Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
6 are Possibly Damaging.
10 are Probably Damaging.
9 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 26 of 26] 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 286817 APN Aff3 0.000 IGL02263 1 38535599 V100A A G missense Het probably damaging 0.998 phenotype 04/16/2015
2 286813 APN Agmo 0.063 IGL02263 12 37357697 N193K T A missense Het probably damaging 0.999 phenotype 04/16/2015
3 286825 APN Dnah8 0.314 IGL02263 17 30729165 I1910V A G missense Het probably benign 0.001 phenotype 04/16/2015
4 286818 APN Dsg2 0.153 IGL02263 18 20590020 S368T T A missense Het possibly damaging 0.700 phenotype 04/16/2015
5 286815 APN Eif2ak4 0.000 IGL02263 2 118461778 T1270A A G missense Het probably benign 0.001 phenotype 04/16/2015
6 286828 APN Ina 0.000 IGL02263 19 47015487 S245P T C missense Het probably damaging 0.999 phenotype 04/16/2015
7 286811 APN Katnb1 1.000 IGL02263 8 95090075 K96R A G missense Het probably damaging 1.000 phenotype 04/16/2015
8 286831 APN Kcnj4 0.101 IGL02263 15 79485787 A G utr 5 prime Het probably benign phenotype 04/16/2015
9 286823 APN Kcnn3 0.534 IGL02263 3 89661218 H601R A G missense Het possibly damaging 0.728 phenotype 04/16/2015
10 286824 APN Lrrc25 0.084 IGL02263 8 70617822 F84L C A missense Het probably benign 0.271 04/16/2015
11 286822 APN Ltb 0.183 IGL02263 17 35196001 Y259C A G missense Het probably damaging 1.000 phenotype 04/16/2015
12 286821 APN Macc1 0.096 IGL02263 12 119446017 N173K T G missense Het possibly damaging 0.871 phenotype 04/16/2015
13 286820 APN Med17 0.966 IGL02263 9 15267476 N466K A T missense Het probably damaging 0.984 phenotype 04/16/2015
14 286810 APN Ncoa2 0.964 IGL02263 1 13174763 N570K A T missense Het probably damaging 0.997 phenotype 04/16/2015
15 286812 APN Olfr1051 0.056 IGL02263 2 86276202 Y95F T A missense Het probably benign 0.008 phenotype 04/16/2015
16 286809 APN Olfr1134 0.175 IGL02263 2 87656199 C241S A T missense Het probably damaging 1.000 phenotype 04/16/2015
17 286816 APN Olfr629 0.084 IGL02263 7 103741055 F62I A T missense Het probably damaging 1.000 phenotype 04/16/2015
18 286829 APN Plb1 0.058 IGL02263 5 32321348 T C splice site Het probably benign phenotype 04/16/2015
19 286808 APN Ptprk 0.000 IGL02263 10 28075114 V12I G A missense Het unknown phenotype 04/16/2015
20 286830 APN Rabggta 0.966 IGL02263 14 55718961 G A splice site Het probably benign phenotype 04/16/2015
21 286814 APN Slc41a2 0.108 IGL02263 10 83313500 V193A A G missense Het possibly damaging 0.816 04/16/2015
22 286826 APN Thbs1 0.000 IGL02263 2 118119880 N665D A G missense Het probably benign 0.060 phenotype 04/16/2015
23 286819 APN Tm9sf1 0.209 IGL02263 14 55642935 T2A T C missense Het possibly damaging 0.947 0.112 04/16/2015
24 286827 APN Traf7 0.566 IGL02263 17 24513046 C193F C A missense Het possibly damaging 0.474 phenotype 04/16/2015
25 286806 APN Vmn1r91 IGL02263 7 20101843 D229G A G missense Het probably benign 0.001 04/16/2015
26 286807 APN Vmn2r7 0.099 IGL02263 3 64691447 V654G A C missense Het probably damaging 0.998 04/16/2015
[records 1 to 26 of 26]