Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
6 are Possibly Damaging.
8 are Probably Damaging.
13 are Probably Benign.
2 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] 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 155648 APN 1700019D03Rik 0.047 IGL01805 G1 1 52925518 D17G T C missense Het possibly damaging 0.522 02/04/2014
2 155640 APN Adam28 0.140 IGL01805 G1 14 68642091 S169R G T missense Het probably benign 0.095 phenotype 02/04/2014
3 155645 APN Aox1 0.000 IGL01805 G1 1 58081513 M855T T C missense Het possibly damaging 0.944 phenotype 02/04/2014
4 155656 APN Apc 0.971 IGL01805 G1 18 34318218 N2688K C A missense Het probably benign 0.023 phenotype 02/04/2014
5 155657 APN Arhgap23 0.000 IGL01805 G1 11 97492602 T A intron Het probably benign phenotype 02/04/2014
6 155658 APN Bpifa6 0.061 IGL01805 G1 2 153984912 T66A A G missense Het probably benign 0.026 02/04/2014
7 155647 APN C1qtnf1 0.000 IGL01805 G1 11 118448167 L221Q T A missense Het probably damaging 1.000 phenotype 02/04/2014
8 155664 APN Ccdc175 0.056 IGL01805 G1 12 72129229 T A splice site Het probably benign 02/04/2014
9 155655 APN Ccl1 0.079 IGL01805 G1 11 82178132 M26I C A missense Het possibly damaging 0.877 phenotype 02/04/2014
10 155662 APN D17Wsu92e 0.000 IGL01805 G1 17 27767906 C T splice site Het probably benign 02/04/2014
11 155642 APN Dnah10 0.000 IGL01805 G1 5 124783921 F2123I T A missense Het probably damaging 1.000 phenotype 02/04/2014
12 155641 APN Dpcr1 0.049 IGL01805 G1 17 35637643 T355S T A missense Het possibly damaging 0.617 02/04/2014
13 155661 APN Fancm 0.935 IGL01805 G1 12 65113861 T C critical splice donor site 2 bp Het probably null phenotype 02/04/2014
14 155644 APN Fstl4 0.155 IGL01805 G1 11 53186357 A647E C A missense Het probably damaging 1.000 phenotype 02/04/2014
15 155660 APN Hmgb4 0.135 IGL01805 G1 4 128260222 G T intron Het probably benign 02/04/2014
16 155665 APN Hr 0.000 IGL01805 G1 14 70565297 A T splice site Het probably benign phenotype 02/04/2014
17 155643 APN Kcna4 0.000 IGL01805 G1 2 107296498 V526L G T missense Het probably damaging 0.996 phenotype 02/04/2014
18 155654 APN Mas1 0.000 IGL01805 G1 17 12842230 Y102C T C missense Het probably damaging 1.000 phenotype 02/04/2014
19 155646 APN Mul1 0.000 IGL01805 G1 4 138439663 P343S C T missense Het possibly damaging 0.696 02/04/2014
20 155652 APN Obscn 0.720 IGL01805 G1 11 59132596 S652G T C missense Het probably damaging 0.992 phenotype 02/04/2014
21 155639 APN Olfr972 0.000 IGL01805 G1 9 39873779 F168S T C missense Het probably damaging 0.998 phenotype 02/04/2014
22 155650 APN Pjvk 0.127 IGL01805 G1 2 76657514 N250I A T missense Het probably benign 0.110 phenotype 02/04/2014
23 155649 APN Pkd2 1.000 IGL01805 G1 5 104483093 I461T T C missense Het probably benign 0.406 phenotype 02/04/2014
24 155663 APN Psen2 0.000 IGL01805 G1 1 180229838 T C splice site 4 bp Het probably null phenotype 02/04/2014
25 155637 APN Ralb 0.000 IGL01805 G1 1 119475995 E81G T C missense Het probably benign 0.028 phenotype 02/04/2014
26 155651 APN Slc15a4 0.073 IGL01805 G1 5 127608836 T261A T C missense Het possibly damaging 0.911 phenotype 02/04/2014
27 155638 APN Vmn2r77 0.079 IGL01805 G1 7 86811187 V574M G A missense Het probably benign 0.178 02/04/2014
28 155653 APN Xrn2 0.967 IGL01805 G1 2 147028143 I251V A G missense Het probably damaging 0.979 phenotype 02/04/2014
29 155659 APN Zfp974 0.061 IGL01805 G1 7 27912264 G A splice site Het probably benign 02/04/2014
[records 1 to 29 of 29]