Incidental Mutations

31 incidental mutations are currently displayed, and affect 31 genes.
2 are Possibly Damaging.
13 are Probably Damaging.
11 are Probably Benign.
5 are Probably Null.
4 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 31 of 31] per page Full List
 
ID question?
Source question?
Gene question?
E-score question?
 
Stock # question?
Gen question?
Quality
-
Vld question?
Strain question?
Chr question?
Position question?
 
Mutation question?
Ref
Var
Type question?
Exon Dist question?
 
Zygosity question?
Predicted Effect question?
PPH Score question?
-
Meta Score question?
 
MGI Phenotype question?
Posted question?
 
1 283877 APN Actn1 0.462 IGL02191 12 80174109 I642V T C missense Het probably benign 0.000 phenotype 04/16/2015
2 283858 APN Adam5 0.053 IGL02191 8 24812423 R185* G A nonsense Het probably null phenotype 04/16/2015
3 283860 APN C2 0.150 IGL02191 17 34866563 I122V T C missense Het probably damaging 0.998 phenotype 04/16/2015
4 283866 APN Camsap1 0.197 IGL02191 2 25929880 I1531T A G missense Het probably damaging 0.972 04/16/2015
5 283881 APN Celsr1 0.735 IGL02191 15 85979004 T1276A T C missense Het possibly damaging 0.693 phenotype 04/16/2015
6 283855 APN Cnot7 0.312 IGL02191 8 40510027 N35K A T missense Het probably benign 0.326 phenotype 04/16/2015
7 283880 APN Cyp2a12 0.084 IGL02191 7 27036611 I482V A G missense Het probably benign 0.002 04/16/2015
8 283854 APN Cyp3a57 0.075 IGL02191 5 145365685 E97G A G missense Het probably damaging 1.000 04/16/2015
9 283864 APN Cyp51 1.000 IGL02191 5 4100147 R192I C A missense Het probably benign 0.047 phenotype 04/16/2015
10 283871 APN Ddx59 1.000 IGL02191 1 136417158 L189P T C missense Het probably damaging 1.000 04/16/2015
11 283874 APN Dnah6 0.141 IGL02191 6 73017797 I4127T A G missense Het probably benign 0.001 phenotype 04/16/2015
12 283856 APN Dock3 0.637 IGL02191 9 106938141 V1217I C T missense Het probably benign 0.000 phenotype 04/16/2015
13 283865 APN Ergic2 0.586 IGL02191 6 148204821 D57G T C missense Het probably null 0.124 phenotype 04/16/2015
14 283875 APN Flvcr2 0.813 IGL02191 12 85786192 K329* A T nonsense Het probably null phenotype 04/16/2015
15 283861 APN Foxp1 1.000 IGL02191 6 98945600 S327G T C missense Het probably damaging 0.993 phenotype 04/16/2015
16 283879 APN Gen1 0.143 IGL02191 12 11242296 H562Q A C missense Het probably benign 0.183 phenotype 04/16/2015
17 283876 APN Gjc2 0.000 IGL02191 11 59177560 V32A A G missense Het probably damaging 0.992 phenotype 04/16/2015
18 283882 APN Grk4 0.169 IGL02191 5 34755189 H574Y C T missense Het probably benign 0.270 phenotype 04/16/2015
19 283867 APN Kif15 0.000 IGL02191 9 122975679 C93S T A missense Het probably damaging 1.000 04/16/2015
20 283863 APN Lrtm1 0.077 IGL02191 14 29021949 I125L A C missense Het probably benign 0.004 04/16/2015
21 283857 APN Mrgprb8 0.000 IGL02191 7 48388779 Y66C A G missense Het probably damaging 1.000 04/16/2015
22 283873 APN Pfn1 1.000 IGL02191 11 70654383 A33V G A missense Het probably damaging 0.980 phenotype 04/16/2015
23 283869 APN Scnn1b 1.000 IGL02191 7 121917513 K492Q A C missense Het probably damaging 0.997 phenotype 04/16/2015
24 283883 APN Slc22a29 0.000 IGL02191 19 8218681 G A unclassified Het probably benign 04/16/2015
25 283853 APN Spocd1 0.143 IGL02191 4 129953587 D523G A G missense Het probably damaging 0.988 phenotype 04/16/2015
26 283859 APN Tmem144 0.072 IGL02191 3 79826852 D181E A T missense Het possibly damaging 0.593 04/16/2015
27 283872 APN Tmem220 0.068 IGL02191 11 67031107 C101Y G A missense Het probably damaging 1.000 04/16/2015
28 283862 APN Tmpo 0.000 IGL02191 10 91161879 V682A A G missense Het probably benign 0.005 phenotype 04/16/2015
29 283868 APN Wdr93 0.064 IGL02191 7 79749220 K34R A G missense Het probably damaging 0.983 04/16/2015
30 283878 APN Zdhhc16 0.530 IGL02191 19 41937691 C8* C A nonsense Het probably null phenotype 04/16/2015
31 283870 APN Zfp318 0.000 IGL02191 17 46396810 R265* C T nonsense Het probably null phenotype 04/16/2015
[records 1 to 31 of 31]