Incidental Mutations

39 incidental mutations are currently displayed, and affect 39 genes.
7 are Possibly Damaging.
17 are Probably Damaging.
10 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 39 of 39] 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 79653 APN 2810474O19Rik 0.000 IGL01401 G1 6 149326896 E480G A G missense Het probably damaging 0.982 11/05/2013
2 79643 APN 4932438A13Rik 1.000 IGL01401 G1 3 36942292 N1051S A G missense Het probably benign 0.000 phenotype 11/05/2013
3 79639 APN Adgrl3 0.000 IGL01401 G1 5 81688669 V758A T C missense Het possibly damaging 0.941 phenotype 11/05/2013
4 79630 APN Arf4 1.000 IGL01401 G1 14 26638454 L12P T C missense Het probably damaging 0.979 phenotype 11/05/2013
5 79657 APN C4bp 0.000 IGL01401 G1 1 130648064 V230E A T missense Het possibly damaging 0.946 11/05/2013
6 79658 APN Carm1 1.000 IGL01401 G1 9 21569582 T A critical splice donor site 2 bp Het probably null phenotype 11/05/2013
7 278341 APN Cd4 0.000 IGL01401 G1 6 124879378 T50I G A missense Het probably benign 0.414 phenotype 04/16/2015
8 79632 APN Ceacam16 0.000 IGL01401 G1 7 19861129 Y8C T C missense Het probably benign 0.000 phenotype 11/05/2013
9 79638 APN Ckap2l 0.273 IGL01401 G1 2 129269216 V687E A T missense Het probably damaging 1.000 phenotype 11/05/2013
10 79633 APN Dcaf4 0.077 IGL01401 G1 12 83541374 D449G A G missense Het probably damaging 1.000 phenotype 11/05/2013
11 79651 APN Dhx38 0.964 IGL01401 G1 8 109552114 Y1113C T C missense Het probably benign 0.150 phenotype 11/05/2013
12 79640 APN Fry 0.572 IGL01401 G1 5 150438788 I161V A G missense Het probably benign 0.000 11/05/2013
13 79629 APN Gm17093 0.310 IGL01401 G1 14 44521527 M169L A C missense Het unknown 11/05/2013
14 79631 APN Gm20721 IGL01401 G1 2 174345502 D999G A G missense Het probably damaging 1.000 11/05/2013
15 79648 APN Grin2b 1.000 IGL01401 G1 6 135736363 H840R T C missense Het probably damaging 1.000 phenotype 11/05/2013
16 79652 APN Hoxc12 0.000 IGL01401 G1 15 102937320 H156Q C A missense Het probably benign 0.000 phenotype 11/05/2013
17 79644 APN Htr3b 0.000 IGL01401 G1 9 48947634 D68G T C missense Het probably damaging 1.000 phenotype 11/05/2013
18 79636 APN Inpp5b 0.229 IGL01401 G1 4 124746087 V99A T C missense Het probably damaging 0.968 phenotype 11/05/2013
19 79635 APN Klhl42 0.000 IGL01401 G1 6 147107743 T360M C T missense Het probably benign 0.026 11/05/2013
20 79641 APN Lmo7 0.162 IGL01401 G1 14 101794277 R36* C T nonsense Het probably null phenotype 11/05/2013
21 79656 APN Lmod3 0.099 IGL01401 G1 6 97252552 N7T T G missense Het probably damaging 0.998 phenotype 11/05/2013
22 278342 APN Malrd1 0.092 IGL01401 G1 2 16101957 G A critical splice donor site 1 bp Het probably null 04/16/2015
23 79634 APN Mthfd2l 0.000 IGL01401 G1 5 91000566 I284K T A missense Het possibly damaging 0.947 11/05/2013
24 79642 APN Myo1e 0.000 IGL01401 G1 9 70327166 I267N T A missense Het probably damaging 0.968 phenotype 11/05/2013
25 79625 APN Olfr1393 0.055 IGL01401 G1 11 49280487 V113E T A missense Het possibly damaging 0.939 phenotype 11/05/2013
26 79628 APN Olfr159 0.120 IGL01401 G1 4 43770112 R300G T C missense Het probably damaging 1.000 phenotype 11/05/2013
27 79649 APN Prkce 0.000 IGL01401 G1 17 86168840 V83A T C missense Het probably damaging 1.000 phenotype 11/05/2013
28 79646 APN Pxdn 0.617 IGL01401 G1 12 30001984 C540F G T missense Het probably damaging 1.000 phenotype 11/05/2013
29 79626 APN Ryr2 1.000 IGL01401 G1 13 11591352 E4448V T A missense Het possibly damaging 0.804 phenotype 11/05/2013
30 79647 APN Scn1a 1.000 IGL01401 G1 2 66289111 N1349K A T missense Het probably damaging 1.000 phenotype 11/05/2013
31 79645 APN Smarcc1 1.000 IGL01401 G1 9 110149965 I172T T C missense Het possibly damaging 0.518 phenotype 11/05/2013
32 79655 APN Syt16 0.000 IGL01401 G1 12 74222663 V92A T C missense Het possibly damaging 0.663 11/05/2013
33 79637 APN Tenm4 1.000 IGL01401 G1 7 96874267 Y1672C A G missense Het probably damaging 1.000 phenotype 11/05/2013
34 79650 APN Tmem131 0.850 IGL01401 G1 1 36799387 Y1486H A G missense Het probably damaging 0.998 11/05/2013
35 79661 APN Tmem132a 1.000 IGL01401 G1 19 10861524 A G splice site Het probably benign phenotype 11/05/2013
36 79654 APN Usp40 0.000 IGL01401 G1 1 87994198 D314E A T missense Het probably damaging 1.000 phenotype 11/05/2013
37 79627 APN Vmn2r79 0.072 IGL01401 G1 7 87037273 V621I G A missense Het probably benign 0.010 11/05/2013
38 79659 APN Wnk4 0.408 IGL01401 G1 11 101276683 A G splice site Het probably benign phenotype 11/05/2013
39 79660 APN Wwc1 0.000 IGL01401 G1 11 35898618 C A critical splice donor site 1 bp Het probably null phenotype 11/05/2013
[records 1 to 39 of 39]