Incidental Mutations

30 incidental mutations are currently displayed, and affect 30 genes.
3 are Possibly Damaging.
11 are Probably Damaging.
12 are Probably Benign.
4 are Probably Null.
2 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 155080 APN Adam9 0.000 IGL01786 G1 8 24996839 H20L T A missense Het probably damaging 1.000 phenotype 02/04/2014
2 278915 APN Ano3 0.175 IGL01786 G1 2 110682715 Q645L T A missense Het probably damaging 0.998 phenotype 04/16/2015
3 278912 APN Clasp1 0.904 IGL01786 G1 1 118497736 L272Q T A missense Het possibly damaging 0.741 phenotype 04/16/2015
4 278916 APN Corin 0.261 IGL01786 G1 5 72339876 N532S T C missense Het probably damaging 0.996 phenotype 04/16/2015
5 155068 APN Ddx1 0.985 IGL01786 G1 12 13229136 D468E A T missense Het probably benign 0.000 phenotype 02/04/2014
6 155077 APN Hk2 1.000 IGL01786 G1 6 82739553 S333P A G missense Het probably benign 0.127 phenotype 02/04/2014
7 155078 APN Kctd19 0.056 IGL01786 G1 8 105390304 T398A T C missense Het probably benign 0.025 02/04/2014
8 155081 APN Klra8 0.015 IGL01786 G1 6 130119068 T A critical splice acceptor site Het probably null phenotype 02/04/2014
9 278918 APN Mcm8 0.787 IGL01786 G1 2 132827948 D314G A G missense Het probably benign 0.046 phenotype 04/16/2015
10 278914 APN Mga 0.721 IGL01786 G1 2 119902912 D80E T A missense Het probably damaging 1.000 phenotype 04/16/2015
11 155071 APN Mylk3 0.285 IGL01786 G1 8 85359317 Q36R T C missense Het probably benign 0.271 phenotype 02/04/2014
12 155067 APN Myom2 0.225 IGL01786 G1 8 15106330 S726P T C missense Het probably damaging 0.987 phenotype 02/04/2014
13 155072 APN Nuf2 0.953 IGL01786 G1 1 169510483 S242G T C missense Het possibly damaging 0.880 phenotype 02/04/2014
14 155079 APN Nup210l 0.225 IGL01786 G1 3 90122776 Y265* T A nonsense Het probably null phenotype 02/04/2014
15 155066 APN Olfr1445 0.119 IGL01786 G1 19 12884277 T132I C T missense Het probably damaging 0.992 phenotype 02/04/2014
16 278909 APN Olfr530 0.043 IGL01786 G1 7 140373125 M162L T A missense Het probably benign 0.000 phenotype 04/16/2015
17 278908 APN Otud3 0.211 IGL01786 G1 4 138896897 D278G T C missense Het probably benign 0.000 04/16/2015
18 155069 APN Papolg 0.892 IGL01786 G1 11 23874488 V298A A G missense Het probably damaging 0.998 phenotype 02/04/2014
19 155076 APN Phc1 1.000 IGL01786 G1 6 122319520 D847G T C missense Het possibly damaging 0.820 phenotype 02/04/2014
20 155075 APN Pkd2l1 0.188 IGL01786 G1 19 44191442 F110L A G missense Het probably damaging 0.960 phenotype 02/04/2014
21 155073 APN Plxnd1 1.000 IGL01786 G1 6 115959935 T1638S T A missense Het probably damaging 1.000 phenotype 02/04/2014
22 278911 APN Polr3a 0.983 IGL01786 G1 14 24484120 Q106* G A nonsense Het probably null phenotype 04/16/2015
23 155082 APN Rnf32 0.076 IGL01786 G1 5 29206814 T C unclassified Het probably benign phenotype 02/04/2014
24 278919 APN Slc30a9 0.722 IGL01786 G1 5 67346238 A G splice site Het probably benign 04/16/2015
25 155070 APN Slc44a2 0.202 IGL01786 G1 9 21352486 Y650C A G missense Het probably damaging 1.000 phenotype 02/04/2014
26 155074 APN Sv2a 1.000 IGL01786 G1 3 96188209 Y306F A T missense Het probably benign 0.078 phenotype 02/04/2014
27 278913 APN Tmem50a 0.155 IGL01786 G1 4 134898447 E153G T C missense Het probably damaging 0.998 phenotype 04/16/2015
28 278917 APN Tor1a 1.000 IGL01786 G1 2 30963703 A G unclassified 4688 bp Het probably null phenotype 04/16/2015
29 278910 APN Tusc5 0.063 IGL01786 G1 11 76680466 V103I G A missense Het probably benign 0.072 phenotype 04/16/2015
30 278907 APN Usp20 0.266 IGL01786 G1 2 31017163 E594G A G missense Het probably benign 0.017 phenotype 04/16/2015
[records 1 to 30 of 30]