Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
13 are Probably Benign.
1 are Probably Null.
1 create premature stop codons.
0 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 102784 APN 4930430A15Rik 0.058 IGL01649 G1 2 111214576 A T splice site Het probably benign 01/21/2014
2 102772 APN 4931429L15Rik 0.000 IGL01649 G1 9 46305818 S220P A G missense Het probably benign 0.001 01/21/2014
3 102761 APN Adam18 0.000 IGL01649 G1 8 24614896 N634S T C missense Het possibly damaging 0.818 phenotype 01/21/2014
4 102786 APN Arhgef18 1.000 IGL01649 G1 8 3441211 T A splice site Het probably benign phenotype 01/21/2014
5 102765 APN Birc6 1.000 IGL01649 G1 17 74604546 S1518G A G missense Het probably benign 0.026 phenotype 01/21/2014
6 102762 APN Cltc 0.953 IGL01649 G1 11 86726400 V341A A G missense Het probably benign 0.156 phenotype 01/21/2014
7 102783 APN Dlg5 1.000 IGL01649 G1 14 24138691 V1721A A G missense Het probably damaging 1.000 phenotype 01/21/2014
8 102782 APN Dnah10 0.000 IGL01649 G1 5 124732489 I274F A T missense Het probably damaging 0.967 phenotype 01/21/2014
9 102760 APN Dock1 1.000 IGL01649 G1 7 134777410 L622Q T A missense Het probably damaging 1.000 phenotype 01/21/2014
10 102774 APN Dysf 0.000 IGL01649 G1 6 84199839 D1960G A G missense Het probably damaging 1.000 phenotype 01/21/2014
11 102767 APN Fat3 0.558 IGL01649 G1 9 16376719 T503A T C missense Het possibly damaging 0.953 phenotype 01/21/2014
12 102769 APN Glb1 0.000 IGL01649 G1 9 114423948 Y73C A G missense Het probably damaging 1.000 phenotype 01/21/2014
13 102781 APN Gm9396 0.895 IGL01649 G1 3 130068619 G T exon Het noncoding transcript 01/21/2014
14 102778 APN Gml2 0.054 IGL01649 G1 15 74824221 E155* G T nonsense Het probably null 01/21/2014
15 102777 APN Ikzf4 0.000 IGL01649 G1 10 128635820 R323C G A missense Het probably damaging 1.000 phenotype 01/21/2014
16 102768 APN Kiz 0.000 IGL01649 G1 2 146889309 T240A A G missense Het probably benign 0.349 phenotype 01/21/2014
17 102759 APN Lzts3 0.162 IGL01649 G1 2 130635431 K480E T C missense Het probably damaging 0.984 01/21/2014
18 102766 APN Mcm7 1.000 IGL01649 G1 5 138169436 H105R T C missense Het probably damaging 0.998 phenotype 01/21/2014
19 102776 APN Mpdz 0.000 IGL01649 G1 4 81303633 L1464P A G missense Het probably damaging 0.979 phenotype 01/21/2014
20 102755 APN Mrgpra9 0.058 IGL01649 G1 7 47235152 L256V A C missense Het probably benign 0.223 01/21/2014
21 102773 APN Mrpl40 0.946 IGL01649 G1 16 18872579 Q127R T C missense Het probably benign 0.019 phenotype 01/21/2014
22 102764 APN Myom2 0.139 IGL01649 G1 8 15113755 R1003L G T missense Het probably benign 0.241 phenotype 01/21/2014
23 102763 APN Nav2 0.629 IGL01649 G1 7 49575729 T1806A A G missense Het probably damaging 0.998 phenotype 01/21/2014
24 102757 APN Olfr248 0.075 IGL01649 G1 1 174391408 L113P T C missense Het probably damaging 1.000 phenotype 01/21/2014
25 102779 APN Pibf1 1.000 IGL01649 G1 14 99187763 Y562F A T missense Het possibly damaging 0.881 01/21/2014
26 102787 APN Ppm1n 0.131 IGL01649 G1 7 19278197 A T splice site Het probably benign 01/21/2014
27 102756 APN Psg17 0.000 IGL01649 G1 7 18816802 V376A A G missense Het possibly damaging 0.599 01/21/2014
28 102771 APN Sept8 0.181 IGL01649 G1 11 53535028 F143I T A missense Het possibly damaging 0.788 phenotype 01/21/2014
29 102780 APN Sestd1 1.000 IGL01649 G1 2 77199045 Y330H A G missense Het probably damaging 1.000 phenotype 01/21/2014
30 102785 APN Sntg1 0.097 IGL01649 G1 1 8681969 C T splice site Het probably benign phenotype 01/21/2014
31 102770 APN Stpg2 0.057 IGL01649 G1 3 139419862 P472Q C A missense Het probably damaging 1.000 01/21/2014
32 102775 APN Thbs1 0.000 IGL01649 G1 2 118114982 K314R A G missense Het probably benign 0.000 phenotype 01/21/2014
33 102758 APN Vav3 0.102 IGL01649 G1 3 109562762 Y508H T C missense Het probably benign 0.000 phenotype 01/21/2014
[records 1 to 33 of 33]