Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
7 are Possibly Damaging.
10 are Probably Damaging.
11 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
1 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 406444 APN 2810004N23Rik 0.531 IGL02977 8 124861191 V57M C T missense Het probably benign 0.012 08/02/2016
2 406427 APN 4933440M02Rik 0.077 IGL02977 7 125331702 T A unclassified Het noncoding transcript 08/02/2016
3 406430 APN 9530053A07Rik 0.120 IGL02977 7 28164372 T2523M C T missense Het possibly damaging 0.827 08/02/2016
4 406435 APN Bmp5 0.388 IGL02977 9 75893799 T404A A G missense Het probably damaging 1.000 phenotype 08/02/2016
5 406434 APN Cep192 0.000 IGL02977 18 67852905 V1660A T C missense Het probably damaging 0.968 08/02/2016
6 406419 APN Csmd2 0.324 IGL02977 4 128493276 Y2121* C A nonsense Het probably null 08/02/2016
7 406443 APN Daam1 1.000 IGL02977 12 71944172 A187T G A missense Het unknown phenotype 08/02/2016
8 406437 APN Dnaja4 0.000 IGL02977 9 54714510 L343P T C missense Het possibly damaging 0.933 08/02/2016
9 406445 APN Dym 0.000 IGL02977 18 75063175 T C critical splice donor site 2 bp Het probably null phenotype 08/02/2016
10 406416 APN F5 1.000 IGL02977 1 164194021 D1355V A T missense Het probably damaging 0.995 phenotype 08/02/2016
11 406423 APN Gcnt1 0.000 IGL02977 19 17329374 I329N A T missense Het probably damaging 1.000 phenotype 08/02/2016
12 406436 APN Gm10110 0.221 IGL02977 14 89897332 T C exon Het noncoding transcript 08/02/2016
13 406441 APN Hdgfl2 0.200 IGL02977 17 56099319 N569S A G missense Het possibly damaging 0.707 phenotype 08/02/2016
14 406432 APN Hivep1 0.717 IGL02977 13 42155936 S551P T C missense Het possibly damaging 0.938 phenotype 08/02/2016
15 406446 APN Hpse2 0.252 IGL02977 19 42789122 G A splice site Het probably benign phenotype 08/02/2016
16 406424 APN Hspe1 0.967 IGL02977 1 55091073 Y88H T C missense Het probably benign 0.300 phenotype 08/02/2016
17 406431 APN Ifi44 0.000 IGL02977 3 151739379 M312K A T missense Het probably benign 0.002 08/02/2016
18 406418 APN Lrp1b 0.000 IGL02977 2 40730735 D3577A T G missense Het probably damaging 0.999 phenotype 08/02/2016
19 406440 APN Mapk13 0.178 IGL02977 17 28776348 G181V G T missense Het probably damaging 1.000 phenotype 08/02/2016
20 406429 APN Olfr1164 0.056 IGL02977 2 88093571 I122V T C missense Het probably benign 0.000 phenotype 08/02/2016
21 406426 APN Olfr464 0.118 IGL02977 11 87914130 S259P A G missense Het possibly damaging 0.478 phenotype 08/02/2016
22 406442 APN Oprl1 0.327 IGL02977 2 181718511 C115F G T missense Het probably damaging 1.000 phenotype 08/02/2016
23 406415 APN Psg22 0.056 IGL02977 7 18719599 D112G A G missense Het probably benign 0.198 08/02/2016
24 406433 APN Rp1l1 0.088 IGL02977 14 64028150 I395N T A missense Het probably benign 0.015 0.099 phenotype 08/02/2016
25 406438 APN Simc1 0.065 IGL02977 13 54526307 S823P T C missense Het probably benign 0.147 08/02/2016
26 406422 APN Slc9b1 0.082 IGL02977 3 135397723 L538P T C missense Het probably damaging 0.995 phenotype 08/02/2016
27 406425 APN Smad2 1.000 IGL02977 18 76289164 Y216N T A missense Het possibly damaging 0.638 phenotype 08/02/2016
28 406439 APN Stxbp2 1.000 IGL02977 8 3641971 I538F A T missense Het probably benign 0.439 phenotype 08/02/2016
29 406420 APN Tonsl 1.000 IGL02977 15 76632873 Q882L T A missense Het probably benign 0.003 phenotype 08/02/2016
30 406414 APN Trav13-2 IGL02977 14 53635307 T80I C T missense Het probably damaging 0.994 08/02/2016
31 406417 APN Uaca 0.151 IGL02977 9 60866380 P388S C T missense Het probably benign 0.001 phenotype 08/02/2016
32 406421 APN Vmn2r116 0.073 IGL02977 17 23388774 R439G A G missense Het possibly damaging 0.901 phenotype 08/02/2016
33 406428 APN Vmn2r18 0.093 IGL02977 5 151586684 A75S C A missense Het probably damaging 1.000 08/02/2016
[records 1 to 33 of 33]