Incidental Mutations

35 incidental mutations are currently displayed, and affect 35 genes.
7 are Possibly Damaging.
15 are Probably Damaging.
9 are Probably Benign.
3 are Probably Null.
0 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 35 of 35] 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 297324 APN Aak1 0.476 IGL02531 6 86956447 H467N C A missense Het unknown phenotype 04/16/2015
2 297313 APN Alb 0.197 IGL02531 5 90467448 D273G A G missense Het probably damaging 1.000 phenotype 04/16/2015
3 297307 APN Arap3 0.789 IGL02531 18 37989751 S531P A G missense Het probably damaging 0.991 phenotype 04/16/2015
4 297330 APN Bmpr2 1.000 IGL02531 1 59845714 T A splice site 6 bp Het probably null phenotype 04/16/2015
5 297321 APN Chd7 0.948 IGL02531 4 8854134 R1902H G A missense Het probably damaging 1.000 phenotype 04/16/2015
6 297322 APN Csgalnact1 0.079 IGL02531 8 68401492 G219V C A missense Het probably damaging 1.000 phenotype 04/16/2015
7 297304 APN Cyp2b13 0.000 IGL02531 7 26061605 H29L A T missense Het possibly damaging 0.545 04/16/2015
8 297312 APN Enpp5 0.000 IGL02531 17 44080952 V91F G T missense Het probably damaging 0.999 phenotype 04/16/2015
9 297298 APN Fam210b 0.000 IGL02531 2 172352755 Y176H T C missense Het probably damaging 0.992 04/16/2015
10 297319 APN Fam83b 0.093 IGL02531 9 76492000 E607G T C missense Het possibly damaging 0.612 04/16/2015
11 297311 APN Gm4788 0.057 IGL02531 1 139774569 K59R T C missense Het probably benign 0.098 04/16/2015
12 297328 APN Hhla1 0.059 IGL02531 15 65967407 C T splice site Het probably benign 04/16/2015
13 297316 APN Kdm3b 0.950 IGL02531 18 34795729 T178A A G missense Het probably benign 0.000 04/16/2015
14 297325 APN Klf1 1.000 IGL02531 8 84904808 F334I T A missense Het probably damaging 0.966 phenotype 04/16/2015
15 297300 APN Klra8 0.050 IGL02531 6 130118970 S220P A G missense Het possibly damaging 0.674 phenotype 04/16/2015
16 297320 APN Medag 0.000 IGL02531 5 149422151 N99S A G missense Het probably benign 0.001 04/16/2015
17 297306 APN Muc6 0.084 IGL02531 7 141636940 T2607A T C missense Het possibly damaging 0.528 phenotype 04/16/2015
18 297297 APN Mug2 0.059 IGL02531 6 122072771 L921R T G missense Het probably damaging 0.998 04/16/2015
19 297305 APN Nacad 0.000 IGL02531 11 6598580 N1385D T C missense Het possibly damaging 0.897 04/16/2015
20 297327 APN Nin 0.000 IGL02531 12 70020932 F1983L A G missense Het probably benign 0.018 phenotype 04/16/2015
21 297303 APN Nipal4 0.116 IGL02531 11 46151325 I176M T C missense Het probably damaging 1.000 phenotype 04/16/2015
22 297301 APN Orc6 1.000 IGL02531 8 85303369 S47P T C missense Het probably damaging 0.997 phenotype 04/16/2015
23 297310 APN Ovch2 0.000 IGL02531 7 107790198 C341Y C T missense Het probably damaging 1.000 04/16/2015
24 297323 APN Polq 0.335 IGL02531 16 37062374 H1633Q T A missense Het possibly damaging 0.754 phenotype 04/16/2015
25 297331 APN Rab23 1.000 IGL02531 1 33738280 T C splice site Het probably benign phenotype 04/16/2015
26 297309 APN Rai14 0.490 IGL02531 15 10574782 S697P A G missense Het probably damaging 0.997 04/16/2015
27 297318 APN Rnf213 0.000 IGL02531 11 119436802 F1872L T C missense Het probably benign 0.000 phenotype 04/16/2015
28 297308 APN Sdhc 1.000 IGL02531 1 171136018 H127R T C missense Het probably damaging 1.000 phenotype 04/16/2015
29 297299 APN Snx9 0.760 IGL02531 17 5891820 V74A T C missense Het probably benign 0.000 phenotype 04/16/2015
30 297315 APN Spata31d1d 0.000 IGL02531 13 59727934 S596P A G missense Het possibly damaging 0.856 04/16/2015
31 297326 APN Syt14 0.000 IGL02531 1 192901934 *78W T C makesense Het probably null phenotype 04/16/2015
32 297314 APN Thoc1 1.000 IGL02531 18 9970258 T203A A G missense Het probably benign 0.000 phenotype 04/16/2015
33 297329 APN Trmt13 0.136 IGL02531 3 116592191 A G critical splice donor site 2 bp Het probably null 04/16/2015
34 297317 APN Ttc28 0.000 IGL02531 5 111225850 I1020V A G missense Het probably damaging 0.995 04/16/2015
35 297302 APN Vmn2r16 0.112 IGL02531 5 109340268 T336A A G missense Het probably damaging 0.989 04/16/2015
[records 1 to 35 of 35]