Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
C |
T |
7: 45,631,584 (GRCm39) |
V1231M |
probably benign |
Het |
Agl |
A |
G |
3: 116,580,177 (GRCm39) |
|
probably null |
Het |
Ak7 |
T |
C |
12: 105,676,404 (GRCm39) |
F35L |
probably benign |
Het |
Aldh1a1 |
A |
G |
19: 20,597,349 (GRCm39) |
N110S |
probably damaging |
Het |
Arhgef5 |
C |
T |
6: 43,260,117 (GRCm39) |
L1368F |
probably damaging |
Het |
Atp5mf |
T |
C |
5: 145,121,365 (GRCm39) |
Y72C |
possibly damaging |
Het |
Atp6v0a2 |
T |
G |
5: 124,784,667 (GRCm39) |
F317V |
probably benign |
Het |
Bank1 |
A |
T |
3: 135,960,690 (GRCm39) |
S56T |
probably benign |
Het |
Cachd1 |
T |
A |
4: 100,775,282 (GRCm39) |
C166S |
probably damaging |
Het |
Cand1 |
A |
G |
10: 119,046,607 (GRCm39) |
I961T |
probably benign |
Het |
Ccdc73 |
G |
A |
2: 104,811,450 (GRCm39) |
|
probably null |
Het |
Cct6b |
A |
T |
11: 82,632,830 (GRCm39) |
|
probably null |
Het |
Chd2 |
A |
C |
7: 73,118,325 (GRCm39) |
S1098A |
probably benign |
Het |
Col6a4 |
A |
T |
9: 105,957,401 (GRCm39) |
V141E |
possibly damaging |
Het |
Col6a5 |
T |
C |
9: 105,807,983 (GRCm39) |
T1022A |
unknown |
Het |
Cr2 |
A |
T |
1: 194,838,243 (GRCm39) |
C698S |
probably damaging |
Het |
Dnaaf5 |
C |
A |
5: 139,170,405 (GRCm39) |
Q786K |
possibly damaging |
Het |
Dnah6 |
T |
C |
6: 73,072,057 (GRCm39) |
D2423G |
probably benign |
Het |
Dnhd1 |
T |
C |
7: 105,370,324 (GRCm39) |
F4583S |
probably damaging |
Het |
Duoxa2 |
A |
T |
2: 122,131,679 (GRCm39) |
T123S |
probably damaging |
Het |
Edem1 |
T |
G |
6: 108,818,595 (GRCm39) |
V201G |
probably damaging |
Het |
Eef1d |
C |
T |
15: 75,775,531 (GRCm39) |
A43T |
possibly damaging |
Het |
Elavl3 |
T |
C |
9: 21,935,974 (GRCm39) |
K249E |
probably damaging |
Het |
Epg5 |
G |
T |
18: 77,992,211 (GRCm39) |
E303* |
probably null |
Het |
Fam83h |
T |
C |
15: 75,874,217 (GRCm39) |
D1040G |
probably damaging |
Het |
Fndc7 |
A |
T |
3: 108,783,975 (GRCm39) |
F211L |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,812,452 (GRCm39) |
T2924A |
possibly damaging |
Het |
Gm5616 |
T |
C |
9: 48,361,983 (GRCm39) |
|
noncoding transcript |
Het |
Gpr135 |
T |
A |
12: 72,116,642 (GRCm39) |
D375V |
probably benign |
Het |
Hgd |
A |
G |
16: 37,452,187 (GRCm39) |
*446W |
probably null |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Htra2 |
A |
G |
6: 83,028,798 (GRCm39) |
L379P |
probably damaging |
Het |
Hypk |
G |
T |
2: 121,288,136 (GRCm39) |
|
probably null |
Het |
Ica1l |
A |
G |
1: 60,049,360 (GRCm39) |
F198L |
probably damaging |
Het |
Igsf11 |
G |
A |
16: 38,845,226 (GRCm39) |
S319N |
probably damaging |
Het |
Il12rb1 |
T |
C |
8: 71,266,012 (GRCm39) |
S213P |
possibly damaging |
Het |
Katnal1 |
C |
T |
5: 148,841,460 (GRCm39) |
V135M |
probably damaging |
Het |
Kcnc4 |
G |
A |
3: 107,354,859 (GRCm39) |
P530S |
probably benign |
Het |
Kcnu1 |
T |
C |
8: 26,403,780 (GRCm39) |
Y24H |
probably damaging |
Het |
Kdm5b |
A |
G |
1: 134,558,538 (GRCm39) |
E1515G |
possibly damaging |
Het |
Kif18a |
A |
T |
2: 109,118,220 (GRCm39) |
M12L |
probably benign |
Het |
Klre1 |
T |
C |
6: 129,561,118 (GRCm39) |
S160P |
probably damaging |
Het |
Lama2 |
A |
T |
10: 27,343,267 (GRCm39) |
H68Q |
probably damaging |
Het |
Lgals8 |
T |
C |
13: 12,468,203 (GRCm39) |
K49R |
possibly damaging |
Het |
Lmf1 |
G |
A |
17: 25,873,445 (GRCm39) |
V317M |
probably damaging |
Het |
Lsr |
T |
C |
7: 30,657,977 (GRCm39) |
T328A |
probably damaging |
Het |
Mark4 |
C |
T |
7: 19,185,582 (GRCm39) |
E51K |
probably benign |
Het |
Mindy2 |
T |
C |
9: 70,541,283 (GRCm39) |
|
probably null |
Het |
Mkks |
G |
A |
2: 136,718,082 (GRCm39) |
T400I |
probably benign |
Het |
Mon2 |
T |
A |
10: 122,841,962 (GRCm39) |
M1544L |
probably benign |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Myo5c |
T |
G |
9: 75,198,198 (GRCm39) |
L1341R |
probably damaging |
Het |
Nin |
T |
C |
12: 70,090,581 (GRCm39) |
R945G |
possibly damaging |
Het |
Nox4 |
T |
C |
7: 86,954,055 (GRCm39) |
V120A |
probably benign |
Het |
Or1s2 |
T |
A |
19: 13,758,706 (GRCm39) |
C243* |
probably null |
Het |
Or2aj4 |
G |
T |
16: 19,385,413 (GRCm39) |
H73Q |
possibly damaging |
Het |
Or2z2 |
A |
T |
11: 58,346,370 (GRCm39) |
V135E |
possibly damaging |
Het |
Or4a66 |
C |
T |
2: 88,531,242 (GRCm39) |
V144I |
probably benign |
Het |
Or7g29 |
T |
C |
9: 19,287,105 (GRCm39) |
E24G |
probably benign |
Het |
Plekha2 |
T |
A |
8: 25,532,778 (GRCm39) |
R398W |
probably damaging |
Het |
Pradc1 |
A |
G |
6: 85,424,173 (GRCm39) |
W58R |
probably damaging |
Het |
Pramel20 |
A |
G |
4: 143,297,559 (GRCm39) |
|
probably benign |
Het |
Prrc2b |
A |
G |
2: 32,107,351 (GRCm39) |
|
probably null |
Het |
Psg19 |
T |
A |
7: 18,528,071 (GRCm39) |
N224I |
probably damaging |
Het |
Ranbp17 |
A |
C |
11: 33,437,746 (GRCm39) |
V164G |
probably benign |
Het |
Rasgrp3 |
A |
G |
17: 75,807,168 (GRCm39) |
S211G |
probably benign |
Het |
Rcc1l |
G |
A |
5: 134,192,615 (GRCm39) |
P270S |
possibly damaging |
Het |
Rfx6 |
T |
A |
10: 51,596,040 (GRCm39) |
|
probably null |
Het |
Rnf222 |
A |
T |
11: 68,783,845 (GRCm39) |
E137D |
probably damaging |
Het |
Selenof |
T |
G |
3: 144,302,584 (GRCm39) |
Y120D |
probably damaging |
Het |
Sema3b |
G |
T |
9: 107,481,012 (GRCm39) |
D108E |
probably damaging |
Het |
Shank3 |
T |
A |
15: 89,384,557 (GRCm39) |
L143Q |
probably damaging |
Het |
Shtn1 |
G |
C |
19: 59,039,305 (GRCm39) |
R45G |
probably damaging |
Het |
Sirt4 |
T |
C |
5: 115,618,373 (GRCm39) |
T234A |
possibly damaging |
Het |
Slc25a30 |
C |
A |
14: 76,000,806 (GRCm39) |
W266L |
probably benign |
Het |
Spata20 |
A |
T |
11: 94,375,412 (GRCm39) |
N127K |
probably damaging |
Het |
Spmip4 |
G |
T |
6: 50,572,817 (GRCm39) |
P32Q |
probably damaging |
Het |
St14 |
C |
T |
9: 31,006,918 (GRCm39) |
G636D |
probably benign |
Het |
Stat5a |
G |
A |
11: 100,756,289 (GRCm39) |
E170K |
probably damaging |
Het |
Sugp2 |
C |
T |
8: 70,695,440 (GRCm39) |
R138C |
probably damaging |
Het |
Sult1e1 |
C |
A |
5: 87,734,589 (GRCm39) |
W119L |
possibly damaging |
Het |
Sv2a |
T |
C |
3: 96,099,874 (GRCm39) |
V608A |
possibly damaging |
Het |
Taok2 |
G |
A |
7: 126,467,304 (GRCm39) |
S167L |
possibly damaging |
Het |
Thoc6 |
T |
C |
17: 23,889,041 (GRCm39) |
H151R |
possibly damaging |
Het |
Tm9sf2 |
T |
C |
14: 122,377,062 (GRCm39) |
S197P |
probably benign |
Het |
Tmem260 |
CAGGGACCGGCATAG |
CAG |
14: 48,749,451 (GRCm39) |
|
probably benign |
Het |
Tmx2 |
G |
A |
2: 84,508,340 (GRCm39) |
P15L |
probably damaging |
Het |
Top1mt |
C |
T |
15: 75,540,474 (GRCm39) |
|
probably null |
Het |
Trpm6 |
T |
A |
19: 18,845,345 (GRCm39) |
S1682T |
probably benign |
Het |
Trrap |
C |
T |
5: 144,740,087 (GRCm39) |
R1171W |
probably damaging |
Het |
Ugt3a1 |
A |
G |
15: 9,361,665 (GRCm39) |
D147G |
probably damaging |
Het |
Utp25 |
G |
A |
1: 192,810,575 (GRCm39) |
H143Y |
probably benign |
Het |
Vnn3 |
A |
G |
10: 23,740,519 (GRCm39) |
H274R |
probably benign |
Het |
Vwf |
C |
A |
6: 125,620,326 (GRCm39) |
T1668K |
|
Het |
Zfp568 |
T |
C |
7: 29,714,608 (GRCm39) |
S162P |
probably damaging |
Het |
Zfp658 |
T |
A |
7: 43,223,890 (GRCm39) |
C722S |
possibly damaging |
Het |
Zfp808 |
T |
A |
13: 62,319,045 (GRCm39) |
H91Q |
probably 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 |
R1837:Syne2
|
UTSW |
12 |
76,014,434 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
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 |
|