Incidental Mutations

33 incidental mutations are currently displayed, and affect 33 genes.
4 are Possibly Damaging.
11 are Probably Damaging.
15 are Probably Benign.
3 are Probably Null.
1 create premature stop codons.
2 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 33 of 33] 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 154320 APN 4932438A13Rik 1.000 IGL01813 G1 3 36928520 S778N G A missense Het possibly damaging 0.901 phenotype 02/04/2014
2 154333 APN Abcb11 0.255 IGL01813 G1 2 69287592 T A splice site Het probably benign phenotype 02/04/2014
3 154306 APN Adgrb2 0.000 IGL01813 G1 4 130012566 V929A T C missense Het probably benign 0.001 phenotype 02/04/2014
4 154323 APN Aldh2 0.000 IGL01813 G1 5 121572073 I400V T C missense Het probably benign 0.001 phenotype 02/04/2014
5 154315 APN Atxn2l 0.921 IGL01813 G1 7 126500253 D84G T C missense Het probably damaging 1.000 phenotype 02/04/2014
6 154327 APN Avpr1a 0.141 IGL01813 G1 10 122449011 N69K T A missense Het probably damaging 1.000 phenotype 02/04/2014
7 154325 APN BC022687 0.101 IGL01813 G1 12 112815559 T272M C T missense Het probably damaging 0.997 02/04/2014
8 154312 APN BC034090 0.059 IGL01813 G1 1 155226339 Q60* G A nonsense Het probably null 02/04/2014
9 154311 APN Bub3 1.000 IGL01813 G1 7 131568633 S295P T C missense Het probably benign 0.341 phenotype 02/04/2014
10 154305 APN Cacna1b 0.000 IGL01813 G1 2 24609890 S161G T C missense Het probably damaging 0.996 phenotype 02/04/2014
11 154310 APN Col6a4 0.000 IGL01813 G1 9 106077253 S296C T A missense Het probably damaging 0.999 02/04/2014
12 278891 APN Cyp4f15 0.245 IGL01813 G1 17 32686157 R38H G A missense Het probably benign 0.014 phenotype 04/16/2015
13 154326 APN Dync2h1 1.000 IGL01813 G1 9 7122799 I2052M T C missense Het probably damaging 1.000 phenotype 02/04/2014
14 154330 APN Gm11627 0.122 IGL01813 G1 11 102578808 T C utr 5 prime Het probably benign 02/04/2014
15 154332 APN Jmjd8 0.000 IGL01813 G1 17 25829238 A T critical splice acceptor site Het probably null phenotype 02/04/2014
16 154328 APN Kmt2c 1.000 IGL01813 G1 5 25290804 V629A A G missense Het possibly damaging 0.819 phenotype 02/04/2014
17 154316 APN Kremen1 0.136 IGL01813 G1 11 5199667 T335A T C missense Het probably benign 0.005 phenotype 02/04/2014
18 154313 APN Olfr109 0.073 IGL01813 G1 17 37466758 E184G A G missense Het probably damaging 1.000 phenotype 02/04/2014
19 154309 APN Olfr282 0.055 IGL01813 G1 15 98437649 Y60C A G missense Het possibly damaging 0.946 phenotype 02/04/2014
20 154324 APN Oosp2 0.070 IGL01813 G1 19 11651483 T85A T C missense Het probably benign 0.140 02/04/2014
21 154317 APN Pex5l 0.463 IGL01813 G1 3 33082055 E5G T C missense Het probably benign 0.016 phenotype 02/04/2014
22 154322 APN Pigk 0.888 IGL01813 G1 3 152742519 Q173L A T missense Het probably damaging 1.000 phenotype 02/04/2014
23 154321 APN Pik3c2g 0.101 IGL01813 G1 6 139622409 N174K T A missense Het possibly damaging 0.551 phenotype 02/04/2014
24 154304 APN Plb1 0.058 IGL01813 G1 5 32329085 H893Y C T missense Het probably damaging 1.000 phenotype 02/04/2014
25 154329 APN Pus7 0.384 IGL01813 G1 5 23760304 T C splice site Het probably benign 02/04/2014
26 154331 APN R3hdm1 0.000 IGL01813 G1 1 128175233 G A critical splice donor site 1 bp Het probably null 02/04/2014
27 154307 APN Samd7 0.139 IGL01813 G1 3 30754286 P83S C T missense Het probably benign 0.004 phenotype 02/04/2014
28 154308 APN Supt5 1.000 IGL01813 G1 7 28323975 Y293F T A missense Het probably damaging 0.994 02/04/2014
29 154318 APN Tbc1d30 0.000 IGL01813 G1 10 121267051 D692G T C missense Het probably benign 0.000 02/04/2014
30 278892 APN Tmpo 0.000 IGL01813 G1 10 91163242 R228C G A missense Het probably benign 0.006 phenotype 04/16/2015
31 154319 APN Tnn 0.491 IGL01813 G1 1 160088438 H1236Q A T missense Het probably damaging 1.000 02/04/2014
32 154314 APN Ubr3 1.000 IGL01813 G1 2 69951570 I667T T C missense Het probably benign 0.342 phenotype 02/04/2014
33 154303 APN Vmn1r183 0.051 IGL01813 G1 7 24055560 F263I T A missense Het probably benign 0.192 02/04/2014
[records 1 to 33 of 33]