Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
3 are Possibly Damaging.
5 are Probably Damaging.
15 are Probably Benign.
1 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 25 of 25] 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 103483 APN Cdc7 1.000 IGL01671 G1 5 106983245 P529S C T missense Het probably damaging 1.000 phenotype 01/21/2014
2 103490 APN Defb45 0.058 IGL01671 G1 2 152593411 K26E T C missense Het probably benign 0.428 01/21/2014
3 103496 APN Dnajb8 0.702 IGL01671 G1 6 88222920 L146S T C missense Het probably benign 0.001 phenotype 01/21/2014
4 103484 APN Egln1 1.000 IGL01671 G1 8 124910715 D399G T C missense Het probably benign 0.022 phenotype 01/21/2014
5 103499 APN Ephb1 0.000 IGL01671 G1 9 101996787 C563S A T missense Het probably damaging 1.000 phenotype 01/21/2014
6 103498 APN Gad2 0.000 IGL01671 G1 2 22623699 Y49* T A nonsense Het probably null phenotype 01/21/2014
7 103501 APN Gga2 1.000 IGL01671 G1 7 121994856 S470P A G missense Het probably benign 0.006 phenotype 01/21/2014
8 103487 APN Gm21276 0.265 IGL01671 G1 7 38764727 G T exon Het noncoding transcript 01/21/2014
9 103480 APN Gm3115 IGL01671 G1 14 4084189 C9Y G A missense Het probably benign 0.049 01/21/2014
10 103485 APN H2-M1 0.068 IGL01671 G1 17 36670438 E235G T C missense Het probably damaging 0.999 01/21/2014
11 103486 APN Hfe2 0.000 IGL01671 G1 3 96528491 V355A T C missense Het probably damaging 0.999 phenotype 01/21/2014
12 103479 APN Hsp90b1 1.000 IGL01671 G1 10 86704325 G41S C T missense Het probably benign 0.066 phenotype 01/21/2014
13 103495 APN Mccc1 1.000 IGL01671 G1 3 35964460 D575G T C missense Het probably benign 0.000 phenotype 01/21/2014
14 103503 APN Metap2 1.000 IGL01671 G1 10 93871478 T C splice site Het probably benign phenotype 01/21/2014
15 103500 APN Myh7 0.812 IGL01671 G1 14 54972924 T1775A T C missense Het probably damaging 0.999 phenotype 01/21/2014
16 103482 APN Olfr1469 0.084 IGL01671 G1 19 13410891 F107L T A missense Het probably benign 0.292 phenotype 01/21/2014
17 103481 APN Olfr170 0.074 IGL01671 G1 16 19605921 I249T A G missense Het probably benign 0.005 phenotype 01/21/2014
18 103491 APN Olfr935 0.061 IGL01671 G1 9 38994853 V194A A G missense Het probably benign 0.054 phenotype 01/21/2014
19 103493 APN Pak7 0.000 IGL01671 G1 2 136116373 D265G T C missense Het possibly damaging 0.887 phenotype 01/21/2014
20 103494 APN Pex1 0.567 IGL01671 G1 5 3624088 I793V A G missense Het probably benign 0.003 phenotype 01/21/2014
21 103492 APN Prkdc 0.963 IGL01671 G1 16 15667745 I479V A G missense Het possibly damaging 0.899 phenotype 01/21/2014
22 103489 APN Rhcg 0.070 IGL01671 G1 7 79598551 I435S A C missense Het probably benign 0.129 phenotype 01/21/2014
23 103488 APN Slc9c1 0.604 IGL01671 G1 16 45560315 T535S A T missense Het probably benign 0.000 phenotype 01/21/2014
24 103497 APN Stab2 0.000 IGL01671 G1 10 86969277 D279G T C missense Het possibly damaging 0.800 phenotype 01/21/2014
25 103502 APN Wdr83 1.000 IGL01671 G1 8 85075819 T C unclassified Het probably benign phenotype 01/21/2014
[records 1 to 25 of 25]