Incidental Mutations

44 incidental mutations are currently displayed, and affect 44 genes.
5 are Possibly Damaging.
19 are Probably Damaging.
14 are Probably Benign.
4 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 179138 APN Akt1 0.935 IGL01886 G1 12 112659158 (GRCm38) V136M C T missense Het probably benign 0.164 phenotype 2014-05-07
2 179141 APN Ankrd34c 0.066 IGL01886 G1 9 89730265 (GRCm38) L8M A T missense Het possibly damaging 0.712 2014-05-07
3 179143 APN Anks6 1.000 IGL01886 G1 4 47044850 (GRCm38) W352L C A missense Het probably damaging 1.000 phenotype 2014-05-07
4 179127 APN Arhgap12 0.000 IGL01886 G1 18 6027613 (GRCm38) N768K A T missense Het probably damaging 1.000 phenotype 2014-05-07
5 279007 APN C130026I21Rik 0.265 IGL01886 G1 1 85254186 (GRCm38) A G intron Het probably benign 2015-04-16
6 179158 APN Clec7a 0.073 IGL01886 G1 6 129463177 (GRCm38) A T splice site Het probably benign 2014-05-07
7 179148 APN Cyp3a13 0.000 IGL01886 G1 5 137898820 (GRCm38) P411S G A missense Het probably damaging 1.000 phenotype 2014-05-07
8 179140 APN Elavl2 0.416 IGL01886 G1 4 91264093 (GRCm38) V129A A G missense Het probably damaging 1.000 phenotype 2014-05-07
9 179145 APN Ercc6 0.372 IGL01886 G1 14 32569580 (GRCm38) S994T T A missense Het possibly damaging 0.904 phenotype 2014-05-07
10 179154 APN Esco1 0.228 IGL01886 G1 18 10595262 (GRCm38) K8I T A missense Het probably damaging 0.999 phenotype 2014-05-07
11 179133 APN Esr1 0.944 IGL01886 G1 10 4856861 (GRCm38) I259K T A missense Het probably damaging 0.984 phenotype 2014-05-07
12 179142 APN Filip1l 0.000 IGL01886 G1 16 57571250 (GRCm38) I734V A G missense Het possibly damaging 0.471 2014-05-07
13 279005 APN Gm10717 0.814 IGL01886 G1 9 3025616 (GRCm38) S67L C T missense Het probably benign 0.002 2015-04-16
14 279004 APN Gm10718 0.575 IGL01886 G1 9 3025118 (GRCm38) Y194F A T missense Het probably benign 0.001 2015-04-16
15 279003 APN Gm21738 0.867 IGL01886 G1 14 19416979 (GRCm38) S144L G A missense Het probably benign 0.011 2015-04-16
16 179144 APN Grin3a 0.000 IGL01886 G1 4 49702814 (GRCm38) I891F T A missense Het probably damaging 1.000 phenotype 2014-05-07
17 179153 APN Kat7 1.000 IGL01886 G1 11 95306133 (GRCm38) T27A T C missense Het probably benign 0.006 phenotype 2014-05-07
18 179157 APN Kdm1a 1.000 IGL01886 G1 4 136561016 (GRCm38) A G critical splice donor site 2 bp Het probably null phenotype 2014-05-07
19 179147 APN Kifc5b 0.324 IGL01886 G1 17 26932117 (GRCm38) V663A T C missense Het probably damaging 0.985 2014-05-07
20 179132 APN Lama1 1.000 IGL01886 G1 17 67807797 (GRCm38) S2314A T G missense Het probably benign 0.358 phenotype 2014-05-07
21 179151 APN Lrrc69 0.083 IGL01886 G1 4 14703984 (GRCm38) V279I C T missense Het probably benign 0.014 2014-05-07
22 179152 APN Mast3 0.000 IGL01886 G1 8 70782139 (GRCm38) L774Q A T missense Het possibly damaging 0.938 2014-05-07
23 179137 APN Med27 0.938 IGL01886 G1 2 29413482 (GRCm38) P9Q C A missense Het probably damaging 0.999 phenotype 2014-05-07
24 179162 APN Myo5a 0.951 IGL01886 G1 9 75169090 (GRCm38) C A splice site Het probably benign phenotype 2014-05-07
25 179150 APN Myoz1 0.000 IGL01886 G1 14 20655309 (GRCm38) K14E T C missense Het probably damaging 0.982 0.229 phenotype 2014-05-07
26 179161 APN Neb 0.831 IGL01886 G1 2 52183845 (GRCm38) T C splice site Het probably benign phenotype 2014-05-07
27 179129 APN Nlrp1a 0.102 IGL01886 G1 11 71123501 (GRCm38) T308A T C missense Het probably benign 0.000 phenotype 2014-05-07
28 179126 APN Olfr364-ps1 0.069 IGL01886 G1 2 37146509 (GRCm38) Y99C A G missense Het probably damaging 1.000 2014-05-07
29 179124 APN Olfr926 0.069 IGL01886 G1 9 38877548 (GRCm38) C124F G T missense Het probably damaging 0.968 phenotype 2014-05-07
30 179159 APN Orc1 1.000 IGL01886 G1 4 108603957 (GRCm38) T A splice site Het probably null phenotype 2014-05-07
31 179146 APN Pnkp 0.965 IGL01886 G1 7 44862207 (GRCm38) A76T G A missense Het probably damaging 1.000 phenotype 2014-05-07
32 179128 APN Polr3h 0.955 IGL01886 G1 15 81917390 (GRCm38) E95G T C missense Het probably damaging 0.999 2014-05-07
33 179136 APN Prpf40b 0.153 IGL01886 G1 15 99304447 (GRCm38) M62K T A missense Het unknown phenotype 2014-05-07
34 179134 APN Prpf8 0.963 IGL01886 G1 11 75495744 (GRCm38) Q1075K C A missense Het probably benign 0.317 phenotype 2014-05-07
35 179135 APN Ptprg 0.000 IGL01886 G1 14 12179280 (GRCm38) K766E A G missense Het probably benign 0.225 phenotype 2014-05-07
36 179125 APN Rabgap1l 0.000 IGL01886 G1 1 160342042 (GRCm38) N778K A T missense Het probably damaging 0.999 phenotype 2014-05-07
37 179149 APN Riok3 0.297 IGL01886 G1 18 12139385 (GRCm38) N204K T A missense Het probably damaging 0.997 phenotype 2014-05-07
38 179139 APN Shank3 0.279 IGL01886 G1 15 89531663 (GRCm38) K650E A G missense Het probably damaging 1.000 phenotype 2014-05-07
39 179131 APN Sim1 1.000 IGL01886 G1 10 50984315 (GRCm38) S758T T A missense Het probably damaging 0.998 phenotype 2014-05-07
40 179155 APN Slu7 1.000 IGL01886 G1 11 43439260 (GRCm38) N171K T G missense Het probably damaging 0.997 phenotype 2014-05-07
41 179156 APN Sult6b2 0.084 IGL01886 G1 6 142790126 (GRCm38) A G critical splice donor site 2 bp Het probably null 2014-05-07
42 179160 APN Taf6l 0.963 IGL01886 G1 19 8778086 (GRCm38) C T critical splice donor site 1 bp Het probably null phenotype 2014-05-07
43 179130 APN Ubtfl1 0.166 IGL01886 G1 9 18409721 (GRCm38) V182M G A missense Het possibly damaging 0.925 2014-05-07
44 279006 APN Vmn2r-ps159 0.519 IGL01886 G1 4 156338254 (GRCm38) C T exon Het noncoding transcript 2015-04-16
[records 1 to 44 of 44]