Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
G |
T |
8: 25,162,136 (GRCm39) |
Y46* |
probably null |
Het |
Adam26b |
A |
C |
8: 43,973,524 (GRCm39) |
C493G |
probably damaging |
Het |
Ak5 |
A |
T |
3: 152,359,252 (GRCm39) |
L182Q |
probably damaging |
Het |
Akt1s1 |
T |
C |
7: 44,498,645 (GRCm39) |
|
probably benign |
Het |
Amhr2 |
G |
T |
15: 102,354,863 (GRCm39) |
G133C |
probably damaging |
Het |
Btbd9 |
A |
T |
17: 30,743,941 (GRCm39) |
L187Q |
probably damaging |
Het |
Ccdc117 |
A |
T |
11: 5,484,385 (GRCm39) |
|
probably benign |
Het |
Ccdc138 |
A |
T |
10: 58,411,542 (GRCm39) |
I637F |
probably damaging |
Het |
Ccdc162 |
A |
G |
10: 41,462,407 (GRCm39) |
|
probably benign |
Het |
Cdc25b |
C |
A |
2: 131,033,533 (GRCm39) |
H157Q |
probably benign |
Het |
Cdon |
A |
G |
9: 35,388,379 (GRCm39) |
|
probably null |
Het |
Cdt1 |
G |
A |
8: 123,298,884 (GRCm39) |
|
probably benign |
Het |
Cep350 |
C |
T |
1: 155,816,458 (GRCm39) |
|
probably null |
Het |
Cfb |
T |
C |
17: 35,078,992 (GRCm39) |
K831R |
probably benign |
Het |
Cldn4 |
C |
A |
5: 134,975,645 (GRCm39) |
|
probably benign |
Het |
Cntnap5b |
T |
C |
1: 99,999,767 (GRCm39) |
|
probably benign |
Het |
Cyp27b1 |
T |
G |
10: 126,884,967 (GRCm39) |
S77A |
probably benign |
Het |
Dlc1 |
T |
C |
8: 37,041,203 (GRCm39) |
D1342G |
possibly damaging |
Het |
Dlgap4 |
A |
G |
2: 156,603,799 (GRCm39) |
H887R |
probably damaging |
Het |
Duox2 |
A |
G |
2: 122,123,139 (GRCm39) |
I503T |
probably damaging |
Het |
Eml4 |
T |
C |
17: 83,770,922 (GRCm39) |
|
probably benign |
Het |
Ermap |
A |
G |
4: 119,042,888 (GRCm39) |
S212P |
probably benign |
Het |
Esrrg |
T |
A |
1: 187,775,538 (GRCm39) |
C22S |
probably benign |
Het |
Evx2 |
T |
A |
2: 74,488,238 (GRCm39) |
Y194F |
possibly damaging |
Het |
Fbn2 |
T |
G |
18: 58,191,461 (GRCm39) |
D1554A |
probably damaging |
Het |
Flrt1 |
G |
A |
19: 7,074,508 (GRCm39) |
|
probably benign |
Het |
Fndc5 |
A |
G |
4: 129,033,630 (GRCm39) |
|
probably benign |
Het |
Frem1 |
A |
T |
4: 82,907,403 (GRCm39) |
I837N |
probably damaging |
Het |
Fzd10 |
G |
T |
5: 128,679,662 (GRCm39) |
A461S |
possibly damaging |
Het |
Ganab |
T |
A |
19: 8,888,477 (GRCm39) |
Y511N |
probably damaging |
Het |
Gbp7 |
A |
G |
3: 142,243,926 (GRCm39) |
|
probably null |
Het |
Gm5919 |
T |
A |
9: 83,765,436 (GRCm39) |
C91S |
unknown |
Het |
Gpr31b |
A |
T |
17: 13,271,093 (GRCm39) |
C25* |
probably null |
Het |
Grb10 |
A |
G |
11: 11,886,755 (GRCm39) |
S505P |
probably damaging |
Het |
Grm4 |
A |
T |
17: 27,654,183 (GRCm39) |
V542E |
probably damaging |
Het |
Gsta5 |
T |
C |
9: 78,206,303 (GRCm39) |
I75T |
possibly damaging |
Het |
Hivep3 |
G |
A |
4: 119,954,531 (GRCm39) |
R949H |
possibly damaging |
Het |
Hycc1 |
C |
T |
5: 24,184,506 (GRCm39) |
G242D |
probably damaging |
Het |
Invs |
A |
T |
4: 48,407,653 (GRCm39) |
M543L |
probably benign |
Het |
Kcnk2 |
T |
C |
1: 188,988,927 (GRCm39) |
|
probably null |
Het |
Kdm6b |
A |
T |
11: 69,295,844 (GRCm39) |
S808T |
unknown |
Het |
Klhl30 |
C |
T |
1: 91,283,228 (GRCm39) |
R277W |
probably damaging |
Het |
Lama1 |
A |
G |
17: 68,080,707 (GRCm39) |
Q1245R |
probably benign |
Het |
Lingo3 |
G |
T |
10: 80,671,169 (GRCm39) |
H254N |
probably benign |
Het |
Lzts1 |
A |
T |
8: 69,588,392 (GRCm39) |
H521Q |
possibly damaging |
Het |
Map3k19 |
A |
C |
1: 127,749,919 (GRCm39) |
I1144S |
possibly damaging |
Het |
Mast2 |
A |
G |
4: 116,165,184 (GRCm39) |
S1411P |
probably damaging |
Het |
Mast2 |
T |
C |
4: 116,170,043 (GRCm39) |
|
probably benign |
Het |
Mesp1 |
G |
T |
7: 79,442,328 (GRCm39) |
S225R |
possibly damaging |
Het |
Micu1 |
A |
G |
10: 59,675,503 (GRCm39) |
T366A |
possibly damaging |
Het |
Mideas |
G |
T |
12: 84,205,077 (GRCm39) |
N834K |
possibly damaging |
Het |
Mknk2 |
T |
C |
10: 80,507,742 (GRCm39) |
|
probably null |
Het |
Msh5 |
A |
G |
17: 35,258,199 (GRCm39) |
L309P |
probably damaging |
Het |
Myo7b |
T |
C |
18: 32,127,962 (GRCm39) |
I577V |
probably benign |
Het |
Myom2 |
T |
A |
8: 15,167,698 (GRCm39) |
D1094E |
probably damaging |
Het |
Nedd1 |
T |
C |
10: 92,527,693 (GRCm39) |
|
probably null |
Het |
Neu4 |
T |
C |
1: 93,950,191 (GRCm39) |
L50S |
probably damaging |
Het |
Noa1 |
T |
C |
5: 77,457,722 (GRCm39) |
Y61C |
probably benign |
Het |
Nr1h4 |
A |
T |
10: 89,342,390 (GRCm39) |
M30K |
probably benign |
Het |
Nsd3 |
A |
G |
8: 26,199,096 (GRCm39) |
I1219V |
probably benign |
Het |
Nup188 |
T |
A |
2: 30,233,478 (GRCm39) |
|
probably null |
Het |
Or10ag2 |
T |
A |
2: 87,248,612 (GRCm39) |
Y71* |
probably null |
Het |
Or5al5 |
A |
G |
2: 85,961,378 (GRCm39) |
S210P |
probably damaging |
Het |
Or6c208 |
T |
A |
10: 129,224,162 (GRCm39) |
I220N |
possibly damaging |
Het |
Or6k2 |
A |
T |
1: 173,986,920 (GRCm39) |
T194S |
probably benign |
Het |
Pbk |
G |
A |
14: 66,051,245 (GRCm39) |
|
probably benign |
Het |
Pcnx2 |
G |
A |
8: 126,487,459 (GRCm39) |
T1848M |
possibly damaging |
Het |
Pdzd7 |
C |
T |
19: 45,033,914 (GRCm39) |
G57R |
possibly damaging |
Het |
Pik3r4 |
C |
A |
9: 105,546,386 (GRCm39) |
|
probably benign |
Het |
Plce1 |
A |
G |
19: 38,766,433 (GRCm39) |
S2153G |
probably damaging |
Het |
Potefam1 |
C |
T |
2: 111,044,928 (GRCm39) |
|
probably null |
Het |
Pphln1 |
G |
A |
15: 93,318,192 (GRCm39) |
V34M |
possibly damaging |
Het |
Prrc2a |
T |
C |
17: 35,375,308 (GRCm39) |
D1114G |
probably damaging |
Het |
Prss16 |
T |
C |
13: 22,193,546 (GRCm39) |
|
probably benign |
Het |
Rtp3 |
T |
C |
9: 110,816,168 (GRCm39) |
K128E |
probably damaging |
Het |
Setd1a |
G |
A |
7: 127,386,382 (GRCm39) |
V336I |
probably damaging |
Het |
Sfpq |
A |
G |
4: 126,916,762 (GRCm39) |
I320V |
possibly damaging |
Het |
Skint5 |
A |
T |
4: 113,620,679 (GRCm39) |
D678E |
unknown |
Het |
Slc12a9 |
G |
A |
5: 137,313,638 (GRCm39) |
P774S |
probably benign |
Het |
Slc25a54 |
C |
G |
3: 109,019,481 (GRCm39) |
L362V |
possibly damaging |
Het |
Smarcd1 |
A |
G |
15: 99,605,267 (GRCm39) |
|
probably null |
Het |
Spata31e5 |
T |
A |
1: 28,816,011 (GRCm39) |
N674Y |
probably damaging |
Het |
Suco |
A |
T |
1: 161,661,683 (GRCm39) |
M916K |
probably damaging |
Het |
Tiam2 |
T |
C |
17: 3,564,973 (GRCm39) |
S1404P |
possibly damaging |
Het |
Topors |
T |
C |
4: 40,260,333 (GRCm39) |
T984A |
unknown |
Het |
Trabd2b |
A |
T |
4: 114,443,767 (GRCm39) |
K308M |
probably damaging |
Het |
Trmo |
A |
T |
4: 46,377,083 (GRCm39) |
|
probably benign |
Het |
Trpc3 |
A |
T |
3: 36,725,654 (GRCm39) |
D107E |
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Uggt2 |
A |
C |
14: 119,295,010 (GRCm39) |
Y539D |
probably benign |
Het |
Wwc2 |
T |
G |
8: 48,353,674 (GRCm39) |
|
probably benign |
Het |
Zdbf2 |
T |
A |
1: 63,344,109 (GRCm39) |
D829E |
possibly damaging |
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 |
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 |
R6307:Scn3a
|
UTSW |
2 |
65,302,685 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|