Incidental Mutations

36 incidental mutations are currently displayed, and affect 35 genes.
9 are Possibly Damaging.
12 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 36 of 36] 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 406760 APN Akr1e1 0.147 IGL02987 13 4593592 D222G T C missense Het probably damaging 0.966 phenotype 08/02/2016
2 406771 APN Apbb1ip 0.000 IGL02987 2 22867637 Y422* T A nonsense Het probably null phenotype 08/02/2016
3 406756 APN Asf1a IGL02987 10 53597271 F28L T C missense Het probably damaging 1.000 phenotype 08/02/2016
4 406778 APN Atp6v1c1 0.870 IGL02987 15 38690562 M319K T A missense Het possibly damaging 0.699 phenotype 08/02/2016
5 406774 APN Bsn 0.287 IGL02987 9 108126304 S301P A G missense Het probably benign 0.030 phenotype 08/02/2016
6 406752 APN Cds1 0.230 IGL02987 5 101812525 I281V A G missense Het possibly damaging 0.853 phenotype 08/02/2016
7 406780 APN Col4a4 0.318 IGL02987 1 82498925 T C splice site Het probably benign phenotype 08/02/2016
8 406766 APN Coq2 0.773 IGL02987 5 100663688 Q103* G A nonsense Het probably null phenotype 08/02/2016
9 406782 APN Dgkh 0.161 IGL02987 14 78589872 A G critical splice donor site 2 bp Het probably null phenotype 08/02/2016
10 406776 APN Dnah9 0.659 IGL02987 11 65841273 R4269L C A missense Het probably benign 0.235 phenotype 08/02/2016
11 406767 APN Dnah9 0.659 IGL02987 11 65855272 I4005T A G missense Het probably damaging 0.981 phenotype 08/02/2016
12 406753 APN F2rl1 0.000 IGL02987 13 95514233 Q47L T A missense Het probably benign 0.001 phenotype 08/02/2016
13 406763 APN Fhod3 0.419 IGL02987 18 25113553 V1272A T C missense Het possibly damaging 0.873 phenotype 08/02/2016
14 406779 APN Gdpd4 0.075 IGL02987 7 97961551 T C splice site Het probably benign 08/02/2016
15 406755 APN Gfral 0.090 IGL02987 9 76197301 V143A A G missense Het possibly damaging 0.821 phenotype 08/02/2016
16 406769 APN Gltp 0.212 IGL02987 5 114674182 F88V A C missense Het probably benign 0.317 phenotype 08/02/2016
17 406759 APN Hectd1 1.000 IGL02987 12 51744767 K2565T T G missense Het probably damaging 1.000 phenotype 08/02/2016
18 406764 APN Jade2 0.526 IGL02987 11 51830481 S207P A G missense Het probably damaging 1.000 08/02/2016
19 406773 APN Khdc3 0.174 IGL02987 9 73102666 I53V A G missense Het possibly damaging 0.559 phenotype 08/02/2016
20 406748 APN Lce1a1 IGL02987 3 92647102 T22A T C missense Het unknown 08/02/2016
21 406765 APN Lgals9 0.072 IGL02987 11 78967477 H196Q A T missense Het possibly damaging 0.926 phenotype 08/02/2016
22 406750 APN Lrrc37a 0.141 IGL02987 11 103500413 N1395K A T missense Het probably benign 0.032 08/02/2016
23 406758 APN Mast1 0.492 IGL02987 8 84925719 V268I C T missense Het possibly damaging 0.754 08/02/2016
24 406770 APN Myh11 1.000 IGL02987 16 14232532 E523A T G missense Het probably damaging 0.996 phenotype 08/02/2016
25 406781 APN Napb 0.146 IGL02987 2 148697511 T C splice site Het probably null phenotype 08/02/2016
26 406751 APN Nlrp4e 0.000 IGL02987 7 23301433 R51H G A missense Het probably damaging 1.000 08/02/2016
27 406747 APN Ola1 0.628 IGL02987 2 73156898 D130G T C missense Het probably benign 0.031 phenotype 08/02/2016
28 406775 APN Olfr891 0.064 IGL02987 9 38180623 S67T A T missense Het possibly damaging 0.888 phenotype 08/02/2016
29 406757 APN Pard3 1.000 IGL02987 8 127389491 C687Y G A missense Het probably damaging 0.977 phenotype 08/02/2016
30 406768 APN Rassf9 0.137 IGL02987 10 102545248 T164A A G missense Het possibly damaging 0.595 phenotype 08/02/2016
31 406754 APN Sema3a 0.852 IGL02987 5 13565896 Y429C A G missense Het probably damaging 1.000 phenotype 08/02/2016
32 406777 APN Slc25a54 0.266 IGL02987 3 109116337 V416A T C missense Het probably benign 0.000 08/02/2016
33 406761 APN Slc30a5 0.280 IGL02987 13 100803915 T631A T C missense Het probably damaging 0.998 phenotype 08/02/2016
34 406762 APN Sorl1 0.583 IGL02987 9 42041053 C736S A T missense Het probably damaging 1.000 phenotype 08/02/2016
35 406749 APN Tet3 0.368 IGL02987 6 83368092 S1788T A T missense Het probably damaging 0.993 phenotype 08/02/2016
36 406772 APN Trim42 0.098 IGL02987 9 97365815 V276A A G missense Het probably benign 0.276 phenotype 08/02/2016
[records 1 to 36 of 36]