Incidental Mutations

31 incidental mutations are currently displayed, and affect 31 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
8 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 31 of 31] 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 153464 APN Aatk 0.317 IGL01758 G1 11 120010819 D860G T C missense Het possibly damaging 0.857 phenotype 02/04/2014
2 153469 APN Acot7 0.241 IGL01758 G1 4 152217793 C121R T C missense Het probably damaging 0.961 0.322 phenotype 02/04/2014
3 153473 APN Adam19 1.000 IGL01758 G1 11 46112924 H193L A T missense Het probably benign 0.014 phenotype 02/04/2014
4 153479 APN AI661453 0.042 IGL01758 G1 17 47466623 T A intron Het probably benign 02/04/2014
5 153487 APN Bod1l 0.789 IGL01758 G1 5 41826610 T C splice site Het probably benign 02/04/2014
6 153486 APN Brd4 1.000 IGL01758 G1 17 32212829 T C unclassified Het probably benign phenotype 02/04/2014
7 153484 APN Capn12 0.186 IGL01758 G1 7 28886623 G A splice site 5 bp Het probably null phenotype 02/04/2014
8 153477 APN Cdh18 0.301 IGL01758 G1 15 23474183 Q713R A G missense Het probably benign 0.198 phenotype 02/04/2014
9 153476 APN Cfap52 0.309 IGL01758 G1 11 67953580 L103Q A T missense Het possibly damaging 0.668 phenotype 02/04/2014
10 153475 APN Dpy19l4 0.147 IGL01758 G1 4 11265846 T475S T A missense Het probably damaging 1.000 02/04/2014
11 153460 APN Fat2 0.000 IGL01758 G1 11 55296209 D1270E A T missense Het probably damaging 1.000 phenotype 02/04/2014
12 153483 APN Hfm1 0.095 IGL01758 G1 5 106904793 K275E T C missense Het probably damaging 0.990 phenotype 02/04/2014
13 153472 APN Ift172 1.000 IGL01758 G1 5 31280714 D426G T C missense Het probably benign 0.000 phenotype 02/04/2014
14 153470 APN Mrc1 0.063 IGL01758 G1 2 14238248 S62P T C missense Het probably damaging 1.000 phenotype 02/04/2014
15 153461 APN Olfr275 0.212 IGL01758 G1 4 52825468 E24* G T nonsense Het probably null phenotype 02/04/2014
16 153463 APN Olfr914 0.083 IGL01758 G1 9 38607293 I276K T A missense Het probably damaging 0.989 phenotype 02/04/2014
17 153490 APN Ptgs2 0.500 IGL01758 G1 1 150101989 A T critical splice acceptor site Het probably null phenotype 02/04/2014
18 153478 APN Rxfp1 0.322 IGL01758 G1 3 79652216 I433F T A missense Het possibly damaging 0.807 phenotype 02/04/2014
19 153488 APN Sbf1 0.335 IGL01758 G1 15 89303215 C T unclassified Het probably benign phenotype 02/04/2014
20 153462 APN Serpinb13 0.063 IGL01758 G1 1 107000754 F368C T G missense Het probably damaging 1.000 phenotype 02/04/2014
21 153468 APN Slc9c1 0.397 IGL01758 G1 16 45541461 S80R T A missense Het probably damaging 0.998 phenotype 02/04/2014
22 153471 APN Spats2l 0.219 IGL01758 G1 1 57879556 V30L G T missense Het probably damaging 0.995 0.030 02/04/2014
23 153465 APN Stat1 0.000 IGL01758 G1 1 52136921 E195G A G missense Het probably damaging 1.000 phenotype 02/04/2014
24 153489 APN Tbx5 0.908 IGL01758 G1 5 119844958 T A unclassified Het probably benign phenotype 02/04/2014
25 153481 APN Tmem165 0.301 IGL01758 G1 5 76204163 T164A A G missense Het probably damaging 0.999 phenotype 02/04/2014
26 153485 APN Trim66 0.184 IGL01758 G1 7 109486045 A T critical splice donor site 2 bp Het probably null 02/04/2014
27 153466 APN Trip10 0.353 IGL01758 G1 17 57261409 V405E T A missense Het possibly damaging 0.507 phenotype 02/04/2014
28 153474 APN Vmn2r92 0.089 IGL01758 G1 17 18152013 C28* T A nonsense Het probably null 02/04/2014
29 153467 APN Wdr60 0.647 IGL01758 G1 12 116218798 P728L G A missense Het possibly damaging 0.824 phenotype 02/04/2014
30 153482 APN Zbtb8a 0.314 IGL01758 G1 4 129357847 C277Y C T missense Het probably damaging 0.999 02/04/2014
31 153480 APN Zfp638 0.536 IGL01758 G1 6 83979526 F1705S T C missense Het probably damaging 0.962 phenotype 02/04/2014
[records 1 to 31 of 31]