Incidental Mutations

32 incidental mutations are currently displayed, and affect 32 genes.
6 are Possibly Damaging.
12 are Probably Damaging.
9 are Probably Benign.
4 are Probably Null.
3 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 32 of 32] 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 102872 APN 4933421I07Rik 0.054 IGL01653 G1 7 42446974 (GRCm38) D119G T C missense Het probably damaging 1.000 2014-01-21
2 102896 APN 5430403G16Rik 0.111 IGL01653 G1 5 109677316 (GRCm38) Y89* A C nonsense Het probably null 2014-01-21
3 102881 APN Apol7c 0.050 IGL01653 G1 15 77526300 (GRCm38) C149R A G missense Het probably damaging 1.000 2014-01-21
4 102877 APN Arfgef1 1.000 IGL01653 G1 1 10159908 (GRCm38) R1235* G A nonsense Het probably null phenotype 2014-01-21
5 102882 APN Bpifb4 0.050 IGL01653 G1 2 153944783 (GRCm38) D285G A G missense Het probably damaging 0.998 2014-01-21
6 102878 APN Cep192 0.000 IGL01653 G1 18 67852972 (GRCm38) H1682Q T A missense Het possibly damaging 0.569 2014-01-21
7 102874 APN Cerk 0.073 IGL01653 G1 15 86149351 (GRCm38) Y290* G T nonsense Het probably null phenotype 2014-01-21
8 102897 APN Cyld 0.000 IGL01653 G1 8 88741370 (GRCm38) I544F A T missense Het probably damaging 0.997 phenotype 2014-01-21
9 102893 APN Dcp1a 0.293 IGL01653 G1 14 30505571 (GRCm38) S134P T C missense Het possibly damaging 0.521 phenotype 2014-01-21
10 332105 APN Epha6 0.000 IGL01653 G1 16 59839303 (GRCm38) N817K A C missense Het probably benign 0.047 phenotype 2015-08-05
11 102900 APN Ephb4 1.000 IGL01653 G1 5 137365741 (GRCm38) A G splice site Het probably benign phenotype 2014-01-21
12 102876 APN Fcgr3 0.000 IGL01653 G1 1 171059280 (GRCm38) L25Q A T missense Het probably damaging 1.000 phenotype 2014-01-21
13 102885 APN Heatr3 0.929 IGL01653 G1 8 88144617 (GRCm38) I83V A G missense Het probably benign 0.000 phenotype 2014-01-21
14 102895 APN Hormad1 0.000 IGL01653 G1 3 95578297 (GRCm38) N265K T A missense Het possibly damaging 0.489 phenotype 2014-01-21
15 102880 APN Kpna1 0.516 IGL01653 G1 16 36020192 (GRCm38) T201A A G missense Het probably benign 0.000 phenotype 2014-01-21
16 102894 APN Krt6b 0.147 IGL01653 G1 15 101679114 (GRCm38) T182S T A missense Het probably damaging 0.999 2014-01-21
17 102890 APN Macc1 0.070 IGL01653 G1 12 119450353 (GRCm38) K755E A G missense Het probably damaging 0.995 phenotype 2014-01-21
18 102884 APN Med12l 0.271 IGL01653 G1 3 59261893 (GRCm38) T1568M C T missense Het probably damaging 1.000 phenotype 2014-01-21
19 102899 APN Muc4 0.099 IGL01653 G1 16 32761348 (GRCm38) G T splice site 5 bp Het probably null phenotype 2014-01-21
20 102883 APN Myt1l 0.000 IGL01653 G1 12 29910771 (GRCm38) S1028P T C missense Het unknown phenotype 2014-01-21
21 102887 APN Nhlrc2 1.000 IGL01653 G1 19 56570850 (GRCm38) R256C C T missense Het probably benign 0.255 2014-01-21
22 102886 APN Olfr1230 0.072 IGL01653 G1 2 89297127 (GRCm38) T48S T A missense Het probably benign 0.084 phenotype 2014-01-21
23 102875 APN Olfr1441 0.121 IGL01653 G1 19 12422372 (GRCm38) R21H G A missense Het probably benign 0.000 phenotype 2014-01-21
24 102879 APN Pfkfb4 0.000 IGL01653 G1 9 108999134 (GRCm38) R79H G A missense Het probably damaging 1.000 phenotype 2014-01-21
25 102898 APN Piezo2 1.000 IGL01653 G1 18 63182833 (GRCm38) T C splice site Het probably benign phenotype 2014-01-21
26 102871 APN Pramel5 0.104 IGL01653 G1 4 144273859 (GRCm38) R49H C T missense Het probably benign 0.015 2014-01-21
27 102889 APN Ralgapb 1.000 IGL01653 G1 2 158462159 (GRCm38) S613T T A missense Het possibly damaging 0.942 2014-01-21
28 102888 APN Ryr1 1.000 IGL01653 G1 7 29078597 (GRCm38) E2158G T C missense Het probably damaging 0.989 phenotype 2014-01-21
29 102873 APN Scgb2b19 0.033 IGL01653 G1 7 33279728 (GRCm38) Y43F T A missense Het probably damaging 0.987 2014-01-21
30 102892 APN Slc17a6 1.000 IGL01653 G1 7 51668022 (GRCm38) T468A A G missense Het possibly damaging 0.922 phenotype 2014-01-21
31 102870 APN Slc36a1 0.633 IGL01653 G1 11 55228321 (GRCm38) D374G A G missense Het possibly damaging 0.734 phenotype 2014-01-21
32 102891 APN Wdtc1 0.000 IGL01653 G1 4 133295232 (GRCm38) D601G T C missense Het probably damaging 1.000 phenotype 2014-01-21
[records 1 to 32 of 32]