Incidental Mutations

46 incidental mutations are currently displayed, and affect 46 genes.
9 are Possibly Damaging.
14 are Probably Damaging.
14 are Probably Benign.
8 are Probably Null.
2 create premature stop codons.
5 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 278144 APN 1110038F14Rik IGL01069 G1 15 76950275 V124I G A missense Het probably damaging 0.999 04/16/2015
2 51041 APN 1700123K08Rik 0.021 IGL01069 G1 5 138562489 A215T C T missense Het probably benign 0.011 06/21/2013
3 278145 APN Aen 0.200 IGL01069 G1 7 78907302 M299I G A missense Het probably damaging 0.960 04/16/2015
4 52048 APN Apc2 0.470 IGL01069 G1 10 80311986 C929Y G A missense Het probably damaging 1.000 phenotype 06/21/2013
5 51042 APN Arap2 0.180 IGL01069 G1 5 62649856 H1156R T C missense Het probably benign 0.000 phenotype 06/21/2013
6 52046 APN Arhgap9 0.248 IGL01069 G1 10 127328952 T582A A G missense Het probably damaging 1.000 phenotype 06/21/2013
7 52218 APN Ccdc57 0.071 IGL01069 G1 11 120861259 H832L T A missense Het probably benign 0.057 06/21/2013
8 51719 APN Ces3b 0.013 IGL01069 G1 8 105091574 S92P T C missense Het probably benign 0.002 06/21/2013
9 51720 APN Ces5a 0.104 IGL01069 G1 8 93525544 A G critical splice donor site 2 bp Het probably null phenotype 06/21/2013
10 278146 APN Cfap206 0.257 IGL01069 G1 4 34721562 S162N C T missense Het probably damaging 1.000 04/16/2015
11 52651 APN Cpb2 0.198 IGL01069 G1 14 75270775 D225E T A missense Het probably damaging 0.999 phenotype 06/21/2013
12 52766 APN Cpne8 0.128 IGL01069 G1 15 90615110 C T critical splice donor site 1 bp Het probably null phenotype 06/21/2013
13 51040 APN Cux2 0.483 IGL01069 G1 5 121867351 T924M G A missense Het possibly damaging 0.843 phenotype 06/21/2013
14 50193 APN Dtl 1.000 IGL01069 G1 1 191561539 T A critical splice acceptor site Het probably null phenotype 06/21/2013
15 51252 APN Dysf 0.000 IGL01069 G1 6 84199785 I1912N T A missense Het possibly damaging 0.935 phenotype 06/21/2013
16 51721 APN Edc4 0.913 IGL01069 G1 8 105887134 F369I T A missense Het probably benign 0.346 phenotype 06/21/2013
17 50413 APN Fibcd1 0.124 IGL01069 G1 2 31821519 E298G T C missense Het probably benign 0.367 phenotype 06/21/2013
18 50849 APN Focad 0.385 IGL01069 G1 4 88326146 H788N C A missense Het unknown 06/21/2013
19 50850 APN Frem1 0.672 IGL01069 G1 4 83013867 R199H C T missense Het probably benign 0.004 phenotype 06/21/2013
20 51867 APN Gadl1 0.147 IGL01069 G1 9 115954839 T C critical splice donor site 2 bp Het probably null 06/21/2013
21 50702 APN Hipk1 0.000 IGL01069 G1 3 103777699 T200I G A missense Het possibly damaging 0.955 phenotype 06/21/2013
22 52423 APN Ighv14-2 0.149 IGL01069 G1 12 113994759 V21I C T missense Het possibly damaging 0.473 06/21/2013
23 50851 APN Kank4 0.099 IGL01069 G1 4 98778395 I605N A T missense Het probably damaging 0.988 06/21/2013
24 52765 APN Krt88 0.145 IGL01069 G1 15 101453627 *172G T G makesense Het probably null 06/21/2013
25 52764 APN Lmf2 0.270 IGL01069 G1 15 89352888 A408S C A missense Het probably benign 0.350 06/21/2013
26 52217 APN Lsm12 0.930 IGL01069 G1 11 102164070 T C utr 3 prime Het probably benign 06/21/2013
27 50412 APN Myo3b 0.751 IGL01069 G1 2 70245391 I580V A G missense Het probably benign 0.215 phenotype 06/21/2013
28 50411 APN Myt1 1.000 IGL01069 G1 2 181825956 M1061T T C missense Het probably damaging 0.996 phenotype 06/21/2013
29 51722 APN Nup133 1.000 IGL01069 G1 8 123930982 R405* G A nonsense Het probably null phenotype 06/21/2013
30 50410 APN Olfr1032 0.093 IGL01069 G1 2 86008547 Y257C A G missense Het probably damaging 1.000 phenotype 06/21/2013
31 52215 APN Olfr1377 0.079 IGL01069 G1 11 50985003 I101F A T missense Het possibly damaging 0.940 phenotype 06/21/2013
32 51865 APN Olfr229 0.095 IGL01069 G1 9 39910606 M268L A T missense Het possibly damaging 0.935 phenotype 06/21/2013
33 52424 APN Pcnx 0.000 IGL01069 G1 12 81918144 R362G A G missense Het probably benign 0.270 phenotype 06/21/2013
34 52425 APN Pomt2 1.000 IGL01069 G1 12 87110304 T747K G T missense Het probably damaging 0.997 phenotype 06/21/2013
35 51446 APN Rgma 0.308 IGL01069 G1 7 73417491 A165T G A missense Het probably damaging 1.000 phenotype 06/21/2013
36 52219 APN Rhbdf2 0.000 IGL01069 G1 11 116601751 D437G T C missense Het possibly damaging 0.801 phenotype 06/21/2013
37 51039 APN Rpl5 0.878 IGL01069 G1 5 107907279 T C critical splice donor site 2 bp Het probably null phenotype 06/21/2013
38 52047 APN Rtkn2 0.227 IGL01069 G1 10 68041664 D518G A G missense Het probably benign 0.005 06/21/2013
39 50701 APN Sclt1 0.347 IGL01069 G1 3 41741991 T C unclassified Het probably benign phenotype 06/21/2013
40 51866 APN Sidt2 0.301 IGL01069 G1 9 45943077 V616I C T missense Het possibly damaging 0.734 phenotype 06/21/2013
41 52216 APN Ska2 1.000 IGL01069 G1 11 87109265 A G unclassified Het probably benign phenotype 06/21/2013
42 51251 APN Slc13a4 0.701 IGL01069 G1 6 35268882 L609F C A missense Het probably damaging 1.000 phenotype 06/21/2013
43 52649 APN Sorbs3 0.000 IGL01069 G1 14 70191155 E390G T C missense Het probably damaging 1.000 phenotype 06/21/2013
44 52650 APN Syt15 0.074 IGL01069 G1 14 34224924 V220A T C missense Het possibly damaging 0.907 phenotype 06/21/2013
45 52220 APN Tob1 0.000 IGL01069 G1 11 94214055 F139S T C missense Het probably damaging 1.000 phenotype 06/21/2013
46 278143 APN Yars2 0.958 IGL01069 G1 16 16306542 R338* C T nonsense Het probably null phenotype 04/16/2015
[records 1 to 46 of 46]