Incidental Mutations

61 incidental mutations are currently displayed, and affect 60 genes.
12 are Possibly Damaging.
22 are Probably Damaging.
18 are Probably Benign.
7 are Probably Null.
2 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 61 of 61] 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 283897 APN Actn4 0.836 IGL02192 7 28898400 M545K A T missense Het possibly damaging 0.925 phenotype 04/16/2015
2 283898 APN Adamtsl1 0.172 IGL02192 4 86228016 E303G A G missense Het probably damaging 1.000 phenotype 04/16/2015
3 283909 APN Anxa13 0.092 IGL02192 15 58348780 A T exon Het noncoding transcript phenotype 04/16/2015
4 283908 APN Ap2b1 1.000 IGL02192 11 83346766 T552I C T missense Het possibly damaging 0.484 phenotype 04/16/2015
5 283915 APN Cars 1.000 IGL02192 7 143571588 S388G T C missense Het probably damaging 0.999 phenotype 04/16/2015
6 283931 APN Cdh18 0.125 IGL02192 15 23460316 D544V A T missense Het probably damaging 1.000 phenotype 04/16/2015
7 283923 APN Chat 0.643 IGL02192 14 32423322 R377G T C missense Het possibly damaging 0.942 phenotype 04/16/2015
8 283927 APN Col14a1 0.000 IGL02192 15 55362402 T154A A G missense Het unknown phenotype 04/16/2015
9 283920 APN Col9a1 0.147 IGL02192 1 24221987 P311S C T missense Het probably damaging 0.999 phenotype 04/16/2015
10 283937 APN Cpsf3 0.965 IGL02192 12 21310193 G T unclassified Het probably benign phenotype 04/16/2015
11 283938 APN Cpsf3 0.965 IGL02192 12 21310196 G T critical splice acceptor site Het probably null phenotype 04/16/2015
12 283942 APN Dock8 0.091 IGL02192 19 25078205 T C critical splice donor site 2 bp Het probably null phenotype 04/16/2015
13 283895 APN Eml6 0.248 IGL02192 11 29805743 I837T A G missense Het probably benign 0.002 04/16/2015
14 283891 APN Epb41 0.000 IGL02192 4 131929717 T792A T C missense Het probably damaging 0.989 phenotype 04/16/2015
15 283906 APN Exph5 0.000 IGL02192 9 53376325 R1569* A T nonsense Het probably null phenotype 04/16/2015
16 283888 APN F13b 0.000 IGL02192 1 139517333 T574S A T missense Het probably damaging 1.000 phenotype 04/16/2015
17 283928 APN Fam160a1 1.000 IGL02192 3 85673326 L524P A G missense Het possibly damaging 0.820 04/16/2015
18 283904 APN Fam184b 0.000 IGL02192 5 45537720 D727E G T missense Het probably benign 0.001 phenotype 04/16/2015
19 283932 APN Fhod3 1.000 IGL02192 18 25056358 L619P T C missense Het probably damaging 1.000 phenotype 04/16/2015
20 283910 APN Fsd1l 0.595 IGL02192 4 53647754 I66V A G missense Het probably benign 0.000 04/16/2015
21 283929 APN Fv1 0.172 IGL02192 4 147870255 D426G A G missense Het possibly damaging 0.904 phenotype 04/16/2015
22 283902 APN Gm3371 IGL02192 14 44403778 A T unclassified Het probably benign 04/16/2015
23 283899 APN Hnf1a 0.734 IGL02192 5 114960118 S142T A T missense Het probably damaging 0.999 phenotype 04/16/2015
24 283896 APN Itgb3 0.885 IGL02192 11 104643939 I541V A G missense Het probably benign 0.000 phenotype 04/16/2015
25 283912 APN Itgbl1 0.078 IGL02192 14 123843926 C239F G T missense Het probably damaging 1.000 phenotype 04/16/2015
26 283901 APN Krt26 0.057 IGL02192 11 99333645 R349Q C T missense Het probably benign 0.296 phenotype 04/16/2015
27 283918 APN Larp1b 0.000 IGL02192 3 40967494 S116I G T missense Het probably benign 0.010 04/16/2015
28 283935 APN Lmtk3 0.681 IGL02192 7 45794509 A G unclassified Het probably benign phenotype 04/16/2015
29 283884 APN Mapk10 0.000 IGL02192 5 102989647 I235V T C missense Het probably damaging 0.973 phenotype 04/16/2015
30 283940 APN Mctp1 0.000 IGL02192 13 76731768 C T intron Het probably benign 04/16/2015
31 283911 APN Megf8 0.936 IGL02192 7 25353860 D1819N G A missense Het probably damaging 1.000 phenotype 04/16/2015
32 283885 APN Muc6 0.104 IGL02192 7 141637804 T2254A T C missense Het possibly damaging 0.907 phenotype 04/16/2015
33 283892 APN Nbr1 0.000 IGL02192 11 101569591 S444T T A missense Het probably damaging 1.000 phenotype 04/16/2015
34 283914 APN Ncor2 1.000 IGL02192 5 125024237 D1956E A T missense Het probably damaging 0.998 phenotype 04/16/2015
35 283917 APN Ndufaf5 0.457 IGL02192 2 140188743 V183A T C missense Het probably benign 0.010 phenotype 04/16/2015
36 283887 APN Nfasc 1.000 IGL02192 1 132570481 T1155M G A missense Het probably damaging 1.000 phenotype 04/16/2015
37 283924 APN Nol12 0.904 IGL02192 15 78937174 E78G A G missense Het probably damaging 0.996 04/16/2015
38 283930 APN Npy5r 0.131 IGL02192 8 66681346 H265L T A missense Het probably benign 0.024 phenotype 04/16/2015
39 283905 APN Olfr1008 0.076 IGL02192 2 85690128 G233D G A missense Het possibly damaging 0.798 phenotype 04/16/2015
40 283890 APN Olfr418 0.096 IGL02192 1 173270850 L225H T A missense Het probably damaging 1.000 phenotype 04/16/2015
41 283934 APN Pop1 0.951 IGL02192 15 34529071 E749G A G missense Het probably benign 0.083 phenotype 04/16/2015
42 283886 APN Ppil3 0.210 IGL02192 1 58438388 I66V T C missense Het probably damaging 0.974 phenotype 04/16/2015
43 283913 APN Prl4a1 0.111 IGL02192 13 28018571 T43K C A missense Het possibly damaging 0.688 phenotype 04/16/2015
44 283936 APN Prop1 0.649 IGL02192 11 50953286 A G splice site Het probably benign phenotype 04/16/2015
45 283921 APN Qrsl1 0.956 IGL02192 10 43885014 I218N A T missense Het probably damaging 1.000 04/16/2015
46 283933 APN Rbm22 1.000 IGL02192 18 60564412 M63K T A missense Het possibly damaging 0.910 phenotype 04/16/2015
47 283926 APN Rictor 1.000 IGL02192 15 6786414 S1056P T C missense Het probably benign 0.002 phenotype 04/16/2015
48 283894 APN Rps6kb2 0.148 IGL02192 19 4157588 T388A T C missense Het probably damaging 0.996 phenotype 04/16/2015
49 283941 APN Slc7a5 1.000 IGL02192 8 121886390 A G intron Het probably benign phenotype 04/16/2015
50 283916 APN Sp100 0.267 IGL02192 1 85708001 D509V A T missense Het probably damaging 0.990 04/16/2015
51 283944 APN Spata18 0.171 IGL02192 5 73672518 G T splice site 5 bp Het probably null ApcMin allele leads to increased intestinal adenoma and adenocarcinoma tumor incidence and size. This double mutation and homozygous KO of the gene alone results in lower internal mitochondrial cristae density in small intestinal mucosal epithelium. [provided by MGI curators] (source: MGI)">phenotype 04/16/2015
52 283903 APN Sspo 0.000 IGL02192 6 48459568 T1254K C A missense Het possibly damaging 0.860 04/16/2015
53 283943 APN Stk19 0.373 IGL02192 17 34832158 A G unclassified Het probably benign phenotype 04/16/2015
54 283900 APN Taar8b 0.103 IGL02192 10 24091364 I311F T A missense Het probably damaging 1.000 04/16/2015
55 283939 APN Themis2 0.000 IGL02192 4 132783347 C A critical splice donor site 1 bp Het probably null phenotype 04/16/2015
56 283893 APN Tll2 0.736 IGL02192 19 41086263 Y937C T C missense Het possibly damaging 0.726 phenotype 04/16/2015
57 283922 APN Trim34a 0.097 IGL02192 7 104247732 M1K T A start codon destroyed Het probably null 1.000 04/16/2015
58 283907 APN Usp50 1.000 IGL02192 2 126778038 T118I G A missense Het possibly damaging 0.944 04/16/2015
59 283919 APN Vps13d 1.000 IGL02192 4 145148858 S1693F G A missense Het probably benign 0.018 phenotype 04/16/2015
60 283889 APN Vps16 0.959 IGL02192 2 130440932 I467N T A missense Het probably damaging 0.980 phenotype 04/16/2015
61 283925 APN Zfp318 0.000 IGL02192 17 46396810 R265* C T nonsense Het probably null phenotype 04/16/2015
[records 1 to 61 of 61]