Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
4 are Possibly Damaging.
10 are Probably Damaging.
10 are Probably Benign.
4 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 28 of 28] 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 1739 APN 1700022I11Rik 0.061 IGL00161 G1 4 42973982 H1105L A T missense Het probably benign 0.403 07/12/2011
2 1410 APN 4930467E23Rik IGL00161 G1 8 19749483 T C splice site Het probably benign 07/12/2011
3 1485 APN Akap13 1.000 IGL00161 G1 7 75725971 V1932E T A missense Het probably damaging 0.994 phenotype 07/12/2011
4 860 APN Alg3 0.246 IGL00161 G1 16 20607858 V211A A G missense Het probably damaging 0.963 phenotype 07/12/2011
5 1276 APN Bsn 0.418 IGL00161 G1 9 108115110 T1148A T C missense Het probably benign 0.006 phenotype 07/12/2011
6 1435 APN Dmbt1 0.256 IGL00161 G1 7 131109628 D1538Y G T missense Het probably damaging 0.999 phenotype 07/12/2011
7 306577 APN Fbxl20 0.257 IGL00161 G1 11 98090674 G396D C T missense Het possibly damaging 0.696 phenotype 04/16/2015
8 688 APN Gsto2 0.000 IGL00161 G1 19 47874967 D94G A G missense Het probably damaging 1.000 phenotype 07/12/2011
9 832 APN Igf2r 0.902 IGL00161 G1 17 12713990 I882V T C missense Het probably benign 0.012 phenotype 07/12/2011
10 763 APN Ltbp1 1.000 IGL00161 G1 17 75310152 C T splice site Het probably benign phenotype 07/12/2011
11 306576 APN Men1 1.000 IGL00161 G1 19 6337207 G A intron 1593 bp Het probably null phenotype 04/16/2015
12 306578 APN Nlrp1b 0.078 IGL00161 G1 11 71181181 A C intron Het probably benign phenotype 04/16/2015
13 809 APN Notch3 0.000 IGL00161 G1 17 32158114 C272* A T nonsense Het probably null phenotype 07/12/2011
14 1871 APN Olfr1230 0.088 IGL00161 G1 2 89296455 C272R A G missense Het probably benign 0.397 phenotype 07/12/2011
15 1324 APN Olfr943 0.074 IGL00161 G1 9 39185092 K305E A G missense Het possibly damaging 0.933 phenotype 07/12/2011
16 1352 APN Pard3 1.000 IGL00161 G1 8 127359818 A G splice site Het probably benign phenotype 07/12/2011
17 1233 APN Pcsk4 0.000 IGL00161 G1 10 80322823 Y532H A G missense Het probably damaging 1.000 phenotype 07/12/2011
18 306579 APN Pkd1l1 1.000 IGL00161 G1 11 8929353 A G critical splice donor site 2 bp Het probably null phenotype 04/16/2015
19 1818 APN Prex1 0.318 IGL00161 G1 2 166638401 Y140H A G missense Het probably damaging 1.000 phenotype 07/12/2011
20 1028 APN Ptpdc1 0.000 IGL00161 G1 13 48587058 R238Q C T missense Het possibly damaging 0.804 phenotype 07/12/2011
21 1314 APN Rdx 0.000 IGL00161 G1 9 52086346 D540G A G missense Het probably damaging 1.000 phenotype 07/12/2011
22 968 APN Rnase10 0.000 IGL00161 G1 14 51009781 D168E T G missense Het possibly damaging 0.910 phenotype 07/12/2011
23 994 APN Slc30a5 0.439 IGL00161 G1 13 100806666 D561E A C missense Het probably damaging 0.998 phenotype 07/12/2011
24 930 APN Spag1 0.617 IGL00161 G1 15 36195416 R252* C T nonsense Het probably null phenotype 07/12/2011
25 1242 APN Stox1 0.239 IGL00161 G1 10 62667913 E121G T C missense Het probably damaging 0.999 phenotype 07/12/2011
26 1486 APN Synm 0.000 IGL00161 G1 7 67734915 M558V T C missense Het probably benign 0.006 0.090 phenotype 07/12/2011
27 1184 APN Tenm2 0.603 IGL00161 G1 11 36206899 C T splice site Het probably benign phenotype 07/12/2011
28 1538 APN Vmn1r64 0.055 IGL00161 G1 7 5883828 T239A T C missense Het probably damaging 0.981 07/12/2011
[records 1 to 28 of 28]