Incidental Mutations

34 incidental mutations are currently displayed, and affect 34 genes.
4 are Possibly Damaging.
15 are Probably Damaging.
10 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
2 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 104905 APN 1700030K09Rik 0.039 IGL01714 G1 8 72455569 T C critical splice donor site 2 bp Het probably null 01/21/2014
2 104891 APN Acvrl1 1.000 IGL01714 G1 15 101137370 I259N T A missense Het probably damaging 1.000 phenotype 01/21/2014
3 104897 APN Ahctf1 1.000 IGL01714 G1 1 179795877 S59P A G missense Het probably damaging 0.990 phenotype 01/21/2014
4 104903 APN Bcas1 0.166 IGL01714 G1 2 170384182 T C splice site Het probably benign phenotype 01/21/2014
5 104882 APN Ccdc33 0.155 IGL01714 G1 9 58029870 N682S T C missense Het possibly damaging 0.907 01/21/2014
6 104895 APN Celf1 0.737 IGL01714 G1 2 91009207 S326P T C missense Het possibly damaging 0.827 0.250 phenotype 01/21/2014
7 104875 APN Cntn1 1.000 IGL01714 G1 15 92253989 C436* T A nonsense Het probably null phenotype 01/21/2014
8 104879 APN Cyp2d40 0.276 IGL01714 G1 15 82761240 D142A T G missense Het possibly damaging 0.553 01/21/2014
9 104887 APN Dnhd1 0.139 IGL01714 G1 7 105720942 L4525F C T missense Het probably damaging 1.000 01/21/2014
10 104901 APN Drosha 0.965 IGL01714 G1 15 12878784 Y732C A G missense Het probably damaging 0.998 phenotype 01/21/2014
11 104894 APN Edn1 1.000 IGL01714 G1 13 42305014 N101S A G missense Het probably benign 0.000 phenotype 01/21/2014
12 104892 APN Faxc 0.166 IGL01714 G1 4 21936688 P108S C T missense Het probably damaging 0.999 01/21/2014
13 104904 APN Glb1l2 0.059 IGL01714 G1 9 26768418 C T critical splice donor site 1 bp Het probably null phenotype 01/21/2014
14 104900 APN Gm20498 0.165 IGL01714 G1 12 81510890 I47T A G missense Het probably damaging 1.000 phenotype 01/21/2014
15 104876 APN Gm4952 0.023 IGL01714 G1 19 12624711 R161L G T missense Het probably benign 0.158 01/21/2014
16 104880 APN Hipk2 0.911 IGL01714 G1 6 38819182 Y51N A T missense Het probably damaging 1.000 phenotype 01/21/2014
17 104896 APN Id4 0.795 IGL01714 G1 13 48261790 I98S T G missense Het probably damaging 1.000 phenotype 01/21/2014
18 104889 APN Klf6 1.000 IGL01714 G1 13 5866659 S268P T C missense Het probably benign 0.251 phenotype 01/21/2014
19 104881 APN Kmt2c 0.879 IGL01714 G1 5 25313400 T2427N G T missense Het probably benign 0.000 phenotype 01/21/2014
20 104884 APN Lrp3 0.215 IGL01714 G1 7 35206071 T G unclassified 4957 bp Het probably null 01/21/2014
21 104898 APN Lrrc66 0.055 IGL01714 G1 5 73629977 I10T A G missense Het probably benign 0.189 01/21/2014
22 104883 APN Mapkap1 1.000 IGL01714 G1 2 34518843 V281G T G missense Het probably damaging 1.000 phenotype 01/21/2014
23 104886 APN Ncor1 1.000 IGL01714 G1 11 62334584 I1054F T A missense Het possibly damaging 0.585 phenotype 01/21/2014
24 104877 APN Olfr1061 0.107 IGL01714 G1 2 86413800 N84S T C missense Het probably benign 0.350 phenotype 01/21/2014
25 104893 APN Ppp1r9b 0.000 IGL01714 G1 11 95005354 T817N C A missense Het probably damaging 0.961 phenotype 01/21/2014
26 104878 APN Prkd2 0.000 IGL01714 G1 7 16863942 I659N T A missense Het probably damaging 0.997 phenotype 01/21/2014
27 104902 APN Radil 0.601 IGL01714 G1 5 142543397 T C unclassified Het probably benign 01/21/2014
28 104888 APN Smarcd1 0.875 IGL01714 G1 15 99712421 T474I C T missense Het probably damaging 0.996 phenotype 01/21/2014
29 104890 APN Srd5a1 0.374 IGL01714 G1 13 69611062 W62* C T nonsense Het probably null phenotype 01/21/2014
30 104873 APN St5 0.524 IGL01714 G1 7 109570062 S9P A G missense Het probably damaging 0.988 phenotype 01/21/2014
31 278786 APN St6galnac2 0.126 IGL01714 G1 11 116685119 D169N C T missense Het probably damaging 0.999 phenotype 04/16/2015
32 104874 APN Ttn 1.000 IGL01714 G1 2 76857179 T A intron Het probably benign phenotype 01/21/2014
33 104885 APN Vmn1r77 0.068 IGL01714 G1 7 12041350 I18F A T missense Het probably benign 0.027 01/21/2014
34 104899 APN Xrcc5 1.000 IGL01714 G1 1 72329984 K332N A T missense Het probably damaging 0.982 phenotype 01/21/2014
[records 1 to 34 of 34]