Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
5 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 33 of 33] 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 84778 APN Adam6b 0.034 IGL01456 G1 12 113491463 D633E T A missense Het probably benign 0.304 11/11/2013
2 84793 APN Akap13 1.000 IGL01456 G1 7 75602847 C242R T C missense Het probably damaging 0.983 phenotype 11/11/2013
3 84783 APN Ap5z1 0.222 IGL01456 G1 5 142468036 L175P T C missense Het probably damaging 0.963 phenotype 11/11/2013
4 84790 APN Arid1b 0.452 IGL01456 G1 17 5291235 E938G A G missense Het probably damaging 0.996 phenotype 11/11/2013
5 84794 APN Arid4a 0.000 IGL01456 G1 12 71067262 N208D A G missense Het probably benign 0.002 phenotype 11/11/2013
6 84792 APN Atr 1.000 IGL01456 G1 9 95950565 H2556R A G missense Het possibly damaging 0.619 phenotype 11/11/2013
7 84791 APN Cald1 1.000 IGL01456 G1 6 34764996 D438V A T missense Het probably damaging 0.999 phenotype 11/11/2013
8 84797 APN Dcbld2 0.000 IGL01456 G1 16 58408873 P40S C T missense Het possibly damaging 0.752 phenotype 11/11/2013
9 84780 APN Dock8 0.168 IGL01456 G1 19 25119499 M590I G A missense Het possibly damaging 0.955 phenotype 11/11/2013
10 84781 APN Gm1818 0.887 IGL01456 G1 12 48555800 A T exon Het noncoding transcript 11/11/2013
11 84799 APN Hace1 0.393 IGL01456 G1 10 45709998 A G splice site Het probably benign phenotype 11/11/2013
12 84771 APN Igkv10-96 0.153 IGL01456 G1 6 68632102 Y70H A G missense Het probably benign 0.042 11/11/2013
13 84773 APN Kdm2a 0.966 IGL01456 G1 19 4351755 H200Q G T missense Het probably damaging 1.000 phenotype 11/11/2013
14 84788 APN Ldha 1.000 IGL01456 G1 7 46850178 D111G A G missense Het possibly damaging 0.793 phenotype 11/11/2013
15 84787 APN Map7 0.195 IGL01456 G1 10 20273804 E567G A G missense Het unknown phenotype 11/11/2013
16 84796 APN Nbeal1 0.426 IGL01456 G1 1 60230628 L375F G T missense Het probably damaging 1.000 11/11/2013
17 84782 APN Nectin3 0.247 IGL01456 G1 16 46458853 E254G T C missense Het probably benign 0.235 phenotype 11/11/2013
18 84784 APN Nlrp4b 0.058 IGL01456 G1 7 10714223 I118F A T missense Het probably benign 0.260 11/11/2013
19 84789 APN Pkhd1 0.319 IGL01456 G1 1 20199459 V3287D A T missense Het probably damaging 0.999 phenotype 11/11/2013
20 84785 APN Ptpre 0.276 IGL01456 G1 7 135669802 V375G T G missense Het probably damaging 1.000 phenotype 11/11/2013
21 84774 APN Rabgap1 0.543 IGL01456 G1 2 37541175 E746G A G missense Het probably damaging 0.988 11/11/2013
22 84776 APN Sh2b2 0.914 IGL01456 G1 5 136224467 C311Y C T missense Het probably damaging 0.981 phenotype 11/11/2013
23 84786 APN Skor1 0.408 IGL01456 G1 9 63145490 T399I G A missense Het probably damaging 0.997 11/11/2013
24 84795 APN Sptbn2 0.000 IGL01456 G1 19 4746749 T1792A A G missense Het probably damaging 0.998 phenotype 11/11/2013
25 84777 APN Tiparp 0.487 IGL01456 G1 3 65552609 G442* G T nonsense Het probably null phenotype 11/11/2013
26 84801 APN Tln1 1.000 IGL01456 G1 4 43543432 G A unclassified Het probably benign phenotype 11/11/2013
27 84800 APN Tmc7 0.107 IGL01456 G1 7 118547310 C A splice site Het probably benign 11/11/2013
28 84779 APN Top2a 0.990 IGL01456 G1 11 99011030 L458Q A T missense Het probably damaging 1.000 phenotype 11/11/2013
29 84798 APN Tpte 0.089 IGL01456 G1 8 22345052 A G splice site Het probably benign phenotype 11/11/2013
30 84772 APN Unc13a 1.000 IGL01456 G1 8 71644567 R1228W G A missense Het probably damaging 0.998 phenotype 11/11/2013
31 84770 APN Vipr1 1.000 IGL01456 G1 9 121665178 T275M C T missense Het probably damaging 0.992 phenotype 11/11/2013
32 84775 APN Vmn1r177 0.408 IGL01456 G1 7 23866328 P41Q G T missense Het possibly damaging 0.579 11/11/2013
33 84769 APN Vmn2r4 0.052 IGL01456 G1 3 64406395 N388K A T missense Het probably damaging 0.988 11/11/2013
[records 1 to 33 of 33]