Incidental Mutations

41 incidental mutations are currently displayed, and affect 41 genes.
6 are Possibly Damaging.
16 are Probably Damaging.
15 are Probably Benign.
2 are Probably Null.
0 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 41 of 41] 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 179518 APN 4931408C20Rik 0.000 IGL01901 G1 1 26682584 F1172L A G missense Het probably benign 0.132 05/07/2014
2 179542 APN Adam2 0.000 IGL01901 G1 14 66035229 A G splice site Het probably benign phenotype 05/07/2014
3 179513 APN Aldh1a7 0.275 IGL01901 G1 19 20717739 Y154S T G missense Het probably damaging 0.991 05/07/2014
4 179511 APN BC117090 0.009 IGL01901 G1 16 36334263 A11S C A missense Het probably damaging 1.000 05/07/2014
5 179527 APN Casc3 0.918 IGL01901 G1 11 98823121 D393G A G missense Het probably damaging 0.998 phenotype 05/07/2014
6 179538 APN Cd180 0.000 IGL01901 G1 13 102706428 I661V A G missense Het probably benign 0.036 phenotype 05/07/2014
7 179524 APN Cdh1 1.000 IGL01901 G1 8 106657760 S287P T C missense Het probably damaging 0.994 phenotype 05/07/2014
8 179529 APN Clnk 0.106 IGL01901 G1 5 38794978 N6S T C missense Het probably damaging 0.995 phenotype 05/07/2014
9 179533 APN Cyp17a1 0.263 IGL01901 G1 19 46671092 V100M C T missense Het possibly damaging 0.638 phenotype 05/07/2014
10 179528 APN Ddhd2 0.348 IGL01901 G1 8 25748594 V53A A G missense Het probably damaging 0.962 phenotype 05/07/2014
11 179544 APN Elovl7 0.292 IGL01901 G1 13 108274393 T A critical splice donor site 2 bp Het probably null 05/07/2014
12 279050 APN Gm10717 0.581 IGL01901 G1 9 3025616 S67L C T missense Het probably benign 0.002 04/16/2015
13 279049 APN Gm10718 0.354 IGL01901 G1 9 3025118 Y194F A T missense Het probably benign 0.001 04/16/2015
14 179521 APN Gm14180 0.370 IGL01901 G1 11 99734227 S22P A G missense Het unknown 05/07/2014
15 279048 APN Gm21738 0.533 IGL01901 G1 14 19416979 S144L G A missense Het probably benign 0.011 04/16/2015
16 179547 APN Golga5 0.347 IGL01901 G1 12 102479802 G A critical splice donor site 1 bp Het probably null phenotype 05/07/2014
17 179535 APN Gpr162 0.345 IGL01901 G1 6 124861407 F93L A T missense Het possibly damaging 0.955 phenotype 05/07/2014
18 179545 APN Kcnh8 0.302 IGL01901 G1 17 52894120 G A splice site Het probably benign phenotype 05/07/2014
19 179520 APN Lamp3 0.360 IGL01901 G1 16 19673419 F358L A T missense Het probably damaging 1.000 phenotype 05/07/2014
20 179539 APN Mdn1 0.973 IGL01901 G1 4 32669591 D409E T G missense Het probably damaging 0.999 05/07/2014
21 179541 APN Ms4a10 0.034 IGL01901 G1 19 10963010 D211G T C missense Het probably benign 0.000 phenotype 05/07/2014
22 179525 APN Ms4a3 0.056 IGL01901 G1 19 11639266 E4G T C missense Het possibly damaging 0.855 phenotype 05/07/2014
23 179546 APN Myo15 0.000 IGL01901 G1 11 60527434 A G utr 3 prime Het probably benign phenotype 05/07/2014
24 179514 APN Olfr1257 0.083 IGL01901 G1 2 89881482 I219V A G missense Het probably damaging 1.000 phenotype 05/07/2014
25 179522 APN Olfr1448 0.129 IGL01901 G1 19 12919583 H242R T C missense Het probably damaging 0.980 phenotype 05/07/2014
26 179523 APN Olfr612 0.110 IGL01901 G1 7 103538970 L88Q A T missense Het probably damaging 0.977 phenotype 05/07/2014
27 179512 APN Olfr638 0.128 IGL01901 G1 7 104004067 H264R A G missense Het probably damaging 1.000 phenotype 05/07/2014
28 179517 APN Olfr698 0.116 IGL01901 G1 7 106752545 V281A A G missense Het possibly damaging 0.520 phenotype 05/07/2014
29 179530 APN Olfr815 0.043 IGL01901 G1 10 129901853 F286L A G missense Het probably benign 0.190 phenotype 05/07/2014
30 179526 APN Penk 0.000 IGL01901 G1 4 4134465 I61V T C missense Het probably benign 0.024 phenotype 05/07/2014
31 179516 APN Pkhd1 0.301 IGL01901 G1 1 20220083 K2860N T A missense Het probably benign 0.114 phenotype 05/07/2014
32 179540 APN Prtg 0.428 IGL01901 G1 9 72855066 P492S C T missense Het probably damaging 0.998 phenotype 05/07/2014
33 179543 APN Tdrd7 0.668 IGL01901 G1 4 45989225 T C splice site Het probably benign phenotype 05/07/2014
34 179536 APN Terf2ip 1.000 IGL01901 G1 8 112012068 N196S A G missense Het probably benign 0.000 phenotype 05/07/2014
35 179534 APN Tgtp1 0.083 IGL01901 G1 11 48987555 N108D T C missense Het possibly damaging 0.872 05/07/2014
36 179532 APN Thumpd3 0.548 IGL01901 G1 6 113059971 H277R A G missense Het probably benign 0.094 05/07/2014
37 179531 APN Tshz2 1.000 IGL01901 G1 2 169885536 L215Q T A missense Het possibly damaging 0.865 phenotype 05/07/2014
38 179515 APN Ube3c 0.367 IGL01901 G1 5 29668007 V1015E T A missense Het probably damaging 0.999 05/07/2014
39 179537 APN Utrn 0.000 IGL01901 G1 10 12640928 K2307N T A missense Het probably damaging 1.000 phenotype 05/07/2014
40 179519 APN Vmn1r75 0.100 IGL01901 G1 7 11880812 Y157C A G missense Het probably damaging 0.999 05/07/2014
41 279051 APN Vmn2r-ps159 0.854 IGL01901 G1 4 156338254 C T exon Het noncoding transcript 04/16/2015
[records 1 to 41 of 41]