Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
A |
C |
10: 10,283,214 (GRCm39) |
M164R |
possibly damaging |
Het |
Alg10b |
T |
A |
15: 90,111,656 (GRCm39) |
C167S |
probably benign |
Het |
Ap2m1 |
C |
A |
16: 20,358,113 (GRCm39) |
R44S |
probably damaging |
Het |
Atrip |
T |
C |
9: 108,902,964 (GRCm39) |
S37G |
probably benign |
Het |
Bicra |
C |
T |
7: 15,705,987 (GRCm39) |
V1485M |
probably benign |
Het |
Brca2 |
C |
T |
5: 150,480,579 (GRCm39) |
T2755I |
probably damaging |
Het |
C1qtnf7 |
A |
T |
5: 43,673,313 (GRCm39) |
|
probably benign |
Het |
Ccdc7a |
C |
T |
8: 129,618,860 (GRCm39) |
A895T |
possibly damaging |
Het |
Cep290 |
T |
C |
10: 100,354,529 (GRCm39) |
M871T |
probably benign |
Het |
Col19a1 |
A |
G |
1: 24,318,904 (GRCm39) |
V1062A |
unknown |
Het |
Col24a1 |
T |
A |
3: 145,021,103 (GRCm39) |
Y491* |
probably null |
Het |
Cyp2c66 |
A |
T |
19: 39,102,520 (GRCm39) |
I50F |
probably benign |
Het |
Dbn1 |
C |
A |
13: 55,625,639 (GRCm39) |
R261L |
probably benign |
Het |
Dlat |
G |
A |
9: 50,562,208 (GRCm39) |
A272V |
probably damaging |
Het |
Dlgap3 |
A |
T |
4: 127,130,127 (GRCm39) |
E967V |
possibly damaging |
Het |
Dnhd1 |
A |
G |
7: 105,369,456 (GRCm39) |
M4360V |
probably benign |
Het |
Dock7 |
C |
T |
4: 98,877,464 (GRCm39) |
R1058Q |
unknown |
Het |
Dpp4 |
T |
A |
2: 62,195,340 (GRCm39) |
I313F |
probably benign |
Het |
Dus1l |
C |
T |
11: 120,683,858 (GRCm39) |
V197I |
possibly damaging |
Het |
Eef2k |
TATTCATTCATTCATTCATTCATTCATTCA |
TATTCATTCATTCATTCATTCATTCA |
7: 120,499,453 (GRCm39) |
|
probably benign |
Het |
Fat3 |
A |
G |
9: 15,826,537 (GRCm39) |
S324P |
probably benign |
Het |
Fkbp9 |
C |
T |
6: 56,855,181 (GRCm39) |
H567Y |
possibly damaging |
Het |
Galnt10 |
C |
A |
11: 57,672,065 (GRCm39) |
P452T |
probably damaging |
Het |
Glb1 |
A |
T |
9: 114,246,084 (GRCm39) |
D45V |
probably damaging |
Het |
Grm1 |
A |
T |
10: 10,573,826 (GRCm39) |
V904E |
possibly damaging |
Het |
Gsdma3 |
T |
G |
11: 98,526,071 (GRCm39) |
V274G |
probably damaging |
Het |
Gsn |
A |
G |
2: 35,194,600 (GRCm39) |
E681G |
probably damaging |
Het |
Hpdl |
A |
G |
4: 116,678,062 (GRCm39) |
L133P |
probably damaging |
Het |
Ighv1-75 |
A |
G |
12: 115,797,655 (GRCm39) |
L89P |
probably damaging |
Het |
Igsf21 |
T |
A |
4: 139,755,407 (GRCm39) |
Q416L |
probably damaging |
Het |
Il23a |
G |
C |
10: 128,132,829 (GRCm39) |
R143G |
probably benign |
Het |
Ildr1 |
A |
G |
16: 36,528,659 (GRCm39) |
T35A |
probably benign |
Het |
Ints13 |
G |
T |
6: 146,463,326 (GRCm39) |
H235Q |
probably damaging |
Het |
Lama4 |
C |
T |
10: 38,924,101 (GRCm39) |
T503I |
probably benign |
Het |
Mapk13 |
T |
A |
17: 28,997,075 (GRCm39) |
L289Q |
probably damaging |
Het |
Med13l |
T |
C |
5: 118,887,024 (GRCm39) |
S1642P |
probably benign |
Het |
Megf6 |
T |
A |
4: 154,343,617 (GRCm39) |
S713R |
probably damaging |
Het |
Mical3 |
A |
G |
6: 120,959,529 (GRCm39) |
V922A |
possibly damaging |
Het |
Mug1 |
C |
T |
6: 121,857,864 (GRCm39) |
T1119M |
probably damaging |
Het |
Myo18a |
T |
A |
11: 77,733,080 (GRCm39) |
M1370K |
possibly damaging |
Het |
Ndufa12 |
A |
G |
10: 94,056,692 (GRCm39) |
E140G |
probably damaging |
Het |
Nek4 |
T |
A |
14: 30,706,401 (GRCm39) |
D696E |
probably benign |
Het |
Oas1f |
A |
G |
5: 120,994,429 (GRCm39) |
T317A |
probably benign |
Het |
Or2r11 |
A |
G |
6: 42,437,029 (GRCm39) |
I308T |
probably benign |
Het |
Or6c210 |
T |
C |
10: 129,495,705 (GRCm39) |
I10T |
probably benign |
Het |
Pcdh17 |
C |
T |
14: 84,683,683 (GRCm39) |
P50L |
probably benign |
Het |
Pgs1 |
A |
G |
11: 117,894,256 (GRCm39) |
E261G |
probably benign |
Het |
Pira12 |
T |
G |
7: 3,897,612 (GRCm39) |
R494S |
probably damaging |
Het |
Ppp1r1a |
T |
C |
15: 103,439,857 (GRCm39) |
E145G |
possibly damaging |
Het |
Ppp1r37 |
T |
C |
7: 19,295,783 (GRCm39) |
E58G |
probably benign |
Het |
Ptprc |
A |
T |
1: 138,047,901 (GRCm39) |
V77E |
|
Het |
Rhag |
A |
G |
17: 41,139,416 (GRCm39) |
E117G |
probably benign |
Het |
Sh3d19 |
C |
T |
3: 86,028,483 (GRCm39) |
S653L |
probably benign |
Het |
Sirpd |
C |
A |
3: 15,385,813 (GRCm39) |
E30* |
probably null |
Het |
Slc35a5 |
C |
T |
16: 44,972,939 (GRCm39) |
|
probably null |
Het |
Smc4 |
C |
T |
3: 68,929,655 (GRCm39) |
R510* |
probably null |
Het |
Sorcs1 |
A |
G |
19: 50,248,190 (GRCm39) |
|
probably null |
Het |
Sp140 |
A |
G |
1: 85,569,461 (GRCm39) |
N357S |
probably damaging |
Het |
Spic |
T |
A |
10: 88,514,421 (GRCm39) |
T60S |
possibly damaging |
Het |
Steap1 |
C |
A |
5: 5,786,517 (GRCm39) |
A307S |
probably benign |
Het |
Stk3 |
A |
T |
15: 35,114,791 (GRCm39) |
S40R |
probably damaging |
Het |
Taar1 |
T |
C |
10: 23,796,676 (GRCm39) |
C125R |
probably damaging |
Het |
Tep1 |
T |
A |
14: 51,076,443 (GRCm39) |
K1664* |
probably null |
Het |
Tmem198b |
C |
A |
10: 128,638,273 (GRCm39) |
V97L |
possibly damaging |
Het |
Xirp2 |
C |
A |
2: 67,347,379 (GRCm39) |
P3207T |
possibly damaging |
Het |
Zbtb38 |
C |
G |
9: 96,570,355 (GRCm39) |
S243T |
possibly damaging |
Het |
Zbtb38 |
T |
A |
9: 96,570,356 (GRCm39) |
S243C |
probably damaging |
Het |
Zfp692 |
C |
T |
11: 58,199,638 (GRCm39) |
R76W |
probably benign |
Het |
Zwilch |
A |
T |
9: 64,054,170 (GRCm39) |
L509H |
probably damaging |
Het |
|
Other mutations in Or14c39 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01575:Or14c39
|
APN |
7 |
86,344,501 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01751:Or14c39
|
APN |
7 |
86,343,997 (GRCm39) |
missense |
probably benign |
|
IGL02417:Or14c39
|
APN |
7 |
86,344,027 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02534:Or14c39
|
APN |
7 |
86,343,939 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02830:Or14c39
|
APN |
7 |
86,344,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R0281:Or14c39
|
UTSW |
7 |
86,344,068 (GRCm39) |
missense |
probably benign |
0.00 |
R0423:Or14c39
|
UTSW |
7 |
86,344,434 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0555:Or14c39
|
UTSW |
7 |
86,344,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Or14c39
|
UTSW |
7 |
86,344,084 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0662:Or14c39
|
UTSW |
7 |
86,343,838 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1710:Or14c39
|
UTSW |
7 |
86,344,318 (GRCm39) |
missense |
probably benign |
0.00 |
R2144:Or14c39
|
UTSW |
7 |
86,344,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R4400:Or14c39
|
UTSW |
7 |
86,343,798 (GRCm39) |
missense |
probably benign |
0.10 |
R4615:Or14c39
|
UTSW |
7 |
86,343,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R4762:Or14c39
|
UTSW |
7 |
86,344,329 (GRCm39) |
missense |
probably benign |
0.01 |
R4785:Or14c39
|
UTSW |
7 |
86,343,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Or14c39
|
UTSW |
7 |
86,343,796 (GRCm39) |
missense |
probably damaging |
0.99 |
R4908:Or14c39
|
UTSW |
7 |
86,344,395 (GRCm39) |
missense |
probably benign |
0.00 |
R4983:Or14c39
|
UTSW |
7 |
86,343,687 (GRCm39) |
missense |
probably benign |
0.01 |
R5010:Or14c39
|
UTSW |
7 |
86,343,793 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5024:Or14c39
|
UTSW |
7 |
86,344,089 (GRCm39) |
missense |
probably benign |
0.05 |
R5157:Or14c39
|
UTSW |
7 |
86,344,440 (GRCm39) |
missense |
probably benign |
0.19 |
R5627:Or14c39
|
UTSW |
7 |
86,344,347 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6327:Or14c39
|
UTSW |
7 |
86,343,760 (GRCm39) |
missense |
probably benign |
0.09 |
R6375:Or14c39
|
UTSW |
7 |
86,344,267 (GRCm39) |
missense |
probably benign |
0.01 |
R6775:Or14c39
|
UTSW |
7 |
86,344,357 (GRCm39) |
missense |
probably benign |
0.02 |
R7257:Or14c39
|
UTSW |
7 |
86,344,012 (GRCm39) |
missense |
probably damaging |
0.99 |
R7383:Or14c39
|
UTSW |
7 |
86,343,960 (GRCm39) |
missense |
probably damaging |
0.97 |
R8475:Or14c39
|
UTSW |
7 |
86,344,361 (GRCm39) |
missense |
probably benign |
0.21 |
R9034:Or14c39
|
UTSW |
7 |
86,343,969 (GRCm39) |
missense |
probably benign |
0.41 |
R9134:Or14c39
|
UTSW |
7 |
86,344,588 (GRCm39) |
nonsense |
probably null |
|
R9588:Or14c39
|
UTSW |
7 |
86,343,948 (GRCm39) |
missense |
probably damaging |
1.00 |
|