Incidental Mutations

18 incidental mutations are currently displayed, and affect 18 genes.
6 are Possibly Damaging.
3 are Probably Damaging.
7 are Probably Benign.
2 are Probably Null.
2 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 8439 APN 2410089E03Rik 1.000 IGL00756 G1 15 8264447 A G splice site Het probably benign phenotype 12/06/2012
2 8480 APN 4932438A13Rik 0.882 IGL00756 G1 3 36908218 H489Q C A missense Het probably damaging 0.998 phenotype 12/06/2012
3 8563 APN Acvr2a 0.000 IGL00756 G1 2 48873052 A T splice site Het probably benign phenotype 12/06/2012
4 9808 APN Col19a1 1.000 IGL00756 G1 1 24322942 K583N T A missense Het possibly damaging 0.850 phenotype 12/06/2012
5 9896 APN Crot 0.174 IGL00756 G1 5 8976072 R305L C A missense Het probably damaging 1.000 phenotype 12/06/2012
6 9930 APN Ctnnal1 0.267 IGL00756 G1 4 56829544 N428K A T missense Het possibly damaging 0.902 phenotype 12/06/2012
7 10046 APN Dab1 0.635 IGL00756 G1 4 104727878 K405R A G missense Het probably benign 0.000 phenotype 12/06/2012
8 10228 APN Dnah6 0.241 IGL00756 G1 6 73123771 F2016L A C missense Het possibly damaging 0.763 phenotype 12/06/2012
9 10780 APN Fgfrl1 1.000 IGL00756 G1 5 108705953 K309E A G missense Het possibly damaging 0.913 phenotype 12/06/2012
10 11186 APN Gucy1b2 0.204 IGL00756 G1 14 62403209 H749R T C missense Het probably benign 0.000 phenotype 12/06/2012
11 12014 APN Mki67 0.585 IGL00756 G1 7 135698731 S1525T A T missense Het possibly damaging 0.757 phenotype 12/06/2012
12 10334 APN Mob1a 0.222 IGL00756 G1 6 83332486 Y72N T A missense Het probably damaging 1.000 phenotype 12/06/2012
13 12794 APN Ntrk1 1.000 IGL00756 G1 3 87783697 E387K C T missense Het probably benign 0.055 phenotype 12/06/2012
14 13714 APN Qser1 0.253 IGL00756 G1 2 104787671 M932T A G missense Het possibly damaging 0.551 12/06/2012
15 13755 APN Rarb 0.000 IGL00756 G1 14 16443791 E166* C A nonsense Het probably null phenotype 12/06/2012
16 14453 APN Thnsl1 0.099 IGL00756 G1 2 21212612 H392Q T A missense Het probably benign 0.023 12/06/2012
17 14492 APN Tmem171 0.079 IGL00756 G1 13 98686426 R288S T A missense Het probably benign 0.000 12/06/2012
18 14912 APN Zc4h2 IGL00756 G1 X 95642201 R186* T A nonsense Het probably null phenotype 12/06/2012
[records 1 to 18 of 18]