Incidental Mutations

32 incidental mutations are currently displayed, and affect 32 genes.
5 are Possibly Damaging.
12 are Probably Damaging.
11 are Probably Benign.
4 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 32 of 32] 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 90601 APN 5330417C22Rik 0.080 IGL01552 G1 3 108481312 W252R A G missense Het possibly damaging 0.478 phenotype 12/09/2013
2 90618 APN Arl8a 0.656 IGL01552 G1 1 135152868 T C critical splice donor site 2 bp Het probably null 0.959 12/09/2013
3 90599 APN Bivm 0.128 IGL01552 G1 1 44126773 N128D A G missense Het probably benign 0.397 12/09/2013
4 90606 APN Chil3 0.292 IGL01552 G1 3 106148848 G330V C A missense Het probably damaging 0.982 phenotype 12/09/2013
5 90597 APN Dscaml1 0.600 IGL01552 G1 9 45447908 H155R A G missense Het probably damaging 0.998 phenotype 12/09/2013
6 90614 APN Etl4 0.809 IGL01552 G1 2 20778189 V687D T A missense Het probably damaging 0.988 phenotype 12/09/2013
7 90620 APN Fbxw10 0.069 IGL01552 G1 11 62857684 A T critical splice acceptor site Het probably null phenotype 12/09/2013
8 90598 APN Gfpt2 0.000 IGL01552 G1 11 49805005 E21* G T nonsense Het probably null 12/09/2013
9 90610 APN Gm10197 0.240 IGL01552 G1 19 53371691 V26I C T missense Het possibly damaging 0.455 12/09/2013
10 90600 APN Gm4788 0.060 IGL01552 G1 1 139739302 Y412H A G missense Het probably damaging 0.997 12/09/2013
11 90593 APN Gm6614 0.061 IGL01552 G1 6 141987706 K451R T C missense Het possibly damaging 0.543 12/09/2013
12 90612 APN Golim4 0.078 IGL01552 G1 3 75956195 E35G T C missense Het probably damaging 1.000 phenotype 12/09/2013
13 90622 APN Igdcc4 0.248 IGL01552 G1 9 65122502 A G intron Het probably benign 12/09/2013
14 90619 APN Ino80d 1.000 IGL01552 G1 1 63057977 A G utr 3 prime Het probably benign 12/09/2013
15 90603 APN Ipo13 0.961 IGL01552 G1 4 117900964 M734T A G missense Het probably benign 0.161 phenotype 12/09/2013
16 90592 APN Klk1b27 0.051 IGL01552 G1 7 44054615 L61F C T missense Het probably damaging 0.999 phenotype 12/09/2013
17 90605 APN Lamtor5 1.000 IGL01552 G1 3 107279008 V31A T C missense Het probably benign 0.027 phenotype 12/09/2013
18 90615 APN Lrp1 1.000 IGL01552 G1 10 127588510 L769* A T nonsense Het probably null phenotype 12/09/2013
19 90604 APN Nipsnap1 0.356 IGL01552 G1 11 4889124 S135C A T missense Het probably damaging 0.998 phenotype 12/09/2013
20 90595 APN Olfr1277 0.090 IGL01552 G1 2 111269912 G152C C A missense Het probably damaging 1.000 phenotype 12/09/2013
21 90596 APN Pparg 1.000 IGL01552 G1 6 115490122 H452L A T missense Het probably benign 0.001 phenotype 12/09/2013
22 90609 APN Rab34 1.000 IGL01552 G1 11 78191438 A202V C T missense Het probably damaging 0.997 phenotype 12/09/2013
23 90602 APN Ryr3 0.436 IGL01552 G1 2 112825883 T1923S T A missense Het possibly damaging 0.532 phenotype 12/09/2013
24 90608 APN Sall4 1.000 IGL01552 G1 2 168756123 S266P A G missense Het probably damaging 1.000 0.123 phenotype 12/09/2013
25 90594 APN Sh2d4b 0.051 IGL01552 G1 14 40860648 Q195R T C missense Het probably benign 0.000 12/09/2013
26 90617 APN Sik2 0.728 IGL01552 G1 9 50917522 C A splice site Het probably benign phenotype 12/09/2013
27 90591 APN Slc25a36 0.288 IGL01552 G1 9 97079233 V111A A G missense Het probably benign 0.007 12/09/2013
28 90616 APN Sptbn5 0.248 IGL01552 G1 2 120054422 A T unclassified Het probably benign 12/09/2013
29 90613 APN Tac2 0.084 IGL01552 G1 10 127726101 E25K G A missense Het possibly damaging 0.798 phenotype 12/09/2013
30 90607 APN Tnc 0.000 IGL01552 G1 4 63970408 V1807A A G missense Het probably damaging 0.999 phenotype 12/09/2013
31 90621 APN Top3b 0.288 IGL01552 G1 16 16887823 T C splice site Het probably benign phenotype 12/09/2013
32 90611 APN Zfp827 0.902 IGL01552 G1 8 79076191 E464G A G missense Het probably damaging 1.000 12/09/2013
[records 1 to 32 of 32]