Incidental Mutations

39 incidental mutations are currently displayed, and affect 38 genes.
8 are Possibly Damaging.
16 are Probably Damaging.
11 are Probably Benign.
4 are Probably Null.
1 create premature stop codons.
0 are critical splice junction mutations.
Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 39 of 39] 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 84375 APN 0610010F05Rik 0.191 IGL01444 G1 11 23620225 (GRCm38) T G splice site Het probably benign 2013-11-11
2 84348 APN Adad1 0.311 IGL01444 G1 3 37092034 (GRCm38) N517I A T missense Het probably damaging 1.000 phenotype 2013-11-11
3 84347 APN Adam25 0.079 IGL01444 G1 8 40754921 (GRCm38) R408H G A missense Het probably benign 0.000 phenotype 2013-11-11
4 84344 APN Ang 0.133 IGL01444 G1 14 51101667 (GRCm38) Y88* C A nonsense Het probably null phenotype 2013-11-11
5 84353 APN Ankrd42 0.062 IGL01444 G1 7 92610585 (GRCm38) T327A T C missense Het probably damaging 0.957 2013-11-11
6 84354 APN Birc6 1.000 IGL01444 G1 17 74631687 (GRCm38) D2696G A G missense Het probably damaging 0.998 phenotype 2013-11-11
7 84339 APN Chd3 0.000 IGL01444 G1 11 69348742 (GRCm38) T1717M G A missense Het probably benign 0.285 phenotype 2013-11-11
8 84362 APN Csmd1 0.000 IGL01444 G1 8 16200055 (GRCm38) M970L T A missense Het probably benign 0.001 phenotype 2013-11-11
9 84351 APN Dhx32 0.159 IGL01444 G1 7 133748977 (GRCm38) I121M T C missense Het possibly damaging 0.759 phenotype 2013-11-11
10 84356 APN Dnah11 0.671 IGL01444 G1 12 118020232 (GRCm38) S2506F G A missense Het possibly damaging 0.907 phenotype 2013-11-11
11 84361 APN Dscam 1.000 IGL01444 G1 16 96673709 (GRCm38) I1218F T A missense Het possibly damaging 0.951 phenotype 2013-11-11
12 84343 APN Duox1 0.000 IGL01444 G1 2 122340090 (GRCm38) L1197P T C missense Het probably damaging 0.980 phenotype 2013-11-11
13 84376 APN Eps8l2 0.000 IGL01444 G1 7 141361375 (GRCm38) T C splice site Het probably benign phenotype 2013-11-11
14 84340 APN Exoc3 0.963 IGL01444 G1 13 74206935 (GRCm38) K49R T C missense Het probably damaging 1.000 phenotype 2013-11-11
15 84349 APN Exoc8 1.000 IGL01444 G1 8 124895841 (GRCm38) T596S T A missense Het possibly damaging 0.842 phenotype 2013-11-11
16 84355 APN F13a1 0.000 IGL01444 G1 13 36918577 (GRCm38) G391R C T missense Het probably null 1.000 phenotype 2013-11-11
17 84371 APN Fam35a 0.082 IGL01444 G1 14 34237557 (GRCm38) V823F C A missense Het probably damaging 1.000 2013-11-11
18 84365 APN Fat3 0.519 IGL01444 G1 9 15998848 (GRCm38) S1953T A T missense Het probably damaging 0.997 phenotype 2013-11-11
19 84366 APN Gls2 0.000 IGL01444 G1 10 128201347 (GRCm38) N252K C A missense Het probably damaging 0.999 phenotype 2013-11-11
20 84345 APN Gm5346 0.061 IGL01444 G1 8 43626433 (GRCm38) D251E A T missense Het probably benign 0.058 2013-11-11
21 84373 APN Haus2 0.937 IGL01444 G1 2 120615942 (GRCm38) R115K G A missense Het probably benign 0.002 phenotype 2013-11-11
22 84369 APN Ift122 1.000 IGL01444 G1 6 115884379 (GRCm38) K262E A G missense Het probably benign 0.083 phenotype 2013-11-11
23 84358 APN Islr2 1.000 IGL01444 G1 9 58198378 (GRCm38) C533Y C T missense Het probably damaging 1.000 phenotype 2013-11-11
24 84367 APN Lrp2 1.000 IGL01444 G1 2 69443716 (GRCm38) F3997I A T missense Het possibly damaging 0.936 phenotype 2013-11-11
25 84357 APN Nt5c1a 0.153 IGL01444 G1 4 123216169 (GRCm38) R354W C T missense Het probably damaging 0.997 phenotype 2013-11-11
26 84341 APN Olfr776 0.062 IGL01444 G1 10 129261335 (GRCm38) C125S T A missense Het probably damaging 1.000 phenotype 2013-11-11
27 84364 APN Pcolce 0.105 IGL01444 G1 5 137607476 (GRCm38) S200R A T missense Het probably damaging 0.980 phenotype 2013-11-11
28 84346 APN Plec 0.738 IGL01444 G1 15 76179297 (GRCm38) V2213A A G missense Het possibly damaging 0.455 phenotype 2013-11-11
29 84350 APN Prmt3 0.390 IGL01444 G1 7 49780372 (GRCm38) D74E T A missense Het probably benign 0.001 phenotype 2013-11-11
30 84372 APN Ptk7 1.000 IGL01444 G1 17 46565387 (GRCm38) F1046S A G missense Het probably damaging 1.000 phenotype 2013-11-11
31 84342 APN Ranbp2 1.000 IGL01444 G1 10 58475300 (GRCm38) Y887H T C missense Het possibly damaging 0.790 phenotype 2013-11-11
32 84360 APN Sez6l2 0.000 IGL01444 G1 7 126961883 (GRCm38) E447K G A missense Het possibly damaging 0.912 phenotype 2013-11-11
33 84374 APN Snrnp70 0.962 IGL01444 G1 7 45387236 (GRCm38) C T splice site 154 bp Het probably null phenotype 2013-11-11
34 84368 APN Timm10 0.973 IGL01444 G1 2 84829864 (GRCm38) V49E T A missense Het probably damaging 1.000 phenotype 2013-11-11
35 84377 APN Tox2 0.000 IGL01444 G1 2 163225466 (GRCm38) T C utr 5 prime Het probably benign 2013-11-11
36 84363 APN Usp20 0.000 IGL01444 G1 2 30998789 (GRCm38) M1K T A start codon destroyed Het probably null 1.000 phenotype 2013-11-11
37 84370 APN Usp32 1.000 IGL01444 G1 11 85059164 (GRCm38) L223V A C missense Het probably damaging 0.966 2013-11-11
38 84359 APN Zeb1 0.929 IGL01444 G1 18 5767138 (GRCm38) S550P T C missense Het probably benign 0.000 0.061 phenotype 2013-11-11
39 84352 APN Zeb1 0.929 IGL01444 G1 18 5767906 (GRCm38) A806S G T missense Het probably damaging 0.997 phenotype 2013-11-11
[records 1 to 39 of 39]