Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530064D06Rik |
C |
T |
17: 48,473,558 (GRCm39) |
V120M |
possibly damaging |
Het |
Abca6 |
T |
C |
11: 110,109,793 (GRCm39) |
D646G |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 31,060,403 (GRCm39) |
R141Q |
probably damaging |
Het |
Arid1b |
A |
G |
17: 5,364,293 (GRCm39) |
T554A |
possibly damaging |
Het |
Atp2a3 |
G |
T |
11: 72,873,652 (GRCm39) |
V824L |
probably null |
Het |
Bet1 |
T |
C |
6: 4,077,895 (GRCm39) |
I115V |
possibly damaging |
Het |
Cdc23 |
C |
A |
18: 34,784,742 (GRCm39) |
V7L |
unknown |
Het |
Cfap65 |
A |
G |
1: 74,945,600 (GRCm39) |
S1373P |
probably damaging |
Het |
Chd9 |
T |
C |
8: 91,711,002 (GRCm39) |
L353P |
probably damaging |
Het |
Chil3 |
C |
A |
3: 106,071,405 (GRCm39) |
|
probably null |
Het |
Comp |
C |
T |
8: 70,833,950 (GRCm39) |
T655M |
probably damaging |
Het |
Dctd |
T |
C |
8: 48,564,751 (GRCm39) |
Y18H |
probably damaging |
Het |
Ddx39b |
G |
A |
17: 35,472,005 (GRCm39) |
G348D |
possibly damaging |
Het |
Dhx36 |
A |
T |
3: 62,379,420 (GRCm39) |
S889R |
probably benign |
Het |
Dtx2 |
T |
C |
5: 136,041,044 (GRCm39) |
Y150H |
probably damaging |
Het |
Epx |
A |
G |
11: 87,763,506 (GRCm39) |
F238S |
probably damaging |
Het |
Ergic2 |
T |
C |
6: 148,097,512 (GRCm39) |
T154A |
probably benign |
Het |
Esco1 |
A |
G |
18: 10,594,734 (GRCm39) |
I184T |
probably benign |
Het |
Esf1 |
G |
T |
2: 139,998,991 (GRCm39) |
A495E |
possibly damaging |
Het |
Esf1 |
T |
C |
2: 140,000,499 (GRCm39) |
Y429C |
possibly damaging |
Het |
Fcho1 |
C |
A |
8: 72,169,820 (GRCm39) |
R101L |
probably benign |
Het |
Foxn4 |
T |
A |
5: 114,394,988 (GRCm39) |
D313V |
probably damaging |
Het |
Gm11568 |
T |
C |
11: 99,748,798 (GRCm39) |
M1T |
probably null |
Het |
Gphn |
T |
A |
12: 78,670,063 (GRCm39) |
|
probably null |
Het |
Grid2 |
C |
T |
6: 64,297,136 (GRCm39) |
Q500* |
probably null |
Het |
Igsf10 |
A |
G |
3: 59,233,694 (GRCm39) |
S1680P |
probably damaging |
Het |
Ints12 |
T |
C |
3: 132,806,538 (GRCm39) |
M155T |
possibly damaging |
Het |
Invs |
A |
T |
4: 48,396,307 (GRCm39) |
M327L |
possibly damaging |
Het |
Kdm3a |
T |
C |
6: 71,598,346 (GRCm39) |
E180G |
probably damaging |
Het |
Mgat3 |
G |
A |
15: 80,095,499 (GRCm39) |
V109M |
possibly damaging |
Het |
Mrgprb3 |
A |
G |
7: 48,292,762 (GRCm39) |
V263A |
probably benign |
Het |
Mroh7 |
A |
T |
4: 106,547,515 (GRCm39) |
V1109D |
probably benign |
Het |
Myo15b |
A |
T |
11: 115,757,482 (GRCm39) |
T1111S |
probably benign |
Het |
Myo19 |
G |
T |
11: 84,794,037 (GRCm39) |
A654S |
possibly damaging |
Het |
Mypn |
A |
T |
10: 62,954,307 (GRCm39) |
V1224D |
probably damaging |
Het |
Nalcn |
A |
G |
14: 123,560,706 (GRCm39) |
|
probably null |
Het |
Or2a52 |
G |
T |
6: 43,144,273 (GRCm39) |
A94S |
probably benign |
Het |
Or52e7 |
A |
T |
7: 104,684,618 (GRCm39) |
Y71F |
probably damaging |
Het |
Or8c10 |
G |
A |
9: 38,279,358 (GRCm39) |
C172Y |
possibly damaging |
Het |
Pdcd2 |
A |
G |
17: 15,743,084 (GRCm39) |
I247T |
possibly damaging |
Het |
Pik3c2a |
A |
T |
7: 115,941,636 (GRCm39) |
N1571K |
probably damaging |
Het |
Plagl2 |
T |
C |
2: 153,077,964 (GRCm39) |
T6A |
probably benign |
Het |
Ros1 |
T |
A |
10: 52,040,037 (GRCm39) |
Y318F |
possibly damaging |
Het |
Sdccag8 |
C |
A |
1: 176,652,458 (GRCm39) |
H70N |
probably damaging |
Het |
Skint1 |
A |
G |
4: 111,886,630 (GRCm39) |
R359G |
probably benign |
Het |
Slc44a5 |
A |
T |
3: 153,953,424 (GRCm39) |
I269L |
probably benign |
Het |
Suclg1 |
C |
A |
6: 73,240,963 (GRCm39) |
T164K |
probably benign |
Het |
Tgds |
C |
A |
14: 118,353,491 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,643,877 (GRCm39) |
D13117G |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,701,081 (GRCm39) |
|
probably benign |
Het |
Vmn2r28 |
A |
T |
7: 5,483,671 (GRCm39) |
I843N |
possibly damaging |
Het |
Vmn2r52 |
A |
T |
7: 9,893,392 (GRCm39) |
Y582* |
probably null |
Het |
Vps33b |
G |
T |
7: 79,924,389 (GRCm39) |
K65N |
probably damaging |
Het |
Zfp1010 |
A |
G |
2: 176,957,364 (GRCm39) |
F45L |
probably damaging |
Het |
|
Other mutations in Slfn10-ps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00773:Slfn10-ps
|
APN |
11 |
82,926,355 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL00826:Slfn10-ps
|
APN |
11 |
82,926,085 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL01022:Slfn10-ps
|
APN |
11 |
82,926,353 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL01409:Slfn10-ps
|
APN |
11 |
82,926,322 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL01664:Slfn10-ps
|
APN |
11 |
82,926,761 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL01700:Slfn10-ps
|
APN |
11 |
82,919,938 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02093:Slfn10-ps
|
APN |
11 |
82,923,016 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02253:Slfn10-ps
|
APN |
11 |
82,919,890 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02364:Slfn10-ps
|
APN |
11 |
82,923,117 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02466:Slfn10-ps
|
APN |
11 |
82,921,090 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02636:Slfn10-ps
|
APN |
11 |
82,920,971 (GRCm39) |
unclassified |
noncoding transcript |
|
R0055:Slfn10-ps
|
UTSW |
11 |
82,921,126 (GRCm39) |
unclassified |
noncoding transcript |
|
R0055:Slfn10-ps
|
UTSW |
11 |
82,921,126 (GRCm39) |
unclassified |
noncoding transcript |
|
R0069:Slfn10-ps
|
UTSW |
11 |
82,926,368 (GRCm39) |
unclassified |
noncoding transcript |
|
R0069:Slfn10-ps
|
UTSW |
11 |
82,926,368 (GRCm39) |
unclassified |
noncoding transcript |
|
R0164:Slfn10-ps
|
UTSW |
11 |
82,926,128 (GRCm39) |
unclassified |
noncoding transcript |
|
R0362:Slfn10-ps
|
UTSW |
11 |
82,926,600 (GRCm39) |
unclassified |
noncoding transcript |
|
R0382:Slfn10-ps
|
UTSW |
11 |
82,920,360 (GRCm39) |
unclassified |
noncoding transcript |
|
R0597:Slfn10-ps
|
UTSW |
11 |
82,926,479 (GRCm39) |
unclassified |
noncoding transcript |
|
R0812:Slfn10-ps
|
UTSW |
11 |
82,926,388 (GRCm39) |
unclassified |
noncoding transcript |
|
R0904:Slfn10-ps
|
UTSW |
11 |
82,926,235 (GRCm39) |
unclassified |
noncoding transcript |
|
R1552:Slfn10-ps
|
UTSW |
11 |
82,920,676 (GRCm39) |
unclassified |
noncoding transcript |
|
R1703:Slfn10-ps
|
UTSW |
11 |
82,920,869 (GRCm39) |
unclassified |
noncoding transcript |
|
R2127:Slfn10-ps
|
UTSW |
11 |
82,921,168 (GRCm39) |
unclassified |
noncoding transcript |
|
R2151:Slfn10-ps
|
UTSW |
11 |
82,926,511 (GRCm39) |
unclassified |
noncoding transcript |
|
R2302:Slfn10-ps
|
UTSW |
11 |
82,919,756 (GRCm39) |
unclassified |
noncoding transcript |
|
R3114:Slfn10-ps
|
UTSW |
11 |
82,919,955 (GRCm39) |
unclassified |
noncoding transcript |
|
R4293:Slfn10-ps
|
UTSW |
11 |
82,926,260 (GRCm39) |
unclassified |
noncoding transcript |
|
R4929:Slfn10-ps
|
UTSW |
11 |
82,920,345 (GRCm39) |
unclassified |
noncoding transcript |
|
R4970:Slfn10-ps
|
UTSW |
11 |
82,921,207 (GRCm39) |
unclassified |
noncoding transcript |
|
R5290:Slfn10-ps
|
UTSW |
11 |
82,919,851 (GRCm39) |
unclassified |
noncoding transcript |
|
R5306:Slfn10-ps
|
UTSW |
11 |
82,926,355 (GRCm39) |
unclassified |
noncoding transcript |
|
R5444:Slfn10-ps
|
UTSW |
11 |
82,926,113 (GRCm39) |
unclassified |
noncoding transcript |
|
|