap96
|
UTSW |
8 |
46,421,198 (GRCm39) |
missense |
probably damaging |
0.99 |
R0055:Cfap96
|
UTSW |
8 |
46,421,198 (GRCm39) |
missense |
probably damaging |
0.99 |
R0894:Cfap96
|
UTSW |
8 |
46,409,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Cfap96
|
UTSW |
8 |
46,409,515 (GRCm39) |
missense |
probably benign |
0.19 |
R4600:Cfap96
|
UTSW |
8 |
46,423,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R4601:Cfap96
|
UTSW |
8 |
46,423,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R4602:Cfap96
|
UTSW |
8 |
46,423,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R4603:Cfap96
|
UTSW |
8 |
46,423,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R4610:Cfap96
|
UTSW |
8 |
46,423,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R4734:Cfap96
|
UTSW |
8 |
46,423,454 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4829:Cfap96
|
UTSW |
8 |
46,420,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R5259:Cfap96
|
UTSW |
8 |
46,415,373 (GRCm39) |
missense |
probably benign |
0.04 |
R7031:Cfap96
|
UTSW |
8 |
46,421,140 (GRCm39) |
missense |
probably benign |
0.02 |
R7032:Cfap96
|
UTSW |
8 |
46,409,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R7177:Cfap96
|
UTSW |
8 |
46,423,444 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7488:Cfap96
|
UTSW |
8 |
46,415,331 (GRCm39) |
missense |
probably benign |
|
R7611:Cfap96
|
UTSW |
8 |
46,423,488 (GRCm39) |
missense |
probably damaging |
0.96 |
R7877:Cfap96
|
UTSW |
8 |
46,423,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Cfap96
|
UTSW |
8 |
46,415,403 (GRCm39) |
missense |
probably benign |
0.37 |
R9495:Cfap96
|
UTSW |
8 |
46,409,458 (GRCm39) |
missense |
probably damaging |
1.00 |
|