Incidental Mutations

20 incidental mutations are currently displayed, and affect 20 genes.
3 are Possibly Damaging.
5 are Probably Damaging.
9 are Probably Benign.
0 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 20 of 20] 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 103267 APN Col19a1 1.000 IGL01664 G1 1 24561335 Y42F T A missense Het unknown phenotype 01/21/2014
2 103271 APN Ddx31 0.843 IGL01664 G1 2 28875835 T C splice site Het probably benign phenotype 01/21/2014
3 103261 APN Fbln2 0.000 IGL01664 G1 6 91233457 D128N G A missense Het probably damaging 0.963 phenotype 01/21/2014
4 103255 APN Fgf7 0.000 IGL01664 G1 2 126035987 M91I G T missense Het probably benign 0.006 phenotype 01/21/2014
5 103268 APN Gm28539 IGL01664 G1 16 18836773 H31R A G missense Het possibly damaging 0.711 01/21/2014
6 103259 APN Hivep1 0.514 IGL01664 G1 13 42159279 V1665G T G missense Het probably benign 0.176 phenotype 01/21/2014
7 103270 APN Ifih1 0.124 IGL01664 G1 2 62611700 T C splice site Het probably benign phenotype 01/21/2014
8 103263 APN Il10 0.773 IGL01664 G1 1 131021477 R125L G T missense Het possibly damaging 0.947 phenotype 01/21/2014
9 103256 APN Kalrn 0.933 IGL01664 G1 16 34294161 R574H C T missense Het probably damaging 1.000 phenotype 01/21/2014
10 103260 APN Lmln 0.126 IGL01664 G1 16 33080987 E251G A G missense Het probably benign 0.028 phenotype 01/21/2014
11 103266 APN Olfr1507 0.066 IGL01664 G1 14 52490545 N57D T C missense Het probably benign 0.014 phenotype 01/21/2014
12 103253 APN Olfr668 0.261 IGL01664 G1 7 104925104 Y220C T C missense Het probably damaging 1.000 phenotype 01/21/2014
13 103264 APN Olfr681 0.464 IGL01664 G1 7 105122216 L253Q T A missense Het probably damaging 1.000 phenotype 01/21/2014
14 103262 APN Otol1 0.000 IGL01664 G1 3 70027797 D374G A G missense Het probably benign 0.006 01/21/2014
15 103257 APN Pcdhb15 0.079 IGL01664 G1 18 37474261 V182A T C missense Het probably benign 0.353 phenotype 01/21/2014
16 103272 APN Polr3e 0.954 IGL01664 G1 7 120931317 T C splice site Het probably benign 01/21/2014
17 103265 APN Sectm1a 0.057 IGL01664 G1 11 121069044 S149T A T missense Het possibly damaging 0.548 phenotype 01/21/2014
18 103254 APN Slfn10-ps 0.083 IGL01664 G1 11 83035935 A G unclassified Het noncoding transcript 01/21/2014
19 103269 APN Sox1ot 0.497 IGL01664 G1 8 12430670 A G exon Het noncoding transcript 01/21/2014
20 103258 APN Tnik 0.000 IGL01664 G1 3 28638479 G895C G T missense Het probably damaging 0.995 phenotype 01/21/2014
[records 1 to 20 of 20]