Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
6 are Possibly Damaging.
5 are Probably Damaging.
12 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 26 of 26] 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 5813 APN Amigo2 0.198 IGL00587 G1 15 97245446 M365R A C missense Het possibly damaging 0.836 04/20/2012
2 9104 APN Atat1 0.280 IGL00587 G1 17 35897883 D352G T C missense Het probably benign 0.044 phenotype 12/06/2012
3 6905 APN Bbs12 0.097 IGL00587 G1 3 37320197 T265A A G missense Het probably damaging 1.000 phenotype 04/20/2012
4 332717 APN Cd300c 0.000 IGL00587 G1 11 114959790 N62K A T missense Het probably benign 0.000 08/05/2015
5 9572 APN Cdk5rap3 1.000 IGL00587 G1 11 96913399 S43P A G missense Het probably damaging 1.000 phenotype 12/06/2012
6 332718 APN Chchd6 0.070 IGL00587 G1 6 89569417 A T splice site Het probably null 08/05/2015
7 7286 APN Cr2 0.186 IGL00587 G1 1 195154251 R868Q C T missense Het possibly damaging 0.759 phenotype 04/20/2012
8 9990 APN Cyp2d9 0.067 IGL00587 G1 15 82455143 S126P T C missense Het possibly damaging 0.894 12/06/2012
9 10406 APN Dsg3 0.428 IGL00587 G1 18 20539654 I794N T A missense Het probably damaging 0.995 phenotype 12/06/2012
10 6861 APN Fga 0.266 IGL00587 G1 3 83030289 S158C A T missense Het possibly damaging 0.623 phenotype 04/20/2012
11 26796 APN Gm14240 IGL00587 G1 2 156052950 T C unclassified Het probably null 04/17/2013
12 11496 APN Itga1 0.608 IGL00587 G1 13 115012249 V279L C A missense Het probably damaging 1.000 phenotype 12/06/2012
13 4310 APN Kdm1b 0.469 IGL00587 G1 13 47068540 V485A T C missense Het probably benign 0.012 phenotype 04/20/2012
14 11972 APN Mfap3l 0.089 IGL00587 G1 8 60671909 V395A T C missense Het probably benign 0.285 12/06/2012
15 12370 APN Nlrp14 0.157 IGL00587 G1 7 107181767 V57E T A missense Het probably benign 0.099 phenotype 12/06/2012
16 12892 APN P2ry12 0.098 IGL00587 G1 3 59217882 I124K A T missense Het probably damaging 1.000 phenotype 12/06/2012
17 12914 APN Paxip1 1.000 IGL00587 G1 5 27772552 A G utr 3 prime Het probably benign phenotype 12/06/2012
18 4006 APN Prkdc 0.958 IGL00587 G1 16 15652358 T C splice site Het probably benign phenotype 04/20/2012
19 10356 APN Rab28 0.176 IGL00587 G1 5 41703456 R52G T C missense Het probably benign 0.303 phenotype 12/06/2012
20 7304 APN Rrp15 0.955 IGL00587 G1 1 186721548 T C critical splice acceptor site Het probably null phenotype 04/20/2012
21 7013 APN Sel1l2 0.538 IGL00587 G1 2 140243944 L539F G A missense Het possibly damaging 0.952 04/20/2012
22 14462 APN Ticam2 0.000 IGL00587 G1 18 46560813 E69G T C missense Het probably benign 0.044 phenotype 12/06/2012
23 7396 APN Zcchc2 0.252 IGL00587 G1 1 106030263 S821R T A missense Het probably benign 0.250 04/20/2012
24 6432 APN Zcchc4 0.135 IGL00587 G1 5 52816169 S379T T A missense Het probably benign 0.052 04/20/2012
25 3916 APN Zfp53 0.085 IGL00587 G1 17 21508338 V211A T C missense Het probably benign 0.000 phenotype 04/20/2012
26 4182 APN Zmym2 0.646 IGL00587 G1 14 56903360 S219A T G missense Het possibly damaging 0.861 phenotype 04/20/2012
[records 1 to 26 of 26]