Incidental Mutations

46 incidental mutations are currently displayed, and affect 46 genes.
7 are Possibly Damaging.
16 are Probably Damaging.
17 are Probably Benign.
6 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 46 of 46] 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 365814 APN A930018P22Rik 0.090 IGL02971 2 104123219 T130I C T missense Het probably benign 0.015 12/18/2015
2 365824 APN Ahi1 0.835 IGL02971 10 21000551 L787P T C missense Het possibly damaging 0.933 phenotype 12/18/2015
3 365823 APN Atf3 0.000 IGL02971 1 191177443 S10P A G missense Het probably benign 0.000 phenotype 12/18/2015
4 365813 APN Cdr2l 0.208 IGL02971 11 115390900 N77S A G missense Het probably damaging 0.999 12/18/2015
5 365804 APN Cnp 0.000 IGL02971 11 100576699 D156G A G missense Het probably benign 0.255 phenotype 12/18/2015
6 365822 APN Cntn3 0.000 IGL02971 6 102168933 D982E A T missense Het probably damaging 0.998 12/18/2015
7 365821 APN Col22a1 0.000 IGL02971 15 72006738 L190S A G missense Het probably damaging 0.999 phenotype 12/18/2015
8 365831 APN Csmd3 0.000 IGL02971 15 47913929 C T splice site Het probably benign 12/18/2015
9 365795 APN Dnah5 0.828 IGL02971 15 28384461 D3117G A G missense Het probably damaging 0.999 phenotype 12/18/2015
10 365811 APN Dock5 0.578 IGL02971 14 67757109 E1834G T C missense Het probably null 0.999 phenotype 12/18/2015
11 365803 APN Eea1 0.440 IGL02971 10 96041527 T1368A A G missense Het probably benign 0.373 12/18/2015
12 365830 APN Fam83f 0.059 IGL02971 15 80672149 V78A T C missense Het probably benign 0.000 12/18/2015
13 365802 APN Fcgbp 0.000 IGL02971 7 28101473 V1315I G A missense Het probably damaging 0.999 12/18/2015
14 365826 APN Fsd2 0.000 IGL02971 7 81548923 Y364* A T nonsense Het probably null phenotype 12/18/2015
15 365819 APN Gm21976 0.063 IGL02971 13 98302549 G16R G A missense Het probably null 0.354 12/18/2015
16 365818 APN Guca2b 0.090 IGL02971 4 119657688 S59P A G missense Het probably damaging 1.000 phenotype 12/18/2015
17 365807 APN Hars2 0.944 IGL02971 18 36786178 E123G A G missense Het probably damaging 1.000 0.456 phenotype 12/18/2015
18 365806 APN Hdac2 1.000 IGL02971 10 37000374 K462* A T nonsense Het probably null phenotype 12/18/2015
19 365836 APN Huwe1 1.000 IGL02971 X 151927626 T A splice site Het probably benign phenotype 12/18/2015
20 365816 APN Iqgap3 0.284 IGL02971 3 88090304 N262K T A missense Het probably benign 0.301 12/18/2015
21 365820 APN Kat6b 0.869 IGL02971 14 21669758 S1502G A G missense Het probably damaging 0.997 phenotype 12/18/2015
22 365800 APN Mapkapk3 0.000 IGL02971 9 107257080 D328E A T missense Het probably benign 0.002 phenotype 12/18/2015
23 365797 APN Mgea5 1.000 IGL02971 19 45762243 F671S A G missense Het probably damaging 0.999 phenotype 12/18/2015
24 365796 APN Naca 0.758 IGL02971 10 128041568 C T intron Het probably benign phenotype 12/18/2015
25 365798 APN Npffr1 0.000 IGL02971 10 61614139 V64A T C missense Het probably damaging 1.000 phenotype 12/18/2015
26 365792 APN Olfr331 0.063 IGL02971 11 58502385 L57P A G missense Het probably damaging 1.000 phenotype 12/18/2015
27 365794 APN Olfr918 0.185 IGL02971 9 38673268 M72L T A missense Het probably damaging 0.963 phenotype 12/18/2015
28 365817 APN Pcca 1.000 IGL02971 14 122889533 D718G A G missense Het probably damaging 0.963 phenotype 12/18/2015
29 365801 APN Pde6a 0.000 IGL02971 18 61264255 D670A A C missense Het probably damaging 0.999 phenotype 12/18/2015
30 365827 APN Pramel7 0.080 IGL02971 2 87490073 E292V T A missense Het probably benign 0.028 12/18/2015
31 365829 APN Prmt9 0.668 IGL02971 8 77565069 M357L A C missense Het probably benign 0.001 12/18/2015
32 365812 APN Ptgfr 0.086 IGL02971 3 151835326 S182T A T missense Het probably benign 0.004 phenotype 12/18/2015
33 365810 APN Rtraf 1.000 IGL02971 14 19816192 M152K A T missense Het possibly damaging 0.955 12/18/2015
34 365799 APN Satb1 1.000 IGL02971 17 51742689 D579G T C missense Het possibly damaging 0.615 phenotype 12/18/2015
35 365833 APN Serpinb6a 0.000 IGL02971 13 33931470 A G critical splice donor site 2 bp Het probably null phenotype 12/18/2015
36 365815 APN Slc5a9 0.075 IGL02971 4 111890300 I297V T C missense Het possibly damaging 0.579 12/18/2015
37 365832 APN Slf1 0.000 IGL02971 13 77047104 T A splice site Het probably benign phenotype 12/18/2015
38 365809 APN St8sia2 0.119 IGL02971 7 73966811 V139M C T missense Het probably damaging 1.000 phenotype 12/18/2015
39 365828 APN Tas2r114 0.060 IGL02971 6 131689280 M262V T C missense Het probably benign 0.001 phenotype 12/18/2015
40 365834 APN Tmem147 0.387 IGL02971 7 30729422 A G unclassified Het probably benign 12/18/2015
41 365835 APN Tmem220 0.068 IGL02971 11 67034107 A G critical splice acceptor site Het probably null 12/18/2015
42 365825 APN Uspl1 0.920 IGL02971 5 149188346 N35S A G missense Het possibly damaging 0.836 12/18/2015
43 365808 APN Vmn1r170 0.056 IGL02971 7 23606334 I54F A T missense Het possibly damaging 0.810 12/18/2015
44 365791 APN Vmn2r121 0.084 IGL02971 X 124127894 I810L T G missense Het probably damaging 0.999 12/18/2015
45 365805 APN Wbp2nl 0.000 IGL02971 15 82305744 T46S A T missense Het possibly damaging 0.605 phenotype 12/18/2015
46 365793 APN Zfp955b 0.082 IGL02971 17 33300966 M57K T A missense Het probably benign 0.109 12/18/2015
[records 1 to 46 of 46]