Incidental Mutations

48 incidental mutations are currently displayed, and affect 46 genes.
11 are Possibly Damaging.
19 are Probably Damaging.
12 are Probably Benign.
4 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 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 298842 APN Aff4 1.000 IGL02567 11 53372751 S199R C A missense Het possibly damaging 0.637 phenotype 04/16/2015
2 298870 APN Ano1 1.000 IGL02567 7 144611625 L621P A G missense Het probably damaging 1.000 phenotype 04/16/2015
3 298883 APN Calcr 0.000 IGL02567 6 3691564 V404M C T missense Het probably damaging 1.000 phenotype 04/16/2015
4 298845 APN Carmil3 0.663 IGL02567 14 55498882 S635G A G missense Het possibly damaging 0.934 04/16/2015
5 298885 APN Ccl12 0.000 IGL02567 11 82102621 S28R C A missense Het possibly damaging 0.894 phenotype 04/16/2015
6 298857 APN Cdc45 1.000 IGL02567 16 18798729 M200I C T missense Het probably benign 0.059 0.196 phenotype 04/16/2015
7 298866 APN Cdhr3 0.064 IGL02567 12 33038901 N761D T C missense Het probably benign 0.021 04/16/2015
8 298888 APN Col14a1 0.000 IGL02567 15 55344961 T C critical splice donor site 2 bp Het probably null phenotype 04/16/2015
9 298862 APN Col28a1 0.083 IGL02567 6 8014819 K862R T C missense Het possibly damaging 0.912 phenotype 04/16/2015
10 298886 APN Cyp2c66 0.150 IGL02567 19 39186640 C T utr 3 prime Het probably benign 04/16/2015
11 298876 APN D5Ertd615e 0.156 IGL02567 5 45163416 T C exon Het noncoding transcript 04/16/2015
12 298868 APN Deup1 0.000 IGL02567 9 15575283 E367G T C missense Het probably damaging 1.000 04/16/2015
13 298869 APN Dpp8 0.293 IGL02567 9 65078776 Y849* T G nonsense Het probably null phenotype 04/16/2015
14 298874 APN Efhc1 0.106 IGL02567 1 20972964 V369E T A missense Het probably damaging 0.983 phenotype 04/16/2015
15 298860 APN Epg5 0.946 IGL02567 18 78033073 Y2562C A G missense Het probably damaging 1.000 phenotype 04/16/2015
16 298872 APN Fam189a1 0.061 IGL02567 7 64786731 M101L T A missense Het possibly damaging 0.955 04/16/2015
17 298887 APN Fbln5 0.162 IGL02567 12 101761800 A G critical splice donor site 2 bp Het probably null phenotype 04/16/2015
18 298878 APN Frem1 0.761 IGL02567 4 83000055 M551K A T missense Het probably damaging 0.999 phenotype 04/16/2015
19 298861 APN Gba2 0.000 IGL02567 4 43567281 S889G T C missense Het probably benign 0.000 phenotype 04/16/2015
20 298873 APN Golph3 0.000 IGL02567 15 12349421 R176* C T nonsense Het probably null phenotype 04/16/2015
21 298871 APN Got2 0.642 IGL02567 8 95872201 F191Y A T missense Het probably benign 0.056 phenotype 04/16/2015
22 298889 APN Gtf2ird2 0.094 IGL02567 5 134213048 G T unclassified Het probably benign 04/16/2015
23 298879 APN Hist4h4 0.929 IGL02567 6 136804274 R36W G A missense Het probably damaging 0.971 phenotype 04/16/2015
24 298875 APN Hivep3 0.000 IGL02567 4 120133956 T2218A A G missense Het probably damaging 0.987 phenotype 04/16/2015
25 298865 APN Htr1f 0.000 IGL02567 16 64926248 G227D C T missense Het probably benign 0.446 phenotype 04/16/2015
26 298856 APN Ifi202b 0.062 IGL02567 1 173963804 S436N C T missense Het possibly damaging 0.838 04/16/2015
27 298864 APN Nf1 1.000 IGL02567 11 79547143 V2109D T A missense Het probably damaging 0.999 phenotype 04/16/2015
28 298859 APN Opa1 1.000 IGL02567 16 29588286 D29E C A missense Het probably benign 0.014 phenotype 04/16/2015
29 298880 APN Papln 0.000 IGL02567 12 83778837 P631S C T missense Het probably benign 0.003 04/16/2015
30 298882 APN Pde4c 0.000 IGL02567 8 70747921 M352K T A missense Het probably benign 0.110 phenotype 04/16/2015
31 298867 APN Pigu 1.000 IGL02567 2 155331192 T129A T C missense Het possibly damaging 0.702 phenotype 04/16/2015
32 298855 APN Pla2g4c 0.093 IGL02567 7 13346040 H424Q T A missense Het probably damaging 0.998 phenotype 04/16/2015
33 298858 APN Ptpn13 0.213 IGL02567 5 103562291 L1564R T G missense Het probably damaging 1.000 phenotype 04/16/2015
34 298851 APN Rbm5 0.916 IGL02567 9 107744274 D642G T C missense Het probably damaging 0.997 phenotype 04/16/2015
35 298848 APN Rnf111 1.000 IGL02567 9 70459005 T384A T C missense Het probably damaging 0.997 phenotype 04/16/2015
36 298854 APN Scn11a 0.150 IGL02567 9 119804489 T393A T C missense Het probably damaging 0.992 phenotype 04/16/2015
37 298877 APN Sned1 0.080 IGL02567 1 93274347 K619M A T missense Het probably damaging 0.964 04/16/2015
38 298852 APN Srrm1 1.000 IGL02567 4 135325104 P658L G A missense Het unknown 04/16/2015
39 298863 APN Syt9 0.000 IGL02567 7 107436661 Y295C A G missense Het probably damaging 1.000 phenotype 04/16/2015
40 298843 APN Taar7f 0.106 IGL02567 10 24050425 Y306N T A missense Het probably damaging 0.974 04/16/2015
41 298844 APN Tmem107 1.000 IGL02567 11 69071019 L25V T G missense Het possibly damaging 0.786 phenotype 04/16/2015
42 298881 APN Wdr24 1.000 IGL02567 17 25824348 I48S T G missense Het probably damaging 0.990 04/16/2015
43 298884 APN Zc3hc1 0.627 IGL02567 6 30374849 D231G T C missense Het probably benign 0.000 phenotype 04/16/2015
44 298846 APN Zfp142 0.000 IGL02567 1 74578147 S342C T A missense Het possibly damaging 0.843 phenotype 04/16/2015
45 298849 APN Zfp142 0.000 IGL02567 1 74578149 K341T T G missense Het possibly damaging 0.923 phenotype 04/16/2015
46 298850 APN Zfp142 0.000 IGL02567 1 74578150 K341E T C missense Het possibly damaging 0.923 phenotype 04/16/2015
47 298853 APN Zfp804b 0.173 IGL02567 5 6769989 I989L T A missense Het probably benign 0.016 04/16/2015
48 298847 APN Zfyve9 0.816 IGL02567 4 108674523 V1095G A C missense Het probably damaging 1.000 phenotype 04/16/2015
[records 1 to 48 of 48]