Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap11 |
A |
T |
14: 78,750,787 (GRCm39) |
S533R |
probably benign |
Het |
Amph |
C |
T |
13: 19,288,461 (GRCm39) |
Q317* |
probably null |
Het |
Bach2 |
A |
G |
4: 32,562,279 (GRCm39) |
T249A |
possibly damaging |
Het |
Cacna2d3 |
A |
G |
14: 28,703,137 (GRCm39) |
C845R |
probably damaging |
Het |
Calml4 |
A |
G |
9: 62,778,622 (GRCm39) |
K12E |
probably benign |
Het |
Chrd |
C |
T |
16: 20,556,283 (GRCm39) |
R615W |
probably damaging |
Het |
Chst15 |
T |
A |
7: 131,870,798 (GRCm39) |
K246* |
probably null |
Het |
Cmtr2 |
G |
A |
8: 110,948,235 (GRCm39) |
D182N |
probably benign |
Het |
Cyp2d9 |
C |
A |
15: 82,338,525 (GRCm39) |
C186* |
probably null |
Het |
Cyp3a13 |
G |
T |
5: 137,909,892 (GRCm39) |
|
probably null |
Het |
Dcaf17 |
A |
T |
2: 70,912,332 (GRCm39) |
I320F |
probably damaging |
Het |
Ddx10 |
T |
C |
9: 53,145,297 (GRCm39) |
I227V |
possibly damaging |
Het |
Dlc1 |
G |
T |
8: 37,405,302 (GRCm39) |
N162K |
probably benign |
Het |
Dnhd1 |
G |
A |
7: 105,317,670 (GRCm39) |
R455H |
probably benign |
Het |
Drg2 |
G |
T |
11: 60,355,679 (GRCm39) |
A306S |
probably benign |
Het |
Dsg1a |
A |
T |
18: 20,465,076 (GRCm39) |
R422S |
probably damaging |
Het |
Ehbp1l1 |
A |
G |
19: 5,766,452 (GRCm39) |
V353A |
probably damaging |
Het |
Emilin2 |
T |
C |
17: 71,617,756 (GRCm39) |
S34G |
probably benign |
Het |
Enpp2 |
C |
A |
15: 54,702,910 (GRCm39) |
W862L |
probably damaging |
Het |
Exoc2 |
T |
C |
13: 31,119,485 (GRCm39) |
I139V |
probably benign |
Het |
Fhad1 |
C |
T |
4: 141,691,936 (GRCm39) |
R400H |
probably benign |
Het |
Fv1 |
C |
T |
4: 147,954,595 (GRCm39) |
T387M |
probably damaging |
Het |
Gatad1 |
T |
A |
5: 3,693,701 (GRCm39) |
D156V |
probably damaging |
Het |
Gm4744 |
A |
G |
6: 40,927,367 (GRCm39) |
|
probably benign |
Het |
Gm4799 |
G |
A |
10: 82,790,469 (GRCm39) |
|
noncoding transcript |
Het |
Hadha |
A |
G |
5: 30,333,804 (GRCm39) |
F405S |
probably benign |
Het |
Ifit3 |
T |
C |
19: 34,565,651 (GRCm39) |
V399A |
probably benign |
Het |
Il1rapl1 |
G |
T |
X: 86,348,469 (GRCm39) |
Y150* |
probably null |
Het |
Kirrel1 |
T |
C |
3: 86,997,779 (GRCm39) |
E248G |
probably benign |
Het |
Krt72 |
C |
A |
15: 101,686,769 (GRCm39) |
K392N |
probably damaging |
Het |
Loxhd1 |
G |
A |
18: 77,444,528 (GRCm39) |
G309D |
probably damaging |
Het |
Mc3r |
T |
G |
2: 172,091,300 (GRCm39) |
I174S |
probably benign |
Het |
Me3 |
A |
G |
7: 89,282,273 (GRCm39) |
D52G |
probably benign |
Het |
Med12l |
T |
C |
3: 59,168,256 (GRCm39) |
|
probably null |
Het |
Mgat5 |
G |
A |
1: 127,325,378 (GRCm39) |
|
probably null |
Het |
Mphosph10 |
A |
T |
7: 64,039,252 (GRCm39) |
F239L |
probably damaging |
Het |
Mrps7 |
T |
C |
11: 115,495,023 (GRCm39) |
S13P |
probably benign |
Het |
Nexn |
T |
C |
3: 151,943,323 (GRCm39) |
T527A |
possibly damaging |
Het |
Nlrp1b |
G |
A |
11: 71,046,885 (GRCm39) |
H1156Y |
probably damaging |
Het |
Nostrin |
A |
G |
2: 68,989,129 (GRCm39) |
E120G |
probably damaging |
Het |
Nsun2 |
A |
G |
13: 69,779,706 (GRCm39) |
E624G |
probably damaging |
Het |
Oga |
T |
C |
19: 45,767,079 (GRCm39) |
D99G |
probably null |
Het |
Or4c102 |
G |
A |
2: 88,422,492 (GRCm39) |
V115I |
possibly damaging |
Het |
Or4k2 |
A |
G |
14: 50,424,539 (GRCm39) |
I45T |
probably damaging |
Het |
Or52n4b |
G |
A |
7: 108,143,782 (GRCm39) |
V15I |
probably benign |
Het |
Or5p70 |
A |
C |
7: 107,995,289 (GRCm39) |
K321Q |
probably benign |
Het |
Phldb2 |
T |
C |
16: 45,598,146 (GRCm39) |
N802S |
probably damaging |
Het |
Pik3c2g |
T |
C |
6: 139,789,796 (GRCm39) |
|
probably null |
Het |
Pikfyve |
T |
A |
1: 65,304,443 (GRCm39) |
I1670N |
possibly damaging |
Het |
Pld5 |
A |
G |
1: 175,803,087 (GRCm39) |
F393L |
probably benign |
Het |
Plekhg1 |
C |
A |
10: 3,907,361 (GRCm39) |
D759E |
probably benign |
Het |
Plekhm1 |
A |
G |
11: 103,277,888 (GRCm39) |
S403P |
probably benign |
Het |
Pop1 |
T |
C |
15: 34,510,503 (GRCm39) |
F432L |
probably benign |
Het |
Ptpn13 |
T |
C |
5: 103,664,230 (GRCm39) |
I406T |
probably benign |
Het |
Ptpn5 |
G |
T |
7: 46,739,623 (GRCm39) |
D185E |
probably benign |
Het |
Rad50 |
G |
T |
11: 53,578,978 (GRCm39) |
Q527K |
possibly damaging |
Het |
Scn7a |
A |
G |
2: 66,530,507 (GRCm39) |
F613L |
probably benign |
Het |
Sh3bp2 |
T |
C |
5: 34,712,920 (GRCm39) |
|
probably null |
Het |
Slc22a3 |
G |
A |
17: 12,725,991 (GRCm39) |
T74I |
probably benign |
Het |
Slc23a4 |
A |
G |
6: 34,932,057 (GRCm39) |
L272P |
probably damaging |
Het |
Slc26a8 |
T |
C |
17: 28,857,536 (GRCm39) |
D869G |
possibly damaging |
Het |
Slc5a11 |
T |
A |
7: 122,859,731 (GRCm39) |
V291E |
probably damaging |
Het |
Slc6a19 |
C |
A |
13: 73,832,167 (GRCm39) |
A470S |
probably benign |
Het |
Slfn8 |
A |
G |
11: 82,894,006 (GRCm39) |
S878P |
probably damaging |
Het |
Smchd1 |
A |
G |
17: 71,672,089 (GRCm39) |
M1655T |
possibly damaging |
Het |
Srgap2 |
A |
G |
1: 131,220,437 (GRCm39) |
L179P |
probably damaging |
Het |
Tbx2 |
A |
G |
11: 85,725,622 (GRCm39) |
D191G |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,796,351 (GRCm39) |
Y485H |
probably damaging |
Het |
Trim12c |
T |
A |
7: 103,990,095 (GRCm39) |
|
probably benign |
Het |
Trpc6 |
A |
G |
9: 8,610,170 (GRCm39) |
T213A |
probably damaging |
Het |
Upp1 |
T |
A |
11: 9,084,708 (GRCm39) |
|
probably null |
Het |
Vmn1r46 |
A |
T |
6: 89,953,198 (GRCm39) |
I16L |
probably benign |
Het |
Vmn2r75 |
A |
T |
7: 85,814,850 (GRCm39) |
D214E |
possibly damaging |
Het |
Vmn2r95 |
T |
A |
17: 18,660,118 (GRCm39) |
Y177N |
probably damaging |
Het |
Vmn2r99 |
T |
G |
17: 19,582,521 (GRCm39) |
I42S |
possibly damaging |
Het |
Zeb1 |
A |
T |
18: 5,761,399 (GRCm39) |
K232N |
possibly damaging |
Het |
Zfp280b |
T |
C |
10: 75,875,603 (GRCm39) |
I494T |
probably damaging |
Het |
Zfp804a |
A |
G |
2: 82,066,143 (GRCm39) |
D38G |
probably damaging |
Het |
|
Other mutations in Sec16a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00337:Sec16a
|
APN |
2 |
26,329,499 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00435:Sec16a
|
APN |
2 |
26,320,113 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00469:Sec16a
|
APN |
2 |
26,318,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01622:Sec16a
|
APN |
2 |
26,328,915 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01623:Sec16a
|
APN |
2 |
26,328,915 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02158:Sec16a
|
APN |
2 |
26,306,644 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02188:Sec16a
|
APN |
2 |
26,326,020 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02445:Sec16a
|
APN |
2 |
26,312,052 (GRCm39) |
missense |
probably benign |
|
IGL02568:Sec16a
|
APN |
2 |
26,326,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02710:Sec16a
|
APN |
2 |
26,320,142 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02735:Sec16a
|
APN |
2 |
26,318,149 (GRCm39) |
splice site |
probably benign |
|
IGL02964:Sec16a
|
APN |
2 |
26,309,735 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03027:Sec16a
|
APN |
2 |
26,313,601 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03073:Sec16a
|
APN |
2 |
26,329,195 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03297:Sec16a
|
APN |
2 |
26,329,202 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03339:Sec16a
|
APN |
2 |
26,325,945 (GRCm39) |
missense |
probably benign |
|
H8562:Sec16a
|
UTSW |
2 |
26,331,517 (GRCm39) |
missense |
probably benign |
|
IGL03050:Sec16a
|
UTSW |
2 |
26,305,759 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4486001:Sec16a
|
UTSW |
2 |
26,315,785 (GRCm39) |
missense |
|
|
R0039:Sec16a
|
UTSW |
2 |
26,313,926 (GRCm39) |
missense |
probably benign |
0.03 |
R0095:Sec16a
|
UTSW |
2 |
26,315,772 (GRCm39) |
splice site |
probably null |
|
R0095:Sec16a
|
UTSW |
2 |
26,315,772 (GRCm39) |
splice site |
probably null |
|
R0189:Sec16a
|
UTSW |
2 |
26,314,426 (GRCm39) |
splice site |
probably null |
|
R0255:Sec16a
|
UTSW |
2 |
26,321,198 (GRCm39) |
missense |
probably damaging |
0.97 |
R0278:Sec16a
|
UTSW |
2 |
26,318,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R0739:Sec16a
|
UTSW |
2 |
26,331,063 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0743:Sec16a
|
UTSW |
2 |
26,309,734 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1446:Sec16a
|
UTSW |
2 |
26,313,579 (GRCm39) |
missense |
probably benign |
0.00 |
R1466:Sec16a
|
UTSW |
2 |
26,321,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R1466:Sec16a
|
UTSW |
2 |
26,321,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R1524:Sec16a
|
UTSW |
2 |
26,318,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R1584:Sec16a
|
UTSW |
2 |
26,321,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R1649:Sec16a
|
UTSW |
2 |
26,315,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R1744:Sec16a
|
UTSW |
2 |
26,329,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Sec16a
|
UTSW |
2 |
26,320,144 (GRCm39) |
missense |
probably benign |
0.00 |
R1973:Sec16a
|
UTSW |
2 |
26,316,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Sec16a
|
UTSW |
2 |
26,329,092 (GRCm39) |
missense |
probably benign |
0.27 |
R2073:Sec16a
|
UTSW |
2 |
26,330,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Sec16a
|
UTSW |
2 |
26,330,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Sec16a
|
UTSW |
2 |
26,330,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Sec16a
|
UTSW |
2 |
26,303,757 (GRCm39) |
intron |
probably benign |
|
R2472:Sec16a
|
UTSW |
2 |
26,329,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:Sec16a
|
UTSW |
2 |
26,329,037 (GRCm39) |
missense |
probably benign |
0.00 |
R2520:Sec16a
|
UTSW |
2 |
26,331,368 (GRCm39) |
nonsense |
probably null |
|
R2571:Sec16a
|
UTSW |
2 |
26,329,343 (GRCm39) |
missense |
probably benign |
0.08 |
R3105:Sec16a
|
UTSW |
2 |
26,328,433 (GRCm39) |
missense |
probably benign |
0.14 |
R3508:Sec16a
|
UTSW |
2 |
26,315,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R3809:Sec16a
|
UTSW |
2 |
26,331,825 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3912:Sec16a
|
UTSW |
2 |
26,304,399 (GRCm39) |
missense |
probably damaging |
0.97 |
R4292:Sec16a
|
UTSW |
2 |
26,312,167 (GRCm39) |
missense |
probably benign |
0.01 |
R4293:Sec16a
|
UTSW |
2 |
26,312,167 (GRCm39) |
missense |
probably benign |
0.01 |
R4294:Sec16a
|
UTSW |
2 |
26,312,167 (GRCm39) |
missense |
probably benign |
0.01 |
R4576:Sec16a
|
UTSW |
2 |
26,321,131 (GRCm39) |
nonsense |
probably null |
|
R4611:Sec16a
|
UTSW |
2 |
26,331,817 (GRCm39) |
missense |
probably benign |
0.04 |
R4627:Sec16a
|
UTSW |
2 |
26,321,080 (GRCm39) |
splice site |
probably null |
|
R4627:Sec16a
|
UTSW |
2 |
26,319,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4662:Sec16a
|
UTSW |
2 |
26,320,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Sec16a
|
UTSW |
2 |
26,302,970 (GRCm39) |
intron |
probably benign |
|
R4906:Sec16a
|
UTSW |
2 |
26,331,979 (GRCm39) |
unclassified |
probably benign |
|
R4967:Sec16a
|
UTSW |
2 |
26,302,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4983:Sec16a
|
UTSW |
2 |
26,329,531 (GRCm39) |
missense |
probably benign |
|
R5033:Sec16a
|
UTSW |
2 |
26,309,661 (GRCm39) |
missense |
probably benign |
0.00 |
R5251:Sec16a
|
UTSW |
2 |
26,329,357 (GRCm39) |
missense |
probably benign |
0.00 |
R5391:Sec16a
|
UTSW |
2 |
26,330,044 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5457:Sec16a
|
UTSW |
2 |
26,330,280 (GRCm39) |
missense |
probably benign |
0.01 |
R5530:Sec16a
|
UTSW |
2 |
26,329,264 (GRCm39) |
missense |
probably benign |
0.00 |
R5645:Sec16a
|
UTSW |
2 |
26,329,907 (GRCm39) |
missense |
probably benign |
0.01 |
R5661:Sec16a
|
UTSW |
2 |
26,329,649 (GRCm39) |
missense |
probably benign |
0.01 |
R5770:Sec16a
|
UTSW |
2 |
26,304,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R5830:Sec16a
|
UTSW |
2 |
26,330,853 (GRCm39) |
missense |
probably benign |
0.15 |
R5866:Sec16a
|
UTSW |
2 |
26,309,650 (GRCm39) |
missense |
probably benign |
0.00 |
R5875:Sec16a
|
UTSW |
2 |
26,323,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R5906:Sec16a
|
UTSW |
2 |
26,328,843 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5922:Sec16a
|
UTSW |
2 |
26,305,651 (GRCm39) |
missense |
probably benign |
0.05 |
R6076:Sec16a
|
UTSW |
2 |
26,313,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Sec16a
|
UTSW |
2 |
26,316,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R6295:Sec16a
|
UTSW |
2 |
26,318,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Sec16a
|
UTSW |
2 |
26,315,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6309:Sec16a
|
UTSW |
2 |
26,328,583 (GRCm39) |
missense |
probably benign |
0.00 |
R6459:Sec16a
|
UTSW |
2 |
26,313,512 (GRCm39) |
missense |
probably benign |
0.04 |
R6520:Sec16a
|
UTSW |
2 |
26,316,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R6631:Sec16a
|
UTSW |
2 |
26,329,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R6657:Sec16a
|
UTSW |
2 |
26,315,876 (GRCm39) |
nonsense |
probably null |
|
R6750:Sec16a
|
UTSW |
2 |
26,330,030 (GRCm39) |
missense |
probably benign |
0.00 |
R6852:Sec16a
|
UTSW |
2 |
26,331,431 (GRCm39) |
missense |
probably damaging |
0.99 |
R6860:Sec16a
|
UTSW |
2 |
26,320,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R6967:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6970:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6991:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6993:Sec16a
|
UTSW |
2 |
26,313,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R7009:Sec16a
|
UTSW |
2 |
26,326,014 (GRCm39) |
nonsense |
probably null |
|
R7057:Sec16a
|
UTSW |
2 |
26,315,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R7186:Sec16a
|
UTSW |
2 |
26,330,715 (GRCm39) |
nonsense |
probably null |
|
R7227:Sec16a
|
UTSW |
2 |
26,328,935 (GRCm39) |
missense |
probably benign |
0.01 |
R7234:Sec16a
|
UTSW |
2 |
26,329,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R7259:Sec16a
|
UTSW |
2 |
26,331,604 (GRCm39) |
missense |
probably benign |
0.00 |
R7326:Sec16a
|
UTSW |
2 |
26,329,729 (GRCm39) |
missense |
unknown |
|
R7371:Sec16a
|
UTSW |
2 |
26,331,734 (GRCm39) |
missense |
probably benign |
|
R7388:Sec16a
|
UTSW |
2 |
26,318,376 (GRCm39) |
missense |
|
|
R7414:Sec16a
|
UTSW |
2 |
26,313,643 (GRCm39) |
missense |
|
|
R7417:Sec16a
|
UTSW |
2 |
26,311,409 (GRCm39) |
missense |
|
|
R7501:Sec16a
|
UTSW |
2 |
26,331,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R7558:Sec16a
|
UTSW |
2 |
26,329,746 (GRCm39) |
missense |
|
|
R7696:Sec16a
|
UTSW |
2 |
26,305,645 (GRCm39) |
critical splice donor site |
probably null |
|
R7981:Sec16a
|
UTSW |
2 |
26,311,384 (GRCm39) |
critical splice donor site |
probably null |
|
R8117:Sec16a
|
UTSW |
2 |
26,331,441 (GRCm39) |
missense |
probably benign |
0.00 |
R8131:Sec16a
|
UTSW |
2 |
26,300,958 (GRCm39) |
missense |
|
|
R8163:Sec16a
|
UTSW |
2 |
26,306,433 (GRCm39) |
missense |
|
|
R8825:Sec16a
|
UTSW |
2 |
26,313,586 (GRCm39) |
missense |
|
|
R8855:Sec16a
|
UTSW |
2 |
26,329,852 (GRCm39) |
missense |
probably benign |
0.16 |
R9165:Sec16a
|
UTSW |
2 |
26,313,645 (GRCm39) |
missense |
|
|
R9216:Sec16a
|
UTSW |
2 |
26,304,401 (GRCm39) |
missense |
|
|
R9283:Sec16a
|
UTSW |
2 |
26,313,904 (GRCm39) |
missense |
|
|
R9506:Sec16a
|
UTSW |
2 |
26,319,384 (GRCm39) |
critical splice donor site |
probably null |
|
R9581:Sec16a
|
UTSW |
2 |
26,328,647 (GRCm39) |
missense |
|
|
R9772:Sec16a
|
UTSW |
2 |
26,329,417 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0011:Sec16a
|
UTSW |
2 |
26,305,655 (GRCm39) |
missense |
probably damaging |
1.00 |
X0034:Sec16a
|
UTSW |
2 |
26,306,709 (GRCm39) |
missense |
probably benign |
0.07 |
X0062:Sec16a
|
UTSW |
2 |
26,306,709 (GRCm39) |
missense |
probably benign |
0.07 |
Z1088:Sec16a
|
UTSW |
2 |
26,329,105 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Sec16a
|
UTSW |
2 |
26,328,760 (GRCm39) |
missense |
|
|
Z1177:Sec16a
|
UTSW |
2 |
26,329,333 (GRCm39) |
missense |
probably damaging |
0.99 |
|