Incidental Mutations

26 incidental mutations are currently displayed, and affect 26 genes.
6 are Possibly Damaging.
8 are Probably Damaging.
9 are Probably Benign.
2 are Probably Null.
1 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 26 of 26] 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 300308 APN 1110004E09Rik 0.300 IGL02607 16 90929947 T98M G A missense Het probably damaging 1.000 phenotype 04/16/2015
2 300309 APN Abca17 0.000 IGL02607 17 24327705 W307* C T nonsense Het probably null 04/16/2015
3 300321 APN Cit 0.955 IGL02607 5 115859209 I84V A G missense Het probably benign 0.000 phenotype 04/16/2015
4 300327 APN Cltc 0.953 IGL02607 11 86706714 D1132G T C missense Het probably benign 0.003 phenotype 04/16/2015
5 300323 APN Cobll1 0.339 IGL02607 2 65151085 S54T A T missense Het probably damaging 0.977 04/16/2015
6 300324 APN Dcstamp 0.599 IGL02607 15 39754584 R130G A G missense Het possibly damaging 0.942 phenotype 04/16/2015
7 300328 APN Dennd4a 0.451 IGL02607 9 64862327 M439V A G missense Het probably damaging 0.993 phenotype 04/16/2015
8 300318 APN Dnajc15 0.000 IGL02607 14 77840216 I110F T A missense Het probably damaging 1.000 phenotype 04/16/2015
9 300310 APN Dock1 1.000 IGL02607 7 134851513 F824L T C missense Het probably benign 0.134 phenotype 04/16/2015
10 300315 APN Eml2 0.000 IGL02607 7 19206111 H617R A G missense Het probably damaging 1.000 04/16/2015
11 300322 APN Fgd6 0.434 IGL02607 10 94044448 Q388L A T missense Het possibly damaging 0.944 04/16/2015
12 300331 APN Fkbp4 0.726 IGL02607 6 128434470 A T splice site Het probably benign phenotype 04/16/2015
13 300314 APN Fmnl3 0.667 IGL02607 15 99324772 L431Q A T missense Het probably damaging 1.000 phenotype 04/16/2015
14 300329 APN Gng8 0.293 IGL02607 7 16894934 T C splice site Het probably benign phenotype 04/16/2015
15 300320 APN Hmcn1 0.000 IGL02607 1 150744995 I1155F T A missense Het possibly damaging 0.879 phenotype 04/16/2015
16 300325 APN Muc4 0.085 IGL02607 16 32775819 C3135F G T missense Het possibly damaging 0.734 phenotype 04/16/2015
17 300306 APN Mycbp2 1.000 IGL02607 14 103285273 G685D C T missense Het probably damaging 1.000 phenotype 04/16/2015
18 300312 APN Olfr1389 0.275 IGL02607 11 49430512 F12S T C missense Het probably damaging 0.997 phenotype 04/16/2015
19 300307 APN Pcdhb8 0.063 IGL02607 18 37357581 I771F A T missense Het probably benign 0.005 04/16/2015
20 300330 APN Pkn2 1.000 IGL02607 3 142794101 A G critical splice donor site 2 bp Het probably null phenotype 04/16/2015
21 300316 APN Rrn3 1.000 IGL02607 16 13806563 V420L G T missense Het possibly damaging 0.650 phenotype 04/16/2015
22 300319 APN Samm50 0.952 IGL02607 15 84207838 Y338F A T missense Het probably benign 0.085 phenotype 04/16/2015
23 300317 APN Slc2a7 0.088 IGL02607 4 150154705 T129I C T missense Het probably benign 0.000 phenotype 04/16/2015
24 300326 APN Tbc1d8 0.000 IGL02607 1 39379511 I806V T C missense Het probably benign 0.045 04/16/2015
25 300313 APN Tex2 0.000 IGL02607 11 106546747 E699G T C missense Het unknown 04/16/2015
26 300311 APN Vmn2r85 0.071 IGL02607 10 130426421 K150E T C missense Het possibly damaging 0.895 04/16/2015
[records 1 to 26 of 26]