Incidental Mutations

44 incidental mutations are currently displayed, and affect 44 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
18 are Probably Benign.
6 are Probably Null.
1 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 44 of 44] 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 409878 APN Abca3 1.000 IGL03118 17 24400450 G921S G A missense Het probably benign 0.174 phenotype 08/02/2016
2 409865 APN Abca8b 0.000 IGL03118 11 109947181 T1082A T C missense Het possibly damaging 0.659 phenotype 08/02/2016
3 409890 APN AF366264 0.543 IGL03118 8 13838096 C T utr 5 prime Het probably benign 08/02/2016
4 409894 APN B9d2 1.000 IGL03118 7 25681476 T C critical splice donor site 2 bp Het probably null phenotype 08/02/2016
5 409855 APN Bfsp1 0.198 IGL03118 2 143827333 E442G T C missense Het possibly damaging 0.942 phenotype 08/02/2016
6 409893 APN Bpifb5 0.000 IGL03118 2 154236753 C T splice site Het probably benign 08/02/2016
7 409873 APN Ccl1 0.090 IGL03118 11 82178070 I47T A G missense Het probably damaging 1.000 phenotype 08/02/2016
8 409867 APN Cln3 0.000 IGL03118 7 126575397 I285V T C missense Het probably null 0.002 phenotype 08/02/2016
9 409852 APN Cyp4a12b 0.054 IGL03118 4 115432976 R242I G T missense Het possibly damaging 0.536 08/02/2016
10 409856 APN Dcc 1.000 IGL03118 18 71420273 T771A T C missense Het probably benign 0.001 phenotype 08/02/2016
11 409868 APN Erbb4 1.000 IGL03118 1 68042719 D1052G T C missense Het probably benign 0.106 phenotype 08/02/2016
12 409881 APN Fcnb 0.000 IGL03118 2 28076618 N301S T C missense Het probably benign 0.061 phenotype 08/02/2016
13 409871 APN Gm28043 IGL03118 17 29634731 E403A A C missense Het probably damaging 1.000 phenotype 08/02/2016
14 409892 APN Gria4 0.638 IGL03118 9 4793804 A G splice site Het probably benign phenotype 08/02/2016
15 409851 APN Ighv5-12 IGL03118 12 113702578 M1L T A start codon destroyed Het probably benign 0.008 08/02/2016
16 409891 APN Il17rd 0.000 IGL03118 14 27093395 A G critical splice acceptor site Het probably null phenotype 08/02/2016
17 409857 APN Kcnn3 0.432 IGL03118 3 89667161 L660Q T A missense Het probably damaging 1.000 phenotype 08/02/2016
18 409869 APN Lcor 0.253 IGL03118 19 41558369 P131S C T missense Het probably damaging 0.985 phenotype 08/02/2016
19 409872 APN Leng1 0.600 IGL03118 7 3665410 N13S T C missense Het probably damaging 1.000 08/02/2016
20 409877 APN Loxhd1 0.202 IGL03118 18 77380464 V827A T C missense Het probably damaging 1.000 phenotype 08/02/2016
21 409860 APN Mapk13 0.215 IGL03118 17 28777735 Y208C A G missense Het probably benign 0.138 phenotype 08/02/2016
22 409862 APN Mybpc3 0.717 IGL03118 2 91124503 V453A T C missense Het probably damaging 0.997 phenotype 08/02/2016
23 409859 APN Odam 0.092 IGL03118 5 87885754 S15P T C missense Het unknown 08/02/2016
24 409853 APN Olfr26 0.067 IGL03118 9 38855230 H56L A T missense Het probably damaging 0.999 phenotype 08/02/2016
25 409882 APN Olfr323 0.088 IGL03118 11 58625443 V201D A T missense Het probably damaging 0.993 phenotype 08/02/2016
26 409888 APN Pcdhb19 0.059 IGL03118 18 37499565 T C intron Het probably benign phenotype 08/02/2016
27 409886 APN Per2 0.309 IGL03118 1 91444619 Y244* G T nonsense Het probably null phenotype 08/02/2016
28 409880 APN Pik3ca 1.000 IGL03118 3 32459935 I857F A T missense Het probably damaging 0.998 phenotype 08/02/2016
29 409876 APN Pold1 0.973 IGL03118 7 44539400 I447F T A missense Het probably benign 0.175 phenotype 08/02/2016
30 409879 APN Ppm1f 1.000 IGL03118 16 16914078 W131R T A missense Het probably null 0.032 phenotype 08/02/2016
31 409870 APN Ppp2r2c 0.371 IGL03118 5 36926316 Y67C A G missense Het probably damaging 1.000 phenotype 08/02/2016
32 409875 APN Psmb10 0.392 IGL03118 8 105936900 H155Q A T missense Het probably damaging 0.998 phenotype 08/02/2016
33 409885 APN Ptbp3 0.291 IGL03118 4 59501470 A149V G A missense Het probably benign 0.031 phenotype 08/02/2016
34 409864 APN Pygb 0.223 IGL03118 2 150820811 V566E T A missense Het probably benign 0.015 phenotype 08/02/2016
35 409884 APN Rictor 1.000 IGL03118 15 6759518 R205Q G A missense Het possibly damaging 0.932 phenotype 08/02/2016
36 409863 APN Ryr1 1.000 IGL03118 7 29015786 R4638W T A missense Het unknown phenotype 08/02/2016
37 409887 APN Sept3 0.100 IGL03118 15 82284514 G A splice site 5 bp Het probably null phenotype 08/02/2016
38 409858 APN Serpina3b 0.059 IGL03118 12 104131054 D198V A T missense Het probably benign 0.215 08/02/2016
39 409866 APN Slc27a6 0.049 IGL03118 18 58556743 H94N C A missense Het probably benign 0.001 phenotype 08/02/2016
40 409883 APN Taf2 1.000 IGL03118 15 55052163 V456M C T missense Het probably damaging 1.000 phenotype 08/02/2016
41 409854 APN Tbpl2 0.372 IGL03118 2 24087289 E238G T C missense Het probably benign 0.225 phenotype 08/02/2016
42 409874 APN Ttn 1.000 IGL03118 2 76754207 V20440I C T missense Het possibly damaging 0.837 phenotype 08/02/2016
43 409889 APN Zfp638 0.882 IGL03118 6 83935018 T A splice site Het probably benign phenotype 08/02/2016
44 409861 APN Zfp865 0.127 IGL03118 7 5034645 T C intron Het probably benign 08/02/2016
[records 1 to 44 of 44]