Incidental Mutations

37 incidental mutations are currently displayed, and affect 37 genes.
3 are Possibly Damaging.
18 are Probably Damaging.
14 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 37 of 37] 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 281824 APN 1700021P04Rik 0.065 IGL02147 19 24064963 T C exon Het noncoding transcript 04/16/2015
2 281832 APN Acadsb 0.000 IGL02147 7 131425881 T A splice site Het probably benign phenotype 04/16/2015
3 281822 APN Ambra1 0.856 IGL02147 2 91767719 H75R A G missense Het probably benign 0.008 phenotype 04/16/2015
4 281826 APN Arhgef28 0.000 IGL02147 13 97961314 I931F T A missense Het probably damaging 0.999 phenotype 04/16/2015
5 281819 APN Cdk5 0.633 IGL02147 5 24420320 N165D T C missense Het probably benign 0.015 phenotype 04/16/2015
6 281802 APN Col4a2 1.000 IGL02147 8 11408140 Y272F A T missense Het probably benign 0.285 phenotype 04/16/2015
7 281801 APN Csde1 0.960 IGL02147 3 103039934 D67E T A missense Het probably damaging 1.000 04/16/2015
8 281806 APN Dhx34 0.320 IGL02147 7 16204003 H724R T C missense Het probably benign 0.006 phenotype 04/16/2015
9 281823 APN Dhx57 0.175 IGL02147 17 80260323 D777G T C missense Het possibly damaging 0.953 04/16/2015
10 281809 APN Fat3 0.576 IGL02147 9 15995985 V2907G A C missense Het probably damaging 0.999 phenotype 04/16/2015
11 281828 APN Fst 0.871 IGL02147 13 114454360 Y290C T C missense Het probably damaging 1.000 phenotype 04/16/2015
12 281817 APN Gm5065 0.315 IGL02147 7 5359733 I121N T A missense Het probably damaging 1.000 04/16/2015
13 281814 APN Ighg2b 0.061 IGL02147 12 113306391 *336R A T makesense Het probably null 0.976 04/16/2015
14 281803 APN Igkv4-92 0.128 IGL02147 6 68755252 S46N C T missense Het probably damaging 1.000 04/16/2015
15 281810 APN Kdm2b 1.000 IGL02147 5 122947835 E238K C T missense Het probably damaging 0.992 phenotype 04/16/2015
16 281805 APN Lmtk2 0.480 IGL02147 5 144156936 M244V A G missense Het possibly damaging 0.782 phenotype 04/16/2015
17 281798 APN Mcoln1 0.195 IGL02147 8 3508379 F211S T C missense Het probably benign 0.000 phenotype 04/16/2015
18 281829 APN Mib2 0.000 IGL02147 4 155657687 R209L C A missense Het probably benign 0.000 phenotype 04/16/2015
19 281830 APN Msx3 0.000 IGL02147 7 140048885 V39L C A missense Het possibly damaging 0.455 04/16/2015
20 281827 APN Mtnr1b 0.000 IGL02147 9 15863376 F129S A G missense Het probably damaging 0.960 phenotype 04/16/2015
21 281799 APN Nr3c2 1.000 IGL02147 8 76909067 S266G A G missense Het probably damaging 0.984 phenotype 04/16/2015
22 281808 APN Nup160 0.967 IGL02147 2 90703941 L703F G T missense Het probably benign 0.170 phenotype 04/16/2015
23 281800 APN Olfr1093 0.298 IGL02147 2 86786150 N140S A G missense Het probably benign 0.193 phenotype 04/16/2015
24 281812 APN Olfr95 0.064 IGL02147 17 37210986 Y289F T A missense Het probably damaging 1.000 phenotype 04/16/2015
25 281821 APN Pcyt1a 1.000 IGL02147 16 32462098 N105K T A missense Het probably damaging 0.998 phenotype 04/16/2015
26 281833 APN Pdhx 1.000 IGL02147 2 103030341 A G unclassified Het probably benign phenotype 04/16/2015
27 281807 APN Qpct 0.297 IGL02147 17 79070716 V105A T C missense Het probably damaging 0.989 phenotype 04/16/2015
28 281820 APN Ros1 0.138 IGL02147 10 52120895 F1227C A C missense Het probably damaging 1.000 phenotype 04/16/2015
29 281815 APN Rrp12 0.953 IGL02147 19 41886181 V342E A T missense Het probably damaging 1.000 04/16/2015
30 281834 APN Sart3 0.969 IGL02147 5 113762943 A G splice site Het probably benign phenotype 04/16/2015
31 281813 APN Slc6a18 0.000 IGL02147 13 73668162 K366M T A missense Het probably damaging 0.969 phenotype 04/16/2015
32 281816 APN Smarca4 1.000 IGL02147 9 21635703 N175D A G missense Het probably damaging 0.984 phenotype 04/16/2015
33 281804 APN Sox14 0.405 IGL02147 9 99875545 K47R T C missense Het probably damaging 0.999 phenotype 04/16/2015
34 281811 APN Trcg1 0.070 IGL02147 9 57245849 I592F A T missense Het probably benign 0.201 04/16/2015
35 281825 APN Ush2a 0.595 IGL02147 1 188864703 M3880T T C missense Het probably benign 0.000 phenotype 04/16/2015
36 281818 APN Usp20 0.000 IGL02147 2 31006401 F172S T C missense Het probably damaging 0.999 phenotype 04/16/2015
37 281831 APN Vmn2r4 0.074 IGL02147 3 64398361 C T splice site Het probably benign 04/16/2015
[records 1 to 37 of 37]