Incidental Mutations

37 incidental mutations are currently displayed, and affect 37 genes.
6 are Possibly Damaging.
15 are Probably Damaging.
14 are Probably Benign.
2 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 37 of 37] 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 412783 APN Abcb1b 0.385 IGL03195 5 8853607 D1086G A G missense Het possibly damaging 0.835 phenotype 08/02/2016
2 412799 APN Ahcyl2 0.808 IGL03195 6 29906769 T C splice site Het probably benign phenotype 08/02/2016
3 412774 APN Ankrd42 0.059 IGL03195 7 92591858 Q431L T A missense Het probably benign 0.332 08/02/2016
4 412767 APN Arhgap12 0.000 IGL03195 18 6031766 F592I A T missense Het probably damaging 1.000 phenotype 08/02/2016
5 412797 APN Arhgef28 0.000 IGL03195 13 97951563 A G splice site 6 bp Het probably null phenotype 08/02/2016
6 412778 APN Boc 0.000 IGL03195 16 44492821 F560S A G missense Het probably damaging 0.993 phenotype 08/02/2016
7 412780 APN Ccdc81 0.102 IGL03195 7 89896708 V96E A T missense Het probably benign 0.047 08/02/2016
8 412781 APN Cep162 0.152 IGL03195 9 87225786 S517N C T missense Het probably benign 0.001 08/02/2016
9 412766 APN Cntnap5a 0.000 IGL03195 1 116157448 N372S A G missense Het probably benign 0.003 phenotype 08/02/2016
10 412772 APN Dnah7a 0.132 IGL03195 1 53419607 R3791C G A missense Het probably damaging 1.000 08/02/2016
11 412792 APN Fdxr 0.941 IGL03195 11 115276092 Q57R T C missense Het probably benign 0.294 phenotype 08/02/2016
12 412798 APN G3bp2 1.000 IGL03195 5 92068508 A G splice site Het probably benign 08/02/2016
13 412775 APN Gm595 0.057 IGL03195 X 48872948 Q296L T A missense Het possibly damaging 0.787 08/02/2016
14 412794 APN Hmcn1 0.000 IGL03195 1 150802909 T487I G A missense Het probably benign 0.060 phenotype 08/02/2016
15 412787 APN Kpna7 0.449 IGL03195 5 144997037 I282N A T missense Het probably damaging 0.998 phenotype 08/02/2016
16 412791 APN Lif 0.383 IGL03195 11 4269201 Y160F A T missense Het probably damaging 0.999 phenotype 08/02/2016
17 412769 APN Lrp1b 0.000 IGL03195 2 41471122 D556E A T missense Het possibly damaging 0.948 phenotype 08/02/2016
18 412786 APN Myom2 0.105 IGL03195 8 15111844 E954* G T nonsense Het probably null phenotype 08/02/2016
19 412776 APN Nr6a1 1.000 IGL03195 2 38742936 I171N A T missense Het probably damaging 1.000 phenotype 08/02/2016
20 412788 APN Nup210 0.000 IGL03195 6 91015850 R1059L C A missense Het probably benign 0.317 phenotype 08/02/2016
21 412768 APN Olfr1109 0.078 IGL03195 2 87092569 V276E A T missense Het probably damaging 0.995 phenotype 08/02/2016
22 412779 APN Olfr225 0.055 IGL03195 11 59613803 V280M G A missense Het probably damaging 0.999 08/02/2016
23 412764 APN Olfr698 0.078 IGL03195 7 106752773 I205T A G missense Het probably benign 0.000 phenotype 08/02/2016
24 412765 APN Olfr743 0.078 IGL03195 14 50533420 T3A A G missense Het probably benign 0.000 phenotype 08/02/2016
25 412770 APN Olfr987 0.064 IGL03195 2 85331520 I126N A T missense Het probably damaging 1.000 phenotype 08/02/2016
26 412782 APN Ostm1 0.308 IGL03195 10 42698217 V302A T C missense Het probably damaging 0.997 phenotype 08/02/2016
27 412771 APN Oxct1 1.000 IGL03195 15 4101189 M388V A G missense Het possibly damaging 0.505 phenotype 08/02/2016
28 412784 APN Ppp6r2 0.168 IGL03195 15 89268555 V300I G A missense Het possibly damaging 0.502 phenotype 08/02/2016
29 412789 APN Prmt1 1.000 IGL03195 7 44977571 Y205C T C missense Het probably damaging 0.982 phenotype 08/02/2016
30 412796 APN Slc45a4 0.000 IGL03195 15 73584423 V636G A C missense Het possibly damaging 0.889 08/02/2016
31 412777 APN Spata18 0.173 IGL03195 5 73671248 L270Q T A missense Het probably damaging 1.000 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 08/02/2016
32 412795 APN Stard9 0.146 IGL03195 2 120705802 D4151N G A missense Het probably damaging 0.999 08/02/2016
33 412790 APN Thsd7b 0.125 IGL03195 1 129628909 C334Y G A missense Het probably damaging 1.000 08/02/2016
34 412773 APN Tmtc3 0.769 IGL03195 10 100459034 V406M C T missense Het probably benign 0.003 phenotype 08/02/2016
35 412793 APN Trpc5 0.000 IGL03195 X 144382728 M900L T A missense Het probably benign 0.000 phenotype 08/02/2016
36 412785 APN Ttc9c 0.101 IGL03195 19 8815980 K99E T C missense Het probably benign 0.310 08/02/2016
37 412763 APN Vmn1r73 0.067 IGL03195 7 11757080 E275G A G missense Het probably damaging 1.000 08/02/2016
[records 1 to 37 of 37]