Incidental Mutations

30 incidental mutations are currently displayed, and affect 30 genes.
5 are Possibly Damaging.
15 are Probably Damaging.
7 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 30 of 30] 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 13252 APN 4930402F06Rik 0.000 IGL00786 G1 2 35375839 N242S T C missense Het probably benign 0.053 12/06/2012
2 13290 APN Akap9 0.391 IGL00786 G1 5 4070522 A3646E C A missense Het probably damaging 0.998 phenotype 12/06/2012
3 13292 APN Akt1 0.939 IGL00786 G1 12 112657671 G233V C A missense Het probably damaging 1.000 phenotype 12/06/2012
4 13318 APN B3gat3 1.000 IGL00786 G1 19 8926785 E320G A G missense Het probably benign 0.440 phenotype 12/06/2012
5 13327 APN Bpifa5 0.052 IGL00786 G1 2 154167252 C238Y G A missense Het probably damaging 1.000 12/06/2012
6 13242 APN Camkmt 0.000 IGL00786 G1 17 85096491 V47A T C missense Het probably damaging 0.987 phenotype 12/06/2012
7 13345 APN Ccnl2 IGL00786 G1 4 155820880 R284W C T missense Het probably damaging 0.999 phenotype 12/06/2012
8 13363 APN Chl1 0.467 IGL00786 G1 6 103675145 V341F G T missense Het probably damaging 1.000 phenotype 12/06/2012
9 13391 APN Cst3 0.161 IGL00786 G1 2 148872877 C93* A T nonsense Het probably null phenotype 12/06/2012
10 13395 APN Ctsh 0.000 IGL00786 G1 9 90064238 V119A T C missense Het probably damaging 1.000 phenotype 12/06/2012
11 13418 APN Dmap1 1.000 IGL00786 G1 4 117676396 R225Q C T missense Het possibly damaging 0.673 phenotype 12/06/2012
12 13441 APN Ehbp1 0.567 IGL00786 G1 11 22100460 S479P A G missense Het possibly damaging 0.794 phenotype 12/06/2012
13 13447 APN Eml2 0.000 IGL00786 G1 7 19202582 Y528C A G missense Het probably damaging 1.000 12/06/2012
14 277962 APN Faim 0.594 IGL00786 G1 9 98992165 G15R G A missense Het probably damaging 1.000 phenotype 04/16/2015
15 13486 APN G6pc3 0.000 IGL00786 G1 11 102193105 M186V A G missense Het probably benign 0.014 phenotype 12/06/2012
16 13517 APN Gpr37 0.141 IGL00786 G1 6 25669318 V509A A G missense Het possibly damaging 0.654 phenotype 12/06/2012
17 13529 APN Heatr5b 0.279 IGL00786 G1 17 78824634 H347N G T missense Het possibly damaging 0.946 12/06/2012
18 13546 APN Idh1 0.000 IGL00786 G1 1 65166243 S188P A G missense Het probably damaging 0.999 phenotype 12/06/2012
19 13618 APN Mphosph8 0.567 IGL00786 G1 14 56672544 V118A T C missense Het probably benign 0.002 12/06/2012
20 13623 APN Mthfsd 0.104 IGL00786 G1 8 121104468 R91Q C T missense Het probably damaging 1.000 12/06/2012
21 13667 APN Otor 0.098 IGL00786 G1 2 143079926 V86I G A missense Het probably damaging 0.974 phenotype 12/06/2012
22 13680 APN Pdk2 0.000 IGL00786 G1 11 95031935 T140S T A missense Het probably benign 0.000 phenotype 12/06/2012
23 13694 APN Pnliprp2 0.114 IGL00786 G1 19 58760497 N78S A G missense Het probably benign 0.000 phenotype 12/06/2012
24 13823 APN Rimbp3 0.241 IGL00786 G1 16 17211688 T992M C T missense Het probably damaging 0.991 phenotype 12/06/2012
25 13941 APN Sdad1 0.966 IGL00786 G1 5 92303773 A T splice site Het probably null 12/06/2012
26 14015 APN Sidt2 0.175 IGL00786 G1 9 45949803 S71P A G missense Het possibly damaging 0.695 phenotype 12/06/2012
27 14100 APN Slc44a2 0.000 IGL00786 G1 9 21345935 V390E T A missense Het probably damaging 0.964 phenotype 12/06/2012
28 14491 APN Tmem168 0.099 IGL00786 G1 6 13602675 I231V T C missense Het probably benign 0.057 12/06/2012
29 14712 APN Uhrf1bp1 0.000 IGL00786 G1 17 27879292 I136N T A missense Het probably damaging 0.989 12/06/2012
30 14777 APN Vim 0.632 IGL00786 G1 2 13578510 T C critical splice donor site 2 bp Het probably null phenotype 12/06/2012
[records 1 to 30 of 30]