Incidental Mutations

33 incidental mutations are currently displayed, and affect 32 genes.
2 are Possibly Damaging.
13 are Probably Damaging.
10 are Probably Benign.
5 are Probably Null.
3 create premature stop codons.
2 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 104977 APN 4932438A13Rik 1.000 IGL01717 G1 3 37034736 S4112G A G missense Het probably benign 0.000 phenotype 01/21/2014
2 104980 APN Aif1 0.319 IGL01717 G1 17 35171555 M73K A T missense Het probably damaging 0.997 phenotype 01/21/2014
3 104982 APN Alk 0.185 IGL01717 G1 17 72603382 I110V T C missense Het probably benign 0.000 phenotype 01/21/2014
4 104961 APN Aoah 0.000 IGL01717 G1 13 20999977 S404P T C missense Het probably damaging 0.986 phenotype 01/21/2014
5 104979 APN Bhlhe41 0.265 IGL01717 G1 6 145863037 S350P A G missense Het possibly damaging 0.930 phenotype 01/21/2014
6 104965 APN Capn12 0.000 IGL01717 G1 7 28889105 D540G A G missense Het probably benign 0.000 phenotype 01/21/2014
7 104964 APN Chd6 0.739 IGL01717 G1 2 160965259 Y2012H A G missense Het possibly damaging 0.956 phenotype 01/21/2014
8 104974 APN Col1a1 1.000 IGL01717 G1 11 94950777 T1284A A G missense Het unknown phenotype 01/21/2014
9 104986 APN Col24a1 0.000 IGL01717 G1 3 145524263 T C splice site Het probably benign phenotype 01/21/2014
10 104983 APN Col4a5 IGL01717 G1 X 141639238 V1070D T A missense Het unknown phenotype 01/21/2014
11 104975 APN Col6a5 0.887 IGL01717 G1 9 105940273 T280A T C missense Het unknown phenotype 01/21/2014
12 104970 APN Dicer1 1.000 IGL01717 G1 12 104702787 L1212* A T nonsense Het probably null phenotype 01/21/2014
13 104963 APN Gigyf1 0.440 IGL01717 G1 5 137525691 V1041E T A missense Het probably damaging 0.999 01/21/2014
14 104972 APN Gm4978 IGL01717 G1 9 69450873 C T unclassified Het probably benign 01/21/2014
15 104988 APN Gnai1 0.000 IGL01717 G1 5 18291461 A G critical splice donor site 2 bp Het probably null phenotype 01/21/2014
16 104981 APN Golgb1 0.812 IGL01717 G1 16 36915502 R1704* C T nonsense Het probably null phenotype 01/21/2014
17 104991 APN Incenp 1.000 IGL01717 G1 19 9893265 A G splice site Het probably benign phenotype 01/21/2014
18 104989 APN Lrrc39 0.525 IGL01717 G1 3 116579497 A T unclassified Het probably benign 01/21/2014
19 104978 APN Man2a2 0.326 IGL01717 G1 7 80367365 K319E T C missense Het probably damaging 1.000 phenotype 01/21/2014
20 104969 APN Neb 0.785 IGL01717 G1 2 52189867 D83G T C missense Het probably damaging 1.000 phenotype 01/21/2014
21 104968 APN Osbpl6 0.479 IGL01717 G1 2 76588594 I732T T C missense Het probably damaging 0.997 phenotype 01/21/2014
22 104976 APN Pacs1 0.000 IGL01717 G1 19 5167972 K130N T A missense Het probably damaging 0.999 phenotype 01/21/2014
23 104990 APN Pappa2 0.000 IGL01717 G1 1 158857132 A G critical splice donor site 2 bp Het probably null phenotype 01/21/2014
24 104967 APN Pole2 1.000 IGL01717 G1 12 69213849 M186V T C missense Het probably damaging 0.999 phenotype 01/21/2014
25 104987 APN Rwdd4a 0.110 IGL01717 G1 8 47544105 T C splice site Het probably benign 01/21/2014
26 104966 APN Sel1l3 0.000 IGL01717 G1 5 53200168 Y161H A G missense Het probably damaging 0.988 01/21/2014
27 104984 APN Sf3a2 0.963 IGL01717 G1 10 80804692 Q446* C T nonsense Het probably null 01/21/2014
28 104971 APN Slc26a3 0.547 IGL01717 G1 12 31463477 I466T T C missense Het probably benign 0.111 phenotype 01/21/2014
29 104962 APN Slc29a4 0.000 IGL01717 G1 5 142718746 I348F A T missense Het probably damaging 0.997 0.913 phenotype 01/21/2014
30 104985 APN Tbl1xr1 0.841 IGL01717 G1 3 22193171 A G splice site Het probably benign phenotype 01/21/2014
31 104973 APN Tlr5 0.198 IGL01717 G1 1 182975398 I756F A T missense Het probably damaging 0.997 phenotype 01/21/2014
32 278793 APN Ttn 1.000 IGL01717 G1 2 76730402 L29218F T A missense Het probably damaging 1.000 phenotype 04/16/2015
33 278794 APN Ttn 1.000 IGL01717 G1 2 76730404 L29218I A T missense Het probably damaging 0.999 phenotype 04/16/2015
[records 1 to 33 of 33]