Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
8 are Possibly Damaging.
11 are Probably Damaging.
14 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 35 of 35] 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 78732 APN 2010300C02Rik 0.000 IGL01376 G1 1 37628344 L207P A G missense Het probably damaging 0.993 11/05/2013
2 78737 APN 4930568D16Rik 0.107 IGL01376 G1 2 35355628 I61K A T missense Het probably benign 0.363 11/05/2013
3 78714 APN Acot12 0.077 IGL01376 G1 13 91784671 Y521C A G missense Het probably damaging 0.980 11/05/2013
4 78731 APN Anxa7 0.158 IGL01376 G1 14 20460456 N313D T C missense Het probably benign 0.002 phenotype 11/05/2013
5 78715 APN Cdk14 0.000 IGL01376 G1 5 5010839 I327M T C missense Het probably damaging 1.000 phenotype 11/05/2013
6 78727 APN Clca3b 0.062 IGL01376 G1 3 144826051 N664S T C missense Het possibly damaging 0.597 11/05/2013
7 78734 APN Cpb1 0.000 IGL01376 G1 3 20270324 L62R A C missense Het probably benign 0.001 phenotype 11/05/2013
8 78741 APN Eef2 0.967 IGL01376 G1 10 81178049 G A unclassified Het probably benign phenotype 11/05/2013
9 78742 APN Enox1 0.000 IGL01376 G1 14 77251843 T C intron Het probably benign phenotype 11/05/2013
10 78721 APN Esco1 0.371 IGL01376 G1 18 10594892 C131* A T nonsense Het probably null phenotype 11/05/2013
11 78735 APN Etv1 0.427 IGL01376 G1 12 38857040 D347V A T missense Het probably damaging 1.000 phenotype 11/05/2013
12 78740 APN Fat1 1.000 IGL01376 G1 8 45026841 I2975V A G missense Het probably benign 0.004 phenotype 11/05/2013
13 78738 APN Ghsr 0.000 IGL01376 G1 3 27371828 E11G A G missense Het probably benign 0.000 phenotype 11/05/2013
14 78736 APN Gins4 1.000 IGL01376 G1 8 23227327 D166G T C missense Het probably benign 0.384 phenotype 11/05/2013
15 78719 APN Iglv2 IGL01376 G1 16 19260565 H62N G T missense Het possibly damaging 0.605 11/05/2013
16 78722 APN Irf2bp1 0.706 IGL01376 G1 7 19006027 S531P T C missense Het possibly damaging 0.856 11/05/2013
17 78716 APN Lrig3 0.268 IGL01376 G1 10 125994466 F144L T A missense Het probably benign 0.014 phenotype 11/05/2013
18 78739 APN Magi1 0.325 IGL01376 G1 6 94283093 R77Q C T missense Het possibly damaging 0.861 phenotype 11/05/2013
19 78730 APN Mlkl 0.086 IGL01376 G1 8 111319747 L298P A G missense Het probably damaging 0.999 phenotype 11/05/2013
20 78718 APN Ndc1 0.950 IGL01376 G1 4 107375197 L193P T C missense Het probably damaging 1.000 phenotype 11/05/2013
21 78733 APN Npas3 0.909 IGL01376 G1 12 54044586 T308S A T missense Het probably benign 0.014 phenotype 11/05/2013
22 78717 APN Nt5dc3 0.000 IGL01376 G1 10 86834164 Q541L A T missense Het probably benign 0.048 11/05/2013
23 78712 APN Olfr1084 0.472 IGL01376 G1 2 86639609 V33G A C missense Het probably benign 0.004 phenotype 11/05/2013
24 78711 APN Olfr1115 0.068 IGL01376 G1 2 87252873 V312A T C missense Het possibly damaging 0.579 0.179 phenotype 11/05/2013
25 78720 APN Parp10 0.123 IGL01376 G1 15 76241677 T437K G T missense Het probably benign 0.093 phenotype 11/05/2013
26 78713 APN Phf3 0.000 IGL01376 G1 1 30830485 V494A A G missense Het possibly damaging 0.615 phenotype 11/05/2013
27 278320 APN Prpf8 0.958 IGL01376 G1 11 75494295 A794D C A missense Het possibly damaging 0.940 phenotype 04/16/2015
28 78710 APN Sars2 0.878 IGL01376 G1 7 28749883 Y307N T A missense Het probably damaging 1.000 phenotype 11/05/2013
29 78725 APN Serping1 0.101 IGL01376 G1 2 84770185 V271E A T missense Het probably damaging 1.000 phenotype 11/05/2013
30 78723 APN Sgpl1 1.000 IGL01376 G1 10 61114070 P117S G A missense Het probably damaging 1.000 phenotype 11/05/2013
31 78726 APN Slc38a1 0.133 IGL01376 G1 15 96585556 L297R A C missense Het probably damaging 1.000 phenotype 11/05/2013
32 78729 APN Strbp 0.465 IGL01376 G1 2 37645651 M15T A G missense Het probably damaging 1.000 phenotype 11/05/2013
33 78743 APN Tdp2 0.673 IGL01376 G1 13 24836949 A G splice site 3 bp Het probably null phenotype 11/05/2013
34 78724 APN Tex10 0.954 IGL01376 G1 4 48456740 Y657C T C missense Het possibly damaging 0.901 phenotype 11/05/2013
35 78728 APN Xrcc4 0.359 IGL01376 G1 13 90062050 S92T A T missense Het probably benign 0.003 phenotype 11/05/2013
[records 1 to 35 of 35]