Incidental Mutations

27 incidental mutations are currently displayed, and affect 27 genes.
6 are Possibly Damaging.
10 are Probably Damaging.
9 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 27 of 27] 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 302781 APN 6530409C15Rik IGL02667 6 28217671 A G unclassified Het noncoding transcript 04/16/2015
2 302765 APN Akr1e1 0.087 IGL02667 13 4595667 P174L G A missense Het possibly damaging 0.647 phenotype 04/16/2015
3 302767 APN Arf5 0.206 IGL02667 6 28425199 N95K C A missense Het probably damaging 0.995 phenotype 04/16/2015
4 302785 APN Atl3 0.000 IGL02667 19 7509416 F39L T C missense Het possibly damaging 0.716 phenotype 04/16/2015
5 302779 APN Atp2a3 0.140 IGL02667 11 72975339 H262N C A missense Het probably benign 0.001 phenotype 04/16/2015
6 302764 APN Cyp2a12 0.084 IGL02667 7 27031158 S183P T C missense Het probably damaging 0.999 04/16/2015
7 302776 APN Dicer1 1.000 IGL02667 12 104714906 R449S T A missense Het probably damaging 0.998 phenotype 04/16/2015
8 302777 APN Dlec1 0.000 IGL02667 9 119127466 I736T T C missense Het probably benign 0.233 phenotype 04/16/2015
9 302771 APN Eny2 0.893 IGL02667 15 44429588 M12K T A missense Het possibly damaging 0.842 04/16/2015
10 302768 APN Fbxl21 0.000 IGL02667 13 56537129 R349C C T missense Het probably benign 0.070 phenotype 04/16/2015
11 302782 APN Gstm2 0.105 IGL02667 3 107986108 L13P A G missense Het probably damaging 1.000 phenotype 04/16/2015
12 302783 APN Gucy2g 0.000 IGL02667 19 55206177 T936M G A missense Het possibly damaging 0.639 phenotype 04/16/2015
13 302769 APN Mbp 0.257 IGL02667 18 82554615 K12N G T missense Het probably damaging 1.000 phenotype 04/16/2015
14 302786 APN Mon1b 0.085 IGL02667 8 113638823 R261L G T missense Het possibly damaging 0.899 04/16/2015
15 302789 APN Myo18a 1.000 IGL02667 11 77857852 A G splice site Het probably benign phenotype 04/16/2015
16 302766 APN Nr2f2 1.000 IGL02667 7 70357985 S117G T C missense Het probably damaging 0.995 phenotype 04/16/2015
17 302788 APN Pi4k2b 0.195 IGL02667 5 52750605 T C splice site Het probably benign phenotype 04/16/2015
18 302780 APN Pi4ka 1.000 IGL02667 16 17295461 F1504L A G missense Het possibly damaging 0.823 phenotype 04/16/2015
19 302784 APN Ppm1d 1.000 IGL02667 11 85332285 W239R T C missense Het probably damaging 1.000 phenotype 04/16/2015
20 302787 APN Setd1b 1.000 IGL02667 5 123157497 S1043T T A missense Het unknown phenotype 04/16/2015
21 302770 APN Tgfbrap1 1.000 IGL02667 1 43067620 I298V T C missense Het probably benign 0.035 phenotype 04/16/2015
22 302773 APN Tmem190 0.000 IGL02667 7 4783158 D20E T A missense Het probably benign 0.056 phenotype 04/16/2015
23 302775 APN Tph2 0.302 IGL02667 10 115080045 C408S A T missense Het probably benign 0.425 phenotype 04/16/2015
24 302774 APN Trmt44 0.083 IGL02667 5 35571052 Y295D A C missense Het probably damaging 1.000 phenotype 04/16/2015
25 302778 APN Trpm2 0.111 IGL02667 10 77935942 R621H C T missense Het probably damaging 1.000 phenotype 04/16/2015
26 302772 APN Ubn1 0.633 IGL02667 16 5062599 E134G A G missense Het probably damaging 0.997 phenotype 04/16/2015
27 302790 APN Zcchc11 0.000 IGL02667 4 108558708 T C splice site Het probably benign phenotype 04/16/2015
[records 1 to 27 of 27]