Incidental Mutations

21 incidental mutations are currently displayed, and affect 21 genes.
3 are Possibly Damaging.
7 are Probably Damaging.
10 are Probably Benign.
1 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 21 of 21] 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 27568 APN 2810474O19Rik 0.000 IGL00767 G1 6 149334750 T C utr 3 prime Het probably benign 04/17/2013
2 8970 APN Anpep 0.000 IGL00767 G1 7 79840890 S293A A C missense Het probably benign 0.001 phenotype 12/06/2012
3 10138 APN Dgkh 0.000 IGL00767 G1 14 78587261 T A splice site Het probably benign phenotype 12/06/2012
4 10190 APN Dlg5 1.000 IGL00767 G1 14 24165285 T657S T A missense Het probably damaging 0.995 phenotype 12/06/2012
5 8444 APN Hpf1 0.000 IGL00767 G1 8 60896802 I155V A G missense Het probably benign 0.000 12/06/2012
6 11436 APN Il12rb2 0.000 IGL00767 G1 6 67303562 I554V T C missense Het possibly damaging 0.628 phenotype 12/06/2012
7 10668 APN Mindy2 0.150 IGL00767 G1 9 70634003 A G critical splice donor site 2 bp Het probably null 12/06/2012
8 12765 APN Nostrin 0.273 IGL00767 G1 2 69175775 T268A A G missense Het probably benign 0.004 phenotype 12/06/2012
9 12775 APN Npy6r 0.000 IGL00767 G1 18 44276318 T269A A G missense Het probably benign 0.008 phenotype 12/06/2012
10 12793 APN Nt5dc3 0.000 IGL00767 G1 10 86820273 T A splice site Het probably benign 12/06/2012
11 12880 APN Osgin2 0.348 IGL00767 G1 4 16006377 H106Y G A missense Het probably damaging 0.998 12/06/2012
12 12967 APN Pdlim3 0.484 IGL00767 G1 8 45896790 G46R G A missense Het probably damaging 1.000 phenotype 12/06/2012
13 12968 APN Pdpk1 1.000 IGL00767 G1 17 24106861 K147N T G missense Het possibly damaging 0.869 phenotype 12/06/2012
14 12981 APN Pfkfb3 1.000 IGL00767 G1 2 11488754 D137G T C missense Het probably damaging 1.000 phenotype 12/06/2012
15 13087 APN Polg 1.000 IGL00767 G1 7 79451925 P1048S G A missense Het probably damaging 1.000 phenotype 12/06/2012
16 13206 APN Ptcd3 1.000 IGL00767 G1 6 71903448 I97K A T missense Het probably damaging 0.965 12/06/2012
17 26573 APN Serpinb10 0.000 IGL00767 G1 1 107536077 V30F G T missense Het possibly damaging 0.930 04/17/2013
18 14268 APN Stk17b 0.129 IGL00767 G1 1 53764023 A G splice site Het probably benign phenotype 12/06/2012
19 14471 APN Tll1 1.000 IGL00767 G1 8 64071321 R444C G A missense Het probably damaging 1.000 phenotype 12/06/2012
20 14621 APN Ttbk2 1.000 IGL00767 G1 2 120745745 V848A A G missense Het probably benign 0.000 phenotype 12/06/2012
21 10386 APN Ttn 1.000 IGL00767 G1 2 76885673 T C intron Het probably benign phenotype 12/06/2012
[records 1 to 21 of 21]