Incidental Mutations

32 incidental mutations are currently displayed, and affect 32 genes.
5 are Possibly Damaging.
15 are Probably Damaging.
9 are Probably Benign.
3 are Probably Null.
3 create premature stop codons.
0 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 182663 APN Alms1 0.000 IGL01976 G1 6 85622665 V1960A T C missense Het possibly damaging 0.732 phenotype 05/07/2014
2 182659 APN Asph 0.000 IGL01976 G1 4 9475471 N537K A T missense Het probably damaging 0.982 phenotype 05/07/2014
3 182687 APN Bnip2 0.000 IGL01976 G1 9 70000834 T C splice site Het probably benign phenotype 05/07/2014
4 182684 APN Cc2d2a 0.894 IGL01976 G1 5 43683115 Q104K C A missense Het probably benign 0.019 phenotype 05/07/2014
5 182661 APN Cd300ld IGL01976 G1 11 114987444 S81P A G missense Het probably damaging 1.000 05/07/2014
6 182689 APN Clec4a1 0.057 IGL01976 G1 6 122928074 T C splice site Het probably benign 05/07/2014
7 182679 APN Dnajb8 0.685 IGL01976 G1 6 88222526 S15P T C missense Het probably damaging 0.988 phenotype 05/07/2014
8 182672 APN Erp27 0.073 IGL01976 G1 6 136919989 V72L C A missense Het probably damaging 0.988 phenotype 05/07/2014
9 182678 APN Gm13103 0.075 IGL01976 G1 4 143852793 N316S A G missense Het probably benign 0.175 05/07/2014
10 182658 APN Gpr156 0.000 IGL01976 G1 16 37979033 T131A A G missense Het probably damaging 0.974 phenotype 05/07/2014
11 182666 APN Grk1 0.000 IGL01976 G1 8 13415993 V479A T C missense Het probably damaging 0.998 phenotype 05/07/2014
12 182677 APN Hist1h2ba IGL01976 G1 13 23933999 D53V T A missense Het possibly damaging 0.544 phenotype 05/07/2014
13 182673 APN Hspg2 1.000 IGL01976 G1 4 137561926 D3784G A G missense Het probably damaging 1.000 phenotype 05/07/2014
14 182669 APN Irf2 0.254 IGL01976 G1 8 46807225 K26M A T missense Het probably damaging 0.999 phenotype 05/07/2014
15 182667 APN Irx6 0.127 IGL01976 G1 8 92676089 C27* C A nonsense Het probably null phenotype 05/07/2014
16 182676 APN Izumo1r IGL01976 G1 9 14901679 C99Y C T missense Het probably damaging 1.000 phenotype 05/07/2014
17 182660 APN Klrb1a 0.000 IGL01976 G1 6 128618109 T132S T A missense Het probably benign 0.356 05/07/2014
18 182688 APN Mmp13 0.229 IGL01976 G1 9 7278974 C T splice site Het probably benign phenotype 05/07/2014
19 182674 APN Myo5b 0.782 IGL01976 G1 18 74698277 R766Q G A missense Het probably damaging 1.000 phenotype 05/07/2014
20 182683 APN Myt1 1.000 IGL01976 G1 2 181795739 L81P T C missense Het probably damaging 1.000 phenotype 05/07/2014
21 182662 APN Nfat5 0.921 IGL01976 G1 8 107367559 V793I G A missense Het probably damaging 0.997 phenotype 05/07/2014
22 182685 APN Nup210 0.000 IGL01976 G1 6 91053614 V108A A G missense Het possibly damaging 0.887 phenotype 05/07/2014
23 182664 APN Olfr32 0.081 IGL01976 G1 2 90138924 S72P A G missense Het probably damaging 1.000 phenotype 05/07/2014
24 182665 APN Omd 0.071 IGL01976 G1 13 49589643 Y56* T A nonsense Het probably null phenotype 05/07/2014
25 182682 APN Psmd9 0.157 IGL01976 G1 5 123234634 E60G A G missense Het probably damaging 0.987 phenotype 05/07/2014
26 182671 APN Rab11fip1 0.098 IGL01976 G1 8 27152797 E658G T C missense Het possibly damaging 0.565 phenotype 05/07/2014
27 182681 APN Smchd1 0.754 IGL01976 G1 17 71394725 K1091* T A nonsense Het probably null phenotype 05/07/2014
28 182668 APN Supt16 0.966 IGL01976 G1 14 52182307 N111K A T missense Het possibly damaging 0.705 phenotype 05/07/2014
29 182675 APN Trrap 1.000 IGL01976 G1 5 144856989 T3666A A G missense Het probably benign 0.004 phenotype 05/07/2014
30 182680 APN Ttn 1.000 IGL01976 G1 2 76785751 D8289G T C missense Het probably damaging 0.997 phenotype 05/07/2014
31 182670 APN Ush2a 0.432 IGL01976 G1 1 188911241 S4267T T A missense Het probably benign 0.035 phenotype 05/07/2014
32 182686 APN Usp50 1.000 IGL01976 G1 2 126709466 E31V T A missense Het probably benign 0.102 05/07/2014
[records 1 to 32 of 32]