Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
T |
G |
5: 125,589,716 (GRCm39) |
M446R |
possibly damaging |
Het |
Abca16 |
A |
G |
7: 120,140,500 (GRCm39) |
N1599S |
probably benign |
Het |
Ankib1 |
G |
A |
5: 3,763,146 (GRCm39) |
Q528* |
probably null |
Het |
Ano10 |
A |
T |
9: 122,088,606 (GRCm39) |
L347M |
possibly damaging |
Het |
Bag6 |
T |
C |
17: 35,361,992 (GRCm39) |
|
probably benign |
Het |
Bpnt1 |
T |
C |
1: 185,086,191 (GRCm39) |
V182A |
possibly damaging |
Het |
Capn13 |
G |
T |
17: 73,638,053 (GRCm39) |
T450N |
probably benign |
Het |
Cbr3 |
A |
T |
16: 93,480,331 (GRCm39) |
E40V |
probably benign |
Het |
Cdk10 |
T |
C |
8: 123,955,126 (GRCm39) |
I159T |
probably damaging |
Het |
Cela3b |
T |
C |
4: 137,152,382 (GRCm39) |
D65G |
possibly damaging |
Het |
Csf2rb |
T |
G |
15: 78,219,502 (GRCm39) |
|
probably benign |
Het |
Cyp2b19 |
C |
T |
7: 26,462,886 (GRCm39) |
T256I |
possibly damaging |
Het |
Dpp9 |
T |
C |
17: 56,497,713 (GRCm39) |
H687R |
probably benign |
Het |
Elovl1 |
T |
C |
4: 118,288,467 (GRCm39) |
V108A |
probably benign |
Het |
Emb |
T |
A |
13: 117,408,614 (GRCm39) |
N318K |
probably damaging |
Het |
Ermp1 |
A |
G |
19: 29,617,339 (GRCm39) |
L36P |
probably damaging |
Het |
Esco2 |
T |
G |
14: 66,064,044 (GRCm39) |
H380P |
possibly damaging |
Het |
Gm9747 |
G |
A |
1: 82,211,809 (GRCm39) |
|
probably benign |
Het |
Golga1 |
A |
G |
2: 38,910,138 (GRCm39) |
M603T |
probably benign |
Het |
Hsph1 |
A |
G |
5: 149,550,743 (GRCm39) |
V411A |
probably benign |
Het |
Igsf21 |
C |
T |
4: 139,834,675 (GRCm39) |
G66S |
possibly damaging |
Het |
Ints11 |
T |
C |
4: 155,969,655 (GRCm39) |
|
probably null |
Het |
Jakmip1 |
G |
T |
5: 37,258,112 (GRCm39) |
A253S |
probably damaging |
Het |
Met |
A |
G |
6: 17,540,576 (GRCm39) |
Y834C |
probably damaging |
Het |
Mgl2 |
A |
G |
11: 70,024,984 (GRCm39) |
T2A |
probably benign |
Het |
Myh2 |
G |
T |
11: 67,088,170 (GRCm39) |
V1929L |
probably benign |
Het |
Myh8 |
T |
C |
11: 67,192,536 (GRCm39) |
S1472P |
probably benign |
Het |
Myo1e |
T |
C |
9: 70,248,555 (GRCm39) |
|
probably benign |
Het |
Ndufaf7 |
A |
G |
17: 79,244,931 (GRCm39) |
I17V |
probably benign |
Het |
Or4a47 |
T |
C |
2: 89,666,152 (GRCm39) |
T46A |
probably damaging |
Het |
Or5ak22 |
C |
T |
2: 85,230,515 (GRCm39) |
D121N |
probably damaging |
Het |
Or5h25 |
A |
T |
16: 58,930,284 (GRCm39) |
S230T |
probably damaging |
Het |
Or7g18 |
T |
A |
9: 18,786,617 (GRCm39) |
|
probably benign |
Het |
Or8b50 |
A |
G |
9: 38,517,850 (GRCm39) |
I30V |
probably null |
Het |
Or8k1 |
T |
G |
2: 86,047,505 (GRCm39) |
D183A |
probably damaging |
Het |
Ppef2 |
T |
C |
5: 92,383,679 (GRCm39) |
E477G |
probably benign |
Het |
Scmh1 |
T |
A |
4: 120,387,097 (GRCm39) |
|
probably benign |
Het |
Scn1a |
C |
A |
2: 66,116,281 (GRCm39) |
D1473Y |
probably damaging |
Het |
Sdr42e1 |
C |
T |
8: 118,389,676 (GRCm39) |
V322I |
probably benign |
Het |
Slco1a7 |
G |
T |
6: 141,658,940 (GRCm39) |
T552K |
possibly damaging |
Het |
Spta1 |
G |
A |
1: 174,035,960 (GRCm39) |
A1089T |
probably damaging |
Het |
Sufu |
T |
C |
19: 46,464,059 (GRCm39) |
Y424H |
probably damaging |
Het |
Tgs1 |
T |
C |
4: 3,585,183 (GRCm39) |
F108L |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,805,308 (GRCm39) |
N177S |
probably benign |
Het |
Tyk2 |
T |
C |
9: 21,031,872 (GRCm39) |
D401G |
probably damaging |
Het |
Vav1 |
T |
C |
17: 57,614,067 (GRCm39) |
F650L |
possibly damaging |
Het |
Wdr12 |
T |
C |
1: 60,119,718 (GRCm39) |
H385R |
probably damaging |
Het |
Xab2 |
T |
C |
8: 3,660,880 (GRCm39) |
M745V |
probably benign |
Het |
|
Other mutations in Or6c6c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02041:Or6c6c
|
APN |
10 |
129,541,104 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02245:Or6c6c
|
APN |
10 |
129,541,608 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02341:Or6c6c
|
APN |
10 |
129,541,358 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02433:Or6c6c
|
APN |
10 |
129,541,445 (GRCm39) |
missense |
probably benign |
0.01 |
authen
|
UTSW |
10 |
129,541,668 (GRCm39) |
missense |
probably benign |
0.00 |
R0111:Or6c6c
|
UTSW |
10 |
129,541,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Or6c6c
|
UTSW |
10 |
129,541,008 (GRCm39) |
missense |
probably benign |
0.38 |
R0326:Or6c6c
|
UTSW |
10 |
129,541,638 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0374:Or6c6c
|
UTSW |
10 |
129,541,516 (GRCm39) |
missense |
probably benign |
0.00 |
R1573:Or6c6c
|
UTSW |
10 |
129,541,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R1663:Or6c6c
|
UTSW |
10 |
129,541,160 (GRCm39) |
missense |
probably benign |
0.44 |
R1778:Or6c6c
|
UTSW |
10 |
129,541,574 (GRCm39) |
missense |
probably benign |
0.01 |
R1789:Or6c6c
|
UTSW |
10 |
129,541,476 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1906:Or6c6c
|
UTSW |
10 |
129,541,365 (GRCm39) |
missense |
probably benign |
0.00 |
R2108:Or6c6c
|
UTSW |
10 |
129,541,490 (GRCm39) |
missense |
probably benign |
|
R2211:Or6c6c
|
UTSW |
10 |
129,541,320 (GRCm39) |
missense |
probably benign |
|
R2432:Or6c6c
|
UTSW |
10 |
129,540,794 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2902:Or6c6c
|
UTSW |
10 |
129,541,320 (GRCm39) |
missense |
probably benign |
|
R4114:Or6c6c
|
UTSW |
10 |
129,541,668 (GRCm39) |
missense |
probably benign |
0.00 |
R5149:Or6c6c
|
UTSW |
10 |
129,541,377 (GRCm39) |
missense |
probably benign |
0.00 |
R5153:Or6c6c
|
UTSW |
10 |
129,541,026 (GRCm39) |
missense |
probably benign |
0.05 |
R5846:Or6c6c
|
UTSW |
10 |
129,540,756 (GRCm39) |
missense |
probably damaging |
0.99 |
R6553:Or6c6c
|
UTSW |
10 |
129,540,932 (GRCm39) |
missense |
probably benign |
0.07 |
R7676:Or6c6c
|
UTSW |
10 |
129,541,155 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8161:Or6c6c
|
UTSW |
10 |
129,540,753 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9266:Or6c6c
|
UTSW |
10 |
129,541,547 (GRCm39) |
missense |
probably benign |
0.17 |
R9318:Or6c6c
|
UTSW |
10 |
129,541,283 (GRCm39) |
missense |
probably benign |
0.00 |
R9334:Or6c6c
|
UTSW |
10 |
129,541,683 (GRCm39) |
missense |
probably benign |
0.00 |
R9746:Or6c6c
|
UTSW |
10 |
129,541,208 (GRCm39) |
missense |
probably damaging |
0.97 |
|