Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
4 are Possibly Damaging.
9 are Probably Damaging.
10 are Probably Benign.
1 are Probably Null.
0 create premature stop codons.
0 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 25 of 25] 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 415304 APN A530099J19Rik 0.000 IGL03272 13 19729537 A T exon Het noncoding transcript 08/02/2016
2 415311 APN Acp2 0.364 IGL03272 2 91204233 C T splice site Het probably benign phenotype 08/02/2016
3 415309 APN B4galnt3 0.069 IGL03272 6 120216306 D413G T C missense Het probably damaging 1.000 phenotype 08/02/2016
4 415305 APN Chd2 0.487 IGL03272 7 73453166 D1357G T C missense Het possibly damaging 0.936 phenotype 08/02/2016
5 415295 APN Dsg1b 0.000 IGL03272 18 20397389 L367P T C missense Het probably benign 0.255 phenotype 08/02/2016
6 415301 APN Emsy 0.456 IGL03272 7 98593762 F1057I A T missense Het probably damaging 0.975 08/02/2016
7 415310 APN Fam171a2 0.120 IGL03272 11 102444118 F64L A T missense Het possibly damaging 0.578 08/02/2016
8 415300 APN Fat4 1.000 IGL03272 3 39009703 S4603P T C missense Het probably benign 0.000 phenotype 08/02/2016
9 415306 APN Fyco1 0.000 IGL03272 9 123829603 T503A T C missense Het probably benign 0.005 phenotype 08/02/2016
10 415294 APN Gpr179 0.115 IGL03272 11 97336593 T1579A T C missense Het possibly damaging 0.890 phenotype 08/02/2016
11 415290 APN Itgae 0.000 IGL03272 11 73133854 T C splice site 1631 bp Het probably null phenotype 08/02/2016
12 415303 APN Lrriq3 0.090 IGL03272 3 155101058 I115F A T missense Het probably damaging 0.988 08/02/2016
13 415297 APN Mmrn1 0.000 IGL03272 6 60988435 D1149G A G missense Het probably damaging 1.000 phenotype 08/02/2016
14 415307 APN Mylk 0.000 IGL03272 16 34979189 K1650Q A C missense Het probably benign 0.087 phenotype 08/02/2016
15 415312 APN Nrap 0.000 IGL03272 19 56345568 T C intron Het probably benign 08/02/2016
16 415289 APN Olfr193 0.065 IGL03272 16 59110556 V18G A C missense Het probably benign 0.012 phenotype 08/02/2016
17 415292 APN Ovgp1 0.000 IGL03272 3 105981325 D332E T A missense Het probably damaging 0.992 phenotype 08/02/2016
18 415298 APN Pou2f1 1.000 IGL03272 1 165896480 I296K A T missense Het possibly damaging 0.672 phenotype 08/02/2016
19 415313 APN Psd4 0.000 IGL03272 2 24405680 A G splice site Het probably benign 08/02/2016
20 415299 APN Satb2 1.000 IGL03272 1 56845643 Q433R T C missense Het probably damaging 0.996 phenotype 08/02/2016
21 415291 APN Serpinb9f 0.090 IGL03272 13 33327916 N134I A T missense Het probably damaging 1.000 08/02/2016
22 415308 APN Slc6a3 0.000 IGL03272 13 73540929 N124S A G missense Het probably damaging 0.979 phenotype 08/02/2016
23 415302 APN Spta1 0.884 IGL03272 1 174214144 N1360S A G missense Het probably benign 0.075 phenotype 08/02/2016
24 415296 APN Strc 0.203 IGL03272 2 121371751 T1212I G A missense Het probably damaging 0.995 phenotype 08/02/2016
25 415293 APN Tmtc3 0.761 IGL03272 10 100457080 K472R T C missense Het probably benign 0.003 phenotype 08/02/2016
[records 1 to 25 of 25]