Incidental Mutations

15 incidental mutations are currently displayed, and affect 15 genes.
3 are Possibly Damaging.
7 are Probably Damaging.
5 are Probably Benign.
0 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 15 of 15] 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 90873 APN Crym 0.000 IGL01562 G1 7 120195399 V199A A G missense Het probably damaging 0.980 phenotype 12/09/2013
2 90867 APN Dsel 0.123 IGL01562 G1 1 111860319 T829A T C missense Het probably benign 0.000 phenotype 12/09/2013
3 90864 APN Frg1 0.108 IGL01562 G1 8 41416909 K18R T C missense Het possibly damaging 0.919 phenotype 12/09/2013
4 90863 APN H2-M10.5 0.053 IGL01562 G1 17 36773776 S131G A G missense Het possibly damaging 0.533 12/09/2013
5 90875 APN Ift172 1.000 IGL01562 G1 5 31267247 I701N A T missense Het probably damaging 0.966 phenotype 12/09/2013
6 90874 APN Il5ra 0.083 IGL01562 G1 6 106731904 I292V T C missense Het probably benign 0.003 phenotype 12/09/2013
7 90872 APN Nup98 1.000 IGL01562 G1 7 102185918 S243P A G missense Het probably damaging 0.990 phenotype 12/09/2013
8 90870 APN Pramef25 0.058 IGL01562 G1 4 143950865 L48S A G missense Het probably damaging 1.000 12/09/2013
9 90869 APN Ptgis 0.000 IGL01562 G1 2 167206830 Y422C T C missense Het probably damaging 1.000 0.214 phenotype 12/09/2013
10 90866 APN Senp2 1.000 IGL01562 G1 16 22009687 C16R T C missense Het probably damaging 0.996 phenotype 12/09/2013
11 90871 APN St7 0.155 IGL01562 G1 6 17922035 L411Q T A missense Het probably damaging 0.994 phenotype 12/09/2013
12 90876 APN Tanc2 1.000 IGL01562 G1 11 105780069 Y164F A T missense Het probably benign 0.001 phenotype 12/09/2013
13 90877 APN Ttc23l 0.072 IGL01562 G1 15 10551390 T C splice site Het probably benign 12/09/2013
14 90868 APN Vmn2r66 0.201 IGL01562 G1 7 85007287 Q174K G T missense Het probably benign 0.033 12/09/2013
15 90865 APN Wrap73 0.726 IGL01562 G1 4 154145337 E55G A G missense Het possibly damaging 0.626 phenotype 12/09/2013
[records 1 to 15 of 15]