Incidental Mutations

32 incidental mutations are currently displayed, and affect 31 genes.
7 are Possibly Damaging.
15 are Probably Damaging.
8 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 32 of 32] 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 285175 APN Abca12 1.000 IGL02222 1 71282886 R1682W T A missense Het probably benign 0.398 phenotype 04/16/2015
2 285186 APN Angptl6 0.226 IGL02222 9 20873907 M450K A T missense Het probably damaging 0.990 phenotype 04/16/2015
3 285179 APN Armc12 0.095 IGL02222 17 28538720 N275K C A missense Het probably damaging 0.999 04/16/2015
4 285197 APN Cd27 0.000 IGL02222 6 125234532 H144R T C missense Het probably damaging 0.977 phenotype 04/16/2015
5 285172 APN Cenpf 0.631 IGL02222 1 189654444 K1880E T C missense Het probably benign 0.000 phenotype 04/16/2015
6 285183 APN Dchs1 1.000 IGL02222 7 105764887 I907N A T missense Het probably damaging 0.995 phenotype 04/16/2015
7 285171 APN Dpy19l4 0.084 IGL02222 4 11281116 F443C A C missense Het possibly damaging 0.934 04/16/2015
8 285196 APN Eif3i 0.961 IGL02222 4 129592088 D315N C T missense Het possibly damaging 0.892 04/16/2015
9 285180 APN Fam217a 0.087 IGL02222 13 34911119 L128P A G missense Het probably damaging 1.000 04/16/2015
10 285178 APN Fam46b 0.183 IGL02222 4 133486553 V245A T C missense Het probably damaging 0.989 04/16/2015
11 285181 APN Fetub 0.061 IGL02222 16 22932328 L62F C T missense Het probably damaging 1.000 phenotype 04/16/2015
12 285187 APN Fmn1 0.402 IGL02222 2 113593109 I1047F A T missense Het probably damaging 1.000 phenotype 04/16/2015
13 285194 APN G2e3 0.628 IGL02222 12 51363233 H267R A G missense Het probably damaging 1.000 phenotype 04/16/2015
14 285200 APN Gigyf2 0.935 IGL02222 1 87410863 A G splice site 3820 bp Het probably null phenotype 04/16/2015
15 285185 APN Gm10650 0.129 IGL02222 3 128040140 T C exon Het noncoding transcript 04/16/2015
16 285177 APN Grip1 1.000 IGL02222 10 119999809 T470I C T missense Het probably damaging 1.000 phenotype 04/16/2015
17 285176 APN Hmcn1 0.000 IGL02222 1 150806401 D466A T G missense Het probably benign 0.049 phenotype 04/16/2015
18 285195 APN Lrrc63 0.083 IGL02222 14 75086140 Y548C T C missense Het probably damaging 0.986 04/16/2015
19 285199 APN Naaa 0.000 IGL02222 5 92259550 T C unclassified Het probably benign phenotype 04/16/2015
20 285191 APN Parpbp 0.000 IGL02222 10 88140085 E55D T A missense Het possibly damaging 0.947 04/16/2015
21 285190 APN Pnpt1 1.000 IGL02222 11 29130842 A29T G A missense Het probably benign 0.003 phenotype 04/16/2015
22 285188 APN Pnpt1 1.000 IGL02222 11 29159327 D691V A T missense Het possibly damaging 0.708 phenotype 04/16/2015
23 285174 APN Pramef6 0.049 IGL02222 4 143895846 M313T A G missense Het possibly damaging 0.942 04/16/2015
24 285170 APN Psg25 0.056 IGL02222 7 18529727 N57S T C missense Het probably damaging 0.999 04/16/2015
25 285184 APN Selenbp2 0.309 IGL02222 3 94699962 V168E T A missense Het probably damaging 0.996 04/16/2015
26 285198 APN Syne2 0.319 IGL02222 12 75952843 E2337K G A missense Het probably damaging 0.963 phenotype 04/16/2015
27 285173 APN Synj2 0.122 IGL02222 17 6037480 T1269A A G missense Het probably benign 0.037 phenotype 04/16/2015
28 285182 APN Tnfrsf13c 0.161 IGL02222 15 82223163 V144L C A missense Het probably damaging 0.979 phenotype 04/16/2015
29 285193 APN Uspl1 0.954 IGL02222 5 149194044 V132L G T missense Het probably benign 0.254 04/16/2015
30 285169 APN Vmn2r58 0.363 IGL02222 7 41864025 Y398F T A missense Het possibly damaging 0.811 04/16/2015
31 285189 APN Vps13a 0.000 IGL02222 19 16682175 T1663S T A missense Het probably benign 0.060 phenotype 04/16/2015
32 285192 APN Ythdc1 0.969 IGL02222 5 86828043 R503H G A missense Het possibly damaging 0.724 04/16/2015
[records 1 to 32 of 32]