Incidental Mutations

19 incidental mutations are currently displayed, and affect 19 genes.
5 are Possibly Damaging.
6 are Probably Damaging.
8 are Probably Benign.
0 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 19 of 19] 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 304196 APN Adad1 0.280 IGL02703 3 37064241 Q60L A T missense Het probably damaging 0.999 phenotype 04/16/2015
2 304193 APN AI593442 0.107 IGL02703 9 52678118 L53R A C missense Het probably damaging 0.999 04/16/2015
3 304205 APN Bmp2 1.000 IGL02703 2 133561404 S292A T G missense Het probably benign 0.000 phenotype 04/16/2015
4 304199 APN Cd37 0.000 IGL02703 7 45235525 D186G T C missense Het probably benign 0.070 phenotype 04/16/2015
5 304194 APN Cenpf 0.673 IGL02703 1 189659758 I626V T C missense Het probably benign 0.135 phenotype 04/16/2015
6 304191 APN Faim 0.491 IGL02703 9 98992201 S49T T A missense Het probably benign 0.093 phenotype 04/16/2015
7 304190 APN Glrb 1.000 IGL02703 3 80850993 E371A T G missense Het probably benign 0.188 phenotype 04/16/2015
8 304204 APN Kcne2 IGL02703 16 92296950 S122P T C missense Het possibly damaging 0.674 phenotype 04/16/2015
9 304200 APN Mon1b 0.106 IGL02703 8 113638823 R261L G T missense Het possibly damaging 0.899 04/16/2015
10 304207 APN Olfr1047 0.102 IGL02703 2 86228979 T A utr 5 prime Het probably benign phenotype 04/16/2015
11 304189 APN Olfr1420 0.097 IGL02703 19 11896242 T74A A G missense Het possibly damaging 0.956 phenotype 04/16/2015
12 304198 APN Olfr453 0.095 IGL02703 6 42744076 I13S T G missense Het possibly damaging 0.899 phenotype 04/16/2015
13 304197 APN Pex1 0.568 IGL02703 5 3615120 H573Q C A missense Het probably benign 0.243 phenotype 04/16/2015
14 304192 APN Plxna1 0.867 IGL02703 6 89356943 S235P A G missense Het probably damaging 1.000 phenotype 04/16/2015
15 304202 APN Rbm12 0.899 IGL02703 2 156095560 C T intron Het probably benign 0.637 phenotype 04/16/2015
16 304201 APN Slc41a2 0.203 IGL02703 10 83254847 K491R T C missense Het probably damaging 0.999 04/16/2015
17 304195 APN Sugct 0.139 IGL02703 13 17452540 T243P T G missense Het possibly damaging 0.936 phenotype 04/16/2015
18 304206 APN Tnfaip3 0.000 IGL02703 10 19007032 D212E G T missense Het probably damaging 0.978 phenotype 04/16/2015
19 304203 APN Trim68 0.069 IGL02703 7 102684079 V132A A G missense Het probably damaging 0.990 phenotype 04/16/2015
[records 1 to 19 of 19]