Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
5 are Possibly Damaging.
17 are Probably Damaging.
12 are Probably Benign.
1 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 35 of 35] 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 103719 APN Abcc1 0.141 IGL01678 G1 16 14405019 M186K T A missense Het probably null 0.956 phenotype 01/21/2014
2 103704 APN Adamts3 1.000 IGL01678 G1 5 89707856 N385S T C missense Het probably damaging 0.999 phenotype 01/21/2014
3 103709 APN Adamts6 0.876 IGL01678 G1 13 104313688 V299A T C missense Het probably damaging 1.000 phenotype 01/21/2014
4 103715 APN Angel1 0.203 IGL01678 G1 12 86717026 E500G T C missense Het probably benign 0.000 01/21/2014
5 103722 APN Car9 0.000 IGL01678 G1 4 43512941 T C splice site Het probably benign phenotype 01/21/2014
6 103699 APN Colec11 0.065 IGL01678 G1 12 28594868 F209S A G missense Het probably damaging 0.995 phenotype 01/21/2014
7 103708 APN Dock10 0.612 IGL01678 G1 1 80543352 Y1179H A G missense Het probably damaging 0.999 phenotype 01/21/2014
8 103697 APN Ece1 0.653 IGL01678 G1 4 137962733 W697R T A missense Het probably damaging 1.000 phenotype 01/21/2014
9 103705 APN Eml2 0.000 IGL01678 G1 7 19186122 M117K T A missense Het probably benign 0.380 01/21/2014
10 103724 APN Flii 1.000 IGL01678 G1 11 60716846 G T unclassified Het probably benign phenotype 01/21/2014
11 103710 APN Frmpd1 0.000 IGL01678 G1 4 45243717 D63E T A missense Het probably damaging 1.000 01/21/2014
12 103712 APN Ftmt 0.000 IGL01678 G1 18 52332134 H174L A T missense Het probably damaging 0.982 phenotype 01/21/2014
13 103711 APN Gm438 0.055 IGL01678 G1 4 144777873 M236K A T missense Het probably benign 0.197 01/21/2014
14 103714 APN Gm960 0.077 IGL01678 G1 19 4672165 I76L T A missense Het possibly damaging 0.944 phenotype 01/21/2014
15 103702 APN Gpr37l1 0.080 IGL01678 G1 1 135167053 V151A A G missense Het probably damaging 0.999 phenotype 01/21/2014
16 103707 APN Inppl1 0.862 IGL01678 G1 7 101832596 T180A T C missense Het probably benign 0.094 phenotype 01/21/2014
17 103692 APN Klhdc4 0.095 IGL01678 G1 8 121796938 D513G T C missense Het possibly damaging 0.725 01/21/2014
18 103721 APN Klrb1a 0.000 IGL01678 G1 6 128618448 A G splice site Het probably benign 01/21/2014
19 103718 APN Nit1 0.462 IGL01678 G1 1 171342694 V270A A G missense Het probably damaging 0.974 phenotype 01/21/2014
20 103695 APN Olfr774 0.064 IGL01678 G1 10 129238668 D173A A C missense Het possibly damaging 0.938 phenotype 01/21/2014
21 103716 APN Phox2b 1.000 IGL01678 G1 5 67098919 Y8F T A missense Het probably damaging 0.998 phenotype 01/21/2014
22 103698 APN Psg20 0.078 IGL01678 G1 7 18680870 S364C T A missense Het probably damaging 0.999 01/21/2014
23 103700 APN Rab38 0.582 IGL01678 G1 7 88430532 V44E T A missense Het probably damaging 1.000 phenotype 01/21/2014
24 103723 APN Rapgef4 0.650 IGL01678 G1 2 72242225 T C splice site Het probably benign phenotype 01/21/2014
25 103713 APN Ror1 1.000 IGL01678 G1 4 100425968 P410L C T missense Het possibly damaging 0.684 phenotype 01/21/2014
26 103693 APN Rptn 0.083 IGL01678 G1 3 93396811 N484D A G missense Het probably benign 0.001 01/21/2014
27 103696 APN Sirpb1a 0.060 IGL01678 G1 3 15411310 S142R G T missense Het probably damaging 1.000 01/21/2014
28 103717 APN Smox 0.341 IGL01678 G1 2 131512059 R17H G A missense Het possibly damaging 0.906 phenotype 01/21/2014
29 103720 APN Trpm7 1.000 IGL01678 G1 2 126816799 C1146S A T missense Het probably damaging 0.993 phenotype 01/21/2014
30 103706 APN Upf3a 0.000 IGL01678 G1 8 13791930 A155V C T missense Het probably benign 0.210 phenotype 01/21/2014
31 103691 APN Vmn1r212 0.069 IGL01678 G1 13 22883911 V84D A T missense Het probably damaging 1.000 01/21/2014
32 103694 APN Vmn2r40 IGL01678 G1 7 8920106 N419D T C missense Het probably damaging 0.994 01/21/2014
33 103703 APN Wdr92 0.299 IGL01678 G1 11 17232790 V317A T C missense Het probably benign 0.000 phenotype 01/21/2014
34 103725 APN Zfp143 0.954 IGL01678 G1 7 110080351 C A splice site Het probably benign phenotype 01/21/2014
35 103701 APN Zmat4 0.092 IGL01678 G1 8 23902048 C7S T A missense Het probably damaging 1.000 01/21/2014
[records 1 to 35 of 35]