Incidental Mutations

34 incidental mutations are currently displayed, and affect 34 genes.
6 are Possibly Damaging.
15 are Probably Damaging.
9 are Probably Benign.
3 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 34 of 34] 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 289006 APN 4930402H24Rik 0.160 IGL02339 2 130739465 S546P A G missense Het probably damaging 0.972 phenotype 04/16/2015
2 288994 APN Aass 0.325 IGL02339 6 23093966 V119F C A missense Het probably damaging 0.989 phenotype 04/16/2015
3 289004 APN Abcg5 0.249 IGL02339 17 84673604 I186V T C missense Het possibly damaging 0.952 phenotype 04/16/2015
4 288997 APN B4gat1 0.579 IGL02339 19 5039418 E148K G A missense Het probably benign 0.000 phenotype 04/16/2015
5 288982 APN Ccr6 0.000 IGL02339 17 8256253 T97S A T missense Het probably benign 0.012 phenotype 04/16/2015
6 289014 APN Cd209f 0.237 IGL02339 8 4104483 A C critical splice donor site 2 bp Het probably null 04/16/2015
7 289002 APN Chst1 0.305 IGL02339 2 92613577 D131E T A missense Het possibly damaging 0.737 phenotype 04/16/2015
8 288998 APN Dennd4a 0.607 IGL02339 9 64842561 R145* C T nonsense Het probably null phenotype 04/16/2015
9 288986 APN Dnah6 0.202 IGL02339 6 73101898 Y2361H A G missense Het probably benign 0.001 phenotype 04/16/2015
10 289010 APN Dpp6 0.108 IGL02339 5 27652230 T333I C T missense Het probably damaging 0.969 phenotype 04/16/2015
11 288995 APN Glt8d1 0.000 IGL02339 14 31008810 T91K C A missense Het probably damaging 0.997 phenotype 04/16/2015
12 288991 APN Gm4952 0.024 IGL02339 19 12626911 R229Q G A missense Het probably damaging 0.981 04/16/2015
13 289008 APN Gm5117 0.907 IGL02339 8 31738226 T C exon Het noncoding transcript 04/16/2015
14 289009 APN Gp5 0.000 IGL02339 16 30309190 E222G T C missense Het probably damaging 0.997 phenotype 04/16/2015
15 289011 APN Herc2 0.870 IGL02339 7 56121722 D1077E T A missense Het probably benign 0.014 phenotype 04/16/2015
16 288996 APN Hfe 0.137 IGL02339 13 23704390 E171G T C missense Het probably damaging 0.981 phenotype 04/16/2015
17 288999 APN Hsp90b1 1.000 IGL02339 10 86701814 V209A A G missense Het probably damaging 0.999 phenotype 04/16/2015
18 289013 APN Ktn1 0.000 IGL02339 14 47683378 A T splice site Het probably benign phenotype 04/16/2015
19 288981 APN Med13 0.938 IGL02339 11 86288939 I1394M T C missense Het probably benign 0.164 phenotype 04/16/2015
20 288993 APN Meioc 0.183 IGL02339 11 102668448 S65R T G missense Het probably benign 0.184 phenotype 04/16/2015
21 288988 APN Myof 0.228 IGL02339 19 37972213 Y460C T C missense Het possibly damaging 0.458 phenotype 04/16/2015
22 288983 APN Olfr1276 0.091 IGL02339 2 111257243 T43S A T missense Het probably benign 0.004 phenotype 04/16/2015
23 288987 APN Pms1 0.000 IGL02339 1 53275165 Y74H A G missense Het possibly damaging 0.778 phenotype 04/16/2015
24 289000 APN Ptprn2 0.407 IGL02339 12 116722104 Q61P A C missense Het probably damaging 0.998 phenotype 04/16/2015
25 288990 APN Rab29 0.463 IGL02339 1 131872142 T152A A G missense Het probably benign 0.084 04/16/2015
26 288989 APN Rest 1.000 IGL02339 5 77275288 H313R A G missense Het probably damaging 0.999 phenotype 04/16/2015
27 289003 APN Slc9a5 0.139 IGL02339 8 105358459 Y531H T C missense Het probably damaging 0.997 04/16/2015
28 289007 APN St3gal3 0.000 IGL02339 4 117958562 T148A T C missense Het probably damaging 1.000 phenotype 04/16/2015
29 288985 APN Stxbp5 1.000 IGL02339 10 9816297 V368I C T missense Het possibly damaging 0.888 phenotype 04/16/2015
30 289012 APN Taf1c 0.904 IGL02339 8 119604280 D33G T C missense Het probably damaging 1.000 phenotype 04/16/2015
31 289001 APN Trim38 0.038 IGL02339 13 23788230 R178Q G A missense Het probably damaging 0.999 phenotype 04/16/2015
32 289005 APN Uvssa 0.184 IGL02339 5 33414849 K704N A T missense Het probably damaging 1.000 phenotype 04/16/2015
33 288992 APN Vmn1r69 0.078 IGL02339 7 10580718 Q29* G A nonsense Het probably null 04/16/2015
34 288984 APN Ypel2 0.250 IGL02339 11 86940603 D119G T C missense Het possibly damaging 0.903 04/16/2015
[records 1 to 34 of 34]