Incidental Mutations

25 incidental mutations are currently displayed, and affect 25 genes.
4 are Possibly Damaging.
8 are Probably Damaging.
12 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 290623 APN 2410089E03Rik 1.000 IGL02363 15 8218437 H1490L A T missense Het possibly damaging 0.675 phenotype 04/16/2015
2 290625 APN Ak8 0.106 IGL02363 2 28812898 S425P T C missense Het probably damaging 0.964 phenotype 04/16/2015
3 290631 APN Comt 0.000 IGL02363 16 18411131 D153G T C missense Het probably benign 0.210 phenotype 04/16/2015
4 290628 APN Exoc6 0.000 IGL02363 19 37608954 I601T T C missense Het probably damaging 0.999 phenotype 04/16/2015
5 290611 APN F11 0.117 IGL02363 8 45241531 C598S A T missense Het probably damaging 1.000 phenotype 04/16/2015
6 290629 APN Galnt13 0.185 IGL02363 2 55112860 D524Y G T missense Het probably damaging 0.997 phenotype 04/16/2015
7 290613 APN Glb1l3 0.074 IGL02363 9 26853644 E157G T C missense Het probably damaging 1.000 04/16/2015
8 290616 APN Hc 0.654 IGL02363 2 35000835 H1323R T C missense Het probably benign 0.000 phenotype 04/16/2015
9 290612 APN Hsd3b5 0.063 IGL02363 3 98630105 I32V T C missense Het probably benign 0.078 04/16/2015
10 290621 APN Il6ra 0.000 IGL02363 3 89871253 S430P A G missense Het probably benign 0.001 phenotype 04/16/2015
11 290619 APN Lama2 0.294 IGL02363 10 27366066 T298K G T missense Het probably damaging 1.000 phenotype 04/16/2015
12 290632 APN Nedd4l 0.882 IGL02363 18 65208045 T C splice site Het probably benign phenotype 04/16/2015
13 290626 APN Ntrk3 1.000 IGL02363 7 78453337 D405G T C missense Het probably benign 0.244 phenotype 04/16/2015
14 290617 APN Opn5 0.208 IGL02363 17 42557491 D371G T C missense Het probably benign 0.000 phenotype 04/16/2015
15 290618 APN Pcdh15 0.000 IGL02363 10 74317086 A408S G T missense Het probably damaging 0.979 phenotype 04/16/2015
16 290627 APN Pim3 0.000 IGL02363 15 88862913 V54A T C missense Het probably benign 0.345 phenotype 04/16/2015
17 290622 APN Prdm5 0.000 IGL02363 6 65794319 F38S T C missense Het probably damaging 0.999 phenotype 04/16/2015
18 290630 APN Ptgs2 0.705 IGL02363 1 150105709 C T splice site 4383 bp Het probably null phenotype 04/16/2015
19 290614 APN Rnf185 0.163 IGL02363 11 3418015 I221T A G missense Het possibly damaging 0.787 04/16/2015
20 290620 APN Slc27a2 0.000 IGL02363 2 126578950 F318L T C missense Het possibly damaging 0.585 phenotype 04/16/2015
21 290624 APN Spata1 0.098 IGL02363 3 146487364 Y124C T C missense Het possibly damaging 0.956 04/16/2015
22 290633 APN Tmie 0.056 IGL02363 9 110870753 G T splice site Het probably benign phenotype 04/16/2015
23 290615 APN Tph2 0.270 IGL02363 10 115079981 K429R T C missense Het probably benign 0.013 phenotype 04/16/2015
24 290610 APN Usp32 1.000 IGL02363 11 85044787 Y388H A G missense Het probably benign 0.006 04/16/2015
25 290609 APN Vmn2r60 0.100 IGL02363 7 42195154 Q647L A T missense Het probably benign 0.018 04/16/2015
[records 1 to 25 of 25]