Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
16 are Probably Benign.
1 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 304177 APN Abtb1 0.293 IGL02702 6 88838138 V337I C T missense Het probably benign 0.000 phenotype 04/16/2015
2 304156 APN Adam11 0.000 IGL02702 11 102777038 V750I G A missense Het probably benign 0.264 phenotype 04/16/2015
3 304184 APN Alms1 0.000 IGL02702 6 85599849 V129A T C missense Het probably benign 0.119 phenotype 04/16/2015
4 304176 APN Cacna1d 0.805 IGL02702 14 30123533 K560* T A nonsense Het probably null phenotype 04/16/2015
5 304188 APN Cntn1 1.000 IGL02702 15 92291601 A G splice site Het probably benign phenotype 04/16/2015
6 304183 APN Cpne2 0.147 IGL02702 8 94570023 V530A T C missense Het probably benign 0.031 phenotype 04/16/2015
7 304181 APN Fbxo21 0.199 IGL02702 5 118000510 L507P T C missense Het probably damaging 0.999 phenotype 04/16/2015
8 304154 APN Fndc4 0.000 IGL02702 5 31293735 K204R T C missense Het probably damaging 0.998 phenotype 04/16/2015
9 304170 APN Gnrhr 0.150 IGL02702 5 86182269 N297K G T missense Het possibly damaging 0.687 phenotype 04/16/2015
10 304164 APN Grin2b 1.000 IGL02702 6 135739132 F729S A G missense Het probably damaging 0.992 phenotype 04/16/2015
11 304163 APN Hdac3 1.000 IGL02702 18 37941094 R359L C A missense Het probably benign 0.001 phenotype 04/16/2015
12 304157 APN Met 1.000 IGL02702 6 17534143 S662P T C missense Het possibly damaging 0.921 phenotype 04/16/2015
13 304182 APN Mphosph9 0.000 IGL02702 5 124259989 E1081D T A missense Het probably damaging 1.000 04/16/2015
14 304180 APN Mycbp2 1.000 IGL02702 14 103220124 T1546P T G missense Het probably benign 0.007 phenotype 04/16/2015
15 304158 APN Nlrp9a 0.079 IGL02702 7 26564956 M767K T A missense Het possibly damaging 0.673 04/16/2015
16 304178 APN Olfm5 0.086 IGL02702 7 104154357 Y300H A G missense Het probably damaging 1.000 04/16/2015
17 304162 APN Olfr911-ps1 0.058 IGL02702 9 38524560 V276D T A missense Het probably damaging 0.996 phenotype 04/16/2015
18 304155 APN Pcf11 0.957 IGL02702 7 92661618 N178K A T missense Het possibly damaging 0.762 phenotype 04/16/2015
19 304179 APN Polr3a 1.000 IGL02702 14 24470877 I571M T C missense Het probably benign 0.073 phenotype 04/16/2015
20 304174 APN Ppef2 0.000 IGL02702 5 92231819 R557W T A missense Het probably benign 0.008 phenotype 04/16/2015
21 304185 APN Prelid3a 0.235 IGL02702 18 67473794 D85E T A missense Het probably damaging 1.000 04/16/2015
22 304161 APN Rb1cc1 1.000 IGL02702 1 6240023 E215G A G missense Het probably damaging 0.994 phenotype 04/16/2015
23 304172 APN Rbm12 0.910 IGL02702 2 156095560 C T intron Het probably benign 0.637 phenotype 04/16/2015
24 304159 APN Recql4 1.000 IGL02702 15 76707285 G501R C T missense Het probably damaging 0.999 phenotype 04/16/2015
25 304187 APN Sema3e 0.551 IGL02702 5 14233726 T C splice site Het probably benign phenotype 04/16/2015
26 304173 APN Shisa6 0.000 IGL02702 11 66219962 L318V A C missense Het probably damaging 0.999 04/16/2015
27 304186 APN Slu7 1.000 IGL02702 11 43438892 T C splice site Het probably benign phenotype 04/16/2015
28 304160 APN Spink12 0.000 IGL02702 18 44104769 V38A T C missense Het probably benign 0.001 04/16/2015
29 304167 APN Syne2 0.296 IGL02702 12 76097924 D1549G A G missense Het probably damaging 0.999 phenotype 04/16/2015
30 304169 APN Tet1 0.000 IGL02702 10 62879752 V88A A G missense Het possibly damaging 0.831 phenotype 04/16/2015
31 304175 APN Tmem200a 0.073 IGL02702 10 25993603 G256D C T missense Het probably damaging 1.000 04/16/2015
32 304168 APN Ttn 1.000 IGL02702 2 76884491 G T intron Het probably benign phenotype 04/16/2015
33 304166 APN Ugt2b34 0.107 IGL02702 5 86892891 I391V T C missense Het probably benign 0.213 04/16/2015
34 304165 APN Zfp292 0.544 IGL02702 4 34809415 L1215I A T missense Het probably benign 0.137 04/16/2015
35 304171 APN Zfp410 0.236 IGL02702 12 84325776 N125K C A missense Het probably damaging 0.999 04/16/2015
[records 1 to 35 of 35]