Incidental Mutations

39 incidental mutations are currently displayed, and affect 39 genes.
5 are Possibly Damaging.
15 are Probably Damaging.
14 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 39 of 39] 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 417005 APN Abcb4 0.000 IGL03335 5 8935258 V713A T C missense Het probably benign 0.002 phenotype 08/02/2016
2 417018 APN Actr8 1.000 IGL03335 14 29978557 V31A T C missense Het probably benign 0.000 08/02/2016
3 417007 APN Alcam 0.370 IGL03335 16 52291003 Y244* A C nonsense Het probably null phenotype 08/02/2016
4 417000 APN Ankrd24 0.511 IGL03335 10 81647133 S972G A G missense Het probably benign 0.177 08/02/2016
5 416996 APN Aox1 0.000 IGL03335 1 58076160 V768E T A missense Het probably damaging 0.984 phenotype 08/02/2016
6 417022 APN Btbd11 0.261 IGL03335 10 85658358 A T utr 3 prime Het probably benign 08/02/2016
7 417019 APN C130060K24Rik 0.071 IGL03335 6 65453117 T C critical splice donor site 2 bp Het probably null 08/02/2016
8 416993 APN Carmil2 0.151 IGL03335 8 105697029 I1212V A G missense Het probably benign 0.136 phenotype 08/02/2016
9 416999 APN Catsper1 0.156 IGL03335 19 5336311 R191C C T missense Het probably damaging 0.971 phenotype 08/02/2016
10 417001 APN Cenpe 1.000 IGL03335 3 135243625 V57D T A missense Het probably benign 0.000 phenotype 08/02/2016
11 417021 APN Cpsf3 0.969 IGL03335 12 21306887 T C splice site 6 bp Het probably null phenotype 08/02/2016
12 416988 APN Cubn 1.000 IGL03335 2 13360329 S1633P A G missense Het probably damaging 0.998 phenotype 08/02/2016
13 416985 APN Dsg1c 0.000 IGL03335 18 20283697 R885Q G A missense Het probably benign 0.006 phenotype 08/02/2016
14 417010 APN Egfl6 IGL03335 X 166538693 G272W C A missense Het probably damaging 1.000 phenotype 08/02/2016
15 416990 APN Ermard 0.149 IGL03335 17 15059406 L486P T C missense Het probably damaging 1.000 phenotype 08/02/2016
16 416987 APN F13b 0.000 IGL03335 1 139522386 L595F A T missense Het probably damaging 0.997 phenotype 08/02/2016
17 416992 APN Foxm1 1.000 IGL03335 6 128372568 N350S A G missense Het possibly damaging 0.921 phenotype 08/02/2016
18 417023 APN Fras1 0.000 IGL03335 5 96733944 T C splice site Het probably benign phenotype 08/02/2016
19 417009 APN Gpr152 0.000 IGL03335 19 4143771 T437N C A missense Het possibly damaging 0.691 08/02/2016
20 417014 APN Icmt 1.000 IGL03335 4 152300697 Y205* T A nonsense Het probably null phenotype 08/02/2016
21 416994 APN Ints8 0.964 IGL03335 4 11216460 F844I A T missense Het probably damaging 0.997 phenotype 08/02/2016
22 417017 APN Mep1a 0.000 IGL03335 17 43477173 D664V T A missense Het possibly damaging 0.633 phenotype 08/02/2016
23 416986 APN Muc4 0.088 IGL03335 16 32753021 N966K T A missense Het probably benign 0.015 phenotype 08/02/2016
24 417004 APN Myo7b 0.000 IGL03335 18 31985020 Q851L T A missense Het possibly damaging 0.807 phenotype 08/02/2016
25 417008 APN Pdzd2 0.140 IGL03335 15 12373764 H2095R T C missense Het probably benign 0.001 phenotype 08/02/2016
26 417013 APN Phldb1 0.143 IGL03335 9 44728069 L4P A G missense Het possibly damaging 0.955 08/02/2016
27 417012 APN Pkd1l2 0.000 IGL03335 8 117065745 T436I G A missense Het probably benign 0.070 0.072 phenotype 08/02/2016
28 417003 APN Pnpla8 0.225 IGL03335 12 44283164 N166K T A missense Het probably benign 0.026 phenotype 08/02/2016
29 417006 APN Rapgef2 1.000 IGL03335 3 79099185 M137T A G missense Het probably damaging 0.995 phenotype 08/02/2016
30 417002 APN Rbm15b 0.534 IGL03335 9 106884339 H877Y G A missense Het probably damaging 0.994 phenotype 08/02/2016
31 416998 APN Rbm45 0.937 IGL03335 2 76376433 L263P T C missense Het probably damaging 0.995 phenotype 08/02/2016
32 417011 APN Rprd1b 0.951 IGL03335 2 158074964 V288A T C missense Het probably damaging 1.000 08/02/2016
33 416997 APN Tmtc3 0.675 IGL03335 10 100466254 V278L C A missense Het probably damaging 0.974 phenotype 08/02/2016
34 416989 APN Tomm70a 0.969 IGL03335 16 57149926 T556A A G missense Het probably damaging 0.996 phenotype 08/02/2016
35 417016 APN Trpc7 0.138 IGL03335 13 56887691 E143G T C missense Het probably damaging 1.000 phenotype 08/02/2016
36 417020 APN Trpm3 0.119 IGL03335 19 22926071 G T critical splice donor site 1 bp Het probably null phenotype 08/02/2016
37 416995 APN Ugt2b34 0.171 IGL03335 5 86906640 E94G T C missense Het probably benign 0.288 08/02/2016
38 417015 APN Vmn1r174 0.070 IGL03335 7 23754512 V201A T C missense Het probably benign 0.411 08/02/2016
39 416991 APN Zfp352 0.000 IGL03335 4 90224346 F241S T C missense Het probably damaging 0.993 08/02/2016
[records 1 to 39 of 39]