Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts17 |
T |
C |
7: 66,559,124 (GRCm39) |
F305L |
probably damaging |
Het |
Ankrd12 |
T |
C |
17: 66,291,398 (GRCm39) |
H1345R |
probably benign |
Het |
Bloc1s5 |
A |
T |
13: 38,787,859 (GRCm39) |
M175K |
probably damaging |
Het |
C9 |
T |
A |
15: 6,526,613 (GRCm39) |
M549K |
probably benign |
Het |
Cfap52 |
A |
G |
11: 67,845,007 (GRCm39) |
|
probably benign |
Het |
Cntnap2 |
A |
T |
6: 46,998,670 (GRCm39) |
K907N |
possibly damaging |
Het |
Cox8c |
T |
A |
12: 102,865,752 (GRCm39) |
|
probably null |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Cyp26b1 |
A |
T |
6: 84,551,294 (GRCm39) |
N307K |
possibly damaging |
Het |
Cyp2s1 |
T |
C |
7: 25,515,849 (GRCm39) |
|
probably benign |
Het |
Dpysl2 |
G |
A |
14: 67,061,847 (GRCm39) |
T253I |
probably damaging |
Het |
Efr3b |
C |
T |
12: 4,033,391 (GRCm39) |
V139I |
probably benign |
Het |
Egflam |
T |
A |
15: 7,252,293 (GRCm39) |
I835F |
probably damaging |
Het |
Eif5a |
A |
T |
11: 69,809,989 (GRCm39) |
H51Q |
possibly damaging |
Het |
Fancd2 |
T |
A |
6: 113,539,422 (GRCm39) |
I637N |
probably damaging |
Het |
Gpr173 |
T |
A |
X: 151,130,092 (GRCm39) |
H127L |
probably damaging |
Het |
Klc3 |
T |
C |
7: 19,130,969 (GRCm39) |
I203V |
probably benign |
Het |
Lsg1 |
T |
C |
16: 30,390,060 (GRCm39) |
K352E |
probably benign |
Het |
Man2a2 |
G |
A |
7: 80,009,388 (GRCm39) |
A822V |
probably damaging |
Het |
Med12l |
G |
T |
3: 58,984,510 (GRCm39) |
D483Y |
probably damaging |
Het |
Mlh1 |
A |
G |
9: 111,058,943 (GRCm39) |
Y694H |
probably benign |
Het |
Mmrn1 |
A |
G |
6: 60,935,160 (GRCm39) |
R219G |
possibly damaging |
Het |
Nsd1 |
T |
C |
13: 55,450,646 (GRCm39) |
|
probably benign |
Het |
Or2y1f |
A |
T |
11: 49,184,555 (GRCm39) |
M136L |
possibly damaging |
Het |
Or8k33 |
C |
T |
2: 86,384,224 (GRCm39) |
M81I |
possibly damaging |
Het |
Pax3 |
A |
T |
1: 78,098,424 (GRCm39) |
S322T |
possibly damaging |
Het |
Pkhd1 |
T |
A |
1: 20,187,944 (GRCm39) |
I3455F |
probably damaging |
Het |
Plekhb2 |
T |
C |
1: 34,916,022 (GRCm39) |
V187A |
possibly damaging |
Het |
Pot1a |
A |
T |
6: 25,794,592 (GRCm39) |
F31I |
probably damaging |
Het |
Rpap1 |
A |
T |
2: 119,613,720 (GRCm39) |
|
probably benign |
Het |
Scmh1 |
T |
A |
4: 120,385,343 (GRCm39) |
|
probably benign |
Het |
Scn2a |
A |
G |
2: 65,560,522 (GRCm39) |
T1251A |
probably damaging |
Het |
Siglecf |
T |
C |
7: 43,001,634 (GRCm39) |
V148A |
probably benign |
Het |
Slit3 |
A |
G |
11: 35,598,969 (GRCm39) |
*1524W |
probably null |
Het |
Spp2 |
T |
A |
1: 88,338,868 (GRCm39) |
L25* |
probably null |
Het |
Sptbn4 |
T |
C |
7: 27,090,976 (GRCm39) |
Q1405R |
probably damaging |
Het |
Traf3ip2 |
G |
T |
10: 39,522,902 (GRCm39) |
A463S |
possibly damaging |
Het |
Trappc11 |
T |
C |
8: 47,960,617 (GRCm39) |
E27G |
probably damaging |
Het |
Vmn2r12 |
C |
T |
5: 109,233,858 (GRCm39) |
V785I |
probably damaging |
Het |
Zc3h8 |
A |
G |
2: 128,785,846 (GRCm39) |
|
probably benign |
Het |
Zfp57 |
T |
A |
17: 37,317,056 (GRCm39) |
S45T |
probably damaging |
Het |
|
Other mutations in Son |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00531:Son
|
APN |
16 |
91,461,210 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01024:Son
|
APN |
16 |
91,452,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01066:Son
|
APN |
16 |
91,457,024 (GRCm39) |
intron |
probably benign |
|
IGL01083:Son
|
APN |
16 |
91,454,279 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01115:Son
|
APN |
16 |
91,456,346 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01467:Son
|
APN |
16 |
91,454,165 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01506:Son
|
APN |
16 |
91,454,174 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01933:Son
|
APN |
16 |
91,454,903 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02156:Son
|
APN |
16 |
91,452,992 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02473:Son
|
APN |
16 |
91,455,683 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02498:Son
|
APN |
16 |
91,453,713 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02517:Son
|
APN |
16 |
91,452,099 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02865:Son
|
APN |
16 |
91,448,640 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03180:Son
|
APN |
16 |
91,453,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Son
|
UTSW |
16 |
91,448,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0036:Son
|
UTSW |
16 |
91,457,054 (GRCm39) |
intron |
probably benign |
|
R0037:Son
|
UTSW |
16 |
91,461,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Son
|
UTSW |
16 |
91,456,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Son
|
UTSW |
16 |
91,455,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0048:Son
|
UTSW |
16 |
91,455,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0056:Son
|
UTSW |
16 |
91,475,043 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0227:Son
|
UTSW |
16 |
91,453,761 (GRCm39) |
missense |
probably damaging |
0.99 |
R0256:Son
|
UTSW |
16 |
91,453,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0302:Son
|
UTSW |
16 |
91,453,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R0815:Son
|
UTSW |
16 |
91,452,372 (GRCm39) |
missense |
probably damaging |
0.98 |
R1225:Son
|
UTSW |
16 |
91,454,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1255:Son
|
UTSW |
16 |
91,461,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1457:Son
|
UTSW |
16 |
91,453,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R1459:Son
|
UTSW |
16 |
91,452,230 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1535:Son
|
UTSW |
16 |
91,456,622 (GRCm39) |
missense |
probably damaging |
0.99 |
R1587:Son
|
UTSW |
16 |
91,456,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Son
|
UTSW |
16 |
91,454,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R1629:Son
|
UTSW |
16 |
91,454,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1711:Son
|
UTSW |
16 |
91,457,114 (GRCm39) |
intron |
probably benign |
|
R2138:Son
|
UTSW |
16 |
91,456,260 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2245:Son
|
UTSW |
16 |
91,444,848 (GRCm39) |
splice site |
probably null |
|
R2351:Son
|
UTSW |
16 |
91,454,547 (GRCm39) |
missense |
probably damaging |
0.98 |
R2434:Son
|
UTSW |
16 |
91,451,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2871:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2872:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2889:Son
|
UTSW |
16 |
91,456,787 (GRCm39) |
unclassified |
probably benign |
|
R3712:Son
|
UTSW |
16 |
91,453,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R3913:Son
|
UTSW |
16 |
91,456,999 (GRCm39) |
intron |
probably benign |
|
R4172:Son
|
UTSW |
16 |
91,456,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4301:Son
|
UTSW |
16 |
91,455,299 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4302:Son
|
UTSW |
16 |
91,455,299 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4770:Son
|
UTSW |
16 |
91,455,756 (GRCm39) |
missense |
probably damaging |
0.96 |
R4881:Son
|
UTSW |
16 |
91,472,397 (GRCm39) |
missense |
probably benign |
0.31 |
R5020:Son
|
UTSW |
16 |
91,453,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Son
|
UTSW |
16 |
91,454,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Son
|
UTSW |
16 |
91,452,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R5153:Son
|
UTSW |
16 |
91,451,910 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5215:Son
|
UTSW |
16 |
91,453,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R5243:Son
|
UTSW |
16 |
91,451,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Son
|
UTSW |
16 |
91,452,627 (GRCm39) |
missense |
probably damaging |
0.99 |
R5529:Son
|
UTSW |
16 |
91,452,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Son
|
UTSW |
16 |
91,468,301 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5763:Son
|
UTSW |
16 |
91,454,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R5766:Son
|
UTSW |
16 |
91,461,875 (GRCm39) |
intron |
probably benign |
|
R5788:Son
|
UTSW |
16 |
91,456,940 (GRCm39) |
intron |
probably benign |
|
R5992:Son
|
UTSW |
16 |
91,455,792 (GRCm39) |
missense |
probably benign |
0.04 |
R6314:Son
|
UTSW |
16 |
91,457,298 (GRCm39) |
intron |
probably benign |
|
R6371:Son
|
UTSW |
16 |
91,471,629 (GRCm39) |
|
|
|
R6429:Son
|
UTSW |
16 |
91,455,054 (GRCm39) |
missense |
probably benign |
0.33 |
R6451:Son
|
UTSW |
16 |
91,454,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R6489:Son
|
UTSW |
16 |
91,452,044 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6513:Son
|
UTSW |
16 |
91,456,835 (GRCm39) |
intron |
probably benign |
|
R6753:Son
|
UTSW |
16 |
91,454,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R6916:Son
|
UTSW |
16 |
91,451,673 (GRCm39) |
missense |
probably damaging |
0.97 |
R7070:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7079:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7110:Son
|
UTSW |
16 |
91,453,406 (GRCm39) |
missense |
probably benign |
0.01 |
R7120:Son
|
UTSW |
16 |
91,467,414 (GRCm39) |
missense |
unknown |
|
R7120:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7167:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7205:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R7208:Son
|
UTSW |
16 |
91,458,990 (GRCm39) |
missense |
unknown |
|
R7219:Son
|
UTSW |
16 |
91,461,889 (GRCm39) |
missense |
unknown |
|
R7249:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7328:Son
|
UTSW |
16 |
91,455,278 (GRCm39) |
missense |
probably benign |
0.33 |
R7330:Son
|
UTSW |
16 |
91,453,486 (GRCm39) |
unclassified |
probably benign |
|
R7374:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7405:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7420:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7424:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7464:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7514:Son
|
UTSW |
16 |
91,451,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R7555:Son
|
UTSW |
16 |
91,455,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R7645:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R7716:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7718:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7778:Son
|
UTSW |
16 |
91,453,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7824:Son
|
UTSW |
16 |
91,453,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7856:Son
|
UTSW |
16 |
91,456,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R7870:Son
|
UTSW |
16 |
91,453,486 (GRCm39) |
unclassified |
probably benign |
|
R7928:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7972:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7978:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8000:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8192:Son
|
UTSW |
16 |
91,452,437 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8221:Son
|
UTSW |
16 |
91,453,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8227:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R8233:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8255:Son
|
UTSW |
16 |
91,461,824 (GRCm39) |
missense |
unknown |
|
R8292:Son
|
UTSW |
16 |
91,453,545 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8407:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8468:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R8495:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R8772:Son
|
UTSW |
16 |
91,454,826 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8796:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8862:Son
|
UTSW |
16 |
91,453,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Son
|
UTSW |
16 |
91,455,057 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8972:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8991:Son
|
UTSW |
16 |
91,453,608 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8991:Son
|
UTSW |
16 |
91,453,366 (GRCm39) |
missense |
probably benign |
0.04 |
R9086:Son
|
UTSW |
16 |
91,467,418 (GRCm39) |
missense |
unknown |
|
R9138:Son
|
UTSW |
16 |
91,452,006 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9232:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9241:Son
|
UTSW |
16 |
91,454,122 (GRCm39) |
missense |
probably damaging |
0.96 |
R9258:Son
|
UTSW |
16 |
91,474,570 (GRCm39) |
missense |
unknown |
|
R9328:Son
|
UTSW |
16 |
91,452,645 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9420:Son
|
UTSW |
16 |
91,454,508 (GRCm39) |
missense |
probably damaging |
0.98 |
R9468:Son
|
UTSW |
16 |
91,454,439 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9500:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9516:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9595:Son
|
UTSW |
16 |
91,454,241 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9679:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9719:Son
|
UTSW |
16 |
91,456,440 (GRCm39) |
missense |
probably damaging |
0.96 |
R9749:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9772:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9782:Son
|
UTSW |
16 |
91,444,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R9788:Son
|
UTSW |
16 |
91,453,699 (GRCm39) |
unclassified |
probably benign |
|
RF007:Son
|
UTSW |
16 |
91,456,257 (GRCm39) |
missense |
possibly damaging |
0.53 |
RF041:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
Z1176:Son
|
UTSW |
16 |
91,452,689 (GRCm39) |
missense |
possibly damaging |
0.80 |
|