Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
5 are Possibly Damaging.
7 are Probably Damaging.
12 are Probably Benign.
3 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 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 91122 APN Abcf3 0.120 IGL01570 G1 16 20559998 S54P T C missense Het probably damaging 1.000 12/09/2013
2 91125 APN Adam5 0.058 IGL01570 G1 8 24810823 V230A A G missense Het probably damaging 0.996 phenotype 12/09/2013
3 91129 APN Arid4b 1.000 IGL01570 G1 13 14186809 T A unclassified Het probably benign phenotype 12/09/2013
4 91128 APN Cep250 0.000 IGL01570 G1 2 155967663 T G splice site Het probably benign phenotype 12/09/2013
5 91109 APN Col28a1 0.077 IGL01570 G1 6 8014540 D955V T A missense Het probably damaging 0.993 phenotype 12/09/2013
6 91115 APN Gm7676 0.176 IGL01570 G1 8 13896311 A G exon Het noncoding transcript 12/09/2013
7 91116 APN Hao1 0.090 IGL01570 G1 2 134554200 S45P A G missense Het probably damaging 0.967 phenotype 12/09/2013
8 91121 APN Hars2 0.937 IGL01570 G1 18 36787592 I163L A T missense Het probably benign 0.035 phenotype 12/09/2013
9 91124 APN Iqgap1 0.000 IGL01570 G1 7 80723061 Y1510C T C missense Het possibly damaging 0.765 phenotype 12/09/2013
10 91130 APN Itga4 1.000 IGL01570 G1 2 79322634 G A critical splice acceptor site Het probably null phenotype 12/09/2013
11 91110 APN Kif18b 1.000 IGL01570 G1 11 102912391 H498Y G A missense Het probably benign 0.041 12/09/2013
12 91114 APN Kin 0.959 IGL01570 G1 2 10091952 T204M C T missense Het probably benign 0.048 phenotype 12/09/2013
13 91127 APN Lmo7 0.249 IGL01570 G1 14 101902371 T C critical splice donor site 2 bp Het probably null phenotype 12/09/2013
14 91118 APN Ltbp2 0.806 IGL01570 G1 12 84794033 T1009I G A missense Het probably benign 0.052 phenotype 12/09/2013
15 91107 APN Mad1l1 1.000 IGL01570 G1 5 140117277 S489P A G missense Het probably benign 0.001 phenotype 12/09/2013
16 91126 APN Memo1 1.000 IGL01570 G1 17 74217108 A G splice site Het probably benign phenotype 12/09/2013
17 91120 APN Myocd 1.000 IGL01570 G1 11 65200807 H103L T A missense Het probably benign 0.003 phenotype 12/09/2013
18 91106 APN Nhlrc2 1.000 IGL01570 G1 19 56574787 F273I T A missense Het possibly damaging 0.874 12/09/2013
19 91105 APN Olfr385 0.142 IGL01570 G1 11 73589383 M118I C A missense Het probably benign 0.345 phenotype 12/09/2013
20 91104 APN Olfr481 0.088 IGL01570 G1 7 108081273 T160S A T missense Het probably benign 0.383 phenotype 12/09/2013
21 91113 APN Olfr978 0.122 IGL01570 G1 9 39994329 I173T T C missense Het probably damaging 0.994 phenotype 12/09/2013
22 91119 APN Pappa2 0.000 IGL01570 G1 1 158814540 Y1315* A C nonsense Het probably null phenotype 12/09/2013
23 91111 APN Pdzk1ip1 0.116 IGL01570 G1 4 115089017 P25S C T missense Het possibly damaging 0.930 12/09/2013
24 91108 APN Ppp2r5d 0.218 IGL01570 G1 17 46687917 V73D A T missense Het possibly damaging 0.638 phenotype 12/09/2013
25 278580 APN Psmg2 0.952 IGL01570 G1 18 67653223 V218I G A missense Het probably benign 0.000 04/16/2015
26 91112 APN Qars 0.963 IGL01570 G1 9 108511539 T266M C T missense Het probably damaging 0.999 12/09/2013
27 91117 APN Slc26a2 0.231 IGL01570 G1 18 61198260 C700G A C missense Het possibly damaging 0.802 phenotype 12/09/2013
28 91123 APN Zfp638 0.876 IGL01570 G1 6 83947847 A724E C A missense Het probably damaging 1.000 phenotype 12/09/2013
[records 1 to 28 of 28]