Incidental Mutations

38 incidental mutations are currently displayed, and affect 38 genes.
10 are Possibly Damaging.
11 are Probably Damaging.
14 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 38 of 38] 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 179410 APN 9330159F19Rik 0.064 IGL01896 G1 10 29225158 F509Y T A missense Het possibly damaging 0.838 05/07/2014
2 179409 APN Acot11 0.129 IGL01896 G1 4 106771367 I75F T A missense Het probably damaging 1.000 phenotype 05/07/2014
3 179397 APN Atp1a2 1.000 IGL01896 G1 1 172286011 N427Y T A missense Het probably damaging 1.000 phenotype 05/07/2014
4 179392 APN Cd19 0.755 IGL01896 G1 7 126414350 D89G T C missense Het possibly damaging 0.740 phenotype 05/07/2014
5 179387 APN Clca1 0.101 IGL01896 G1 3 145015677 T378S T A missense Het possibly damaging 0.790 phenotype 05/07/2014
6 179403 APN Cltc 0.962 IGL01896 G1 11 86725133 C436S A T missense Het probably damaging 0.998 phenotype 05/07/2014
7 179407 APN Def8 0.211 IGL01896 G1 8 123459895 V429M G A missense Het probably benign 0.292 05/07/2014
8 179411 APN Dnah9 0.450 IGL01896 G1 11 66130666 D311E A T missense Het possibly damaging 0.891 phenotype 05/07/2014
9 179413 APN Dpy19l4 0.089 IGL01896 G1 4 11267752 K396R T C missense Het possibly damaging 0.807 05/07/2014
10 179404 APN Eif4b 0.959 IGL01896 G1 15 102095286 S597P T C missense Het probably benign 0.226 05/07/2014
11 179384 APN Ezh1 0.000 IGL01896 G1 11 101213755 N155K A T missense Het probably benign 0.004 phenotype 05/07/2014
12 179408 APN Glud1 0.938 IGL01896 G1 14 34319905 S157G A G missense Het probably benign 0.004 phenotype 05/07/2014
13 279034 APN Gm10718 0.730 IGL01896 G1 9 3025118 Y194F A T missense Het probably benign 0.001 04/16/2015
14 279033 APN Gm21738 0.872 IGL01896 G1 14 19416979 S144L G A missense Het probably benign 0.011 04/16/2015
15 179401 APN Gm5600 0.117 IGL01896 G1 7 113707984 T C exon Het noncoding transcript 05/07/2014
16 179399 APN Hnf4g 0.202 IGL01896 G1 3 3651410 V298E T A missense Het probably damaging 0.999 phenotype 05/07/2014
17 179414 APN Hspd1 1.000 IGL01896 G1 1 55079109 R446Q C T missense Het probably benign 0.012 phenotype 05/07/2014
18 179394 APN Lyst 0.366 IGL01896 G1 13 13635577 I611V A G missense Het probably benign 0.043 phenotype 05/07/2014
19 179389 APN Map4k3 0.000 IGL01896 G1 17 80613931 E524G T C missense Het probably benign 0.130 phenotype 05/07/2014
20 179405 APN Mepe 0.059 IGL01896 G1 5 104338269 D425G A G missense Het possibly damaging 0.845 phenotype 05/07/2014
21 179388 APN Myo1a 0.128 IGL01896 G1 10 127719904 V921L G T missense Het probably benign 0.000 phenotype 05/07/2014
22 179393 APN Plxdc1 0.496 IGL01896 G1 11 97924582 M470K A T missense Het probably damaging 0.983 05/07/2014
23 179415 APN Prim1 0.957 IGL01896 G1 10 128022889 Y222C A G missense Het probably damaging 1.000 phenotype 05/07/2014
24 179396 APN Ptpn13 0.289 IGL01896 G1 5 103501523 N264S A G missense Het possibly damaging 0.781 phenotype 05/07/2014
25 179406 APN Qrsl1 0.957 IGL01896 G1 10 43876504 D441G T C missense Het probably benign 0.018 05/07/2014
26 179400 APN Samd9l 0.000 IGL01896 G1 6 3375120 Q714K G T missense Het probably benign 0.016 phenotype 05/07/2014
27 179402 APN Scrib 1.000 IGL01896 G1 15 76066118 E293G T C missense Het possibly damaging 0.745 phenotype 05/07/2014
28 179398 APN Slc12a2 0.000 IGL01896 G1 18 57896308 N255K T A missense Het probably benign 0.065 phenotype 05/07/2014
29 179390 APN Slc6a6 0.000 IGL01896 G1 6 91726069 I141T T C missense Het probably damaging 0.972 phenotype 05/07/2014
30 179385 APN Slc9a1 0.000 IGL01896 G1 4 133418059 L485P T C missense Het probably damaging 0.998 phenotype 05/07/2014
31 179383 APN Slfn8 0.103 IGL01896 G1 11 83003696 Y706N A T missense Het probably damaging 1.000 05/07/2014
32 179386 APN Tlr5 0.360 IGL01896 G1 1 182974879 F583L T C missense Het possibly damaging 0.637 phenotype 05/07/2014
33 179395 APN Tmprss15 0.000 IGL01896 G1 16 79090790 V43A A G missense Het probably benign 0.216 phenotype 05/07/2014
34 179417 APN Ttc24 0.069 IGL01896 G1 3 88070413 T C critical splice acceptor site Het probably null 05/07/2014
35 179412 APN Ttc7 0.771 IGL01896 G1 17 87359124 T606A A G missense Het probably damaging 0.994 phenotype 05/07/2014
36 179416 APN Ubap2 0.196 IGL01896 G1 4 41202362 P689T G T missense Het possibly damaging 0.848 phenotype 05/07/2014
37 279035 APN Vmn2r-ps159 0.608 IGL01896 G1 4 156338254 C T exon Het noncoding transcript 04/16/2015
38 179391 APN Wfdc8 0.000 IGL01896 G1 2 164605780 M120K A T missense Het probably damaging 0.999 phenotype 05/07/2014
[records 1 to 38 of 38]