Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl10 |
G |
T |
2: 154,394,962 (GRCm39) |
G305W |
probably damaging |
Het |
Actr3b |
A |
T |
5: 26,030,157 (GRCm39) |
T74S |
probably benign |
Het |
Add2 |
A |
G |
6: 86,095,540 (GRCm39) |
E652G |
probably damaging |
Het |
Alg9 |
T |
A |
9: 50,717,615 (GRCm39) |
V83D |
probably damaging |
Het |
Atp13a2 |
T |
A |
4: 140,721,643 (GRCm39) |
Y244* |
probably null |
Het |
BB014433 |
C |
G |
8: 15,092,629 (GRCm39) |
V75L |
unknown |
Het |
Bcr |
A |
G |
10: 75,003,932 (GRCm39) |
|
probably benign |
Het |
Begain |
G |
A |
12: 109,001,249 (GRCm39) |
|
probably benign |
Het |
Bzw1 |
A |
G |
1: 58,439,277 (GRCm39) |
K67E |
probably damaging |
Het |
Ccdc141 |
T |
C |
2: 76,842,009 (GRCm39) |
E1474G |
probably benign |
Het |
Cdc73 |
T |
A |
1: 143,543,395 (GRCm39) |
T314S |
possibly damaging |
Het |
Cfap206 |
T |
C |
4: 34,728,813 (GRCm39) |
T31A |
probably damaging |
Het |
Cfap58 |
G |
A |
19: 48,017,578 (GRCm39) |
E813K |
probably damaging |
Het |
Clstn2 |
C |
A |
9: 97,465,593 (GRCm39) |
A133S |
probably benign |
Het |
Col14a1 |
A |
T |
15: 55,245,891 (GRCm39) |
D465V |
unknown |
Het |
Col2a1 |
C |
T |
15: 97,894,522 (GRCm39) |
|
probably benign |
Het |
Dab2 |
A |
G |
15: 6,365,957 (GRCm39) |
|
probably benign |
Het |
Eme1 |
T |
C |
11: 94,536,787 (GRCm39) |
D464G |
probably benign |
Het |
Eml6 |
T |
C |
11: 29,699,802 (GRCm39) |
|
probably null |
Het |
Ern1 |
C |
A |
11: 106,349,783 (GRCm39) |
L44F |
probably damaging |
Het |
Fam111a |
T |
A |
19: 12,564,816 (GRCm39) |
S188R |
probably benign |
Het |
Fam151b |
A |
T |
13: 92,610,639 (GRCm39) |
|
probably benign |
Het |
Fmo6 |
T |
C |
1: 162,750,379 (GRCm39) |
N226D |
probably benign |
Het |
Ggt1 |
A |
G |
10: 75,415,128 (GRCm39) |
D214G |
probably benign |
Het |
Gm14226 |
A |
G |
2: 154,866,930 (GRCm39) |
I296V |
probably benign |
Het |
Gm9915 |
A |
T |
1: 42,269,847 (GRCm39) |
|
noncoding transcript |
Het |
Heatr5b |
T |
C |
17: 79,128,180 (GRCm39) |
D485G |
possibly damaging |
Het |
Helz2 |
A |
T |
2: 180,871,082 (GRCm39) |
I2785N |
probably damaging |
Het |
Htt |
C |
T |
5: 34,976,367 (GRCm39) |
T723M |
probably benign |
Het |
Hydin |
C |
A |
8: 111,296,257 (GRCm39) |
H3595Q |
probably benign |
Het |
Il6ra |
T |
C |
3: 89,797,579 (GRCm39) |
D96G |
probably benign |
Het |
Kif5a |
G |
A |
10: 127,072,684 (GRCm39) |
Q702* |
probably null |
Het |
Klhdc7a |
G |
T |
4: 139,694,381 (GRCm39) |
P189T |
probably benign |
Het |
Krt7 |
A |
G |
15: 101,317,463 (GRCm39) |
D252G |
probably benign |
Het |
Lad1 |
C |
A |
1: 135,757,444 (GRCm39) |
D394E |
probably benign |
Het |
Lhx8 |
A |
T |
3: 154,033,692 (GRCm39) |
C38S |
possibly damaging |
Het |
Lta4h |
C |
T |
10: 93,305,037 (GRCm39) |
T280M |
probably damaging |
Het |
Magi2 |
A |
T |
5: 20,670,825 (GRCm39) |
T163S |
probably damaging |
Het |
Med1 |
G |
T |
11: 98,060,238 (GRCm39) |
D230E |
probably damaging |
Het |
Mmp1b |
A |
T |
9: 7,386,409 (GRCm39) |
F171I |
probably damaging |
Het |
Mprip |
T |
C |
11: 59,657,571 (GRCm39) |
V801A |
probably damaging |
Het |
Mtrf1 |
A |
G |
14: 79,639,273 (GRCm39) |
E135G |
possibly damaging |
Het |
Muc5ac |
T |
A |
7: 141,360,823 (GRCm39) |
M1378K |
probably benign |
Het |
Myo3a |
A |
T |
2: 22,467,604 (GRCm39) |
Q286L |
possibly damaging |
Het |
Ndor1 |
C |
T |
2: 25,138,408 (GRCm39) |
G391R |
probably damaging |
Het |
Nefl |
C |
T |
14: 68,324,075 (GRCm39) |
R438C |
probably damaging |
Het |
Nlrp3 |
G |
A |
11: 59,439,742 (GRCm39) |
V440I |
probably benign |
Het |
Notch3 |
A |
T |
17: 32,343,296 (GRCm39) |
L1959Q |
probably damaging |
Het |
Noto |
A |
G |
6: 85,401,159 (GRCm39) |
T63A |
probably benign |
Het |
Oc90 |
G |
A |
15: 65,761,529 (GRCm39) |
T163M |
probably damaging |
Het |
Or1l4 |
T |
A |
2: 37,092,114 (GRCm39) |
M287K |
probably benign |
Het |
Or4c114 |
A |
T |
2: 88,905,176 (GRCm39) |
Y86* |
probably null |
Het |
Or5an10 |
A |
G |
19: 12,275,740 (GRCm39) |
V252A |
probably damaging |
Het |
Pdpr |
C |
A |
8: 111,861,366 (GRCm39) |
P787T |
probably damaging |
Het |
Phlda1 |
A |
G |
10: 111,343,092 (GRCm39) |
Q276R |
probably benign |
Het |
Ptpn21 |
T |
G |
12: 98,699,885 (GRCm39) |
K10Q |
probably damaging |
Het |
Ptprb |
A |
G |
10: 116,177,531 (GRCm39) |
E1364G |
probably benign |
Het |
Rabep1 |
T |
A |
11: 70,795,484 (GRCm39) |
W237R |
probably damaging |
Het |
Rai1 |
A |
T |
11: 60,080,224 (GRCm39) |
K1429N |
probably damaging |
Het |
Rapgef1 |
A |
G |
2: 29,627,438 (GRCm39) |
I1027M |
probably damaging |
Het |
Rit1 |
C |
G |
3: 88,636,477 (GRCm39) |
T127S |
probably damaging |
Het |
Rpap1 |
A |
C |
2: 119,600,366 (GRCm39) |
|
probably null |
Het |
Senp7 |
T |
A |
16: 55,978,879 (GRCm39) |
C471S |
probably benign |
Het |
Slc16a14 |
A |
G |
1: 84,890,120 (GRCm39) |
V395A |
probably benign |
Het |
Slc45a1 |
C |
T |
4: 150,722,916 (GRCm39) |
G323S |
probably benign |
Het |
Tap1 |
C |
T |
17: 34,407,083 (GRCm39) |
A77V |
possibly damaging |
Het |
Ticam1 |
T |
C |
17: 56,577,799 (GRCm39) |
E432G |
possibly damaging |
Het |
Tmem192 |
C |
A |
8: 65,416,992 (GRCm39) |
|
probably benign |
Het |
Trub1 |
T |
C |
19: 57,441,461 (GRCm39) |
V28A |
probably benign |
Het |
Ttc21b |
A |
T |
2: 66,028,106 (GRCm39) |
L1121H |
probably benign |
Het |
Ttc38 |
A |
G |
15: 85,735,764 (GRCm39) |
D290G |
probably damaging |
Het |
Ulk1 |
C |
T |
5: 110,937,247 (GRCm39) |
G683D |
probably damaging |
Het |
Vmn1r122 |
A |
T |
7: 20,867,291 (GRCm39) |
F255I |
probably benign |
Het |
Vmn2r68 |
T |
A |
7: 84,882,886 (GRCm39) |
I289F |
probably damaging |
Het |
Vps39 |
A |
T |
2: 120,155,878 (GRCm39) |
L514H |
probably damaging |
Het |
Wdr48 |
T |
G |
9: 119,734,482 (GRCm39) |
S134A |
probably damaging |
Het |
Yap1 |
A |
T |
9: 7,962,350 (GRCm39) |
Y139N |
probably damaging |
Het |
Ylpm1 |
T |
C |
12: 85,076,107 (GRCm39) |
V486A |
possibly damaging |
Het |
Zbtb38 |
T |
C |
9: 96,569,048 (GRCm39) |
T679A |
probably benign |
Het |
Zfp292 |
A |
G |
4: 34,810,264 (GRCm39) |
S927P |
probably damaging |
Het |
Zfp324 |
C |
T |
7: 12,704,156 (GRCm39) |
T115I |
probably benign |
Het |
Zfp523 |
T |
A |
17: 28,413,967 (GRCm39) |
I34N |
probably damaging |
Het |
Zfp945 |
A |
T |
17: 23,070,247 (GRCm39) |
C551S |
probably damaging |
Het |
Zfp958 |
A |
G |
8: 4,678,590 (GRCm39) |
H205R |
probably damaging |
Het |
Zfp974 |
G |
A |
7: 27,609,781 (GRCm39) |
P648L |
possibly damaging |
Het |
|
Other mutations in Syne2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00329:Syne2
|
APN |
12 |
76,078,474 (GRCm39) |
unclassified |
probably benign |
|
IGL00595:Syne2
|
APN |
12 |
75,972,420 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL00672:Syne2
|
APN |
12 |
76,110,958 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00781:Syne2
|
APN |
12 |
76,070,836 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00823:Syne2
|
APN |
12 |
76,036,016 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01014:Syne2
|
APN |
12 |
75,952,051 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01074:Syne2
|
APN |
12 |
76,078,361 (GRCm39) |
nonsense |
probably null |
|
IGL01074:Syne2
|
APN |
12 |
76,033,785 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01324:Syne2
|
APN |
12 |
76,090,526 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01325:Syne2
|
APN |
12 |
75,973,288 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01331:Syne2
|
APN |
12 |
75,976,027 (GRCm39) |
splice site |
probably benign |
|
IGL01338:Syne2
|
APN |
12 |
76,107,000 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01373:Syne2
|
APN |
12 |
76,033,881 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01446:Syne2
|
APN |
12 |
76,088,149 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01556:Syne2
|
APN |
12 |
76,134,589 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01585:Syne2
|
APN |
12 |
75,995,834 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01629:Syne2
|
APN |
12 |
76,051,377 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01686:Syne2
|
APN |
12 |
75,956,110 (GRCm39) |
missense |
probably benign |
|
IGL01935:Syne2
|
APN |
12 |
75,972,087 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01941:Syne2
|
APN |
12 |
76,013,994 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01956:Syne2
|
APN |
12 |
76,144,748 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01967:Syne2
|
APN |
12 |
75,988,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01990:Syne2
|
APN |
12 |
76,101,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02000:Syne2
|
APN |
12 |
76,062,419 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02063:Syne2
|
APN |
12 |
76,098,874 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02069:Syne2
|
APN |
12 |
75,974,186 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02120:Syne2
|
APN |
12 |
75,993,480 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02222:Syne2
|
APN |
12 |
75,999,617 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02223:Syne2
|
APN |
12 |
76,155,079 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02321:Syne2
|
APN |
12 |
75,965,773 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02488:Syne2
|
APN |
12 |
76,012,512 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02491:Syne2
|
APN |
12 |
76,118,953 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02525:Syne2
|
APN |
12 |
76,147,777 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02578:Syne2
|
APN |
12 |
76,069,053 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02615:Syne2
|
APN |
12 |
76,143,768 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02702:Syne2
|
APN |
12 |
76,144,698 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02726:Syne2
|
APN |
12 |
76,062,356 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02795:Syne2
|
APN |
12 |
76,013,323 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02803:Syne2
|
APN |
12 |
76,078,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02814:Syne2
|
APN |
12 |
75,992,150 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03013:Syne2
|
APN |
12 |
75,976,111 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03131:Syne2
|
APN |
12 |
76,104,264 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03152:Syne2
|
APN |
12 |
76,012,486 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03216:Syne2
|
APN |
12 |
75,989,735 (GRCm39) |
splice site |
probably benign |
|
IGL03228:Syne2
|
APN |
12 |
76,026,686 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03259:Syne2
|
APN |
12 |
76,035,853 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03374:Syne2
|
APN |
12 |
76,121,360 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03375:Syne2
|
APN |
12 |
75,972,209 (GRCm39) |
missense |
possibly damaging |
0.57 |
3-1:Syne2
|
UTSW |
12 |
75,977,406 (GRCm39) |
missense |
probably benign |
0.02 |
B5639:Syne2
|
UTSW |
12 |
75,976,564 (GRCm39) |
missense |
probably benign |
|
K3955:Syne2
|
UTSW |
12 |
75,977,439 (GRCm39) |
missense |
probably damaging |
1.00 |
P0026:Syne2
|
UTSW |
12 |
75,926,994 (GRCm39) |
splice site |
probably benign |
|
PIT4514001:Syne2
|
UTSW |
12 |
76,151,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R0089:Syne2
|
UTSW |
12 |
76,010,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Syne2
|
UTSW |
12 |
76,144,734 (GRCm39) |
nonsense |
probably null |
|
R0113:Syne2
|
UTSW |
12 |
76,080,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R0113:Syne2
|
UTSW |
12 |
75,977,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R0141:Syne2
|
UTSW |
12 |
75,988,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R0211:Syne2
|
UTSW |
12 |
76,144,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R0219:Syne2
|
UTSW |
12 |
76,088,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Syne2
|
UTSW |
12 |
76,144,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Syne2
|
UTSW |
12 |
76,144,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R0279:Syne2
|
UTSW |
12 |
76,142,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R0319:Syne2
|
UTSW |
12 |
76,110,936 (GRCm39) |
missense |
probably damaging |
0.99 |
R0325:Syne2
|
UTSW |
12 |
76,009,415 (GRCm39) |
missense |
probably benign |
0.00 |
R0329:Syne2
|
UTSW |
12 |
76,013,727 (GRCm39) |
missense |
probably benign |
|
R0330:Syne2
|
UTSW |
12 |
76,013,727 (GRCm39) |
missense |
probably benign |
|
R0361:Syne2
|
UTSW |
12 |
75,965,384 (GRCm39) |
missense |
probably benign |
0.22 |
R0363:Syne2
|
UTSW |
12 |
76,118,981 (GRCm39) |
missense |
probably damaging |
0.98 |
R0367:Syne2
|
UTSW |
12 |
75,926,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R0371:Syne2
|
UTSW |
12 |
75,980,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Syne2
|
UTSW |
12 |
75,968,000 (GRCm39) |
nonsense |
probably null |
|
R0388:Syne2
|
UTSW |
12 |
76,033,749 (GRCm39) |
missense |
probably benign |
0.41 |
R0411:Syne2
|
UTSW |
12 |
76,106,358 (GRCm39) |
splice site |
probably null |
|
R0432:Syne2
|
UTSW |
12 |
75,995,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R0469:Syne2
|
UTSW |
12 |
75,900,923 (GRCm39) |
critical splice donor site |
probably null |
|
R0492:Syne2
|
UTSW |
12 |
76,028,837 (GRCm39) |
critical splice donor site |
probably null |
|
R0496:Syne2
|
UTSW |
12 |
76,085,714 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0504:Syne2
|
UTSW |
12 |
76,080,365 (GRCm39) |
splice site |
probably benign |
|
R0505:Syne2
|
UTSW |
12 |
76,146,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R0510:Syne2
|
UTSW |
12 |
75,900,923 (GRCm39) |
critical splice donor site |
probably null |
|
R0518:Syne2
|
UTSW |
12 |
76,155,636 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0539:Syne2
|
UTSW |
12 |
76,070,895 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0552:Syne2
|
UTSW |
12 |
75,977,778 (GRCm39) |
missense |
probably benign |
0.00 |
R0557:Syne2
|
UTSW |
12 |
75,976,075 (GRCm39) |
missense |
probably benign |
0.04 |
R0567:Syne2
|
UTSW |
12 |
75,937,004 (GRCm39) |
missense |
probably damaging |
0.98 |
R0599:Syne2
|
UTSW |
12 |
76,144,734 (GRCm39) |
nonsense |
probably null |
|
R0602:Syne2
|
UTSW |
12 |
76,144,734 (GRCm39) |
nonsense |
probably null |
|
R0608:Syne2
|
UTSW |
12 |
76,010,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Syne2
|
UTSW |
12 |
75,959,127 (GRCm39) |
splice site |
probably null |
|
R0636:Syne2
|
UTSW |
12 |
75,977,757 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0647:Syne2
|
UTSW |
12 |
75,934,977 (GRCm39) |
missense |
probably benign |
|
R0654:Syne2
|
UTSW |
12 |
76,144,734 (GRCm39) |
nonsense |
probably null |
|
R0658:Syne2
|
UTSW |
12 |
76,141,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R0666:Syne2
|
UTSW |
12 |
75,969,787 (GRCm39) |
missense |
probably damaging |
0.99 |
R0707:Syne2
|
UTSW |
12 |
76,028,837 (GRCm39) |
critical splice donor site |
probably null |
|
R0714:Syne2
|
UTSW |
12 |
76,144,734 (GRCm39) |
nonsense |
probably null |
|
R0841:Syne2
|
UTSW |
12 |
76,121,209 (GRCm39) |
splice site |
probably benign |
|
R0848:Syne2
|
UTSW |
12 |
76,144,734 (GRCm39) |
nonsense |
probably null |
|
R0848:Syne2
|
UTSW |
12 |
76,144,733 (GRCm39) |
frame shift |
probably null |
|
R1077:Syne2
|
UTSW |
12 |
76,088,809 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1103:Syne2
|
UTSW |
12 |
76,156,609 (GRCm39) |
missense |
probably benign |
0.00 |
R1144:Syne2
|
UTSW |
12 |
76,013,298 (GRCm39) |
missense |
probably benign |
0.04 |
R1194:Syne2
|
UTSW |
12 |
75,981,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R1247:Syne2
|
UTSW |
12 |
76,014,264 (GRCm39) |
missense |
probably benign |
0.39 |
R1276:Syne2
|
UTSW |
12 |
75,987,963 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1343:Syne2
|
UTSW |
12 |
76,080,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Syne2
|
UTSW |
12 |
75,993,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Syne2
|
UTSW |
12 |
76,098,952 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1448:Syne2
|
UTSW |
12 |
76,067,099 (GRCm39) |
splice site |
probably null |
|
R1522:Syne2
|
UTSW |
12 |
76,150,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R1528:Syne2
|
UTSW |
12 |
76,012,874 (GRCm39) |
missense |
probably benign |
0.00 |
R1636:Syne2
|
UTSW |
12 |
76,051,506 (GRCm39) |
missense |
probably benign |
0.01 |
R1637:Syne2
|
UTSW |
12 |
76,042,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Syne2
|
UTSW |
12 |
75,951,033 (GRCm39) |
nonsense |
probably null |
|
R1654:Syne2
|
UTSW |
12 |
76,147,868 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1714:Syne2
|
UTSW |
12 |
76,101,713 (GRCm39) |
missense |
probably benign |
0.26 |
R1750:Syne2
|
UTSW |
12 |
76,099,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R1772:Syne2
|
UTSW |
12 |
75,985,503 (GRCm39) |
missense |
probably benign |
0.19 |
R1797:Syne2
|
UTSW |
12 |
76,010,557 (GRCm39) |
missense |
probably benign |
0.00 |
R1830:Syne2
|
UTSW |
12 |
76,156,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Syne2
|
UTSW |
12 |
76,141,053 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1913:Syne2
|
UTSW |
12 |
75,946,020 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1944:Syne2
|
UTSW |
12 |
76,121,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Syne2
|
UTSW |
12 |
75,999,644 (GRCm39) |
missense |
probably benign |
|
R1958:Syne2
|
UTSW |
12 |
76,016,319 (GRCm39) |
missense |
probably benign |
0.11 |
R2018:Syne2
|
UTSW |
12 |
76,121,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R2037:Syne2
|
UTSW |
12 |
76,072,343 (GRCm39) |
missense |
probably benign |
0.04 |
R2067:Syne2
|
UTSW |
12 |
75,935,116 (GRCm39) |
critical splice donor site |
probably null |
|
R2073:Syne2
|
UTSW |
12 |
76,062,353 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2099:Syne2
|
UTSW |
12 |
76,026,747 (GRCm39) |
missense |
probably benign |
0.06 |
R2102:Syne2
|
UTSW |
12 |
76,074,853 (GRCm39) |
missense |
probably benign |
0.01 |
R2134:Syne2
|
UTSW |
12 |
75,999,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R2135:Syne2
|
UTSW |
12 |
75,999,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R2157:Syne2
|
UTSW |
12 |
76,141,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R2173:Syne2
|
UTSW |
12 |
76,147,763 (GRCm39) |
splice site |
probably benign |
|
R2248:Syne2
|
UTSW |
12 |
76,143,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R2276:Syne2
|
UTSW |
12 |
75,974,240 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2277:Syne2
|
UTSW |
12 |
75,974,240 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2278:Syne2
|
UTSW |
12 |
75,974,240 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2279:Syne2
|
UTSW |
12 |
75,974,240 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2483:Syne2
|
UTSW |
12 |
76,142,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R2877:Syne2
|
UTSW |
12 |
76,047,605 (GRCm39) |
missense |
probably benign |
0.00 |
R2884:Syne2
|
UTSW |
12 |
76,010,533 (GRCm39) |
missense |
probably benign |
0.00 |
R3119:Syne2
|
UTSW |
12 |
75,956,058 (GRCm39) |
missense |
probably benign |
0.01 |
R3499:Syne2
|
UTSW |
12 |
76,101,752 (GRCm39) |
splice site |
probably null |
|
R3827:Syne2
|
UTSW |
12 |
76,033,805 (GRCm39) |
missense |
probably benign |
0.02 |
R3847:Syne2
|
UTSW |
12 |
76,095,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R3849:Syne2
|
UTSW |
12 |
76,092,839 (GRCm39) |
nonsense |
probably null |
|
R3850:Syne2
|
UTSW |
12 |
76,095,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R3859:Syne2
|
UTSW |
12 |
75,976,558 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3861:Syne2
|
UTSW |
12 |
76,013,253 (GRCm39) |
missense |
probably damaging |
0.98 |
R4078:Syne2
|
UTSW |
12 |
76,082,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R4116:Syne2
|
UTSW |
12 |
75,977,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R4326:Syne2
|
UTSW |
12 |
75,999,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R4335:Syne2
|
UTSW |
12 |
76,074,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R4410:Syne2
|
UTSW |
12 |
76,141,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R4412:Syne2
|
UTSW |
12 |
76,152,834 (GRCm39) |
missense |
probably benign |
0.01 |
R4444:Syne2
|
UTSW |
12 |
76,069,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R4595:Syne2
|
UTSW |
12 |
76,013,845 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4604:Syne2
|
UTSW |
12 |
76,014,484 (GRCm39) |
missense |
probably damaging |
0.99 |
R4606:Syne2
|
UTSW |
12 |
76,036,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R4651:Syne2
|
UTSW |
12 |
76,036,013 (GRCm39) |
missense |
probably damaging |
0.99 |
R4656:Syne2
|
UTSW |
12 |
76,078,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R4675:Syne2
|
UTSW |
12 |
75,996,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Syne2
|
UTSW |
12 |
76,067,165 (GRCm39) |
missense |
probably benign |
0.19 |
R4791:Syne2
|
UTSW |
12 |
75,956,018 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4799:Syne2
|
UTSW |
12 |
75,945,941 (GRCm39) |
missense |
probably benign |
0.04 |
R4836:Syne2
|
UTSW |
12 |
76,026,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R4880:Syne2
|
UTSW |
12 |
76,026,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R4881:Syne2
|
UTSW |
12 |
76,026,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R4899:Syne2
|
UTSW |
12 |
75,900,875 (GRCm39) |
missense |
probably benign |
0.03 |
R4934:Syne2
|
UTSW |
12 |
75,946,046 (GRCm39) |
missense |
probably benign |
0.14 |
R4981:Syne2
|
UTSW |
12 |
75,987,993 (GRCm39) |
missense |
probably damaging |
0.98 |
R4996:Syne2
|
UTSW |
12 |
75,990,724 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5056:Syne2
|
UTSW |
12 |
75,955,905 (GRCm39) |
unclassified |
probably benign |
|
R5066:Syne2
|
UTSW |
12 |
76,013,325 (GRCm39) |
missense |
probably benign |
0.05 |
R5095:Syne2
|
UTSW |
12 |
75,999,600 (GRCm39) |
missense |
probably damaging |
0.99 |
R5151:Syne2
|
UTSW |
12 |
76,090,484 (GRCm39) |
missense |
probably benign |
0.06 |
R5193:Syne2
|
UTSW |
12 |
76,141,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Syne2
|
UTSW |
12 |
75,985,515 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5288:Syne2
|
UTSW |
12 |
76,146,112 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5402:Syne2
|
UTSW |
12 |
76,106,213 (GRCm39) |
missense |
probably damaging |
0.98 |
R5434:Syne2
|
UTSW |
12 |
76,018,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R5441:Syne2
|
UTSW |
12 |
76,035,917 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5488:Syne2
|
UTSW |
12 |
75,934,946 (GRCm39) |
missense |
probably benign |
0.13 |
R5497:Syne2
|
UTSW |
12 |
75,927,163 (GRCm39) |
missense |
probably benign |
0.19 |
R5506:Syne2
|
UTSW |
12 |
75,985,495 (GRCm39) |
missense |
probably benign |
0.01 |
R5509:Syne2
|
UTSW |
12 |
75,968,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R5518:Syne2
|
UTSW |
12 |
75,991,944 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5561:Syne2
|
UTSW |
12 |
76,141,232 (GRCm39) |
nonsense |
probably null |
|
R5581:Syne2
|
UTSW |
12 |
75,991,859 (GRCm39) |
missense |
probably benign |
0.01 |
R5625:Syne2
|
UTSW |
12 |
76,141,886 (GRCm39) |
missense |
probably benign |
0.06 |
R5642:Syne2
|
UTSW |
12 |
75,965,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R5665:Syne2
|
UTSW |
12 |
76,154,991 (GRCm39) |
critical splice donor site |
probably null |
|
R5666:Syne2
|
UTSW |
12 |
75,997,733 (GRCm39) |
missense |
probably benign |
0.16 |
R5670:Syne2
|
UTSW |
12 |
75,997,733 (GRCm39) |
missense |
probably benign |
0.16 |
R5691:Syne2
|
UTSW |
12 |
76,074,630 (GRCm39) |
frame shift |
probably null |
|
R5696:Syne2
|
UTSW |
12 |
76,040,919 (GRCm39) |
missense |
probably benign |
0.00 |
R5720:Syne2
|
UTSW |
12 |
76,014,441 (GRCm39) |
missense |
probably benign |
0.03 |
R5739:Syne2
|
UTSW |
12 |
76,044,239 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5840:Syne2
|
UTSW |
12 |
75,927,065 (GRCm39) |
splice site |
probably null |
|
R5846:Syne2
|
UTSW |
12 |
76,074,898 (GRCm39) |
missense |
probably benign |
0.01 |
R5850:Syne2
|
UTSW |
12 |
76,144,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R5889:Syne2
|
UTSW |
12 |
76,119,026 (GRCm39) |
nonsense |
probably null |
|
R5912:Syne2
|
UTSW |
12 |
75,955,721 (GRCm39) |
critical splice donor site |
probably null |
|
R5931:Syne2
|
UTSW |
12 |
76,055,639 (GRCm39) |
missense |
probably benign |
0.37 |
R5985:Syne2
|
UTSW |
12 |
76,012,933 (GRCm39) |
missense |
probably damaging |
0.96 |
R5988:Syne2
|
UTSW |
12 |
75,976,191 (GRCm39) |
critical splice donor site |
probably null |
|
R5990:Syne2
|
UTSW |
12 |
76,070,918 (GRCm39) |
missense |
probably benign |
0.10 |
R6038:Syne2
|
UTSW |
12 |
75,925,158 (GRCm39) |
nonsense |
probably null |
|
R6038:Syne2
|
UTSW |
12 |
75,925,158 (GRCm39) |
nonsense |
probably null |
|
R6132:Syne2
|
UTSW |
12 |
75,991,921 (GRCm39) |
missense |
probably benign |
0.14 |
R6136:Syne2
|
UTSW |
12 |
75,952,099 (GRCm39) |
missense |
probably benign |
0.24 |
R6229:Syne2
|
UTSW |
12 |
75,967,994 (GRCm39) |
missense |
probably benign |
0.00 |
R6252:Syne2
|
UTSW |
12 |
76,016,210 (GRCm39) |
missense |
probably benign |
0.39 |
R6271:Syne2
|
UTSW |
12 |
75,937,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6320:Syne2
|
UTSW |
12 |
76,108,424 (GRCm39) |
missense |
probably damaging |
0.96 |
R6339:Syne2
|
UTSW |
12 |
76,035,927 (GRCm39) |
missense |
probably benign |
0.34 |
R6380:Syne2
|
UTSW |
12 |
76,151,754 (GRCm39) |
missense |
probably damaging |
0.98 |
R6394:Syne2
|
UTSW |
12 |
76,037,269 (GRCm39) |
missense |
probably benign |
0.09 |
R6419:Syne2
|
UTSW |
12 |
76,143,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R6426:Syne2
|
UTSW |
12 |
75,969,857 (GRCm39) |
missense |
probably null |
0.97 |
R6434:Syne2
|
UTSW |
12 |
76,088,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R6437:Syne2
|
UTSW |
12 |
76,037,188 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6466:Syne2
|
UTSW |
12 |
75,990,675 (GRCm39) |
missense |
probably damaging |
0.97 |
R6501:Syne2
|
UTSW |
12 |
76,074,621 (GRCm39) |
splice site |
probably null |
|
R6552:Syne2
|
UTSW |
12 |
75,937,015 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6744:Syne2
|
UTSW |
12 |
76,121,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R6810:Syne2
|
UTSW |
12 |
75,989,659 (GRCm39) |
missense |
probably benign |
0.00 |
R6831:Syne2
|
UTSW |
12 |
76,013,568 (GRCm39) |
missense |
probably benign |
0.39 |
R6861:Syne2
|
UTSW |
12 |
75,956,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R6875:Syne2
|
UTSW |
12 |
76,082,404 (GRCm39) |
missense |
probably damaging |
0.99 |
R6892:Syne2
|
UTSW |
12 |
76,009,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R6899:Syne2
|
UTSW |
12 |
76,142,503 (GRCm39) |
splice site |
probably null |
|
R6906:Syne2
|
UTSW |
12 |
76,042,760 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6909:Syne2
|
UTSW |
12 |
76,110,969 (GRCm39) |
missense |
probably benign |
0.04 |
R6925:Syne2
|
UTSW |
12 |
75,900,906 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6949:Syne2
|
UTSW |
12 |
76,012,771 (GRCm39) |
missense |
probably benign |
0.00 |
R6952:Syne2
|
UTSW |
12 |
75,974,205 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6996:Syne2
|
UTSW |
12 |
76,074,786 (GRCm39) |
missense |
probably damaging |
0.99 |
R7080:Syne2
|
UTSW |
12 |
76,099,501 (GRCm39) |
missense |
probably benign |
0.00 |
R7083:Syne2
|
UTSW |
12 |
75,990,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R7090:Syne2
|
UTSW |
12 |
75,989,125 (GRCm39) |
missense |
probably benign |
|
R7144:Syne2
|
UTSW |
12 |
76,052,152 (GRCm39) |
missense |
probably benign |
0.03 |
R7154:Syne2
|
UTSW |
12 |
76,106,231 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7177:Syne2
|
UTSW |
12 |
76,018,654 (GRCm39) |
nonsense |
probably null |
|
R7190:Syne2
|
UTSW |
12 |
76,113,361 (GRCm39) |
missense |
probably benign |
0.01 |
R7206:Syne2
|
UTSW |
12 |
76,051,531 (GRCm39) |
missense |
probably benign |
0.02 |
R7208:Syne2
|
UTSW |
12 |
76,078,172 (GRCm39) |
splice site |
probably null |
|
R7230:Syne2
|
UTSW |
12 |
75,980,674 (GRCm39) |
missense |
probably benign |
0.12 |
R7260:Syne2
|
UTSW |
12 |
75,991,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R7272:Syne2
|
UTSW |
12 |
76,095,417 (GRCm39) |
missense |
probably benign |
0.00 |
R7296:Syne2
|
UTSW |
12 |
76,149,810 (GRCm39) |
missense |
probably benign |
0.00 |
R7322:Syne2
|
UTSW |
12 |
76,030,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R7329:Syne2
|
UTSW |
12 |
76,013,758 (GRCm39) |
missense |
probably benign |
0.01 |
R7332:Syne2
|
UTSW |
12 |
76,014,529 (GRCm39) |
critical splice donor site |
probably null |
|
R7381:Syne2
|
UTSW |
12 |
75,973,263 (GRCm39) |
missense |
probably benign |
0.11 |
R7401:Syne2
|
UTSW |
12 |
76,014,155 (GRCm39) |
missense |
probably damaging |
0.98 |
R7403:Syne2
|
UTSW |
12 |
75,962,020 (GRCm39) |
missense |
not run |
|
R7429:Syne2
|
UTSW |
12 |
76,087,184 (GRCm39) |
nonsense |
probably null |
|
R7429:Syne2
|
UTSW |
12 |
75,980,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R7430:Syne2
|
UTSW |
12 |
76,087,184 (GRCm39) |
nonsense |
probably null |
|
R7430:Syne2
|
UTSW |
12 |
75,980,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R7438:Syne2
|
UTSW |
12 |
76,062,337 (GRCm39) |
missense |
probably benign |
0.04 |
R7447:Syne2
|
UTSW |
12 |
76,074,853 (GRCm39) |
missense |
probably benign |
0.01 |
R7466:Syne2
|
UTSW |
12 |
76,092,960 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7493:Syne2
|
UTSW |
12 |
76,012,654 (GRCm39) |
missense |
probably benign |
0.00 |
R7502:Syne2
|
UTSW |
12 |
76,141,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R7543:Syne2
|
UTSW |
12 |
75,953,616 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7569:Syne2
|
UTSW |
12 |
75,974,164 (GRCm39) |
missense |
probably benign |
0.00 |
R7599:Syne2
|
UTSW |
12 |
76,013,145 (GRCm39) |
missense |
probably benign |
0.04 |
R7618:Syne2
|
UTSW |
12 |
75,992,108 (GRCm39) |
missense |
probably benign |
0.01 |
R7639:Syne2
|
UTSW |
12 |
75,981,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R7698:Syne2
|
UTSW |
12 |
75,995,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R7702:Syne2
|
UTSW |
12 |
76,037,161 (GRCm39) |
missense |
probably benign |
0.16 |
R7737:Syne2
|
UTSW |
12 |
75,989,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R7742:Syne2
|
UTSW |
12 |
76,106,209 (GRCm39) |
missense |
probably benign |
0.02 |
R7753:Syne2
|
UTSW |
12 |
76,085,697 (GRCm39) |
missense |
probably benign |
0.43 |
R7755:Syne2
|
UTSW |
12 |
76,044,181 (GRCm39) |
missense |
probably benign |
0.19 |
R7757:Syne2
|
UTSW |
12 |
76,108,553 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7790:Syne2
|
UTSW |
12 |
75,975,877 (GRCm39) |
splice site |
probably null |
|
R7808:Syne2
|
UTSW |
12 |
76,030,501 (GRCm39) |
splice site |
probably null |
|
R7809:Syne2
|
UTSW |
12 |
76,014,230 (GRCm39) |
missense |
probably benign |
0.00 |
R7811:Syne2
|
UTSW |
12 |
76,030,501 (GRCm39) |
splice site |
probably null |
|
R7834:Syne2
|
UTSW |
12 |
76,014,021 (GRCm39) |
missense |
probably benign |
0.00 |
R7853:Syne2
|
UTSW |
12 |
76,078,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R7867:Syne2
|
UTSW |
12 |
76,030,501 (GRCm39) |
splice site |
probably null |
|
R7896:Syne2
|
UTSW |
12 |
76,082,397 (GRCm39) |
missense |
probably damaging |
0.99 |
R7903:Syne2
|
UTSW |
12 |
76,110,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R7944:Syne2
|
UTSW |
12 |
75,951,079 (GRCm39) |
missense |
probably damaging |
0.98 |
R7945:Syne2
|
UTSW |
12 |
75,951,079 (GRCm39) |
missense |
probably damaging |
0.98 |
R7963:Syne2
|
UTSW |
12 |
76,067,174 (GRCm39) |
missense |
probably benign |
0.38 |
R7996:Syne2
|
UTSW |
12 |
76,051,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R7998:Syne2
|
UTSW |
12 |
76,134,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Syne2
|
UTSW |
12 |
75,977,512 (GRCm39) |
missense |
probably benign |
0.39 |
R8016:Syne2
|
UTSW |
12 |
75,989,681 (GRCm39) |
missense |
probably benign |
0.19 |
R8140:Syne2
|
UTSW |
12 |
75,959,127 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8141:Syne2
|
UTSW |
12 |
76,108,442 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8206:Syne2
|
UTSW |
12 |
76,062,365 (GRCm39) |
missense |
probably benign |
0.03 |
R8258:Syne2
|
UTSW |
12 |
75,996,143 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8259:Syne2
|
UTSW |
12 |
75,996,143 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8320:Syne2
|
UTSW |
12 |
76,150,604 (GRCm39) |
missense |
probably damaging |
0.99 |
R8464:Syne2
|
UTSW |
12 |
76,012,546 (GRCm39) |
missense |
probably benign |
0.39 |
R8465:Syne2
|
UTSW |
12 |
75,900,898 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8486:Syne2
|
UTSW |
12 |
76,088,881 (GRCm39) |
nonsense |
probably null |
|
R8488:Syne2
|
UTSW |
12 |
76,012,546 (GRCm39) |
missense |
probably benign |
0.39 |
R8511:Syne2
|
UTSW |
12 |
76,055,647 (GRCm39) |
missense |
probably benign |
0.03 |
R8540:Syne2
|
UTSW |
12 |
76,141,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R8711:Syne2
|
UTSW |
12 |
76,104,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R8722:Syne2
|
UTSW |
12 |
75,972,095 (GRCm39) |
missense |
probably benign |
0.04 |
R8827:Syne2
|
UTSW |
12 |
76,095,357 (GRCm39) |
missense |
probably benign |
0.00 |
R8867:Syne2
|
UTSW |
12 |
75,989,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R8878:Syne2
|
UTSW |
12 |
75,952,067 (GRCm39) |
missense |
probably benign |
|
R8924:Syne2
|
UTSW |
12 |
75,943,444 (GRCm39) |
missense |
probably damaging |
0.97 |
R8966:Syne2
|
UTSW |
12 |
76,146,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R9007:Syne2
|
UTSW |
12 |
76,146,224 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9019:Syne2
|
UTSW |
12 |
75,999,618 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9057:Syne2
|
UTSW |
12 |
75,937,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R9067:Syne2
|
UTSW |
12 |
75,950,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R9081:Syne2
|
UTSW |
12 |
76,016,290 (GRCm39) |
nonsense |
probably null |
|
R9091:Syne2
|
UTSW |
12 |
75,977,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R9123:Syne2
|
UTSW |
12 |
76,040,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Syne2
|
UTSW |
12 |
75,937,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R9148:Syne2
|
UTSW |
12 |
75,937,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R9163:Syne2
|
UTSW |
12 |
76,009,349 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9192:Syne2
|
UTSW |
12 |
76,156,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R9248:Syne2
|
UTSW |
12 |
76,154,230 (GRCm39) |
intron |
probably benign |
|
R9270:Syne2
|
UTSW |
12 |
75,977,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R9292:Syne2
|
UTSW |
12 |
75,997,823 (GRCm39) |
missense |
probably benign |
|
R9397:Syne2
|
UTSW |
12 |
76,040,849 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9454:Syne2
|
UTSW |
12 |
76,141,844 (GRCm39) |
nonsense |
probably null |
|
R9454:Syne2
|
UTSW |
12 |
76,067,275 (GRCm39) |
missense |
probably damaging |
0.99 |
R9478:Syne2
|
UTSW |
12 |
76,154,387 (GRCm39) |
missense |
probably damaging |
0.96 |
R9492:Syne2
|
UTSW |
12 |
75,995,839 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9573:Syne2
|
UTSW |
12 |
75,927,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R9611:Syne2
|
UTSW |
12 |
76,080,460 (GRCm39) |
missense |
probably benign |
0.05 |
R9623:Syne2
|
UTSW |
12 |
75,986,760 (GRCm39) |
missense |
probably benign |
0.12 |
R9647:Syne2
|
UTSW |
12 |
76,151,875 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9652:Syne2
|
UTSW |
12 |
76,101,620 (GRCm39) |
missense |
probably benign |
0.00 |
R9667:Syne2
|
UTSW |
12 |
75,926,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R9701:Syne2
|
UTSW |
12 |
76,037,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R9794:Syne2
|
UTSW |
12 |
76,047,617 (GRCm39) |
missense |
probably benign |
0.04 |
R9802:Syne2
|
UTSW |
12 |
76,037,197 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Syne2
|
UTSW |
12 |
76,020,061 (GRCm39) |
missense |
probably benign |
0.41 |
X0026:Syne2
|
UTSW |
12 |
76,147,790 (GRCm39) |
missense |
possibly damaging |
0.78 |
X0061:Syne2
|
UTSW |
12 |
75,974,285 (GRCm39) |
critical splice donor site |
probably null |
|
X0066:Syne2
|
UTSW |
12 |
76,143,701 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Syne2
|
UTSW |
12 |
76,087,157 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Syne2
|
UTSW |
12 |
76,014,315 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Syne2
|
UTSW |
12 |
76,020,197 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Syne2
|
UTSW |
12 |
76,144,748 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Syne2
|
UTSW |
12 |
76,110,912 (GRCm39) |
missense |
possibly damaging |
0.51 |
|