Incidental Mutations

42 incidental mutations are currently displayed, and affect 42 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
17 are Probably Benign.
6 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 42 of 42] 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 89806 APN Adamts17 0.061 IGL01532 G1 7 66908601 N264K C A missense Het probably damaging 1.000 phenotype 12/03/2013
2 89786 APN Adgrl3 0.000 IGL01532 G1 5 81694569 T260I C T missense Het probably damaging 1.000 phenotype 12/03/2013
3 89805 APN Ambra1 0.887 IGL01532 G1 2 91885632 K769N G T missense Het probably damaging 1.000 phenotype 12/03/2013
4 89794 APN Arel1 0.602 IGL01532 G1 12 84934162 V357A A G missense Het possibly damaging 0.459 12/03/2013
5 89793 APN Atp11b 0.221 IGL01532 G1 3 35849502 C76* T A nonsense Het probably null phenotype 12/03/2013
6 89808 APN AW112010 0.130 IGL01532 G1 19 11048069 C A exon Het noncoding transcript 12/03/2013
7 278559 APN Bfar 0.100 IGL01532 G1 16 13687387 A T splice site Het probably benign 04/16/2015
8 89804 APN Ccdc70 0.056 IGL01532 G1 8 21973283 L30V T G missense Het probably damaging 0.999 12/03/2013
9 89811 APN Chrm5 0.090 IGL01532 G1 2 112479232 R513Q C T missense Het probably benign 0.000 phenotype 12/03/2013
10 89814 APN Crem 0.449 IGL01532 G1 18 3276732 T7I G A missense Het probably benign 0.017 phenotype 12/03/2013
11 89816 APN Cyp4f39 0.441 IGL01532 G1 17 32470954 C T splice site Het probably benign phenotype 12/03/2013
12 89785 APN Dlg5 1.000 IGL01532 G1 14 24158592 T849A T C missense Het probably benign 0.000 phenotype 12/03/2013
13 89796 APN Dock8 0.106 IGL01532 G1 19 25169441 G1428V G T missense Het probably damaging 0.993 phenotype 12/03/2013
14 89781 APN Eomes 1.000 IGL01532 G1 9 118482249 I380T T C missense Het probably damaging 1.000 phenotype 12/03/2013
15 89802 APN Fam13a 0.000 IGL01532 G1 6 58940295 D532G T C missense Het probably damaging 0.963 12/03/2013
16 89803 APN Fopnl 0.112 IGL01532 G1 16 14304511 S130P A G missense Het probably benign 0.004 12/03/2013
17 89790 APN Gm10061 IGL01532 G1 16 89151302 *55L G T makesense Het probably null 12/03/2013
18 89813 APN Gm27438 IGL01532 G1 2 87252925 T G utr 3 prime Het probably benign 12/03/2013
19 89787 APN Gpalpp1 IGL01532 G1 14 76102502 K124E T C missense Het probably benign 0.001 12/03/2013
20 89812 APN Hgs 0.208 IGL01532 G1 11 120477509 T A splice site Het probably null phenotype 12/03/2013
21 89792 APN Hpn 0.000 IGL01532 G1 7 31103513 M121L T A missense Het possibly damaging 0.509 phenotype 12/03/2013
22 89818 APN Il1r1 0.091 IGL01532 G1 1 40294928 T C critical splice donor site 2 bp Het probably null phenotype 12/03/2013
23 89783 APN Jag2 1.000 IGL01532 G1 12 112914363 C583S A T missense Het probably damaging 0.975 phenotype 12/03/2013
24 89799 APN Katnal2 0.000 IGL01532 G1 18 77012000 H146R T C missense Het probably benign 0.000 12/03/2013
25 89819 APN Ldah 0.000 IGL01532 G1 12 8220596 T C splice site Het probably benign phenotype 12/03/2013
26 89791 APN Lvrn 0.539 IGL01532 G1 18 46900484 Y921N T A missense Het probably damaging 1.000 12/03/2013
27 89798 APN Muc5b 0.173 IGL01532 G1 7 141870006 Y4572C A G missense Het possibly damaging 0.956 phenotype 12/03/2013
28 89800 APN Myo16 0.380 IGL01532 G1 8 10400551 S518G A G missense Het probably benign 0.002 phenotype 12/03/2013
29 89784 APN Ncf1 0.000 IGL01532 G1 5 134226593 N148S T C missense Het probably benign 0.027 phenotype 12/03/2013
30 89810 APN Nes 0.522 IGL01532 G1 3 87978347 D1260E T G missense Het possibly damaging 0.544 phenotype 12/03/2013
31 89820 APN Nup210 0.000 IGL01532 G1 6 91085999 C A splice site Het probably benign phenotype 12/03/2013
32 89809 APN Olfr548-ps1 0.077 IGL01532 G1 7 102542656 L240P T C missense Het probably damaging 1.000 12/03/2013
33 89789 APN Rnf31 1.000 IGL01532 G1 14 55602623 Q968K C A missense Het probably damaging 0.991 phenotype 12/03/2013
34 89817 APN Ros1 0.148 IGL01532 G1 10 52090938 A G splice site Het probably benign phenotype 12/03/2013
35 89807 APN Ryk 1.000 IGL01532 G1 9 102897266 Y400H T C missense Het probably benign 0.380 phenotype 12/03/2013
36 89821 APN Slc4a5 0.745 IGL01532 G1 6 83273040 T A splice site Het probably null phenotype 12/03/2013
37 89815 APN Sptssb IGL01532 G1 3 69820869 A G utr 3 prime Het probably benign phenotype 12/03/2013
38 89801 APN Sstr5 0.140 IGL01532 G1 17 25491331 D308G T C missense Het probably damaging 0.997 phenotype 12/03/2013
39 89795 APN Taf2 1.000 IGL01532 G1 15 55049486 W493R A G missense Het possibly damaging 0.944 phenotype 12/03/2013
40 89782 APN Vmn2r28 0.123 IGL01532 G1 7 5486464 I459L T A missense Het probably benign 0.155 0.090 12/03/2013
41 89788 APN Vti1b 0.178 IGL01532 G1 12 79165138 L1W A C start codon destroyed Het probably null 1.000 phenotype 12/03/2013
42 89797 APN Wdr1 1.000 IGL01532 G1 5 38535187 Y125C T C missense Het probably damaging 1.000 phenotype 12/03/2013
[records 1 to 42 of 42]