Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
1 are Possibly Damaging.
12 are Probably Damaging.
12 are Probably Benign.
8 are Probably Null.
0 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33] 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 91640 APN Abcc12 0.066 IGL01593 G1 8 86557650 I310N A T missense Het probably damaging 1.000 phenotype 12/09/2013
2 91659 APN Ackr4 0.000 IGL01593 G1 9 104085931 C T intron Het probably benign phenotype 12/09/2013
3 91637 APN Ankib1 0.000 IGL01593 G1 5 3732590 D346E A T missense Het probably benign 0.003 12/09/2013
4 91656 APN Armc4 0.238 IGL01593 G1 18 7127345 K956R T C missense Het probably benign 0.004 phenotype 12/09/2013
5 91661 APN Asap2 0.150 IGL01593 G1 12 21213202 A273S G T missense Het probably null 0.026 phenotype 12/09/2013
6 91660 APN Atp6v0d2 0.000 IGL01593 G1 4 19881436 R219L C A missense Het probably damaging 1.000 phenotype 12/09/2013
7 91650 APN Atp6v1e2 0.203 IGL01593 G1 17 86944299 F224I A T missense Het probably damaging 0.997 12/09/2013
8 91657 APN Bnc2 1.000 IGL01593 G1 4 84276241 T C unclassified 4 bp Het probably null phenotype 12/09/2013
9 91665 APN Btbd11 0.227 IGL01593 G1 10 85654475 T A splice site Het probably benign 12/09/2013
10 91651 APN Cd33 0.000 IGL01593 G1 7 43530281 L241P A G missense Het possibly damaging 0.907 phenotype 12/09/2013
11 91668 APN Clec4g 0.052 IGL01593 G1 8 3719474 A T critical splice donor site 2 bp Het probably null phenotype 12/09/2013
12 91667 APN Dym 0.000 IGL01593 G1 18 75114781 C T splice site Het probably benign phenotype 12/09/2013
13 91643 APN Enpp5 0.000 IGL01593 G1 17 44080721 T14A A G missense Het probably benign 0.000 phenotype 12/09/2013
14 91669 APN Ggt1 0.108 IGL01593 G1 10 75585287 T C critical splice donor site 2 bp Het probably null phenotype 12/09/2013
15 91645 APN Gm17541 IGL01593 G1 12 4689868 T A intron Het probably benign 12/09/2013
16 91647 APN Gpr39 0.000 IGL01593 G1 1 125677451 I39F A T missense Het probably benign 0.002 phenotype 12/09/2013
17 91654 APN Kcnb1 0.000 IGL01593 G1 2 167106207 F240L G T missense Het probably damaging 1.000 phenotype 12/09/2013
18 91658 APN Kcnt1 0.213 IGL01593 G1 2 25898754 V400E T A missense Het probably damaging 0.997 phenotype 12/09/2013
19 91639 APN Klhdc7a 0.000 IGL01593 G1 4 139966814 I274T A G missense Het probably damaging 0.998 12/09/2013
20 91653 APN Lrwd1 0.860 IGL01593 G1 5 136134629 L71Q A T missense Het probably damaging 1.000 phenotype 12/09/2013
21 91663 APN Mycbp2 1.000 IGL01593 G1 14 103291287 A T critical splice donor site 2 bp Het probably null phenotype 12/09/2013
22 91649 APN Nckap1 1.000 IGL01593 G1 2 80520570 M725K A T missense Het probably benign 0.058 phenotype 12/09/2013
23 91644 APN Olfr1535 0.058 IGL01593 G1 13 21555219 I268F T A missense Het probably damaging 0.976 phenotype 12/09/2013
24 91662 APN Pole2 1.000 IGL01593 G1 12 69223099 C T splice site 5 bp Het probably null phenotype 12/09/2013
25 91638 APN Prss32 0.070 IGL01593 G1 17 23856008 T111A A G missense Het probably benign 0.008 12/09/2013
26 91664 APN Rgs9 0.000 IGL01593 G1 11 109249049 A G splice site Het probably benign phenotype 12/09/2013
27 91641 APN Slc2a4 0.786 IGL01593 G1 11 69944828 C361R A G missense Het probably damaging 0.979 phenotype 12/09/2013
28 91655 APN Ston1 0.220 IGL01593 G1 17 88637010 G615R G A missense Het probably null 1.000 phenotype 12/09/2013
29 91642 APN Tas2r139 0.000 IGL01593 G1 6 42140957 W8G T G missense Het probably benign 0.011 phenotype 12/09/2013
30 91652 APN Tmem101 0.138 IGL01593 G1 11 102155878 L55Q A T missense Het probably damaging 0.999 12/09/2013
31 91666 APN Tnni3k 0.208 IGL01593 G1 3 154941029 T C splice site 3 bp Het probably null phenotype 12/09/2013
32 91646 APN Uba2 1.000 IGL01593 G1 7 34146264 V478A A G missense Het probably damaging 0.963 phenotype 12/09/2013
33 91648 APN Vps13a 0.000 IGL01593 G1 19 16762181 D52G T C missense Het probably damaging 0.980 phenotype 12/09/2013
[records 1 to 33 of 33]