Incidental Mutations

39 incidental mutations are currently displayed, and affect 39 genes.
6 are Possibly Damaging.
18 are Probably Damaging.
11 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 39 of 39] 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 103134 APN 9130011E15Rik 1.000 IGL01660 G1 19 45940476 L393H A T missense Het probably damaging 1.000 01/21/2014
2 103130 APN Acta2 0.150 IGL01660 G1 19 34251791 I66T A G missense Het probably damaging 0.977 phenotype 01/21/2014
3 103151 APN Actl11 0.062 IGL01660 G1 9 107929048 V190A T C missense Het probably benign 0.000 01/21/2014
4 103137 APN Ankub1 0.000 IGL01660 G1 3 57690396 Y51F T A missense Het possibly damaging 0.928 01/21/2014
5 103143 APN Ccdc63 0.135 IGL01660 G1 5 122110964 S434L G A missense Het possibly damaging 0.810 01/21/2014
6 103146 APN Cdan1 1.000 IGL01660 G1 2 120725653 I711F T A missense Het possibly damaging 0.633 phenotype 01/21/2014
7 103145 APN Cep170b 0.443 IGL01660 G1 12 112744160 N1474K C A missense Het probably damaging 1.000 01/21/2014
8 103140 APN Cyp2c40 0.119 IGL01660 G1 19 39786810 S333P A G missense Het probably damaging 0.987 01/21/2014
9 103153 APN Dars 0.939 IGL01660 G1 1 128415344 A G splice site Het probably benign phenotype 01/21/2014
10 103156 APN Dock3 0.724 IGL01660 G1 9 107032364 T A splice site Het probably benign phenotype 01/21/2014
11 103141 APN Dsp 1.000 IGL01660 G1 13 38176495 I359V A G missense Het possibly damaging 0.904 phenotype 01/21/2014
12 103144 APN Fut8 0.000 IGL01660 G1 12 77450258 L414* T G nonsense Het probably null phenotype 01/21/2014
13 103126 APN Gja1 1.000 IGL01660 G1 10 56388448 Y301C A G missense Het probably damaging 1.000 phenotype 01/21/2014
14 103120 APN Glipr1l1 0.048 IGL01660 G1 10 112072279 S161P T C missense Het probably damaging 0.974 01/21/2014
15 103155 APN Gpat4 0.330 IGL01660 G1 8 23175338 A T critical splice donor site 2 bp Het probably null phenotype 01/21/2014
16 103154 APN Grhl1 0.000 IGL01660 G1 12 24608578 T A splice site 6 bp Het probably null phenotype 01/21/2014
17 103124 APN Hectd3 0.000 IGL01660 G1 4 116996372 V181A T C missense Het possibly damaging 0.910 phenotype 01/21/2014
18 103136 APN Htr2a 0.067 IGL01660 G1 14 74705754 I258N T A missense Het probably damaging 1.000 phenotype 01/21/2014
19 103148 APN Hyou1 1.000 IGL01660 G1 9 44381117 D83E T A missense Het possibly damaging 0.748 phenotype 01/21/2014
20 103129 APN Myh10 1.000 IGL01660 G1 11 68785889 L862Q T A missense Het probably benign 0.001 phenotype 01/21/2014
21 103149 APN Nkx2-2 1.000 IGL01660 G1 2 147185913 S36G T C missense Het probably benign 0.026 phenotype 01/21/2014
22 103139 APN Nsun2 0.895 IGL01660 G1 13 69623249 V326E T A missense Het probably benign 0.007 phenotype 01/21/2014
23 103147 APN Nuak2 0.089 IGL01660 G1 1 132331570 V362A T C missense Het probably benign 0.120 phenotype 01/21/2014
24 103128 APN Nyap2 0.000 IGL01660 G1 1 81191927 C133Y G A missense Het probably damaging 0.993 phenotype 01/21/2014
25 103135 APN Oas2 0.083 IGL01660 G1 5 120741223 T351A T C missense Het probably benign 0.001 phenotype 01/21/2014
26 103119 APN Olfr1025-ps1 0.068 IGL01660 G1 2 85918564 I213T T C missense Het probably benign 0.250 01/21/2014
27 103133 APN Olfr279 0.074 IGL01660 G1 15 98498195 T241I C T missense Het probably damaging 0.998 phenotype 01/21/2014
28 103123 APN Pde4d 0.000 IGL01660 G1 13 109938072 I404F A T missense Het probably damaging 0.998 phenotype 01/21/2014
29 103127 APN Pga5 0.069 IGL01660 G1 19 10675092 S95P A G missense Het probably damaging 1.000 01/21/2014
30 103150 APN Pitpnm2 0.000 IGL01660 G1 5 124123194 D947E A T missense Het probably damaging 0.999 phenotype 01/21/2014
31 103142 APN Pla2g10 IGL01660 G1 16 13728086 R28H C T missense Het probably damaging 1.000 phenotype 01/21/2014
32 103138 APN Prlr 0.468 IGL01660 G1 15 10317590 D84G A G missense Het probably damaging 1.000 phenotype 01/21/2014
33 103125 APN Rbm15b 0.532 IGL01660 G1 9 106885709 G420D C T missense Het probably damaging 1.000 phenotype 01/21/2014
34 103132 APN Tbcd 0.955 IGL01660 G1 11 121605327 T1063A A G missense Het probably benign 0.008 phenotype 01/21/2014
35 103131 APN Tmc2 0.266 IGL01660 G1 2 130260224 Q770* C T nonsense Het probably null phenotype 01/21/2014
36 103157 APN Tpo 0.393 IGL01660 G1 12 30119400 T C splice site Het probably benign phenotype 01/21/2014
37 103152 APN Vim 0.664 IGL01660 G1 2 13574813 N128D A G missense Het probably damaging 1.000 phenotype 01/21/2014
38 103121 APN Vmn1r21 0.192 IGL01660 G1 6 57844237 I74N A T missense Het probably damaging 0.990 01/21/2014
39 103122 APN Vmn2r52 0.108 IGL01660 G1 7 10159180 I677M A C missense Het probably damaging 0.968 01/21/2014
[records 1 to 39 of 39]