Incidental Mutations

45 incidental mutations are currently displayed, and affect 44 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
19 are Probably Benign.
7 are Probably Null.
4 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 45 of 45] 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 291689 APN 0610040J01Rik 0.114 IGL02389 5 63896483 S11N G A missense Het probably null 1.000 04/16/2015
2 291695 APN Aqp9 0.127 IGL02389 9 71122906 I200V T C missense Het possibly damaging 0.796 phenotype 04/16/2015
3 291658 APN BC100530 0.057 IGL02389 16 36367486 V6F C A missense Het possibly damaging 0.842 04/16/2015
4 291693 APN Cntn2 0.262 IGL02389 1 132525321 E411G T C missense Het probably damaging 0.993 phenotype 04/16/2015
5 291692 APN Csgalnact1 0.075 IGL02389 8 68401492 G219V C A missense Het probably damaging 1.000 phenotype 04/16/2015
6 291681 APN Dennd3 0.192 IGL02389 15 73567056 D1091G A G missense Het probably damaging 0.999 04/16/2015
7 291697 APN Dock2 0.000 IGL02389 11 34698740 T C splice site Het probably benign phenotype 04/16/2015
8 291669 APN Dscam 1.000 IGL02389 16 96640897 I1577F T A missense Het probably benign 0.267 phenotype 04/16/2015
9 291684 APN Egflam 0.000 IGL02389 15 7250078 N482K A T missense Het probably benign 0.008 phenotype 04/16/2015
10 291668 APN Fam216a 0.000 IGL02389 5 122367511 T129A T C missense Het probably damaging 0.986 04/16/2015
11 291677 APN Fbxo40 0.117 IGL02389 16 36969774 M325V T C missense Het probably benign 0.259 phenotype 04/16/2015
12 291663 APN Fbxw8 0.414 IGL02389 5 118128955 V148M C T missense Het possibly damaging 0.569 phenotype 04/16/2015
13 291667 APN Fcgbp 0.000 IGL02389 7 28075171 R57C C T missense Het probably damaging 0.998 04/16/2015
14 291699 APN Gnpnat1 1.000 IGL02389 14 45380931 A G splice site 6 bp Het probably null 0.976 phenotype 04/16/2015
15 291676 APN Gria2 0.533 IGL02389 3 80709422 T408A T C missense Het probably benign 0.142 phenotype 04/16/2015
16 291691 APN H2-T3 0.000 IGL02389 17 36186608 M59T A G missense Het probably benign 0.009 phenotype 04/16/2015
17 291694 APN Jakmip1 0.742 IGL02389 5 37100843 Q278* C T nonsense Het probably null phenotype 04/16/2015
18 291665 APN Krtap21-1 0.071 IGL02389 16 89403424 G110D C T missense Het unknown 04/16/2015
19 291698 APN Myo7a 0.000 IGL02389 7 98106991 C T critical splice donor site 1 bp Het probably null phenotype 04/16/2015
20 291671 APN Nlrp9c 0.000 IGL02389 7 26394207 Q11L T A missense Het probably benign 0.000 04/16/2015
21 291666 APN Olfr1442 0.054 IGL02389 19 12674535 D110V A T missense Het probably benign 0.002 phenotype 04/16/2015
22 291674 APN Olfr298 0.096 IGL02389 7 86489128 L141P A G missense Het probably damaging 0.975 phenotype 04/16/2015
23 291660 APN Olfr767 0.054 IGL02389 10 129079230 I244M A C missense Het probably damaging 0.972 phenotype 04/16/2015
24 291664 APN Olfr790 0.132 IGL02389 10 129501070 M62K T A missense Het probably benign 0.000 phenotype 04/16/2015
25 291670 APN Pdzd8 0.000 IGL02389 19 59301393 I525T A G missense Het probably benign 0.001 04/16/2015
26 291680 APN Pign 0.818 IGL02389 1 105646781 L280* A T nonsense Het probably null phenotype 04/16/2015
27 291679 APN Pik3r4 1.000 IGL02389 9 105650331 I294M T G missense Het possibly damaging 0.883 phenotype 04/16/2015
28 291675 APN Pkhd1 0.150 IGL02389 1 20117720 I3455F T A missense Het probably damaging 0.992 phenotype 04/16/2015
29 291661 APN Prmt3 0.730 IGL02389 7 49848758 Q471* C T nonsense Het probably null phenotype 04/16/2015
30 291688 APN Prrc2c 0.356 IGL02389 1 162692870 F2006L A G missense Het probably damaging 0.999 04/16/2015
31 291673 APN Ptger3 0.076 IGL02389 3 157567171 R52C C T missense Het probably damaging 0.997 phenotype 04/16/2015
32 291702 APN Rfx2 0.706 IGL02389 17 56808325 T C splice site Het probably benign phenotype 04/16/2015
33 291662 APN Sh3bp4 0.000 IGL02389 1 89145148 F573L T C missense Het probably damaging 0.987 phenotype 04/16/2015
34 291700 APN Slc18a2 1.000 IGL02389 19 59263301 G T splice site Het probably benign phenotype 04/16/2015
35 291687 APN Slc26a8 0.545 IGL02389 17 28638650 I840F T A missense Het probably benign 0.002 phenotype 04/16/2015
36 291672 APN Slc5a4b 0.147 IGL02389 10 76072465 Y364* A T nonsense Het probably null 04/16/2015
37 291686 APN Slitrk1 0.000 IGL02389 14 108912322 I319T A G missense Het probably benign 0.000 phenotype 04/16/2015
38 291678 APN Stxbp5l 0.000 IGL02389 16 37208205 A499T C T missense Het probably benign 0.001 phenotype 04/16/2015
39 291682 APN Tnks2 0.000 IGL02389 19 36884103 S951R T A missense Het probably benign 0.322 phenotype 04/16/2015
40 291690 APN Trim30c 0.057 IGL02389 7 104382174 F478S A G missense Het probably benign 0.001 04/16/2015
41 291701 APN Tyro3 0.000 IGL02389 2 119804864 C T splice site Het probably benign phenotype 04/16/2015
42 291659 APN Vmn1r34 0.074 IGL02389 6 66637058 L232Q A T missense Het probably damaging 1.000 04/16/2015
43 291696 APN Zfp148 1.000 IGL02389 16 33495446 C215S T A missense Het probably damaging 0.999 phenotype 04/16/2015
44 291685 APN Zzef1 0.000 IGL02389 11 72899538 V2106D T A missense Het possibly damaging 0.893 04/16/2015
45 291683 APN Zzef1 0.000 IGL02389 11 72891217 P1995S C T missense Het probably benign 0.000 04/16/2015
[records 1 to 45 of 45]