Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
6 are Possibly Damaging.
10 are Probably Damaging.
16 are Probably Benign.
2 are Probably Null.
0 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 35 of 35] 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 364655 APN Akap13 1.000 IGL02944 7 75608657 Q343R A G missense Het probably benign 0.000 phenotype 12/18/2015
2 364654 APN Antxr1 0.000 IGL02944 6 87188159 N432I T A missense Het possibly damaging 0.929 phenotype 12/18/2015
3 364670 APN Arhgap15 0.347 IGL02944 2 44142350 T C critical splice donor site 2 bp Het probably null phenotype 12/18/2015
4 364672 APN Atp6v1h 0.912 IGL02944 1 5093355 T A splice site Het probably benign phenotype 12/18/2015
5 364642 APN Cav2 0.252 IGL02944 6 17281457 Y33H T C missense Het probably damaging 0.993 phenotype 12/18/2015
6 364666 APN Ccdc175 0.026 IGL02944 12 72117893 D585V T A missense Het probably benign 0.016 12/18/2015
7 364644 APN Coro7 0.132 IGL02944 16 4635412 D271G T C missense Het probably benign 0.143 phenotype 12/18/2015
8 364657 APN Cylc1 IGL02944 X 111123604 D551E T A missense Het possibly damaging 0.911 12/18/2015
9 364652 APN Dnah1 0.000 IGL02944 14 31300871 I1103N A T missense Het possibly damaging 0.877 phenotype 12/18/2015
10 364659 APN Gm44 IGL02944 X 90892262 K41E A G missense Het probably benign 0.001 12/18/2015
11 364662 APN Gmds 1.000 IGL02944 13 32338452 Y11F T A missense Het probably benign 0.000 phenotype 12/18/2015
12 364658 APN Igkv13-54-1 0.087 IGL02944 6 69617390 C T exon Het noncoding transcript 12/18/2015
13 364656 APN Irf8 0.000 IGL02944 8 120755125 T318A A G missense Het probably benign 0.002 phenotype 12/18/2015
14 364671 APN Lrrc40 0.125 IGL02944 3 158041665 G A intron Het probably benign 12/18/2015
15 364645 APN Mbd1 0.000 IGL02944 18 74277410 G428E G A missense Het probably damaging 1.000 phenotype 12/18/2015
16 364669 APN Myom2 0.222 IGL02944 8 15104065 A T critical splice acceptor site Het probably null phenotype 12/18/2015
17 364661 APN Nav2 0.714 IGL02944 7 49420256 R287W C T missense Het probably damaging 0.993 phenotype 12/18/2015
18 364649 APN Nfs1 0.975 IGL02944 2 156127768 D320N C T missense Het probably damaging 1.000 phenotype 12/18/2015
19 364653 APN Nlrp9a 0.100 IGL02944 7 26558651 T565S A T missense Het probably benign 0.284 12/18/2015
20 364664 APN Nod1 0.000 IGL02944 6 54924947 I951N A T missense Het possibly damaging 0.675 phenotype 12/18/2015
21 364648 APN Olfr353 0.229 IGL02944 2 36890788 E20A T G missense Het possibly damaging 0.835 phenotype 12/18/2015
22 364639 APN Olfr675 0.225 IGL02944 7 105024923 L19P A G missense Het probably damaging 0.999 phenotype 12/18/2015
23 364640 APN Olfr694 0.084 IGL02944 7 106689269 L154P A G missense Het probably damaging 0.997 phenotype 12/18/2015
24 364638 APN Olfr924 0.074 IGL02944 9 38848752 I213F A T missense Het possibly damaging 0.878 phenotype 12/18/2015
25 364660 APN Pkhd1l1 0.253 IGL02944 15 44501531 Y689H T C missense Het probably damaging 1.000 12/18/2015
26 364643 APN Ppp2r5c 0.259 IGL02944 12 110567800 I366V A G missense Het probably benign 0.016 phenotype 12/18/2015
27 364665 APN Ppp3cb 0.000 IGL02944 14 20528235 Y149C T C missense Het probably damaging 1.000 phenotype 12/18/2015
28 364651 APN Prdm1 1.000 IGL02944 10 44441811 S354G T C missense Het probably benign 0.000 phenotype 12/18/2015
29 364667 APN Ralgapa1 0.796 IGL02944 12 55757951 Q520L T A missense Het probably benign 0.009 phenotype 12/18/2015
30 364663 APN Slc25a54 0.275 IGL02944 3 109080615 Y24F A T missense Het probably benign 0.137 12/18/2015
31 364650 APN Slfn3 0.000 IGL02944 11 83213011 V236E T A missense Het probably damaging 0.986 phenotype 12/18/2015
32 364668 APN Syt6 0.120 IGL02944 3 103575549 A G unclassified Het probably benign phenotype 12/18/2015
33 364641 APN Trim30a 0.079 IGL02944 7 104435777 N75K G T missense Het probably benign 0.194 phenotype 12/18/2015
34 364647 APN Vmn1r175 0.081 IGL02944 7 23809166 E12G T C missense Het probably damaging 0.972 12/18/2015
35 364646 APN Xylt1 0.253 IGL02944 7 117634757 T504S A T missense Het probably benign 0.001 phenotype 12/18/2015
[records 1 to 35 of 35]