Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
3 are Possibly Damaging.
8 are Probably Damaging.
12 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 27 of 27] 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 104110 APN Actl6a 1.000 IGL01691 G1 3 32720200 M282K T A missense Het possibly damaging 0.944 phenotype 01/21/2014
2 104106 APN Adam22 1.000 IGL01691 G1 5 8092742 N831S T C missense Het probably damaging 1.000 phenotype 01/21/2014
3 104115 APN Adamdec1 0.086 IGL01691 G1 14 68573107 R200Q C T missense Het probably damaging 0.998 phenotype 01/21/2014
4 104121 APN Asb15 0.000 IGL01691 G1 6 24567272 I531V A G missense Het probably benign 0.018 phenotype 01/21/2014
5 104114 APN Btrc 0.000 IGL01691 G1 19 45512678 D223E T A missense Het probably benign 0.004 phenotype 01/21/2014
6 104124 APN Ccdc30 0.000 IGL01691 G1 4 119393564 E161V T A missense Het probably damaging 0.959 01/21/2014
7 104127 APN Cd38 0.000 IGL01691 G1 5 43903586 G A splice site Het probably benign phenotype 01/21/2014
8 104108 APN Clec2d 0.000 IGL01691 G1 6 129184222 F94S T C missense Het probably damaging 1.000 phenotype 01/21/2014
9 104125 APN Cwf19l1 0.861 IGL01691 G1 19 44120872 C T critical splice donor site 1 bp Het probably null phenotype 01/21/2014
10 104122 APN Dnah2 0.000 IGL01691 G1 11 69539443 N96K A T missense Het probably benign 0.000 phenotype 01/21/2014
11 104102 APN Ephb6 0.663 IGL01691 G1 6 41614515 R202H G A missense Het probably benign 0.259 phenotype 01/21/2014
12 104112 APN Gm43191 IGL01691 G1 3 116677967 I218L T A missense Het probably benign 0.002 01/21/2014
13 104103 APN Gm7168 0.102 IGL01691 G1 17 13948878 S169N G A missense Het probably damaging 0.965 01/21/2014
14 104111 APN Gm7964 0.919 IGL01691 G1 7 83756136 T C exon Het noncoding transcript 01/21/2014
15 104128 APN Kif20b 0.856 IGL01691 G1 19 34935743 T C splice site Het probably benign phenotype 01/21/2014
16 104105 APN Kmt2e 1.000 IGL01691 G1 5 23497091 T906A A G missense Het probably benign 0.000 phenotype 01/21/2014
17 104113 APN Mboat2 0.000 IGL01691 G1 12 24954222 N341D A G missense Het probably damaging 1.000 01/21/2014
18 104120 APN Msh6 1.000 IGL01691 G1 17 87985479 V554A T C missense Het probably benign 0.000 phenotype 01/21/2014
19 104116 APN Ndc80 0.963 IGL01691 G1 17 71508639 T384A T C missense Het possibly damaging 0.716 phenotype 01/21/2014
20 104104 APN Olfr1537 0.132 IGL01691 G1 9 39238019 T135I G A missense Het probably benign 0.001 phenotype 01/21/2014
21 104107 APN Olfr366 0.096 IGL01691 G1 2 37220026 C179F G T missense Het probably damaging 0.999 phenotype 01/21/2014
22 104119 APN Ptpn5 0.000 IGL01691 G1 7 47083158 H312Q G T missense Het probably benign 0.266 phenotype 01/21/2014
23 104117 APN Rftn2 0.000 IGL01691 G1 1 55214286 V53I C T missense Het probably damaging 0.996 0.100 01/21/2014
24 104109 APN Rgs20 0.000 IGL01691 G1 1 4916922 T124A T C missense Het probably benign 0.003 phenotype 01/21/2014
25 104118 APN Sox18 1.000 IGL01691 G1 2 181671350 S58G T C missense Het possibly damaging 0.845 phenotype 01/21/2014
26 104123 APN Togaram2 0.088 IGL01691 G1 17 71729490 M1012V A G missense Het probably null 0.024 01/21/2014
27 104126 APN Usp48 0.958 IGL01691 G1 4 137623272 A T critical splice acceptor site Het probably null phenotype 01/21/2014
[records 1 to 27 of 27]