Incidental Mutations

13 incidental mutations are currently displayed, and affect 13 genes.
1 are Possibly Damaging.
4 are Probably Damaging.
5 are Probably Benign.
3 are Probably Null.
2 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 13 of 13] 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 9352 APN Cage1 0.092 IGL00648 G1 13 38022993 S398* G T nonsense Het probably null 12/06/2012
2 9358 APN Calr 1.000 IGL00648 G1 8 84842702 T A unclassified Het probably benign phenotype 12/06/2012
3 9744 APN Cmah 0.113 IGL00648 G1 13 24460276 K459* A T nonsense Het probably null phenotype 12/06/2012
4 10443 APN Edem1 0.578 IGL00648 G1 6 108851207 T A splice site Het probably null 12/06/2012
5 10469 APN Elp4 0.971 IGL00648 G1 2 105842366 A T splice site Het probably benign phenotype 12/06/2012
6 10322 APN Fam3b 0.052 IGL00648 G1 16 97478399 G110E C T missense Het probably damaging 0.987 phenotype 12/06/2012
7 277840 APN Fmnl3 0.726 IGL00648 G1 15 99322670 T577I G A missense Het probably damaging 0.999 phenotype 04/16/2015
8 12260 APN Nbea 1.000 IGL00648 G1 3 56009260 S860P A G missense Het probably damaging 0.979 phenotype 12/06/2012
9 12378 APN Nlrp1a 0.092 IGL00648 G1 11 71092957 T1082A T C missense Het probably benign 0.001 phenotype 12/06/2012
10 12917 APN Pbrm1 1.000 IGL00648 G1 14 31052283 I469F A T missense Het probably damaging 1.000 phenotype 12/06/2012
11 13224 APN Ptprq 0.261 IGL00648 G1 10 107646716 L999F G A missense Het probably benign 0.105 phenotype 12/06/2012
12 14343 APN Taar6 0.194 IGL00648 G1 10 23985508 V47M C T missense Het probably benign 0.152 phenotype 12/06/2012
13 14544 APN Tom1l2 0.248 IGL00648 G1 11 60261116 Y155C T C missense Het possibly damaging 0.925 phenotype 12/06/2012
[records 1 to 13 of 13]