Incidental Mutations

28 incidental mutations are currently displayed, and affect 28 genes.
8 are Possibly Damaging.
8 are Probably Damaging.
12 are Probably Benign.
0 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 28 of 28] 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 90098 APN Clca4b 0.071 IGL01539 G1 3 144926157 M196L T A missense Het probably benign 0.000 phenotype 12/03/2013
2 90106 APN Cyp4a14 0.059 IGL01539 G1 4 115487177 N497S T C missense Het possibly damaging 0.710 phenotype 12/03/2013
3 90114 APN Eif3b 1.000 IGL01539 G1 5 140430253 T C splice site Het probably benign phenotype 12/03/2013
4 90113 APN Gm5724 0.062 IGL01539 G1 6 141727607 S402P A G missense Het possibly damaging 0.880 12/03/2013
5 90110 APN Grin2c 0.353 IGL01539 G1 11 115250106 Q1062R T C missense Het probably benign 0.319 phenotype 12/03/2013
6 90107 APN Ina 0.000 IGL01539 G1 19 47015464 E237G A G missense Het probably damaging 0.961 phenotype 12/03/2013
7 90112 APN Lmx1b 0.908 IGL01539 G1 2 33639498 D83G T C missense Het possibly damaging 0.947 phenotype 12/03/2013
8 90115 APN Macf1 1.000 IGL01539 G1 4 123395908 A G splice site Het probably benign phenotype 12/03/2013
9 90101 APN Muc6 0.084 IGL01539 G1 7 141650041 M406L T A missense Het probably benign 0.073 phenotype 12/03/2013
10 90102 APN Myo15b 0.063 IGL01539 G1 11 115863473 I933T T C missense Het probably benign 0.428 12/03/2013
11 90090 APN Olfr1226 0.066 IGL01539 G1 2 89193492 F181L A G missense Het possibly damaging 0.810 phenotype 12/03/2013
12 90094 APN Olfr773 0.062 IGL01539 G1 10 129186935 N162S T C missense Het probably benign 0.042 phenotype 12/03/2013
13 90117 APN Pde1b 0.000 IGL01539 G1 15 103525345 A T splice site Het probably benign phenotype 12/03/2013
14 90093 APN Rab29 0.000 IGL01539 G1 1 131870707 R75Q G A missense Het probably damaging 1.000 12/03/2013
15 90103 APN Scn10a 0.162 IGL01539 G1 9 119638698 I792N A T missense Het probably damaging 0.989 phenotype 12/03/2013
16 90096 APN Serpinb6a 0.000 IGL01539 G1 13 33930134 V70D A T missense Het probably damaging 0.996 phenotype 12/03/2013
17 90095 APN Spg20 0.288 IGL01539 G1 3 55117302 D106G A G missense Het possibly damaging 0.946 phenotype 12/03/2013
18 90111 APN Sucla2 0.908 IGL01539 G1 14 73591121 E359G A G missense Het probably damaging 0.974 phenotype 12/03/2013
19 90104 APN Sycp2 0.000 IGL01539 G1 2 178374695 Y658C T C missense Het probably damaging 0.995 phenotype 12/03/2013
20 90109 APN Tenm2 0.515 IGL01539 G1 11 36106827 T811S T A missense Het possibly damaging 0.889 phenotype 12/03/2013
21 90092 APN Trim66 0.143 IGL01539 G1 7 109455066 M1312I C A missense Het probably benign 0.017 12/03/2013
22 90100 APN Tspan18 0.000 IGL01539 G1 2 93210853 S135P A G missense Het probably damaging 0.997 12/03/2013
23 90116 APN Ube2j1 0.000 IGL01539 G1 4 33043993 T C splice site Het probably benign phenotype 12/03/2013
24 90108 APN Ubr1 0.836 IGL01539 G1 2 120926013 V711G A C missense Het possibly damaging 0.792 phenotype 12/03/2013
25 90099 APN Veph1 0.000 IGL01539 G1 3 66158075 T524A T C missense Het probably benign 0.001 phenotype 12/03/2013
26 90091 APN Vmn1r222 0.082 IGL01539 G1 13 23232889 F51L A T missense Het probably benign 0.446 12/03/2013
27 90097 APN Vwf 0.160 IGL01539 G1 6 125590262 V338L G T missense Het possibly damaging 0.848 phenotype 12/03/2013
28 90105 APN Zfp770 0.207 IGL01539 G1 2 114197093 A165E G T missense Het probably damaging 0.989 12/03/2013
[records 1 to 28 of 28]