Incidental Mutations

44 incidental mutations are currently displayed, and affect 44 genes.
5 are Possibly Damaging.
13 are Probably Damaging.
21 are Probably Benign.
5 are Probably Null.
0 create premature stop codons.
3 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 44 of 44] 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 1046 APN Abcb5 0.217 IGL00092 G1 12 118928695 D443G T C missense Het probably benign 0.091 phenotype 07/12/2011
2 1973 APN Atg16l1 1.000 IGL00092 G1 1 87765397 I28T T C missense Het possibly damaging 0.679 phenotype 07/12/2011
3 1826 APN Bpi 0.000 IGL00092 G1 2 158274796 V371E T A missense Het probably damaging 0.999 phenotype 07/12/2011
4 1292 APN Cd109 0.000 IGL00092 G1 9 78616969 V55G T G missense Het probably damaging 0.998 phenotype 07/12/2011
5 28450 APN Cd300c2 0.000 IGL00092 G1 11 115001549 T C utr 5 prime Het probably benign phenotype 04/17/2013
6 1526 APN Cic 0.954 IGL00092 G1 7 25292124 R1280C C T missense Het probably damaging 1.000 phenotype 07/12/2011
7 306527 APN Cngb1 1.000 IGL00092 G1 8 95242184 G A splice site Het probably benign phenotype 04/16/2015
8 306525 APN Cntn4 0.373 IGL00092 G1 6 106506225 C247F G T missense Het probably damaging 1.000 phenotype 04/16/2015
9 1687 APN Disp3 0.000 IGL00092 G1 4 148241534 V1256I C T missense Het probably benign 0.101 07/12/2011
10 1979 APN Farsb 0.970 IGL00092 G1 1 78462993 S338T A T missense Het probably benign 0.081 phenotype 07/12/2011
11 1912 APN Fcnb 0.000 IGL00092 G1 2 28076801 N240S T C missense Het probably benign 0.036 phenotype 07/12/2011
12 306516 APN Flg2 0.095 IGL00092 G1 3 93219855 S5G A G missense Het possibly damaging 0.904 04/16/2015
13 1151 APN Git1 1.000 IGL00092 G1 11 77505957 L635P T C missense Het probably benign 0.000 phenotype 07/12/2011
14 1860 APN Gm21985 IGL00092 G1 2 112351334 W685G T G missense Het probably damaging 0.997 07/12/2011
15 1379 APN Gpt2 0.095 IGL00092 G1 8 85512324 V262A T C missense Het probably benign 0.000 phenotype 07/12/2011
16 1996 APN Hecw2 0.224 IGL00092 G1 1 53830737 V1444A A G missense Het probably damaging 1.000 phenotype 07/12/2011
17 306523 APN Herc1 0.000 IGL00092 G1 9 66483966 V4017A T C missense Het probably benign 0.016 phenotype 04/16/2015
18 1677 APN Klhl17 0.255 IGL00092 G1 4 156233690 T129A T C missense Het possibly damaging 0.659 phenotype 07/12/2011
19 879 APN Krt84 0.096 IGL00092 G1 15 101528735 D331A T G missense Het probably damaging 1.000 phenotype 07/12/2011
20 1075 APN Lrrc9 0.167 IGL00092 G1 12 72486243 T963M C T missense Het possibly damaging 0.632 07/12/2011
21 770 APN Mtcl1 0.236 IGL00092 G1 17 66344319 V935I C T missense Het probably benign 0.001 phenotype 07/12/2011
22 306522 APN Muc4 0.072 IGL00092 G1 16 32754086 G1321R G A missense Het probably benign 0.354 phenotype 04/16/2015
23 1169 APN Myocd 1.000 IGL00092 G1 11 65180944 T C critical splice acceptor site Het probably null phenotype 07/12/2011
24 1042 APN Nid1 0.281 IGL00092 G1 13 13476392 N505D A G missense Het probably damaging 0.999 phenotype 07/12/2011
25 1027 APN Ninj1 0.151 IGL00092 G1 13 49193734 A T critical splice acceptor site Het probably null phenotype 07/12/2011
26 306517 APN Olfr1375 0.077 IGL00092 G1 11 51048400 Q98K C A missense Het probably benign 0.002 phenotype 04/16/2015
27 713 APN Olfr1426 0.068 IGL00092 G1 19 12087993 D266E A T missense Het probably benign 0.277 phenotype 07/12/2011
28 1472 APN Olfr307 0.102 IGL00092 G1 7 86336061 V112I C T missense Het probably benign 0.002 phenotype 07/12/2011
29 1288 APN Plscr2 0.000 IGL00092 G1 9 92290632 T A splice site Het probably benign 07/12/2011
30 306521 APN Ppfia2 0.000 IGL00092 G1 10 106819492 T307A A G missense Het probably benign 0.248 phenotype 04/16/2015
31 1636 APN Sart3 0.970 IGL00092 G1 5 113746669 R625G T C missense Het probably benign 0.000 phenotype 07/12/2011
32 1791 APN Sohlh2 0.589 IGL00092 G1 3 55207815 L407H T A missense Het probably damaging 1.000 phenotype 07/12/2011
33 306518 APN Sorcs1 0.139 IGL00092 G1 19 50190054 S877P A G missense Het probably damaging 0.999 phenotype 04/16/2015
34 306524 APN Stat1 0.000 IGL00092 G1 1 52122595 M1T T C start codon destroyed Het probably null 0.500 phenotype 04/16/2015
35 1707 APN Szt2 0.420 IGL00092 G1 4 118384250 C T splice site Het probably benign phenotype 07/12/2011
36 306526 APN Tarsl2 0.116 IGL00092 G1 7 65652259 G T critical splice acceptor site Het probably null 04/16/2015
37 1852 APN Terb2 0.070 IGL00092 G1 2 122198386 S141R T A missense Het probably benign 0.296 07/12/2011
38 2000 APN Tgfbrap1 1.000 IGL00092 G1 1 43060123 Y177C T C missense Het probably damaging 0.975 phenotype 07/12/2011
39 915 APN Trappc9 0.000 IGL00092 G1 15 73026026 I169N A T missense Het possibly damaging 0.794 phenotype 07/12/2011
40 306520 APN Trim47 0.000 IGL00092 G1 11 116106194 L578P A G missense Het probably damaging 1.000 04/16/2015
41 306519 APN Usp34 0.595 IGL00092 G1 11 23436020 R2149H G A missense Het probably damaging 0.978 04/16/2015
42 827 APN Vmn2r90 0.130 IGL00092 G1 17 17733496 S641P T C missense Het probably benign 0.002 07/12/2011
43 1331 APN Vwa5a 0.000 IGL00092 G1 9 38737814 T A splice site 6 bp Het probably null 07/12/2011
44 1163 APN Zzef1 0.000 IGL00092 G1 11 72875126 I1493N T A missense Het probably benign 0.023 07/12/2011
[records 1 to 44 of 44]