Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Adamts10 |
C |
T |
17: 33,762,668 (GRCm39) |
A549V |
probably benign |
Het |
Akap13 |
T |
C |
7: 75,259,074 (GRCm39) |
M566T |
probably benign |
Het |
Alb |
A |
G |
5: 90,615,225 (GRCm39) |
T246A |
probably benign |
Het |
Cyfip1 |
C |
T |
7: 55,558,140 (GRCm39) |
R806C |
probably damaging |
Het |
Cyp11a1 |
T |
A |
9: 57,925,644 (GRCm39) |
I195N |
probably damaging |
Het |
Dclre1a |
C |
G |
19: 56,526,826 (GRCm39) |
Q863H |
|
Het |
Ddx19a |
A |
G |
8: 111,705,188 (GRCm39) |
V311A |
probably benign |
Het |
Dnajc13 |
A |
T |
9: 104,057,330 (GRCm39) |
F1557I |
probably damaging |
Het |
Eml6 |
T |
A |
11: 29,755,181 (GRCm39) |
T865S |
possibly damaging |
Het |
Esrrg |
T |
A |
1: 187,943,104 (GRCm39) |
I382K |
possibly damaging |
Het |
Fam149a |
G |
A |
8: 45,811,837 (GRCm39) |
T22M |
|
Het |
Fam227b |
A |
T |
2: 125,958,019 (GRCm39) |
Y249N |
probably damaging |
Het |
Fanci |
G |
A |
7: 79,095,472 (GRCm39) |
V1217I |
probably benign |
Het |
Fermt2 |
A |
G |
14: 45,742,023 (GRCm39) |
Y108H |
probably benign |
Het |
Gkn1 |
A |
T |
6: 87,325,160 (GRCm39) |
V83E |
probably damaging |
Het |
Glmp |
T |
A |
3: 88,233,002 (GRCm39) |
S47T |
probably benign |
Het |
Greb1 |
T |
C |
12: 16,734,457 (GRCm39) |
H1511R |
probably damaging |
Het |
Grid1 |
G |
A |
14: 35,043,664 (GRCm39) |
D340N |
probably damaging |
Het |
Htra3 |
A |
T |
5: 35,836,372 (GRCm39) |
C107S |
probably damaging |
Het |
Ighv1-58 |
T |
C |
12: 115,275,835 (GRCm39) |
Q101R |
probably benign |
Het |
Igtp |
T |
A |
11: 58,096,947 (GRCm39) |
|
probably null |
Het |
Il1rap |
T |
C |
16: 26,533,696 (GRCm39) |
S531P |
probably damaging |
Het |
Kcnd3 |
A |
T |
3: 105,367,039 (GRCm39) |
H303L |
probably damaging |
Het |
Kcnj3 |
G |
T |
2: 55,485,039 (GRCm39) |
S379I |
probably benign |
Het |
Lrrc36 |
T |
C |
8: 106,176,093 (GRCm39) |
S156P |
possibly damaging |
Het |
Mical3 |
G |
T |
6: 120,991,822 (GRCm39) |
D250E |
|
Het |
Msh3 |
T |
C |
13: 92,483,334 (GRCm39) |
T270A |
probably damaging |
Het |
Myrfl |
A |
G |
10: 116,658,746 (GRCm39) |
W404R |
probably damaging |
Het |
Nol7 |
T |
C |
13: 43,554,985 (GRCm39) |
F206S |
probably damaging |
Het |
Obi1 |
T |
C |
14: 104,745,418 (GRCm39) |
H86R |
probably damaging |
Het |
Or12e13 |
A |
T |
2: 87,663,655 (GRCm39) |
I91F |
possibly damaging |
Het |
Or2ag1 |
A |
G |
7: 106,473,050 (GRCm39) |
I134T |
probably benign |
Het |
Paox |
A |
G |
7: 139,706,503 (GRCm39) |
E141G |
probably benign |
Het |
Plod1 |
A |
T |
4: 147,997,734 (GRCm39) |
H658Q |
probably damaging |
Het |
Pou4f1 |
T |
C |
14: 104,704,087 (GRCm39) |
D115G |
probably damaging |
Het |
Ppp1r26 |
G |
T |
2: 28,342,802 (GRCm39) |
E811* |
probably null |
Het |
Qsox1 |
C |
T |
1: 155,666,829 (GRCm39) |
R220K |
probably damaging |
Het |
Rabgap1l |
C |
T |
1: 160,085,105 (GRCm39) |
V781I |
probably damaging |
Het |
Rad50 |
T |
C |
11: 53,541,354 (GRCm39) |
D1294G |
possibly damaging |
Het |
Rbp7 |
C |
T |
4: 149,537,371 (GRCm39) |
V97I |
probably benign |
Het |
Rrad |
C |
T |
8: 105,355,222 (GRCm39) |
R262Q |
possibly damaging |
Het |
Sdcbp2 |
T |
C |
2: 151,429,150 (GRCm39) |
V183A |
probably benign |
Het |
Slfn2 |
C |
G |
11: 82,960,427 (GRCm39) |
I135M |
possibly damaging |
Het |
Sntg1 |
T |
A |
1: 8,484,491 (GRCm39) |
D443V |
possibly damaging |
Het |
Tas2r105 |
G |
A |
6: 131,663,913 (GRCm39) |
Q172* |
probably null |
Het |
Tfdp2 |
A |
G |
9: 96,172,637 (GRCm39) |
R44G |
probably damaging |
Het |
Thbd |
A |
T |
2: 148,248,480 (GRCm39) |
C463S |
probably damaging |
Het |
Tnxb |
T |
C |
17: 34,897,646 (GRCm39) |
V807A |
possibly damaging |
Het |
Trim68 |
T |
A |
7: 102,327,808 (GRCm39) |
K382* |
probably null |
Het |
Vmn2r110 |
T |
A |
17: 20,803,823 (GRCm39) |
I251F |
probably damaging |
Het |
Vmn2r61 |
A |
T |
7: 41,915,325 (GRCm39) |
R91* |
probably null |
Het |
Vmn2r-ps117 |
G |
A |
17: 19,044,943 (GRCm39) |
W453* |
probably null |
Het |
Zc3h18 |
T |
C |
8: 123,134,193 (GRCm39) |
V553A |
unknown |
Het |
Zfp609 |
C |
T |
9: 65,610,561 (GRCm39) |
A801T |
possibly damaging |
Het |
Zfp791 |
A |
G |
8: 85,837,327 (GRCm39) |
F179S |
probably benign |
Het |
Zyg11a |
A |
T |
4: 108,041,628 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ighv6-5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02532:Ighv6-5
|
APN |
12 |
114,380,424 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02928:Ighv6-5
|
APN |
12 |
114,380,412 (GRCm39) |
missense |
probably benign |
0.42 |
IGL03117:Ighv6-5
|
APN |
12 |
114,380,320 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02991:Ighv6-5
|
UTSW |
12 |
114,380,315 (GRCm39) |
missense |
probably benign |
|
R0020:Ighv6-5
|
UTSW |
12 |
114,380,241 (GRCm39) |
missense |
probably null |
1.00 |
R4386:Ighv6-5
|
UTSW |
12 |
114,380,337 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5067:Ighv6-5
|
UTSW |
12 |
114,380,191 (GRCm39) |
splice site |
probably null |
|
R6154:Ighv6-5
|
UTSW |
12 |
114,380,362 (GRCm39) |
missense |
probably benign |
0.04 |
R7133:Ighv6-5
|
UTSW |
12 |
114,380,395 (GRCm39) |
missense |
probably benign |
0.00 |
R7617:Ighv6-5
|
UTSW |
12 |
114,380,626 (GRCm39) |
critical splice donor site |
probably benign |
|
R8047:Ighv6-5
|
UTSW |
12 |
114,380,191 (GRCm39) |
splice site |
probably null |
|
|