Incidental Mutations

47 incidental mutations are currently displayed, and affect 47 genes.
9 are Possibly Damaging.
18 are Probably Damaging.
15 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 47 of 47] 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 412055 APN Adgrg2 0.000 IGL03177 X 160438263 I23T T C missense Het possibly damaging 0.528 phenotype 08/02/2016
2 412033 APN Ank2 1.000 IGL03177 3 126955870 E503D C A missense Het probably damaging 0.998 phenotype 08/02/2016
3 412050 APN Anxa7 0.137 IGL03177 14 20456586 I451V T C missense Het probably benign 0.411 phenotype 08/02/2016
4 412041 APN Capn10 0.295 IGL03177 1 92934982 F37L T C missense Het probably benign 0.020 phenotype 08/02/2016
5 412032 APN Cyp4f13 0.130 IGL03177 17 32946914 I30T A G missense Het possibly damaging 0.879 phenotype 08/02/2016
6 412031 APN Ddx27 0.968 IGL03177 2 167027920 N392D A G missense Het possibly damaging 0.763 phenotype 08/02/2016
7 412026 APN Dhx30 1.000 IGL03177 9 110088010 H479R T C missense Het possibly damaging 0.752 phenotype 08/02/2016
8 412043 APN Dnah5 0.779 IGL03177 15 28295399 Y1426C A G missense Het probably damaging 0.970 phenotype 08/02/2016
9 412065 APN Dnajc2 0.954 IGL03177 5 21775081 A G splice site Het probably benign phenotype 08/02/2016
10 412061 APN Fbxw8 0.580 IGL03177 5 118128980 C A splice site Het probably benign phenotype 08/02/2016
11 412054 APN Grik5 0.268 IGL03177 7 25015454 T705I G A missense Het probably damaging 1.000 phenotype 08/02/2016
12 412028 APN H2-M3 0.000 IGL03177 17 37270316 V19F G T missense Het possibly damaging 0.861 phenotype 08/02/2016
13 412040 APN Hapln2 0.100 IGL03177 3 88022771 C266F C A missense Het probably damaging 1.000 phenotype 08/02/2016
14 412062 APN Hist1h2ab IGL03177 13 23751526 T A unclassified Het probably benign phenotype 08/02/2016
15 412063 APN Hspbp1 0.135 IGL03177 7 4664701 A T critical splice donor site 2 bp Het probably null phenotype 08/02/2016
16 412039 APN Jak3 0.838 IGL03177 8 71682370 V549D T A missense Het probably damaging 1.000 phenotype 08/02/2016
17 412027 APN Mark1 0.278 IGL03177 1 184944907 S49P A G missense Het probably damaging 0.999 08/02/2016
18 412048 APN Mdfic 0.438 IGL03177 6 15770451 V152A T C missense Het probably damaging 1.000 phenotype 08/02/2016
19 412034 APN Mgat4a 0.264 IGL03177 1 37444887 V501L C A missense Het probably damaging 0.997 phenotype 08/02/2016
20 412021 APN Mlxip 0.167 IGL03177 5 123445981 P536T C A missense Het possibly damaging 0.856 phenotype 08/02/2016
21 412057 APN Mrpl2 0.886 IGL03177 17 46649037 T213S A T missense Het probably damaging 0.990 phenotype 08/02/2016
22 412060 APN Nos1ap 0.000 IGL03177 1 170390730 C A critical splice donor site 1 bp Het probably null 08/02/2016
23 412042 APN Olfr1247 0.136 IGL03177 2 89609482 V207I C T missense Het probably benign 0.026 phenotype 08/02/2016
24 412045 APN Olfr786 0.060 IGL03177 10 129436815 M1T T C start codon destroyed Het probably null 0.820 phenotype 08/02/2016
25 412025 APN Olfr914 0.056 IGL03177 9 38606571 Y35* T A nonsense Het probably null phenotype 08/02/2016
26 412046 APN P2rx2 0.000 IGL03177 5 110341613 I251V T C missense Het probably damaging 0.998 phenotype 08/02/2016
27 412064 APN Parva 1.000 IGL03177 7 112572933 T A splice site Het probably benign phenotype 08/02/2016
28 412037 APN Phf10 0.000 IGL03177 17 14946231 T459I G A missense Het probably damaging 0.996 phenotype 08/02/2016
29 412020 APN Prg4 0.126 IGL03177 1 150455603 T A intron Het probably benign phenotype 08/02/2016
30 412051 APN Pum3 0.965 IGL03177 19 27390212 I639N A T missense Het probably benign 0.291 phenotype 08/02/2016
31 412035 APN Rlf 1.000 IGL03177 4 121148079 K1235* T A nonsense Het probably null phenotype 08/02/2016
32 412059 APN Ryr3 0.331 IGL03177 2 113028671 I46F T A missense Het probably benign 0.388 phenotype 08/02/2016
33 412047 APN Sall3 1.000 IGL03177 18 80972968 S582P A G missense Het probably benign 0.002 phenotype 08/02/2016
34 412030 APN Scn3b 0.000 IGL03177 9 40270042 Y17S A C missense Het probably benign 0.002 phenotype 08/02/2016
35 412038 APN Senp8 0.439 IGL03177 9 59737328 C169R A G missense Het probably damaging 1.000 phenotype 08/02/2016
36 412036 APN Sgsm1 0.000 IGL03177 5 113250993 A1025T C T missense Het probably damaging 1.000 08/02/2016
37 412029 APN Six1 0.850 IGL03177 12 73043740 E217G T C missense Het possibly damaging 0.679 phenotype 08/02/2016
38 412044 APN Slc38a8 0.067 IGL03177 8 119485512 D364G T C missense Het probably damaging 1.000 phenotype 08/02/2016
39 412052 APN Stk10 0.125 IGL03177 11 32614592 E801V A T missense Het probably damaging 1.000 phenotype 08/02/2016
40 412058 APN Ston2 0.420 IGL03177 12 91647657 I659N A T missense Het probably damaging 1.000 phenotype 08/02/2016
41 412024 APN Stxbp4 0.000 IGL03177 11 90571753 Q331R T C missense Het probably benign 0.013 08/02/2016
42 412053 APN Synpo2 1.000 IGL03177 3 123121215 V54E A T missense Het probably damaging 0.998 08/02/2016
43 412049 APN Tax1bp1 0.182 IGL03177 6 52736947 D237G A G missense Het possibly damaging 0.955 phenotype 08/02/2016
44 412056 APN Tmigd1 0.000 IGL03177 11 76906948 Y39H T C missense Het probably benign 0.062 08/02/2016
45 412023 APN Vmn1r15 0.194 IGL03177 6 57258473 T109A A G missense Het probably benign 0.269 08/02/2016
46 412019 APN Vmn1r209 0.140 IGL03177 13 22805854 Y222C T C missense Het possibly damaging 0.464 08/02/2016
47 412022 APN Zfp809 0.134 IGL03177 9 22235051 D12G A G missense Het probably damaging 0.993 phenotype 08/02/2016
[records 1 to 47 of 47]