Incidental Mutations

39 incidental mutations are currently displayed, and affect 38 genes.
8 are Possibly Damaging.
16 are Probably Damaging.
10 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 0.197 IGL01444 G1 11 23620225 T G splice site Het probably benign 11/11/2013
2 84348 APN Adad1 0.218 IGL01444 G1 3 37092034 N517I A T missense Het probably damaging 1.000 phenotype 11/11/2013
3 84347 APN Adam25 0.106 IGL01444 G1 8 40754921 R408H G A missense Het probably benign 0.000 phenotype 11/11/2013
4 84344 APN Ang 0.256 IGL01444 G1 14 51101667 Y88* C A nonsense Het probably null phenotype 11/11/2013
5 84353 APN Ankrd42 0.123 IGL01444 G1 7 92610585 T327A T C missense Het probably damaging 0.957 11/11/2013
6 84354 APN Birc6 1.000 IGL01444 G1 17 74631687 D2696G A G missense Het probably damaging 0.998 phenotype 11/11/2013
7 84339 APN Chd3 0.466 IGL01444 G1 11 69348742 T1717M G A missense Het probably benign 0.285 phenotype 11/11/2013
8 84362 APN Csmd1 0.387 IGL01444 G1 8 16200055 M970L T A missense Het probably benign 0.001 phenotype 11/11/2013
9 84351 APN Dhx32 0.181 IGL01444 G1 7 133748977 I121M T C missense Het possibly damaging 0.759 phenotype 11/11/2013
10 84356 APN Dnah11 0.543 IGL01444 G1 12 118020232 S2506F G A missense Het possibly damaging 0.907 phenotype 11/11/2013
11 84361 APN Dscam 1.000 IGL01444 G1 16 96673709 I1218F T A missense Het possibly damaging 0.951 phenotype 11/11/2013
12 84343 APN Duox1 0.000 IGL01444 G1 2 122340090 L1197P T C missense Het probably damaging 0.980 phenotype 11/11/2013
13 84376 APN Eps8l2 0.000 IGL01444 G1 7 141361375 T C Het phenotype 11/11/2013
14 84340 APN Exoc3 0.968 IGL01444 G1 13 74206935 K49R T C missense Het probably damaging 1.000 phenotype 11/11/2013
15 84349 APN Exoc8 0.859 IGL01444 G1 8 124895841 T596S T A missense Het possibly damaging 0.842 phenotype 11/11/2013
16 84355 APN F13a1 0.000 IGL01444 G1 13 36918577 G391R C T missense Het probably null 1.000 phenotype 11/11/2013
17 84371 APN Fam35a 0.174 IGL01444 G1 14 34237557 V823F C A missense Het probably damaging 1.000 11/11/2013
18 84365 APN Fat3 0.457 IGL01444 G1 9 15998848 S1953T A T missense Het probably damaging 0.997 phenotype 11/11/2013
19 84366 APN Gls2 0.266 IGL01444 G1 10 128201347 N252K C A missense Het probably damaging 0.999 phenotype 11/11/2013
20 84345 APN Gm5346 0.083 IGL01444 G1 8 43626433 D251E A T missense Het probably benign 0.058 11/11/2013
21 84373 APN Haus2 0.895 IGL01444 G1 2 120615942 R115K G A missense Het probably benign 0.002 phenotype 11/11/2013
22 84369 APN Ift122 1.000 IGL01444 G1 6 115884379 K262E A G missense Het probably benign 0.083 phenotype 11/11/2013
23 84358 APN Islr2 1.000 IGL01444 G1 9 58198378 C533Y C T missense Het probably damaging 1.000 phenotype 11/11/2013
24 84367 APN Lrp2 1.000 IGL01444 G1 2 69443716 F3997I A T missense Het possibly damaging 0.936 phenotype 11/11/2013
25 84357 APN Nt5c1a 0.199 IGL01444 G1 4 123216169 R354W C T missense Het probably damaging 0.997 phenotype 11/11/2013
26 84341 APN Olfr776 0.038 IGL01444 G1 10 129261335 C125S T A missense Het probably damaging 1.000 phenotype 11/11/2013
27 84364 APN Pcolce 0.186 IGL01444 G1 5 137607476 S200R A T missense Het probably damaging 0.980 phenotype 11/11/2013
28 84346 APN Plec 0.870 IGL01444 G1 15 76179297 V2213A A G missense Het possibly damaging 0.455 phenotype 11/11/2013
29 84350 APN Prmt3 0.621 IGL01444 G1 7 49780372 D74E T A missense Het probably benign 0.001 phenotype 11/11/2013
30 84372 APN Ptk7 1.000 IGL01444 G1 17 46565387 F1046S A G missense Het probably damaging 1.000 phenotype 11/11/2013
31 84342 APN Ranbp2 1.000 IGL01444 G1 10 58475300 Y887H T C missense Het possibly damaging 0.790 phenotype 11/11/2013
32 84360 APN Sez6l2 0.000 IGL01444 G1 7 126961883 E447K G A missense Het possibly damaging 0.912 phenotype 11/11/2013
33 84374 APN Snrnp70 0.955 IGL01444 G1 7 45387236 C T unclassified 154 bp Het probably null phenotype 11/11/2013
34 84368 APN Timm10 0.978 IGL01444 G1 2 84829864 V49E T A missense Het probably damaging 1.000 phenotype 11/11/2013
35 84377 APN Tox2 0.295 IGL01444 G1 2 163225466 T C utr 5 prime Het probably benign 11/11/2013
36 84363 APN Usp20 0.241 IGL01444 G1 2 30998789 M1K T A start codon destroyed Het probably null 0.999 phenotype 11/11/2013
37 84370 APN Usp32 0.805 IGL01444 G1 11 85059164 L223V A C missense Het probably damaging 0.966 11/11/2013
38 84352 APN Zeb1 0.774 IGL01444 G1 18 5767906 A806S G T missense Het probably damaging 0.997 phenotype 11/11/2013
39 84359 APN Zeb1 0.774 IGL01444 G1 18 5767138 S550P T C missense Het probably benign 0.000 0.072 phenotype 11/11/2013
[records 1 to 39 of 39]