Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
C |
10: 79,843,221 (GRCm39) |
L1232P |
probably damaging |
Het |
Akap6 |
A |
T |
12: 53,188,351 (GRCm39) |
I1922F |
possibly damaging |
Het |
Ankdd1a |
C |
T |
9: 65,415,343 (GRCm39) |
A227T |
possibly damaging |
Het |
Arpc5 |
T |
C |
1: 152,647,206 (GRCm39) |
V103A |
possibly damaging |
Het |
Atp9a |
C |
A |
2: 168,510,090 (GRCm39) |
V430F |
probably benign |
Het |
Bod1 |
A |
G |
11: 31,616,932 (GRCm39) |
S110P |
probably damaging |
Het |
Cacna1c |
C |
A |
6: 118,590,914 (GRCm39) |
V1453F |
probably damaging |
Het |
Capn8 |
T |
A |
1: 182,435,264 (GRCm39) |
M414K |
probably damaging |
Het |
Cbl |
A |
T |
9: 44,069,809 (GRCm39) |
|
probably null |
Het |
Ccdc42 |
A |
T |
11: 68,479,106 (GRCm39) |
Q98L |
probably damaging |
Het |
Ccn3 |
T |
C |
15: 54,611,421 (GRCm39) |
|
probably null |
Het |
Cd200 |
C |
A |
16: 45,217,545 (GRCm39) |
V49L |
probably benign |
Het |
Celsr1 |
A |
G |
15: 85,812,531 (GRCm39) |
S2060P |
probably benign |
Het |
Ces1g |
A |
T |
8: 94,057,820 (GRCm39) |
H160Q |
possibly damaging |
Het |
Chrnb2 |
G |
T |
3: 89,668,831 (GRCm39) |
H161Q |
probably damaging |
Het |
Ctns |
G |
A |
11: 73,082,559 (GRCm39) |
T57I |
probably benign |
Het |
Cyp3a25 |
A |
T |
5: 145,931,766 (GRCm39) |
M114K |
possibly damaging |
Het |
D630003M21Rik |
A |
G |
2: 158,057,871 (GRCm39) |
F536L |
probably benign |
Het |
Dcc |
C |
T |
18: 71,943,826 (GRCm39) |
R275Q |
probably benign |
Het |
Dmxl2 |
A |
T |
9: 54,289,990 (GRCm39) |
H2508Q |
possibly damaging |
Het |
Elf5 |
C |
A |
2: 103,269,757 (GRCm39) |
Q113K |
probably damaging |
Het |
Fam83a |
T |
G |
15: 57,849,507 (GRCm39) |
V17G |
possibly damaging |
Het |
Farsa |
T |
C |
8: 85,587,674 (GRCm39) |
|
probably null |
Het |
Fat2 |
G |
C |
11: 55,172,106 (GRCm39) |
T2869S |
possibly damaging |
Het |
Fgg |
A |
T |
3: 82,920,283 (GRCm39) |
Q354L |
probably damaging |
Het |
Folh1 |
T |
C |
7: 86,372,517 (GRCm39) |
D679G |
probably damaging |
Het |
Gbp4 |
T |
A |
5: 105,270,975 (GRCm39) |
R83* |
probably null |
Het |
Gm17482 |
T |
A |
6: 115,204,311 (GRCm39) |
|
probably benign |
Het |
Hmgxb4 |
T |
A |
8: 75,749,927 (GRCm39) |
V481D |
possibly damaging |
Het |
Ifi207 |
A |
C |
1: 173,552,619 (GRCm39) |
Y926D |
probably damaging |
Het |
Ikzf5 |
T |
A |
7: 130,993,377 (GRCm39) |
N264Y |
probably damaging |
Het |
Kat6a |
T |
A |
8: 23,430,384 (GRCm39) |
M1913K |
unknown |
Het |
Krt33b |
A |
T |
11: 99,915,694 (GRCm39) |
C351S |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,427,944 (GRCm39) |
D543G |
probably damaging |
Het |
Lrrfip2 |
C |
T |
9: 111,053,021 (GRCm39) |
R339W |
probably damaging |
Het |
Mapk3 |
T |
G |
7: 126,363,454 (GRCm39) |
M276R |
probably benign |
Het |
Mgst1 |
T |
C |
6: 138,127,827 (GRCm39) |
V137A |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,558,884 (GRCm39) |
T2470A |
unknown |
Het |
Muc4 |
C |
T |
16: 32,575,237 (GRCm39) |
S1274F |
possibly damaging |
Het |
Myo5c |
A |
C |
9: 75,180,198 (GRCm39) |
K713T |
possibly damaging |
Het |
Myzap |
T |
C |
9: 71,466,146 (GRCm39) |
D170G |
possibly damaging |
Het |
Naa50 |
T |
C |
16: 43,979,831 (GRCm39) |
V113A |
probably damaging |
Het |
Neu3 |
T |
C |
7: 99,462,929 (GRCm39) |
T265A |
probably benign |
Het |
Nin |
T |
C |
12: 70,061,631 (GRCm39) |
T2078A |
possibly damaging |
Het |
Nomo1 |
G |
A |
7: 45,683,260 (GRCm39) |
|
probably benign |
Het |
Nprl3 |
A |
G |
11: 32,189,828 (GRCm39) |
L273P |
probably damaging |
Het |
Oaf |
T |
A |
9: 43,136,216 (GRCm39) |
H120L |
possibly damaging |
Het |
Or10s1 |
T |
C |
9: 39,985,824 (GRCm39) |
S78P |
probably damaging |
Het |
Or13p4 |
C |
T |
4: 118,547,145 (GRCm39) |
R168H |
probably benign |
Het |
Or8b36 |
ATTGCTGTTT |
ATTGCTGTTTGCTGTTT |
9: 37,937,836 (GRCm39) |
|
probably null |
Het |
Or8k21 |
T |
C |
2: 86,145,468 (GRCm39) |
H54R |
probably benign |
Het |
Pcdhga3 |
T |
A |
18: 37,809,674 (GRCm39) |
|
probably benign |
Het |
Polq |
G |
A |
16: 36,837,718 (GRCm39) |
|
probably null |
Het |
Prdm8 |
C |
T |
5: 98,333,162 (GRCm39) |
P243L |
possibly damaging |
Het |
Prim2 |
T |
C |
1: 33,701,373 (GRCm39) |
D138G |
probably benign |
Het |
Prl2c5 |
A |
G |
13: 13,365,175 (GRCm39) |
E107G |
probably benign |
Het |
Prr14l |
T |
A |
5: 32,984,869 (GRCm39) |
H1542L |
probably damaging |
Het |
Rab26 |
T |
C |
17: 24,749,072 (GRCm39) |
E203G |
probably damaging |
Het |
Rtkn2 |
A |
T |
10: 67,871,662 (GRCm39) |
H350L |
possibly damaging |
Het |
Scara3 |
T |
C |
14: 66,175,710 (GRCm39) |
D19G |
probably benign |
Het |
Sdcbp |
A |
G |
4: 6,385,059 (GRCm39) |
M93V |
probably benign |
Het |
Sema6a |
C |
A |
18: 47,382,231 (GRCm39) |
R772L |
probably damaging |
Het |
Slc5a7 |
T |
C |
17: 54,584,006 (GRCm39) |
K428R |
probably benign |
Het |
Sptbn2 |
G |
A |
19: 4,774,674 (GRCm39) |
G109D |
probably damaging |
Het |
Tmppe |
T |
C |
9: 114,233,812 (GRCm39) |
L37P |
probably benign |
Het |
Tuba1a |
T |
C |
15: 98,849,410 (GRCm39) |
T56A |
probably benign |
Het |
Tut4 |
T |
A |
4: 108,412,817 (GRCm39) |
I1506N |
probably damaging |
Het |
Vmn2r111 |
A |
G |
17: 22,792,070 (GRCm39) |
I62T |
probably benign |
Het |
Vmn2r73 |
A |
G |
7: 85,506,828 (GRCm39) |
I828T |
probably damaging |
Het |
Vmn2r79 |
T |
A |
7: 86,686,976 (GRCm39) |
W786R |
probably damaging |
Het |
Zp1 |
G |
A |
19: 10,894,084 (GRCm39) |
T405M |
probably null |
Het |
|
Other mutations in Scn3a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00953:Scn3a
|
APN |
2 |
65,327,736 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01086:Scn3a
|
APN |
2 |
65,300,503 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01141:Scn3a
|
APN |
2 |
65,325,457 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01150:Scn3a
|
APN |
2 |
65,327,709 (GRCm39) |
splice site |
probably null |
|
IGL01564:Scn3a
|
APN |
2 |
65,291,790 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01594:Scn3a
|
APN |
2 |
65,291,775 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01751:Scn3a
|
APN |
2 |
65,291,596 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01803:Scn3a
|
APN |
2 |
65,352,127 (GRCm39) |
unclassified |
probably benign |
|
IGL01822:Scn3a
|
APN |
2 |
65,325,608 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02063:Scn3a
|
APN |
2 |
65,291,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02142:Scn3a
|
APN |
2 |
65,356,965 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02198:Scn3a
|
APN |
2 |
65,338,833 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02501:Scn3a
|
APN |
2 |
65,356,899 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02608:Scn3a
|
APN |
2 |
65,354,510 (GRCm39) |
nonsense |
probably null |
|
IGL02645:Scn3a
|
APN |
2 |
65,344,871 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02653:Scn3a
|
APN |
2 |
65,291,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03077:Scn3a
|
APN |
2 |
65,367,016 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03099:Scn3a
|
APN |
2 |
65,367,016 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03299:Scn3a
|
APN |
2 |
65,327,860 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03327:Scn3a
|
APN |
2 |
65,367,016 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03346:Scn3a
|
APN |
2 |
65,367,016 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03355:Scn3a
|
APN |
2 |
65,290,912 (GRCm39) |
missense |
possibly damaging |
0.91 |
curtsey
|
UTSW |
2 |
65,295,180 (GRCm39) |
missense |
probably damaging |
1.00 |
dip
|
UTSW |
2 |
65,354,523 (GRCm39) |
missense |
probably benign |
0.01 |
Regime
|
UTSW |
2 |
65,355,194 (GRCm39) |
missense |
possibly damaging |
0.93 |
Willpower
|
UTSW |
2 |
65,356,098 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0019:Scn3a
|
UTSW |
2 |
65,292,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R0316:Scn3a
|
UTSW |
2 |
65,291,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Scn3a
|
UTSW |
2 |
65,338,918 (GRCm39) |
missense |
probably damaging |
0.97 |
R0414:Scn3a
|
UTSW |
2 |
65,356,326 (GRCm39) |
splice site |
probably benign |
|
R0609:Scn3a
|
UTSW |
2 |
65,366,854 (GRCm39) |
missense |
probably damaging |
0.96 |
R0613:Scn3a
|
UTSW |
2 |
65,302,628 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0645:Scn3a
|
UTSW |
2 |
65,355,194 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0665:Scn3a
|
UTSW |
2 |
65,314,755 (GRCm39) |
missense |
probably null |
0.00 |
R0667:Scn3a
|
UTSW |
2 |
65,314,755 (GRCm39) |
missense |
probably null |
0.00 |
R0710:Scn3a
|
UTSW |
2 |
65,299,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R1202:Scn3a
|
UTSW |
2 |
65,336,491 (GRCm39) |
missense |
probably benign |
0.07 |
R1440:Scn3a
|
UTSW |
2 |
65,359,785 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1447:Scn3a
|
UTSW |
2 |
65,300,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R1564:Scn3a
|
UTSW |
2 |
65,344,979 (GRCm39) |
missense |
probably damaging |
0.98 |
R1595:Scn3a
|
UTSW |
2 |
65,329,323 (GRCm39) |
missense |
probably damaging |
0.99 |
R1775:Scn3a
|
UTSW |
2 |
65,302,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R1781:Scn3a
|
UTSW |
2 |
65,302,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Scn3a
|
UTSW |
2 |
65,314,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R1924:Scn3a
|
UTSW |
2 |
65,291,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Scn3a
|
UTSW |
2 |
65,291,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Scn3a
|
UTSW |
2 |
65,351,210 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2174:Scn3a
|
UTSW |
2 |
65,337,550 (GRCm39) |
missense |
probably damaging |
0.99 |
R2656:Scn3a
|
UTSW |
2 |
65,356,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R2680:Scn3a
|
UTSW |
2 |
65,366,880 (GRCm39) |
missense |
probably benign |
0.04 |
R3882:Scn3a
|
UTSW |
2 |
65,312,623 (GRCm39) |
missense |
probably benign |
0.03 |
R4019:Scn3a
|
UTSW |
2 |
65,356,295 (GRCm39) |
intron |
probably benign |
|
R4106:Scn3a
|
UTSW |
2 |
65,325,379 (GRCm39) |
missense |
probably benign |
0.07 |
R4108:Scn3a
|
UTSW |
2 |
65,325,379 (GRCm39) |
missense |
probably benign |
0.07 |
R4109:Scn3a
|
UTSW |
2 |
65,325,379 (GRCm39) |
missense |
probably benign |
0.07 |
R4225:Scn3a
|
UTSW |
2 |
65,366,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R4419:Scn3a
|
UTSW |
2 |
65,297,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R4552:Scn3a
|
UTSW |
2 |
65,354,523 (GRCm39) |
missense |
probably benign |
0.01 |
R4687:Scn3a
|
UTSW |
2 |
65,295,074 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4780:Scn3a
|
UTSW |
2 |
65,336,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Scn3a
|
UTSW |
2 |
65,291,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R4856:Scn3a
|
UTSW |
2 |
65,291,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R4886:Scn3a
|
UTSW |
2 |
65,291,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R4914:Scn3a
|
UTSW |
2 |
65,291,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Scn3a
|
UTSW |
2 |
65,291,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4918:Scn3a
|
UTSW |
2 |
65,291,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Scn3a
|
UTSW |
2 |
65,302,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R5101:Scn3a
|
UTSW |
2 |
65,291,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R5128:Scn3a
|
UTSW |
2 |
65,338,862 (GRCm39) |
missense |
probably benign |
0.08 |
R5132:Scn3a
|
UTSW |
2 |
65,298,548 (GRCm39) |
missense |
probably benign |
0.09 |
R5297:Scn3a
|
UTSW |
2 |
65,299,378 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5595:Scn3a
|
UTSW |
2 |
65,291,057 (GRCm39) |
missense |
probably benign |
|
R5699:Scn3a
|
UTSW |
2 |
65,337,608 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5730:Scn3a
|
UTSW |
2 |
65,325,604 (GRCm39) |
missense |
probably benign |
0.00 |
R5735:Scn3a
|
UTSW |
2 |
65,314,803 (GRCm39) |
missense |
probably benign |
0.09 |
R5735:Scn3a
|
UTSW |
2 |
65,312,622 (GRCm39) |
missense |
probably damaging |
0.98 |
R5855:Scn3a
|
UTSW |
2 |
65,295,074 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5888:Scn3a
|
UTSW |
2 |
65,327,742 (GRCm39) |
missense |
probably benign |
0.06 |
R5898:Scn3a
|
UTSW |
2 |
65,345,039 (GRCm39) |
missense |
probably damaging |
0.96 |
R5935:Scn3a
|
UTSW |
2 |
65,295,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R5970:Scn3a
|
UTSW |
2 |
65,325,125 (GRCm39) |
intron |
probably benign |
|
R6214:Scn3a
|
UTSW |
2 |
65,325,380 (GRCm39) |
missense |
probably benign |
0.29 |
R6215:Scn3a
|
UTSW |
2 |
65,325,380 (GRCm39) |
missense |
probably benign |
0.29 |
R6235:Scn3a
|
UTSW |
2 |
65,291,679 (GRCm39) |
missense |
probably damaging |
0.97 |
R6355:Scn3a
|
UTSW |
2 |
65,291,643 (GRCm39) |
missense |
probably damaging |
0.99 |
R6376:Scn3a
|
UTSW |
2 |
65,291,843 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6517:Scn3a
|
UTSW |
2 |
65,327,907 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6775:Scn3a
|
UTSW |
2 |
65,352,159 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6893:Scn3a
|
UTSW |
2 |
65,356,098 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6986:Scn3a
|
UTSW |
2 |
65,338,962 (GRCm39) |
missense |
probably damaging |
0.97 |
R7065:Scn3a
|
UTSW |
2 |
65,295,199 (GRCm39) |
missense |
probably benign |
|
R7078:Scn3a
|
UTSW |
2 |
65,327,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7146:Scn3a
|
UTSW |
2 |
65,313,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R7240:Scn3a
|
UTSW |
2 |
65,299,386 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7294:Scn3a
|
UTSW |
2 |
65,302,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R7352:Scn3a
|
UTSW |
2 |
65,356,045 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7636:Scn3a
|
UTSW |
2 |
65,328,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R7708:Scn3a
|
UTSW |
2 |
65,313,512 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7733:Scn3a
|
UTSW |
2 |
65,338,994 (GRCm39) |
missense |
probably benign |
0.08 |
R7761:Scn3a
|
UTSW |
2 |
65,359,798 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7792:Scn3a
|
UTSW |
2 |
65,297,334 (GRCm39) |
nonsense |
probably null |
|
R7828:Scn3a
|
UTSW |
2 |
65,338,918 (GRCm39) |
missense |
probably damaging |
0.97 |
R7875:Scn3a
|
UTSW |
2 |
65,327,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:Scn3a
|
UTSW |
2 |
65,366,859 (GRCm39) |
missense |
probably damaging |
0.96 |
R7958:Scn3a
|
UTSW |
2 |
65,336,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R7965:Scn3a
|
UTSW |
2 |
65,336,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Scn3a
|
UTSW |
2 |
65,361,154 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8345:Scn3a
|
UTSW |
2 |
65,329,335 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8356:Scn3a
|
UTSW |
2 |
65,291,017 (GRCm39) |
missense |
probably benign |
0.08 |
R8456:Scn3a
|
UTSW |
2 |
65,291,017 (GRCm39) |
missense |
probably benign |
0.08 |
R8527:Scn3a
|
UTSW |
2 |
65,327,863 (GRCm39) |
missense |
probably damaging |
0.99 |
R8688:Scn3a
|
UTSW |
2 |
65,356,047 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8731:Scn3a
|
UTSW |
2 |
65,298,507 (GRCm39) |
nonsense |
probably null |
|
R8901:Scn3a
|
UTSW |
2 |
65,352,252 (GRCm39) |
missense |
probably benign |
0.00 |
R8910:Scn3a
|
UTSW |
2 |
65,338,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R9011:Scn3a
|
UTSW |
2 |
65,352,170 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9364:Scn3a
|
UTSW |
2 |
65,291,596 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9460:Scn3a
|
UTSW |
2 |
65,300,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R9496:Scn3a
|
UTSW |
2 |
65,312,493 (GRCm39) |
critical splice donor site |
probably null |
|
R9542:Scn3a
|
UTSW |
2 |
65,366,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R9563:Scn3a
|
UTSW |
2 |
65,291,595 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Scn3a
|
UTSW |
2 |
65,355,191 (GRCm39) |
nonsense |
probably null |
|
X0062:Scn3a
|
UTSW |
2 |
65,297,345 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Scn3a
|
UTSW |
2 |
65,329,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|