Incidental Mutations

20 incidental mutations are currently displayed, and affect 20 genes.
4 are Possibly Damaging.
5 are Probably Damaging.
7 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 20 of 20] 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 8690 APN AI314180 0.399 IGL00799 G1 4 58828047 I981F T A missense Het possibly damaging 0.949 12/06/2012
2 9286 APN Boc 0.000 IGL00799 G1 16 44492955 D515E G T missense Het probably benign 0.003 phenotype 12/06/2012
3 9600 APN Cenpe 1.000 IGL00799 G1 3 135228917 T A critical splice donor site 2 bp Het probably null phenotype 12/06/2012
4 9920 APN Ctcf 1.000 IGL00799 G1 8 105677336 D608G A G missense Het unknown phenotype 12/06/2012
5 10050 APN Dab2ip 0.440 IGL00799 G1 2 35707775 I99V A G missense Het probably benign 0.247 phenotype 12/06/2012
6 10452 APN Ehd2 0.172 IGL00799 G1 7 15963467 A139T C T missense Het possibly damaging 0.888 phenotype 12/06/2012
7 10637 APN Fam151b 0.000 IGL00799 G1 13 92477853 K42N C A missense Het probably damaging 0.999 12/06/2012
8 10916 APN Gapvd1 1.000 IGL00799 G1 2 34699860 D1002E A T missense Het probably benign 0.001 12/06/2012
9 10992 APN Gm13124 0.057 IGL00799 G1 4 144555273 H316Q A T missense Het probably benign 0.129 12/06/2012
10 11192 APN Gusb 0.128 IGL00799 G1 5 129999381 Y290C T C missense Het probably damaging 0.999 phenotype 12/06/2012
11 11322 APN Hoxd10 0.618 IGL00799 G1 2 74692442 S155G A G missense Het probably benign 0.063 phenotype 12/06/2012
12 11328 APN Hp 0.178 IGL00799 G1 8 109575618 A G unclassified 2095 bp Het probably null phenotype 12/06/2012
13 11412 APN Ift122 1.000 IGL00799 G1 6 115877536 S112P T C missense Het probably damaging 0.999 phenotype 12/06/2012
14 11486 APN Iqgap2 0.000 IGL00799 G1 13 95657944 A G splice site Het probably benign phenotype 12/06/2012
15 12114 APN Mtbp 1.000 IGL00799 G1 15 55617508 L290* T A nonsense Het probably null phenotype 12/06/2012
16 12778 APN Nr5a2 1.000 IGL00799 G1 1 136890798 D330V T A missense Het probably damaging 1.000 phenotype 12/06/2012
17 13717 APN R3hdm1 0.000 IGL00799 G1 1 128174963 L157Q T A missense Het probably damaging 1.000 12/06/2012
18 13727 APN Rad21 1.000 IGL00799 G1 15 51976125 D116E A T missense Het possibly damaging 0.764 phenotype 12/06/2012
19 14062 APN Slc23a3 0.000 IGL00799 G1 1 75133281 I114N A T missense Het possibly damaging 0.921 12/06/2012
20 14318 APN Syne1 1.000 IGL00799 G1 10 5347878 I1140L A G missense Het probably benign 0.001 phenotype 12/06/2012
[records 1 to 20 of 20]