Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm3 |
T |
C |
3: 59,784,571 (GRCm39) |
L348P |
probably damaging |
Het |
Adamts15 |
C |
A |
9: 30,816,111 (GRCm39) |
C616F |
probably damaging |
Het |
Adarb1 |
T |
C |
10: 77,158,099 (GRCm39) |
N116S |
probably damaging |
Het |
Add2 |
C |
T |
6: 86,095,639 (GRCm39) |
S437L |
probably damaging |
Het |
Adra1d |
T |
A |
2: 131,388,069 (GRCm39) |
R495S |
probably benign |
Het |
Agk |
C |
T |
6: 40,364,429 (GRCm39) |
T309I |
probably damaging |
Het |
Aqr |
T |
C |
2: 113,992,133 (GRCm39) |
Y81C |
probably damaging |
Het |
Bak1 |
G |
A |
17: 27,240,242 (GRCm39) |
Q142* |
probably null |
Het |
Bckdha |
A |
G |
7: 25,330,845 (GRCm39) |
V307A |
probably damaging |
Het |
Camk2n2 |
C |
A |
16: 20,438,948 (GRCm39) |
G72V |
probably benign |
Het |
Cd276 |
A |
T |
9: 58,434,845 (GRCm39) |
|
probably benign |
Het |
Cd2ap |
G |
A |
17: 43,149,649 (GRCm39) |
Q122* |
probably null |
Het |
Cdan1 |
T |
A |
2: 120,561,907 (GRCm39) |
|
probably benign |
Het |
Cdh3 |
T |
C |
8: 107,263,547 (GRCm39) |
S156P |
probably benign |
Het |
Chil4 |
T |
A |
3: 106,117,959 (GRCm39) |
|
probably benign |
Het |
Col11a1 |
C |
T |
3: 113,951,791 (GRCm39) |
R1074C |
probably damaging |
Het |
Depp1 |
G |
A |
6: 116,628,683 (GRCm39) |
V9M |
possibly damaging |
Het |
Fcrlb |
T |
C |
1: 170,735,096 (GRCm39) |
T344A |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,861,829 (GRCm39) |
|
probably benign |
Het |
Fras1 |
G |
T |
5: 96,912,835 (GRCm39) |
V3380F |
possibly damaging |
Het |
Galnt9 |
A |
G |
5: 110,767,119 (GRCm39) |
D530G |
possibly damaging |
Het |
Gja10 |
A |
T |
4: 32,601,135 (GRCm39) |
S416R |
probably benign |
Het |
Gm10549 |
T |
A |
18: 33,603,841 (GRCm39) |
V108E |
unknown |
Het |
Hook3 |
A |
T |
8: 26,558,687 (GRCm39) |
L59Q |
probably damaging |
Het |
Hpf1 |
T |
A |
8: 61,353,154 (GRCm39) |
D178E |
probably benign |
Het |
Hsd17b7 |
T |
C |
1: 169,788,698 (GRCm39) |
N173S |
possibly damaging |
Het |
Hsph1 |
A |
G |
5: 149,553,454 (GRCm39) |
F236L |
probably damaging |
Het |
Kcnk12 |
G |
T |
17: 88,053,537 (GRCm39) |
T375K |
probably benign |
Het |
Klra3 |
A |
T |
6: 130,304,033 (GRCm39) |
S220T |
probably damaging |
Het |
Lhx1 |
A |
T |
11: 84,414,967 (GRCm39) |
L12Q |
probably damaging |
Het |
Lnx1 |
A |
G |
5: 74,766,710 (GRCm39) |
L468P |
probably damaging |
Het |
Ltbp3 |
T |
A |
19: 5,803,970 (GRCm39) |
C827* |
probably null |
Het |
Mical1 |
C |
T |
10: 41,354,210 (GRCm39) |
A53V |
probably damaging |
Het |
Mmp10 |
A |
T |
9: 7,506,502 (GRCm39) |
H326L |
probably benign |
Het |
Mpl |
A |
T |
4: 118,300,729 (GRCm39) |
M600K |
possibly damaging |
Het |
Muc5b |
T |
A |
7: 141,419,230 (GRCm39) |
D4004E |
possibly damaging |
Het |
Myo5b |
A |
T |
18: 74,710,680 (GRCm39) |
H98L |
possibly damaging |
Het |
Nbeal1 |
A |
G |
1: 60,323,251 (GRCm39) |
T2110A |
probably damaging |
Het |
Nedd4l |
C |
A |
18: 65,345,862 (GRCm39) |
R825S |
probably damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Or4k35 |
A |
T |
2: 111,100,622 (GRCm39) |
I30N |
possibly damaging |
Het |
Or52e19 |
T |
A |
7: 102,959,432 (GRCm39) |
L168Q |
probably damaging |
Het |
Or8k41 |
A |
T |
2: 86,313,483 (GRCm39) |
I201N |
probably damaging |
Het |
Otog |
A |
T |
7: 45,940,361 (GRCm39) |
|
probably null |
Het |
Parp2 |
T |
A |
14: 51,056,836 (GRCm39) |
L320H |
probably damaging |
Het |
Poglut3 |
T |
C |
9: 53,307,150 (GRCm39) |
Y365H |
probably damaging |
Het |
Poln |
A |
T |
5: 34,264,494 (GRCm39) |
|
probably benign |
Het |
Pomt1 |
T |
A |
2: 32,131,680 (GRCm39) |
V123E |
probably damaging |
Het |
Prom2 |
T |
C |
2: 127,374,802 (GRCm39) |
Y578C |
probably damaging |
Het |
Prss23 |
T |
C |
7: 89,159,599 (GRCm39) |
T157A |
probably damaging |
Het |
Sdk1 |
T |
A |
5: 141,598,950 (GRCm39) |
V205E |
probably damaging |
Het |
Sdk1 |
A |
G |
5: 142,147,681 (GRCm39) |
K1771R |
probably benign |
Het |
Sidt1 |
A |
T |
16: 44,102,234 (GRCm39) |
S309T |
possibly damaging |
Het |
Sirpa |
T |
A |
2: 129,457,432 (GRCm39) |
F169I |
probably damaging |
Het |
Slc8a1 |
T |
C |
17: 81,955,916 (GRCm39) |
N374S |
probably damaging |
Het |
Sp110 |
C |
T |
1: 85,523,831 (GRCm39) |
|
probably null |
Het |
Stard9 |
A |
G |
2: 120,509,934 (GRCm39) |
|
probably null |
Het |
Synpr |
A |
G |
14: 13,563,082 (GRCm38) |
N105S |
probably damaging |
Het |
Tbc1d16 |
T |
C |
11: 119,046,927 (GRCm39) |
Y440C |
probably damaging |
Het |
Trabd |
A |
G |
15: 88,969,824 (GRCm39) |
I313V |
possibly damaging |
Het |
Trappc10 |
T |
C |
10: 78,046,610 (GRCm39) |
R430G |
probably damaging |
Het |
Trim50 |
A |
G |
5: 135,387,743 (GRCm39) |
E145G |
probably benign |
Het |
Uba2 |
A |
T |
7: 33,862,624 (GRCm39) |
F105I |
probably damaging |
Het |
Uba3 |
A |
G |
6: 97,176,230 (GRCm39) |
V92A |
possibly damaging |
Het |
Uhmk1 |
T |
C |
1: 170,038,628 (GRCm39) |
K153R |
probably damaging |
Het |
Vmn2r3 |
T |
C |
3: 64,194,810 (GRCm39) |
K8R |
possibly damaging |
Het |
Vmn2r3 |
T |
A |
3: 64,182,893 (GRCm39) |
M269L |
probably benign |
Het |
Xpot |
G |
T |
10: 121,443,543 (GRCm39) |
|
probably benign |
Het |
Zfp128 |
A |
G |
7: 12,624,949 (GRCm39) |
Y439C |
probably benign |
Het |
Zfy1 |
T |
A |
Y: 725,620 (GRCm39) |
H715L |
possibly damaging |
Het |
Zmym1 |
A |
C |
4: 126,941,872 (GRCm39) |
L839V |
probably damaging |
Het |
|
Other mutations in Pola2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01403:Pola2
|
APN |
19 |
6,009,121 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01704:Pola2
|
APN |
19 |
5,992,047 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01807:Pola2
|
APN |
19 |
6,003,187 (GRCm39) |
splice site |
probably benign |
|
IGL02039:Pola2
|
APN |
19 |
5,998,497 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02639:Pola2
|
APN |
19 |
6,003,802 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4403001:Pola2
|
UTSW |
19 |
6,009,074 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0189:Pola2
|
UTSW |
19 |
5,992,370 (GRCm39) |
splice site |
probably benign |
|
R1467:Pola2
|
UTSW |
19 |
5,992,093 (GRCm39) |
nonsense |
probably null |
|
R1467:Pola2
|
UTSW |
19 |
5,992,093 (GRCm39) |
nonsense |
probably null |
|
R1521:Pola2
|
UTSW |
19 |
5,998,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R1682:Pola2
|
UTSW |
19 |
6,003,091 (GRCm39) |
critical splice donor site |
probably null |
|
R1934:Pola2
|
UTSW |
19 |
6,003,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Pola2
|
UTSW |
19 |
6,001,208 (GRCm39) |
missense |
probably benign |
0.01 |
R4833:Pola2
|
UTSW |
19 |
6,003,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R5643:Pola2
|
UTSW |
19 |
6,011,198 (GRCm39) |
missense |
probably benign |
0.03 |
R5644:Pola2
|
UTSW |
19 |
6,011,198 (GRCm39) |
missense |
probably benign |
0.03 |
R6192:Pola2
|
UTSW |
19 |
6,003,802 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7509:Pola2
|
UTSW |
19 |
6,011,194 (GRCm39) |
missense |
probably benign |
0.26 |
R8217:Pola2
|
UTSW |
19 |
6,013,855 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8954:Pola2
|
UTSW |
19 |
5,998,452 (GRCm39) |
missense |
probably damaging |
0.98 |
R9225:Pola2
|
UTSW |
19 |
6,000,492 (GRCm39) |
missense |
probably benign |
0.04 |
R9336:Pola2
|
UTSW |
19 |
5,991,029 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9783:Pola2
|
UTSW |
19 |
5,990,904 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Pola2
|
UTSW |
19 |
6,003,856 (GRCm39) |
missense |
probably benign |
0.01 |
|