Incidental Mutations

34 incidental mutations are currently displayed, and affect 34 genes.
7 are Possibly Damaging.
16 are Probably Damaging.
9 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 34 of 34] 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 29609 APN Acot9 0.139 IGL00987 G1 X 155295181 I241T T C missense Het probably benign 0.005 04/17/2013
2 27044 APN Atp5g3 0.290 IGL00987 G1 2 73909926 R19* T A nonsense Het probably null phenotype 04/17/2013
3 29474 APN Celf4 1.000 IGL00987 G1 18 25486950 D420G T C missense Het probably damaging 1.000 phenotype 04/17/2013
4 29010 APN Cideb 0.072 IGL00987 G1 14 55754560 R179L C A missense Het possibly damaging 0.783 phenotype 04/17/2013
5 29376 APN Cmtr1 0.967 IGL00987 G1 17 29697169 R591H G A missense Het probably benign 0.007 04/17/2013
6 28101 APN Dync1li2 0.230 IGL00987 G1 8 104442498 S34T A T missense Het possibly damaging 0.954 phenotype 04/17/2013
7 27962 APN Eri2 0.183 IGL00987 G1 7 119791166 Y80H A G missense Het probably damaging 1.000 04/17/2013
8 27045 APN Eya2 0.843 IGL00987 G1 2 165754481 E304G A G missense Het probably damaging 1.000 phenotype 04/17/2013
9 26781 APN Fam135a 0.181 IGL00987 G1 1 24055898 L130V A C missense Het probably damaging 1.000 04/17/2013
10 29608 APN Fancb 0.231 IGL00987 G1 X 164991598 K410N A T missense Het probably damaging 1.000 phenotype 04/17/2013
11 27180 APN Gabpb2 0.000 IGL00987 G1 3 95200191 V191G A C missense Het probably damaging 0.997 phenotype 04/17/2013
12 27179 APN Gfm1 1.000 IGL00987 G1 3 67438560 H197R A G missense Het possibly damaging 0.791 phenotype 04/17/2013
13 28673 APN Gm11595 0.093 IGL00987 G1 11 99772539 V105A A G missense Het unknown 04/17/2013
14 27359 APN Hectd3 0.000 IGL00987 G1 4 116999643 D462E T A missense Het probably damaging 0.982 0.647 phenotype 04/17/2013
15 306671 APN Herc1 0.000 IGL00987 G1 9 66408052 V1139L G T missense Het probably benign 0.072 phenotype 04/16/2015
16 306670 APN Itgal 0.144 IGL00987 G1 7 127302011 F190L T C missense Het probably damaging 0.989 phenotype 04/16/2015
17 306672 APN Krt87 0.074 IGL00987 G1 15 101438446 H109Y G A missense Het probably benign 0.002 04/16/2015
18 29114 APN Lmf2 0.200 IGL00987 G1 15 89354568 Y115C T C missense Het probably benign 0.000 04/17/2013
19 28674 APN Papolg 0.916 IGL00987 G1 11 23876377 Y259F T A missense Het possibly damaging 0.934 phenotype 04/17/2013
20 29211 APN Parn 0.950 IGL00987 G1 16 13667603 I10V T C missense Het probably benign 0.000 phenotype 04/17/2013
21 29555 APN Pdcd11 0.967 IGL00987 G1 19 47114550 T A intron Het probably benign phenotype 04/17/2013
22 29210 APN Phldb2 0.000 IGL00987 G1 16 45763102 Q1003L T A missense Het possibly damaging 0.782 04/17/2013
23 27554 APN Pigg 0.083 IGL00987 G1 5 108342078 F850I T A missense Het probably damaging 1.000 0.871 phenotype 04/17/2013
24 27043 APN Pkp4 0.000 IGL00987 G1 2 59308357 L317P T C missense Het probably damaging 0.984 phenotype 04/17/2013
25 28675 APN Polr2a 0.968 IGL00987 G1 11 69743794 T C splice site Het probably benign phenotype 04/17/2013
26 27360 APN Prdm16 0.771 IGL00987 G1 4 154341969 T453M G A missense Het possibly damaging 0.887 phenotype 04/17/2013
27 28910 APN Rnf144b 0.000 IGL00987 G1 13 47207493 E36D A T missense Het possibly damaging 0.567 04/17/2013
28 28911 APN Ryr2 1.000 IGL00987 G1 13 11735502 T1961I G A missense Het probably damaging 0.986 phenotype 04/17/2013
29 28442 APN Sash1 1.000 IGL00987 G1 10 8751413 K305I T A missense Het probably damaging 1.000 phenotype 04/17/2013
30 28909 APN Tbc1d7 0.810 IGL00987 G1 13 43159321 I32N A T missense Het probably damaging 0.998 phenotype 04/17/2013
31 28441 APN Thop1 0.472 IGL00987 G1 10 81081695 F623L T C missense Het probably damaging 0.993 phenotype 04/17/2013
32 26780 APN Thsd7b 0.239 IGL00987 G1 1 129613279 G297R G A missense Het probably damaging 1.000 04/17/2013
33 27361 APN Tln1 1.000 IGL00987 G1 4 43551297 C A unclassified Het probably benign phenotype 04/17/2013
34 27961 APN Vmn1r183 0.056 IGL00987 G1 7 24055224 N151D A G missense Het probably damaging 1.000 04/17/2013
[records 1 to 34 of 34]