Incidental Mutations

52 incidental mutations are currently displayed, and affect 51 genes.
5 are Possibly Damaging.
23 are Probably Damaging.
20 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 52 of 52] 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 291762 APN Adgre1 0.182 IGL02398 17 57402824 C160* T A nonsense Het probably null phenotype 04/16/2015
2 291773 APN Alkbh8 0.000 IGL02398 9 3345870 P197S C T missense Het possibly damaging 0.773 phenotype 04/16/2015
3 291778 APN Ankef1 0.068 IGL02398 2 136555782 N761T A C missense Het probably damaging 0.983 04/16/2015
4 291780 APN Ankrd7 0.000 IGL02398 6 18866697 Y72C A G missense Het probably damaging 0.987 04/16/2015
5 291768 APN Cfap36 0.000 IGL02398 11 29222833 M231L T G missense Het probably benign 0.000 04/16/2015
6 291772 APN Cog7 1.000 IGL02398 7 121964209 C227R A G missense Het probably damaging 0.999 phenotype 04/16/2015
7 291784 APN Csgalnact1 0.072 IGL02398 8 68401492 G219V C A missense Het probably damaging 1.000 phenotype 04/16/2015
8 291743 APN Cspg4 0.000 IGL02398 9 56886686 E568D A T missense Het probably benign 0.433 phenotype 04/16/2015
9 291745 APN Cwc27 0.000 IGL02398 13 104804254 T199I G A missense Het possibly damaging 0.825 phenotype 04/16/2015
10 291769 APN Cyp26a1 1.000 IGL02398 19 37700019 I330V A G missense Het probably benign 0.000 phenotype 04/16/2015
11 291782 APN Dcaf7 1.000 IGL02398 11 106053753 V254A T C missense Het probably benign 0.028 phenotype 04/16/2015
12 291775 APN Dhrs7 0.080 IGL02398 12 72664692 R24C G A missense Het probably damaging 0.999 phenotype 04/16/2015
13 291771 APN Ehmt2 1.000 IGL02398 17 34908479 C838S T A missense Het probably damaging 0.997 phenotype 04/16/2015
14 291785 APN Fn1 1.000 IGL02398 1 71618670 A T splice site Het probably null phenotype 04/16/2015
15 291761 APN Gjb3 1.000 IGL02398 4 127326062 S226C T A missense Het probably benign 0.001 phenotype 04/16/2015
16 291742 APN Gm14496 0.000 IGL02398 2 181996170 I346V A G missense Het probably benign 0.092 04/16/2015
17 291754 APN Gm5926 IGL02398 X 32651386 D224G A G missense Het probably damaging 0.995 04/16/2015
18 291739 APN Gm8050 IGL02398 14 6717330 E172G T C missense Het probably damaging 0.999 04/16/2015
19 291752 APN Higd1a IGL02398 9 121852524 R22W G A missense Het probably damaging 0.999 04/16/2015
20 291777 APN Hmcn1 0.000 IGL02398 1 150802897 L491S A G missense Het possibly damaging 0.781 phenotype 04/16/2015
21 291774 APN Igsf9b 0.869 IGL02398 9 27333130 S794P T C missense Het possibly damaging 0.543 04/16/2015
22 291744 APN Irgm2 0.000 IGL02398 11 58219929 I161F A T missense Het probably damaging 0.999 phenotype 04/16/2015
23 291749 APN Lrp8 0.658 IGL02398 4 107847494 V304F G T missense Het probably damaging 0.967 phenotype 04/16/2015
24 291779 APN Lrp8 0.658 IGL02398 4 107869048 S850R C A missense Het probably damaging 0.999 phenotype 04/16/2015
25 291770 APN Lrrc9 0.212 IGL02398 12 72466903 M513L A T missense Het probably benign 0.000 04/16/2015
26 291783 APN Myo18b 1.000 IGL02398 5 112830312 V1248E A T missense Het possibly damaging 0.922 phenotype 04/16/2015
27 291741 APN Myo1b 0.195 IGL02398 1 51757891 N945K A T missense Het probably damaging 0.995 04/16/2015
28 291748 APN Nipbl 0.964 IGL02398 15 8327090 L1604P A G missense Het probably damaging 1.000 phenotype 04/16/2015
29 291764 APN Oas1f 0.056 IGL02398 5 120851505 Y169F A T missense Het probably benign 0.000 04/16/2015
30 291766 APN Ogfod3 0.098 IGL02398 11 121203025 T53I G A missense Het probably benign 0.059 04/16/2015
31 291760 APN Olfr1054 0.084 IGL02398 2 86332524 Y277* A T nonsense Het probably null phenotype 04/16/2015
32 291740 APN Olfr444 0.061 IGL02398 6 42956112 I205F A T missense Het probably benign 0.017 phenotype 04/16/2015
33 291753 APN Olfr584 0.094 IGL02398 7 103086106 C191Y G A missense Het probably damaging 1.000 phenotype 04/16/2015
34 291786 APN Parp8 0.000 IGL02398 13 116910863 A G critical splice donor site 2 bp Het probably null 04/16/2015
35 291763 APN Pde4dip 1.000 IGL02398 3 97766781 Y273C T C missense Het probably benign 0.000 phenotype 04/16/2015
36 291759 APN Pgbd5 0.000 IGL02398 8 124384518 A54T C T missense Het probably damaging 1.000 phenotype 04/16/2015
37 291790 APN Pglyrp4 0.000 IGL02398 3 90739117 G A splice site Het probably benign phenotype 04/16/2015
38 291781 APN Piezo1 1.000 IGL02398 8 122486563 S1819R A T missense Het probably benign 0.214 phenotype 04/16/2015
39 291787 APN Polr1a 1.000 IGL02398 6 71936556 T C splice site Het probably benign phenotype 04/16/2015
40 291756 APN Polr1b 1.000 IGL02398 2 129102966 I61V A G missense Het probably benign 0.028 phenotype 04/16/2015
41 291758 APN Prlhr 0.078 IGL02398 19 60467315 A271E G T missense Het probably damaging 0.995 phenotype 04/16/2015
42 291788 APN Rad23b 1.000 IGL02398 4 55350360 C T utr 5 prime Het probably benign phenotype 04/16/2015
43 291746 APN Rad51ap1 0.000 IGL02398 6 126928151 S132R A T missense Het probably damaging 0.999 04/16/2015
44 291789 APN Ros1 0.167 IGL02398 10 52144884 T A splice site Het probably benign phenotype 04/16/2015
45 291757 APN Ryr3 0.507 IGL02398 2 112847422 D1327G T C missense Het probably benign 0.051 phenotype 04/16/2015
46 291755 APN Slit1 0.000 IGL02398 19 41602237 V1332G A C missense Het probably damaging 1.000 phenotype 04/16/2015
47 291767 APN Tmem178b 0.230 IGL02398 6 40207527 M120V A G missense Het probably damaging 0.997 04/16/2015
48 291776 APN Trim25 0.000 IGL02398 11 88999804 C106R T C missense Het probably damaging 1.000 phenotype 04/16/2015
49 291751 APN Trim35 0.078 IGL02398 14 66309248 Y488C A G missense Het probably damaging 1.000 phenotype 04/16/2015
50 291750 APN Tsc2 1.000 IGL02398 17 24621729 H326Q A T missense Het probably damaging 0.999 phenotype 04/16/2015
51 291765 APN Yap1 1.000 IGL02398 9 7950535 I315K A T missense Het probably benign 0.059 phenotype 04/16/2015
52 291747 APN Zfp654 0.737 IGL02398 16 64786018 V607A A G missense Het probably benign 0.001 04/16/2015
[records 1 to 52 of 52]