Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap9 |
A |
T |
5: 4,100,545 (GRCm39) |
T2736S |
probably benign |
Het |
AW209491 |
T |
C |
13: 14,811,957 (GRCm39) |
V270A |
probably benign |
Het |
Best3 |
A |
T |
10: 116,838,450 (GRCm39) |
K169N |
probably damaging |
Het |
Cabyr |
A |
G |
18: 12,883,816 (GRCm39) |
K101R |
probably damaging |
Het |
Cfhr4 |
C |
T |
1: 139,701,764 (GRCm39) |
V117I |
probably damaging |
Het |
Chd5 |
A |
T |
4: 152,461,079 (GRCm39) |
D1223V |
possibly damaging |
Het |
Commd2 |
T |
C |
3: 57,559,064 (GRCm39) |
D4G |
probably benign |
Het |
Cox5b-ps |
T |
C |
13: 21,685,294 (GRCm39) |
T99A |
probably benign |
Het |
Cyp3a41a |
A |
T |
5: 145,652,320 (GRCm39) |
F60I |
possibly damaging |
Het |
D6Ertd527e |
G |
C |
6: 87,088,839 (GRCm39) |
S334T |
unknown |
Het |
Dnmbp |
C |
A |
19: 43,855,974 (GRCm39) |
A261S |
probably benign |
Het |
Fcgbp |
A |
C |
7: 27,800,832 (GRCm39) |
T1293P |
probably benign |
Het |
Gal3st2b |
A |
C |
1: 93,868,777 (GRCm39) |
N336T |
probably benign |
Het |
Gm10309 |
T |
C |
17: 86,806,494 (GRCm39) |
T7A |
unknown |
Het |
Gm10322 |
A |
T |
10: 59,451,931 (GRCm39) |
H16L |
possibly damaging |
Het |
Gpr17 |
A |
G |
18: 32,080,199 (GRCm39) |
L288P |
probably damaging |
Het |
Ighe |
T |
C |
12: 113,235,899 (GRCm39) |
I142M |
|
Het |
Lrrc7 |
T |
C |
3: 157,946,138 (GRCm39) |
K187R |
probably benign |
Het |
Lrrk2 |
T |
A |
15: 91,696,527 (GRCm39) |
D2438E |
probably benign |
Het |
Map3k20 |
G |
A |
2: 72,232,403 (GRCm39) |
S353N |
possibly damaging |
Het |
Moxd2 |
T |
A |
6: 40,863,000 (GRCm39) |
D102V |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,972,686 (GRCm39) |
E2120G |
possibly damaging |
Het |
Or4f4-ps1 |
T |
A |
2: 111,330,267 (GRCm39) |
C223* |
probably null |
Het |
Or5p79 |
A |
G |
7: 108,221,654 (GRCm39) |
I212V |
probably benign |
Het |
Or6c5c |
T |
C |
10: 129,299,463 (GRCm39) |
V306A |
probably benign |
Het |
Pcdhb5 |
A |
T |
18: 37,454,510 (GRCm39) |
T297S |
probably benign |
Het |
Pdcd2l |
A |
C |
7: 33,892,356 (GRCm39) |
L171R |
possibly damaging |
Het |
Ppp4r3b |
T |
C |
11: 29,138,113 (GRCm39) |
S154P |
probably benign |
Het |
Prc1 |
T |
G |
7: 79,962,047 (GRCm39) |
M515R |
probably benign |
Het |
Samsn1 |
T |
G |
16: 75,673,457 (GRCm39) |
T140P |
probably damaging |
Het |
Slc34a1 |
G |
A |
13: 55,556,940 (GRCm39) |
V379M |
probably damaging |
Het |
Stab2 |
T |
A |
10: 86,686,651 (GRCm39) |
R2298* |
probably null |
Het |
Trim10 |
G |
A |
17: 37,187,890 (GRCm39) |
V369M |
probably damaging |
Het |
Trpv6 |
T |
C |
6: 41,599,901 (GRCm39) |
N585S |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,586,617 (GRCm39) |
D21765N |
possibly damaging |
Het |
Ubxn6 |
A |
G |
17: 56,376,189 (GRCm39) |
L349P |
probably damaging |
Het |
Vdac3 |
A |
T |
8: 23,077,575 (GRCm39) |
S37R |
probably damaging |
Het |
Vmn1r124 |
G |
A |
7: 20,993,720 (GRCm39) |
L275F |
probably benign |
Het |
Wdr17 |
A |
T |
8: 55,101,375 (GRCm39) |
I964N |
probably damaging |
Het |
Zdhhc22 |
A |
G |
12: 87,030,396 (GRCm39) |
F184S |
possibly damaging |
Het |
Zfp512 |
A |
G |
5: 31,623,669 (GRCm39) |
H124R |
probably benign |
Het |
Zswim4 |
T |
C |
8: 84,939,354 (GRCm39) |
T843A |
probably damaging |
Het |
|
Other mutations in Rbm34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:Rbm34
|
APN |
8 |
127,696,736 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02505:Rbm34
|
APN |
8 |
127,676,071 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03166:Rbm34
|
APN |
8 |
127,697,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R0081:Rbm34
|
UTSW |
8 |
127,676,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R1186:Rbm34
|
UTSW |
8 |
127,692,197 (GRCm39) |
nonsense |
probably null |
|
R1257:Rbm34
|
UTSW |
8 |
127,697,643 (GRCm39) |
missense |
possibly damaging |
0.45 |
R1867:Rbm34
|
UTSW |
8 |
127,697,631 (GRCm39) |
missense |
probably benign |
0.17 |
R1868:Rbm34
|
UTSW |
8 |
127,697,631 (GRCm39) |
missense |
probably benign |
0.17 |
R4008:Rbm34
|
UTSW |
8 |
127,676,037 (GRCm39) |
missense |
probably benign |
0.00 |
R4395:Rbm34
|
UTSW |
8 |
127,676,131 (GRCm39) |
missense |
probably benign |
0.03 |
R4823:Rbm34
|
UTSW |
8 |
127,697,655 (GRCm39) |
missense |
probably benign |
0.01 |
R4903:Rbm34
|
UTSW |
8 |
127,678,087 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4964:Rbm34
|
UTSW |
8 |
127,678,087 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4966:Rbm34
|
UTSW |
8 |
127,678,087 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5605:Rbm34
|
UTSW |
8 |
127,676,169 (GRCm39) |
missense |
probably benign |
0.05 |
R5734:Rbm34
|
UTSW |
8 |
127,696,880 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6515:Rbm34
|
UTSW |
8 |
127,688,682 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8263:Rbm34
|
UTSW |
8 |
127,692,139 (GRCm39) |
missense |
probably benign |
0.03 |
R8544:Rbm34
|
UTSW |
8 |
127,696,821 (GRCm39) |
missense |
probably benign |
0.00 |
R8915:Rbm34
|
UTSW |
8 |
127,679,908 (GRCm39) |
splice site |
probably benign |
|
R8957:Rbm34
|
UTSW |
8 |
127,692,208 (GRCm39) |
missense |
probably benign |
0.00 |
R9005:Rbm34
|
UTSW |
8 |
127,686,332 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9131:Rbm34
|
UTSW |
8 |
127,679,928 (GRCm39) |
missense |
probably damaging |
0.97 |
|