Incidental Mutations

22 incidental mutations are currently displayed, and affect 22 genes.
3 are Possibly Damaging.
6 are Probably Damaging.
10 are Probably Benign.
3 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 22 of 22] 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 28857 APN Arrdc3 0.380 IGL00933 G1 13 80891055 T A splice site Het probably benign phenotype 04/17/2013
2 27441 APN Brca2 1.000 IGL00933 G1 5 150542404 S1878G A G missense Het probably benign 0.035 phenotype 04/17/2013
3 26657 APN Cpa6 0.132 IGL00933 G1 1 10337370 H314R T C missense Het probably benign 0.026 phenotype 04/17/2013
4 29513 APN Ehbp1l1 1.000 IGL00933 G1 19 5717933 I1114T A G missense Het probably benign 0.332 phenotype 04/17/2013
5 29514 APN Eml3 0.812 IGL00933 G1 19 8936398 W73* G A nonsense Het probably null 04/17/2013
6 26658 APN Fmo4 0.081 IGL00933 G1 1 162794023 Q540K G T missense Het probably benign 0.001 phenotype 04/17/2013
7 28539 APN Fstl4 0.117 IGL00933 G1 11 53186761 G782R G A missense Het possibly damaging 0.800 phenotype 04/17/2013
8 28179 APN Itga11 0.135 IGL00933 G1 9 62769305 I925T T C missense Het possibly damaging 0.580 phenotype 04/17/2013
9 28743 APN Itsn2 0.000 IGL00933 G1 12 4707540 F1411C T G missense Het probably damaging 1.000 phenotype 04/17/2013
10 27107 APN Lmna 1.000 IGL00933 G1 3 88482549 C590S A T missense Het possibly damaging 0.725 phenotype 04/17/2013
11 27106 APN Magi3 0.411 IGL00933 G1 3 104015847 Y1185H A G missense Het probably benign 0.000 04/17/2013
12 29151 APN Marf1 0.147 IGL00933 G1 16 14117357 Y1516H A G missense Het probably damaging 1.000 phenotype 04/17/2013
13 28856 APN Mast4 0.239 IGL00933 G1 13 102735366 D2306G T C missense Het probably damaging 0.973 phenotype 04/17/2013
14 26915 APN Ncoa6 1.000 IGL00933 G1 2 155415397 V742A A G missense Het probably damaging 0.997 phenotype 04/17/2013
15 26916 APN Nol4l 0.917 IGL00933 G1 2 153477936 F175S A G missense Het probably damaging 0.958 04/17/2013
16 28344 APN Olfr826 0.076 IGL00933 G1 10 130180214 M222K A T missense Het probably benign 0.056 phenotype 04/17/2013
17 27260 APN Orm2 0.049 IGL00933 G1 4 63364152 T C splice site Het probably benign 04/17/2013
18 28180 APN Pik3cb 0.960 IGL00933 G1 9 99101286 T90S T A missense Het probably damaging 0.962 phenotype 04/17/2013
19 27829 APN Plekhg2 0.482 IGL00933 G1 7 28360689 P1072S G A missense Het probably benign 0.008 04/17/2013
20 28953 APN Rgr 0.117 IGL00933 G1 14 37038918 Y227* A T nonsense Het probably null phenotype 04/17/2013
21 27636 APN Snd1 0.922 IGL00933 G1 6 28512986 T C critical splice donor site 2 bp Het probably null phenotype 04/17/2013
22 28181 APN Zfp560 0.000 IGL00933 G1 9 20348808 S253P A G missense Het probably benign 0.002 04/17/2013
[records 1 to 22 of 22]