Incidental Mutations

22 incidental mutations are currently displayed, and affect 22 genes.
5 are Possibly Damaging.
7 are Probably Damaging.
6 are Probably Benign.
3 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 22 of 22] 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 103305 APN 9530053A07Rik 0.152 IGL01666 G1 7 28153292 V1335M G A missense Het probably damaging 0.999 01/21/2014
2 103304 APN 9530077C05Rik 0.184 IGL01666 G1 9 22431698 D163G A G missense Het probably benign 0.078 01/21/2014
3 103311 APN Adgrb3 0.464 IGL01666 G1 1 25460751 A664S C A missense Het probably damaging 0.959 phenotype 01/21/2014
4 103316 APN Ankrd61 0.107 IGL01666 G1 5 143891136 L297F T A missense Het probably damaging 1.000 01/21/2014
5 103315 APN Chrnd 0.514 IGL01666 G1 1 87198736 S513C A T missense Het possibly damaging 0.548 phenotype 01/21/2014
6 103313 APN Col24a1 0.287 IGL01666 G1 3 145344686 V645M G A missense Het possibly damaging 0.930 phenotype 01/21/2014
7 103317 APN Csn3 0.000 IGL01666 G1 5 87930157 V174A T C missense Het unknown phenotype 01/21/2014
8 103314 APN D630039A03Rik 0.029 IGL01666 G1 4 57910570 V81I C T missense Het possibly damaging 0.864 01/21/2014
9 103312 APN Deptor 0.143 IGL01666 G1 15 55149379 R54Q G A missense Het probably damaging 1.000 01/21/2014
10 103302 APN Ell 1.000 IGL01666 G1 8 70585813 H400R A G missense Het probably benign 0.000 phenotype 01/21/2014
11 103321 APN Itga2 0.000 IGL01666 G1 13 114837091 A G critical splice donor site 2 bp Het probably null phenotype 01/21/2014
12 103307 APN Itpr3 0.000 IGL01666 G1 17 27117178 I2293V A G missense Het probably benign 0.019 phenotype 01/21/2014
13 103318 APN Mrps27 0.848 IGL01666 G1 13 99409816 E241G A G missense Het probably damaging 1.000 phenotype 01/21/2014
14 103319 APN Mut 1.000 IGL01666 G1 17 40958811 L687P T C missense Het probably damaging 1.000 phenotype 01/21/2014
15 103309 APN Myh9 1.000 IGL01666 G1 15 77761931 A1951T C T missense Het probably benign 0.312 phenotype 01/21/2014
16 103322 APN Oca2 0.235 IGL01666 G1 7 56314811 G A splice site 5 bp Het probably null phenotype 01/21/2014
17 103301 APN Olfr135 0.044 IGL01666 G1 17 38208889 L215F C T missense Het probably benign 0.110 phenotype 01/21/2014
18 103308 APN Olfr215 0.061 IGL01666 G1 6 116582335 I204F T A missense Het possibly damaging 0.930 phenotype 01/21/2014
19 103303 APN Ptgdr2 0.124 IGL01666 G1 19 10940910 F264L T C missense Het probably benign 0.393 phenotype 01/21/2014
20 103320 APN Ptpn23 1.000 IGL01666 G1 9 110386545 T1384A T C missense Het possibly damaging 0.948 phenotype 01/21/2014
21 103310 APN Rasgrf2 0.378 IGL01666 G1 13 92038210 D170E A T missense Het probably damaging 0.998 phenotype 01/21/2014
22 103306 APN Rnf20 0.942 IGL01666 G1 4 49654486 Q848* C T nonsense Het probably null phenotype 01/21/2014
[records 1 to 22 of 22]