Incidental Mutations

29 incidental mutations are currently displayed, and affect 29 genes.
5 are Possibly Damaging.
7 are Probably Damaging.
13 are Probably Benign.
3 are Probably Null.
2 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 29 of 29] 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 300639 APN A430033K04Rik 0.070 IGL02615 5 138646140 E96* G T nonsense Het probably null 04/16/2015
2 300625 APN Adck5 0.000 IGL02615 15 76589167 S72L C T missense Het possibly damaging 0.686 04/16/2015
3 300622 APN Afdn 1.000 IGL02615 17 13825976 H404R A G missense Het probably benign 0.002 phenotype 04/16/2015
4 300633 APN Aph1c 0.000 IGL02615 9 66819406 V222E A T missense Het possibly damaging 0.941 phenotype 04/16/2015
5 300641 APN Armc8 0.716 IGL02615 9 99527069 T C splice site Het probably benign 04/16/2015
6 300637 APN Bcl2l13 0.088 IGL02615 6 120862867 D42V A T missense Het probably damaging 0.979 phenotype 04/16/2015
7 300630 APN Bhlhe22 0.000 IGL02615 3 18054900 T38I C T missense Het possibly damaging 0.747 phenotype 04/16/2015
8 300623 APN Ccdc51 0.417 IGL02615 9 109089435 T31S A T missense Het probably benign 0.000 04/16/2015
9 300640 APN Ctbp2 1.000 IGL02615 7 132995347 I669T A G missense Het probably benign 0.345 phenotype 04/16/2015
10 300635 APN Dennd4c 1.000 IGL02615 4 86821467 T998A A G missense Het probably benign 0.001 04/16/2015
11 300628 APN Dpp4 0.000 IGL02615 2 62359328 Y410C T C missense Het probably damaging 1.000 phenotype 04/16/2015
12 300617 APN Gli2 1.000 IGL02615 1 118844398 N526Y T A missense Het probably damaging 1.000 phenotype 04/16/2015
13 300626 APN Gm12394 IGL02615 4 42793027 M368I C T missense Het probably benign 0.020 04/16/2015
14 300614 APN Ighv1-64 0.205 IGL02615 12 115507687 I70T A G missense Het possibly damaging 0.899 04/16/2015
15 300642 APN Mphosph10 0.956 IGL02615 7 64381045 A T splice site Het probably benign phenotype 04/16/2015
16 300634 APN Mrps34 0.952 IGL02615 17 24895793 A G unclassified 3646 bp Het probably null phenotype 04/16/2015
17 300629 APN Myo1f 0.156 IGL02615 17 33604656 I1053L A T missense Het probably benign 0.000 phenotype 04/16/2015
18 300618 APN Nckap5l 0.266 IGL02615 15 99429382 P142L G A missense Het possibly damaging 0.890 04/16/2015
19 300638 APN Platr26 0.360 IGL02615 2 71730426 T A exon Het noncoding transcript 04/16/2015
20 300616 APN Rag2 0.234 IGL02615 2 101629568 Y74* T A nonsense Het probably null phenotype 04/16/2015
21 300627 APN Rnf213 0.000 IGL02615 11 119440789 M2275L A T missense Het probably damaging 0.959 phenotype 04/16/2015
22 300631 APN Rsbn1 1.000 IGL02615 3 103953752 L498Q T A missense Het probably damaging 0.999 04/16/2015
23 300620 APN Scp2 0.129 IGL02615 4 108107631 V62A A G missense Het probably benign 0.402 phenotype 04/16/2015
24 300624 APN Spag17 0.000 IGL02615 3 100072085 I1421V A G missense Het probably benign 0.094 phenotype 04/16/2015
25 300621 APN St6galnac4 0.000 IGL02615 2 32594204 H138R A G missense Het probably benign 0.328 phenotype 04/16/2015
26 300615 APN Syne2 0.239 IGL02615 12 76096994 M1045K T A missense Het probably damaging 1.000 phenotype 04/16/2015
27 300619 APN Tbxas1 0.061 IGL02615 6 39027866 T349M C T missense Het probably damaging 1.000 phenotype 04/16/2015
28 300636 APN U2surp 0.955 IGL02615 9 95493231 D146A T G missense Het probably benign 0.002 04/16/2015
29 300632 APN Usp38 0.000 IGL02615 8 80985151 M752V T C missense Het probably benign 0.002 04/16/2015
[records 1 to 29 of 29]