Incidental Mutations

36 incidental mutations are currently displayed, and affect 36 genes.
7 are Possibly Damaging.
17 are Probably Damaging.
10 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 36 of 36] 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 411283 APN 1700017D01Rik 0.063 IGL03156 19 11105750 I102K A T missense Het possibly damaging 0.801 08/02/2016
2 411275 APN 4930430A15Rik 0.059 IGL03156 2 111200412 D12G T C missense Het possibly damaging 0.904 08/02/2016
3 411267 APN Abca16 0.000 IGL03156 7 120423851 I70T T C missense Het possibly damaging 0.690 08/02/2016
4 411286 APN Acot11 0.136 IGL03156 4 106754136 Y365H A G missense Het probably damaging 0.999 phenotype 08/02/2016
5 411263 APN Bdp1 1.000 IGL03156 13 100061036 V947A A G missense Het probably benign 0.438 phenotype 08/02/2016
6 411278 APN Ccdc159 0.000 IGL03156 9 21929475 V113L G T missense Het probably benign 0.000 08/02/2016
7 411269 APN Cep350 0.962 IGL03156 1 155858042 D3035G T C missense Het probably damaging 1.000 phenotype 08/02/2016
8 411287 APN Clca1 0.078 IGL03156 3 145013911 I433F T A missense Het probably damaging 0.999 phenotype 08/02/2016
9 411261 APN Cntn5 0.000 IGL03156 9 9673877 Y740C T C missense Het probably damaging 1.000 phenotype 08/02/2016
10 411292 APN Dennd5a 0.241 IGL03156 7 109919255 C A splice site Het probably benign phenotype 08/02/2016
11 411258 APN Des 0.565 IGL03156 1 75362996 E333K G A missense Het probably damaging 0.997 phenotype 08/02/2016
12 411260 APN Dnah7a 0.152 IGL03156 1 53605824 R1018G T C missense Het probably damaging 0.968 08/02/2016
13 411259 APN Eif2b2 1.000 IGL03156 12 85219721 A54S G T missense Het probably damaging 0.999 phenotype 08/02/2016
14 411266 APN Gm7276 0.094 IGL03156 18 77185603 C T unclassified Het probably benign 08/02/2016
15 411290 APN Hsbp1l1 IGL03156 18 80235519 A G splice site Het probably benign 08/02/2016
16 411280 APN Iars 1.000 IGL03156 13 49703179 G303S G A missense Het possibly damaging 0.870 phenotype 08/02/2016
17 411284 APN Il18r1 0.000 IGL03156 1 40498368 E431G A G missense Het possibly damaging 0.916 phenotype 08/02/2016
18 411271 APN Lrrc14b 0.068 IGL03156 13 74363904 V19A A G missense Het probably benign 0.000 08/02/2016
19 411281 APN Map1lc3a 0.268 IGL03156 2 155277009 I31N T A missense Het probably damaging 0.999 phenotype 08/02/2016
20 411257 APN Obscn 0.741 IGL03156 11 59054896 Y4163C T C missense Het probably damaging 1.000 phenotype 08/02/2016
21 411288 APN Olfr478 0.136 IGL03156 7 108032351 T A utr 5 prime Het probably benign phenotype 08/02/2016
22 411285 APN Pcsk1 1.000 IGL03156 13 75131951 T632A A G missense Het probably benign 0.000 phenotype 08/02/2016
23 411273 APN Ppp1r15a 0.183 IGL03156 7 45525171 L71P A G missense Het possibly damaging 0.820 phenotype 08/02/2016
24 411276 APN Ptgs2 0.751 IGL03156 1 150105477 F504V T G missense Het probably damaging 0.999 0.531 phenotype 08/02/2016
25 411272 APN Rimbp2 0.000 IGL03156 5 128771757 R908S T G missense Het probably damaging 0.998 phenotype 08/02/2016
26 411274 APN Rnh1 0.111 IGL03156 7 141163183 N268S T C missense Het probably damaging 0.997 phenotype 08/02/2016
27 411291 APN Sap30l 0.338 IGL03156 11 57806168 T C critical splice donor site 2 bp Het probably null 08/02/2016
28 411277 APN Scara3 0.151 IGL03156 14 65931154 R338H C T missense Het probably damaging 0.999 phenotype 08/02/2016
29 411279 APN Serpina12 0.000 IGL03156 12 104037899 Y158C T C missense Het probably damaging 1.000 phenotype 08/02/2016
30 411282 APN Tmem237 0.102 IGL03156 1 59109127 D148E A T missense Het probably damaging 1.000 phenotype 08/02/2016
31 411262 APN Trmt13 0.143 IGL03156 3 116585802 D232G T C missense Het probably benign 0.002 08/02/2016
32 411264 APN Zan 0.070 IGL03156 5 137463939 T993S T A missense Het unknown phenotype 08/02/2016
33 411268 APN Zfp236 1.000 IGL03156 18 82680702 L85F G A missense Het probably damaging 1.000 08/02/2016
34 411270 APN Zfp352 0.000 IGL03156 4 90224087 D155N G A missense Het possibly damaging 0.574 08/02/2016
35 411289 APN Zfp867 0.102 IGL03156 11 59465008 T C splice site Het probably benign 08/02/2016
36 411265 APN Zmiz2 1.000 IGL03156 11 6399536 F399L T C missense Het probably damaging 0.999 phenotype 08/02/2016
[records 1 to 36 of 36]