Incidental Mutations

42 incidental mutations are currently displayed, and affect 42 genes.
5 are Possibly Damaging.
18 are Probably Damaging.
14 are Probably Benign.
5 are Probably Null.
1 create premature stop codons.
2 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 88204 APN 9430007A20Rik 0.064 IGL01469 G1 4 144528622 Q204R A G missense Het possibly damaging 0.919 11/18/2013
2 88195 APN Actn2 0.779 IGL01469 G1 13 12310910 E60K C T missense Het possibly damaging 0.500 phenotype 11/18/2013
3 88208 APN Alpk1 0.000 IGL01469 G1 3 127677752 T C splice site 1768 bp Het probably null phenotype 11/18/2013
4 88225 APN Ccdc107 0.064 IGL01469 G1 4 43495751 N218S A G missense Het probably benign 0.370 phenotype 11/18/2013
5 88219 APN Cdh23 0.619 IGL01469 G1 10 60597725 M60K A T missense Het probably benign 0.033 phenotype 11/18/2013
6 88224 APN Cenpe 1.000 IGL01469 G1 3 135228806 Q378R A G missense Het probably damaging 0.996 phenotype 11/18/2013
7 88228 APN Dnah8 0.486 IGL01469 G1 17 30683714 T A splice site Het probably benign phenotype 11/18/2013
8 88197 APN Eif2b4 1.000 IGL01469 G1 5 31187767 D190G T C missense Het probably benign 0.019 phenotype 11/18/2013
9 88202 APN Fmo5 0.147 IGL01469 G1 3 97651568 N448S A G missense Het probably benign 0.190 phenotype 11/18/2013
10 88223 APN Gal3st2c 0.107 IGL01469 G1 1 94009317 N328S A G missense Het probably benign 0.184 0.090 11/18/2013
11 88216 APN Gbf1 1.000 IGL01469 G1 19 46279364 E1271V A T missense Het probably damaging 1.000 phenotype 11/18/2013
12 88215 APN Ifitm6 0.000 IGL01469 G1 7 141016812 V16D A T missense Het probably damaging 0.975 11/18/2013
13 88193 APN Ighv2-4 0.094 IGL01469 G1 12 113653346 A G splice site Het probably null 11/18/2013
14 88194 APN Kng2 0.000 IGL01469 G1 16 22999827 K305I T A missense Het probably damaging 1.000 11/18/2013
15 88214 APN Lrp1 1.000 IGL01469 G1 10 127584414 R900Q C T missense Het probably damaging 0.999 phenotype 11/18/2013
16 88220 APN Maml1 1.000 IGL01469 G1 11 50266526 M274T A G missense Het probably damaging 0.999 phenotype 11/18/2013
17 88211 APN Med23 1.000 IGL01469 G1 10 24882597 E278G A G missense Het probably damaging 0.998 phenotype 11/18/2013
18 88218 APN Myo1h 1.000 IGL01469 G1 5 114361269 T164A A G missense Het probably damaging 1.000 11/18/2013
19 88226 APN Ncoa2 0.963 IGL01469 G1 1 13186869 S135R A T missense Het probably benign 0.017 phenotype 11/18/2013
20 88221 APN Nrbf2 0.523 IGL01469 G1 10 67270140 L41P A G missense Het probably damaging 0.979 11/18/2013
21 88209 APN Olfr108 0.053 IGL01469 G1 17 37445535 S5T T A missense Het probably benign 0.003 phenotype 11/18/2013
22 88190 APN Olfr341 0.067 IGL01469 G1 2 36479824 Y102C T C missense Het probably benign 0.440 0.200 phenotype 11/18/2013
23 88198 APN Olfr514 0.114 IGL01469 G1 7 108825327 V224A A G missense Het probably benign 0.295 phenotype 11/18/2013
24 88213 APN Olfr678 0.152 IGL01469 G1 7 105070388 M307K T A missense Het probably benign 0.055 phenotype 11/18/2013
25 88192 APN Olfr782 0.091 IGL01469 G1 10 129350580 M6V A G missense Het probably benign 0.000 phenotype 11/18/2013
26 88230 APN Otoa 0.000 IGL01469 G1 7 121155273 T C critical splice donor site 2 bp Het probably null phenotype 11/18/2013
27 88191 APN Pih1d3 0.000 IGL01469 G1 1 31223429 D164V A T missense Het probably damaging 0.986 phenotype 11/18/2013
28 88229 APN Plxnb1 0.000 IGL01469 G1 9 109105415 T C intron Het probably benign phenotype 11/18/2013
29 88227 APN Ppp1r42 0.000 IGL01469 G1 1 10003233 A T critical splice donor site 2 bp Het probably null phenotype 11/18/2013
30 88189 APN Rad54l2 1.000 IGL01469 G1 9 106722758 K100M T A missense Het probably damaging 1.000 phenotype 11/18/2013
31 88201 APN Rnf112 0.000 IGL01469 G1 11 61451341 T308S T A missense Het possibly damaging 0.941 phenotype 11/18/2013
32 88199 APN Scaper 0.695 IGL01469 G1 9 55859767 D466G T C missense Het probably damaging 1.000 11/18/2013
33 88206 APN Sgsm2 0.311 IGL01469 G1 11 74853871 I796L T A missense Het possibly damaging 0.908 phenotype 11/18/2013
34 88217 APN Shank3 0.252 IGL01469 G1 15 89521274 L476P T C missense Het probably damaging 0.997 phenotype 11/18/2013
35 88203 APN Shkbp1 0.000 IGL01469 G1 7 27355941 T6A T C missense Het probably benign 0.000 11/18/2013
36 88210 APN Slc14a2 0.000 IGL01469 G1 18 78155566 I783N A T missense Het probably damaging 0.979 phenotype 11/18/2013
37 88207 APN Stat1 0.000 IGL01469 G1 1 52147370 D447G A G missense Het possibly damaging 0.873 phenotype 11/18/2013
38 88222 APN Tekt3 0.000 IGL01469 G1 11 63073468 I208S T G missense Het probably damaging 1.000 phenotype 11/18/2013
39 88205 APN Tenm3 0.558 IGL01469 G1 8 48236423 V2043E A T missense Het probably damaging 1.000 phenotype 11/18/2013
40 88212 APN Tgm3 0.000 IGL01469 G1 2 130024494 Y111H T C missense Het probably damaging 0.999 phenotype 11/18/2013
41 88200 APN Tph2 0.257 IGL01469 G1 10 115079759 R459* T A nonsense Het probably null phenotype 11/18/2013
42 88196 APN Vmn2r109 0.083 IGL01469 G1 17 20541409 Y562C T C missense Het probably damaging 1.000 11/18/2013
[records 1 to 42 of 42]