Incidental Mutations

48 incidental mutations are currently displayed, and affect 48 genes.
8 are Possibly Damaging.
20 are Probably Damaging.
15 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 48 of 48] 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 282754 APN Aass 0.000 IGL02167 6 23122722 T A intron Het probably benign phenotype 04/16/2015
2 282739 APN Cacna1f 0.000 IGL02167 X 7616019 Y581H T C missense Het probably damaging 0.997 phenotype 04/16/2015
3 282762 APN Camsap1 0.197 IGL02167 2 25934300 R1416H C T missense Het probably damaging 0.998 04/16/2015
4 282765 APN Ccdc117 0.277 IGL02167 11 5531333 E266G T C missense Het possibly damaging 0.847 04/16/2015
5 282743 APN Ccdc9 0.073 IGL02167 7 16284359 L8* A T nonsense Het probably null 04/16/2015
6 282741 APN Cited2 IGL02167 10 17724270 S109P T C missense Het probably benign 0.003 phenotype 04/16/2015
7 282761 APN Cnot4 1.000 IGL02167 6 35056224 D286G T C missense Het possibly damaging 0.491 phenotype 04/16/2015
8 282779 APN Col5a1 1.000 IGL02167 2 28018556 I52T T C missense Het probably benign 0.000 phenotype 04/16/2015
9 282764 APN Cry2 0.855 IGL02167 2 92433821 N68S T C missense Het possibly damaging 0.932 phenotype 04/16/2015
10 282737 APN Cul4a 0.397 IGL02167 8 13122826 F153S T C missense Het probably damaging 1.000 phenotype 04/16/2015
11 282745 APN Ddr1 0.925 IGL02167 17 35690071 S261G T C missense Het possibly damaging 0.554 phenotype 04/16/2015
12 282756 APN Depdc5 1.000 IGL02167 5 32903801 R324Q G A missense Het probably damaging 1.000 phenotype 04/16/2015
13 282773 APN Dmgdh 0.000 IGL02167 13 93720627 A G splice site Het probably benign phenotype 04/16/2015
14 282736 APN Epha8 0.000 IGL02167 4 136931094 M990K A T missense Het probably damaging 1.000 phenotype 04/16/2015
15 282742 APN Gpr137c 0.087 IGL02167 14 45279955 G383C G T missense Het probably damaging 0.981 04/16/2015
16 282734 APN Hydin 0.741 IGL02167 8 110418423 I802N T A missense Het possibly damaging 0.956 phenotype 04/16/2015
17 282744 APN Ifne 0.000 IGL02167 4 88879828 Y118H A G missense Het possibly damaging 0.577 phenotype 04/16/2015
18 282778 APN Kansl2 0.935 IGL02167 15 98533515 T C splice site Het probably benign 04/16/2015
19 282746 APN Lig4 1.000 IGL02167 8 9971821 N653I T A missense Het probably benign 0.061 phenotype 04/16/2015
20 282772 APN Nagk 0.000 IGL02167 6 83801106 D246G A G missense Het probably damaging 0.979 phenotype 04/16/2015
21 282757 APN Nav1 0.938 IGL02167 1 135470961 S628P A G missense Het probably damaging 1.000 phenotype 04/16/2015
22 282752 APN Ncoa3 0.949 IGL02167 2 166070136 Y1401C A G missense Het probably damaging 0.998 phenotype 04/16/2015
23 282776 APN Ndufa9 1.000 IGL02167 6 126844785 A G splice site Het probably benign phenotype 04/16/2015
24 282758 APN Nynrin 0.000 IGL02167 14 55863335 R194L G T missense Het probably damaging 0.996 04/16/2015
25 282735 APN Olfr1115 0.069 IGL02167 2 87252198 C87Y G A missense Het probably benign 0.177 phenotype 04/16/2015
26 282750 APN Olfr17 0.112 IGL02167 7 107097661 R65S A T missense Het probably benign 0.090 phenotype 04/16/2015
27 282733 APN Olfr45 0.066 IGL02167 7 140691751 V282D T A missense Het probably damaging 0.976 phenotype 04/16/2015
28 282780 APN Orc2 0.964 IGL02167 1 58483639 A T unclassified Het probably benign phenotype 04/16/2015
29 282747 APN Oxgr1 0.000 IGL02167 14 120021930 R288S T A missense Het probably damaging 0.968 phenotype 04/16/2015
30 282775 APN Prkcg 0.000 IGL02167 7 3322581 T C critical splice donor site 2 bp Het probably null phenotype 04/16/2015
31 282738 APN Prox1 1.000 IGL02167 1 190161280 N323D T C missense Het probably benign 0.134 phenotype 04/16/2015
32 282759 APN Prrt1 0.066 IGL02167 17 34631855 E215A A C missense Het possibly damaging 0.675 phenotype 04/16/2015
33 282740 APN Rab2b 0.164 IGL02167 14 52268696 D103G T C missense Het probably damaging 0.994 phenotype 04/16/2015
34 282766 APN Sardh 0.101 IGL02167 2 27191975 N846K G T missense Het probably damaging 0.979 phenotype 04/16/2015
35 282767 APN Slc38a8 0.089 IGL02167 8 119487360 T248S T A missense Het probably benign 0.028 phenotype 04/16/2015
36 282777 APN Slc6a18 0.000 IGL02167 13 73666472 T C critical splice acceptor site Het probably null phenotype 04/16/2015
37 282753 APN Smcp 0.081 IGL02167 3 92584199 T114A T C missense Het unknown phenotype 04/16/2015
38 282755 APN Tmem8 0.085 IGL02167 17 26119071 S450P T C missense Het probably damaging 0.997 04/16/2015
39 282768 APN Trpv1 0.414 IGL02167 11 73254797 N754D A G missense Het probably damaging 0.999 phenotype 04/16/2015
40 282760 APN Txnrd1 1.000 IGL02167 10 82881911 H243L A T missense Het probably benign 0.012 phenotype 04/16/2015
41 282749 APN Wdfy3 0.917 IGL02167 5 101961157 M125V T C missense Het probably damaging 0.976 phenotype 04/16/2015
42 282774 APN Wnk2 0.405 IGL02167 13 49071125 T C critical splice acceptor site Het probably null phenotype 04/16/2015
43 282748 APN Wrn 0.517 IGL02167 8 33317555 M292V T C missense Het probably damaging 0.998 phenotype 04/16/2015
44 282751 APN Zbtb17 1.000 IGL02167 4 141461829 L20P T C missense Het possibly damaging 0.938 phenotype 04/16/2015
45 282763 APN Zfp608 0.819 IGL02167 18 54988224 H97R T C missense Het probably damaging 0.997 04/16/2015
46 282771 APN Zfp68 0.803 IGL02167 5 138606367 M565L T A missense Het probably benign 0.002 04/16/2015
47 282769 APN Zfp687 0.724 IGL02167 3 95010530 T644A T C missense Het probably benign 0.000 phenotype 04/16/2015
48 282770 APN Zfp777 0.294 IGL02167 6 48044526 G54D C T missense Het probably damaging 0.982 04/16/2015
[records 1 to 48 of 48]