Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
4 are Possibly Damaging.
13 are Probably Damaging.
14 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 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 89578 APN 1500002C15Rik IGL01526 G1 4 155734171 G T unclassified Het probably benign 12/03/2013
2 89556 APN 4933430I17Rik 0.000 IGL01526 G1 4 62532621 R107L G T missense Het possibly damaging 0.711 12/03/2013
3 89584 APN 9130204L05Rik 0.117 IGL01526 G1 3 91088305 T A utr 3 prime Het probably benign 12/03/2013
4 89566 APN Acvr1 1.000 IGL01526 G1 2 58458985 D388E A T missense Het probably benign 0.198 phenotype 12/03/2013
5 89553 APN Art3 0.054 IGL01526 G1 5 92414340 S354P T C missense Het probably damaging 0.994 phenotype 12/03/2013
6 89576 APN Bpnt1 0.339 IGL01526 G1 1 185345394 S102* C A nonsense Het probably null phenotype 12/03/2013
7 89574 APN C530008M17Rik 0.000 IGL01526 G1 5 76857631 M613K T A missense Het unknown 12/03/2013
8 278554 APN Ces1a 0.000 IGL01526 G1 8 93045098 P24T G T missense Het probably damaging 0.999 04/16/2015
9 89562 APN Cfap65 0.503 IGL01526 G1 1 74911078 S1171T A T missense Het probably damaging 0.999 phenotype 12/03/2013
10 89575 APN Csn2 0.056 IGL01526 G1 5 87694979 H47R T C missense Het possibly damaging 0.921 phenotype 12/03/2013
11 89554 APN Gm14496 0.000 IGL01526 G1 2 181995665 D177E T A missense Het probably benign 0.117 12/03/2013
12 89569 APN Hmbs 1.000 IGL01526 G1 9 44339548 V126A A G missense Het possibly damaging 0.907 phenotype 12/03/2013
13 89571 APN Ica1l 0.000 IGL01526 G1 1 60015757 M105T A G missense Het probably damaging 0.986 phenotype 12/03/2013
14 89559 APN Morc2a 1.000 IGL01526 G1 11 3650428 E17K G A missense Het probably benign 0.003 phenotype 12/03/2013
15 89581 APN Mroh8 0.917 IGL01526 G1 2 157238312 T C splice site Het probably benign phenotype 12/03/2013
16 89572 APN Mroh9 0.000 IGL01526 G1 1 163055603 L436I G T missense Het probably damaging 0.990 12/03/2013
17 89565 APN Nup54 0.959 IGL01526 G1 5 92417475 D461G T C missense Het probably benign 0.120 phenotype 12/03/2013
18 89573 APN Olfr1123 0.215 IGL01526 G1 2 87418975 D309V A T missense Het probably damaging 0.993 phenotype 12/03/2013
19 89567 APN Olfr315 0.070 IGL01526 G1 11 58778297 T57A A G missense Het probably benign 0.210 phenotype 12/03/2013
20 89582 APN Pcid2 1.000 IGL01526 G1 8 13085319 G A unclassified Het probably benign phenotype 12/03/2013
21 89558 APN Ppp1r3b 0.377 IGL01526 G1 8 35384718 R237L G T missense Het probably benign 0.073 phenotype 12/03/2013
22 89561 APN Prdm11 0.784 IGL01526 G1 2 93012757 V119A A G missense Het probably damaging 0.999 12/03/2013
23 89563 APN Serpina5 0.000 IGL01526 G1 12 104101890 V70E T A missense Het probably damaging 0.999 phenotype 12/03/2013
24 89568 APN Skap2 1.000 IGL01526 G1 6 51907914 D249N C T missense Het probably benign 0.196 phenotype 12/03/2013
25 89583 APN Slc22a29 0.000 IGL01526 G1 19 8207178 A T splice site Het probably benign 12/03/2013
26 89579 APN Slc4a1ap 0.581 IGL01526 G1 5 31528227 T283K C A missense Het possibly damaging 0.860 12/03/2013
27 89564 APN Slc6a21 0.050 IGL01526 G1 7 45287796 I575S T G missense Het probably damaging 0.999 12/03/2013
28 89557 APN Smpd1 0.290 IGL01526 G1 7 105554775 W82G T G missense Het probably benign 0.014 phenotype 12/03/2013
29 89577 APN Snx14 1.000 IGL01526 G1 9 88381500 M897L T A missense Het probably damaging 0.988 phenotype 12/03/2013
30 89570 APN Tjp1 1.000 IGL01526 G1 7 65322658 V586A A G missense Het probably damaging 1.000 phenotype 12/03/2013
31 89580 APN Tmc8 0.055 IGL01526 G1 11 117792084 T C splice site Het probably benign phenotype 12/03/2013
32 89555 APN Trim34a 0.098 IGL01526 G1 7 104260499 Y298C A G missense Het probably damaging 0.999 12/03/2013
33 89560 APN Ube3c 0.000 IGL01526 G1 5 29667962 V1000A T C missense Het probably damaging 0.991 12/03/2013
[records 1 to 33 of 33]