Incidental Mutations

18 incidental mutations are currently displayed, and affect 18 genes.
3 are Possibly Damaging.
7 are Probably Damaging.
7 are Probably Benign.
1 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 18 of 18] 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 9846 APN Cops6 1.000 IGL00814 G1 5 138163378 R58L G T missense Het probably damaging 1.000 phenotype 12/06/2012
2 10466 APN Elmo1 0.000 IGL00814 G1 13 20286724 M262K T A missense Het probably damaging 0.970 phenotype 12/06/2012
3 277981 APN Faim 0.450 IGL00814 G1 9 98992165 G15R G A missense Het probably damaging 1.000 phenotype 04/16/2015
4 11144 APN Gria4 0.602 IGL00814 G1 9 4472202 M429K A T missense Het probably damaging 0.979 phenotype 12/06/2012
5 277980 APN Hipk2 0.943 IGL00814 G1 6 38818549 R262W G A missense Het probably damaging 1.000 phenotype 04/16/2015
6 11622 APN Kif23 0.972 IGL00814 G1 9 61937107 I143K A T missense Het possibly damaging 0.948 phenotype 12/06/2012
7 11920 APN Mbtd1 1.000 IGL00814 G1 11 93943840 S615T T A missense Het possibly damaging 0.942 phenotype 12/06/2012
8 12394 APN Nlrp9c 0.000 IGL00814 G1 7 26384750 S468N C T missense Het probably benign 0.228 12/06/2012
9 12791 APN Nt5c2 0.290 IGL00814 G1 19 46897648 D212E A T missense Het probably benign 0.017 phenotype 12/06/2012
10 12852 APN Olfr596 0.079 IGL00814 G1 7 103309807 I29L A T missense Het probably benign 0.026 12/06/2012
11 12934 APN Pck2 0.203 IGL00814 G1 14 55548299 T C unclassified Het probably benign phenotype 12/06/2012
12 12950 APN Pdcd6ip 0.000 IGL00814 G1 9 113687653 Q230R T C missense Het probably damaging 0.967 phenotype 12/06/2012
13 8463 APN Pomk 0.198 IGL00814 G1 8 25983596 T110A T C missense Het probably benign 0.210 phenotype 12/06/2012
14 13200 APN Psg23 0.000 IGL00814 G1 7 18614683 W66* C T nonsense Het probably null phenotype 12/06/2012
15 13836 APN Rnf144b 0.000 IGL00814 G1 13 47220488 T C splice site Het probably benign 12/06/2012
16 277982 APN Sppl2c 0.078 IGL00814 G1 11 104186979 G202S G A missense Het possibly damaging 0.828 04/16/2015
17 14454 APN Thnsl2 0.091 IGL00814 G1 6 71139883 L95R A C missense Het probably damaging 1.000 phenotype 12/06/2012
18 14656 APN Ttn 1.000 IGL00814 G1 2 76807167 V12248A A G missense Het probably benign 0.296 phenotype 12/06/2012
[records 1 to 18 of 18]